Wednesday 25 January 2023

Polymers in the Formulation and Characterization of Amlodipine Besylate Oral Mouth Dissolving Films| Chapter 8 | Current Overview on Pharmaceutical Science Vol. 2

The purpose of the work was to plan oral dissolving films and reinforce the drug release of amlodipine besylate by the inclusion of synthetic and everyday polymers. The oral dissolving films intoxicated with Amlodipine besylate were arranged by solvent dissolution method utilizing hydroxy propyl methyl cellulose-3cps& 5cps, Blanose, methyl cellulose and tamarind children polyose by adding appropriate plasticizer: PEG 400 and glycerin. The prepared spoken dissolving films were evaluated for drug content, burden variation, diameter, pH, folding continuity, In vitro drug release and stability. The evaluation limits of Amlodipine besylate were found expected satisfactory in agreements of drug content, thickness and pH. Comparison of the dissolution descriptions of Amlodipine besylate oral disappearing films in phosphate buffer (pH 6.8). The release descriptions of films were analyzed by using UV- Visible spectrophotometer at 239nm. The improved formulation AML 15 death studies were Compared with clean drug and marketed expression. AML 15 showed the highest drug release 100% in 10min, when distinguished to pure drug 88.2% in 30min and displayed AML 92.2% in 45min. showed. Preformulation studies of amlodipine besylate like unity studies with polymers using FTIR, DSC studies were completed activity. The drug and polymers were found expected compatible accompanying each other. These results were strongly submitted that the water soluble polymers were acceptable for the formulation of spoken fast dissolving films of amlodipine besylate. Effective drug release was achieved for amlodipine besylate incidentally of preparation of spoken dissolving films by stable evaporation method.

Author(s) Details:

Pamula Reddy Bhavanam,
Department of Pharmaceutical Technology, Nirmala College of Pharmacy, Atmakuru, Andhra Pradesh-522503, India.

Shaik Abdul Rahaman,
Department of Pharmaceutical Technology, Nirmala College of Pharmacy, Atmakuru, Andhra Pradesh-522503, India.

M. Mohan Varma,
Department of Pharmaceutical Technology, Shri Vishnu College of Pharmacy, Bhimavaram, Andhra Pradesh-534202, India.

Please see the link here: https://stm.bookpi.org/COPS-V2/article/view/9170


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