首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Chitosan/poly (lactic acid)-coated piceatannol nanoparticles exert an in vitro apoptosis activity on liver, lung and breast cancer cell lines
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Chitosan/poly (lactic acid)-coated piceatannol nanoparticles exert an in vitro apoptosis activity on liver, lung and breast cancer cell lines

机译:壳聚糖/聚(乳酸)包被的皮甲环醇纳米颗粒对肝,肺和乳腺癌细胞系具有体外凋亡活性

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The aim of the study was to synthesize nanoparticles (NPs) with chitosan (CS), and poly (lactic acid) (PLA) as a carrier for the drug piceatannol (PIC). The synthesized nanoparticles form the composite of polymeric-drug nanoparticles (CS/PLA-PIC NPs) by dropping method. The preliminary and stability studies were determined for the polymers drug-loading capacity and encapsulation efficiencies. The in vitro drug release study showed that NPs provided a continuous release of the entrapped PIC. The NPs found to be a good scavenger for DPPH, SOD and NO radicals. MTT and LDH assays revealed higher cytotoxic efficacy of CS/PLA–PIC NPs in HepG2, A549 and MCF7 cells compared to CS-PLA NPs and PIC. Dual staining results showed the early/late-stages of apoptotic and necrotic cells. Furthermore, cells treated with CS/PLA-PIC NPs showed fragmenting DNA and also demonstrated for apoptotic cells percentage by flow cytometry. These results suggested that upon CS/PLA–PIC NPs exposure leads to decrease in cancer cell viability due to apoptosis.
机译:该研究的目的是用壳聚糖(CS)和聚乳酸(PLA)合成吡咯烷醇(PIC)的载体来合成纳米颗粒(NPs)。合成的纳米颗粒通过滴落法形成聚合物-药物纳米颗粒(CS / PLA-PIC NPs)的复合物。对聚合物的载药量和包封效率进行了初步和稳定性研究。体外药物释放研究表明,NP可连续释放被包裹的PIC。发现NP是DPPH,SOD和NO自由基的良好清除剂。 MTT和LDH分析显示,与CS-PLA NP和PIC相比,CS / PLA-PIC NP在HepG2,A549和MCF7细胞中具有更高的细胞毒性。双重染色结果显示凋亡和坏死细胞的早期/晚期。此外,用CS / PLA-PIC NPs处理的细胞显示出片段化的DNA,并且通过流式细胞术还显示出凋亡细胞的百分比。这些结果表明,由于细胞凋亡,CS / PLA-PIC NPs暴露导致癌细胞生存能力下降。

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