EVALUATION OF NEW BENZOPORPHYRIN DERIVATIVES WITH ENHANCED PDT EFFICACY*

Photochemistry and Photobiology - Tập 62 Số 4 - Trang 764-768 - 1995
Ravindra K. Pandeyi1, William R. Potter1, Isabelle Meunier2, Adam B. Sumlin1, Kevin M. Smith2
1Chemistry Division, PDT Center, Department of Radiation Biology, Division of Radiation Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA
2Department of Chemistry, University of California, Davis, CA 95616 USA

Tóm tắt

Abstract— A first report on the biological evaluation of a series of isomerically pure benzoporphyrin derivatives (cis‐ and frarcs‐isomers) as methyl esters is described. In preliminary in vivo studies, the n‐bexyl ether analogues of both cis‐ and trans‐isomers of benzoporphyrin derivatives were found to be more active than the industrially prepared benzoporphyrin derivative, a mixture of monocarboxylic acids (BPDMA, Quadralogic Technologies, Vancouver). Further studies with 4‐de‐vinyl‐4‐(I‐hexyloxyethyl) benzoporphyrin derivative showed that, like BPDMA, it had reduced residual skin phototoxicity compared in mice with Photofrin®. The uptake and clearance characteristics of BPDMA were also compared with the 4‐(1‐hexyloxyethyl)‐derivative by in vivo reflection spectroscopy.

Từ khóa


Tài liệu tham khảo

Dougherty T. J., 1990, Photodynamic Therapy of Neoplastic Disease, 1

10.1117/12.978017

Richter A. M., 1987, Preliminary studies on a more effective phototoxic agent than hematoporphyrin, J. Natl. Cancer Inst., 79, 1327

10.1111/j.1751-1097.1991.tb08468.x

10.1016/1011-1344(93)80131-R

10.1016/S0960-894X(00)80176-6

10.1016/S0960-894X(00)80433-3

10.1038/bjc.1991.18

10.1039/p19940000961

10.1117/12.60948

10.1007/978-1-4684-4406-3_2

Note: The BPDMA used in our study was dissolved in 1% Tween 80.The clinical material prepared by Quadralogic Technologies is generally delivered in liposomes.

10.1038/bjc.1987.98