Acute toxicity is a dose-limiting factor for intravenous polymyxin B: A safety and pharmacokinetic study in healthy Chinese subjects

•A single-dose (at 0.75 or 1.5 mg/kg) clinical trial of polymyxin B was firstly conducted in healthy Chinese subjects.•Acute toxicity (including neurotoxicity) is a dose-limiting factor for intravenous polymyxin B.•It’s important to monitor the adverse reactions and the polymyxin B daily dose should...

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Vydané v:The Journal of infection Ročník 82; číslo 2; s. 207 - 215
Hlavní autori: Liu, Xiaofen, Chen, Yuancheng, Yang, Haijing, Li, Jian, Yu, Jicheng, Yu, Zhenwei, Cao, Guoying, Wu, Xiaojie, Wang, Yu, Wu, Hailan, Fan, Yaxin, Wang, Jingjing, Wu, Jufang, Jin, Yi, Guo, Beining, Hu, Jiali, Bian, Xingchen, Li, Xin, Zhang, Jing
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England Elsevier Ltd 01.02.2021
Predmet:
Administration, Intravenous
Anti-Bacterial Agents - adverse effects
China
Female
Healthy Volunteers
Humans
Male
Neurotoxicity
Pharmacokinetics
Polymyxin
Polymyxin B - adverse effects
Safety
Urinary recovery
China
Neurotoxicity
Safety
Polymyxin
Pharmacokinetics
Urinary recovery
ISSN:0163-4453, 1532-2742, 1532-2742
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Shrnutí:•A single-dose (at 0.75 or 1.5 mg/kg) clinical trial of polymyxin B was firstly conducted in healthy Chinese subjects.•Acute toxicity (including neurotoxicity) is a dose-limiting factor for intravenous polymyxin B.•It’s important to monitor the adverse reactions and the polymyxin B daily dose should not exceed 3 mg/kg in general.•Our pharmacokinetic and safety results may benefit the design of Phase I clinical trials for new-generation polymyxins. Polymyxin B is a last-line antibiotic for multidrug-resistant gram-negative bacterial infections. However, limited safety and pharmacokinetic information is available. We investigated the safety and pharmacokinetics of intravenous polymyxin B in healthy subjects. An open-label, single-dose clinical trial was conducted in healthy Chinese subjects. Polymyxin B (sulphate) was administered intravenously at 0.75 or 1.5 mg/kg (n = 10 per dose, 5 males and 5 females) to examine the safety and pharmacokinetics. One female subject in the 1.5-mg/kg group discontinued due to abdominal pain during administration. The most frequently reported adverse events were perioral paraesthesia, dizziness, and numbness of extremities (7/10 subjects in the 0.75-mg/kg group, all subjects in the 1.5-mg/kg group). All neurotoxicity-related events dissipated without treatment within a maximum of 23 h. Notably, abdominal pain (3/5) and vulvar pruritus (2/5), colpitis (2/5) or abnormal uterine bleeding (1/5) were reported in female subjects receiving the 1.5-mg/kg dose. In the 0.75-mg/kg group, the total clearance, volume of distribution and half-life of polymyxin B were 0.028±0.002 L/h/kg, 0.219±0.023 L/kg and 5.44±0.741 h, respectively; similar values were observed in the 1.5-mg/kg group. Urinary recovery was 3.7 ± 1.1% and 8.1 ± 1.3% in the 0.75- and 1.5-mg/kg groups, respectively. Population pharmacokinetics of polymyxin B was consistent with a three-compartment model. The clearance and distribution of the central compartment were 0.027 L/h/kg and 0.071 L/kg, respectively. This study is the first to examine the safety and pharmacokinetics of polymyxin B in healthy subjects. Our results highlight that acute toxicity is a dose-limiting factor for intravenous polymyxin B.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0163-4453
1532-2742
1532-2742
DOI:10.1016/j.jinf.2021.01.006