| Literature DB >> 28952260 |
Yu-Jiao Zhao1, Wen-Hui Xu2, Xiao-Li Shen3, Jun-Sheng Tian1, Xue-Mei Qin1.
Abstract
This research is to establish TLC and UPLC methods for simultaneous determination of 3 atractylenolides in Atractylodes macrocephala. Silica gel GF254 plate was used for identification of A. macrocephala, and UPLC-PDA gradient elution method was used to simultaneously determine atractylenolide Ⅰ, Ⅱ and Ⅲ. The Waters BEH C₁₈ column(2.1 mm×100 mm,1.7 μm)with acetonitrile-water as mobile phase and the wavelength of UV detector of 235 nm were performed. The quality control study showed that the characteristic for identification by TLC was distinct and highly specific. The method of content determination was in accordance with the regulations. The quantitative evaluation of atractylenolide Ⅰ,Ⅱ and Ⅲ was in good linear range(r>0.999 9), and the average recovery was 93.48%(RSD 1.4%),94.97%(RSD 1.6%),92.71%(RSD 1.2%),respectively. TLC identification was in good specificity and repeatability, and the UPLC-PDA method for the simultaneous determination of 3 atractylenolides was simple and reliable for the quality control of A.macrocephala. Copyright© by the Chinese Pharmaceutical Association.Entities:
Keywords: Atractylodes macrocephala ; TLC ; UPLC ; atractylenolide ; quality control
Mesh:
Substances:
Year: 2017 PMID: 28952260 DOI: 10.19540/j.cnki.cjcmm.20161222.074
Source DB: PubMed Journal: Zhongguo Zhong Yao Za Zhi ISSN: 1001-5302