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Journal of Medicine and Pharmacy","Tạp chí Y Dược học Cần Thơ",{"EN":487,"VI":488},"\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">04\u002F10\u002F2015 Ministry of Information and Communications allowed Can Tho journal of medicine and pharmacy to operate (102 \u002FGP-BTTTT)\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">07\u002F16\u002F2015 Can Tho journal of medicine and pharmacy is internationally recognized: ISSN 2354-1210\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">In 2016, The journal has been included in the list of medical science journals by The State Council for professorship which is awarded a work score of 0-0.5 points for a published article.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Can Tho Journal of Medicine and Pharmacy welcome original works that haven’t been submitted or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":490},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[494],{"id":495,"createTime":28,"updateTime":28,"relativeEntities":496,"slug":28,"properties":497,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":507,"parentIds":508,"statistic":28},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":498,"address":501,"country":504,"abbreviation":505},{"EN":499,"VI":500},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":502,"VI":503},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":15},{"VOID":506},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":32,"impactFactorByYear":512,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":514,"totalPublicationByYear":515,"totalCitation":520,"totalCitationByYear":521,"totalCitationPerPublication":108,"totalCitationPerPublicationByYear":523,"hindexLast5Year":45,"hindex":45},{"2022":513,"2023":111,"2024":106},0.01,1556,{"2020":47,"2021":516,"2022":517,"2023":518,"2024":519,"2025":122},57,306,801,358,161,{"2021":146,"2022":280,"2023":522},99,{"2021":524,"2022":318,"2023":104},0.23,{"impactFactor":28,"impactFactorByYear":28,"i10Index":123,"i10IndexLast5Year":123,"totalPublication":526,"totalPublicationByYear":527,"totalCitation":526,"totalCitationByYear":528,"totalCitationPerPublication":40,"totalCitationPerPublicationByYear":531,"hindexLast5Year":49,"hindex":49},476,{"0":205,"2019":123,"2021":139,"2022":459,"2023":451,"2024":357,"2025":49,"2026":48},{"2021":42,"2022":123,"2023":161,"2024":529,"2025":360,"2026":530},136,83,{"2021":105,"2022":513,"2023":532,"2024":127,"2025":533,"2026":534},0.62,25.43,13.83,{"id":536,"createTime":537,"updateTime":382,"relativeEntities":538,"slug":539,"properties":540,"entityType":25,"verifyStatus":26,"verifyTime":28,"verifyNote":28,"languages":552,"translateLanguages":28,"viewCount":133,"subjectFields":553,"manageAffiliations":554,"indexDatabases":555,"url":556,"thumbnailPath":557,"statistic":558,"gsStatistic":594,"type":55,"analyzePriority":28},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":541,"issn":542,"title":544,"introduce":547,"gsId":550},{"VOID":15},{"VOID":543},"25252445",{"EN":545,"VI":546},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":548,"VI":549},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. 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studies have shown that short-wavelength blue visible light induces retinal injury and may be a risk factor for age related macular degeneration. A2E is a blue light absorbing retinal chromophore that accumulates with age. Our previous in vitro studies have determined that, although A2E itself has a low phototoxic efficiency, the oxidation products of A2E that are formed in the presence of visible light can contribute to observed retinal pigment epithelial photodamage. The purpose of this study was to investigate the effects of blue light on retinal phototoxicity and its relationship to A2E, oxidized A2E and its isomers. Sprague-Dawley albino rats were dark adapted for 24 h. Control rats remained in the dark while experimental rats were exposed to blue light (λ = 450 nm, 3.1 mW cm−2) for 6 h. Isolated retinas were homogenized in Folch extraction mixture and then in chloroform. The dried extracts were reconstituted and divided for determination of organic soluble compound. Esters of fatty acids were determined with GC-MS, A2E and other chromophores using HPLC, and A2E oxidation products with LC-MS. Exposure of rat eyes to blue light did not significantly change the fatty acid composition of the retina. The A2E concentration (normalized to fatty acid content) in blue light exposed animals was found to be lower than the A2E concentration in control rats. The concentrations of all-trans-retinal-ethanolamine adduct and iso-A2E a precursor and an isomer of A2E respectively, were also lower after blue-light exposure than in the retinas of rats housed in the dark. On the other hand, the amount of oxidized forms of A2E was higher in the animals exposed to blue light. We conclude that in the rat eye, blue-light exposure promotes oxidation of A2E and iso-A2E to the products that are toxic to retinal tissue. Although high concentrations of A2E may be cytotoxic to the retina, the phototoxicity associated with blue light damage to the retina is in part a result of the formation of toxic A2E oxides. 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Sci., 2000, 41, 2303–2308.",{"VOID":1011},"10.1039\u002Fc0pp00133c","PUBLICATION","Auto Verify","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1039\u002Fc0pp00133c",[1016,1032,1047,1060,1075,1088,1101],{"id":1017,"sortIndex":32,"researcher":28,"roles":1018,"affiliations":1020,"properties":1029,"displayName":1031,"givenName":28,"familyName":28},"db10f9bf-9a58-4e5b-a132-ff4247ccc822",[1019],"AUTHOR",[1021],{"id":1022,"sortIndex":32,"affiliation":1023,"properties":28},"e19c38e4-960a-4d25-a89a-14b929b3d0c8",{"id":1022,"createTime":28,"updateTime":28,"relativeEntities":1024,"slug":28,"properties":1025,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1028,"statistic":28},[],{"title":1026},{"VI":1027},"Laboratory of Pharmacology, National Institute of Environmental Health Sciences, Research Triangle Park, USA",[],{"title":1030},{"VI":1031},"A. R. 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Collier",{"id":1048,"sortIndex":123,"researcher":28,"roles":1049,"affiliations":1050,"properties":1057,"displayName":1059,"givenName":28,"familyName":28},"1eef50c7-9201-4cdc-beda-269380688feb",[1019],[1051],{"id":1037,"sortIndex":32,"affiliation":1052,"properties":28},{"id":1037,"createTime":28,"updateTime":28,"relativeEntities":1053,"slug":28,"properties":1054,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1056,"statistic":28},[],{"title":1055},{"VI":1042},[],{"title":1058},{"VI":1059},"E. Martin",{"id":1061,"sortIndex":42,"researcher":28,"roles":1062,"affiliations":1063,"properties":1072,"displayName":1074,"givenName":28,"familyName":28},"8ee3e484-fe50-4da7-9934-04d7de9ee171",[1019],[1064],{"id":1065,"sortIndex":32,"affiliation":1066,"properties":28},"42ee25db-3b44-4789-a030-fc124441fd2f",{"id":1065,"createTime":28,"updateTime":28,"relativeEntities":1067,"slug":28,"properties":1068,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1071,"statistic":28},[],{"title":1069},{"VI":1070},"Laboratory of Structural Biology, National Institute of Environmental Health Sciences, Research Triangle Park, USA",[],{"title":1073},{"VI":1074},"F. B. 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Chignell",{"id":1102,"sortIndex":48,"researcher":28,"roles":1103,"affiliations":1104,"properties":1113,"displayName":1115,"givenName":28,"familyName":28},"a4750a5a-f50e-47aa-9c5f-60dd84dcf6f9",[1019],[1105],{"id":1106,"sortIndex":32,"affiliation":1107,"properties":28},"64daac88-529d-41ff-80dc-41d72c0c080d",{"id":1106,"createTime":28,"updateTime":28,"relativeEntities":1108,"slug":28,"properties":1109,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1112,"statistic":28},[],{"title":1110},{"VI":1111},"Department of Natural Sciences, Fordham University, New York, USA",[],{"title":1114},{"VI":1115},"J. E. 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Comparative spectroscopic (absorption and fluorescence) and kinetic investigations of the stimulated photochromic and solvatochromic behavior were carried out in different media. SP embedded in a rigid thin film of poly(methylmethacrylate) might be exploited profitably as an optical sensor for the identification of a solvent’s nature. Furthermore, thermodynamic parameters, in particular, Gibbs’ free energy change (ΔG°), were derived using density functional theory quantum chemical calculations with the SP and merocyanine coloured form. The model used was the B3LYP\u002F6-31G(d,p)\u002F SCRF = (SMD, solvent) and its time-dependent extension procedure was used to quantitatively explain the structural isomerization in response to a variety of stimuli, such as light, solvent nature, lanthanide(III) ions, and macromolecular support. These findings might be useful for the design of photoswitchable and energy transfer materials and their related fields.",{"EN":1178},"Lanthanide complexes of spiropyran photoswitch and sensor: spectroscopic investigations and computational modelling",{"VOID":1180},"A. Mustafa, Chem. Rev., 1948, 43, 509–523.