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十二烷基硫酸钠诱导番红与三嵌段共聚物F127的结合增强:一种作为高效药物递送载体的混合胶束系统

Enhanced Binding of Phenosafranin to Triblock Copolymer F127 Induced by Sodium Dodecyl Sulfate: A Mixed Micellar System as an Efficient Drug Delivery Vehicle.

作者信息

Mondal Ramakanta, Ghosh Narayani, Mukherjee Saptarshi

机构信息

Department of Chemistry, Indian Institute of Science Education and Research Bhopal , Bhopal Bypass Road, Bhauri, Bhopal 462 066, Madhya Pradesh, India.

出版信息

J Phys Chem B. 2016 Mar 24;120(11):2968-76. doi: 10.1021/acs.jpcb.6b00759. Epub 2016 Mar 14.

DOI:10.1021/acs.jpcb.6b00759
PMID:26936205
Abstract

In this study, we explored the interaction of a cationic phenazinium dye, phenosafranin (PSF, here used as a model drug), with pluronic block copolymer F127, both in the presence and in the absence of the anionic surfactant sodium dodecyl sulfate (SDS), which forms mixed micelles with F127. We applied both steady-state and time-resolved spectroscopic techniques, along with isothermal titration calorimetry (ITC), to demonstrate the binding of the probe PSF to both the pluronic and F127/SDS mixed micelles. Dynamic light scattering (DLS) study revealed that, upon interaction with SDS, the hydrodynamic diameter (dH) of F127 micelles decreased due to the formation of the mixed micelles. The PSF penetrated to the more hydrophobic interior of the mixed micellar system as compared to F127 micelles alone. Micropolarity and fluorescence-quenching experiments revealed that PSF is more deeply seated in the case of F127/SDS mixed micelles. Through a partition coefficient, lifetime measurements, and time-resolved anisotropy experiments, we also established that the partitioning of the probe within the F127 micelles in the presence of SDS is almost double than that in its absence. ITC data corroborates the fact that the binding of PSF is the strongest and most thermodynamically favorable when mixed micelles are formed, which enables our system to serve as an excellent drug delivery vehicle when compared to F127 alone.

摘要

在本研究中,我们探究了阳离子吩嗪染料番红(PSF,此处用作模型药物)与普朗尼克嵌段共聚物F127在存在和不存在阴离子表面活性剂十二烷基硫酸钠(SDS)的情况下的相互作用,SDS与F127形成混合胶束。我们应用了稳态和时间分辨光谱技术以及等温滴定量热法(ITC),以证明探针PSF与普朗尼克和F127/SDS混合胶束的结合。动态光散射(DLS)研究表明,与SDS相互作用时,由于形成了混合胶束,F127胶束的流体力学直径(dH)减小。与单独的F127胶束相比,PSF渗透到混合胶束体系更疏水的内部。微极性和荧光猝灭实验表明,在F127/SDS混合胶束的情况下,PSF所处位置更深。通过分配系数、寿命测量和时间分辨各向异性实验,我们还确定,在存在SDS的情况下,探针在F127胶束内的分配几乎是不存在SDS时的两倍。ITC数据证实了这样一个事实,即当形成混合胶束时,PSF的结合最强且在热力学上最有利,与单独的F127相比,这使我们的体系能够作为一种出色的药物递送载体。

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