Literature DB >> 22459459

Quantitative determination of deferiprone in human plasma by reverse phase high performance liquid chromatography and its application to pharmacokinetic study.

Mateen Abbas1, Rakhshanda Nawaz, Tahira Iqbal, Muhammad Alim, Muhammad Rafique Asi.   

Abstract

Deferiprone (1, 2 dimethyl-3-hydroxypyrid-4-one) is considered to be the standard iron chelator. Pharmacokinetic studies of generic formulations are required in local condition before placed on the market. High performance liquid chromatographic (HPLC) method was used for quantification of deferiprone in human plasma using UV/VIS detector. Chromatographic separation was carried out on C(18) column, with a mobile phase of methanol-buffer (18:82, v/v), pH 3.5, and caffeine was used as an internal standard. The calibration curve was linear over the range 0.25-10 μg/mL in human plasma (R(2) = 0.9994). After oral administration of deferiprone (500 mg) to human, the plasma concentration-time curve of deferiprone was conformed to two-compartment open model. The deferiprone plasma concentration showed a rapid absorption and average area under the plasma concentration-time curve (AUC) of deferiprone was 17.0 ± 1.23 h.μg/ml. Average absorption and elimination half-life values of deferiprone of 24 volunteers were 0.62 ± 0.12 and 2.65 ± 0.43 hours. This study confirms the rapid absorption of deferiprone in humans. AUC was similar to that previously reported but C(max) was slightly lower than that stated in the literature.

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Year:  2012        PMID: 22459459

Source DB:  PubMed          Journal:  Pak J Pharm Sci        ISSN: 1011-601X            Impact factor:   0.684


  2 in total

1.  A ratiometric fluorometric and colorimetric probe for the β-thalassemia drug deferiprone based on the use of gold nanoclusters and carbon dots.

Authors:  Yanying Wang; Lei Mao; Wei Liu; Fang Ding; Ping Zou; Xianxiang Wang; Qingbiao Zhao; Hanbing Rao
Journal:  Mikrochim Acta       Date:  2018-09-01       Impact factor: 5.833

2.  Quality by design approach for green HPLC method development for simultaneous analysis of two thalassemia drugs in biological fluid with pharmacokinetic study.

Authors:  Michel Y Fares; Maha A Hegazy; Ghada M El-Sayed; Maha M Abdelrahman; Nada S Abdelwahab
Journal:  RSC Adv       Date:  2022-05-09       Impact factor: 4.036

  2 in total

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