\nR. Klajn, Chem. Soc. Rev., 2014, 43, 148–184 and references cited therein.\nS. Aiken, R. J. L. Edgar, C. D. Gabbutt, B. Mark Heron and P. A. Hobson, Dyes Pigm., 2018, 149, 92–121\nPi.-X. Wang, Fu.-Q. Bai, Z.-X. Zhang, Y.-P. Wang, J. Wang and H.-X. Zhang, Org. Electron., 2017, 45, 33–41.\nY. Sheng, J. Leszczynski, A. A. Garcia, R. Rosario, D. Gust and J. Springer, J. Phys. Chem. B, 2004, 108, 16233–16243.\nS. Yagi, S. Nakamura, D. Watanabe and H. Nakazumi, Dyes Pigm., 2009, 80, 98–105.\nA. Samoladas, D. Bikiaris, T. Zorba, K. M. Paraskevopoulos and A. Jannakoudakis, Dyes Pigm., 2008, 76, 386–393.\nJ. Piard, J. Chem. Educ., 2014, 91, 2105–2111 and references cited therein.\nH. S. 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Acta, Part A, 2012, 86, 600–604.\nF. Nourmohammadian and A. A. Abdi, Spectrochim. Acta, Part A, 2016, 153, 53–62.\nD. Y. Hur, T. J. Park and E. Ju. Shin, Spectrochim. Acta, Part A, 2014, 114, 541–547.\nA. O. Bulanov, L. D. Popov, I. N. Shcherbakov, V. A. Kogan, V. A. Barachevsky, V. V. Lukov, S. N. Borisenko and Yu. N. Tkachenko, Spectrochim. Acta, Part A, 2008, 71, 1146–1152.\nPhotochromism, in Techniques in Chemistry, ed. R.C. Bertelson and G.H. Brown, Wiley-Interscience, New York, NY, USA, 1971, vol. 3, pp. 45–294.\nS. V. Paramonov, V. Vladimir Lokshin and O. A. Fedorova, J. Photochem. Photobiol., C, 2011, 12, 209–236.\nJ. Malkin, A. S. Dvornikov, K. D. Straub and P. M. Rentzepis, Res. Chem. Intermed., 1993, 19, 159–167.\nR. F. Khairutdinov and J. K. Hurst, Langmuir, 2001, 17, 6881–6886.\nA. V. Chernyshev, N. A. Voloshin, A. V. Metelitsa, V. V. Tkachev, S. M. Aldoshin, E. Solov’eva, I. A. Rostovtseva and V. I. Minkin, J. Photochem. Photobiol., A, 2013, 265, 1–9.\nM. S. A. Abdel-Mottaleb and S. N. Ali, Int. J. Photoenergy, 2016, 2016, 1–8.\nJ. Hobley, V. Malatesta, R. Millini, L. Montanari and W. O. Neil Parker Jr., Phys. Chem. Chem. Phys., 1999, 1, 3259–3267.\nJ. Ho and M. Z. Ertem, Calculating Free Energy Changes in Continuum Solvation Models, J. Phys. Chem. B, 2016, 120, 1319–1329.\nR. F. Ribeiro, A. V. Marenich, C. J. Cramer and D. G. Truhlar, J. Phys. Chem. B, 2011, 115, 14556–14562.\nA. V. Marenich, C. J. Cramer and D. G. Truhlar, J. Phys. Chem. B, 2009, 113 (18), 6378–6396.\nJ. H. Jensen, Molecular Modelling Basics, CRC Press, Taylor and Francis, NY, 2010, ch. 2, p. 72.\nM. S. Attia, M. M. H. Khalil, M. S. A. Abdel-Mottaleb, M. B. Lukyanova, Yu. A. Alekseenko and B. Lukyanov, Int. J. Photoenergy, 2006, 2006, 1–9.\nA. Fissi, O. Pieroni, N. Angelini and F. Lenci, Macromolecules, 1999, 32, 7116–7121.\nM. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, T. Keith, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, O. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski and D. J. Fox, GAUSSIAN 16, Revision A.03, Gaussian Inc., Wallingford, Conn, USA, 2015.\nY. Shao, L. F. Molnar, Y. Jung, J. Kussmann, C. Ochsenfeld, S. T. Brown, A. T. B. Gilbert, L. V. 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W. Taft, J. Org. Chem., 1983, 48, 2877–2887.\nJ. H. Jensen, Molecular Modeling Basics, CRC Press, Taylor and Francis, NY, 2010, ch. 3, p. 95.\nE. Bakeir, G. M. Attia, M. Lukyanova, B. Lukyanov and M. S. A. Abdel-Mottaleb, Res. Lett. Phys. Chem., 2008, 2008, 314898.\nR. G. Parr and W. Yang, J. Am. Chem. Soc., 1984, 106, 4049–4050.\nC.-Y. Lee, C.-H. Hu, S.-L. Cheng, C.-C. Chu and V. K. S. Hsiao, J. Lumin., 2015, 159, 246–250.",{"VOID":1182},"10.1039\u002Fc7pp00226b","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1039\u002Fc7pp00226b",[1185,1200,1215,1228,1241],{"id":1186,"sortIndex":32,"researcher":28,"roles":1187,"affiliations":1188,"properties":1197,"displayName":1199,"givenName":28,"familyName":28},"df12adb9-01b6-4379-bdec-fdde2ea889ea",[1019],[1189],{"id":1190,"sortIndex":32,"affiliation":1191,"properties":28},"6b1fcd56-6fae-4b50-bbc2-9a1c91e346a4",{"id":1190,"createTime":28,"updateTime":28,"relativeEntities":1192,"slug":28,"properties":1193,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1196,"statistic":28},[],{"title":1194},{"VI":1195},"Nano\u002FPhotochemistry, Solar Chemistry and Computational Chemistry Labs, Department of Chemistry, Faculty of Science, Ain Shams University, Cairo, Egypt",[],{"title":1198},{"VI":1199},"M. S. A. Abdel-Mottaleb",{"id":1201,"sortIndex":40,"researcher":28,"roles":1202,"affiliations":1203,"properties":1212,"displayName":1214,"givenName":28,"familyName":28},"d1ac008c-a6b8-407f-8eb1-21c73ab006fe",[1019],[1204],{"id":1205,"sortIndex":32,"affiliation":1206,"properties":28},"d3cef475-be59-46d5-8dbe-12d8c57129f5",{"id":1205,"createTime":28,"updateTime":28,"relativeEntities":1207,"slug":28,"properties":1208,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1211,"statistic":28},[],{"title":1209},{"VI":1210},"Department of Chemistry, Faculty of Education, Ain Shams University, Heliopolis, Egypt",[],{"title":1213},{"VI":1214},"M. 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This proxy may not only provide information on variation of stratospheric ozone and solar UV in the period preceding and during the Antarctic ozone hole (1974–present day), but also on the development and variation of the stratospheric ozone layer and solar surface UV during the evolution of life on Earth. Sporopollenin and cutin are highly resistant biopolymers, preserving well in the geological record and contain the phenolic acids p-coumaric (pCA) and ferulic acid (FA). pCA and FA represent a good perspective for a plant-based proxy for past surface UV radiation since they are induced by solar UV-B via the phenylpropanoid pathway (PPP). UV-B absorption by these monomers in the wall of pollen and spores and in cuticles may prevent damage to the cellular metabolism. Increased pCAand FA in pollen of Vicia faba exposed to enhanced UV-B was found in greenhouse experiments. Further correlative evidence comes from UV-absorbing compounds in spores from 1960–2000 comparing exposure of land plants (Lycopodium species) to solar UV before and during ozone depletion and comparing plants from Antarctica (severe ozone depletion), Arctic, and other latitudes with less or negligible ozone depletion. Wood-derived compounds guaiacyl (G), syringyl (S), and p-hydroxyphenyl (P) are produced via the PPP. The proportions of P, G, and S in the lignin differ between various plant groups (e.g. dicotyledons\u002Fmonocotyledons, gymnosperms\u002F angiosperms). It is hypothesized that this lignin composition and derived physiological and physical properties of lignin (such as tree-ring wood density) has potential as a proxy for palaeo-UV climate. However validation by exposure of trees to enhanced UV is lacking. pCAand FA also form part of cutin polymers and are found in extant and fossil Ginkgo leaf cuticles as shown by thermally-assisted hydrolysis and methylation (THM)-pyrolysis-GC-MS. Potentially, the time scale for reconstruction of ozone column thickness and UV-B based on the UAC UV proxy may be decadal, centennial, millennial and possibly billenial. For further development of the UACs and pCA and FA-based UV proxy, it is necessary to obtain the UV dose–response (content of UACs, pCA and FA in sporopollenin and cutin) relationships for validation, based on outdoor UV radiation manipulations experiments with plants, and comparative analysis of stored plants (herbaria) or fossil material of the same or related plant species.",{"EN":1314},"UV-B absorbing compounds in present-day and fossil pollen, spores, cuticles, seed coats and wood: evaluation of a proxy for solar UV radiation",{"VOID":1316},"V. E. Fioletov, G. E. 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Newsham, Metabolic recovery of the Antarctic liverwort Cephaloziella varians during spring snowmelt Polar Biol. 2007 30 1115–1122.",{"VOID":1318},"10.1039\u002Fb904515e","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1039\u002Fb904515e",[1321,1336,1349,1362],{"id":1322,"sortIndex":32,"researcher":28,"roles":1323,"affiliations":1324,"properties":1333,"displayName":1335,"givenName":28,"familyName":28},"abc07749-fb57-4c27-8338-5781ad0aaba9",[1019],[1325],{"id":1326,"sortIndex":32,"affiliation":1327,"properties":28},"5052147e-5ab6-438a-a7d6-352591c21b11",{"id":1326,"createTime":28,"updateTime":28,"relativeEntities":1328,"slug":28,"properties":1329,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1332,"statistic":28},[],{"title":1330},{"VI":1331},"Department Systems Ecology, Institute of Ecological Science, Faculty of Earth and Life Sciences, Vrije Universiteit, Amsterdam, The Netherlands",[],{"title":1334},{"VI":1335},"J. Rozema",{"id":1337,"sortIndex":40,"researcher":28,"roles":1338,"affiliations":1339,"properties":1346,"displayName":1348,"givenName":28,"familyName":28},"a49f4b95-cb78-4530-8f99-a6d2e499bc7e",[1019],[1340],{"id":1326,"sortIndex":32,"affiliation":1341,"properties":28},{"id":1326,"createTime":28,"updateTime":28,"relativeEntities":1342,"slug":28,"properties":1343,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1345,"statistic":28},[],{"title":1344},{"VI":1331},[],{"title":1347},{"VI":1348},"P. Blokker",{"id":1350,"sortIndex":123,"researcher":28,"roles":1351,"affiliations":1352,"properties":1359,"displayName":1361,"givenName":28,"familyName":28},"d2a9c1ae-6dc6-44e3-92ed-3b1329937ef8",[1019],[1353],{"id":1326,"sortIndex":32,"affiliation":1354,"properties":28},{"id":1326,"createTime":28,"updateTime":28,"relativeEntities":1355,"slug":28,"properties":1356,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1358,"statistic":28},[],{"title":1357},{"VI":1331},[],{"title":1360},{"VI":1361},"M. A. Mayoral Fuertes",{"id":1363,"sortIndex":42,"researcher":28,"roles":1364,"affiliations":1365,"properties":1372,"displayName":1374,"givenName":28,"familyName":28},"7fdd42f0-9ee1-4551-af3b-3124541f2060",[1019],[1366],{"id":1326,"sortIndex":32,"affiliation":1367,"properties":28},{"id":1326,"createTime":28,"updateTime":28,"relativeEntities":1368,"slug":28,"properties":1369,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1371,"statistic":28},[],{"title":1370},{"VI":1331},[],{"title":1373},{"VI":1374},"R. 