Degradation Study of Ketorolactromethamine by a Validated UPLC Method

Mohammad Nasir Uddin, Md. Al-Amin, Md. Nazmul Haque Mijan, Suman Das

Abstrak


UPLC stability indicating method was developed for determining ketorolac tromethamine in its degradation study at different conditions. An isocratic mobile phase composition of 60:10:30 (v/v) containing CH3OH, CH3CN and 5mM NaH2PO4 and C18 column were used at a flow rate of 0.20 mL min-1. Satisfactory retention time was found 2.13±0.05 min at 320 nm when monitored by DAD detector. Forced degradation studies of ketorolac tromethamine was also performed at the following conditions: acid and basic hydrolysis, heat (50-70°C for 1 hr), photolytic (UV and sunlight for up to 3 hr), oxidation (3% hydrogen peroxide for 1 hr). Forced degradation study revealed that ketorolac degraded significantly under thermal conditions. In 1N acid and base hydrolysis, degradation was moderately significant and comparable. It was degraded marginally in 0.1N acid-base hydrolysis which was comparable to oxidative conditions. But in photolytic condition ketorolac shows insignificant degradation. Method was also applied to pharmaceutical formulation.

Keywords: UPLC, Ketorolac tromethamine, pharmaceutical formulation, Forced degradation


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Referensi


Rang H, Dale M, Ritter J and Flower R, Pharmacology, 6th Ed., Churchill Livingstone, Elsevier, 2007, 227-230.

Wang Z, Dsida R and Avram M, Determination of ketorolac in human plasma by reversed – phase high-performance liquid chromatography using solid-phase extraction and ultraviolet detection, J. Chromatography B, 2001, 755 (1-2), 383-386.

Warner TD, Mitchell JA (2004) Cyclooxygenases: new forms, new inhibitors, and lessons from the clinic. FASEB J 18: 790-804.

Galán-Herrera JF, Poo JL, Maya-Barrios JA, de Lago A, Oliva I, et al. (2008), Bioavailability of two sublingual formulations of ketorolac tromethamine 30 mg: a randomized, open-label, single-dose, two-period crossover comparison in healthy Mexican adult volunteers. Clin Ther 30: 1667-1674.

Jayant B. Dave, Pratik J. Vyas, Chhagan N. Patel, A validated stability‑indicating high performance liquid chromatographic method for moxifloxacin hydrochloride and ketorolac tromethamine eye drops and its application in pH dependent degradation kinetics, Chronicles of Young Scientists, 2013, 4(1), 24-31.

Martindale, The Complete Drug Reference, 35th Edition, (ISBN: 9780853696872) 2007.

Committee on the Safety of Medicines, Medicines Control Agency: Ketorolac: new restrictions on dose and duration of treatment. Current Problems in Pharmacovigilance, 1993, 19, 5-8.

Strom BL, Berlin JA, Kinman JL, Spitz PW, Hennessy S, Feldman H, Kimmel S, Carson JL. Parenteral Ketorolac and risk of gastrointestinal and operative site bleeding: a postmarketing surveillance study, the journal of American medical association. JAMA, 1996, 275, 376-82.

Kamath, B. V.; Shivram, K.; Shah, A. C.; Determination of diclofenac sodium, famotidine and ketorolac tromethamine by flow injection analysis using dichloronitrophenol, J. Pharm. Biomed. Anal., 1994, 12, 343-346.

E. Manal, A.El-Brashy, A. Fatma, W. Talaat, Spectrofluorometric Determination of Ketorolac Tromethamine Via Its Oxidation with Cerium(IV) in Pharmaceutical Preparations and Biological Fluids J. AOAC Int., 2007, 90, 941-947.

M.S. Prakash, S. Meena, Fluorophotometric. Determination of Ketororlac Tromethamine, Indian Drugs, 1996, 12, 343-346.

