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pH响应性超支化聚合物肽杂化材料的制备与自组装

Preparation and Self-Assembly of pH-Responsive Hyperbranched Polymer Peptide Hybrid Materials.

作者信息

Qin Yan, Yi Jianguo, Zhang Yue

机构信息

Hebei Key Laboratory of Functional Polymers, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China.

出版信息

Nanomaterials (Basel). 2023 May 25;13(11):1725. doi: 10.3390/nano13111725.

Abstract

In recent years, the coupling of structurally and functionally controllable polymers with biologically active peptide materials to obtain polymer-peptide hybrids with excellent properties and biocompatibility has led to important research progress in the field of polymers. In this study, a pH-responsive hyperbranched polymer hPDPA was prepared by combining atom transfer radical polymerization (ATRP) with self-condensation vinyl polymerization (SCVP) using a three-component reaction of Passerini to obtain a monomeric initiator ABMA containing functional groups. The pH-responsive polymer peptide hybrids hPDPA/PArg/HA were obtained by using the molecular recognition of polyarginine (β-CD-PArg) peptide modified with β-cyclodextrin (β-CD) on the hyperbranched polymer, followed by the electrostatic adsorption of hyaluronic acid (HA). The two hybrid materials, hPDPA/PArg/HA and hPDPA/PArg/HA could self-assemble to form vesicles with narrow dispersion and nanoscale dimensions in phosphate-buffered (PB) at pH = 7.4. The assemblies exhibited low toxicity as drug carriers of β-lapachone (β-lapa), and the synergistic therapy based on ROS and NO generated by β-lapa had significant inhibitory effects on cancer cells.

摘要

近年来,将结构和功能可控的聚合物与生物活性肽材料偶联,以获得具有优异性能和生物相容性的聚合物-肽杂化材料,这在聚合物领域取得了重要的研究进展。在本研究中,通过原子转移自由基聚合(ATRP)与自缩合乙烯基聚合(SCVP)相结合,利用Passerini三组分反应制备了一种pH响应性超支化聚合物hPDPA,以获得含官能团的单体引发剂ABMA。通过用β-环糊精(β-CD)修饰的聚精氨酸(β-CD-PArg)肽在超支化聚合物上的分子识别,随后进行透明质酸(HA)的静电吸附,获得了pH响应性聚合物肽杂化材料hPDPA/PArg/HA。这两种杂化材料hPDPA/PArg/HA和hPDPA/PArg/HA在pH = 7.4的磷酸盐缓冲液(PB)中可自组装形成具有窄分散性和纳米尺寸的囊泡。这些组装体作为β-拉帕醌(β-lapa)的药物载体表现出低毒性,并且基于β-lapa产生的活性氧(ROS)和一氧化氮(NO)的协同治疗对癌细胞具有显著的抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/10254404/1238658347c1/nanomaterials-13-01725-sch001.jpg

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