DEVELOPMENT AND VALIDATION OF HPLC METHOD FOR ESTIMATION OF BRIMONIDINE TARTRATE AS BULK DRUG AND IN OPHTHALMIC FORMULATION

Authors

  • S S Mandan MET’s Institute of Nashik Shirpur, India (MH)
  • A V Nerpagar MET’s Institute of Nashik Shirpur, India (MH)
  • U D Laddha MET’s Institute of Nashik Shirpur, India (MH)

Abstract

The optimized reverse phase high performance liquid chromatographic method was developed for estimation of Brimonidine Tartrate in bulk drug and pharmaceutical dosage form. Chromatography was performed on Kromasil C 18 ( 250 mm X 4.6 mm i.d. , 5 μm particle size) column with mobile phase citric acid monohydrate buffer:water:methanol (30:50:20 v/v/v) and  pH 3 was maintained by using triethylamine. The flow rate was 1.0 ml/min. Elute was detected at 246 nm and it effectively separated at Retention Time of 5.96 min. The LOD and LOQ was 1.47 and 4.47 μg/ml respectively. A linear response was observed over the concentration range 40-80 μg/ml for Brimonidine Tartrate. Thus the proposed HPLC method was found accurate, specific, precise, robust and reproducible.

DOI

https://doi.org/10.22270/jddt.v7i7.1616

Author Biographies

S S Mandan, MET’s Institute of Nashik Shirpur, India (MH)

MET’s Institute of Nashik Shirpur, India (MH)

A V Nerpagar, MET’s Institute of Nashik Shirpur, India (MH)

MET’s Institute of Nashik Shirpur, India (MH)

U D Laddha, MET’s Institute of Nashik Shirpur, India (MH)

MET’s Institute of Nashik Shirpur, India (MH)

References

Rathore K, Kumar R, Sisodia S, Timolol maleate a gold standard drug in glaucoma used as ocular films and inserts an overview, Int J Pharm Sci Rev Res, 2010, 3, 23-29.

Phogat A, Kumar M, Mahadevan N, Simultaneous estimation of Brimonidine Tartrate and Timolol Maleate in Nanoparticles Formulation by RP-HPLC, Int J Recent Adv Pharm Res, 2011, 3, 31-36.

Jiang S, Chappa A, Proksch J, A rapid and sensitive LC/MS/MS assay for quantitation of brimonidine in ocular fluid and tissue , J Chromatogr B Anal Technol Biomed Life Sci, 2009, 3, 107-114.

Sethi PD, Quantitative analysis of pharmaceutical formulation, HPLC, 2011, 1, 38-70.

ICH Harmonised Tripartite Guideline Validation of Analytical Procedures, Text and Methodology, 2005, Q2, R1.

Published

2017-12-22
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How to Cite

1.
Mandan SS, Nerpagar AV, Laddha UD. DEVELOPMENT AND VALIDATION OF HPLC METHOD FOR ESTIMATION OF BRIMONIDINE TARTRATE AS BULK DRUG AND IN OPHTHALMIC FORMULATION. J. Drug Delivery Ther. [Internet]. 2017 Dec. 22 [cited 2025 Oct. 19];7(7):146-59. Available from: https://jddtonline.info/index.php/jddt/article/view/1616

How to Cite

1.
Mandan SS, Nerpagar AV, Laddha UD. DEVELOPMENT AND VALIDATION OF HPLC METHOD FOR ESTIMATION OF BRIMONIDINE TARTRATE AS BULK DRUG AND IN OPHTHALMIC FORMULATION. J. Drug Delivery Ther. [Internet]. 2017 Dec. 22 [cited 2025 Oct. 19];7(7):146-59. Available from: https://jddtonline.info/index.php/jddt/article/view/1616