Mediation of in Vitro Cytochrome P450 Activity by Common Pharmaceutical Excipients

2013 ◽  
Vol 10 (7) ◽  
pp. 2739-2748 ◽  
Author(s):  
Philip Martin ◽  
Marco Giardiello ◽  
Tom O. McDonald ◽  
Steven P. Rannard ◽  
Andrew Owen

Author(s):  
Michaela Šadibolová ◽  
Risto O. Juvonen ◽  
Seppo Auriola ◽  
Iva Boušová


2018 ◽  
Vol 39 (5) ◽  
pp. 275-279
Author(s):  
Yuki Asai ◽  
Yukiko Sakakibara ◽  
Rina Inoue ◽  
Rikako Inoue ◽  
Masayuki Nadai ◽  
...  


2012 ◽  
Vol 41 (2) ◽  
pp. 390-397 ◽  
Author(s):  
Lies De Bock ◽  
Koen Boussery ◽  
Myriam Van Winckel ◽  
Peter De Paepe ◽  
Xavier Rogiers ◽  
...  


2005 ◽  
Vol 316 (2) ◽  
pp. 822-829 ◽  
Author(s):  
Wolfgang E. Thasler ◽  
Rania Dayoub ◽  
Marcus Mühlbauer ◽  
Claus Hellerbrand ◽  
Thomas Singer ◽  
...  


1999 ◽  
Vol 66 (1) ◽  
pp. 51-55 ◽  
Author(s):  
W.M ZWEERS-ZEILMAKER ◽  
A.S.J.P.A.M VAN MIERT ◽  
G.J HORBACH ◽  
R.F WITKAMP


Nanoscale ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 5171-5181 ◽  
Author(s):  
Raphaël Cornu ◽  
Nathalie Rougier ◽  
Yann Pellequer ◽  
Alf Lamprecht ◽  
Paul Hamon ◽  
...  

This study emphasizes the interest to set up relevant in vitro models using human hepatic cells to evaluate the hepatotoxicity of nanomedicines.





2003 ◽  
Vol 22 (2) ◽  
pp. 65-71 ◽  
Author(s):  
Margarita Kataropoulou ◽  
Catherine Henderson ◽  
Helen Grant

The use of primary hepatocyte cultures as in vitro models for studying xenobiotic metabolism and toxicity is limited by the loss of liver-specific differentiated functions with time in culture and the inability of the cells to proliferate. The aim of this study was to investigate the effect of incorporating 20% chondroitin-6-sulphate (Ch6SO4), a glycosaminoglycan (GAG), into collagen gels (0.3% w/v) and crosslinking the gels with either 1-ethyl-3-(3-di methylaminopropyl) carbodiimide (EDAC) or 1,6-diaminohexane (DAH) on the expression of glutathione-Stransferases (GSTs) and the activity of cytochrome P450 in hepatocytes cultured for 48 hours and 7 days. Hepatocytes were isolated from male Sprague–Dawley rats by collagenase perfusion. Cell homogenates were immunoblotted against class α and π GST subunits. To measure cytochrome P450 activity, testosterone hydroxylation was assessed. Viability of the cultured cells was assessed by confocal laser scanning microscopy using the vital stain carboxyfluorescein diacetate (CFDA). Cells cultured on gels crosslinked with EDAC were dead by 48 hours as judged by lack of CFDA-derived fluorescence and absence of GST bands on the immunoblots. The viability and morphology of the cells were unaffected by any of the other components of the substrata tested. Expression of GSTs indicated that the hepatocyte phenotype was stable for at least 48 hours. The addition of GAG did not improve the phenotype at either 48 hours or 7 days in culture, but the combination of GAG and DAH crosslinking improved GST expression in the 7-day cultures. However, the hepatocyte cytochrome P450 activity did not show any improvement on any of the gels. The combination of GAG and DAH crosslinking provided the most stable substratum environment in terms of GST expression in hepatocytes.



2014 ◽  
Vol 22 (2) ◽  
pp. 155-160 ◽  
Author(s):  
Min Song ◽  
HyunHee Do ◽  
Oh Kwang Kwon ◽  
Eun-Ju Yang ◽  
Jong-Sup Bae ◽  
...  


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