Molecular interactions between novel synthesized biodegradable ionic liquids with antidepressant drug

Chemical Thermodynamics and Thermal Analysis - Tập 3 - Trang 100012 - 2021
Manoj Kumar Banjare1,2, Kamalakanta Behera3, Ramesh Kumar Banjare2,4, Siddharth Pandey5, Kallol K. Ghosh1, Yevgen Karpichev6
1School of Studies in Chemistry, Pt. Ravishankar Shukla University, Raipur, (C.G.) 492010, India
2MATS School of Sciences, MATS University, Pagaria Complex, Pandri, Raipur (C.G.) 492004, India
3Department of Applied Chemistry (CBFS-ASAS) Amity University, Gurgaon, Manesar, Panchgaon, Haryana 122413, India
4Departments of Chemistry, Raipur Institute of Technology, Raipur (C.G.) 492001, India
5Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, 110016, India
6Department of Chemistry and Biotechnology, Tallinn University of Technology (TalTech), Tallinn 12618, Estonia

Tài liệu tham khảo

Alam, 2011, Effect of KCl on the micellization and clouding phenomenon of the amphiphilic phenothiazine drug promethazine hydrochloride: some thermodynamic properties, J. Chem. Eng. Data, 56, 1540, 10.1021/je101156d Sankaranarayanan, 2011, Dual fluorescence of dothiepin, doxepin drugs-effect of solvents and β-cyclodextrin, J. Mol. Liq, 161, 107, 10.1016/j.molliq.2011.04.016 Alam, 2007, Kabir-ud-Din, Surface and micellar properties of some amphiphilic drugs in the presence of additives, J. Chem. Eng. Data, 52, 1326, 10.1021/je700045r Matijevic, 1958, The properties of ionized monolayers. Part 1. Sodium dodecyl sulphate at the air/water interface, Chem. Soc. Faraday Trans., 54, 1382, 10.1039/TF9585401382 Alam, 2010, Thermodynamics at the cloud point of phenothiazine drug chlorpromazine hydrochloride-additive systems, J. Chem. Eng. Data, 55, 1693, 10.1021/je9007487 Schreier, 2000, Review Surface active drugs: self-association and interaction with membranes and surfactants. Physicochemical and biological aspects, Biochim. Biophys. Acta, 1508, 210, 10.1016/S0304-4157(00)00012-5 Purushothaman, 2016, Dependence of norfloxacin diffusion across bilayers on lipid composition, Soft Matter, 12, 2135, 10.1039/C5SM02371H Mangiapia, 2017, Effect of benzocaine and propranolol on phospholipid-based bilayers, Phys. Chem. Chem. Phys., 19, 32057, 10.1039/C7CP06077G Kartzung, 2004 Geetha, 2003, Surface characteristics of comblike copolymers from hexadecylacrylamide and acrylic acid at the air/water interface, Langmuir, 19, 9051, 10.1021/la034784g Schreier, 2000, Surface active drugs: self-association and interaction with membranes and surfactants. Physicochemical and biological aspects, Biochim. Biophys. Acta, 210, 210, 10.1016/S0304-4157(00)00012-5 Hijo, 2016, Applications of ionic liquids in the food and bioproducts industries, ACS Sustain. Chem. Eng., 4, 5347, 10.1021/acssuschemeng.6b00560 Egorova, 2017, Biological activity of ionic liquids and their application in pharmaceutics and medicine, Chem. Rev., 117, 7132, 10.1021/acs.chemrev.6b00562 Behera, 2007, Modulating properties of aqueous sodium dodecyl sulfate by adding hydrophobic ionic liquid, J. Colloid Interface Sci., 316, 803, 10.1016/j.jcis.2007.07.072 Jordana, 2015, Biodegradation of ionic liquids - a critical review, Chem. Soc. Rev., 44, 8200, 10.1039/C5CS00444F Markiewicz, 2016, Readily biodegradable and low-toxic biocompatible ionic liquids for cellulose processing, RSC Adv., 6, 87325, 10.1039/C6RA14435G Clarke, 2018, Green and sustainable solvents in chemical processes, Chem. Rev., 118, 747, 10.1021/acs.chemrev.7b00571 Choudhury, 2013, Green chemistry and the textile industry, J. Textile Progr., 45, 3, 10.1080/00405167.2013.807601 Wu, 2019, Assessment of the toxicity and biodegradation of amino acid-based ionic liquids, RSC Adv., 9, 10100, 10.1039/C8RA06929H Tao, 2006, Preparation, characterization and application of amino acid-based green ionic liquids, Green Chem., 8, 639, 10.1039/b600813e Gomes, 2019, Biocompatible ionic liquids: fundamental behaviours and applications, Chem. Soc. Rev., 48, 4317, 10.1039/C9CS00016J Fresta, 2002, Puglisi, combining molecular modeling with experimental methodologies: