Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans

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Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans. / Christiansen, Martin Lau; Müllertz, Anette; Garmer, Mats; Kristensen, Jakob; Jacobsen, Jette; Abrahamsson, Bertil; Holm, Rene.

In: Journal of Pharmaceutical Sciences, Vol. 104, No. 1, 01.2015, p. 135-143.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Christiansen, ML, Müllertz, A, Garmer, M, Kristensen, J, Jacobsen, J, Abrahamsson, B & Holm, R 2015, 'Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans', Journal of Pharmaceutical Sciences, vol. 104, no. 1, pp. 135-143. https://doi.org/10.1002/jps.24270

APA

Christiansen, M. L., Müllertz, A., Garmer, M., Kristensen, J., Jacobsen, J., Abrahamsson, B., & Holm, R. (2015). Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans. Journal of Pharmaceutical Sciences, 104(1), 135-143. https://doi.org/10.1002/jps.24270

Vancouver

Christiansen ML, Müllertz A, Garmer M, Kristensen J, Jacobsen J, Abrahamsson B et al. Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans. Journal of Pharmaceutical Sciences. 2015 Jan;104(1):135-143. https://doi.org/10.1002/jps.24270

Author

Christiansen, Martin Lau ; Müllertz, Anette ; Garmer, Mats ; Kristensen, Jakob ; Jacobsen, Jette ; Abrahamsson, Bertil ; Holm, Rene. / Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans. In: Journal of Pharmaceutical Sciences. 2015 ; Vol. 104, No. 1. pp. 135-143.

Bibtex

@article{585b411f9c8d4f48adf9803d6781f67c,
title = "Evaluation of the use of G{\"o}ttingen minipigs to predict food effects on the oral absorption of drugs in humans",
abstract = "This study investigated the oral absorption of drugs in minipigs to predict food effects in man. The protocol was based on a previously described model in dogs and further investigated the food source (i.e., US FDA breakfast or a nutritional drink) and food quantities. Two poorly soluble compounds were investigated [pravastatin (negative food effect) and atazanavir (positive food effect)] in G{\"o}ttingen minipigs after seven different food regimens. The gastric emptying rate was evaluated by coadministration of acetaminophen. In short, the results demonstrated longer gastric emptying times in minipigs when compared with humans, within a range from 2.3 to 8.4 h dependent on the food regimen. There were no significant differences in drug absorption between fed and fasted state for the two compounds. The study showed that the dog protocol could not be transferred directly to minipigs, but needs further investigation and adjustments in order to get a valid model using G{\"o}ttingen minipigs for the evaluation of food effects on drug absorption in humans.",
author = "Christiansen, {Martin Lau} and Anette M{\"u}llertz and Mats Garmer and Jakob Kristensen and Jette Jacobsen and Bertil Abrahamsson and Rene Holm",
note = "{\textcopyright} 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.",
year = "2015",
month = jan,
doi = "10.1002/jps.24270",
language = "English",
volume = "104",
pages = "135--143",
journal = "Journal of Pharmaceutical Sciences",
issn = "0022-3549",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans

AU - Christiansen, Martin Lau

AU - Müllertz, Anette

AU - Garmer, Mats

AU - Kristensen, Jakob

AU - Jacobsen, Jette

AU - Abrahamsson, Bertil

AU - Holm, Rene

N1 - © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.

PY - 2015/1

Y1 - 2015/1

N2 - This study investigated the oral absorption of drugs in minipigs to predict food effects in man. The protocol was based on a previously described model in dogs and further investigated the food source (i.e., US FDA breakfast or a nutritional drink) and food quantities. Two poorly soluble compounds were investigated [pravastatin (negative food effect) and atazanavir (positive food effect)] in Göttingen minipigs after seven different food regimens. The gastric emptying rate was evaluated by coadministration of acetaminophen. In short, the results demonstrated longer gastric emptying times in minipigs when compared with humans, within a range from 2.3 to 8.4 h dependent on the food regimen. There were no significant differences in drug absorption between fed and fasted state for the two compounds. The study showed that the dog protocol could not be transferred directly to minipigs, but needs further investigation and adjustments in order to get a valid model using Göttingen minipigs for the evaluation of food effects on drug absorption in humans.

AB - This study investigated the oral absorption of drugs in minipigs to predict food effects in man. The protocol was based on a previously described model in dogs and further investigated the food source (i.e., US FDA breakfast or a nutritional drink) and food quantities. Two poorly soluble compounds were investigated [pravastatin (negative food effect) and atazanavir (positive food effect)] in Göttingen minipigs after seven different food regimens. The gastric emptying rate was evaluated by coadministration of acetaminophen. In short, the results demonstrated longer gastric emptying times in minipigs when compared with humans, within a range from 2.3 to 8.4 h dependent on the food regimen. There were no significant differences in drug absorption between fed and fasted state for the two compounds. The study showed that the dog protocol could not be transferred directly to minipigs, but needs further investigation and adjustments in order to get a valid model using Göttingen minipigs for the evaluation of food effects on drug absorption in humans.

U2 - 10.1002/jps.24270

DO - 10.1002/jps.24270

M3 - Journal article

C2 - 25417837

VL - 104

SP - 135

EP - 143

JO - Journal of Pharmaceutical Sciences

JF - Journal of Pharmaceutical Sciences

SN - 0022-3549

IS - 1

ER -

ID: 138171604