Antimicrobial activity assessment of time-dependent release bilayer tablets of amoxicillin trihydrate

被引:7
作者
Beg, Sarwar [1 ]
Nayak, Amit Kumar [2 ]
Kohli, Kanchan [1 ]
Swain, Suryakanta [3 ]
Hasnain, M. S. [2 ]
机构
[1] Hamdard Univ, Fac Pharm, Dept Pharmaceut, New Delhi 110062, India
[2] Seemanta Inst Pharmaceut Sci, Dept Pharmaceut, Odisha, India
[3] Roland Inst Pharmaceut Sci, Dept Pharmaceut, Berhampur, Odisha, India
关键词
Chronotherapeutics; Time-dependent release; In vitro dissolution; Minimum inhibitory concentration; Zone of inhibition; PULSATILE DELIVERY; SUSTAINED-RELEASE; COLONIC DELIVERY; COMBINATION; POLYMETHACRYLATES; CLARITHROMYCIN; HYDROGELS; SYSTEM;
D O I
10.1590/S1984-82502012000200010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of present study was the assessment of antimicrobial activity of prepared time-dependent release bilayer tablets of amoxicillin trihydrate and in vitro evaluation of drug release by antimicrobial assay using agar plate diffusion method. The bilayer tablets comprised of a delayed and sustained release layer. Direct compression method was used for the preparation of bilayer tablets containing Eudragit-L100 D55 as delayed release polymer, and HPMCK4M and HPMCK15 as sustained release polymers. The prepared bilayer tablets containing amoxicillin trihydrate were evaluated for hardness, thickness, friability, weight variation and drug content. Further, in vitro drug release was assessed by antimicrobial assay using S. aureus and E. coli as test microorganisms. The aliquot samples of in vitro drug release study were found to be effective against both microorganisms for 16 hours due to sustained action. The in vitro drug release study and antimicrobial assay showed that bilayer tablets have sustained release profile of drug delivery with time-dependent burst release after a lag-time of 2 hours. The lower MIC value (2 mu g/mL) of prepared bilayer tablets vis-a-vis marketed preparation (5 mu g/mL) represented its good antimicrobial activity.
引用
收藏
页码:265 / 272
页数:8
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