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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2014, Vol. 19 ›› Issue (3): 246-253.

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Effects of Lycium barbarum Polysaccharide on doxorubicin pharmacokinetics in dogs

YU Jian, XIN Yan-fei , GU Li-qiang, GAO Hai-yan, ZHANG Sheng, YOU Zhen-qiang, WEN Lei, CHEN Guo-can, CHEN Yun-xiang, XUAN Yao-xian   

  1. Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou 310013,Zhejiang,China
  • Received:2013-03-26 Revised:2014-02-16 Online:2014-03-26 Published:2014-04-10
  • Contact: Xin Yan-fei, male, correspondece author, investigator, research area: pharmacokinetic.Tel: 0571-87568012 E-mail:xinyanfei@gmail.com。Xuan Yao-xian, female, correspondece author, investigator, Tel: +86-571-87568016 E-mail: nndsvc@mail.hz.zj.cn
  • Supported by:
    Zhejiang Provincial Bureau of Traditional Chinese Medicine (2013ZZ003);the Sciences Technology Department of Zhejiang Province (2012C37098,2013F20005) and Ministry of Science and Technology of China (2011ZX09301-003)

Abstract: AIM: To investigate whether Lycium barbarum Polysaccharide (LBP) could modify the pharmacokinetic property of the doxorubicin (DOX) in Beagle dogs.METHODS: Eight Beagle dogs were treated with LBP capsule (20 mg/kg) or vehicle for 12 continuous days. Plasma concentration of DOX in two groups is monitored after i.v. bolus injection of DOX (1.5 mg/kg) at day 7 and was determined by reverse phase-high performance liquid chromatography with a fluorescence detector. Furthermore, the enzyme activity of cytochrome P450 3A (CYP 3A) in two groups were evaluated.RESULTS: Compared with DOX group, LBP did not modify the pharmacokinetic profiles such as the area under curve and the clearance of DOX in the LPB+DOX group. However, it is proved that LBP could inhibit the activity of CYP 3A , which is a critical metabolizing enzyme of DOX. There is a slight paradox between the inhibition of LBP to CYP 3A and no influence of LBP to pharmacokinetic profiles of intravenous DOX.CONCLUSION: Co-administration of LBP inhibits CYP 3A, the metabolizing enzyme of DOX, but does not affect the pharmacokinetic profiles of intravenous DOX.

Key words: Lycuim barbarum Polysaccharide, cardiotoxicity, herb-drug interaction

CLC Number: