色谱

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高效液相色谱-荧光检测法测定人血浆中匹伐他汀的含量

OJHA Ashwini, GUTTIKAR Swati, VAYEDA Chintan, PADH Harish

  

  1. B.V.Patel, Pharmaceutical Education & Research Development (PERD) Centre, Ahmedabad, Gujarat, India

  • 收稿日期:2007-05-08 修回日期:2007-06-28 出版日期:2007-09-30 发布日期:1985-03-25
  • 通讯作者: Harish Padh

Determination of Pitavastatin from Human Plasma Using High Performance Liquid Chromatography with Fluorescence Detection

OJHA Ashwini, GUTTIKAR Swati, VAYEDA Chintan, PADH Harish

  

  1. B.V.Patel, Pharmaceutical Education & Research Development (PERD) Centre, Ahmedabad, Gujarat, India

  • Received:2007-05-08 Revised:2007-06-28 Online:2007-09-30 Published:1985-03-25
  • Contact: Harish Padh

摘要:

Pitavastatin belongs to the class of coenzyme A reductase inhibitors. Very few methods of assaying pitavastatin from human plasma are available in literature. An analytical method is presented for the determination of the drug from human plasma making use of the fluorescent property of the drug. The drug is extracted from plasma using ethyl acetate under neutral condition and then analyzed by reversed-phase high performance liquid chromatography (HPLC) with fluorescence detection (λEx 245 nm; λEm 420 nm). Analysis of pitavastatin was carried out on a C18 HPLC column using a gradient flow of mobile phase (0.01 mol/L monobasic potassium phosphate (pH 3.20)-acetonitrile, 63∶37, v/v). Fluorescein isothiocyanate was used as internal standard. The dynamic range of assay was 3 to 50 ng/mL. The intraday precision was less than 10% and accuracy ranged from 95.2% to 112.6%. The same for interday check was less than 12% and 92.8% to 105.1%, respectively. The drug was found to be stable under the assay conditions. The developed method is simple, precise, accurate, and stable. This indicates that it can be applied to routine analysis of this drug in human subjects where there are large numbers of samples without the need of specialized instruments like column switching.

关键词: fluorescein isothiocyanate, fluorescence detection, human plasma , pitavastatin, high performance liquid chromatography (HPLC)

Abstract:

Pitavastatin belongs to the class of coenzyme A reductase inhibitors. Very few methods of assaying pitavastatin from human plasma are available in literature. An analytical method is presented for the determination of the drug from human plasma making use of the fluorescent property of the drug. The drug is extracted from plasma using ethyl acetate under neutral condition and then analyzed by reversed-phase high performance liquid chromatography (HPLC) with fluorescence detection (λEx 245 nm; λEm 420 nm). Analysis of pitavastatin was carried out on a C18 HPLC column using a gradient flow of mobile phase (0.01 mol/L monobasic potassium phosphate (pH 3.20)-acetonitrile, 63∶37, v/v). Fluorescein isothiocyanate was used as internal standard. The dynamic range of assay was 3 to 50 ng/mL. The intraday precision was less than 10% and accuracy ranged from 95.2% to 112.6%. The same for interday check was less than 12% and 92.8% to 105.1%, respectively. The drug was found to be stable under the assay conditions. The developed method is simple, precise, accurate, and stable. This indicates that it can be applied to routine analysis of this drug in human subjects where there are large numbers of samples without the need of specialized instruments like column switching.

Key words: fluorescein isothiocyanate, fluorescence detection, human plasma , pitavastatin, high performance liquid chromatography (HPLC)