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Author

M. B. Sufi

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Open access 2026

To study the effect of various superdisintegrants and binders in the Formulation and Evaluation of Labetalol Rapid Disintegrating Tablet

The objective of the present study was to formulate and evaluate the Rapid disintegrating tablets (RDTs) of Labetalol hydrochloride by direct compression method and revealing the effect of various super disintegrates and binders on the performance of tablets. Fourteen different formulations (F1–F14) were prepared using...

M. B. Sufi, Shaikh Riyaj Khayumsab, Rajlaxmi S. Deolekar · 0 citations
Open access 2026

Formulation and Evaluation of Mouth Dissolving Film of Irbesartan

The main objective of the present study was to formulate and evaluate Irbesartan based mouth dissolving film in order to achieve rapid drug release for the geriatric and dysphagic patients to increase patient compliance. The solvent casting method was used to prepare mouth dissolving films by employing HPMC E5, HPMC E1...

M. B. Sufi, M. Tabish, Rajlaxmi Deolekara · 0 citations
Open access 2026

To Develop and Validate the Stability Indicating Method for Ezetimibe and Rosuvastatin Using HPLC Method

F Forced degradation studies conducted in acidic, alkaline, oxidative and photolytic conditions proved that the RP-HPLC method was suitable for identifying degradation products from Rosuvastatin and Ezetimibe, the latter being relatively more susceptible to degradation than Rosuvastatin.

M. B. Sufi, Sakshi Bobade, Rajlaxmi Deolekara · 0 citations
Open access 2026

To develop and validate the stability indicating method for repaglinide and voglibose using HPLC method

The forced degradation studies were carried out under acidic, alkaline, oxidative, neutral and photolytic conditions, showing adequate separation of degradation peaks from the drug peak thus proving the forced degradation method to be stability indicating.

M. B. Sufi, Shantanu Burange, Rajlaxmi S. Deolekar · 0 citations
Open access 2026

To develop and validate the stability indicating method for Empagliflozin and Linagliptin using HPLC method

The developed RP HPLC method is simple, rapid, selective, accurate, economical, and can be used for routine pharmaceutical quality control, stability testing and analysis of combined Linagliptin and Empagliflozin formulation.

M. B. Sufi, Vaishnavi Daldale, Irshad Ahmed · 0 citations

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