bioactive markers based pharmacokinetic evaluation of extracts of a traditional medicinal plant, piper sarmentosum提取物的生物活性标记基于药代动力学评价传统的药用植物,派珀sarmentosum.pdfVIP
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bioactive markers based pharmacokinetic evaluation of extracts of a traditional medicinal plant, piper sarmentosum提取物的生物活性标记基于药代动力学评价传统的药用植物,派珀sarmentosum
Hindawi Publishing Corporation
Evidence-Based Complementary and Alternative Medicine
Volume 2011, Article ID 980760, 7 pages
doi:10.1093/ecam/nep143
Original Article
Bioactive Markers Based Pharmacokinetic Evaluation of
Extracts of a Traditional Medicinal Plant, Piper sarmentosum
Khalid Hussain, Zhari Ismail, Amirin Sadikun, and Pazillah Ibrahim
Department of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Universiti Sains Malaysia,
Pulau Pinang 11800, Malaysia
Correspondence should be addressed to Khalid Hussain, hussain 761@
Received 4 February 2009; Accepted 25 August 2009
Copyright © 2011 Khalid Hussain et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
In vitro assays are economical and easy to perform but to establish relevance of their results to real clinical outcome in animals
or human, pharmacokinetics is prerequisite. Despite various in vitro pharmacological activities of extracts of Piper sarmentosum,
there is no report of pharmacokinetics. Therefore, the present study aimed to evaluate ethanol extract of fruit of the plant in dose of
500 mg kg−1 orally for pharmacokinetics. Sprague-Dawley rats were randomly divided into groups 1, 2, and 3 (each n = 6) to study
absorption, distribution and excretion, respectively. High performance liquid chromatography (HPLC) with ultraviolet detection
was applied to quantify pellitorine, sarmentine and sarmentosine in plasma, tissues, feces and urine to calculate pharmacokinetic
parameters. Pellitorine exhibited maximum plasma concentration (Cmax ) 34.77 ng mL−1 ± 1.040, time to achieve Cmax (Tmax ) 8 h,
mean resident time (MRT) 26.00 ± 0.149
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