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细胞毒性肽两亲物自组装成超分子膜用于癌症治疗。

Self-assembly of cytotoxic peptide amphiphiles into supramolecular membranes for cancer therapy.

机构信息

Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA.

出版信息

Adv Healthc Mater. 2013 Jan;2(1):126-33. doi: 10.1002/adhm.201200118. Epub 2012 Jul 31.

Abstract

Peptide amphiphiles (PAs) provide a versatile platform for the design of complex and functional material constructs for biomedical applications. The hierarchical self-assembly of PAs with biopolymers is used to create robust hybrid membranes with molecular order on the micron scale. Fabrication of membranes by assembling hyaluronic acid with positively charged PA nanostructures containing anti-cancer PAs bearing a (KLAKLAK)(2) peptide sequence is reported here. Changes in membrane microstructure as the positively charged PA nanostructures vary from cylindrical nanofibers to spherical aggregates are characterized. Results indicate that formation of highly aligned fibrous membranes requires a threshold concentration of nanofibers in solution. Additionally, variation of PA nanostructure morphology from spherical aggregates to cylindrical nanofibers allows membranes to act either as reservoirs for sustained release of cytotoxicity upon enzymatic degradation or as membranes with surface-bound cytotoxicity, respectively. Thus, the self-assembly processes of these PA-biopolymer membranes can be potentially used to design delivery platforms for anti-cancer therapeutics.

摘要

肽两亲物(PAs)为设计用于生物医学应用的复杂且功能化的材料结构提供了一个通用的平台。通过将 PAs 与生物聚合物进行分级自组装,可以在微米尺度上构建具有分子有序性的坚固混合膜。本文报道了通过组装透明质酸与含有抗癌肽(KLAKLAK)(2)肽序列的带正电荷的 PA 纳米结构来制造膜。表征了带正电荷的 PA 纳米结构从圆柱状纳米纤维到球形聚集体的变化对膜微观结构的影响。结果表明,形成高度取向的纤维状膜需要溶液中纳米纤维的阈值浓度。此外,从球形聚集体到圆柱状纳米纤维的 PA 纳米结构形态的变化使得膜可以分别作为在酶降解时持续释放细胞毒性的储库或作为具有表面结合细胞毒性的膜。因此,这些 PA-生物聚合物膜的自组装过程可用于设计抗癌治疗药物的递送平台。

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