Issue 73, 2017, Issue in Progress

pH sensitive mesoporous nanohybrids with charge-reversal properties for anticancer drug delivery

Abstract

The surface/interface state of nanomaterials plays a key role on their biomedical applications. Nanotechnology offers a versatile means to develop nanoparticles with well-defined architecture. In this study, mesoporous silica nanoparticles were firstly loaded with an anticancer drug (doxorubicin, DOX), which were then decorated with a cationic oligomer (low molecular weight polyethyleneimine, LPEI) to acquire an increased surface charge. The resulting particles were further self-assembled with negative-charged bovine serum albumin (BSA) as natural protein nanoblocks to offer surface charge tunability. The resulting mesoporous nanohybrids (MDPB) acquired charge-reversal ability, which presented negative charge under biological conditions (beneficial to biocompatibility), while displaying a positive-charged state under acidic conditions mimicking the tumor extracellular microenvironment (favoring cell uptake or tumor penetration). Furthermore, the nanohybrids not only allowed for an effective loading of DOX drug, but also accelerated its release under acidic tumor microenvironments in a sustainable way. In vitro biological study indicated that the DOX-free nanoparticles were biocompatible, while MDPB exerted good cytotoxicity against cancer cells, suggesting their promise for therapeutic delivery application.

Graphical abstract: pH sensitive mesoporous nanohybrids with charge-reversal properties for anticancer drug delivery

Article information

Article type
Paper
Submitted
26 May 2017
Accepted
26 Aug 2017
First published
28 Sep 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 46045-46050

pH sensitive mesoporous nanohybrids with charge-reversal properties for anticancer drug delivery

B. Wu, S. Deng, S. Zhang, J. Jiang, B. Han and Y. Li, RSC Adv., 2017, 7, 46045 DOI: 10.1039/C7RA05912D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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