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免疫治疗维生素 E 纳米乳通过调节 Th1 和 Th2 免疫应答增强紫杉醇在乳腺癌细胞中的抗增殖活性。

Immunotherapeutic vitamin E nanoemulsion synergies the antiproliferative activity of paclitaxel in breast cancer cells via modulating Th1 and Th2 immune response.

机构信息

Pharmaceutics Division, CSIR-Central Drug Research Institute, Lucknow, UP 226031, India.

Laboratory Animals Facility, CSIR-Central Drug Research Institute, Lucknow, UP 226031, India.

出版信息

J Control Release. 2014 Dec 28;196:295-306. doi: 10.1016/j.jconrel.2014.10.010. Epub 2014 Oct 22.

Abstract

Paclitaxel (PTX) is used as first line treatment for metastatic breast cancer but the relief comes at a heavy cost in terms of accompanying adverse effects. The pharmaceutical credentials of PTX are further dampened by the intrinsically low aqueous solubility. In order to sideline such insidious tendencies, PTX was incorporated in a vitamin E nanoemulsion using high pressure homogenization. The encapsulation efficiency of PTX in nanoemulsion was 97.81±2.7% and a sustained drug release profile was obtained. PTX loaded nanoemulsion exhibited higher cytotoxicity in breast cancer cell line (MCF-7) when compared to free PTX and marketed formulation (Taxol). Cell cycle arrest study depicted that MCF-7 cells treated with PTX loaded nanoemulsion showed high arrest in G2-M phase. Moreover blank nanoemulsion induced additional apoptosis in breast cancer cells through G1-S arrest by disrupting mitochondrial membrane potential. Cytokine estimation study in macrophages showed that both PTX loaded nanoemulsion and blank nanoemulsion enhanced secretion of IL-12 and downregulated secretion of IL-4 and IL-10. Results suggest that inclusion of vitamin E in nanoemulsion opened multiple complementary molecular effects which not only magnified the principle antiproliferative activity of PTX but also independently showcased potential in restoring the proactive nature of the breast cancer slackened chronic immune response. In-vivo anticancer activity showed significantly improved efficacy of PTX loaded nanoemlsion compare to Taxol and free PTX. The list of plausible advantages of PTX nanoemulsification was further substantiated by acceptable haemolytic potential, reduced in-vivo toxicity and conveniently modified pharmacokinetic profile in which the AUC and MRT were extended considerably. Overall, there were strong evidences that developed formulation can serve as a viable alternative to currently available PTX options.

摘要

紫杉醇(PTX)被用作转移性乳腺癌的一线治疗药物,但随之而来的不良反应也带来了沉重的代价。PTX 的内在低水溶性进一步降低了其药物性能。为了规避这种潜在的趋势,将 PTX 包封在维生素 E 纳米乳中,采用高压匀质法。纳米乳中 PTX 的包封效率为 97.81±2.7%,并获得了持续的药物释放曲线。与游离 PTX 和市售制剂(Taxol)相比,载 PTX 的纳米乳在乳腺癌细胞系(MCF-7)中表现出更高的细胞毒性。细胞周期阻滞研究表明,用载 PTX 的纳米乳处理的 MCF-7 细胞在 G2-M 期有较高的阻滞。此外,空白纳米乳通过破坏线粒体膜电位,在 G1-S 期诱导乳腺癌细胞发生额外的凋亡。巨噬细胞细胞因子评估研究表明,载 PTX 的纳米乳和空白纳米乳均增强了 IL-12 的分泌,并下调了 IL-4 和 IL-10 的分泌。结果表明,维生素 E 的加入在纳米乳中开启了多种互补的分子效应,不仅放大了 PTX 的主要抗增殖活性,而且独立展示了恢复乳腺癌松弛慢性免疫反应的主动状态的潜力。体内抗癌活性研究表明,与 Taxol 和游离 PTX 相比,载 PTX 的纳米乳具有显著提高的疗效。PTX 纳米乳的优势还包括可接受的溶血潜力、降低的体内毒性以及方便修饰的药代动力学特征,其中 AUC 和 MRT 得到了极大的延长。总的来说,有强有力的证据表明,所开发的制剂可以作为目前可用的 PTX 选择的可行替代品。

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