شماره ركورد :
143883
عنوان مقاله :
طولاني رهش نمودن پروپرانولول هيدروكلرايد به روش پراكندگي جامد
عنوان به زبان ديگر :
Sustain release formulation of propranolol hydrochloride by solid dispersion technique
پديد آورندگان :
حسن زاده ، داود نويسنده دانشكده داروسازي-دانشگاه علوم پزشكي تبريز ,
رتبه نشريه :
-
تعداد صفحه :
8
از صفحه :
67
تا صفحه :
74
كليدواژه :
پروپرانولول هيدروكلرايد , پزشكي , Solid dispersion , آهسته رهش , Propranolo hydrochloride , پراكندگي جامد , اودراژيت , Eudragit , علوم دارويي , Sustained Release
چكيده لاتين :
Sustained release formulations have many advantages over the conventional dosage forms. There are various techniques to control the release rate of drugs, among which, controlling drugʹs dissolution rate is most popular due to its success and low cost. Although there are numerous studies to produce sustained release formulations, little studies were carried out to use solid dispersion technique to produce sustained release formulations. Propranolol is a (Beta) adrenergic receptor blocker that has some adverse effects. These side effects could be reduced by reduction of usage frequency and producing steady pharmacological effects by preparing sustain release formulation. In this study we tried to use solid dispersion technique to slow down the release rate in water from its tablet formulation. Solid dispersion formulations were prepared using molten-solvent technique. The final obtained powder was compressed into tablets and their dissolution were investigated at pH 1.2 and 6.8. FT-IR was used to find any interaction between the drug and excipient. The results showed that solid dispersions produced harder tablets than that of physical mixtures formulations. The amount of eduragit had no significant effect on release rate. It was interesting to note that solid dispersions containing PEG 6000 and eudragit had slow release rate. This indicates that the presence of PEG 6000 to slow down the release of propranolol from eudragit solid dispersion matrices is necessary. It was found that type of Eudragit had not significant effect on the release rate of propranolol from solid dispersions. Ethylcelllose alone was not able to decrease the release rate. Although PEG 6000 is hydrophilic excipient, the reduced release rate in presence of PEG 6000 is due to the enhance effect of PEG 6000 on the hardness of tablets. FT-IR study showed no interaction between the drug and excipients.
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