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拉帕替尼/紫杉醇聚电解质纳米胶囊克服卵巢癌多药耐药性。

Lapatinib/Paclitaxel polyelectrolyte nanocapsules for overcoming multidrug resistance in ovarian cancer.

机构信息

Laboratory of General Physiology, Department of Biological and Environmental Sciences and Technologies, University of Salento, Lecce, Italy.

出版信息

Nanomedicine. 2012 Aug;8(6):891-9. doi: 10.1016/j.nano.2011.10.014. Epub 2011 Nov 16.

Abstract

The sonication-assisted layer-by-layer (SLBL) technology was developed to combine necessary factors for an efficient drug-delivery system: (i) control of nanocolloid size within 100 - 300 nm, (ii) high drug content (70% wt), (iii) shell biocompatibility and biodegradability, (iv) sustained controlled release, and (v) multidrug-loaded system. Stable nanocolloids of Paclitaxel (PTX) and lapatinib were prepared by the SLBL method. In a multidrug-resistant (MDR) ovarian cancer cell line, OVCAR-3, lapatinib/PTX nanocolloids mediated an enhanced cell growth inhibition in comparison with the PTX-only treatment. A series of in vitro cell assays were used to test the efficacy of these formulations. The small size and functional versatility of these nanoparticles, combined with their ability to incorporate various drugs, indicates that lapatinib/PTX nanocolloids may have in vivo therapeutic applications.

摘要

超声辅助层层(SLBL)技术被开发出来,以结合高效药物输送系统的必要因素:(i)控制纳米胶体大小在 100-300nm 范围内,(ii)高药物含量(70wt%),(iii)壳的生物相容性和可生物降解性,(iv)持续的控制释放,和(v)多药装载系统。紫杉醇(PTX)和拉帕替尼的稳定纳米胶体通过 SLBL 方法制备。在多药耐药(MDR)卵巢癌细胞系 OVCAR-3 中,与仅用 PTX 治疗相比,拉帕替尼/PTX 纳米胶体介导的细胞生长抑制增强。一系列体外细胞试验用于测试这些制剂的功效。这些纳米粒子的小尺寸和多功能性,结合它们能够结合各种药物的能力,表明拉帕替尼/PTX 纳米胶体可能具有体内治疗应用。

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