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pH/还原敏感型多柔比星前药胶束的制备及体外性能评价
引用本文:刘慎欢,杨福伟,蔡瑶,邱立朋,陈敬华.pH/还原敏感型多柔比星前药胶束的制备及体外性能评价[J].中国药学杂志,2021,56(1):36-41.
作者姓名:刘慎欢  杨福伟  蔡瑶  邱立朋  陈敬华
作者单位:江南大学药学院, 江苏 无锡 214122
基金项目:国家自然科学基金项目资助(81503007,21574059)
摘    要:目的 本实验以聚乙二醇(polyethylene glycol,PEG)和多柔比星(doxorubicin,DOX)合成的刺激敏感型前药聚合物(PEG-DOX)包载美法仑(melphalan,MEL),制备MEL/PEG-DOX纳米胶束,考察其体外协同抗肿瘤作用.方法 通过希夫碱反应将PEG化的二硫代二丙酸二酰肼(TP...

关 键 词:聚乙二醇  纳米前药  多柔比星  美法仑
收稿时间:2020-03-10

Preparation and in Vitro Performance Evaluation of pH/Reduction-Sensitive Doxorubicin Prodrug Micelles
LIU Shen-huan,YANG Fu-wei,CAI Yao,QIU Li-peng,CHEN Jing-hua.Preparation and in Vitro Performance Evaluation of pH/Reduction-Sensitive Doxorubicin Prodrug Micelles[J].Chinese Pharmaceutical Journal,2021,56(1):36-41.
Authors:LIU Shen-huan  YANG Fu-wei  CAI Yao  QIU Li-peng  CHEN Jing-hua
Institution:School of Parmaceutical Science,Jiangnan University, Wuxi 214122, China
Abstract:OBJECTIVE To synthesize a stimulus-sensitive precursor polymer (PEG-DOX) from polyethylene glycol and doxorubicin, encapsulate melphalan(MEL) to prepare MEL/PEG-DOX nanometer micelles, and investigate its synergistic anti-tumor effect in vitro. METHODS Through Schiff base reaction, the pegylated dithionyl hydrazide (TPH) was combined with DOX to form a pH/reduction sensitive PEG-DOX prodrug nanocarrier, and MEL/PEG-DOX loaded micelle was prepared by its self-assembly property.The morphology was observed by transmission electron microscopy, the particle size and potential were measured by particle size analyzer, drug loading and encapsulation rate were measured by ultrafiltration, drug release of micelles was evaluated by dialysis, and cytotoxicity was evaluated by MTT. RESULTS The stimulation response PEG-DOX precursor polymer was verified by H-NMR.The mean particle size of peg-dox carrier was (188±2.4) nm, and the polydispersion coefficient (PDI) was (0.255±0.008). The mean particle size of MEL/PEG-DOX loaded micelles was (299.7±2.4) nm, the polydispersion coefficient (PDI) was 0.301±0.03, and the Zeta potential was (-0.385±0.02) mV. DOX drug-polymer interactions (14.85±0.24)%, the encapsulation rate was (85.78±0.37)%, MEL drug-polymer interactions (7.36±0.36)%, the encapsulation rate was (38.79±0.42)%.The results of drug release experiments in vitro showed that MEL/PEG-DOX micelles were sensitive to reduction and pH, and the reduction sensitivity was greater than that of pH. Cytotoxicity analysis showed that DOX and MEL were released together in cells, achieving the joint killing of tumor cells. CONCLUSION MEL/PEG-DOX can be specifically released in the tumor microenvironment, which has a coordinating effect on tumor cells and a good application prospect.
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