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A CL resonance energy transfer (CRET) occurs between CdS QDs as a donor and Rh B as an energy acceptor. Based on the strong specific quenching effect of meropenem on the CL intensity, a novel chemosensor for meropenem sensing was developed. Under the optimized conditions, the quenched CL emission intensity was proportional to the concentration of meropenem in the range of 0.002-10.0 mg L−1 with a detection limit (3s) of 0.8 µg L−1 Moreover, the feasibility of the induced CL system was studied via the meropenem determination in environmental water samples.",{"EN":1435},"A novel and sensitive chemosensor based on a KMnO4–rhodamine B–CdS quantum dot chemiluminescence system for meropenem detection",{"VOID":1437},"J. L. Blumer, Int. J. Antimicrob. Agents, 1997, 8, 73–92.\nM. Carlier V. Stove J. A. Roberts E. Van De Velde J. J. De Waele and A. G. Verstraete, Int. J. Antimicrob. Agents, 2012, 40, 416–422.\nR. Denooz and C. Charlier, J. Chromatogr. B: Biomed. Appl., 2008, 864, 161–167.\nA. S. L. Mendez M. Steppe and E. E. S. Schapoval, J. Pharm. Biomed. Anal., 2003, 33, 947–954.\nL. Venkateswara Rao G. Ramu M. Sravan Kumar and C. Rambabu, Int. J. PharmTech Res., 2012, 4, 957–962.\nE. Dailly R. Bouquié G. Deslandes P. Jolliet and R. Le Floch, J. Chromatogr. B: Biomed. Appl., 2011, 879, 1137–1142.\nB. C. McWhinney S. C. Wallis T. Hillister J. A. Roberts J. Lipman and J. P. J. Ungerer, J. Chromatogr. B: Biomed. Appl., 2010, 878, 2039–2043.\nY. Ozkan L. Kuukguzel S. A. Ozkan and H. Y. Aboul-Enein, Biomed. Chromatogr., 2001, 15, 263–266.\nM. Ehrlich F. D. Daschner and K. Kümmerer, J. Chromatogr. B: Biomed. Appl., 2001, 751, 357–363.\nT. Ohmori A. Suzuki T. Niwa H. Ushikoshi K. Shirai S. Yoshida S. Ogura and Y. Itoh, J. Chromatogr. B: Biomed. Appl., 2011, 879, 1038–1042.\nD. Singh and G. Maheshwari, Med. Chem. Res., 2013, 22, 5680–5684.\nS. R. Narala and K. Saraswathi, Int. J. ChemTech Res., 2011, 3, 605–609.\nJ. Cielecka-Piontek M. Paczkowska K. Lewandowska B. Barszcz P. Zalewski and P. Garbacki, Chem. Cent. J., 2013, 7, 7–98.\nY. Mrestani R. Neubert and F. Nagel, J. Pharm. Biomed. Anal., 1999, 20, 899–903.\nT. Kitahashi and I. Furuta, J. Chromatogr. Sci., 2005, 43, 430–433.\nY.-W. Chou Y.-H. Yang J.-H. Chen C.-C. Kuo and S.-H. Chen, J. Chromatogr. B: Biomed. Appl., 2007, 856, 294–301.\nA. S. L. Mendez V. Weisheimer T. P. Oppe M. Steppe and E. E. S. Schapoval, J. Pharm. Biomed. Anal., 2005, 37, 649–653.\nM. A. Al-Meshal M. A. Ramadan K. M. Lotfi and A. M. Shibl, J. Clin. Pharm. Ther., 1995, 20, 159–163.\nA. R. Khataee M. Fathinia A. Hasanzadeh M. Iranifam and L. Moradkhannejhad, J. Lumin., 2014, 149, 272–279.\nM. Iranifam, TrAC, Trends Anal. Chem., 2014, 59, 156–183.\nM. Iranifam M. Fathinia T. Sadeghi Rad Y. Hanifehpour A. R. Khataee and S. W. Joo, Talanta, 2013, 107, 263–269.\nC. Guo H. Zeng X. Ding D. He J. Li R. Yang and L. Qu, J. Lumin., 2013, 134, 888–892.\nM. Iranifam, TrAC, Trends Anal. Chem., 2013, 51, 51–70.\nB. Liu Y. He C. Duan N. Li and H. Cui, J. Photochem. Photobiol., A, 2011, 217, 62–67.\nJ. Hassanzadeh M. Amjadi J. L. Manzoori and M. H. Sorouraddin, Spectrochim. Acta, Part A, 2013, 107, 296–302.\nJ. Hassanzadeh and M. Amjadi, Luminescence, 2015, 30, 439–443.\nA. Patterson, Phys. Rev., 1939, 56, 978.\nA. Khataee A. Hasanzadeh M. Iranifam and S. W. Joo, Sens. Actuators, B, 2015, 215, 272–282.\nA. Khataee R. Lotfi and A. Hasanzadeh, RSC Adv., 2015, 5, 82645–82653.\nL. Xi W. X. W. Tan C. Boothroyd and Y. M. Lam, Chem. Mater., 2008, 20, 5444–5452.\nZ. B. Yu Y. P. Xie G. Liu G. Q. M. Lu X. L. Ma and H.-M. Cheng, J. Mater. Chem. A, 2013, 1, 2773–2776.\nA. A. Aghuy M. Zakeri M. Moayed and M. Mazinani, Corros. Sci., 2015, 94, 368–376.\nB. Ayoubi-Feiz S. Aber A. Khataee and E. Alipour, Environ. Sci. Pollut. Res., 2014, 21, 8555–8564.\nA. Ghasemi and M. Mousavinia, Ceram. Int., 2014, 40, 2825–2834.\nM. Koneswaran and R. Narayanaswamy, Sens. Actuators, B, 2009, 139, 104–109.\nW. Zhao Y. Fung O. Waisum and M. Cheung, Anal. Sci., 2010, 26, 879–884.\nJ. L. Adcock N. W. Barnett C. J. Barrow and P. S. Francis, Anal. Chim. Acta, 2014, 807, 9–28.\nM. Amjadi J. Hassanzadeh and J. L. Manzoori, Microchim. Acta, 2014, 181, 1851–1856.\nH. Chen R. Li L. Lin G. Guo and J.-M. Lin, Talanta, 2010, 81, 1688–1696.\nZ. Wang J. Li B. Liu J. Hu X. Yao and J. Li, J. Phys. Chem. B, 2005, 109, 23304–23311.\nH. Chen L. Lin H. Li and J.-M. Lin, Coord. Chem. Rev., 2014, 263, 86–100.\nA. Sproul and M. Green, J. Appl. Phys., 1991, 70, 846–854.\nJ. L. Adcock N. W. Barnett C. J. Barrow and P. S. Francis, Anal. Chim. Acta, 2014, 807, 9–28.\nThe United states Pharmacopeia and The National Formulary, The United States Pharmacopeial Convention, Rockville, 34th edn, 2011, pp. 3425-3428",{"VOID":1439},"10.1039\u002Fc6pp00320f","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1039\u002Fc6pp00320f",[1442,1466,1479],{"id":1443,"sortIndex":32,"researcher":28,"roles":1444,"affiliations":1445,"properties":1463,"displayName":1465,"givenName":28,"familyName":28},"87b90079-0d83-4ab0-bcf8-1b8c8236029b",[1019],[1446,1454],{"id":1447,"sortIndex":32,"affiliation":1448,"properties":28},"613cc29c-1c94-47e3-aea0-01a29d8d371f",{"id":1447,"createTime":28,"updateTime":28,"relativeEntities":1449,"slug":28,"properties":1450,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1453,"statistic":28},[],{"title":1451},{"VI":1452},"Research Laboratory of Advanced Water and Wastewater Treatment Processes, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran",[],{"id":1455,"sortIndex":40,"affiliation":1456,"properties":1462},"06cc23cb-ddf6-4e41-a4c1-733a7e4557e5",{"id":1455,"createTime":28,"updateTime":28,"relativeEntities":1457,"slug":28,"properties":1458,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1461,"statistic":28},[],{"title":1459},{"VI":1460},"Department of Materials Science and Nanotechnology, Near East University, Mersin 10, Turkey",[],{},{"title":1464},{"VI":1465},"Alireza Khataee",{"id":1467,"sortIndex":40,"researcher":28,"roles":1468,"affiliations":1469,"properties":1476,"displayName":1478,"givenName":28,"familyName":28},"51426c23-ccf6-45bd-b14a-27fec21210f2",[1019],[1470],{"id":1447,"sortIndex":32,"affiliation":1471,"properties":28},{"id":1447,"createTime":28,"updateTime":28,"relativeEntities":1472,"slug":28,"properties":1473,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1475,"statistic":28},[],{"title":1474},{"VI":1452},[],{"title":1477},{"VI":1478},"Roya Lotfi",{"id":1480,"sortIndex":123,"researcher":28,"roles":1481,"affiliations":1482,"properties":1489,"displayName":1491,"givenName":28,"familyName":28},"0c9fc952-a6a1-41b3-bc40-7263b8f42abd",[1019],[1483],{"id":1447,"sortIndex":32,"affiliation":1484,"properties":28},{"id":1447,"createTime":28,"updateTime":28,"relativeEntities":1485,"slug":28,"properties":1486,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1488,"statistic":28},[],{"title":1487},{"VI":1452},[],{"title":1490},{"VI":1491},"Aliyeh