A New Gold Nanoparticles and Paclitaxel Co-Delivery System for Enhanced Anti-Cancer Effect Through Chemo-Photothermal Combination

被引:6
|
作者
Zhan, Honglei [1 ]
Song, Wenjing [1 ]
Gu, Mingyang [1 ]
Zhao, He [1 ]
Liu, Yujia [1 ]
Liu, Bingnan [1 ]
Wang, Jihui [1 ,2 ]
机构
[1] Dalian Polytech Univ, Sch Bioengn, Dept Biotechnol, Dalian 116034, Liaoning, Peoples R China
[2] Dongguan Univ Technol, Sch Chem Engn & Energy Technol, Dongguan 523808, Guangzhou Provi, Peoples R China
关键词
Gold Nanoparticles; Chemo-Photothermal Combination; Anti-Cancer Efficiency; Nanocrystals; Functionalization; TARGETED DELIVERY; DRUG NANOCRYSTALS; DOXORUBICIN; THERAPY; CHITOSAN; GROWTH; SILVER;
D O I
10.1166/jbn.2022.3309
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Limited chemotherapeutic efficiency, drug resistance and side effect are primary obstacles for cancer treatment. The development of co-delivery system with synergistic treatment modes should be a promising strategy. Here, we fabricated a multi-functionalized nanocarrier with a combination of chemotherapeutic agent and gold nanoparticles (AuNPs), which could integrate chemo-photothermal therapy and improve entire anti-cancer index. Particularly, Paclitaxel nanocrystals (PTX NC) were first fabricated as a platform, on surface of which AuNPs were decorated and polydopamine (PDA) layer act as capping, stabilizing and hydrophilic agents for PTX NC, providing a bridge connecting AuNPs to PTX. These AuNPs decorated PTX NC exhibited good physico-chemical properties like optimal sizes, stability and photothermal efficiency. Compared to other PTX formulations, they displayed considerably improved biocompatibility, selectivity, intracellular uptake, cytotoxicity, apoptosis induction activity and P-glycoprotein (Pgp) inhibitory capability, owing to a synergistic/cooperative effect from AuNPs, PTX and NIR treatment, photothermal- triggered drug release and nano-scaled structure. Mitochondria-mediated signaling pathway is underlying mechanism for cytotoxic and apoptotic effect from AuNPs decorated PTX NC, in terms of Mitochondria damage, a loss of Mitochondrial membrane potential, intensified oxidative stress, DNA breakage, Caspase 3 activation, up-regulated expression in pro-apoptotic genes like p53, Caspase 3 and Bax and down- regulated level in anti-apoptotic gene like Bcl-2.
引用
收藏
页码:957 / 975
页数:19
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