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聚乙二醇化聚谷氨酸肽树枝状聚合物的合成及其在溶解血栓中的应用。

Synthesis of PEGylated polyglutamic acid peptide dendrimer and its application in dissolving thrombus.

机构信息

State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province and Department of Chemistry, Lanzhou University, Lanzhou 730000, PR China; Longnan Teacher's College, Longnan, 742500, PR China.

State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province and Department of Chemistry, Lanzhou University, Lanzhou 730000, PR China.

出版信息

Colloids Surf B Biointerfaces. 2017 Nov 1;159:284-292. doi: 10.1016/j.colsurfb.2017.08.009. Epub 2017 Aug 4.

Abstract

Nattokinase (NK) has been used as a new generation thrombolytic drug, due to its high safety, low cost and low side effects. However, it is sensitive to external environment and may lose the enzyme activity easily. Peptide dendrimer possesses functional groups on its surface, adjustable sizes, biodegradability, biocompatibility, and low toxicity, which could be used as ideal carrier for drug protection and delivery. Demonstrated for the first time in this paper, a PEGylated dendrimer (G-PEG-G) composed of polyglutamic acid is designed and synthesized as delivery platform of NK for thrombus treatment. A panel of PEGylated dendrimers with three different generations of 2, 3, 4 was prepared to investigate the effect of dendrimer architecture on the properties and therapeutic efficacy of the resultant NK-loaded delivery systems in terms of the morphology, dimension and enzyme activity. The results demonstrated that the NK-loaded G-PEG-G (G-PEG-G/NK ratio of 6/1), of all the formulations, displayed the optimal enzyme activity for dissolving thrombus in vitro, thus offering great potential for the treatment of thrombus.

摘要

纳豆激酶(NK)已被用作新一代溶栓药物,因其安全性高、成本低、副作用低。然而,它对外界环境敏感,可能容易失去酶活性。肽树状大分子在其表面具有官能团、可调节的大小、生物降解性、生物相容性和低毒性,可用作药物保护和递送的理想载体。本文首次设计并合成了一种由聚谷氨酸组成的聚乙二醇化树状大分子(G-PEG-G),用作 NK 的递送平台,用于血栓治疗。制备了一系列具有 2、3、4 代三种不同代数的聚乙二醇化树状大分子,以研究树状大分子结构对 NK 载药递释系统的形态、尺寸和酶活性的影响。结果表明,在所制备的所有制剂中,NK 负载的 G-PEG-G(G-PEG-G/NK 比为 6/1)具有最佳的体外溶栓酶活性,因此具有治疗血栓的巨大潜力。

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