Related Experiment Video
Updated: Sep 13, 2025

Transduction and Expansion of Primary T Cells in Nine Days with Maintenance of Central Memory Phenotype
Published on: March 18, 2020
The Pharmacokinetics of Tulathromycin Following Subcutaneous Administration in Rhesus Macaques (Macaca mulatta)
Jacob D Herford1, Luke A Wittenburg2, Rebecca L Sammak1
11Primate Medicine Department, California National Primate Research Center, University of California, Davis, California; and.
Abstract:
Campylobacter jejuni is a pathogenic bacterium commonly associated with enteritis and diarrhea in rhesus macaques (Macaca mulatta). The standard therapy at the California National Primate Research Center is oral azithromycin, a second-generation macrolide, given daily for 5 d. Oral treatment administration can be difficult with some animals. Poor oral compliance for antibiotics can result in treatment failure and potentially select for antibiotic resistance. Tulathromycin, a newer-generation macrolide, may offer an injectable alternative to azithromycin. The aim of the current study is to quantify the pharmacokinetics of tulathromycin in plasma in rhesus macaques. Six rhesus macaques were each given a single 2.5 mg/kg dose SC of tulathromycin, and serial blood samples were collected at 0, 0.25, 0.5, 0.75, 1.0, 1.5, 2, 4, 8, 12, 24, 48, 72, 96, 120, and 168 h, to quantify the concentration of tulathromycin in plasma over time. Results show that Cmax = 1,280 ± 395 ng/mL, Tmax = 1.25 ± 0.5 h, t1/2 = 77.2 ± 15.4 h, and AUC0-168 = 6,557.4 ± 875.4 h·ng/mL. There are no published Clinical and Laboratory Sciences Institute breakpoints for tulathromycin against C. jejuni, but based on an independently established minimum inhibitory concentration of 500 ng/mL, these data suggest that 2.5 mg/kg tulathromycin can be given subcutaneously to achieve potential therapeutic levels in rhesus macaques, possibly providing an alternative to oral azithromycin.
Insights
Tulathromycin offers a potential injectable alternative for treating Campylobacter jejuni infections in rhesus macaques when oral azithromycin is challenging. Pharmacokinetic data suggest a 2.5 mg/kg subcutaneous dose can achieve therapeutic levels.
Area of Science:
- Veterinary Pharmacology
- Primate Medicine
- Infectious Diseases
Background:
- Campylobacter jejuni causes enteritis in rhesus macaques, often treated with oral azithromycin.
- Poor oral compliance with azithromycin can lead to treatment failure and antibiotic resistance.
- Tulathromycin, a newer macrolide, presents a potential injectable alternative.
Purpose of the Study:
- To quantify the pharmacokinetics of tulathromycin in rhesus macaque plasma.
- To evaluate tulathromycin as a potential alternative to azithromycin for C. jejuni infections.
Main Methods:
- Six rhesus macaques received a single 2.5 mg/kg subcutaneous dose of tulathromycin.
- Serial blood samples were collected over 168 hours to measure plasma tulathromycin concentrations.
Main Results:
- Peak plasma concentration (Cmax) was 1,280 ± 395 ng/mL.
- Time to peak concentration (Tmax) was 1.25 ± 0.5 hours.
- Half-life (t1/2) was 77.2 ± 15.4 hours, and AUC0-168 was 6,557.4 ± 875.4 h·ng/mL.
Conclusions:
- The pharmacokinetic profile suggests that a 2.5 mg/kg subcutaneous dose of tulathromycin can achieve therapeutic levels in rhesus macaques.
- Tulathromycin may offer a viable injectable alternative to oral azithromycin for treating C. jejuni infections in this species.
More Related Videos
Related Concept Videos
Noncompartmental Analysis: Mean Transit, Absorption and Dissolution Time
One of the key parameters is the mean transit time (MTT), which refers to the total duration required for drug molecules to transit through the body. MTT is determined by calculating the ratio of the area under the moment curve to the area...
Drug Concentration Versus Time Correlation
Two pivotal parameters are the minimum effective concentration (MEC) and the minimum toxic concentration (MTC). The MEC is the...
Chronopharmacokinetics: Time-Dependent Pharmacokinetics
Time-dependent pharmacokinetics refers to non-cyclical changes in drug rate processes over a period of time. It can lead to nonlinear pharmacokinetics, where the relationship between drug concentration and time is not proportional. Non-cyclical...
Pharmacokinetics: Overview
Bioavailability: Overview
Factors Influencing Drug Absorption: Presystemic Elimination