mechanism of membrane permeation and accumulation of of loxacin, Bioorg. Med. Chem., 10, 3871, 10.1016/S0968-0896(02)00350-4 Kabir-ud-Din, 2011, Mixed micelles of amphiphilic drug promethazine hydrochloride and surfactants (conventional and emini) at 293.15 K to 308.15 K: composition, interaction and stability of the aggregates, J. Colloid Interface Sci., 354, 700, 10.1016/j.jcis.2010.11.005 Kabir-ud-Din, 2013, Mixed micelle formation between amphiphilic drug amitriptyline hydrochloride and surfactants (Conventional and Gemini) at 293.15−308.15 K, J. Phys. Chem., 114, 459 Mahajan, 2012, An investigation of drug binding ability of a surface active ionic liquid: micellization, electrochemical, and spectroscopic studies, Langmuir, 28, 17238, 10.1021/la303193n Péteilh, 2014, Surfactant behavior of ionic liquids involving a drug: from molecular interactions to self-assembly, Langmuir, 30, 1229, 10.1021/la404166y Farooq, 2018, Interaction of a surface-active ionic liquid with an antidepressant drug: micellization and spectroscopic studies, J. Sol. Chem., 47, 68, 10.1007/s10953-018-0739-7 Banjare, 2018, Self-assembly of a short-chain ionic liquid within deep eutectic solvents, RSC Adv., 8, 7969, 10.1039/C7RA13557B Banjare, 2018, Self-aggregation of bio-surfactants within ionic liquid 1-ethyl-3-methylimidazolium bromide: a comparative study and potential application in antidepressants drug aggregation, Spectrochim. Acta Part A, 199, 376, 10.1016/j.saa.2018.03.079 Pandya, 2020, An example of green surfactant systems based on inherently biodegradable IL-derived amphiphilic oximes, J. Mol. Liq., 305, 10.1016/j.molliq.2020.112857 Akhtera, 2019, Synthesis and characterization of cationic surfactants and their interactions with drug and metal complexes, Heliyon, 5, e01885, 10.1016/j.heliyon.2019.e01885 Zha, 2018, Study of interaction between ionic liquids and orange g in aqueous solution with UV-vis spectroscopy and conductivity meter, Spectrochim. Acta Part A, 196, 178, 10.1016/j.saa.2018.02.015 Terdale, 2007, Thermodynamic studies of drug−α-cyclodextrin interactions in water at 298.15 K:  promazine hydrochloride/chlorpromazine hydrochloride + α-cyclodextrin + H2O systems, J. Phys. Chem. B, 111, 13645, 10.1021/jp0754381 Yadav, 2017, Biophysical studies on the interactions between antidepressant drugs and bile salts, J. Mol. Liq., 233, 23, 10.1016/j.molliq.2017.02.102 Sharma, 2012, An investigation of binding ability of ionic surfactants with trifluoperazine dihydrochloride: insights from surface tension, electronic absorption and fluorescence measurements, RSC Adv., 2, 9571, 10.1039/c2ra21020g Du, 2014, Interaction of ionic liquid [Bmin][CF3SO3] with lysozyme investigated by two-dimensional fourier transform infrared spectroscopy, ACS Sustain. Chem. Eng., 2, 1420, 10.1021/sc500218e Reshma, 2019, Antidepressant drug-protein interactions studied by spectroscopic methods based on fluorescent carbon quantum dots, Heliyon, 5, e01631, 10.1016/j.heliyon.2019.e01631 Sharma, 2020, Multi-spectroscopic monitoring of molecular interactions between an amino acid-functionalized ionic liquid and potential anti-Alzheimer's drugs, RSC Adv., 10, 38873, 10.1039/D0RA06323A Bhardwaj, 2014, Drug-surfactant interaction: thermo-acoustic investigation of sodium dodecyl sulfate and antimicrobial drug (levofloxacin) for potential pharmaceutical application, RSC Adv., 4, 24935, 10.1039/C4RA02177K Akhter, 2019, Synthesis and characterization of cationic surfactants and their interactions with drug and metal complexes, Heliyon, 5, e01885, 10.1016/j.heliyon.2019.e01885 Dinache, 2020, Spectroscopic characterization of emulsions generated with a new laser-assisted device, Molecules, 25, 1729, 10.3390/molecules25071729 Singh, 2017, Aggregation and morphological aptitude of drug-based ionic liquids in aqueous solution, ACS Omega, 7, 3296, 10.1021/acsomega.7b00578 Qamar, 2016, The interaction of a model active pharmaceutical with cationic surfactant and the subsequent design of drug based ionic liquid surfactants, J. Colloid Interface Sci., 1, 117, 10.1016/j.jcis.2016.07.054