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International Journal of Pharmaceutical Investigation
Home»JPHI»Vol 3 Issue 1»Formulation and Evaluation of Buccal film of Ivabradine hydrochloride for the Treatment of Stable Angina Pectoris
Vol 3 Issue 1

Formulation and Evaluation of Buccal film of Ivabradine hydrochloride for the Treatment of Stable Angina Pectoris

March 18, 2013Updated:May 30, 20232 Mins Read
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International Journal of Pharmaceutical Investigation, 2013, 3, 1, 47-53.
DOI: 10.4103/2230-973X.108963
Published: March 2013
Type: Original Article

Authors: 

Mohasin Lodhi
Department of Pharmaceutics, Shree Devi College of Pharmacy, Kenjar Village, Mangalore, Karnataka, India

Akhilesh Dubey
Department of Pharmaceutics, Shree Devi College of Pharmacy, Kenjar Village, Mangalore, Karnataka, India

Reema Narayan
Department of Pharmaceutics, Shree Devi College of Pharmacy, Kenjar Village, Mangalore, Karnataka, India

Prabhakara Prabhu
Department of Pharmaceutics, Shree Devi College of Pharmacy, Kenjar Village, Mangalore, Karnataka, India

Sneh Priya
Department of Pharmaceutics, NGSM Institute of Pharmaceutical Sciences, Mangalore, Karnataka, India

ABSTRACT

Background: Ivabradine hydrochloride is an anti-anginal drug with a biological half-life of about 2 h and repeated daily administration is needed to maintain effective plasma level. Present investigation of buccal films of Ivabradine hydrochloride is an attempt to avoid the repeated administration and release of drug in more controlled fashion, thereby, to improve the bioavailability. Materials and Methods: Buccal patches were fabricated by solvent casting technique and were evaluated for its physical properties like physical appearance, weight uniformity, thickness, swelling index, surface pH, mucoadhesive time and folding endurance, in vitro and ex vivo release studies. Results: A combination of hydroxypropyl methyl cellulose (HPMC) K15M and K100M with carbopol 940, PEG 6000 gave promising results. Further, the drug content of all the formulations was determined and was found to be uniform. All the formulations were subjected to in vitro release study using phosphate buffer pH 6.6. Patches exhibited drug release in the range of 90.36% ± 0.854 to 98.37% ± 0.589 at the end of six hrs . The best formulations (F2 and F5) containing the composition of HPMC K15-37.50 mg, carbopol-0.42 mg, PEG6000-16.87 mg, Aspertane-0.28 mg, Tween-0.0023 mg and HPMC K100-37.50 mg, carbopol-0.42 mg, PEG6000-16.87 mg, Aspertane-0.28 mg, Tween-0.0023 mg respectively exhibited in vitro drug release of 97.61% ± 0.589 and 98.37% ± 0.114 respectively. The results of ex vivo diffusion using goat cheek pouch revealed that the drug release rate was retarded up to seven hrs. Films prepared with permeation enhancer (Tween 80) showed faster drug release. Finally, stability studies were carried out by using human saliva for the optimized formulation (F2-F5). Conclusion: The present study indicated enormous potential of mucoadhesive buccal patches containing Ivabradine for systemic delivery with an added advantage of circumventing hepatic first pass metabolism. Further work is recommended to support its efficacy claims by long term pharmacokinetic and pharmacodynamic studies in human beings.

Keywords:Hydroxypropyl methyl cellulose K15 and K100, Ivabradine hydrochlorid, Mucoadhesive buccal films, Solvent casting.

Original Article
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