Synthesis and In vitro Evaluation of Doxorubicin loaded Polymeric Nanoparticles on Cancer Cells

Nimra Batool, Tayyaba Saif, Tahira Anwar, Sajjad Ullah, Sikandar Hayat, Malik Ihsan Ullah Khan
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Abstract

Cancer is the second biggest mortality rate globally. Most of anti-cancer drugs are hydrophobic and when they are administered in the body, they get clear from the blood. That’s why polymeric nanoparticles (NPs) have been used for delivering anti-cancer drugs to targeted sites. Biodegradable and self-assembled nature, PEG-PLGA has been used as a nanocarrier for biomedical applications. We developed PEG-PLGA NP for the doxorubicin (DOX) delivery to cancerous cells. The successful PEG-PLGA synthesis was confirmed by its 1 H NMR spectrum. All NPs displayed individual spherical morphology and 100 nm size range with -18.5mV zeta potential. Drug release profile showed DOX had sustained release pattern from DOX@NPs. In vitro, MTT assay and apoptosis analysis revealed that low-dose DOX@NPs exhibited more toxic effects on cancerous cells as compared to DOX alone. Overall results demonstrate that polymeric-based nanosystems increase the efficacy of DOX on cancer cells.
负载多柔比星的聚合物纳米粒子的合成及对癌细胞的体外评估
癌症是全球死亡率第二高的疾病。大多数抗癌药物都是疏水性的,进入人体后会被血液清除。因此,聚合物纳米粒子(NPs)被用于将抗癌药物输送到靶点。PEG-PLGA 具有生物可降解性和自组装性,已被用作生物医学应用的纳米载体。我们开发了 PEG-PLGA NP,用于向癌细胞递送多柔比星(DOX)。其 1 H NMR 光谱证实了 PEG-PLGA 的成功合成。所有 NPs 均呈独立球形,尺寸范围为 100 nm,Zeta 电位为 -18.5mV。药物释放曲线显示 DOX 具有从 DOX@NPs 中持续释放的模式。体外 MTT 试验和细胞凋亡分析表明,与单用 DOX 相比,低剂量 DOX@NPs 对癌细胞的毒性更强。总体结果表明,基于聚合物的纳米系统提高了 DOX 对癌细胞的疗效。
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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