Implementation of PLGA-based nanoparticles for treatment of Colorectal Cancer

Rajiv Sharma, A. Gill, S. Gautam, Amanda Frank, Neha Bajwa, P. Singh
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Abstract

Colorectal cancer is more prevalent in females than males. There are many anticancer drugs accessible for use, but their therapeutic importance is constrained by factors including poor solubility, low absorption, and multi-drug resistance. This review highlights how PLGA may be used to develop polymeric-targeted drug delivery systems that specifically target colorectal cancer. The PLGA polymer, which is disseminated in the colon together with drugs in a regulated and targeted manner, has the distinct characteristics of smart degradation in a biological system. Its degradability is dependent on multiple glycolide units; therefore, a lower glycol concentration improves degradability and vice versa. Also, PLGA facilitates drug delivery in colorectal cancer, enhances the efficacy of the drug, improves the sustained release profile of a drug, improves bioavailability due to prolonged retention time in the colon, enhances solubility, etc. To develop the formulation for improving the cytotoxic impact of various anticancer drugs, the surface modification of PLGA can be carried out by introducing a copolymer. By emphasizing their crucial characterization to demonstrate their therapeutic potential, this literature work has also shed light on recent patents and advancements in PLGA application.
基于plga的纳米颗粒治疗结直肠癌的实现
结直肠癌在女性中比男性更普遍。有许多抗癌药物可供使用,但其治疗重要性受到溶解度差、吸收低和多重耐药等因素的限制。这篇综述强调了PLGA如何用于开发特异性靶向结直肠癌的聚合物靶向药物递送系统。PLGA聚合物在生物系统中具有明显的智能降解特性,与药物一起以调控和靶向的方式散布在结肠中。它的可降解性取决于多个糖苷单元;因此,乙二醇浓度越低,降解性越好,反之亦然。此外,PLGA促进了结直肠癌中的药物递送,提高了药物的疗效,改善了药物的缓释谱,由于延长了在结肠中的滞留时间而提高了生物利用度,增强了溶解度等。为了开发改善各种抗癌药物细胞毒性作用的配方,可以通过引入共聚物对PLGA进行表面改性。通过强调其关键特征来展示其治疗潜力,本文献工作也揭示了PLGA应用的最新专利和进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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