<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>127</id><JournalTitle>FORMULATION AND EVALUATION OF IMMEDIATE RELEASE (IR) TABLETS OF VALACYCLOVIR</JournalTitle><Abstract>The objective of this research work was to formulate, develop and evaluate the immediate release (IR) tablets of
valacyclovir 500 mg. The tablets were prepared by direct compression method. For the Immediate release formulation the
disintegration time of the tablet must be optimised in order to have a faster release of drug in the dissolution profile. The
disintegration time is managed by using the superdisintegrants like sodium starch glycollate and HPC in the formulation. The
formulation Trails were optimised by incorporating varying composition of HPC as binder, Sodium starch glycollate as
Superdisintegrants, Talc as Glidant and Magnesium Stearate as Lubricant. The different excipients were tested for their
compatibility with Valacyclovir, which revealed that there was no chemical and physical interaction occurred. The
preformulation parameters such as bulk density, tapped density, compressibility index and Hausner ratio were analysed for
prepared granules before compression. The thickness, hardness, friability, weight variation, disintegration time and drug
content uniformity was evaluated for tablets. The effect of these variables on the drug release profile of Valacyclovir was also
studied. The in-vitro drug release studied were performed in the USP Apparatus-II (Paddle) using water with phosphate buffer
PH 6.8 as a dissolution media at 50rpm speed and temperature of 37Â°C Â± 2Â°c. The sampling was done at periodic time
intervals of 5, 10,15,20,25 and 30 minutes and was replaced with equal volume of dissolution media after each withdrawal.
The cumulative amount of drug release at different time interval was estimated using UV method based on the evaluation
result F7 trial formulation was selected as the best formulation. These results indicated that the selected formulation was stable
during the test period of accelerated stability studies.</Abstract><Email>ritudubi@gmail.com</Email><articletype>Research</articletype><volume>9</volume><issue>2</issue><year>2019</year><keyword>Immediate Release Formulation,Valacyclovir,Anti-viral,Preformulation</keyword><AUTHORS>Ritu Dabi,Sunil Shah,Hemant Kumar Sharma</AUTHORS><afflication>College of Pharmacy, Sri Satya Sai University of Technology & Medical Sciences Sehore-466001, Madhya Pradesh, India,College of Pharmacy, Sri Satya Sai University of Technology & Medical Sciences Sehore-466001, Madhya Pradesh, India,College of Pharmacy, Sri Satya Sai University of Technology & Medical Sciences Sehore-466001, Madhya Pradesh, India</afflication></Article></Articles>