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. 2016 Jul 22;60(8):4464–4470. doi: 10.1128/AAC.02708-15

TABLE 1.

Pharmacokinetic and pharmacodynamic parameters for single doses of colistin methanesulfonate, tigecycline, and imipenema

Antimicrobial (dose [mg/kg], route of administration) Drug form Cmax (mg/liter) t1/2 (h) AUC0–24 (mg · h/liter) AUC0–24/MICb
TMIC (h, %)b
Ab9 Ab186 Ab9 Ab186
CMS (20, i.p.) CMS 14.24 1.12 43.24 172.97 172.97 ND ND
tCST 2.87 1.1 14.41 57.63 57.63 ND ND
fCST 0.97 1.01 4.7 18.81 18.81 ND ND
TGC (5, s.c.) tTGC 1.34 2.04 13.75 55 3.44 ND ND
IMP (30, i.m.) tIMP 26.66 0.36 ND ND ND 1.54, 38.5 0.09, 2.25
a

CMS, colistin methanesulfonate; TGC, tigecycline; IMP, imipenem; CST, colistin; tCST, total colistin; fCST, free colistin; tTGC, total tigecycline; tIMP, total imipenem; Cmax, maximum concentration of antimicrobial agent in serum; t1/2, elimination half-life; AUC0–24, area under the concentration-time curve from time zero to 24 h; TMIC, time that the drug concentration remains above the MIC; ND, not determined; i.p., intraperitoneal; s.c., subcutaneous; i.m., intramuscular.

b

For Ab9, the CST, TGC, and IMP MICs were 0.25, 0.25, and 0.5 mg/liter, respectively. For Ab186, the CST, TGC, and IMP MICs were 0.25, 4, and 16 mg/liter, respectively.