In vitro/in vivo evaluation of HPMC/alginate based extended-release matrix tablets of cefpodoxime proxetil

被引:23
作者
Mujtaba, Ali [1 ]
Kohli, Kanchan [2 ]
机构
[1] Northern Border Univ, Coll Pharm, Deparment Pharmaceut, Raffia, Saudi Arabia
[2] Hamdard Univ, Fac Pharm, Dept Pharmaceut, New Delhi 110062, India
关键词
Cefpodoxime proxetil; Extended-release; HPMC K4M; Sodium alginate; Release kinetics; PHARMACOKINETICS; OPTIMIZATION; FORMULATION; DELIVERY; DESIGN; PH;
D O I
10.1016/j.ijbiomac.2016.05.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of this research was to assessment of antimicrobial activity and in vitro/in vivo evaluation of cefpodoxime proxetil extended-release (ER) tablet for once daily administration. The tablets were prepared using combination of biodegradable polysaccharides including hydroxypropyl methylcellulose and sodium alginate as matrix material to achieve pH-independent ER release. The tablets were found within the permissible limits for various physicochemical parameters. The in vitro drug release showed that the drug was released over a period of 24h in a sustained release manner. The drug release followed Higuchi kinetics as these plots showed the highest linearity (R-2 = 0.9833), but a close relationship was also observed with zero-order kinetics (R-2 = 0.9088) and the drug release mechanism was found to be of anomalous or non-Fickian type. Further, in vitro drug release was assessed by antimicrobial assay and it revealed that drug release through 24h periods was above the MIC. In vivo investigation in rabbits showed ER pharmacokinetic profile of cefpodoxime from the matrix tablets. A good correlation of drug absorption in vivo and drug release in vitro (R-2 = 0.9785) was observed. These results suggested that the investigated CFP matrix tablets have a potential for extended-release dosage forms. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:434 / 441
页数:8
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