alexa
Reach Us +3225889658
Determination of Tacrolimus in Rat Whole Blood Utilizing Triple Quadrupole LC/MS | OMICS International | Abstract
ISSN: 2155-9872

Journal of Analytical & Bioanalytical Techniques
Open Access

Like us on:

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Research Article

Determination of Tacrolimus in Rat Whole Blood Utilizing Triple Quadrupole LC/MS

A. R. Suresh Babu*, B. Thippeswamy and A. B. Vinod

A.R.Suresh Babu, Department of Bioanalytical, G7Synergon Pvt Ltd, No537, 9th cross, 5th main, Tatanagar, Sahakaranagar post, Bangalore-560092, India

*Corresponding Author:
Dr. A.R.Suresh Babu
Department of Bioanalytical
G7Synergon Pvt Ltd,
No537, 9th cross, 5th main, Tatanagar
Sahakaranagar post, Bangalore-560092, India
Tel: +91 080-22172700
E-mail: [email protected] ,[email protected]

Received date: January 31, 2011; Accepted date: March 26, 2011; Published date: March 30, 2011

Citation: Babu ARS, Thippeswamy B, Vinod AB (2011) Determination of Tacrolimus in Rat Whole Blood Utilizing Triple Quadrupole LC/MS. J Anal Bioanal Tech 2:118. doi: 10.4172/2155-9872.1000118

Copyright: © 2011 Babu ARS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

A simple, sensitive and rapid method was developed for quantitation of tacrolimus in rat whole blood utilizing triple Quadrupole LC/MS. An aliquot of 0.1 mL of whole blood sample was extracted with t-butyl methyl ether using a Heidolph vortexer. The chromatographic separation was performed by using chromolith fast gradient HPLC RP 18e (2mmX50mm.i.d) column with a mobile phase of 90% methanol and 10% 2mM ammonium acetate buffer followed by MS/MS detection. The analyte was quantitated in negative ionization mode. Multiple reaction monitoring (MRM) using the transition m/z 802.4→560.2 and m/z 808.4→548.6 was performed to quantify tacrolimus with IS (pimecrolimus), respectively. The method had a total chromatographic run time of 2.5 min; and linear calibration curves over the concentration range of 20.931 -1000.703 ng/mL.The lower limit of quantification (LLOQ) was 20.931 ng/mL. Use of sodium citrate (3.85%) as an anticoagulant in rat whole blood and samples were stable for at least the time required to assay the number of samples that could be placed in the auto sampler which is maintaining temperature of 10°C. The between and within batch precision and accuracy of the method were determined by using 6 quality control samples. The highest %CV 478.908 ng/mL (8.01% within run & 3.07 between run), with other %CV<5%. The recovery ranged 23.92% for tacrolimus over range of 50.285 to 798.179 ng/mL and was 18.52% for pimecrolimus respectively. The validated method was successfully applied to the quantification of tacrolimus concentration in rat whole blood.

Keywords

Recommended Conferences
Share This Page
Top