COMPARATIVE STUDY OF REVERSE WET GRANULATION WITH CONVENTIONAL WET GRANULATION IN SOLUBILITY ENHANCEMENT OF SIMVASTATIN

Abstract

Objectives: Simvastatin is a cholesterol- lowering agent widely used in hypercholesterolemia. It belongs to BCS class II drugs having low solubility and high permeability. Simvastatin is practically insoluble in water and poorly absorbed from the gastrointestinal tract. Therefore, it is necessary to introduce an effective method to enhance the solubility and dissolution rate of the drug. The main purpose of this work was to compare the reverse wet granulation with conventional wet granulation in enhancing the solubility of Simvastatin.Methods: The Granules were prepared by both conventional wet granulation in which Simvastatin was added along with other dry excipients and reverse wet granulation in which Simvastatin was added in granulating solvent using water as granulating solvent and Povidone, Lactose, Sodium starch glycolate, Magnesium stearate and Aerosil as an Excipients. The granules were evaluated for flow properties, solubility study, X- ray diffraction and FTIR study.Results: The flow properties of reverse wet granulation were found to be improved as compared to conventional wet granulation. The tablets were formulated from either type of granules which were subjected to a Hardness, Disintegration, Weight variation, Content of active ingredient, Friability, Wetting time and Dissolution test. The Simvastatin tablets of reverse wet granulation resulted in about 1.4 fold increase in dissolution rate when compared to conventional wet granulation tablets. The significant difference between flow properties and dissolution profile in between reverse wet granulation and conventional wet granulation was validated by statistical evaluation.Conclusion: Reverse wet granulation can be successfully used over the conventional wet granulation for solubility enhancement of Simvastatin. The method is easy to adopt. 

Authors and Affiliations

Sonal M. Jagtap, Ashish Y. Pawar, Khanderao R. Jadhav

Keywords

Related Articles

Critical Evaluation of Drug Promotional Literature for Drugs Used in Cardiovascular Diseases

Objective: This study was conducted to critically evaluate the drug promotional literature pertaining to drugs used in cardiovascular disorders using WHO criteria for ethical promotion of drugs. Methods: The brochures we...

CURCUMIN-LOADED MULTI-VALENT LIGANDS CONJUGATED-NANOPARTICLES FOR ANTI-INFLAMMATORY ACTIVITY

Objective: The present study aims to develop curcumin-loaded muti-valent ligands conjugated-nanoparticlesfor targeted cell and study the biological activities including anti-inflammatory activity and kinetic cellular upt...

EFFECTS OF STREPTOZOTOCIN INDUCED DIABETES MELLITUS TYPE 1 ON THE RAT BRAIN ANTIOXIDANT STATUS AND ACTIVITY OF ACETYL-CHOLINESTERASE: A NOVEL AND POTENTIAL TREATMENT BY VITEX NEGUNDO.

Objective: The objective of the present study was to determine the effect of streptozotocin (STZ) induced diabetes type 1 on activity of acetyl-cholinesterase (AChE) in rat brain and on the brain antioxidant status and a...

IDENTIFICATION OF DIFFERENT SAMPLES OF GUGGULU THROUGH SENSORY EVALUATION TECHNIQUE

Objective: Present study is aimed to evaluate an efficacy of the two-Alternative Forced Choice (2-AFC) sensory methods in detecting differences between Fresh and old samples of Guggulu.Methods: Both samples of Guggulu we...

A CASE REPORT ON AYURVEDIC MEDICINE (RED MERCURIC SULPHATE) INDUCED BRONCHIOLITIS OBLITERANS ORGANIZING PNEUMONIA (BOOP) IN SERO POSITIVE RHEUMATOID PATIENT

Bronchiolitis obliterans organizing pneumonia (BOOP) is a lung disease that causes inflammation in the small air tubes (bronchioles) and air sacs (alveoli). It can be caused due to wide range of etiologies like viral inf...

Download PDF file
  • EP ID EP579202
  • DOI -
  • Views 62
  • Downloads 0

How To Cite

Sonal M. Jagtap, Ashish Y. Pawar, Khanderao R. Jadhav (2015). COMPARATIVE STUDY OF REVERSE WET GRANULATION WITH CONVENTIONAL WET GRANULATION IN SOLUBILITY ENHANCEMENT OF SIMVASTATIN. International Journal of Pharmacy and Pharmaceutical Sciences, 7(1), 264-272. https://europub.co.uk/articles/-A-579202