Tumor-Microenvironment-Adaptive Nanoparticles Codeliver Paclitaxel and siRNA to Inhibit Growth and Lung Metastasis of Breast Cancer | |
Tang, Shan2; Meng, Qingshuo2; Sun, Huiping1,2; Su, Jinghan2; Yin, Qi2![]() ![]() ![]() ![]() ![]() ![]() | |
刊名 | ADVANCED FUNCTIONAL MATERIALS
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2016-09-06 | |
卷号 | 26期号:33页码:6033-6046 |
ISSN号 | 1616-301X |
DOI | 10.1002/adfm.201601703 |
文献子类 | Article |
英文摘要 | Prolonged circulation, specific and effective uptake by tumor cells, and rapid intracellular drug release are three main factors for the drug delivery systems to win the battle against metastatic breast cancer. In this work, a tumor microenvironment-adaptive nanoparticle co-loading paclitaxel (PTX) and the anti-metastasis siRNA targeting Twist is prepared. The nanoparticle consists of a pH-sensitive core, a cationic shell, and a matrix metalloproteinase (MMP)-cleavable polyethylene glycol (PEG) corona conjugated via a peptide linker. PEG will be cut away by MMPs at the tumor site, which endows the nanoparticle with smaller particle size and higher positive charge, leading to more efficient cellular uptake in tumor cells and higher intra-tumor accumulation of both PTX and siRNA in the 4T1 tumor-bearing mice models compared to the nanoparticles with irremovable PEG. In addition, acid-triggered drug release in endo/lysosomes is achieved through the pH-sensitive core. As a result, the MMP/pH dual-sensitive nanoparticles significantly inhibit tumor growth and pulmonary metastasis. Therefore, this tumor-microenvironment-adaptive nanoparticle can be a promising codelivery vector for effective therapy of metastatic breast cancer due to simultaneously satisfying the requirements of long circulating time, efficient tumor cell targeting, and fast intracellular drug release. |
资助项目 | National Basic Research Program of China[2014CB931900] ; National Natural Science Foundation of China[81521005] ; National Natural Science Foundation of China[81230029] ; National Natural Science Foundation of China[81302712] ; Youth Innovation Promotion Association of CAS[2015226] |
WOS关键词 | AMINO ESTER NANOPARTICLES ; DRUG-DELIVERY ; GENE DELIVERY ; IN-VIVO ; BIODISTRIBUTION ; THERAPEUTICS ; NANOCARRIERS ; DOXORUBICIN ; PEGYLATION ; EXPRESSION |
WOS研究方向 | Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics |
语种 | 英语 |
出版者 | WILEY-V C H VERLAG GMBH |
WOS记录号 | WOS:000383609100009 |
内容类型 | 期刊论文 |
源URL | [http://119.78.100.183/handle/2S10ELR8/275897] ![]() |
专题 | 药物制剂研究中心 中科院受体结构与功能重点实验室 新药研究国家重点实验室 |
通讯作者 | Yin, Qi; Li, Yaping |
作者单位 | 1.Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China; 2.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res & Ctr Pharmaceut, 501 Haike Rd, Shanghai 201203, Peoples R China; 3.Yantai Univ, Collaborat Innovat Ctr Adv Drug Delivery Syst & B, Sch Pharm, Yantai 264005, Peoples R China |
推荐引用方式 GB/T 7714 | Tang, Shan,Meng, Qingshuo,Sun, Huiping,et al. Tumor-Microenvironment-Adaptive Nanoparticles Codeliver Paclitaxel and siRNA to Inhibit Growth and Lung Metastasis of Breast Cancer[J]. ADVANCED FUNCTIONAL MATERIALS,2016,26(33):6033-6046. |
APA | Tang, Shan.,Meng, Qingshuo.,Sun, Huiping.,Su, Jinghan.,Yin, Qi.,...&Li, Yaping.(2016).Tumor-Microenvironment-Adaptive Nanoparticles Codeliver Paclitaxel and siRNA to Inhibit Growth and Lung Metastasis of Breast Cancer.ADVANCED FUNCTIONAL MATERIALS,26(33),6033-6046. |
MLA | Tang, Shan,et al."Tumor-Microenvironment-Adaptive Nanoparticles Codeliver Paclitaxel and siRNA to Inhibit Growth and Lung Metastasis of Breast Cancer".ADVANCED FUNCTIONAL MATERIALS 26.33(2016):6033-6046. |
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