TY - JOUR
T1 - Assessment of carbapenems in a mouse model of Mycobacterium tuberculosis infection
AU - Jadhav, Ravindra
AU - Gallardo-Macias, Ricardo
AU - Kumar, Gaurav
AU - Daher, Samer S.
AU - Kaushik, Amit
AU - Bigelow, Kristina M.
AU - Nuermberger, Eric L.
AU - Lamichhane, Gyanu
AU - Freundlich, Joel S.
N1 - Publisher Copyright:
© 2021 Jadhav et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2021/5
Y1 - 2021/5
N2 - We present further study of a subset of carbapenems, arising from a previously reported machine learning approach, with regard to their mouse pharmacokinetic profiling and subsequent study in a mouse model of sub-acute Mycobacterium tuberculosis infection. Pharmacokinetic metrics for such small molecules were compared to those for meropenem and biapenem, resulting in the selection of two carbapenems to be assessed for their ability to reduce M. tuberculosis bacterial loads in the lungs of infected mice. The original syntheses of these two carbapenems were optimized to provide multigram quantities of each compound. One of the two experimental carbapenems, JSF-2204, exhibited efficacy equivalent to that of meropenem, while both were inferior to rifampin. The lessons learned in this study point toward the need to further enhance the pharmacokinetic profiles of experimental carbapenems to positively impact in vivo efficacy performance.
AB - We present further study of a subset of carbapenems, arising from a previously reported machine learning approach, with regard to their mouse pharmacokinetic profiling and subsequent study in a mouse model of sub-acute Mycobacterium tuberculosis infection. Pharmacokinetic metrics for such small molecules were compared to those for meropenem and biapenem, resulting in the selection of two carbapenems to be assessed for their ability to reduce M. tuberculosis bacterial loads in the lungs of infected mice. The original syntheses of these two carbapenems were optimized to provide multigram quantities of each compound. One of the two experimental carbapenems, JSF-2204, exhibited efficacy equivalent to that of meropenem, while both were inferior to rifampin. The lessons learned in this study point toward the need to further enhance the pharmacokinetic profiles of experimental carbapenems to positively impact in vivo efficacy performance.
UR - http://www.scopus.com/inward/record.url?scp=85105105973&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85105105973&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0249841
DO - 10.1371/journal.pone.0249841
M3 - Article
C2 - 33939697
AN - SCOPUS:85105105973
SN - 1932-6203
VL - 16
JO - PloS one
JF - PloS one
IS - 5 May
M1 - e0249841
ER -