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用于靶向选择性递药的纳米颗粒包裹药物的受体结合肽。

Receptor binding peptides for target-selective delivery of nanoparticles encapsulated drugs.

机构信息

Centro interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Department of Pharmacy and Istituto di Biostrutture e Bioimmagini -Consiglio Nazionale delle Ricerche (IBB CNR), University of Naples "Federico II", Napoli, Italy.

Department of Nuclear Medicine, Istituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione "G. Pascale", Napoli, Italy.

出版信息

Int J Nanomedicine. 2014 Mar 27;9:1537-57. doi: 10.2147/IJN.S53593. eCollection 2014.

Abstract

Active targeting by means of drug encapsulated nanoparticles decorated with targeting bioactive moieties represents the next frontier in drug delivery; it reduces drug side effects and increases the therapeutic index. Peptides, based on their chemical and biological properties, could have a prevalent role to direct drug encapsulated nanoparticles, such as liposomes, micelles, or hard nanoparticles, toward the tumor tissues. A considerable number of molecular targets for peptides are either exclusively expressed or overexpressed on both cancer vasculature and cancer cells. They can be classified into three wide categories: integrins; growth factor receptors (GFRs); and G-protein coupled receptors (GPCRs). Therapeutic agents based on nanovectors decorated with peptides targeting membrane receptors belonging to the GPCR family overexpressed by cancer cells are reviewed in this article. The most studied targeting membrane receptors are considered: somatostatin receptors; cholecystokinin receptors; receptors associated with the Bombesin like peptides family; luteinizing hormone-releasing hormone receptors; and neurotensin receptors. Nanovectors of different sizes and shapes (micelles, liposomes, or hard nanoparticles) loaded with doxorubicin or other cytotoxic drugs and externally functionalized with natural or synthetic peptides are able to target the overexpressed receptors and are described based on their formulation and in vitro and in vivo behaviors.

摘要

通过用靶向生物活性基团修饰的药物包封纳米粒子进行主动靶向,代表了药物输送的下一个前沿领域;它可以降低药物的副作用并提高治疗指数。基于其化学和生物学特性,肽可以在很大程度上发挥作用,将药物包封的纳米粒子(如脂质体、胶束或硬纳米粒子)导向肿瘤组织。许多肽的分子靶标要么仅在癌症血管和癌细胞上表达,要么过表达。它们可以分为三大类:整合素;生长因子受体(GFRs);和 G 蛋白偶联受体(GPCRs)。本文综述了基于肽靶向属于 GPCR 家族的过表达癌细胞的膜受体的纳米载体的治疗剂。被认为是研究最多的靶向膜受体:生长抑素受体;胆囊收缩素受体;与 Bombesin 样肽家族相关的受体;黄体生成素释放激素受体;和神经降压素受体。用阿霉素或其他细胞毒性药物负载并通过天然或合成肽外部功能化的不同大小和形状的纳米载体(胶束、脂质体或硬纳米粒子)能够靶向过表达的受体,并根据其配方以及体外和体内行为进行描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f6/3970945/aeea1c5e7d13/ijn-9-1537Fig1.jpg

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