A Stability-Indicating Reverse Phase High Performance Liquid Chromatography Method For Development And Validation Of Meptazinol

A Stability-Indicating Reverse Phase High Performance Liquid Chromatography Method For Development And Validation Of Meptazinol

Authors

  • Mukesh Patil
  • Ashwini D. Tayade
  • Ashish Jain

Keywords:

Reverse phase high-performance liquid chromatography, UV-visible spectroscopy, method development, validation, meptazinol, international conference

Abstract

Methodology: The UV-Spectroscopic method was developed for the estimation of meptazinol in bulk and tablet dosage form. The solvent selected for the meptazinol UV analysis was methanol, the solution of 10µg/ml was scanned in UV region from 200-400 nm and the λmax value was determined. The RP-HPLC method was developed on HiQ silC18HS (250mm x 4.6 mm, 5  )column using acetonitrile: methanol [90:10] as mobile phase at flow rate 1.2 ml/min and UV detection at 276 nm. Results: The maximum absorbance was observed at 276 nm. The wavelength 276 nm was selected for further analysis of Meptazinol . The calibration curve was determined using drug  concentrations ranging from 10-60 µgm/ml. The system suitability was performed by injecting a standard solution containing 60µg/ml of meptazinol six replicates. For two of them, the peak asymmetric were 2000, and the %RSD of meptazinol was less than 2.

Author Biographies

Mukesh Patil

Shri. D.D. Vispute College of Pharmacy & Research centre

Ashwini D. Tayade

Shri. D.D. Vispute College of Pharmacy & Research centre

Ashish Jain

Shri. D.D. Vispute College of Pharmacy & Research centre

References

Bill, D.J.; Hartley, J.E.; Stephens, R.J. and Thompson, A.M.: The antinociceptive activity of meptazinol depends on both opiate and cholinergic mechanisms. British Journal of Pharmacology 79: 191–199 (1983)

Madhuri A Hinge, Rajvi J. Mahida; Development and Validation of an RP-HPLC Method for Simultaneous Determination of Trimetazidine Hydrochloride and Metoprolol Succinate; International Journal of Chemical and Pharmaceutical Analysis. (2015); 2(2);77-83.

M. A. Naushad, M. Aqil; Development and Validation of the HPLC Method for the Analysis of Trimetazidine Hydrochloride in Bulk Drug and Pharmaceutical Dosage Forms Journal of Analytical Chemistry (2008), 63(10), 965–97

Sreelatha Nagula, Sridhar Thota and Venisetty Raj Kumar; Development and validation of a stability indicating RP-HPLC method for the determination of trimetazidine dihydrochloride, Der Pharma chemica (2014), 6(1), 149-154.

Robinson, J. W. Frame, E. M. S. Frame, G. M. II. Undergraduate instrumental analysis, 6 ed.; CRC publisher, 2004, pp. 1-4, 65-67

2 Braun, R D Introduction to Instrumental analysis, 2nd ed.; pharma Med press, 2012, pp. 1-8, 138-152

Robinson J. W. et.al. Undergraduate Instrumental Analysis; 6th ed., Marcel Dekker Inc.,:New York, 2005: pp. 3.4,65.

Braun. R D Introduction to Instrumental Analysis, 2nd ed., Pharma Med Press, 2012. Pp. 891-892

Skoog. D. A. et al, Principles of Instrumental Analysis: 6th ed., Thomson Learning, 2007, pp 1-3.

Skoog. D. A. et al: Principles of Instrumental Analysis, 6ª ed., Cengage Learning, 2006, Pg no-1-13.

Thomas S., Bharti A.; Sanjeev S.; Ashutosh A, A stability indicating simultaneous dual wavelength UV-HPLC method for the determination of potential impurities in farmprudine active pharmaceutical ingredient J Pharm Biomed Anal 2012, 58111, 136-40

Jain M. Srivastava V. Kumar R., Dang: V. Hinyanna S., Kumar A. et al. Devenim of five potential genotoxic impurities in Dalfumpridine using liquid chromatography / Pharm Biomed Anal. 2016,133, 27-31.

Snyder. L. R.; Kirkland, J. J. Dolan, J. W. Introduction to modern liquid chromatography, 3rd ed.; Wiley publication, 2010, pp 20-35.

