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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2003, Vol. 8 ›› Issue (2): 180-182.

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Determination of nifedipine in plasma by reversed phase high-performance liquid chromatography

ZHOU Mao-Jin, JIAO Jian-Jie, DONG Wei-Lin, MENG-Lin, GAO Wei-Zhen, ZHENG-Yao, LIU Yan-Xia, ZHANG Cai-Li, LOU Jian-Shi   

  1. Department of Pharmacology, Tianjin Medical University, Tianjin 300080
  • Received:2002-11-06 Revised:2002-11-22 Online:2003-04-26 Published:2020-11-25

Abstract: AIM: To develop a HPLC method for the determination of nifedipine in plasma. METHODS: Nitrendipine was used as the internal standard and 1.0 ml lasma was extracted by n-hexane-ethylacetate (3 ∶1)in a two-step extraction.The organic layer was transferred to another tube and evaporated to dryness under a stream of nitrogen gas at 55 ℃.The residue was reconstituted with the mobile phase. RESULTS: the linearity was obtained from 5 to 200 μg·L-1 of nifedipine in plasma with a good correlation (r=0.9999, n=6).The recoveries of nifedipine were 90.13% to 99.43%, and the coefficients of variation of within-day and between-days were 1.43% to 6.61% and 3.85% to 8.79%, and the average absolute recoveries of nifedipine and internal standard were 90.58% and 91.59% for the low, middle and high concentration of check samples, respectively.Endogenous substance did not interfere in the analysis. CONCLUSION:~This method is sensitive, specific and simple and suited for the nifedipine pharmacokinetic study.

Key words: pharmacology, nifedipine, plasma concentration, HPLC

CLC Number: