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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/14611
Title: Enhanced dissolution rate of Ketoprofen by fabricating into smart nanocrystals
Authors: Khan, Jahangir
Bashir, Sajid
Khan, Muhammad Asif
Ghaffar, Rukhsana
Naz, Attiqa
Khan, Wali
Ahmad, Shujat
Ullah, Abid
Ali, Faryal Liaqat
Isreb, Mohammad
Keywords: Nanocrystals
Ketoprofen
DENA
Milling time
characterization
Issue Date: 19-Nov-2019
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciences, Karachi
Citation: Khan, J., Bashir, S., Khan, M. A., Ghaffar, R., Naz, A., Khan, W., ... & Isreb, M. (2019). Enhanced dissolution rate of Ketoprofen by fabricating into smart nanocrystals. Pakistan Journal of Pharmaceutical Sciences, 32.
Abstract: The low bioavailability of Ketoprofen is associated with its hydrophobic nature that can be solved by nanonization. For this purpose, a polymeric solution with drug concentration of 3.5% w/w was formulated. The produced solution was milled for 60 minutes in DENA® mill which contains 0.2µm yttrium reinforced zirconium beads. The Physicochemical properties, characterization including stability studies of the prepared nanoparticles were carried out using pharmacopeial techniques of zeta potential, PXRD, DSC, SEM and TEM. Results suggest that stable crystalline nanocrystals with a size of 169±1.98nm with PDI of 0.194±0.04 and zeta potential of -22.0±2.25mV were produced. Moreover, enhances in-vitro release rate of 78.6% for the processed Ketoprofen was achieved in first 5 min as compared to raw form and marketed drug which released only 22.9% and 33.1% of drug respectively. The 60 days stability studies at 4oC & 25oC revealed that polymers PVP-K30-HPMC-6cps-SDS were effective in stabilizing the nanocrystals. Comparatively stable ketoprofen nanocrystals were successfully produced by DENA® mill with marked enhanced dissolution rate. It proved a useful for commercialization technique due to high drug concentration and retention of distinct characteristics at large scale.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/14611
ISSN: 1011-601X
Appears in Collections:Issue 6 (Supplementary)

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