Title of article :
A validated HPTLC method for determination of terbutaline sulfate in biological samples: Application to pharmacokinetic study
Author/Authors :
Faiyazuddin, Md. Hamdard University - Faculty of Pharmacy - Formulation Research Laboratory, Department of Pharmaceutics, India , Faiyazuddin, Md. Integral University - Faculty of Pharmacy, India , Rauf, Abdul Hamdard University - Faculty of Pharmacy - Formulation Research Laboratory, Department of Pharmaceutics, India , Ahmad, Niyaz Hamdard University - Faculty of Pharmacy - Formulation Research Laboratory, Department of Pharmaceutics, India , Ahmad, Sayeed Hamdard University - Faculty of Pharmacy - Natural Bioactive Research Laboratory, Department of Pharmacognosy Phytochemistry, India , Iqbal, Zeenat Hamdard University - Faculty of Pharmacy - Formulation Research Laboratory, Department of Pharmaceutics, India , Talegaonkar, Sushma Hamdard University - Faculty of Pharmacy - Formulation Research Laboratory, Department of Pharmaceutics, India , Bhatnagar, Aseem Institute of Nuclear Medicine Allied Sciences (INMAS) - Department of Nuclear Medicine, India , Khar, Roop K. Hamdard University - Faculty of Pharmacy - Formulation Research Laboratory, Department of Pharmaceutics, India , Ahmad, Farhan J. Hamdard University - Faculty of Pharmacy - Formulation Research Laboratory, Department of Pharmaceutics, India
From page :
185
To page :
192
Abstract :
Abstract Terbutaline sulfate (TBS) was assayed in biological samples by validated HPTLC method. Densitometric analysis of TBS was carried out at 366 nm on precoated TLC aluminum plates with silica gel 60F254 as a stationary phase and chloroform–methanol (9.0:1.0, v/v) as a mobile phase. TBS was well resolved at RF 0.34 ± 0.02. In all matrices, the calibration curve appeared linear (r^2 P 0.9943) in the tested range of 100–1000 ng spot^-1 with a limit of quantifica-tion of 18.35 ng spot ^-1. Drug recovery from biological fluids averaged P95.92%. In both matrices, rapid degradation of drug favored and the T0.5 of drug ranged from 9.92 to 12.41 h at 4 °C and from 6.31 to 9.13 h at 20 °C. Frozen at 20 °C, this drug was stable for at least 2 months (without losses 10%). The maximum plasma concentration (Cpmax) was found to be 5875.03 ± 114 ng mL ^-1 , which is significantly higher than the maximum saliva concentration (Csmax, 1501.69 ± 96 ng mL ^-1). Therefore, the validated method could be used to carry out pharmacoki- netic studies of the TBS from novel drug delivery systems.
Keywords :
Terbutaline sulfate , High , performance thin , layer chromatography , Biological fluids , Ex vivo stability , Pharmacokinetic study
Journal title :
Saudi Pharmaceutical Journal(SPJ)
Journal title :
Saudi Pharmaceutical Journal(SPJ)
Record number :
2552672
Link To Document :
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