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Improving anti-tumor activity with polymeric micelles entrapping paclitaxel in pulmonary carcinoma

机译:改善与聚合物的抗肿瘤活性胶束诱骗紫杉醇在肺癌

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Nanoscale polymeric micelles have promising applications as drug delivery systems (DDS). In this work, to improve the anti-tumor activity and eliminate toxicity of the commercial formulation (cremophor EL and ethanol) of paclitaxel (PTX), we developed biodegradable poly(ethylene glycol)-poly(s-caprolactone) (MPEG-PCL) micelles entrapping PTX by a simple one-step solid dispersion method, which is without any surfactants or additives and is easy to scale up. In addition, the PTX micelles could be lyophilized into powder without any adjuvant and the re-dissolved PTX micelles are stable and homogeneous. The prepared PTX micelles have a mean particle size of 38.06 ± 2.30 nm, a polydispersity index of 0.168 ± 0.014, a drug loading of 14.89 ± 0.06% and an encapsulation efficiency of 99.25 ± 0.38%. A molecular modeling study implied that PTX interacted with PCL as a core, which was embraced by PEG as a shell. The encapsulation of PTX in polymeric micelles enhanced its cytotoxicity by increasing the uptake by LL/2 cells. A sustained in vitro release behavior and slow extravasation behavior from blood vessels in a transgenic zebrafish model were observed in the PTX micelles. Furthermore, compared with Taxol?, the PTX micelles were more effective in suppressing tumor growth in the subcutaneous LL/2 tumor model. The PTX micelles also inhibited metastases in the pulmonary metastatic LL/2 tumor model and prolonged survival in both mouse models. Pharmacokinetic and tissue distribution studies showed that after PTX was encapsulated in polymeric micelles, the biodistribution pattern of PTX was altered and the PTX concentration in tumors was increased compared with Taxol? after intravenous injection. In conclusion, we have developed a polymeric micelles entrapping PTX that enhanced cytotoxicity in vitro and improved anti-tumor activity in vivo with low systemic toxicity on pulmonary carcinoma. The biodegradable MPEG-PCL micelles entrapping PTX may have promising applications in pulmonary carcinoma therapy.
机译:纳米聚合物胶束有前途应用程序作为药物输送系统(DDS)。这项工作,提高抗肿瘤活性和消除毒性的商业配方(cremophor EL和乙醇)的紫杉醇(PTX),我们开发了可降解聚(乙烯乙二醇)聚(s-caprolactone) (MPEG-PCL)胶束固体诱骗PTX通过一个简单的一步分散的方法,这是没有任何表面活性剂和添加剂和易于扩展。此外,PTX胶束冻干成粉末,没有任何辅助的溶解PTX稳定和胶束同构的。38.06±2.30 nm的平均粒径多分散性指数为0.168±0.014,一种药物加载14.89±0.06%和封装99.25±0.38%的效率。研究暗示PTX与PCL互动核心,由盯住了壳。封装的PTX聚合物胶束增强其细胞毒性增加通过将/ 2细胞吸收。释放行为和缓慢溢出行为从转基因斑马鱼血管PTX胶束模型观察。此外,与紫杉醇相比?胶束更有效地抑制肿瘤增长的皮下肿瘤模型/ 2。PTX微粒也抑制转移肺转移性/ 2肿瘤模型长期生存在小鼠模型。药代动力学和组织分布研究PTX封装后的显示聚合物胶束,biodistribution模式PTX改变和PTX浓度肿瘤是增加与紫杉醇相比?静脉注射。开发出一种聚合物胶束诱骗PTX增强的体外细胞毒性和改善体内抗肿瘤活性较低的系统肺部癌毒性。可生物降解MPEG-PCL胶束诱骗PTX在肺可能应用前景癌的治疗。

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