S. Orlandini, S. Fanalo, S. Furlanetto, A. Marras, S. Pinzauti, Micellar electrokinetic chromatography for the simultaneous determination of ketorolac tromethamine and its impurities: Multivariate optimization and validation, J. Chrom. A., 2004, 1032, 253-263.

J. Sturm, H. Canelo, L. Nunez-Vergara, J. Squella, Voltammetric study of ketorolac and its differential pulse polarographic determination in pharmaceuticals, Talanta, 1997, 44, 931-937.

Chaudhary R, Gangwal S, Jindal K and Khanna S, Reversedphase high-performance liquid chromatography of ketorolac and its application to bioequivalence studies in human serum, J. Chromatography B: Biomedical Sciences and Applications, 1993, 614 (1), 180- 184.

Jones D and Bjorksten A, Detection of ketorolac enantiomers in human plasma using enantioselective liquid chromatography, J. Chromatography B: Biomedical Sciences and Applications, 1994, 661(1), 165-167.

Uddin MN et al. A novel validated UPLC method for the estimation of ketorolac tromethamine in pharmaceutical formulation, Research 2014;1:1237

Sabyasachi Patri, Anil K. Patni, Sunil S. Iyer, Arshad H. Khuroo, Tausif Monif, Sachin Rana, Sudershan Kumar, and Rakesh Jain, A Validated High-Performance Liquid Chromatography-Tandem Mass Spectrometric (LC-MS/MS)Method for Simultaneous Determination of R(+)-Ketorolac and S(−)-Ketorolac in Human Plasma and Its Application to a Bioequivalence Study, Chrom. Res. International. Volume 2011, Article ID 214793, 11 pages.

Devarajan P, Gore S and Chavan S, HPTLC determination of ketorolac tromethamine, J. Pharmaceutical and Biomedical Analysis, 2000, 22 (4), 679-683.

Orlandini S, Furlanetto S, Pinzauti S, D’Orazio G andFanali S, Analysis of ketorolac and its related impurities by capillary electrochromatography, J. Chromatography A, 2004, 1044 (1-2), 295- 303.

Logan, B. K.; Friel, N. P.; Peterson, K. L.; Predmore, B. B.; J. Anal. Toxicol., 1995, 19, 61.

R Singh, A Pathak, P Chawla, Method Development and Validation for Simultaneous Estimation of Ketorolac and Sparfloxacin by RP-HPLC, Indian J. Pharm. Biol. Res. 2013; 1(4):95-101

Bhagyashree RD, KP Bhusari, MR Tajne, MH Ghante, NS Jain, Stability Indicating Method for the Determination of Ketorolac Tromethamine in Pharmaceutical Formulations by HPLC, Indo American Journal of Pharm Research.2014:4(07). 3248-3257

Razzaq SN, Khan IU, Stability indicating hplc method for simultaneous determination of moxifloxacin hydrochloride and Ketorolac tromethamine in pharmaceutical formulations. Quim. Nova. 2012:35( 6), 1216-1221.

Jayant B. Dave, Pratik J. Vyas, Chhagan N. Patel A validated stability‑indicating high performance liquid chromatographic method for moxifloxacin hydrochloride and ketorolac tromethamine eye drops and its application in pH dependent degradation kinetics, Chronicles of Young Scientists, 2013; 4(1), 24-31

ICH Harmonized Tripartite (1996) Validation of Analytical Procedures: Text and Methodology Q2 (R1), Current Step 4 Version, Parent Guidelines on Methodology Dated November 6 1996, Incorporated in November In: International Conference on Harmonisation, Geneva, Switzerland. 2005.

Pradipbhai DK, Raju B, Roshan MB, Deepak N, Gananadhamu S, Prajwal PN, Abhay TS and Srinivas R, Characterization of forced degradation products of ketorolac tromethamine using LC/ESI/Q/TOF/MS/MS and in silico toxicity prediction, J. Mass Spectrom. 2014: 49, 380–391.




DOI: https://doi.org/10.24198/ijpst.v6i1.16508

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