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https://read.qxmd.com/read/28702816/enhancing-the-solubility-of-fenofibrate-by-nanocrystal-formation-and-encapsulation
#1
JOURNAL ARTICLE
Raj Kumar, Prem Felix Siril
Development of techniques to enhance bioavailability of drugs having poor water solubility is a big challenge for pharmaceutical industry. Solubility can be enhanced by particle size reduction and encapsulation using hydrophilic polymers. Fenofibrate (FF) is a drug for regulating lipids. Multi-fold enhancement in solubility of FF has been achieved by nanocrystal formation in the present study. Nanoparticles were prepared by an evaporation-assisted solvent-antisolvent interaction (EASAI) approach. Water-soluble polymers, viz...
January 2018: AAPS PharmSciTech
https://read.qxmd.com/read/27612834/unusual-anti-leukemia-activity-of-nanoformulated-naproxen-and-other-non-steroidal-anti-inflammatory-drugs
#2
JOURNAL ARTICLE
Raj Kumar, Prem Felix Siril, Farideh Javid
The non-steroidal anti-inflammatory drugs (NSAIDs) are the most widely used pharmaceuticals worldwide. Interestingly, many of them have significant anticancer properties too. However, the poor water solubility of certain NSAIDs limits their application for cancer treatment. Nanosizing of such drugs can help to improve the solubility and this may result in enhanced anticancer activities too. Moreover, over dosages and the accompanying side effects of NSAIDs can be minimized by improving their solubility and bioavailability...
December 1, 2016: Materials Science & Engineering. C, Materials for Biological Applications
https://read.qxmd.com/read/19255943/involvement-of-mrp2-mrp2-in-the-species-different-excretion-route-of-benzylpenicillin-between-rat-and-human
#3
COMPARATIVE STUDY
M-K Choi, H Kim, Y-H Han, I-S Song, C-K Shim
1. The purpose of this study was to investigate the involvement of rat Mrp2 and human MRP2 in benzylpenicillin transport using canalicular liver plasma membrane (cLPM) vesicles isolated from Sprague-Dawley or Easai hyperbilirubinemic (EHBR) rats, and MDCKII cells overexpressing MRP2. 2. The adenosine triphosphate (ATP)-dependent uptake of benzylpenicillin and oestradiol-17beta-D-glucuronide (E(2)17betaG), a representative substrate for Mrp2, into EHBR-cLPM vesicles was decreased relative to that seen with control-cLPM vesicles, which may reflect the absence of Mrp2 in the EHBR...
February 2009: Xenobiotica; the Fate of Foreign Compounds in Biological Systems
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