Issue 10, 2021, Issue in Progress

Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug

Abstract

The development of sustained control drug release for delivering hydrophilic drugs has been challenging due to a burst release. Nanofibers are used as materials that enable efficient drug delivery systems. In this study, we designed drug-encapsulated core–shell nanofibers comprising a hydrophilic core of collagen (Col) incorporated with berberine chloride (BC), an anti-inflammatory and anti-cancer agent used as a model drug, and a hydrophobic shell of poly-L-lactic acid (PLLA). Long-term drug release profiles under both the physiological and hydrolysis-accelerated conditions were measured and analyzed using a Korsmeyer–Peppas kinetics model. We found that the Col/PLLA core–shell fiber achieved a controllable long-term release of the hydrophilic drug incorporated inside the core by the slow degradation of the PLLA shell to prevent the burst release while PLLA monolithic fibers showed early release due to the dissolution of drug and the following rapid hydrolysis of fibers. As shown by the results of Col/PLLA core–shell fiber under a hydrolysis-accelerated condition to promote the release of drugs test, it would provide sustained release over 16 days under physiological conditions. Here, the development of the nanomaterial for the long-term drug release of hydrophilic drugs was achieved, leading to its potential medical application including cancer treatment.

Graphical abstract: Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug

Supplementary files

Article information

Article type
Paper
Submitted
30 Sep 2020
Accepted
13 Jan 2021
First published
02 Feb 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 5703-5711

Electrospun collagen core/poly-L-lactic acid shell nanofibers for prolonged release of hydrophilic drug

W. Huang, T. Hibino, S. Suye and S. Fujita, RSC Adv., 2021, 11, 5703 DOI: 10.1039/D0RA08353D

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