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PEO-PPO-PEO 嵌段共聚物胶束作为纳米容器增溶难溶性药物氢氯噻嗪。

Micelles from PEO-PPO-PEO block copolymers as nanocontainers for solubilization of a poorly water soluble drug hydrochlorothiazide.

机构信息

Department of Chemistry, Veer Narmad South Gujarat University, Surat 395 007, India.

出版信息

Colloids Surf B Biointerfaces. 2011 Mar;83(1):49-57. doi: 10.1016/j.colsurfb.2010.10.041. Epub 2010 Nov 2.

Abstract

The effect of molecular characteristics of EO-PO triblock copolymers viz. Pluronic(®) P103 (EO(17)PO(60)PEO(17)), P123 (EO(19)PO(69)EO(19)), and F127 (EO(100)PO(65)EO(100)) on micellar behavior and solubilization of a diuretic drug, hydrochlorothiazide (HCT) was investigated. The critical micellization temperatures (CMTs) and size for empty as well as drug loaded micelles are reported. The CMTs and micelle size depended on the hydrophobicity and molecular weight of the copolymer; a decrease in CMT and increase in size was observed on solubilization. The solubilization of the drug hydrochlorothiazide (HCT) in the block copolymer nanoaggregates at different temperatures (28, 37, 45°C), pH (3.7, 5.0, 6.7) and in the presence of added salt (NaCl) was monitored by using UV-vis spectroscopy and solubility data were used to calculate the solubilization characteristics; micelle-water partition coefficient (P) and thermodynamic parameters of solubilization viz. Gibbs free energy (ΔG(s)°), enthalpy (ΔH(s)°) and entropy (ΔS(s)°). The solubility of the drug in copolymer increases with the trend: P103>P123>F127. The solubilized drug decreased the cloud point (CP) of copolymers. Results show that the drug solubility increases in the presence of salt but significantly enhances with the increase in the temperature and at a lower pH in which drug remains in the non-ionized form.

摘要

考察了 EO-PO 嵌段共聚物(如 Pluronic® P103(EO(17)PO(60)PEO(17))、P123(EO(19)PO(69)EO(19))和 F127(EO(100)PO(65)EO(100))的分子特性对米氏行为和利尿剂药物氢氯噻嗪(HCT)增溶的影响。报道了空胶束和载药胶束的临界胶束温度(CMT)和粒径。CMT 和胶束粒径取决于共聚物的疏水性和分子量;增溶时,CMT 降低,粒径增大。采用紫外可见光谱法监测不同温度(28、37、45°C)、pH(3.7、5.0、6.7)和外加盐(NaCl)存在下药物氢氯噻嗪(HCT)在嵌段共聚物纳米聚集体中的增溶情况,并利用溶解度数据计算增溶特性;胶束-水分配系数(P)和增溶热力学参数,如吉布斯自由能(ΔG(s)°)、焓变(ΔH(s)°)和熵变(ΔS(s)°)。药物在共聚物中的溶解度随 P103>P123>F127 的趋势增加。增溶的药物降低了共聚物的浊点(CP)。结果表明,盐的存在会增加药物的溶解度,但在较低 pH 值和温度升高时,药物仍以非离子形式存在时,药物的溶解度会显著增加。

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