Impact of Blast Overpressure on the Pharmacokinetics of Various Antibiotics in Sprague Dawley Rats

• Published in: Military medicine Vol. 188; no. Supplement_6; pp. 271 - 279
• Main Authors: Rios, Kariana E, Selig, Daniel J, Pavlovic, Radmila, Alamneh, Yonas, Vuong, Chau, Nadeau, Robert John, Pannone, Kristina M, Deluca, Jesse P, Long, Joseph B, Sajja, Venkatasivasai S, Tyner, Stuart, Antonic, Vlado, Getnet, Derese, Bobrov, Alexander G
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 08-11-2023
• Subjects: Antibiotics; Pharmacokinetics
• ISSN: 0026-4075; 1930-613X
• DOI: 10.1093/milmed/usad107

ABSTRACT
Introduction
Combat injuries are complex and multimodal. Most injuries to the extremities occur because of explosive devices such as improvised explosive devices. Blast exposure dramatically increases the risk of infection in combat wounds, and there is limited available information on the best antibiotic treatments for these injuries. We previously demonstrated that mice exposed to blast displayed a delayed clearance of cefazolin from the plasma and liver; further semi-mechanistic modeling determined that cefazolin concentrations in the skin of these mice were reduced. Our objective was to investigate the effects of blast on the pharmacokinetics of antibiotics of different types used for the treatment of combat wounds in the rat model.
Materials and Methods
Male Sprague Dawley rats were exposed to blast overpressure followed by injection of a bolus of animal equivalent doses of an antibiotic (cefazolin, cefepime, ertapenem, or clindamycin) into the tail vein at 1-hour post-blast exposure. Blood was collected at predetermined time points via repeated sampling from the tail vein. Animals were also euthanized at predetermined time points, at which time liver, kidney, skin, and blood via cardiac puncture were collected. Antibiotic concentrations were determined by ultra-performance liquid chromatography–tandem mass spectrometry.
Results
Blast-exposed rats exhibited a similar rate of clearance compared to non-blasted rats in the blood, liver, kidney, and skin, which is inconsistent with the data regarding cefazolin in blast-exposed mice.
Conclusions
Our results in rats do not recapitulate our previous observation of delayed cefazolin clearance in mice following the blast overpressure exposure. Although using rats permitted us to collect multiple blood samples from the same animals, rats may not be a suitable model for measuring the pharmacokinetics of antibiotics following blast. The interpretation of the results may be challenging because of variation in data among rat subjects in the same sample groups.