Literature DB >> 31804919

Probe Cocktail to Assess Transporter Function in Sandwich-Cultured Human Hepatocytes.

Cen Guo1, Kenneth R Brouwer, Paul W Stewart, Caroline Mosley, Kim L R Brouwer.   

Abstract

PURPOSE: Probe substrates are used routinely to assess transporter function in vitro. Administration of multiple probe substrates together as a "cocktail" in sandwich-cultured human hepatocytes (SCHH) could increase the throughput of transporter function assessment in a physiologically-relevant in vitro system. This study was designed to compare transporter function between cocktail and single agent administration in SCHH.
METHODS: Rosuvastatin, digoxin, and metformin were selected as probe substrates of hepatic transporters OATP1B1, OATP1B3, BCRP, P-gp, and OCT1. Total accumulation (Cells+Bile) and biliary excretion index (BEI) values derived from administration of the cocktail were compared to values obtained after administration of single agents in the absence and presence of a model inhibitor, erythromycin estolate.
RESULTS: For rosuvastatin and metformin accumulation, the ratio of means [90% confidence interval (CI)] for cocktail to single agent administration was 100% [94%, 106%] and 90% [82%, 99%], respectively. Therefore, the cocktail and single-agent mode of administration were deemed equivalent per standard equivalence criterion of 80-120% for rosuvastatin and metformin accumulation, but not for digoxin accumulation (77% [62%, 92%]). The ratio of means [90% CI] for rosuvastatin BEI values between the two administration modes (105% [97%, 114%]) also was deemed equivalent. The ratio for digoxin BEI values between the two administration modes was 99% [78%, 120%]. In the presence of erythromycin estolate, the two administration modes were deemed equivalent for evaluation of rosuvastatin, digoxin, and metformin accumulation; the ratio of means [90% CI] was 104% [94%, 115%], 94% [82%, 105%], and 100% [88%, 111%], respectively. However, rosuvastatin and digoxin BEI values were low and quite variable in the presence of the inhibitor, so the BEI results were inconclusive.
CONCLUSIONS: These data suggest that rosuvastatin and metformin can be administered as a cocktail to evaluate the function of OATP1B1, OATP1B3, BCRP, and OCT1 in SCHH, and that digoxin may not be an ideal component of such a cocktail.

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Year:  2019        PMID: 31804919      PMCID: PMC7048373          DOI: 10.18433/jpps30706

Source DB:  PubMed          Journal:  J Pharm Pharm Sci        ISSN: 1482-1826            Impact factor:   2.327


  26 in total

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2.  Simultaneous Assessment of Transporter-Mediated Drug-Drug Interactions Using a Probe Drug Cocktail in Cynomolgus Monkey.

Authors:  Rachel E Kosa; Sarah Lazzaro; Yi-An Bi; Brendan Tierney; Dana Gates; Sweta Modi; Chester Costales; A David Rodrigues; Larry M Tremaine; Manthena V Varma
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3.  Structure-based identification of OATP1B1/3 inhibitors.

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Journal:  Mol Pharmacol       Date:  2013-04-09       Impact factor: 4.436

4.  Drug and bile acid transporters in rosuvastatin hepatic uptake: function, expression, and pharmacogenetics.

Authors:  Richard H Ho; Rommel G Tirona; Brenda F Leake; Hartmut Glaeser; Wooin Lee; Christopher J Lemke; Yi Wang; Richard B Kim
Journal:  Gastroenterology       Date:  2006-03-06       Impact factor: 22.682

5.  Digoxin is not a substrate for organic anion-transporting polypeptide transporters OATP1A2, OATP1B1, OATP1B3, and OATP2B1 but is a substrate for a sodium-dependent transporter expressed in HEK293 cells.

Authors:  Mitchell E Taub; Kirsten Mease; Rucha S Sane; Cory A Watson; Liangfu Chen; Harma Ellens; Brad Hirakawa; Eric L Reyner; Marton Jani; Caroline A Lee
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6.  Functional complementation between a novel mammalian polygenic transport complex and an evolutionarily ancient organic solute transporter, OSTalpha-OSTbeta.

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Journal:  J Biol Chem       Date:  2003-04-28       Impact factor: 5.157

7.  Quantitative Expression of Hepatobiliary Transporters and Functional Uptake of Substrates in Hepatic Two-Dimensional Sandwich Cultures: A Comparative Evaluation of Upcyte and Primary Human Hepatocytes.

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8.  Effects of tetraalkylammonium compounds with different affinities for organic cation transporters on the pharmacokinetics of metformin.

Authors:  Min-Koo Choi; Qing-Ri Jin; Hyo-Eon Jin; Chang-Koo Shim; Doo-Yeoun Cho; Jae-Gook Shin; Im-Sook Song
Journal:  Biopharm Drug Dispos       Date:  2007-12       Impact factor: 1.627

9.  Validation of a microdose probe drug cocktail for clinical drug interaction assessments for drug transporters and CYP3A.

Authors:  T Prueksaritanont; D A Tatosian; X Chu; R Railkar; R Evers; C Chavez-Eng; R Lutz; W Zeng; J Yabut; G H Chan; X Cai; A H Latham; J Hehman; D Stypinski; J Brejda; C Zhou; B Thornton; K P Bateman; I Fraser; S A Stoch
Journal:  Clin Pharmacol Ther       Date:  2016-12-10       Impact factor: 6.875

10.  Effect of silymarin supplement on the pharmacokinetics of rosuvastatin.

Authors:  Jian Wei Deng; Ji-Hong Shon; Ho-Jung Shin; Soo-Jin Park; Chang-Woo Yeo; Hong-Hao Zhou; Im-Sook Song; Jae-Gook Shin
Journal:  Pharm Res       Date:  2008-01-31       Impact factor: 4.200

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