Hasanzadeh",{"url":1440,"publisher":1493,"properties":1534},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1494,"slug":872,"properties":1495,"entityType":25,"verifyStatus":880,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1498,"manageAffiliations":1503,"indexDatabases":1514,"url":28,"thumbnailPath":28,"statistic":1529,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1496,"title":1497},{"VOID":875},{"EN":877},[1499],{"id":883,"createTime":28,"updateTime":28,"relativeEntities":1500,"label":1501,"description":1502,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":886},{},[1504,1509],{"id":890,"createTime":28,"updateTime":28,"relativeEntities":1505,"slug":28,"properties":1506,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1508,"statistic":28},[],{"title":1507},{"EN":894},[896],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":1510,"slug":28,"properties":1511,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1513,"statistic":28},[],{"title":1512},{"EN":902},[896],[1515,1522],{"id":906,"indexDatabase":1516,"url":912,"indexYears":913,"academicFieldIds":1521,"indexDatabaseRanking":916},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":1517,"label":1518,"description":1519,"key":781,"publicationTags":1520,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[915],{"id":918,"indexDatabase":1523,"url":930,"indexYears":28,"academicFieldIds":1528,"indexDatabaseRanking":28},{"id":920,"createTime":28,"updateTime":28,"relativeEntities":1524,"label":1525,"description":1526,"key":927,"publicationTags":1527,"standard":28},[],{"EN":923,"VI":923},{"EN":925,"VI":926},[929,813],[932,933,934],{"impactFactor":32,"impactFactorByYear":1530,"i10Index":940,"i10IndexLast5Year":142,"totalPublication":941,"totalPublicationByYear":1531,"totalCitation":952,"totalCitationByYear":1532,"totalCitationPerPublication":973,"totalCitationPerPublicationByYear":1533,"hindexLast5Year":207,"hindex":207},{"2012":937,"2013":176,"2014":532,"2015":319,"2016":938,"2017":709,"2018":230,"2019":939,"2020":187,"2021":224,"2022":318,"2023":938},{"2002":943,"2003":608,"2004":212,"2005":334,"2006":354,"2007":944,"2008":945,"2009":946,"2010":947,"2011":133,"2012":946,"2013":837,"2014":563,"2015":362,"2016":43,"2017":147,"2018":140,"2019":150,"2020":948,"2021":949,"2022":950,"2023":951,"2024":132},{"2002":954,"2003":955,"2004":956,"2005":957,"2006":958,"2007":959,"2008":960,"2009":961,"2010":350,"2011":962,"2012":963,"2013":964,"2014":965,"2015":966,"2016":967,"2017":968,"2018":969,"2019":970,"2020":971,"2021":972,"2022":155,"2023":129,"2024":40},{"2002":975,"2003":976,"2004":977,"2005":978,"2006":979,"2007":980,"2008":981,"2009":982,"2010":983,"2011":984,"2012":985,"2013":986,"2014":987,"2015":988,"2016":989,"2017":990,"2018":991,"2019":992,"2020":284,"2021":820,"2022":366,"2023":734,"2024":421},{"pages":1535,"volume":1537},{"VOID":1536},"170-177",{"VOID":1538},"16",[916,929],{"id":1541,"createTime":1542,"updateTime":1543,"relativeEntities":1544,"slug":1545,"properties":1546,"entityType":1012,"verifyStatus":26,"verifyTime":1543,"verifyNote":1013,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1555,"fullTextUrl":28,"authors":1556,"publicationType":1116,"publisherRelationship":1609,"citationCount":28,"citationInfo":28,"publishDate":1656,"publishYear":1657,"citationAnalyzeStatus":880,"lastCitationAnalyze":28,"indexDatabases":1658,"openAccess":28,"references":28,"isForceReanalyzing":1167},"007ba2fc-2655-47ca-b24d-f8d7e93de040","2023-12-12T18:43:37.943+00:00","2025-02-22T00:44:02.504+00:00",[],"Milestones-in-the-development-of-photodynamic-therapy-and-fluorescence-diagnosis",{"abstract":1547,"title":1549,"references":1551,"doi":1553},{"EN":1548},"Many reviews on PDT have been published. This field is now so large, and embraces so many subspecialities, from laser technology and optical penetration through diffusing media to a number of medical fields including dermatology, gastroenterology, ophthalmology, blood sterilization and treatment of microbial-viral diseases, that it is impossible to cover all aspects in a single review. Here, we will concentrate on a few basic aspects, all important for the route of development leading PDT to its present state: early work on hematoporphyrin and hematoporphyrin derivative, second and third generation photosensitizers, 5-aminolevulinic acid and its derivatives, oxygen and singlet oxygen, PDT effects on cell organelles, mutagenic potential, the basis for tumour selectivity, cell cooperativity, photochemical internalization, light penetration into tissue and the significance of oxygen depletion, photobleaching of photosensitizers, optimal light sources, effects on the immune system, and, finally, future trends.",{"EN":1550},"Milestones in the development of photodynamic therapy and fluorescence diagnosis",{"VOID":1552},"O. Raab, Über die Wirkung fluoreszierender Stoffe auf Infusorien, Z. Biol., 1900, 39, 524–546.\nR. Ackroyd, C. Kelty, N. Brown, M. Reed, The history of photodetection and photodynamic therapy, Photochem. Photobiol., 2001, 74, 656–669.\nJ. Moan, Q. Peng, An outline of the hundred-year history of PDT, Anticancer Res., 2003, 23, 3591–3600.\nA. F. Taub, Photodynamic therapy in dermatology: history and horizons, J. Drugs Dermatol., 2004, 3, S8–25.\nF. Meyer-Betz, Untersuchung uber die biologische (photodynamische) Wirkung des Hamatoporphyrins und anderer Derivate des Blut- und Gallenfarbstoffs, Dtsch. Arch. Klin. Med., 1913, 112, 476–503.\nF. H. J. Figge, G. S. Weiland, O. J. Manganiello, Cancer detection and therapy. Affinity of neoplastic, embryonic, and traumatized tissues for porphyrins and metalloporphyrins, Proc. Soc. Exp. Biol. Med., 1948, 68, 640–641.\nS. K. Schwartz, K. Absolon, H. Vermund, Some relationships of porphyrins, X-rays and tumours, Univ. Minn. Med. Bull., 1955, 27, 7–8.\nR. L. Lipson, E. J. Baldes, A. M. Olsen, The use of a derivative of hematoporhyrin in tumor detection, J. Natl. Cancer Inst., 1961, 26, 1–11.\nR. Bonnett, M. C. Berenbaum, HPD - a study of its components and their properties, Adv. Exp. Med. 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Capella, A light in multidrug resistance: photodynamic treatment of multidrug-resistant tumors, J. Biomed. Sci., 2003, 10, 361–366.",{"VOID":1554},"10.1039\u002Fb705461k","https:\u002F\u002Flink.springer.com\u002F10.1039\u002Fb705461k",[1557,1572,1587],{"id":1558,"sortIndex":32,"researcher":28,"roles":1559,"affiliations":1560,"properties":1569,"displayName":1571,"givenName":28,"familyName":28},"10763edc-a560-4bdb-a659-ee5009b8f761",[1019],[1561],{"id":1562,"sortIndex":32,"affiliation":1563,"properties":28},"34e83bf9-43ef-4f1e-a099-09f80ac4fe5b",{"id":1562,"createTime":28,"updateTime":28,"relativeEntities":1564,"slug":28,"properties":1565,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1568,"statistic":28},[],{"title":1566},{"VI":1567},"Department of Radiation Biology, Institute for Cancer Research, Rikshospitalet-Radiumhospitalet Medical Center, The Norwegian Radium Hospital, Oslo, Norway",[],{"title":1570},{"VI":1571},"Asta 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we demonstrate the design of multiple fluorophores Coumarin 153 (C153) and Nile Red (NR) encapsulated in semiconducting poly[N-vinylcarbazole] (PVK) polymer nanoparticles (50–70 nm in diameter) by a simple re-precipitation technique, and elucidate their photophysical properties by steady-state and picosecond (ps) time resolved emission spectroscopy. It is interesting to note that multistep cascaded energy transfer occurs from the excited host PVK molecules to NR dye molecules through C153. The energy transfer time constants are found to be 180 ps for PVK→C153, 360 ps for PVK→NR, and 140 ps for the overall energy transfer process from PVK to NR through C153 dye molecules. The multistep energy transfer allows tuning of the wide range emission from 350 nm to 700 nm by changing the relative concentrations of the encapsulated dye molecules. Bright, stable, and white light emission of the dye doped polymer nanoparticles with a quantum yield of 14% is achieved at a particular concentration ratio of the C153:NR dye. The generation of “cool” white emission in suspension and in the solid state film opens up new possibilities to obtain white light OLEDs based on single nanoparticles.",{"EN":1669},"Single and multistep energy transfer processes within doped polymer nanoparticles",{"VOID":1671},"J. L. West and N. J. 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Shinar, On the Mechanism of Conductivity Enhancement in Poly(3,4-Ethylenedioxythiophene):Poly(Styrene Sulfonate) Film through Solvent Treatment, Polymer, 2004, 45, 8443–8450.",{"VOID":1673},"10.1039\u002Fc4pp00086b","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1039\u002Fc4pp00086b",[1676,1691,1706,1719],{"id":1677,"sortIndex":32,"researcher":28,"roles":1678,"affiliations":1679,"properties":1688,"displayName":1690,"givenName":28,"familyName":28},"3c083a52-f76f-4b90-ad89-7e5ab32878c1",[1019],[1680],{"id":1681,"sortIndex":32,"affiliation":1682,"properties":28},"ea2cd797-905e-41ee-be8e-16c6cb2f8e88",{"id":1681,"createTime":28,"updateTime":28,"relativeEntities":1683,"slug":28,"properties":1684,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1687,"statistic":28},[],{"title":1685},{"VI":1686},"Departamento de Química Física, Facultad de Ciencias del Medio Ambiente y Bioquímica e INAMOL, Universidad de Castilla-La Mancha, Toledo, Spain",[],{"title":1689},{"VI":1690},"Cristina Martin",{"id":1692,"sortIndex":40,"researcher":28,"roles":1693,"affiliations":1694,"properties":1703,"displayName":1705,"givenName":28,"familyName":28},"c748896f-dc9f-4d01-9ac3-d1265b2d292d",[1019],[1695],{"id":1696,"sortIndex":32,"affiliation":1697,"properties":28},"88ce2a6a-c994-4d22-a396-c955be721531",{"id":1696,"createTime":28,"updateTime":28,"relativeEntities":1698,"slug":28,"properties":1699,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1702,"statistic":28},[],{"title":1700},{"VI":1701},"Department of Materials Science, Indian Association for the