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Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug
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 co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694765/ https://www.ncbi.nlm.nih.gov/pubmed/35423091 http://dx.doi.org/10.1039/d0ra08353d |
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author | Huang, Wan-Ying Hibino, Toshiya Suye, Shin-ichiro Fujita, Satoshi |
author_facet | Huang, Wan-Ying Hibino, Toshiya Suye, Shin-ichiro Fujita, Satoshi |
author_sort | Huang, Wan-Ying |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8694765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86947652022-04-13 Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug Huang, Wan-Ying Hibino, Toshiya Suye, Shin-ichiro Fujita, Satoshi RSC Adv Chemistry 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. The Royal Society of Chemistry 2021-02-02 /pmc/articles/PMC8694765/ /pubmed/35423091 http://dx.doi.org/10.1039/d0ra08353d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Huang, Wan-Ying Hibino, Toshiya Suye, Shin-ichiro Fujita, Satoshi Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug |
title | Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug |
title_full | Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug |
title_fullStr | Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug |
title_full_unstemmed | Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug |
title_short | Electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug |
title_sort | electrospun collagen core/poly-l-lactic acid shell nanofibers for prolonged release of hydrophilic drug |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694765/ https://www.ncbi.nlm.nih.gov/pubmed/35423091 http://dx.doi.org/10.1039/d0ra08353d |
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