A Stability Indicating Reverse Phase-HPLC Method Development and Validation for the Estimation of Bimatoprost 0.3% & Timolol 0.5% Pharmaceutical Ophthalmic Dosage Form

Author:

Amin Md. S.,Islam Muhammad T.

Publisher

Scientific Research Publishing, Inc.

Subject

General Engineering

Reference12 articles.

1. https://pubchem.ncbi.nlm.nih.gov/compound/Bimatoprost

2. https://pubchem.ncbi.nlm.nih.gov/compound/Timolol

3. Lingayat, V.S., Patil, A. and Patil, V.R. (2022) Development and Validation of RP-HPLC Method for Simultaneous Estimation of Bimatoprost and Timolol Maleate. International Journal of Creative Research Thoughts, 10, c189-c196. https://ijcrt.org/papers/IJCRT22A6255.pdf

4. A Double-Masked, Randomized, Parallel Comparison of a Fixed Combination of Bimatoprost 0.03%/Timolol 0.5% with Non-Fixed Combination use in Patients with Glaucoma or Ocular Hypertension

5. Development and validation of the stability indicating RP-UHPLC method for the determination of the chemical purity and assay of bimatoprost

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