A novel self-assembled micelles based on stearic acid modified schizophyllan for efficient delivery of paclitaxel

胶束 硬脂酸 紫杉醇 化学 药物输送 两亲性 核化学 MTT法 临界胶束浓度 聚合物 有机化学 体外 共聚物 水溶液 生物化学 医学 外科 化疗
作者
Zahra Negahban,Seyed Abbas Shojaosadati,Sepideh Hamedi
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier BV]
卷期号:199: 111524-111524 被引量:34
标识
DOI:10.1016/j.colsurfb.2020.111524
摘要

This study was aimed to design a novel amphiphilic carrier based on schizophyllan (SPG) exopolysacharide for drug delivery. Stearic acid (SA) was used for the esterification of SPG with two degrees of substitutions (SA-SPG0.5 and SA-SPG1). The H NMR and FTIR spectroscopies verified the succesfull esterification of SPG. The polymeric micelles easily self-assembled into nanomicelles by ultrasound method. Fluorescence spectroscopy showed that the critical micelle concentrations (CMCs) of SA-SPG0.5 and SA-SPG1 micelles were 0.068 mg/mL and 0.027 mg/mL, respectively. DLS analyses showed that nanomicelles were ranged from 156 to 175 nm. SEM and TEM images showed that nanomicelles were mostly spherical. Paclitaxel (PTX) as a drug model was successfully loaded into SA-SPG nanomicelles with three different drug/polymer weight ratios of 0.1, 0.2 and 0.3. The highest encapsulation efficiency (75 %) was obtained when the PTX/SA-SPG weight ratio was 0.1. The in vitro release of PTX from SA-SPG micelles represented the sustained release profile over 144 h. MTT assay showed that the PTX-loaded SA-SPG nanomicelles had the higher cytotoxicity against MCF-7 cells than free PTX. These results revealed that the synthesized SA-SPG nanomicelles had a promising potential as a new carrier for efficient delivery of hydrophobic drugs.

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