Preparation and Characterization of Paracetamol Solid Dispersions Using Opened Ring PVP and PEG 4000

Background & Objective: Solid dispersions (SDs) have been traditionally used as an effective method for improving the dissolution properties and bioavailability of poorly water-soluble drugs. The aim of this study was to improve the solubility and dissolution rate of paracetamol by SD technique....

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Main Authors: hossein asgarirad (Author), ali farmoudeh (Author), anahita rezaeiroshan (Author), mohammadjavad rajaei (Author)
Format: Book
Published: Fasa University of Medical Sciences, 2019-09-01T00:00:00Z.
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001 doaj_69fa2b51b8154c45966a3c4a893321eb
042 |a dc 
100 1 0 |a hossein asgarirad  |e author 
700 1 0 |a ali farmoudeh  |e author 
700 1 0 |a anahita rezaeiroshan  |e author 
700 1 0 |a mohammadjavad rajaei  |e author 
245 0 0 |a Preparation and Characterization of Paracetamol Solid Dispersions Using Opened Ring PVP and PEG 4000 
260 |b Fasa University of Medical Sciences,   |c 2019-09-01T00:00:00Z. 
500 |a 2228-5105 
500 |a 2783-1523 
520 |a Background & Objective: Solid dispersions (SDs) have been traditionally used as an effective method for improving the dissolution properties and bioavailability of poorly water-soluble drugs. The aim of this study was to improve the solubility and dissolution rate of paracetamol by SD technique. Materials & methods: The prepared SDs were evaluated by saturation solubility test, In-vitro drug release test, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). Results: The prepared SDs exhibited a statistically significant increase in the solubility of paracetamol compared to that of the free drug (p < 0.05). After 15 min SD tablets had an enhanced cumulative drug release compared to tablets of the free drug (p < 0.05). FTIR study revealed that paracetamol was stable in polymeric dispersions. DSC and SEM microscopy showed that the drugs crystallinity was decreased during the preparation process (amorphous crystal formation). Conclusion: The FTIR spectroscopic test revealed the presence of intermolecular hydrogen bonding between paracetamol and the polymers in the SDs, which could increase the aqueous solubility of the drug. The DSC analysis indicated that the drug was in the amorphous state when dispersed in the polymers. Dissolution studies indicated that the dissolution rates were markedly increased in the SDs compared with those of paracetamol alone, and Better results were obtained with PVP K25. 
546 |a EN 
690 |a solid dispersion 
690 |a peg 4000 
690 |a pvp k25 
690 |a paracetamol 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n Journal of Advanced Biomedical Sciences, Vol 9, Iss 3, Pp 1621-1631 (2019) 
787 0 |n http://jabs.fums.ac.ir/article-1-1944-en.pdf 
787 0 |n https://doaj.org/toc/2228-5105 
787 0 |n https://doaj.org/toc/2783-1523 
856 4 1 |u https://doaj.org/article/69fa2b51b8154c45966a3c4a893321eb  |z Connect to this object online.