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Development and validation of stability-indicating RP-HPLC method for the simultaneous determination of tizanidine HCL and meloxicam in rabbit's plasma

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
High-performance liquid chromatography (HPLC) is a widely used technique for the simultaneous detection and quantification of different drugs. The purpose of the current study was to develop a simple and cost-effective reversed-phase high-performance liquid chromatography (RP-HPLC) method for the simultaneous determination of tizanidine (TZN) HCl and meloxicam (MLX) in rabbit's plasma. Assay of TZN and MLX was performed after extraction of drug from plasma by liquid–liquid extraction technique using methanol and diethyl ether as protein precipitants. Isocratic elution was performed in a Kromasil® C18 column (dimension, 250 × 4.60 mm; particle size, 5 μm) with mobile phase consisting of methanol–water (8:2). Orthophosphoric acid was used to adjust the pH of the mobile phase 3.0, and detection was done at 228 nm. Flow rate was 0.8 mL/min with ambient temperature and average operating pressure of 1400 psig. Retention time of TZN was 2.612 min and that of MLX was 6.960 min with a resolution of 3.18. Both drugs showed satisfactory linearity in the range of 10 to 50 ng/mL with correlation coefficients (R2) of 0.9989 and 0.9972 for TZN and MLX, respectively. The developed method was validated successfully for linearity, system suitability, intra-day and inter-day accuracy, and precision, robustness, and specificity following International Conference on Harmonization (ICH) guidelines. Conclusively, a precise, stable, reproducible, economical, and suitable method for estimation of pharmacokinetic evaluation was developed and validated.
Rocznik
Strony
173--178
Opis fizyczny
Bibliogr. 32 poz., rys., tab.
Twórcy
  • Department of Pharmaceutics, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan
  • Department of Pharmaceutics, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan
  • Department of Pharmaceutics, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan
  • Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan
autor
  • Department of Pharmaceutics, Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan
  • College of Pharmacy, University of Sargodha, Sargodha, Pakistan
autor
  • Department of Pharmaceutical Sciences, Jinnah Sindh Medical College University, Karachi, Pakistan
Bibliografia
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  • [6] Guideline IHT. Validation of Analytical Procedures: Text and Methodology Q2 (R1)(2005). http://www ich org/cache/compo/363-272-1 html. 2010, 1–17.
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  • [19] Kukes, V.; Reikhart, D.; Artnautov, V.; Torshina, E.; Kapashin, A.; Belostotskii, A. Pharm. Chem. J. 2016, 50, 394–403.
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Uwagi
PL
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2019).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-8d32b6d8-31e6-47f8-8b17-fd5218c956b6
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