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Preparation and In Vitro Evaluation of Aceclofenac Loaded Eudragit Microspheres


Affiliations
1 Dept of Pharmaceutics, Hi-Tech College of B Pharmacy, Chandrapur, (Maharashtra), India
2 Dept of Pharmaceutics, Hi-Tech College of B Pharmacy, Chandrapur, (Maharashtra), India
3 Ultra College of Pharmacy, Madhurai, Tamilnadu, India
     

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Aceclofenac is a non-steroidal anti-inflammatory drug. NSAIDs are chemically heterogeneous group of compounds including the sub-class of COX-2 inhibitor. The most available traditional NSAIDs act by inhibiting the prostaglandin synthases enzymes known as the cyclooxygenases. Aceclofenac microspheres were prepared using solvent evaporation technique. The drug : polymer combination such as Eudragit RL 100.The microspheres were evaluated with particle size, size distribution, scanning electron microscopy, encapsulation efficiencies, higuchi release and in vitro drug release study (percent cumulative drug release) using paddle dissolution method.


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  • Preparation and In Vitro Evaluation of Aceclofenac Loaded Eudragit Microspheres

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Authors

Pankaj Pimpalshende
Dept of Pharmaceutics, Hi-Tech College of B Pharmacy, Chandrapur, (Maharashtra), India
S. S. Burle
Dept of Pharmaceutics, Hi-Tech College of B Pharmacy, Chandrapur, (Maharashtra), India
C. Vijay
Ultra College of Pharmacy, Madhurai, Tamilnadu, India

Abstract


Aceclofenac is a non-steroidal anti-inflammatory drug. NSAIDs are chemically heterogeneous group of compounds including the sub-class of COX-2 inhibitor. The most available traditional NSAIDs act by inhibiting the prostaglandin synthases enzymes known as the cyclooxygenases. Aceclofenac microspheres were prepared using solvent evaporation technique. The drug : polymer combination such as Eudragit RL 100.The microspheres were evaluated with particle size, size distribution, scanning electron microscopy, encapsulation efficiencies, higuchi release and in vitro drug release study (percent cumulative drug release) using paddle dissolution method.