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有机添加剂5-甲基水杨酸可诱导水性泊洛沙姆三嵌段共聚物溶液发生自发结构转变:姜黄素与泊洛沙姆胶束和囊泡聚集体相互作用的光谱研究

Organic additive, 5-methylsalicylic acid induces spontaneous structural transformation of aqueous pluronic triblock copolymer solution: a spectroscopic investigation of interaction of curcumin with pluronic micellar and vesicular aggregates.

作者信息

Ghosh Surajit, Kuchlyan Jagannath, Banik Debasis, Kundu Niloy, Roy Arpita, Banerjee Chiranjib, Sarkar Nilmoni

机构信息

Department of Chemistry, Indian Institute of Technology , Kharagpur 721302, WB, India.

出版信息

J Phys Chem B. 2014 Oct 2;118(39):11437-48. doi: 10.1021/jp507378w. Epub 2014 Sep 19.

DOI:10.1021/jp507378w
PMID:25192258
Abstract

This article presents the interaction of curcumin in the microenvironments provided by aggregation of pluronic triblock copolymer P123 into micellar and vesicular assemblies. The formation of vesicles using triblock copolymer P123 and 5-methylsalicylic acid (5 mS) has been successfully characterized by optical spectroscopy, light scattering measurement, and eventually microscopic techniques. Besides, to make a comparative study between the polymeric micelles, we have also investigated the photophysical changes of curcumin in F127 triblock copolymer micelles having variation in poly(ethylene oxide) (PPO) and poly(propylene oxide) (PEO) unit of polymer chain to that of P123. Time-dependent UV-vis measurement suggests that these polymer micelles are able to stabilize poorly water-soluble curcumin by suppressing the degradation rate in micellar nanocavity. However, experimental observations suggest that P123 micelles are more efficient than F127 to perturb excited state intramolecular proton transfer (ESIPT)-related nonradiative decay of curcumin. We also observed that rigid and confined microenvironment of P123/5 mS vesicles enhances emission intensity and lifetime of curcumin more compared to P123 micelles. All the observations suggest that modulation of photophysics of curcumin is responsible due to its interaction with poly(ethylene oxide) or poly(propylene oxide) unit of triblock copolymer.

摘要

本文介绍了姜黄素在普朗尼克三嵌段共聚物P123聚集形成的胶束和囊泡组装体所提供的微环境中的相互作用。利用三嵌段共聚物P123和5-甲基水杨酸(5 mS)形成囊泡的过程已通过光谱学、光散射测量以及最终的显微镜技术成功表征。此外,为了对聚合物胶束进行比较研究,我们还研究了姜黄素在F127三嵌段共聚物胶束中的光物理变化,该胶束的聚合物链中聚环氧乙烷(PPO)和聚环氧丙烷(PEO)单元与P123的有所不同。随时间变化的紫外可见测量表明,这些聚合物胶束能够通过抑制胶束纳米腔内的降解速率来稳定水溶性较差的姜黄素。然而,实验观察表明,P123胶束在干扰姜黄素与激发态分子内质子转移(ESIPT)相关的非辐射衰变方面比F127更有效。我们还观察到,与P123胶束相比,P123/5 mS囊泡的刚性和受限微环境更能增强姜黄素的发射强度和寿命。所有观察结果表明,姜黄素光物理性质的调制是由于其与三嵌段共聚物的聚环氧乙烷或聚环氧丙烷单元相互作用所致。

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