Cultivation of Science, Kolkata, India",[],{"title":1704},{"VI":1705},"Santanu Bhattacharyya",{"id":1707,"sortIndex":123,"researcher":28,"roles":1708,"affiliations":1709,"properties":1716,"displayName":1718,"givenName":28,"familyName":28},"82bb4f22-fe8a-4a4d-b2b7-8dabc1142bea",[1019],[1710],{"id":1696,"sortIndex":32,"affiliation":1711,"properties":28},{"id":1696,"createTime":28,"updateTime":28,"relativeEntities":1712,"slug":28,"properties":1713,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1715,"statistic":28},[],{"title":1714},{"VI":1701},[],{"title":1717},{"VI":1718},"Amitava Patra",{"id":1720,"sortIndex":42,"researcher":28,"roles":1721,"affiliations":1722,"properties":1729,"displayName":1731,"givenName":28,"familyName":28},"bf8ce683-ef22-43fc-903c-493ff45b4ef2",[1019],[1723],{"id":1681,"sortIndex":32,"affiliation":1724,"properties":28},{"id":1681,"createTime":28,"updateTime":28,"relativeEntities":1725,"slug":28,"properties":1726,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1728,"statistic":28},[],{"title":1727},{"VI":1686},[],{"title":1730},{"VI":1731},"Abderrazzak Douhal",{"url":1674,"publisher":1733,"properties":1774},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1734,"slug":872,"properties":1735,"entityType":25,"verifyStatus":880,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1738,"manageAffiliations":1743,"indexDatabases":1754,"url":28,"thumbnailPath":28,"statistic":1769,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1736,"title":1737},{"VOID":875},{"EN":877},[1739],{"id":883,"createTime":28,"updateTime":28,"relativeEntities":1740,"label":1741,"description":1742,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":886},{},[1744,1749],{"id":890,"createTime":28,"updateTime":28,"relativeEntities":1745,"slug":28,"properties":1746,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1748,"statistic":28},[],{"title":1747},{"EN":894},[896],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":1750,"slug":28,"properties":1751,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1753,"statistic":28},[],{"title":1752},{"EN":902},[896],[1755,1762],{"id":906,"indexDatabase":1756,"url":912,"indexYears":913,"academicFieldIds":1761,"indexDatabaseRanking":916},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":1757,"label":1758,"description":1759,"key":781,"publicationTags":1760,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[915],{"id":918,"indexDatabase":1763,"url":930,"indexYears":28,"academicFieldIds":1768,"indexDatabaseRanking":28},{"id":920,"createTime":28,"updateTime":28,"relativeEntities":1764,"label":1765,"description":1766,"key":927,"publicationTags":1767,"standard":28},[],{"EN":923,"VI":923},{"EN":925,"VI":926},[929,813],[932,933,934],{"impactFactor":32,"impactFactorByYear":1770,"i10Index":940,"i10IndexLast5Year":142,"totalPublication":941,"totalPublicationByYear":1771,"totalCitation":952,"totalCitationByYear":1772,"totalCitationPerPublication":973,"totalCitationPerPublicationByYear":1773,"hindexLast5Year":207,"hindex":207},{"2012":937,"2013":176,"2014":532,"2015":319,"2016":938,"2017":709,"2018":230,"2019":939,"2020":187,"2021":224,"2022":318,"2023":938},{"2002":943,"2003":608,"2004":212,"2005":334,"2006":354,"2007":944,"2008":945,"2009":946,"2010":947,"2011":133,"2012":946,"2013":837,"2014":563,"2015":362,"2016":43,"2017":147,"2018":140,"2019":150,"2020":948,"2021":949,"2022":950,"2023":951,"2024":132},{"2002":954,"2003":955,"2004":956,"2005":957,"2006":958,"2007":959,"2008":960,"2009":961,"2010":350,"2011":962,"2012":963,"2013":964,"2014":965,"2015":966,"2016":967,"2017":968,"2018":969,"2019":970,"2020":971,"2021":972,"2022":155,"2023":129,"2024":40},{"2002":975,"2003":976,"2004":977,"2005":978,"2006":979,"2007":980,"2008":981,"2009":982,"2010":983,"2011":984,"2012":985,"2013":986,"2014":987,"2015":988,"2016":989,"2017":990,"2018":991,"2019":992,"2020":284,"2021":820,"2022":366,"2023":734,"2024":421},{"pages":1775,"volume":1777},{"VOID":1776},"1241-1252",{"VOID":1778},"13","2014-09-01",2014,[916,929],{"id":1783,"createTime":1784,"updateTime":1785,"relativeEntities":1786,"slug":1787,"properties":1788,"entityType":1012,"verifyStatus":26,"verifyTime":1785,"verifyNote":1013,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1797,"fullTextUrl":28,"authors":1798,"publicationType":1116,"publisherRelationship":1919,"citationCount":28,"citationInfo":28,"publishDate":1966,"publishYear":1967,"citationAnalyzeStatus":880,"lastCitationAnalyze":28,"indexDatabases":1968,"openAccess":28,"references":28,"isForceReanalyzing":1167},"009c337d-e85b-4f70-8cfb-48fa871ab5fa","2023-12-12T13:47:20.633+00:00","2024-12-21T22:36:13.017+00:00",[],"Rotational-diffusion-of-the-7-diethylamino-4-methylcoumarin-C1-dye-molecule-in-polar-protic-and-aprotic-solvents",{"abstract":1789,"title":1791,"references":1793,"doi":1795},{"EN":1790},"Fluorescence anisotropy decays of the 7-diethylamino-4-methylcoumarin C1 in various polar solvents of different viscosities and hydrogen bond donor\u002Facceptor character have been recorded by means of the fluorescence upconversion and time-correlated single photon counting techniques. The resulting characteristic times for the rotational diffusion fall into two classes with regards to the viscosity-dependency: n-alcohols and “other” solvents. This deviation from the simple Stokes–Einstein–Debye model may be interpreted in terms of rotation of the coumarin molecule under two different hydrodynamic boundary-conditions (“stick” or “slip”) in the two solvent classes. Possible explanations for this behaviour are discussed, and in particular solvent attachment and additional dielectric friction. Both these phenomena may in fact, under certain conditions, explain our findings. Our opinion, however, is that the dielectric friction model offers a more realistic picture of the additional rotational friction experienced by C1 in n-alcohols.",{"EN":1792},"Rotational diffusion of the 7-diethylamino-4-methylcoumarin C1 dye molecule in polar protic and aprotic solvents",{"VOID":1794},"K. B. Eisenthal and K. H. 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J. V. Frankland, M. L. Horng and M. Maroncelli, Dipole solvation in nondipolar solvents: experimental studies of reorganization energies and solvation dynamics, J. Phys. Chem., 1996, 100, 10337–10354.\nL. Cassara, Etude femtoseconde de colorants laser solubles dans l’eau: les coumarines, PhD Thesis, Université Paris 6: Paris, 1996.\nA. J. Cross and J. D. Simon, Rotational dynamics of a solvated dipole: A molecular dynamics study of dielectric friction, J. Chem. Phys., 1987, 86, 7079–7083.\nM. Bruehl and J. T. Hynes, Dielectric friction and solvation dynamics: a molecular dynamics study, J. Phys. Chem., 1992, 96, 4068–4074.\nA. Papazyan and M. Maroncelli, Rotational dielectric friction and dipole solvation: Tests of theory based on simulations of simple model solutions, J. Chem. Phys., 1995, 102, 2888–2919.\nM. G. Kurnikova, D. H. Waldeck and R. D. Coalson, A molecular dynamics study of dielectric friction, J. Chem. Phys., 1996, 105, 628–638.\nN. Balabai, A. Sukharevsky, I. Read, B. Strazisar, M. Kurnikova, R. S. Hartman, R. D. Coalson and D. H. Waldeck, Rotational diffusion of organic solutes: The role of dielectric friction in polar solvents and electrolyte solutions, J. Mol. Liq., 1998, 77, 37–60.\nM. G. Kurnikova, N. Balabai, D. H. Waldeck and R. D. Coalson, Rotational relaxation in polar solvents. Molecular dynamics study of solute-solvent interaction, J. Am. Chem. Soc., 1998, 120, 6121–6130.\nJ. A. Riddick, W. B. Bunger, T. K. Sakano, Organic Solvents, Physical properties and methods of purification, Wiley Interscience, New York, 1986.\nJ. A. Dean, Lange’s Handbook of Chemistry, 15th edition, McGraw-Hill, New York, 1999.\nT. Shinomiya, Dielectric dispersion and intermolecular association for 28 pure liquid alcohols. The position dependence of hydroxyl group in the hydrocarbon chain, Bull. Chem. Soc. Jpn., 1989, 62, 908.\nC. Magallanes, A. Catenaccio and H. Mechette, Relaxation time and viscosity of several n-alcohol\u002Fheptane systems, J. Mol. Liq., 1989, 40, 53.\nF. F. Hanna and I. K. Hakim, Main dielectric dispersion region of mixtures of some long-chain alcohols with non-polar solvents, Z. Naturforsch., 1972, 27A, 1363.\nT. Shinomiya, Dielectric relaxation and intermolecular association for 1-decanol. Temperature and dilution dependences of monomer and three hydrogen-bonded species, Bull. Chem. Soc. Jpn., 1989, 62, 2258.\nJ. Timmermans, Physico-chemical constants of pure organic compounds, Elsevier, New York, 1950.\nC. Wohlfarth, Static dielectric constants of pure liquids and binary liquid mixtures, Springer-Verlag, Berlin, 1991.\nJ.-C. Mialocq, T. Gustavsson and S. Pommeret, Spectroscopie laser femtoseconde dans l’eau, milieu biologique, J. Phys. IV, 1999, 9, 101.\nS. K. Pal, J. Peon and A. H. Zewail, Ultrafast decay and hydration dynamics of DNA bases and mimics, Chem. Phys. Lett., 2002, 363, 57–63.\nJ. Barthel, K. Bachhuber, R. Buchner and H. Hetzenauer, Dielectric spectra of some common solvents in the microwave region. Water and lower alcohols, Chem. Phys. Lett., 1990, 165, 369–373.