Validation and Optimization of a Simple RP-HPLC Method for the Determination of Paracetamol in Human Serum and its Application in a Pharmacokinetic Study with Healthy Bangladeshi Male Volunteers

Abstract

Acetaminophen (paracetamol) is an analgesic and antipyretic agent with minimum anti-inflammatory
properties. In the present study a simple, fast, accurate, precise and reproducible RP-HPLC method has been
developed and validated for the quantification of paracetamol in human serum samples using theophylline as internal
standard. Protein precipitation with perchloric acid was employed in the extraction of paracetamol and theophylline
from biological matrix. The chromatographic separation was accomplished on Phenomenex C18 column with a
mobile phase comprising of 0.05 mM sodium sulfate buffer (pH 2.2 ± 0.02 adjusted with phosphoric acid) and
acetonitrile at a ratio of 93:7 at a flow rate of 1.0 ml/min. The chromatogram was monitored by UV detection at a
wavelength of 254 nm. The method was validated over a linear concentration range of 2-100 μg/ml and limit of
quantification (LOQ) was 1.61 μg/ml with a correlation coefficient (r2) 0.997. The intra-day and inter-day precision
expressed as relative standard deviation were found to be 0.49 - 2.68% and 0.36 - 3.44%, respectively. The average
recovery of paracetamol from serum ranged from 99.0 - 106.4%. The method was successfully applied to a
pharmacokinetic study after oral administration of immediate release paracetamol tablet (1000 mg) in four healthy
Bangladeshi volunteers. The mean Cmax was found to be 11.03 ± 3.21 μg/ml, which occurred at Tmax of 0.88 ± 0.14 hr.
The half life, AUC0-8 and AUC0-∞ values were found to be 3.09 ± 0.71 hr, 31.06 ± 6.57 hr-μg/ml and 37.92 ± 9.51 hr-
μg/ml, respectively.