AI Article Synopsis

  • A rapid and sensitive liquid chromatography/tandem mass spectrometry method was developed to quantify the calcium channel antagonist lacidipine in human plasma, using carbamazepine as an internal standard.
  • The method involved solid-phase extraction and utilized a C(18) column with an acetonitrile-ammonium acetate buffer as the mobile phase, producing a linear calibration curve across a concentration range of 0.05-12.5 ng/mL.
  • The validated protocol demonstrated high precision, accuracy, and a quick run time of 2.2 minutes per sample, allowing the analysis of over 300 plasma samples daily, making it suitable for clinical studies.

Article Abstract

A novel, rapid and sensitive liquid chromatography/tandem mass spectrometry method was developed and validated for the quantification of calcium channel antagonist lacidipine in human plasma. Carbamazepine was used as an internal standard. Analyte and the internal standard were extracted from human plasma by solid-phase extraction technique. The reconstituted samples were chromatographed on a C(18) column by using a mixture of acetonitrile-ammonium acetate buffer (5 mM) (80:20, v/v) as the mobile phase at a flow rate of 1.0 mL/min. The calibration curve obtained was linear (r(2)≥0.9990) over the concentration range of 0.05-12.5 ng/mL. The multiple reaction-monitoring mode was used for quantification of ion transitions at m/z 456.2/354.2 and 237.1/194.1 for the drug and the internal standard, respectively. The results of the intra- and inter-day precision and accuracy studies were well within the acceptable limits. A run time of 2.2 min for each sample made it possible to analyze more than 300 plasma samples per day. The proposed method was found to be applicable to clinical studies.

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Source
http://dx.doi.org/10.1016/j.jpba.2012.02.022DOI Listing

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