Lodba Luxminarayan; Sharma Neha, Viswas Amit, Dr. Khinchi MP. A Review Chromatography Techniques. Asian Journal of Pharmaceutical Research and Development 2017.5(2), 1-08.

Snyder. L. R. et al, Practical HPLC Method Development, 2d ed. Wiley India Pvt. Ltd, 2006, pp 21, 59, 40, 234-251.

Sethi. P. D. HPLC, Quantitative analysis of pharmaceutical formulation, Volume 1: CHS publishers and Distributors, 2019; pp 11, 14, 28 and 38.

Pharmaceutical Guidelines. Analytical Method Validation by Ankut Choudhary: analytical-method-validation.html (Accessed on Mar 05, 2020).

G. Lavanya; M. Sunil: M.M. Eswarudu, M. Chinna Eswaraiah, K. Harisudha and R. Naga Spandana Analytical Method Validation: An Updated Review. International Journal of Pharmaceutical Sciences and Research, 2013, 4(4), 1280-1286.

Ahuja. S.; Dong. M. W. Handbook of Pharmaceutical Analysis by HPLC, Volume 6 Elsevier/Academic Press, 2005, pp 200

Blessy M.; Patel R.D., Prajapati P.N.: Agrawal Y.K. Development of forced degradation and stability indicating studies of drugs A review. J Pharm Anal, 2014, 463), 159-165.

Agranat I, Hava C and John C. Putting chirality to work: the strategy of chiral switches. Nature Reviews Drug Discovery 2002; 1: 753–768

K.G. Mawuenyega, W. Sigurdson, V. Ovod, L. Munsell, T. Kasten, J.C. Morris, K.E. Yarasheski, R.J. Bateman, Science 330 (2010) 1774.

R.T. Bartus, R.L. Dean, B. Beer, A.S. Lippa, Science 217 (1982) 408

J. Wyeth and Brother Ltd. (J.F. Cavalla, A.C, White, inv.) Get. Offen. 194 1534 (April 4, 1970) [Chem. Abstr., 3 (1970) 14727 m].

C. Rudolphi, G. Blaschke, Journal of Chromatography B, 877 (2009) 3787–3791

Rathod K.G. et al. Development and Validation of RP-HPLC Method for Estimation of Dalfampridine, in Bulk and Pharmaceutical Dosage Form, Indo American Journal of Pharmaceutical Research, 2019, 9/17), 614-629.

Vivek Jain; Ritu Dehariyal and Geeta Parkhe Method Development and Validation for Estimation of Dalfampridine in Synthetic Mixture by using UV Spectrophotometry and RP HPLC EASI Pharm & Pharmacol. 2019, 1(4), 84-87

Dharani NR.: Padmini K.: Suakala S. Stability indicating RP-HPLC method development and validation for estimation of Dalfampridinein bulk and formulation. Int. J Ads. Res. 2016, 4191.184-91

Madhumathi CH.: Padmalatha M Snehna 5: Divya C.B: Development and validation of UV spectrophotometery method for the estimation of Dalfampridine in tablets Int J Pharmac Res2014, 2, 1019-26.

Vivekkumar, K. Redasani, Gazalal, Shaikh, Sanjay J. Surana Development and validation of spectroscopic methods for the estimation of Dalfampridine in bulk and in tablet formulation Analytical Chemistry- Aw Indian Journal, 2014, 14(1), 37-41.

LI, W.; HAO, J.; TANG, Y.; CHEN, Y.; QIU, Z. Structural Comparisons of Meptazinol with Opioid Analgesics1. Acta Pharmacologica Sinica 2005, 26 (3), 334–338.

Franklin, R.; Aldridge, A. Studies on the Metabolism of Meptazinol, a New Analgesic Drug. British Journal of Clinical Pharmacology 1976, 3 (3), 497–502

P. D. Sethi Quantitative analysis of pharmaceutical formulations High performance thin layer chromatography, 1" ed.; CBS publisher and distributor: New Delhi, 1996, pp. 3-5, 10, 18-20, 24.27.

Downloads

Published

21-10-2024

Issue

Section

Articles
Loading...