Pharmacy Research Journals

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The intraday and interday precision values were Fast dissolving oral drug delivery system is solid dosage form which disintegrates or dissolves within second when placed in the mouth without need of water or chewing.

In present investigation, an attempt has been made to develop oral fast dissolving film of calcium channel blocker lacidipine.

Although a large number of new drug molecules with varied therapeutic potentials have been discovered in the recent decade, most of them are still in developmental process.

This can be attributed to the limited aqueous solubility which governs the bioavailability of such drug molecules.

Recruitment and retention of network members are essential to maintaining the integrity of the network and achieving its research goals. Pharmacy practice-based research networks (PBRNs) are relatively new compared to their primary care forebears, representing a unique set of research challenges.

Recruitment and retention of network members are essential to maintaining the integrity of the network and achieving its research goals.

The purpose of this review is to focus on various methods of preparation, characterization properties, and applications of nanosuspension.

Pharmacy practice-based research networks (PBRNs) are relatively new compared to their primary care forebears, representing a unique set of research challenges.

The optimized formula F1 showed minimum in vitro disintegration time of 25 second and highest dissolution rate 97.3% in 10 minutes with good mechanical properties.

Based on overall results, the conclusion that lacidipine was successfully prepared as oral fast dissolving film with accepted properties.

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