Pravin Gupta
1*, Manish Kumar
2, Darpan Kaushik
31 Department of Pharmaceutics, Agra Public Pharmacy College, Agra (U.P.), India.
2 Department of Pharmaceutics, Maharishi Markandeshwar College of Pharmacy, Maharishi Markandeshwar University, Mullana-Ambala (Haryana), India.
3 Department of Pharmaceutical Chemistry, Agra Public Pharmacy College, Agra (U.P), India.
Abstract
Purpose: Various floating and
pulsatile drug delivery systems suffer from variations in the gastric transit
time affecting the bioavailability of drugs. The objective of the study was to
develop Pantoprazole Sodium (PAN) microballoons that may prolong the gastric residence
time and could enhance the drug bioavailability.
Methods: Microballoons were
prepared using Eudragit®L100 by adopting emulsion solvent diffusion
method with non-effervescent approach, in
vitro studies were performed and the in
vivo evaluation was carried out employing ethanol induced ulceration
method. Optimization and validation were carried out through Design Expert®
software.
Results: The results
demonstrate an increase in percentage yield, buoyancy, encapsulation efficacy
and swelling. Particles were in the size range 80-100 µm following zero order
release pattern. SEM study revealed their rough surface with spherical shape,
internal cavity and porous walls. DSC thermo gram confirms the encapsulation of
drug in amorphous form. Significant anti ulcer activity was observed for the
prepared microballoons. The calculated ulcer index and protection were
0.20±0.05 and 97.43 % respectively for LRS-O (optimized formulation).
Conclusion: This kind of pH dependent drug delivery may
provide an efficient dosage regimen with enhanced patient compliance.