Chitosan/poly (lactic acid)-coated piceatannol nanoparticles exert an in vitro apoptosis activity on liver, lung and breast cancer cell lines

被引:30
作者
Dhanapal, Jeevitha [1 ]
Ravindrran, Malathy Balaraman [2 ]
机构
[1] Sathyabama Inst Sci & Technol, Dept Biotechnol, Fac Sci & Humanities Life Sci, Chennai 600119, Tamil Nadu, India
[2] Sathyabama Univ Dent Coll & Hosp, Dept Microbiol, Chennai, India
关键词
Apoptosis; chitosan; DNA fragmentation; flow cytometry; nanoparticles; poly(lactic acid); piceatannol; POTENT INDUCER; RESVERATROL; ANALOG; PROGRESSION; LYMPHOMA; DELIVERY; GRAPE; CYCLE; RISK;
D O I
10.1080/21691401.2017.1422130
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:S274 / S282
页数:9
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