1. Academic Validation
  2. Simultaneous determination of 2',3'-dideoxyinosine and the active metabolite, 2',3'-dideoxyadenosine-5'-triphosphate in human peripheral-blood mononuclear cell by HPLC-MS/MS and the application to cell pharmacokinetics

Simultaneous determination of 2',3'-dideoxyinosine and the active metabolite, 2',3'-dideoxyadenosine-5'-triphosphate in human peripheral-blood mononuclear cell by HPLC-MS/MS and the application to cell pharmacokinetics

  • J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Oct 1;1002:337-42. doi: 10.1016/j.jchromb.2015.08.039.
Xu Lan 1 Lei Mingdao 2 Guo Huilin 3 Gan Wei 3 Hu Lvjiang 3 Zhou Yan 4 Li Gang 5
Affiliations

Affiliations

  • 1 Department of Pharmacy, 94 Hospital of Nanjing Military Region, NO 1028 Jinggangshan street, Nanchang 330001, China.
  • 2 Department of Pharmacy, Jiangxi Maternal and Child Health Hospital, NO 318 Bayi Road, Nanchang 330001, China.
  • 3 Department of Pharmacy, Jiangxi University of Traditional Chinese Medicine, NO 818 Xingwan Road, Nanchang 330004, China.
  • 4 Department of Infectious Diseases, The Ninth hospital of Nanchang, No. 167 South Hongdu Road, Nanchang 330002, China.
  • 5 Department of Pharmacy, 94 Hospital of Nanjing Military Region, NO 1028 Jinggangshan street, Nanchang 330001, China. Electronic address: [email protected].
Abstract

A specific and reliable HPLC-MS/MS method was developed and validated for the simultaneous determination of 2',3'-dideoxyinosine (ddI) and the active metabolites, 2',3'-dideoxyadenosine-5'-triphosphate (ddA-TP) in human peripheral-blood mononuclear cell for the first time. The analytes were separated on a HILIC column (100mm×2.1mm, 1.7μm) and a triple-quadrupole mass spectrometry equipped with an electrospray ionization (ESI) source was used for detection. The cell homogenates sample was prepared by the solid phase extraction. The calibration curves were linear over a concentration range of 0.5-200.0ng/mL for ddI and 0.25-100.0ng/mL for ddA-TP. The intra-day and inter-day precision was less than 15% and the relative error (RE) were all within ±15%. The validated method was successfully applied to assess the disposition characteristics of ddI and support cell pharmacokinetics after the patients with AIDS were orally administrated with ddI and tenofovir disoproxyl fumarate (TDF).

Keywords

Cell pharmacokinetics; HPLC–MS/MS; Interaction; dA-TP; ddI.

Figures
Products