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利用导电聚合物纳米粒子包封和储存治疗性纤维蛋白归巢肽,通过电刺激实现程序化释放。

Encapsulation and Storage of Therapeutic Fibrin-Homing Peptides using Conducting Polymer Nanoparticles for Programmed Release by Electrical Stimulation.

机构信息

Departament d'Enginyeria Quı́mica and Barcelona Research Center for Multiscale Science and Engineering, EEBE, Universitat Politècnica de Catalunya, C/Eduard Maristany 10-14, 08019 Barcelona, Spain.

Institute for Bioengineering of Catalonia, The Barcelona Institute of Science and Technology, Baldiri Reixac 10-12, 08028 Barcelona, Spain.

出版信息

ACS Biomater Sci Eng. 2020 Apr 13;6(4):2135-2145. doi: 10.1021/acsbiomaterials.9b01794. Epub 2020 Mar 5.

DOI:10.1021/acsbiomaterials.9b01794
PMID:33455313
Abstract

Cys-Arg-Glu-Lys-Ala (CREKA) is an important fibrin-homing pentapeptide that has been extensively demonstrated for diagnoses and therapies (e.g., image diagnosis of tumors and to inhibit tumor cell migration and invasion). Although CREKA-loaded nanoparticles (NPs) have received major interest as efficient systems for cancer Herein, we report the development of conductive polymer NPs as therapeutic CREKA carriers for controlled dose administration through electric stimuli. Furthermore, the study was extended to CR(Me)EKA, a previously engineered CREKA analogue in which Glu was replaced by -methyl-Glu for improvement of the peptide resistance against proteolysis, which is one of the major weaknesses of therapeutic peptide delivery, and for enhancement of the tumor homing capacity by overstabilizing the bioactive conformation. Particularly, the present work is focused on understanding the interactions between the newly designed nanoengineered materials and biological fluids and the achievement of a modulated peptide release by fine-tuning the electrical . Two different types of stimuli were compared, chronoamperometry versus cyclic voltammetry, the latter being more effective.

摘要

Cys-Arg-Glu-Lys-Ala (CREKA) 是一种重要的纤维蛋白归巢五肽,已被广泛用于诊断和治疗(例如,肿瘤的图像诊断以及抑制肿瘤细胞迁移和侵袭)。尽管载有 CREKA 的纳米颗粒(NPs)已作为有效的癌症治疗系统引起了广泛关注,但此处我们报告了导电聚合物 NPs 的开发,作为通过电刺激进行受控剂量给药的治疗性 CREKA 载体。此外,该研究还扩展到了 CR(Me)EKA,这是一种以前设计的 CREKA 类似物,其中 Glu 被 -甲基-Glu 取代,以提高肽对蛋白水解的抗性,这是治疗性肽递送的主要弱点之一,并且通过过度稳定生物活性构象来增强肿瘤归巢能力。特别是,目前的工作侧重于理解新设计的纳米工程材料与生物流体之间的相互作用,并通过精细调整电来实现调节肽释放。比较了两种不同类型的刺激,计时安培法与循环伏安法,后者更有效。

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