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Merck
  • Simultaneous determination of tazarotene and its active metabolite tazarotenic acid in minipig plasma by LC-MS/MS and its application in pharmacokinetic study after topical administration of tazarotene gel.

Simultaneous determination of tazarotene and its active metabolite tazarotenic acid in minipig plasma by LC-MS/MS and its application in pharmacokinetic study after topical administration of tazarotene gel.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (2015-01-01)
Ying Tong, Hong Pan, Chenglong Sun, Xiaofei Xin, Li Ding, Pengcheng Ma
초록

To study the systemic exposure of tazarotene formulation after topical administration, a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for the simultaneous determination of tazarotene and tazarotenic acid in minipig plasma. Similar extraction recoveries for both analytes were obtained after the plasma samples were acidified by glacial acetic acid (5%) and extracted by ethyl ether-cyclohexane (4:1, v/v). Separation of the analytes was achieved within a short time by the addition of 0.1% formic acid to the mobile phase. Gradient elution was used to avoid the matrix effect. The method was linear over the concentration range of 10-600 pg/mL for both analytes. The data of intra- and inter-run precision and accuracy were lower than 5.2%, 7.3% and 7.3% for both analytes. The developed method can be applied to investigate the transdermal pharmacokinetics and the systemic exposure of tazarotene formulation after topical administration.

MATERIALS
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Ammonium acetate, 99.999% trace metals basis
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Acetic acid, analytical standard
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Cyclohexane, analytical standard
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Acetic acid-12C2, 99.9 atom % 12C
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Acetonitrile solution, contains 0.1 % (v/v) trifluoroacetic acid, suitable for HPLC
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Diethyl ether, contains 1 ppm BHT as inhibitor, anhydrous, ≥99.7%
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Acetic acid, natural, ≥99.5%, FG
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Cyclohexane, anhydrous, 99.5%
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Diethyl ether
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