IN-VITRO DISSOLUTION AND SOME PHYSICAL PROPERTIES OF TWO GENERICS OF LEVAMISOLE BLOUS FORMULATIONS FOR LARGE ANIMALS
Journal Title: Indo American Journal of Pharmaceutical Research - Year 2017, Vol 7, Issue
Abstract
Abstract Physical and dissolution properties of solid oral dosage formulations significantly affect therapeutic outcomes following their use in veterinary medicine. Therapeutic failure of most levamisole boluses for the prevention and treatment of helminth infections have been a recurrent complaint from animal health workers and veterinarians in Nigeria. However, there is dearth of information on the quality of oral bolus formulations of levamisole for veterinary use in Nigeria. Consequently, the purpose of this study was to evaluate physical and dissolution properties of two generic products of levamisole boluses commonly used in large animal practice in Nigeria. Two frequently used generics of levamisole oral boluses for large animal practice (A & B) were evaluated for bolus weight uniformity, hardness, friability, disintegration and dissolution as specified in the United States Pharmacopoeia. The results demonstrated that generic B failed weight uniformity and friability tests, whereas generic A failed friability and disintegration tests. All the products passed dissolution profile test as specified. Consequently, the two products can be used interchangeably, however, generic B is recommended for treating acute enteric helminthosis because of its fast disintegration and dissolution rates as compared to generic A.
DESIGN AND EVALUATION OF CLARITHROMYCIN SUSTAINED RELEASE TABLETS USING ISOLATED NATURAL POLYSACCHARIDE
The present investigation was to isolate natural polymers like tamarind seed polysaccharide, followed by formulation of clarithromycin sustained release tablets. The polymer, drug and dug excipient mixtures were subjecte...
SIMULTANEOUS ESTIMATION OF SOFOSBUVIR AND LEDIPASVIR USING UV SPECTROPHOTOMETRIC AND RP-HPLC METHODS
Abstract The present work includes two simple, inexpensive, rapid, accurate and precise UV spectrophotometric methods and another isocratic RP-HPLC method for estimation of Sofosbuvir (SOFO) and Ledipasvir (LEDI) in bulk...
FORMULATATION DEVELOPMENT AND EVALUATION OF EFFERVESCENT TABLET OF PARACETAMOL AND N-ACETYLCYSTEINE.
Abstract The main aim of the work is to design and develop stable formulation of effervescent tablets of Paracetamol and N-Acetylcysteine and to evaluate respective formulation. The present work is directed to a new phar...
A COMPREHENSIVE REVIEW ON FUTURE PROSPECTS FOR FAST DISSOLVING ORAL FILMS
The ultimate goal of any drug delivery system is the successful delivery of the drug to the body, however patient compliance must not be overlooked. Oral drug delivery is the most widely utilized route of administration...
DEVELOPMENT AND EVALUATION OF EMULGEL FOR WOUND HEALING ACTIVITY
Abstract The study was designed with the aim to evaluate metformin and atorvastatin for its wound Healing activity.Two different formulations of Metformin emulgel and atorvastatin emulgel were formulated using Design exp...