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Arzneimittelforschung 2009; 59(3): 141-145
DOI: 10.1055/s-0031-1296377
Antibiotics · Antimycotics · Antiparasitics · Antiviral Drugs · Chemotherapeutics · Cytostatics
Editio Cantor Verlag Aulendorf (Germany)

Liquid Chromatographic-Mass Spectrometry Analysis and Pharmacokinetic Studies of Erianin for Intravenous Injection in Dogs

Honghua Zhou
1   Center for Instrumental Analysis, China Pharmaceutical University, Nanjing, (The People’s Republic of China)
2   Key Laboratory of Drug Quality Control and Pharmacovigilance (China Pharmaceutical University), Ministry of Education, Nanjing, (The People’s Republic of China)
,
Bingxun Yang
3   Zhejiang Tianhuang Medicinal Plant Pharmaceutical Co., Ltd., Hangzhou, (The People’s Republic of China)
,
Min Hong
4   National Standard Laboratory of Pharmacology for Chinese Materia Medica, Nanjing, (The People’s Republic of China)
,
Renling Ma
1   Center for Instrumental Analysis, China Pharmaceutical University, Nanjing, (The People’s Republic of China)
2   Key Laboratory of Drug Quality Control and Pharmacovigilance (China Pharmaceutical University), Ministry of Education, Nanjing, (The People’s Republic of China)
,
Longsheng Sheng
1   Center for Instrumental Analysis, China Pharmaceutical University, Nanjing, (The People’s Republic of China)
› Author Affiliations
Further Information

Publication History

Publication Date:
13 December 2011 (online)

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Abstract

The purpose of the present study was to examine the pharmacokinetic characteristics of erianin (2-methoxy-5-[2-(3,4,5-trimethoxyphenyl)-ethyl]-phenol, CAS 95041-90-0), a nature product extracted from Dendrobium chrysotoxum, having notable antitumour activity, after intravenous injection of erianin fat emulsion to beagle dogs. An HPLC-MS method was developed to analyze the erianin levels in dog plasma and validated in a pharmacokinetic study. Plasma profiles were obtained after intravenous injection of erianin fat emulsion at the doses 7.5, 15 and 30 mg/kg. The elimination half-life (t1/2) values for erianin were estimated to be 1.41 ± 0.31, 1.66 ± 0.19, 1.60 ± 0.28 h, while the mean area under concentration-time curve (AUC0–∞) values were 1021.3 ± 373.7, 2305.1 ± 597.0 and 3952.1 ± 378.2 ngh/ml, respectively. In conclusion, the present observations indicated that erianin plasma concentrations were clearly dose-proportional for the dose range studied. There was no gender difference in pharmacokinetics for erianin in male and female dogs.

Key words

Antitumour agents - CAS 95041-90-0 - Erianin, dog plasma, HPLC-ESI-MS, pharmacokinetics
 

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