Increase in Dissolution Rate of Simvastatin by Amorphous Solid Dispersion System with Hydroxypropylmethylcellulose Polymer
نویسنده
چکیده
The objective of the present study was to prepare amorphous solid dispersion system simvastatin–hydroxypropylmethylcellulose (HPMC) to enhance the dissolution rate. Amorphous solid dispersion of simvastatin was prepared by solvent technique using HPMC as carrier with ratio of 1:1, 1:3 and 1:5 (w/w). Physicochemical properties of solid dispersions were investigated by X-ray powder diffraction, thermal analysis of differential scanning calorimetry (DSC) and scanning electron microscopy. The dissolution rate profile was performed at 37 ± 0.5 °C and 50 rpm in phosphate buffer solution (pH 7) containing 0,5% sodium laurylsulphate. Powder X-ray diffraction of solid dispersion system exhibited decrease in peak diffraction intensity of simvastatin when increasing the HPMC ratio in solid dispersion system. DSC thermogram of solid dispersion system showed the absence of endothermic peak of simvastatin. All the solid dispersion demonstrated faster dissolution rate in comparison with intact simvastatin and its physical mixture. The dissolution rate of simvastatin from solid dispersion increased with an increased ratio of HPMC polymer. The solid dispersion system of simvastatin with HPMC provide a promising way to improve its dissolution rate.
منابع مشابه
The Effect of PEG Molecular Weights on Dissolution Behavior of Simvastatin in Solid Dispersions
The purpose of the present study was to investigate the effect of polyethylene glycol (PEG) molecular weights (6000, 12000 and 20000) as solid dispersion (SD) carriers on the dissolution behavior of simvastatin. SDs with various drug : carrier ratios were prepared by solvent method and evaluated for dissolution rate. Differential scanning calorimetry (DSC), X-ray diffraction (XRD), infrared spe...
متن کاملThe Effect of PEG Molecular Weights on Dissolution Behavior of Simvastatin in Solid Dispersions
The purpose of the present study was to investigate the effect of polyethylene glycol (PEG) molecular weights (6000, 12000 and 20000) as solid dispersion (SD) carriers on the dissolution behavior of simvastatin. SDs with various drug : carrier ratios were prepared by solvent method and evaluated for dissolution rate. Differential scanning calorimetry (DSC), X-ray diffraction (XRD), infrared spe...
متن کاملEnhancing Dissolution Rate of Carbamazepine via Cogrinding with Crospovidone and Hydroxypropylmethylcellulose
Carbamazepine belongs to the class II biopharmaceutical classification system (BCS) which is characterized by a high per-oral dose, a low aqueous solubility and a high membrane permeability. The bioavailability of such a drug is limited by the dissolution rate. In order to increase the drug dissolution, its solid dispersions were prepared by the cogrinding technique using an insoluble but highl...
متن کاملEnhancing Dissolution Rate of Carbamazepine via Cogrinding with Crospovidone and Hydroxypropylmethylcellulose
Carbamazepine belongs to the class II biopharmaceutical classification system (BCS) which is characterized by a high per-oral dose, a low aqueous solubility and a high membrane permeability. The bioavailability of such a drug is limited by the dissolution rate. In order to increase the drug dissolution, its solid dispersions were prepared by the cogrinding technique using an insoluble but highl...
متن کاملتاثیر گلوسیر 13/50 بر سرعت آزاد شدن ناپروکسن از پراکندگی های جامد تهیه شده با پلی اتیلن گلیکول 4000
Background and purpose: Solubility behavior of a drug is one of the key determinants of its oral bioavailability. The bioavailability may be enhanced by increasing the solubility and dissolution rate of drug by combining the drug with a hydrophilic carrier. Naproxen is a poor water non-soluble analgesic and anti- inflammatory drug. A possible way of overcoming the naproxen low aqueous solubilit...
متن کامل