Fetal Physiologically Based Pharmacokinetic Models: Systems Information on Fetal Cardiac Output and Its Distribution to Different Organs during Development-Reference-Cited by-同舟云学术

Fetal Physiologically Based Pharmacokinetic Models: Systems Information on Fetal Cardiac Output and Its Distribution to Different Organs during Development

Published:2021-01-24 Issue:6 Volume:60 Page:741-757
ISSN:0312-5963
Container-title:Clinical Pharmacokinetics
language:en
Short-container-title:Clin Pharmacokinet

Author:

Abduljalil Khaled^ORCID,Pan Xian,Clayton Ruth,Johnson Trevor N.,Jamei Masoud

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Link

https://link.springer.com/content/pdf/10.1007/s40262-020-00973-0.pdf

Reference93 articles.

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3. Vimpeli T, Huhtala H, Wilsgaard T, Acharya G. Fetal aortic isthmus blood flow and the fraction of cardiac output distributed to the upper body and brain at 11–20 weeks of gestation. Ultrasound Obstet Gynecol. 2009;33:538–44.

4. Finnemore A, Groves A. Physiology of the fetal and transitional circulation. Semin Fetal Neonatal Med. 2015;20:210–6.

5. Gaohua L, Abduljalil K, Jamei M, Johnson TN, Rostami-Hodjegan A. A pregnancy physiologically based pharmacokinetic (p-PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4. Br J Clin Pharmacol. 2012;74:873–85.

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