\nJ. Barthel, K. Bachhuber, R. Buchner, J. B. Gill and M. Kleebauer, Dielectric spectra of some common solvents in the microwave region. Dipolar aprotic solvents and amides, Chem. Phys. Lett., 1990, 167, 62–66.\nI. Kirschenbaum, Physical properties and analysis of heavy water, McGraw-Hill, New York, 1951.\nL. M. Mukherjee and E. Grunwald, Physical properties and hydrogen bonding in the system ethanol–2,2,2-trifluoroethanol, J. Phys. Chem., 1958, 62, 1311.",{"VOID":1796},"10.1039\u002Fb211755j","https:\u002F\u002Flink.springer.com\u002F10.1039\u002Fb211755j",[1799,1823,1836,1849,1871,1893,1906],{"id":1800,"sortIndex":32,"researcher":28,"roles":1801,"affiliations":1802,"properties":1820,"displayName":1822,"givenName":28,"familyName":28},"ccda482a-3e2c-4eac-8225-4ead8fc6ae88",[1019],[1803,1811],{"id":1804,"sortIndex":32,"affiliation":1805,"properties":28},"6b48e8cf-2013-4ed0-89c3-36077989fb9e",{"id":1804,"createTime":28,"updateTime":28,"relativeEntities":1806,"slug":28,"properties":1807,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1810,"statistic":28},[],{"title":1808},{"VI":1809},"DSM\u002FDRECAM\u002FSCM, URA 331 CNRS, Laboratoire Claude Fréjacques, CEA\u002FSaclay, Gif-sur-Yvette Cedex, France",[],{"id":1812,"sortIndex":40,"affiliation":1813,"properties":1819},"a9300486-a750-4287-ae06-4cd86b6fcb01",{"id":1812,"createTime":28,"updateTime":28,"relativeEntities":1814,"slug":28,"properties":1815,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1818,"statistic":28},[],{"title":1816},{"VI":1817},"DSM\u002FDRECAM\u002FSPAM, URA 2453 CNRS, Laboratoire Francis Perrin, CEA\u002FSaclay, Gif-sur-Yvette Cedex, France",[],{},{"title":1821},{"VI":1822},"T. 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All complexes are 10-coordinate. Crystallographic analysis of [M(L1)2(NO3)] (M = Pr, Er) showed that for the smaller Er(iii) ions steric congestion at the metal centre results in two of the Er–N(pyridyl) distances being particularly long, which does not occur with the larger Pr(iii) ion that is better able to accommodate 10-fold coordination. On UV irradiation, both Pr(iii) complexes show, in the visible region of their luminescence spectra, transitions originating from both the 3P0 level (at ca. 21 000 cm-1) and the 1D2 level (at ca. 17 000 cm-1), a consequence of the fact that the lowest triplet state of the coordinated pyrazolylborate ligands lies at ca. 24 000 cm-1 in each case so is high enough in energy to populate both levels. This contrasts with Pr(iii) complexes based on diketonate ligands in which the lower triplet energies of the ligands result in emission from the 1D2 level only. At longer wavelengths, near-infrared luminescence arising from the 1D2 emissive level is observed with lifetimes (in both the solid state and solution) being in the range 50–110 ns. For both Er(iii) complexes, luminescence at 1530 nm occurs following UV excitation of ligand-centred transitions. In CH2Cl2 both complexes gave dual-exponential luminescence, with the major component having a lifetime characteristic of an intact Er(iii) complex (≈ 1.5 μs) and the minor component being much shorter lived (0.2–0.5 μs), suggestive of a species in which a ligand is partially detached and the metal is solvated, with the two forms interconverting slowly. This behaviour is consistent with the steric congestion and long M–N(pyridyl) bonds that were observed in [Er(L1)2(NO3)]. In the solid state both Er(iii) complexes gave very weak luminescence, which could be fitted to a single exponential decay with a lifetime similar to the longer-lived of the solution components.",{"EN":1979},"Photophysical properties of Pr(iii) and Er(iii) complexes of poly(pyrazolyl)borates",{"VOID":1981},"S. Faulkner, B. P. Burton-Pye and S. J. A. Pope, Appl. Spectrosc. Rev., 2005, 41, 1\nS. Tanabe, C. R. Chim., 2002, 5, 815\nG. A. Kumar, R. Riman, E. Snitzer and J. Ballato, J. Appl. Phys., 2004, 95, 40.\nP. L. Jones, A. J. Amoroso, J. C. Jeffery, J. A. McCleverty, E. Psillakis and L. H. Rees, M. D. Ward, Inorg. Chem., 1997, 36, 10.\nN. Armaroli, V. Balzani, F. Barigelletti, M. D. Ward and J. A. McCleverty, Chem. Phys. Lett., 1997, 276, 435.\nN. C. Harden, J. C. Jeffery, J. A. McCleverty, L. H. Rees and M. D. Ward, New J. Chem., 1998, 22, 661.\nD. A. Bardwell, J. C. Jeffery, P. L. Jones, J. A. McCleverty, E. Psillakis, Z. Reeves and M. D. Ward, J. Chem. Soc., Dalton Trans., 1997, 2079.\nN. Armaroli, G. Accorsi, F. Barigelletti, S. M. Couchman, J. S. Fleming, N. C. Harden, J. C. Jeffery, K. L. V. Mann, J. A. McCleverty, L. H. Rees, S. R. Starling and M. D. Ward, Inorg. Chem., 1999, 38, 5769.\nM. D. Ward, J. A. McCleverty, K. L. V. Mann, J. C. Jeffery, G. Motson and J. Hurst, Acta Crystallogr., 1999, C55, 2055\nG. M. Davies, H. Adams, M. D. Ward, Acta Crystallogr., 2005, C61, m221.\nZ. R. Bell, G. R. Motson, J. C. Jeffery, J. A. McCleverty and M. D. Ward, Polyhedron, 2001, 20, 2045.\nA. Beeby, B. P. Burton-Pye, S. Faulkner, J. C. Jeffery, J. A. McCleverty, G. R. Motson and M. D. Ward, J. Chem. Soc., Dalton Trans., 2002, 1923.\nG. M. Davies, R. J. Aarons, G. R. Motson, J. C. Jeffery, H. Adams, S. Faulkner and M. D. Ward, J. Chem. Soc., Dalton Trans., 2004, 1136.\nA. I. Voloshin, N. M. Shavaleev and V. P. Kazakov, J. Lumin., 2001, 93, 199.\nM. P. O. Wolbers, F. C. J. M. van Veggel, B. H. M. Snellink-Ruël, J. W. Hofstraat, F. A. J. Guerts and D. N. Reinhoudt, J. Chem. Soc., Perkin Trans. 2, 1998, 2141.\nJ. Chrysochoos and A. H. Qusti, J. Less-Common Metals, 1986, 126, 169.\nA. H. Qusti and J. Chrysochoos, J. Less-Common Metals, 1985, 112, 291.\nE. B. Sveshnikova and N. T. Timofeev, Opt. Spektrosk., 1980, 48, 503.\nJ. Yu, H. Zhang, L. Fu, R. Deng, L. Zhou, H. Li, F. Liu and H. Fu, Inorg. Chem. Commun., 2003, 6, 852.\nM. P. Hehlen, H. Riesen and H. U. Güdel, Inorg. Chem., 1991, 30, 2273.\nH. Dornauf and J. Heber, J. Lumin., 1979, 20, 271.\nG. L. Hilmes and J. P. Riehl, Inorg. Chem., 1986, 25, 2617.\nD. J. Qian, W. N. Leng, Y. Zhang, Z. Chen and J. van Houten, Spectrochim. Acta, Part A, 2000, 56, 2645.\nJ. R. Darwent, C. D. Flint, P. J. O’Grady, Chem. Phys. Lett., 1986, 127, 547\nT. Yamase, H. Naruke, J. Chem. Soc., Dalton Trans., 1991, 285.\nG. A. Crosby, R. E. Whan, R. M. Alire, J. Chem. Phys., 1961, 34, 743.\nA. S. Batsanov, A. Beeby, J. I. Bruce, J. A. K. Howard, A. M. Kenwright and D. Parker, Chem. Commun., 1999, 1011\nN. Graeppi, D. H. Powell, G. Laurenczy, L. Zékány and A. E. Merbach, Inorg. Chim. Acta, 1995, 235, 311\nL. Helm, A. E. Merbach, Coord. Chem. Rev., 1999, 187, 151.\nN. M. Shavaleev, L. P. Moorcraft, S. J. A. Pope, Z. R. Bell, S. Faulkner and M. D. Ward, Chem. Eur. J., 2003, 9, 5283.\nN. M. Shavaleev, S. J. A. Pope, Z. R. Bell, S. Faulkner and M. D. Ward, Dalton Trans., 2003, 808.\nSiemens SMART Data Collection Software, version 4.050; Siemens Analytical X-ray Instruments Ltd, Madison, WI, 1996.\nSiemens SAINT Data Reduction Software, version 4.050; Siemens Analytical X-ray Instruments Ltd., Madison, WI, 1996.\nSiemens SHELXTL version, An integrated system for solving and refining crystal structures from diffraction data, revision 5.1; Siemens Analytical X-ray Instruments Ltd., Madison, WI, 1996.\nG. M. Sheldrick, SHELXS-97, a Program for Automatic Solution of Crystal Structures; University of Gottingen, Gottingen, Germany, 1997.\nG. M. Sheldrick, SHELXL-97, a Program for Crystal Structure Refinement; University of Gottingen, Gottingen, Germany, 1997.\nA. Beeby and S. Faulkner, Chem. Phys. Lett., 1997, 266, 116.",{"VOID":1983},"10.1039\u002Fb508382f","https:\u002F\u002Flink.springer.com\u002F10.1039\u002Fb508382f",[1986,2001,2014,2029,2042],{"id":1987,"sortIndex":32,"researcher":28,"roles":1988,"affiliations":1989,"properties":1998,"displayName":2000,"givenName":28,"familyName":28},"de3df2b8-4170-4495-9f6b-432f298ec4d4",[1019],[1990],{"id":1991,"sortIndex":32,"affiliation":1992,"properties":28},"ef89fbb6-69ba-4f53-a24c-683de6baf763",{"id":1991,"createTime":28,"updateTime":28,"relativeEntities":1993,"slug":28,"properties":1994,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1997,"statistic":28},[],{"title":1995},{"VI":1996},"Department of Chemistry, University of Sheffield, Sheffield, UK",[],{"title":1999},{"VI":2000},"Graham M. 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A similar factor governs the efficiency of the reaction on direct excitation of either the donor or the acceptor of their components, except that it does not fall to nil below the threshold and the reaction affords higher quantum yields than the selective excitation of the charge-transfer complex.",{"EN":2115},"The factor which determines whether excitation of charge-transfer complexes leads to final net products in comparison with the reactivity on excitation of one of the components",{"VOID":2117},"R. F. Foster, Charge-Transfer Complexes in Organic Chemistry; Academic Press, New York, 1963.\nFor a general review, see: G. J. Kavarnos, Fundamentals of Photoinduced Electron Transfer, VCH, New York, 1993, p. 53.