Volume 39, Issue 7 pp. 864-867
Article

Monitoring of Epidermal Growth Factor Degradation Products by High-Performance Liquid Chromatography

Hyunbin Kim

Hyunbin Kim

College of Pharmacy, Sunchon National University, Suncheon 57922, South Korea

These authors contributed equally to this work.Search for more papers by this author
Chan Seo

Chan Seo

College of Pharmacy, Sunchon National University, Suncheon 57922, South Korea

These authors contributed equally to this work.Search for more papers by this author
Moongi Ji

Moongi Ji

College of Pharmacy, Sunchon National University, Suncheon 57922, South Korea

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Youngbae Kim

Youngbae Kim

College of Pharmacy, Sunchon National University, Suncheon 57922, South Korea

Korea Research Institute of Bioscience and Biotechnology, Jeongup 56212, South Korea

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Jung Dong Kim

Jung Dong Kim

Raphas, Avison Biomedical Research Center, Seoul, South Korea

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Do Hyeon Jeong

Do Hyeon Jeong

Raphas, Avison Biomedical Research Center, Seoul, South Korea

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Wonjae Lee

Wonjae Lee

College of Pharmacy, Chosun University, Gwangju 501-759, South Korea

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Man-Jeong Paik

Corresponding Author

Man-Jeong Paik

College of Pharmacy, Sunchon National University, Suncheon 57922, South Korea

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First published: 07 June 2018
Citations: 1

Abstract

Epidermal growth factor (EGF) has an anti-aging effect of skin. In this study, a HPLC method was developed to monitor of EGF degradation products from pure EGF as a cosmetic raw material. The optimized mobile phase was 7.5 mM sodium phosphate buffer (pH 6.8) at flow rate of 0.6 mL/min. In the method validation of pure EGF, it showed good linearity (r ≥ 0.999) with a detection limit of 0.5 ng/mL. Intra- and inter-day repeatability as a percentage of relative standard deviation (%RSD) varied from 0.01-2.1, and accuracy was 1.1 as the percentage of relative error (%RE). Under optimized conditions, four peaks of pure EGF and three degradation products were observed after storage at room temperature for 12 days. Pure EGF represented as 97.78 ± 0.03% from the total area of the four peaks, whereas the three unknown peaks showed as 0.53 ± 0.01%, 0.61 ± 0.01%, and 1.08 ± 0.01%, respectively. The present method will be useful for the purity and stability tests of EGF in cosmetic materials and products.

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