List of Refereed Journals published by UGC, New Delhi on 28-03-2017-- AJRC (Sr. No.-1025); AJM (Sr. No.-2497); RJET (Sr. No.-7220); RJPP (Sr. No.- 7232): RJPPD (Sr. No.- 7234); RJPT (Sr. No.-7235) (19-Apr-2017)        | List of Refereed Journals published by UGC, New Delhi on 11-01-2017-- Research Journal of Pharmacy and Technology (Sr. No.-275); Asian Journal of Management (Sr. No.-3986); Asian Journal of Research in Chemistry (Sr. No.-4008); Research Journal of Engineering and Technology (Sr. No.-31787); Research (22-Jan-2017)        |

Journal :   Research Journal of Pharmacy and Technology

Volume No. :   3

Issue No. :  1

Year :  2010

Pages :   

ISSN Print :  0974-3618

ISSN Online :  0974-360X


Registration

Allready Registrered
Click to Login

Aceclofenac Extended Release Matrix Tablets: Formulation and In Vitro Evaluation



Address:   1Dept. of Pharmaceutics, Bapatla College of Pharmacy, Bapatla, Guntur Dist, Andhra Pradesh, India – 522101. 2Dept. of Pharmaceutics, Hindu College of Pharmacy, Amaravathi road, Guntur, Andhra Pradesh, India – 522002.
DOI No: Not Available

ABSTRACT:
The objective of the present study was to develop once-daily extended-release matrix tablets of aceclofenac, a non-steroidal anti-inflammatory drug (NSAID) has been indicated for various painful indications, and proved as effective as other NSAIDs with lower indications of gastro-intestinal adverse effects and thus, resulted in a greater compliance with treatment. Natural polymer, xanthan gum was used as matrix former, microcrystalline cellulose (Avicel PH101), dibasic calcium phosphate (DCP) were used as diluents. The matrix tablets were prepared by direct compression, and were subjected to physical characterization and in vitro release studies. The in vitro drug release was carried out using USP apparatus 2 at 100 rpm in 900 ml of 2% SLS acidic dissolution medium (pH 1.2) for 2 hrs, followed by 900 ml alkaline dissolution medium (pH 6.8) for 3-24 hrs. Formulation was optimised on the basis of acceptable tablet properties and in vitro drug release. The results of dissolution studies indicated that formulation F-II (drug to polymer (1:0.3), the most success of the study, exhibited drug release pattern very close to the marketed extended release profile. By applying exponential equation, optimised formula followed korsmeyer-peppas model with non-Fickian anomalous transport mechanism.
KEYWORDS:
Aceclofenac, xanthan gum, matrix tablets, extended release, direct compression
Cite:
Not Available
[View HTML]      [View PDF]



Visitor's No. :   218882