Jia Li, Qiao Ming-Xi, Hu Hai-Yang, Zhao Xiu-Li, Chen Da-Wei
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Yao Xue Xue Bao. 2011 Jul;46(7):839-44.
The dialysis method was employed to prepare blank and doxorubicin (DOX) loaded micelles formed by temperature- and pH- sensitive polyhistidine-co-polyDL-lactide-co-glycolide-co-polyethyleneglycol-co-polyDL-lactide-co-glycolide-co-polyhistidine (PHis-b-PLGA-b-PEG-b-PLGA-b-PHis). The critical micelle concentrations (CMC) of the copolymers were measured with Pyrene Fluorescent Probe Technique. The temperature- and pH- sensitive properties of the blank micelles solution were investigated by optical transmittance measurement. The morphology and diameter of DOX micelles were characterized by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The entrapment rate and drug-loading rate were determined with dialysis method. The in vitro release study was further performed to examine the temperature- and pH-responsive drug release behavior from DOX-loaded micelles. The results indicated that the CMC, entrapment efficiency and drug-loaded amount of the micelles were 7.5 x 10(-3) g x L(-1), 85.2 +/- 3.1% and 10.4 +/- 4.5%, respectively. The DOX micelle was globular-shaped with a mean diameter of 91.1 +/- 15.8 nm. The transmittance of micelle solution consistently increased with the increasing temperature or decreasing pH. In comparison to the drug release profile at physiological conditions (37 degrees C, pH 7.4), the DOX-loaded micelles showed faster drug release rate at higher temperature (41 degrees C), lower pH (pH 7.0, pH 6.5, pH 5.0) or higher temperature and lower pH (41 degrees C, pH 5.0). This indicated that the micelles showed a temperature and pH-triggered drug release pattern. Base on the above results, it can be concluded that PHis-b-PLGA-b-PEG-b-PLGA-b-PHis block copolymer micelles which respond to temperature and pH stimuli are promising smart carriers for anti-tumor drugs with the advantages of temperature- and pH- triggered drug release.
采用透析法制备了由温度和pH敏感的聚组氨酸-聚-DL-丙交酯-乙交酯-聚乙二醇-聚-DL-丙交酯-乙交酯-聚组氨酸(PHis-b-PLGA-b-PEG-b-PLGA-b-PHis)形成的空白胶束和载有阿霉素(DOX)的胶束。用芘荧光探针技术测定共聚物的临界胶束浓度(CMC)。通过透光率测量研究空白胶束溶液的温度和pH敏感特性。用透射电子显微镜(TEM)和动态光散射(DLS)表征DOX胶束的形态和直径。用透析法测定包封率和载药率。进一步进行体外释放研究,以考察载DOX胶束的温度和pH响应药物释放行为。结果表明,胶束的CMC、包封率和载药量分别为7.5×10⁻³ g·L⁻¹、85.2±3.1%和10.4±4.5%。DOX胶束呈球形,平均直径为91.1±15.8 nm。胶束溶液的透光率随温度升高或pH降低而持续增加。与生理条件(37℃,pH 7.4)下的药物释放曲线相比,载DOX胶束在较高温度(41℃)、较低pH(pH 7.0、pH 6.5、pH 5.0)或较高温度和较低pH(41℃,pH 5.0)下显示出更快的药物释放速率。这表明胶束呈现出温度和pH触发的药物释放模式。基于上述结果,可以得出结论,对温度和pH刺激有响应的PHis-b-PLGA-b-PEG-b-PLGA-b-PHis嵌段共聚物胶束是有前景的抗肿瘤药物智能载体,具有温度和pH触发药物释放的优点。