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The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application

A novel synthetic hexapeptide (SFKLRY-NH(2)) that displays angiogenic activity has been identified by positional scanning of a synthetic peptide combinatorial library (PS-SPCL). This study was carried out to investigate the irritation of the SFKLRY-NH(2) on the skin. The tests were performed on the...

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Detalles Bibliográficos
Autores principales: Kim, Dong Ha, Lim, Yun Young, Kim, Hyeong Mi, Kim, So Young, Kim, Beom Joon, Park, Sung-Gil, Lee, Taehoon, Cho, Soo-Muk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Toxicology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834399/
https://www.ncbi.nlm.nih.gov/pubmed/24278589
http://dx.doi.org/10.5487/TR.2012.28.1.051
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author Kim, Dong Ha
Lim, Yun Young
Kim, Hyeong Mi
Kim, So Young
Kim, Beom Joon
Park, Sung-Gil
Lee, Taehoon
Cho, Soo-Muk
author_facet Kim, Dong Ha
Lim, Yun Young
Kim, Hyeong Mi
Kim, So Young
Kim, Beom Joon
Park, Sung-Gil
Lee, Taehoon
Cho, Soo-Muk
author_sort Kim, Dong Ha
collection PubMed
description A novel synthetic hexapeptide (SFKLRY-NH(2)) that displays angiogenic activity has been identified by positional scanning of a synthetic peptide combinatorial library (PS-SPCL). This study was carried out to investigate the irritation of the SFKLRY-NH(2) on the skin. The tests were performed on the basis of Korea Food and Drug Administration (KFDA) guidelines. In results, cell toxicity is not appeared for SFKLRY-NH(2) in HaCaT cells and B16F10 cells. SFKLRY-NH(2) induced no skin irritation at low concentration (10 μM), mild irritation at high concentration (10mM). We consider that this result is helpful for saying about the safety of SFKLRY-NH(2) in clinical use.
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spelling pubmed-38343992013-11-25 The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application Kim, Dong Ha Lim, Yun Young Kim, Hyeong Mi Kim, So Young Kim, Beom Joon Park, Sung-Gil Lee, Taehoon Cho, Soo-Muk Toxicol Res Articles A novel synthetic hexapeptide (SFKLRY-NH(2)) that displays angiogenic activity has been identified by positional scanning of a synthetic peptide combinatorial library (PS-SPCL). This study was carried out to investigate the irritation of the SFKLRY-NH(2) on the skin. The tests were performed on the basis of Korea Food and Drug Administration (KFDA) guidelines. In results, cell toxicity is not appeared for SFKLRY-NH(2) in HaCaT cells and B16F10 cells. SFKLRY-NH(2) induced no skin irritation at low concentration (10 μM), mild irritation at high concentration (10mM). We consider that this result is helpful for saying about the safety of SFKLRY-NH(2) in clinical use. The Korean Society of Toxicology 2012-03 /pmc/articles/PMC3834399/ /pubmed/24278589 http://dx.doi.org/10.5487/TR.2012.28.1.051 Text en Copyright ©2012, The Korean Society of Toxicology
spellingShingle Articles
Kim, Dong Ha
Lim, Yun Young
Kim, Hyeong Mi
Kim, So Young
Kim, Beom Joon
Park, Sung-Gil
Lee, Taehoon
Cho, Soo-Muk
The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application
title The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application
title_full The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application
title_fullStr The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application
title_full_unstemmed The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application
title_short The Safety Evaluation of a Potent Angiogenic Activator, Synthetic Peptide (SFKLRY-NH(2)) for the Skin Application
title_sort safety evaluation of a potent angiogenic activator, synthetic peptide (sfklry-nh(2)) for the skin application
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834399/
https://www.ncbi.nlm.nih.gov/pubmed/24278589
http://dx.doi.org/10.5487/TR.2012.28.1.051
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