Reassessment of tigecycline bone concentrations in volunteers undergoing elective orthopedic procedures
Adult
Male
Minocycline
Tigecycline
Bone and Bones
Mass Spectrometry
Anti-Bacterial Agents
03 medical and health sciences
0302 clinical medicine
Area Under Curve
Humans
Female
Orthopedic Procedures
Chromatography, High Pressure Liquid
DOI:
10.1002/jcph.201
Publication Date:
2013-10-24T08:19:50Z
AUTHORS (7)
ABSTRACT
AbstractThe goal of the this study was to re‐evaluate tigecycline bone concentrations in subjects undergoing elective orthopedic surgery, using multiple doses and a more robust bone assay than was used in a previous study. Each subject received three intravenous doses of tigecycline (one 100‐mg infusion followed by two 50‐mg infusions, each administered over 30 minutes). A single bone sample was collected from each subject at one of the following times: 1, 2, 4, 6, 8, or 12 hours after the third dose. Four blood samples were collected from each subject: before the first dose, before and after the third dose, and within 15 minutes of the collection time of the bone sample. Noncompartmental pharmacokinetic analysis serum and bone area under the curve for the given dose interval (AUCτ) values were 2,402 ng h/mL and 11,465 ng h/g, and maximum concentration (Cmax) values were 974 ng/mL and 2,262 ng/g, respectively. The bone to serum ratio calculated using the AUCτ values was 4.77, confirming tigecycline penetration into bone.
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