Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell Viability

This study proposes an optimization process of the Lithospermum erythrorhizon (LE) extraction with a higher purity of shikonin (SK). The influence of extraction temperature on the concentration of SK is examined, and an in vitro cell viability assay is used to examine the optimal concentration of SK...

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Main Authors: Ching-Wen Lou, Zong-Han Wu, Mong-Chuan Lee, Yueh-Sheng Chen, Jia-Horng Lin
Format: Article
Language:English
Published: MDPI AG 2017-11-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/7/11/1143
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spelling doaj-ec6516c9ba2047568eae71510232ae242020-11-25T02:42:40ZengMDPI AGApplied Sciences2076-34172017-11-01711114310.3390/app7111143app7111143Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell ViabilityChing-Wen Lou0Zong-Han Wu1Mong-Chuan Lee2Yueh-Sheng Chen3Jia-Horng Lin4Innovation Platform of Intelligent and Energy-Saving Textiles, School of Textiles, Tianjin Polytechnic University, Tianjin 300387, ChinaLaboratory of Fiber Application and Manufacturing, Department of Fiber and Composite Materials, Feng Chia University, Taichung 40768, TaiwanGraduate Institute of Biotechnology and Biomedical Engineering, Central Taiwan University of Science and Technology, Taichung 40601, TaiwanDepartment of Biomedical Imaging and Radiological Science, China Medical University, Taichung 40402, TaiwanInnovation Platform of Intelligent and Energy-Saving Textiles, School of Textiles, Tianjin Polytechnic University, Tianjin 300387, ChinaThis study proposes an optimization process of the Lithospermum erythrorhizon (LE) extraction with a higher purity of shikonin (SK). The influence of extraction temperature on the concentration of SK is examined, and an in vitro cell viability assay is used to examine the optimal concentration of SK. Afterwards, polyvinyl alcohol (PVA)/LE solutions at ratios of 90/10, 80/20, and 70/30 w/w are electrospun into LE electrospun nanofibrous membranes (LENMs). The optimal manufacture parameters of LENMs are evaluated based on the test results of in vitro drug release test and cell viability assay. The optimal concentration occurs when the extraction temperature is −10 °C. The purity of the LE extract reaches 53.8% and the concentration of SK is 1.07 mg/mL. Moreover, the cell viability of nanofibrous membranes significantly increases to 136.8% when 0.7 μM SK is used. The diameter of nanofibers of LENM is decreased by 43.9% when the ratio of PVA solution to LE extract is 70/30 (w/w). 80/20 (w/w) LENM has the maximum amount of drug release of 79% for a continuous period of 48 h. In particular, 90/10 (w/w) LENM can create the maximum cell proliferation of 157.5% in a 24-h in vitro cell viability assay. This suggests that LENM has great potential to be used in facilitating tissue regeneration and wound healing.https://www.mdpi.com/2076-3417/7/11/1143electrospinningnanofiberLithospermum erythrorhizon (LE)shikonin (SK)drug release
collection DOAJ
language English
format Article
sources DOAJ
author Ching-Wen Lou
Zong-Han Wu
Mong-Chuan Lee
Yueh-Sheng Chen
Jia-Horng Lin
spellingShingle Ching-Wen Lou
Zong-Han Wu
Mong-Chuan Lee
Yueh-Sheng Chen
Jia-Horng Lin
Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell Viability
Applied Sciences
electrospinning
nanofiber
Lithospermum erythrorhizon (LE)
shikonin (SK)
drug release
author_facet Ching-Wen Lou
Zong-Han Wu
Mong-Chuan Lee
Yueh-Sheng Chen
Jia-Horng Lin
author_sort Ching-Wen Lou
title Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell Viability
title_short Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell Viability
title_full Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell Viability
title_fullStr Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell Viability
title_full_unstemmed Polyvinyl Alcohol/Lithospermum Erythrorhizon Nanofibrous Membrane: Characterizations, In Vitro Drug Release, and Cell Viability
title_sort polyvinyl alcohol/lithospermum erythrorhizon nanofibrous membrane: characterizations, in vitro drug release, and cell viability
publisher MDPI AG
series Applied Sciences
issn 2076-3417
publishDate 2017-11-01
description This study proposes an optimization process of the Lithospermum erythrorhizon (LE) extraction with a higher purity of shikonin (SK). The influence of extraction temperature on the concentration of SK is examined, and an in vitro cell viability assay is used to examine the optimal concentration of SK. Afterwards, polyvinyl alcohol (PVA)/LE solutions at ratios of 90/10, 80/20, and 70/30 w/w are electrospun into LE electrospun nanofibrous membranes (LENMs). The optimal manufacture parameters of LENMs are evaluated based on the test results of in vitro drug release test and cell viability assay. The optimal concentration occurs when the extraction temperature is −10 °C. The purity of the LE extract reaches 53.8% and the concentration of SK is 1.07 mg/mL. Moreover, the cell viability of nanofibrous membranes significantly increases to 136.8% when 0.7 μM SK is used. The diameter of nanofibers of LENM is decreased by 43.9% when the ratio of PVA solution to LE extract is 70/30 (w/w). 80/20 (w/w) LENM has the maximum amount of drug release of 79% for a continuous period of 48 h. In particular, 90/10 (w/w) LENM can create the maximum cell proliferation of 157.5% in a 24-h in vitro cell viability assay. This suggests that LENM has great potential to be used in facilitating tissue regeneration and wound healing.
topic electrospinning
nanofiber
Lithospermum erythrorhizon (LE)
shikonin (SK)
drug release
url https://www.mdpi.com/2076-3417/7/11/1143
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AT jiahornglin polyvinylalcohollithospermumerythrorhizonnanofibrousmembranecharacterizationsinvitrodrugreleaseandcellviability
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