نتایج جستجو برای: p gp inhibition

تعداد نتایج: 1574865  

2015
Shubh Prabhat Gupta Manisha Bhati Kapil Jhajharia Hardik Patel Ashutosh Paliwal Sundeep Franklin

BACKGROUND Microorganisms and their by-products in pulpal and periapical diseases are to be considered as the primary etiological agents of the pulpal necrosis and apical periodontitis. Enterococcus faecalis, which is the most common organism isolated from failed root canals, is a Gram-positive facultative anaerobe. Yeasts can be detected in 7-18% of infected root canals. MATERIALS AND METHOD...

Journal: :Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques 2011
Alaa H Abuznait Shawn G Patrick Amal Kaddoumi

PURPOSE Drug transporters are increasingly recognized as important determinants of variability in drug disposition and therapeutic response, both in pre-clinical and clinical stages of drug development process. The role P-glycoprotein (P-gp) plays in drug interactions via its inhibition is well established. However, much less knowledge is available about drugs effect on P-gp up-regulation. The ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2000
I Kawahara Y Kato H Suzuki M Achira K Ito C L Crespi Y Sugiyama

Our previous report showed that L754.394 and valspodar (PSC833) are potent inhibitors of midazolam hydroxylation in human jejunum microsomes and vectorial transport of vinblastine in Caco-2 cells, respectively. In the present study, to directly examine the interactions of these compounds as well as other substrates with CYP3A4 and P-glycoprotein (P-gp), we performed in vitro inhibition studies ...

2018
Hyun-Jung Moon Hak-Bong Kim Su-Hoon Lee So-Eun Jeun Chi-Dug Kang Sun-Hee Kim

NSAIDs (non-steroidal anti-inflammatory drugs) have potential use as anticancer agents, either alone or in combination with other cancer therapies. We found that NSAIDs including celecoxib (CCB) and ibuprofen (IBU) significantly potentiated the cytotoxicity of Hsp90 inhibitors in human multidrug-resistant (MDR) cells expressing high levels of mutant p53 (mutp53) protein and P-glycoprotein (P-gp...

Journal: :Molecular pharmacology 2002
Sean Ekins Richard B Kim Brenda F Leake Anne H Dantzig Erin G Schuetz Lu-Bin Lan Kazuto Yasuda Robert L Shepard Mark A Winter John D Schuetz James H Wikel Steven A Wrighton

Using in vitro data, we previously built Catalyst 3-dimensional quantitative structure activity relationship (3D-QSAR) models that qualitatively rank and predict IC(50) values for P-glycoprotein (P-gp) inhibitors. These models were derived and tested with data for inhibition of digoxin transport, calcein accumulation, vinblastine accumulation, and vinblastine binding. In the present study, 16 i...

Etoposide, a widely used anticancer drug, exhibits low and variable oral bioavailability mainly because of being substrate for the efflux transporter, P-glycoprotein (P-gp). Therefore, the present study was aimed to investigate the effect of D-α-tocopherol polyethylene glycol 1000 succinate (TPGS) and PEG 400 as P-gp inhibitors on the intestinal absorption of etoposide. Everted sacs of rat smal...

2015
Chuan-jiang Zhu Fang Hua Xiao-lu Zhu Meng Li Hong-xu Wang Xiao-ming Yu Yan Li Hans-Joachim Lehmler

The (-)- and (+)-clausenamide (CLA) enantiomers have different pharmacokinetic effects in animals, but their association with putative stereoselective regulation of P-glycoprotein (P-gp) remains unclear. Using three cells expressing P-gp-Caco-2, KBv and rat brain microvessel endothelial cells(RBMEC), this study investigated the association of CLA enantiomers with P-gp. The results showed that t...

2014
Jeroen J.M.A. Hendrikx Jos H. Beijnen Alfred H. Schinkel

In the past years, the development of oral formulations of the taxane anticancer drugs paclitaxel (Taxol ®) and docetaxel (Taxotere ®) has been the focus of preclinical and clinical research in our groups. A major limitation in the concept of oral administration of paclitaxel and docetaxel is their low oral availability [1]. Paclitaxel and docetaxel have poor aqueous solubility and upon oral ad...

2006
Joseph A. Ludwig Gergely Szakács Scott E. Martin Benjamin F. Chu Carol Cardarelli Zuben E. Sauna Natasha J. Caplen Henry M. Fales Suresh V. Ambudkar John N. Weinstein Michael M. Gottesman

ATP-binding cassette (ABC) proteins include the best known mediators of resistance to anticancer drugs. In particular, ABCB1 [MDR1/P-glycoprotein (P-gp)] extrudes many types of drugs from cancer cells, thereby conferring resistance to those agents. Attempts to overcome P-gp-mediated drug resistance using specific inhibitors of P-gp has had limited success and has faced many therapeutic challeng...

Journal: :Circulation 2001
S R Steinhubl J D Talley G A Braden J E Tcheng P J Casterella D J Moliterno F I Navetta P B Berger J J Popma G Dangas R Gallo D C Sane J F Saucedo G Jia A M Lincoff P Theroux D R Holmes P S Teirstein D J Kereiakes

BACKGROUND The optimal level of platelet inhibition with a glycoprotein (GP) IIb/IIIa antagonist necessary to minimize thrombotic complications in patients undergoing a percutaneous coronary intervention (PCI) is currently unknown. METHODS AND RESULTS Five hundred patients undergoing a PCI with the planned use of a GP IIb/IIIa inhibitor had platelet inhibition measured at 10 minutes, 1 hour, ...

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