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Fast disintegrating tablet of Doxazosin Mesylate nanosuspension: Preparation and characterization
- Source :
- Journal of Drug Delivery Science and Technology. 61:102210
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- Doxazosin Mesylate (DOX) is an antihypertensive drug which possesses poor water solubility and hence low bioavailability. The study objective is to prepare DOX fast disintegrating tablets as a new dosage form for geriatric patients. First, 23 full factorial design using Polyvinyl pyrrolidone k 30, Poloxamer-407 and Sodium Lauryl Sulphate at low and high ratios were used for preparation of DOX nanosuspension as a trial to improve its dissolution properties. Nanosuspension formulations were characterized using Transmission electron microscopy, Differential scanning calorimetry and Fourier transform infrared spectroscopy. Then, the optimized formula was incorporated in fast disintegrating tablets using different superdisintegrants. The tablets were evaluated for hardness, thickness, friability percentage, diameter, weight variation, Wetting time, disintegration time and percentage dissolution after 10 min. A significant reduction (rapidly and efficiently) in mean arterial pressure of hypertensive rats was observed for DOX nanosuspension fast disintegrating tablet using Ac-Di-Sol as a superdisintegrant with 100% dissolution after 10 min.
- Subjects :
- Materials science
Pharmaceutical Science
02 engineering and technology
Factorial experiment
021001 nanoscience & nanotechnology
Friability
030226 pharmacology & pharmacy
Doxazosin Mesylate
Dosage form
Bioavailability
03 medical and health sciences
0302 clinical medicine
Differential scanning calorimetry
Fourier transform infrared spectroscopy
0210 nano-technology
Dissolution
Nuclear chemistry
Subjects
Details
- ISSN :
- 17732247
- Volume :
- 61
- Database :
- OpenAIRE
- Journal :
- Journal of Drug Delivery Science and Technology
- Accession number :
- edsair.doi...........529239d1a3d8c5546c7f5bc728ac6863
- Full Text :
- https://doi.org/10.1016/j.jddst.2020.102210