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基于红细胞的递送系统用于释放具有体外抗肿瘤活性的血红蛋白衍生肽

Red Blood Cell-Based Delivery Systems for the Release of Hemoglobin-Derived Peptides with In Vitro Antitumor Activities.

作者信息

Bonatto Cínthia Caetano, Joanitti Graziella Anselmo, Silva Luciano Paulino

机构信息

Postgraduate Program in Animal Biology, University of Brasilia (UnB), Brasília 70910-900, DF, Brazil.

Embrapa Genetic Resources and Biotechnology, Nanobiotechnology Laboratory (LNANO), Parque Estacao Biologica, Final W5 Norte, Brasília 70770-917, DF, Brazil.

出版信息

Pharmaceuticals (Basel). 2025 Apr 14;18(4):570. doi: 10.3390/ph18040570.

Abstract

This study aimed to develop liposomes derived from lipids obtained from red blood cell membranes for potential use in antitumor applications. Hemoglobin hydrolysates exhibiting peptides with known antitumor activities were encapsulated within these liposomes. The developed liposomal systems were characterized by their physicochemical properties, including size, surface charge, and encapsulation efficiency, and tested in vitro against 4T1 breast cancer cells and NIH3T3 fibroblasts. Results indicated that the liposomes achieved effective encapsulation (88.9%), with nanometer-scale sizes (ranging from 140.7 nm for Blank-Liposomes to 658.3 nm for Pep-Liposomes) and stable colloidal properties. : Although cytotoxicity was limited, the use of liposomes from endogenous components, such as red blood cells, demonstrates promise as a complementary approach in anticancer therapy.

摘要

本研究旨在开发源自红细胞膜脂质的脂质体,以用于潜在的抗肿瘤应用。具有已知抗肿瘤活性肽的血红蛋白水解产物被包裹在这些脂质体中。所开发的脂质体系统通过其物理化学性质进行表征,包括大小、表面电荷和包封效率,并在体外针对4T1乳腺癌细胞和NIH3T3成纤维细胞进行测试。结果表明,脂质体实现了有效的包封(88.9%),具有纳米级大小(从空白脂质体的140.7nm到肽脂质体的658.3nm)和稳定的胶体性质。虽然细胞毒性有限,但使用来自内源性成分(如红细胞)的脂质体显示出作为抗癌治疗补充方法的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/314e/12030676/3ffdeac63da6/pharmaceuticals-18-00570-g001.jpg

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