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Comparative study of different detection methods on prescription design of ginkgo biloba extract with sustained release preparation
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DOI   10.11656/j.issn.1673-9043.2013.03.10
Key Words   Ginkgo biloba extract;UV spectrophotometry;HPLC;sustained release preparation;similarity factor method
Author NameAffiliationE-mail
GUO Ying-xin School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China  
PAN Wei-san School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China  
LI Fei School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China  
ZHAO Qian-qian School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China  
XIAO Wei Jiangsu Kanion Pharmaceut Co Ltd, Lianyungang 222001, China
State Key Laboratory of New-tech for Chinese Medicine Pharmaceutical Process, Lianyungang 222001, China 
 
XU Lu School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China  
YANG Xing-gang School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
State Key Laboratory of New-tech for Chinese Medicine Pharmaceutical Process, Lianyungang 222001, China 
yangxg123@163.com 
Abstract
    [Objective] To investigate the quantitative determination of flavonol glycosides in ginkgo biloba extract using UV spectrophotometry and HPLC, then establish a simple, effective and reliable method for the prescription design of ginkgo biloba extract of sustained release preparation. [Methods] The total flavonoid glycosides were used as the reference compound for UV spectrophotometry. The Quercetin, Kaempferide and Isorhamnetin were used as the reference compound for HPLC. The similarity between UV and HPLC was estimated by the similarity factor method, which was recommended by FDA. [Results] The methodological evaluation showed that those two detection methods met the requirements, and had good similarity. [Conclusion] During the course of prescription design of ginkgo biloba extract of sustained release preparation, the method of UV can be used to determine the content of flavonol glycosides instead of HPLC. This method is simple, accurate and reliable.

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