\nR. A. Marcus, The theory of oxidation-reduction reactions involving electron transfer. I, J. Chem. Phys., 1956, 24, 966–978.\nT. Asahi and N. Mataga, Charge recombination process of ion pair state produced excitation of charge-transfer complex in acetonitrile solution. Essentially different character of its energy gap dependence from that of geminate ion pair formed by encounter between fluorescer and quencher, J. Phys. Chem., 1989, 93, 6576–6578.\nS. Ojima and H. Miyasaka and N. Mataga, Femtosecond–picosecond laser photolysis studies on the dynamics of excited charge-transfer complexes in solution. 2. Ion pair formation processes in the excited state of 1,2,3,4-tetracyanobenzene–aromatic hydrocarbon complexes in polar solvents, J. Phys. Chem., 1990, 94, 5834–5839.\nT. Asahi and N. Mataga, Femtosecond–picosecond laser photolysis studies on the dynamics of excited charge-transfer complexes: aromatic hydrocarbon–acid anhydride,–tetracyanoethylene, and–tetracyanoquinodimethane systems in acetonitrile solutions, J. Phys. Chem., 1991, 95, 1956–1963.\nH. Miyasaka, T. Nagata, M. Kiri and N. Mataga, Femtosecond–picosecond laser photolysis studies on reduction process of excited benzophenone with N-methyldiphenylamine in acetonitrile solution, J. Phys. Chem., 1992, 96, 8060–8065.\nN. Mataga and H. Miyasaka, Photoinduced charge transfer phenomena: femtosecond–picosecond laser photolysis studies, Prog. React. Kinet., 1994, 19, 317–430.\nT. Asahi, M. Ohkohchi and N. Mataga, Energy gap dependence of charge recombination processes of ion pairs produced by excitation of charge-transfer complexes: solvent polarity effects, J. Phys. Chem., 1993, 97, 13132–13137.\nH. Miyasaka, S. Kotani, A. Itaya, G. Schweizer, F. C. DeSchryver and N. Mataga, Temperature effects on the energy gap dependence of charge recombination rates of ion pairs produced by excitation of charge-transfer complexes adsorbed on porous glass, J. Phys. Chem. B, 1997, 101, 7978–7984.\nI. R. Gould, R. Moody and S. Farid, Electron-transfer reactions in the Marcus inverted region: differences in solvation and electronic coupling between excited charge-transfer complexes and geminate radical ion pairs, J. Am. Chem. Soc., 1988, 110, 7242–7244.\nI. R. Gould, J. E. Moser, B. Armitage and S. Farid, Electron-transfer reactions in the Marcus inverted region. Charge recombination versus charge shift reactions, J. Am. Chem. Soc., 1989, 111, 1917–1919.\nI. R. Gould, D. Ege, E. Moser and S. Farid, Efficiencies of photoinduced electron-transfer reactions: role of the Marcus inverted region in return electron transfer within geminate radical-ion pairs, J. Am. Chem. Soc., 1990, 112, 4290–4301.\nI. R. Gould, R. H. Young, R. E. Moody and S. Farid, Contact and solvent-separated radical ion pairs in electron-transfer photochemistry, J. Phys. Chem., 1991, 95, 2068–2080.\nI. R. Gould and S. Farid, Fluorescence of excited charge-transfer complexes and absolute dynamics of radical-ion pairs in acetonitrile, J. Phys. Chem., 1992, 96, 7635–7640.\nI. R. Gould and S. Farid, Steric effects in photoinduced electron-transfer reactions, J. Phys. Chem., 1993, 97, 13067–13072.\nI. R. Gould, D. Noukakis, J. L. Goodman, R. H. Young and S. Farid, A quantitative relationship between radiative and nonradiative electron transfer in radical-ion pairs, J. Am. Chem. Soc., 1993, 115, 3830–3831.\nI. R. Gould, D. Naukakis, L. Gomez-Jahn, J. L. Goodman and S. J. Farid, Explanation of the driving-force dependence of return electron transfer in contact radical-ion pairs, J. Am. Chem. Soc., 1993, 115, 4405–4406.\nI. R. Gould and S. Farid, Concentration-dependent photoinduced electron-transfer reactions. 1:1 and 1:2 radical-ion complexes, J. Am. Chem. Soc., 1993, 115, 4814–4822.\nI. R. Gould, R. H. Young, L. J. Mueller and S. Farid, Mechanisms of exciplex formation. Roles of superexchange, solvent polarity, and driving force for electron transfer, J. Am. Chem. Soc., 1994, 116, 8176–8187.\nB. R. Arnold, D. Noukakis, S. Farid, J. L. Goodman and S. Farid, Dynamics of interconversion of contact and solvent-separated radical-ion pairs, J. Am. Chem. Soc., 1995, 117, 4399–4400.\nB. R. Arnold, S. J. Farid, J. L. Goodman and I. R. Gould, Absolute energies of interconverting contact and solvent separated radical-ion pairs, J. Am. Chem. Soc., 1996, 118, 5482–5283.\nI. R. Gould and S. J. Farid, Dynamics of bimolecular photoinduced electron-transfer reactions, Acc. Chem. Res., 1996, 29, 522–528.\nS. M. Hubig, T. M. Bockmann and J. K. Kochi, Optimized electron transfer in charge-transfer ion pairs. Pronounced inner-sphere behavior of olefin donors, J. Am. Chem. Soc., 1996, 118, 3842–3851.\nO. Nicolet and E. Vauthey, Ultrafast nano-equilibrium charge recombination dynamics of excited donor–acceptor complexes, J. Phys. Chem., 2002, 106, 5553–5562.\nM. Tachiya and S. Murata, Non-Marcus energy gap dependence of back electron transfer in contact ion pairs, J. Am. Chem. Soc., 1994, 116, 2434–2436.\nS. L. Mattes and S. Farid, Photosensitized electron-transfer reactions. Interception of the geminate radical ion pair, J. Am. Chem. Soc., 1983, 105, 1386–1387.\nI. R. Gould, J. E. Moser, D. Ege and S. Farid, Effect of molecular dimension on the rate of return electron transfer within photoinduced geminate radical ion pairs, J. Am. Chem. Soc., 1988, 110, 1991–1993.\nP. J. Dinnocenzo, S. Farid, J. L. Goodman, I. R. Gould, W. P. Todd and S. L. Mattes, Nucleophile-assisted cleavage of the silane cation radicals, J. Am. Chem. Soc., 1989, 111, 8973–8975.\nF. D. Lewis, A. M. Bedell, R. E. Dykstra, J. E. Elbert, I. R. Gould and S. Farid, Photochemical generation, isomerization, and oxygenation of stilbene cation radicals, J. Am. Chem. Soc., 1990, 112, 8055–8064.\nW. P. Todd, J. P. Dinnocenzo, S. Farid, J. L. Goodman and S. Farid, Efficient photoinduced generation of radical cation in solvents of medium and low polarity, J. Am. Chem. Soc., 1991, 113, 3601–3602.\nY. Shirota, J. Nagata and H. Mikawa, The photocycloaddition of acenaphthylene with tetracyanoethylene, Chem. Lett., 1972, 49–50.\nN. Haga, H. Nakajima, H. Takayanagi and K. Tokumaru, Exclusive production of a cycloadduct from selective excitation of charge-transfer complex between acenaphthylene and tetracyanoethylene in crystalline state in contrast to failure of reaction in solution, Chem. Commun., 1997, 1171–1172.\nN. Haga, H. Takayanagi and K. Tokumaru, Photoinduced electron transfer between acenaphthylene and tetracyanoethylene. Effect of irradiation mode on reactivity of the charge-transfer complex and the resulted radical ion pair in solution and crystalline state, J. Org. Chem., 1998, 63, 5372–5384.\nN. Haga, H. Takayanagi and K. Tokumaru, Control of reaction course of the excited state of charge-transfer complexes by free energy for backward electron transfer, Chem. Commun., 1998, 2093–2094.\nN. Haga, K. Takayanagi and K. Tokumaru, Photoinduced electron transfer between acenaphthylene and 1,4-benzoquinones. Formation of dimers of acenaphthylene and 1:1-adducts and effect of excitation mode on reactivity of the charge-transfer complexes, J. Chem. Soc.,Perkin Trans. 2, 2002, 734–745.\nN. Haga, H. Takayanagi and K. Tokumaru, manuscript in preparation.\nH. Chosrowjan, S. Taniguchi, T. Okada, S. Takagi, T. Arai and K. Tokumaru, Electron transfer quenching of S2 state fluorescence of Zn-tetraphenylporphyrin, Chem. Phys. Lett., 1995, 242, 644–649.\nK. Tokumaru, Photochemical and photophysical behaviour of porphyrins and phthalocyanines irradiated with violet or ultraviolet light, J. Porphyrins Phthalocyanines, 2001, 5, 77–86, and references therein.\nS. B. Karki, J. P. Dinnocenzo, S. Farid, J. L. Goodman, I. R. Gould and T. A. Zona, Bond-coupled electron transfer processes: a new strategy for high-efficiency photoinduced electron transfer reactions, J. Am. Chem. Soc., 1997, 119, 431–432.\nN. Haga, H. Takayanagi and K. Tokumaru, Mechanism of photodimerization of acenaphthylene, J. Org. Chem., 1997, 62, 3734–3743.