Targeted delivery of a guanidine-pendant Pt(IV)-backboned poly-prodrug by an anisamide-functionalized polypeptide
文献类型:期刊论文
作者 | Li, Shao-Lu1,2; Wang, Yaoyi2; Zhang, Jingfang2; Wei, Wei3; Lu, Hua2 |
刊名 | JOURNAL OF MATERIALS CHEMISTRY B |
出版日期 | 2017-12-28 |
卷号 | 5期号:48页码:9546-9557 |
ISSN号 | 2050-750X |
DOI | 10.1039/c7tb02513k |
文献子类 | Article |
英文摘要 | We describe here a novel targeting polyion complex (Tg-PIC) system for the delivery and intracellular release of cisplatin. Briefly, a guanidinium-pendant Pt(IV)-backboned poly-prodrug termed P(DSP-Gu) is prepared with excellent aqueous solubility, high drug-loading and high potency. To enable prolonged circulation and selective cellular internalization, P(DSP-Gu) is complexed with anisamide-end-capped poly(ethylene glycol)-block-poly(L-phosphotyrosine)-block-poly(L-leucine) (AA-PEG-PpY-PLeu) to yield Tg-PIC via electrostatic coacervation. Tg-PIC is stabilized by hydrogen bonding between phosphate and guanidinium, the PEG corona, and the helical poly(L-leucine) segment forming the hydrophobic core. The anisamide group, a high affinity ligand recognizing the sigma (sigma) receptors that are overexpressed on many human malignancies including prostate cancer, is incorporated at the surface of the Tg-PIC for active targeting and efficient internalization. In vitro, the Tg-PICs show targeted and efficient internalization into sigma receptor-positive PC3 cells, and can release toxic Pt(II) species due to the degradation of P(DSP-Gu) under the intracellular reducing conditions. In vivo, the Tg-PICs exhibit superior antitumor efficacy with reduced toxicity. Thus, the system holds considerable promise towards more effective and safe nanomedicine. |
WOS关键词 | Ring-opening Polymerization ; Drug-delivery ; Co-delivery ; Prostate-cancer ; Sirna Delivery ; Responsive Polymers ; Anticancer Activity ; Block-copolymers ; In-vitro ; Therapy |
WOS研究方向 | Materials Science |
语种 | 英语 |
WOS记录号 | WOS:000418072200012 |
资助机构 | National Key Research and Development Program of China(2016YFA0201400) ; State High-Tech Development Program of China (863 Program)(2015AA020941) ; National Natural Science Foundation of China(NSFC21434008) ; State Key Laboratory of Biochemical Engineering(2015KF-01) ; China Postdoctoral Science Foundation(2016M600847) ; Postdoctoral Fellowship of Peking-Tsinghua Center for Life Sciences |
源URL | [http://ir.ipe.ac.cn/handle/122111/23476] |
专题 | 过程工程研究所_研究所(批量导入) |
通讯作者 | Lu, Hua |
作者单位 | 1.Tianjin Polytech Univ, Sch Mat Sci & Engn, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China 2.Peking Univ, Key Lab Polymer Chem & Phys, Beijing Natl Lab Mol Sci,Minist Educ, Ctr Soft Matter Sci & Engn,Coll Chem & Mol Engn, Beijing 100871, Peoples R China 3.Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, Beijing 10090, Peoples R China |
推荐引用方式 GB/T 7714 | Li, Shao-Lu,Wang, Yaoyi,Zhang, Jingfang,et al. Targeted delivery of a guanidine-pendant Pt(IV)-backboned poly-prodrug by an anisamide-functionalized polypeptide[J]. JOURNAL OF MATERIALS CHEMISTRY B,2017,5(48):9546-9557. |
APA | Li, Shao-Lu,Wang, Yaoyi,Zhang, Jingfang,Wei, Wei,&Lu, Hua.(2017).Targeted delivery of a guanidine-pendant Pt(IV)-backboned poly-prodrug by an anisamide-functionalized polypeptide.JOURNAL OF MATERIALS CHEMISTRY B,5(48),9546-9557. |
MLA | Li, Shao-Lu,et al."Targeted delivery of a guanidine-pendant Pt(IV)-backboned poly-prodrug by an anisamide-functionalized polypeptide".JOURNAL OF MATERIALS CHEMISTRY B 5.48(2017):9546-9557. |
入库方式: OAI收割
来源:过程工程研究所
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