Dissolution enhancement of valsartan using natural polymers by solid dispersion technique
نویسندگان
چکیده
Solid dispersions have been widely used to enhance the solubility of poorly water soluble drugs. In this study, solid dispersions of valsartan (VAL) with natural polymers such as hupu gum (HG), guar gum (GG) and xanthan gum (XG) were prepared by kneading technique in the weight ratios of 1:1,1:2,1:3 and1:4.The prepared solid dispersions were investigated by X-ray diffraction, infrared spectroscopy, differential scanning caloriemetry and solubility studies. X-ray diffraction and differential scanning caloriemetry have shown that natural polymers inhibit the crystallinity of valsartan. The infrared spectroscopy suggests that there was no chemical interaction between valsartan and natural polymers. Phase solubility studies showed that the drug solubility was increased as the concentration of polymer content was increased. The prepared solid dispersions were analysed for percentage practical yield, drug content and dissolution studies. The results demonstrated that the dissolution of GG/VAL solid dispersions was enhanced greatly at ratios of over 4/1 when compared with that of remaining ratios of GG which shows 97.90% of drug release within 60 minutes.The drug release from the solid dispersions was found to follow the first-order kinetics, Fitment into Hixson Crowell’s cube root model equation suggest the drug release mechanism could be erosion.
منابع مشابه
Investigation of Solid Dispersion Technique in Improvement of Physicochemical Characteristics of Ibuprofen Powder
Ibuprofen solid dispersions were prepared by the solvent and fusion-solvent methods using polyethylene glycol (PEG), polyvinylpyrrolidone (PVP), eudragit RS PO, eudragit RL PO and hydroxypropylmethylcellulose (HPMC) as carriers to improve physicochemical characteristics of ibuprofen. The prepared solid dispersions were evaluated for the flowability, solubility characteristics and dissoluti...
متن کاملSolubility & Dissolution Enhancement of Antihypertensive Agent(S) using Solid Dispersion Techniques
Drugs having poor aqueous solubility present one of the major confronts better absorption for good bioavailability of such drugs. Solid dispersion of Hydrochlorothiazide and valsartan (12.5 mg : 80 mg) in a fixed dose combination was prepared. The major problem with these drugs is their low aqueous solubility, which results into poor bioavailability after oral administration. The purpose of thi...
متن کاملImprovement of Dissolution Characteristics and Bioavailability of Tadalafil by Solid Dispersion Technique Using Water-soluble Polymers
The enhancement of oral bioavailability of poorly water-soluble drugs remains one of the most challenging aspects of drug development. Tadalafil a BCS class II drug is an impotence agent. It is indicated for the treatment of erectile dysfunction and is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type-5 (PDE-5).However, insolubility and poor dissolut...
متن کاملEnhancement of Dissolution Profile of Mefenamic Acid by Solid Dispersion Technique
The oral Bioavailability of BCS (Bio Pharmaceutical Classification System) class II drug with poor solubility and reasonable permeability is limited by drug dissolution. The purpose of this research was to obtain enhancement of the dissolution profile of Mefenamic acid (MA) using solid dispersion technique with hydrophilic polymers such as poly ethylene glycol (PEG), polyvinyl pyrrolidone (PVP)...
متن کاملSolubility enhancement of glimperide: Development of solid dispersion by solvent melt method, characterization and dosage form development
The aim of the present work was to develop immediate release dosage form of the solid dispersion of glimperide (GLIM) for potential enhancement in the bioavailability. The solid dispersions of GLIM were prepared with PEG6000, PVP K30 and Poloxamer 188, in 1:1, 1:3 and 1:5 %w/w ratio by using solvent wetting and solvent melt method. The in vitro dissolution parameters (%DE10min, %DE30min, %DE60m...
متن کامل