Simultaneous Determination of Shikonin, Acetylshikonin and β, β-dimethylacrylshikonin in Arnebia euchroma by RP-HPLC
10.6039/j.issn.1001-0408.2018.04.06
- VernacularTitle:RP-HPLC法同时测定新疆紫草中紫草素、乙酰紫草素、β,β-二甲基丙烯酰紫草素的含量
- Author:
Jianwen SUN
1
;
Xianchun WEN
;
Defu CAI
;
Yue WANG
;
Yonghui WU
Author Information
1. 哈尔滨医科大学公共卫生学院劳动卫生教研室
- Keywords:
Arnebia euchroma;
Shikonin;
Acetylshikonin;
β;
β-dimethylacrylshikonin;
RP-HPLC;
Content
- From:
China Pharmacy
2018;29(4):455-457
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE: To establish a method for the simultaneous determination of shikonin, acetylshikonin and β, β-dimethylacrylshikonin in Arnebia euchroma. METHODS: RP-HPLC method was adopted. The determination was performed on Kromasil 100-5 C18 column with mobile phase consisted of acetonitrile-0. 1％ formic acid solution (80: 20, V/V) at the flow rate of 1. 0 mL/min. The detection wavelength was set at 516 nm, column temperature was 25 ℃, and sample size was 10 μL. RESULTS: The linear ranges of shikonin, acetylshikonin and β, β-dimethylacrylshikonin were 0. 404-10. 100 μg/mL(r=0. 999 8), 5. 350-107. 000 μg/mL(r=0. 999 6), 2. 035-40. 700 μg/mL(r=0. 999 8), respectively. The limit of quantitation was 0. 40, 2. 91, 1. 34 μg/mL, and the limit of detection was 0. 12, 0. 87, 0. 40 μg/mL. RSDs of precision, stability and reproducibility tests were all lower than 2. 0％ (n=6). The recovery rate were 99. 12％-104. 18％ (RSD=1. 85％, n=6), 96. 51％-100. 21％ (RSD=1. 43％, n=6), 98. 11％-102. 51％ (RSD=1. 42％, n=6), respectively. CONCLUSIONS: The method is simple, precise, stable and reproducible. It can be used for simultaneous determination of shikonin, acetylshikonin and β, β-dimethylacrylshikonin in A. euchroma.
