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Sensitive Determination of Pinaverium Bromide in Human Plasma by LC-ESI-MS/MS : Applicability to Oral Bioavailability Determination

LC-ESI-MS/MS를 이용한 생체시료 중 브롬화피나베리움의 고감도 분석 및 이를 이용한 생체이용률 평가

  • Park, Seok (College of Pharmacy, Chung-Ang University) ;
  • Lee, Ye-Rie (Seoul Medical Science Institute, Seoul Clinical Laboratories) ;
  • Kim, Ho-Hyun (Seoul Medical Science Institute, Seoul Clinical Laboratories) ;
  • Lee, Hee-Joo (Seoul Medical Science Institute, Seoul Clinical Laboratories) ;
  • Kim, Yoon-Gyoon (College of Medicine, Dankook University) ;
  • Youm, Jeong-Rok (College of Pharmacy, Chung-Ang University) ;
  • Han, Sang-Beom (College of Pharmacy, Chung-Ang University)
  • Published : 2004.12.20

Abstract

A sensitive method for quantification of pinaverium bromide in human plasma was established using liquid chromatography-electrospray ionization tandem mass spectrometry(LC-ESI-MS/MS). Glimepiride was used as internal standard. Pinaverium bromide and internal standard in plasma sample were extracted using tert-butylmethylether(TBME). A centrifuged upper layer was then evaporated and reconstituted with mobile phase of acetonitrile-5 mM ammonium formate (80/20, pH 3.0). The reconstituted samples were injected into a $C_{18}$ reversed-phase column. Using MS/MS with multiple reaction monitoring (MRM) mode, pinaverium and glimepirde were detected without severe interference from human plasma matrix. Pinaverium produced a protonated precursor ion $([M+H]^+)$ at m/z 510.3 and a corresponding product ion at m/z 228.9. Internal standard produced a protonated precursor ion $([M+H]^+)$ at m/z 491.5 and a corresponding product ion at m/z 352.0. Detection of pinaverium bromide in human plasma was accurate and precise, with limit of quantitation at 0.5 ng/ml. The method has been successfully applied to bioavailability study of pinaverium bromide tablet in Korean healthy male volunteers. Pharmacokinetic parameters such as $AUC_t,\;C_{max},\;T_{max},\;K_{el}\;and\;t_{1/2}$ were calculated.

Keywords

References

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