Issue 12, 2021

Current advances in nanomaterials affecting morphology, structure, and function of erythrocytes

Abstract

In recent decades, nanomaterials have been widely used in the field of biomedicine due to their unique physical and chemical properties, and have shown good prospects for in vitro diagnosis, drug delivery, and imaging. With regard to transporting nanoparticles (NPs) to target tissues or organs in the body intravenously or otherwise, blood is the first tissue that NPs come into contact with and is also considered an important gateway for targeted transport. Erythrocytes are the most numerous cells in the blood, but previous studies based on interactions between erythrocytes and NPs mostly focused on the use of erythrocytes as drug carriers for nanomedicine which were chemically bound or physically adsorbed by NPs, so little is known about the effects of nanoparticles on the morphology, structure, function, and circulation time of erythrocytes in the body. Herein, this review focuses on the mechanisms by which nanoparticles affect the structure and function of erythrocyte membranes, involving the hemocompatibility of NPs, the way that NPs interact with erythrocyte membranes, effects of NPs on erythrocyte surface membrane proteins and their structural morphology and the effect of NPs on erythrocyte lifespan and function. The detailed analysis in this review is expected to shed light on the more advanced biocompatibility of nanomaterials and pave the way for the development of new nanodrugs.

Graphical abstract: Current advances in nanomaterials affecting morphology, structure, and function of erythrocytes

Article information

Article type
Review Article
Submitted
01 Dec 2020
Accepted
27 Jan 2021
First published
10 Feb 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 6958-6971

Current advances in nanomaterials affecting morphology, structure, and function of erythrocytes

Y. Tian, Z. Tian, Y. Dong, X. Wang and L. Zhan, RSC Adv., 2021, 11, 6958 DOI: 10.1039/D0RA10124A

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