TITLE

Formulation and Evaluation of Two-Pulse Drug Delivery System of Amoxicillin Trihydrate

AUTHOR(S)
Kumar, Rohitash; Anvesh, M. S.; Khan, Mohammed S.; Moin, Afrasim; Gowda, D. V.
PUB. DATE
October 2014
SOURCE
Tropical Journal of Pharmaceutical Research;Oct2014, Vol. 13 Issue 10, p1593
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Purpose: To develop a pH-controlled two-pulse drug delivery system of amoxicillin in order to overcome the snag of biological tolerance and to improve bactericidal activity. Methods: The core tablets were compressed and coated with hydroxylpropyl methylcellulose (HPMC) of different viscosities with spray-dried lactose (SDL) as a pore former. The final two-pulse release tablet was prepared with the remaining drug fraction (to be released as the first immediate release pulse) with a disintegrant, giving the final tablet. The tablets were evaluated for pharmaceutical properties including disintegration, thickness, hardness, friability and weight variation and by DSC (differential scanning calorimetry) and FTIR (Fourier transform infrared spectroscopy) studies in order to assess drug/polymer compatibility. The tablets further subjected to in vitro dissolution studies and stability studies. Result: The tablet core disintegrated within 30 to 40 s. Drug content ranged from 97.85 to 98.23. FTIR and DSC studies showed drug-polymer compatibility. The developed two-pulse release tablets had acceptable thickness, hardness, friability and weight variation. In vitro drug release showed prolongation of lag time as polymer viscosity increased. With 25 % HPMC and 75 % SDL, drug release was 97.5 % by the end of 8th, 9th &10th h and viscosity was 100, 400 and 4000 cps respectively. No significant difference in drug release was found as values were within limits of confidence interval (p < 0.05). The formulation was stable. Conclusion: The developed formulation demonstrates the feasibility of a two-phase release of amoxicillin separated by a well-defined time-controlled lag phase which is desirable for chronotherapeutic drug delivery.
ACCESSION #
99493149

 

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