Department of Chemistry, Shahid Beheshti University, G.C., 1983963113, Tehran, Iran.
Int J Pharm. 2012 Nov 1;437(1-2):70-9. doi: 10.1016/j.ijpharm.2012.07.069. Epub 2012 Aug 4.
In this study, a new type of folate-decorated thermoresponsive micelles based on the star-shaped amphiphilic block copolymer 4s[poly(ε-caprolactone)-b-2s(poly(N-isopropylacrylamide-co-acrylamide)-b'-methoxy poly(ethylene glycol)/poly(ethylene glycol)-folate)] (i.e., 4s[PCL-b-2s(P(NIPAAm-co-AAm)-b'-MPEG/PEG-FA)] (PCIAE-FA)), were developed for the tumor-targeted delivery and temperature-induced controlled release of hydrophobic anticancer drugs. These amphiphilic star copolymers are capable of self-assembling into spherical micelles in aqueous solution with an average diameter of 91 nm. The lower critical solution temperature (LCST) of micelles was around 39.7 °C. The anticancer drug, paclitaxel (PTX), was encapsulated into the micelles. In vitro release studies demonstrated that the drug-loaded delivery system (PTX-PCIAE-FA) is relatively stable at physiologic conditions but susceptible to temperatures above LCST which would trigger the release of encapsulated drugs. The cytotoxicity studies showed that the PTX transported by these micelles was higher than that by the commercial PTX formulation Tarvexol(®). The efficacy of this thermoresponsive drug delivery system was also evaluated at temperatures above the LCST; the results demonstrated that the cellular uptake and the cytotoxicity of PTX-loaded micelles increase prominently. These results indicate that these thermoresponsive micelles may offer a very promising carrier to improve the delivery efficiency and cancer specificity of hydrophobic chemotherapeutic drugs.
在这项研究中,开发了一种新型叶酸修饰的温敏胶束,基于星形两亲嵌段共聚物 4s[聚(ε-己内酯)-b-2s(聚(N-异丙基丙烯酰胺-co-丙烯酰胺)-b'-甲氧基聚(乙二醇)/聚(乙二醇)-叶酸)](即 4s[PCL-b-2s(P(NIPAAm-co-AAm)-b'-MPEG/PEG-FA)](PCIAE-FA)),用于肿瘤靶向输送和温度诱导的疏水性抗癌药物的控制释放。这些两亲性星形共聚物能够在水溶液中自组装成平均直径为 91nm 的球形胶束。胶束的低临界溶液温度(LCST)约为 39.7°C。将抗癌药物紫杉醇(PTX)包封到胶束中。体外释放研究表明,载药递送系统(PTX-PCIAE-FA)在生理条件下相对稳定,但易受 LCST 以上温度的影响,这会触发封装药物的释放。细胞毒性研究表明,这些胶束携带的 PTX 高于商业 PTX 制剂 Tarvexol(®)。还评估了该温敏药物递送系统在 LCST 以上温度的疗效;结果表明,载药胶束的细胞摄取和细胞毒性显著增加。这些结果表明,这些温敏胶束可能提供了一种很有前途的载体,以提高疏水性化疗药物的递送效率和癌症特异性。