\nJ. G. Calvert and J. N. Pitts, Jr., Photochemistry, John Wiley & Sons Inc., New York, 1966, p. 734–739.",{"VOID":2119},"10.1039\u002Fb305196j","https:\u002F\u002Flink.springer.com\u002F10.1039\u002Fb305196j",[2122,2137,2152],{"id":2123,"sortIndex":32,"researcher":28,"roles":2124,"affiliations":2125,"properties":2134,"displayName":2136,"givenName":28,"familyName":28},"aa7cbb63-8f53-4dd1-a804-aa83bdad0bf2",[1019],[2126],{"id":2127,"sortIndex":32,"affiliation":2128,"properties":28},"bc29c679-c2d3-4412-a178-46e04bbe1feb",{"id":2127,"createTime":28,"updateTime":28,"relativeEntities":2129,"slug":28,"properties":2130,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2133,"statistic":28},[],{"title":2131},{"VI":2132},"Department of Environmental and Natural Resource Science, Tokyo University of Agriculture and Technology, Fuchu, Tokyo, Japan",[],{"title":2135},{"VI":2136},"Naoki 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order to apply curcumin as a photosensitizer in photodynamic therapy (PDT) one needs a formulation that can solubilize and stabilize the compound. Pluronics® (Pluronic) are reported to both solubilize and stabilize curcumin against hydrolytic degradation. The aim of the present work was therefore to investigate the influence of Pluronic formulation on the photocytotoxicity of curcumin. Interactions between curcumin and Pluronics were investigated by fluorescence emission and absorption spectroscopy. Cell survival was measured with the MTT assay. The location of curcumin in the cells was investigated with fluorescence microscopy, and the cellular uptake was measured with fluorescence emission spectroscopy. Pluronics P123 and F127 in contrast to Pluronic P85 and PEG 400 may solubilize curcumin under noncytotoxic conditions. An inverse relationship between the concentration of Pluronic and the photocytotoxicity of curcumin was observed. Curcumin could rapidly translocate across the cell membrane by passive diffusion. The fluorescence from curcumin in the cells (in the cytoplasm) after 1 hour of incubation was lowered by the presence of Pluronics in the formulation. However, the absolute amount of cell-bound curcumin after 1 hour of incubation was independent of the presence of Pluronics. Curcumin was bound more strongly to cells when incubated with formulations without Pluronics compared to cells incubated with curcumin formulations with Pluronics. Incubation of WiDr cells with curcumin for 6 hours resulted in lysosomal accumulation of curcumin independent of the presence of Pluronics. Lysosomally located curcumin could not be observed in HT1080 cells after 6 hours of incubation. The Pluronics P123 and F127 were found to be suitable for solubilizing and stabilizing curcumin, but inhibited photocytotoxic effects of curcumin unless the Pluronic concentration during treatment of the cells was less than 5–10× above the critical micellar concentration.",{"EN":2225},"The influence of Pluronics® on dark cytotoxicity, photocytotoxicity, localization and uptake of curcumin in cancer cells: studies of curcumin and curcuminoids XLIX",{"VOID":2227},"T. A. Dahl, P. Bilski, K. J. Reszka, C. F. Chignell, Photocytotoxicity of curcumin, Photochem. Photobiol., 1994, 59, 290–294.\nH. H. Tønnesen, J. Karlsen, Studies on curcumin and curcuminoids. VI. Kinetics of curcumin degradation in aqueous solution, Z. Lebensm.-Unters. Forsch., 1985, 180, 402–404.\nH. H. Tønnesen, M. Masson, T. Loftsson, Studies of curcumin and curcuminoids. XXVII. Cyclodextrin complexation: solubility, chemical and photochemical stability, Int. J. Pharm., 2002, 244, 127–135.\nH. H. Tønnesen, J. Karlsen, G. B. van Henegouwen, Studies on curcumin and curcuminoids. VIII. Photochemical stability of curcumin, Z. Lebensm.-Unters. Forsch., 1986, 183, 116–122.\nE. V. Batrakova, A. V. Kabanov, Pluronic block copolymers: evolution of drug delivery concept from inert nanocarriers to biological response modifiers, J. Controlled Release, 2008, 130, 98–106.\nFDA, Inactive Ingredient search for approved drug products, http:\u002F\u002Fwww.accessdata.fda.gov\u002Fscripts\u002Fcder\u002Fiig\u002Findex.cfm, Accessed 24.08.2009.\nE. Batrakova, S. Lee, S. Li, A. Venne, V. Alakhov, A. Kabanov, Fundamental relationships between the composition of Pluronic block copolymers and their hypersensitization effect in MDR cancer cells, Pharm. Res., 1999, 16, 1373–1379.\nR. Singh, S. Kristensen, H. H. Tønnesen, Influence of cosolvents, ionic strength and the method of sample preparation on the solubilization of curcumin by Pluronics and HP-?-cyclodextrin studies of curcumin and curcuminoids, XLIV, Pharmazie, 2012, 67, 131–142.\nH. H. Tønnesen, H. de Vries, J. Karlsen, G. Beijersbergen van Henegouwen, Studies on curcumin and curcuminoids. IX: investigation of the photobiological activity of curcumin using bacterial indicator systems, J. Pharm. Sci., 1987, 76, 371–373.\nE. M. Bruzell, E. Morisbak, H. H. Tønnesen, Studies on curcumin and curcuminoids. XXIX. Photoinduced cytotoxicity of curcumin in selected aqueous preparations, Photochem. Photobiol. Sci., 2005, 4, 523–530.\nT. Haukvik, E. Bruzell, S. Kristensen, H. H. Tønnesen, Photokilling of bacteria by curcumin in different aqueous preparations. Studies on curcumin and curcuminoids XXXVII, Pharmazie, 2009, 64, 666–673.\nT. Haukvik, E. Bruzell, S. Kristensen, H. H. Tønnesen, Photokilling of bacteria by curcumin in selected polyethylene glycol 400 (PEG 400) preparations Studies on curcumin and curcuminoids, XLI, Pharmazie, 2010, 65, 600–606.\nA. B. Hegge, T. Andersen, J. E. Melvik, E. Bruzell, S. Kristensen, H. H. Tønnesen, Formulation and bacterial phototoxicity of curcumin loaded alginate foams for wound treatment applications: studies on curcumin and curcuminoides XLII, J. Pharm. Sci., 2011, 100, 174–185.\nA. Sahu, N. Kasoju, P. Goswami, U. Bora, Encapsulation of curcumin in Pluronic block copolymer micelles for drug delivery applications, J. Biomater. Appl., 2011, 25, 619–639.\nH. J. J. Pabon, Synthesis of curcumin and related compounds, Recl. J. R. Neth. Chem. Soc., 1964, 83, 379–386.\nJ. D. Stoien, R. J. Wang, Effect of near-ultraviolet and visible light on mammalian-cells in culture 2. Formation of toxic photoproducts in tissue-culture medium by blacklight, Proc. Natl. Acad. Sci. U. S. A., 1974, 71, 3961–3965.\nL. Nardo, R. Paderno, A. 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Quitschke, Differential solubility of curcuminoids in serum and albumin solutions: implications for analytical and therapeutic applications, BMC Biotechnol., 2008, 8.\nP. H. Bong, Spectral and photophysical behaviors of curcumin and curcuminoids, Bull. Korean Chem. Soc., 2000, 21, 81–86.\nC. Guo, J. Wang, X. Liang, L. Zheng, H. Liu, Effect of bovine serum albumin on the micellization of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) block copolymers in aqueous solutions by fluorescence spectroscopy, Sci. China, Ser. B: Chem., 2006, 49, 541–549.\nM. Svensson, K. Berggren, A. Veide, F. Tjerneld, Aqueous two-phase systems containing self-associating block copolymers–partitioning of hydrophilic and hydrophobic biomolecules, J. Chromatogr., A, 1999, 839, 71–83.\nT. Minko, E. V. Batrakova, S. Li, Y. L. Li, R. I. Pakunlu, V. Y. Alakhov, A. V. Kabanov, Pluronic block copolymers alter apoptotic signal transduction of doxorubicin in drug-resistant cancer cells, J. Controlled Release, 2005, 105, 269–278.\nE. V. Batrakova, S. Li, W. F. Elmquist, D. W. Miller, V. Y. Alakhov, A. V. Kabanov, Mechanism of sensitization of MDR cancer cells by Pluronic block copolymers: selective energy depletion, Br. J. Cancer, 2001, 85, 1987–1997.\nE. V. Batrakova, S. Li, S. V. Vinogradov, V. Y. Alakhov, D. W. Miller, A. V. Kabanov, Mechanism of pluronic effect on P-glycoprotein efflux system in blood–brain barrier: contributions of energy depletion and membrane fluidization, J. Pharmacol. Exp. Ther., 2001, 299, 483–493.\nA. V. Kabanov, E. V. Batrakova, S. Li, V. Y. Alakhov, Selective energy depletion and sensitization of multiple drug-resistant cancer cells by pluronic block copolymer, Macromol. Symp., 2001, 172, 103–112.\nD. Y. Alakhova, N. Y. Rapoport, E. V. Batrakova, A. A. Timoshin, S. Li, D. Nicholls, V. Y. Alakhov, A. V. Kabanov, Differential metabolic responses to pluronic in MDR and non-MDR cells: a novel pathway for chemosensitization of drug resistant cancers, J. Controlled Release, 2010, 142, 89–100.\nE. V. Batrakova, S. Li, V. Y. Alakhov, D. W. Miller, A. V. Kabanov, Optimal structure requirements for Pluronic block copolymers in modifying P-glycoprotein drug efflux transporter activity in bovine brain microvessel endothelial cells, J. Pharmacol. Exp. Ther., 2003, 304, 845–854.\nZ. Wei, S. Yuan, Y. Chen, S. Yu, J. Hao, J. Luo, X. Sha, X. Fang, Enhanced antitumor efficacy by Paclitaxel-loaded Pluronic P123\u002FF127 mixed micelles against non-small cell lung cancer based on passive tumor targeting and modulation of drug resistance, Eur. J. Pharm. Biopharm., 2010, 75, 341–353.\nA. P. Castano, T. N. Demidova, M. R. Hamblin, Mechanisms in photodynamic therapy: part one-photosensitizers, photochemistry and cellular localization, Photodiagn. Photodyn. Ther., 2005, 1, 279–293.\nA. Kunwar, A. Barik, B. Mishra, K. Rathinasamy, R. Pandey, K. I. Priyadarsini, Quantitative cellular uptake, localization and cytotoxicity of curcumin in normal and tumor cells, Biochim. Biophys. Acta, Gen. Subj., 2008, 1780, 673–679.",{"VOID":2229},"10.1039\u002Fc2pp25249j","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1039\u002Fc2pp25249j",[2232,2247,2260,2273],{"id":2233,"sortIndex":32,"researcher":28,"roles":2234,"affiliations":2235,"properties":2244,"displayName":2246,"givenName":28,"familyName":28},"e1b484f9-dda4-42ed-ba07-8523029173d0",[1019],[2236],{"id":2237,"sortIndex":32,"affiliation":2238,"properties":28},"5c096a43-a4fc-4c5b-9a12-f64ed144c114",{"id":2237,"createTime":28,"updateTime":28,"relativeEntities":2239,"slug":28,"properties":2240,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2243,"statistic":28},[],{"title":2241},{"VI":2242},"School of Pharmacy, Department of Pharmaceutics, University of Oslo, Oslo, Norway",[],{"title":2245},{"VI":2246},"Ravinder 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