首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Urinary Concentrations and Antibacterial Activity of BAL30072 a Novel Siderophore Monosulfactam against Uropathogens after Intravenous Administration in Healthy Subjects
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Urinary Concentrations and Antibacterial Activity of BAL30072 a Novel Siderophore Monosulfactam against Uropathogens after Intravenous Administration in Healthy Subjects

机译:在健康受试者中静脉给药后新型铁载体单磺内酰胺BAL30072对尿毒症的尿液浓度和抗菌活性

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摘要

This annex study to a phase 1 study aimed to correlate urinary concentrations and bactericidal titers (UBTs) of , a novel siderophore monosulfactam, in healthy subjects in order to evaluate which dosage of should be investigated in a clinical study on complicated urinary tract infection (UTI). Three cohorts of a total of 19 healthy male subjects were included in the add-on study and received the following dosages. The 1st cohort received 1 g once a day (q.d.) intravenously (i.v.) (1 h) on day 1 and 1 g thrice daily (t.i.d.) on day 2, the 2nd cohort received 2 g q.d. i.v. (1 h) on day 1 and 2 g t.i.d. on day 2, and the 3rd cohort received 1 g q.d. i.v. (4-h infusion) on day 8. Urine was collected up to 24 h after drug administration. UBTs were determined for seven Escherichia coli isolates (three wild type [WT], CTX-M-15, TEM-3, TEM-5, NDM-1), two Klebsiella pneumoniae isolates (WT, KPC), one Proteus mirabilis isolate (WT), and two Pseudomonas aeruginosa isolates (WT, VIM-1 plus AmpC). Urine drug concentrations were measured by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The median urinary excretions of ranged between 38% and 46% (3 cohorts). The median UBTs after i.v. administration of 1 or 2 g q.d. and after 1 or 2 g t.i.d. showed positive UBTs for 24 h after the lowest dosage (1 g q.d.) for 5 of 7 of the Enterobacteriaceae strains and after the higher dosage of 2 g administered i.v. t.i.d. for all strains tested. After i.v. infusion of 1 g over 4 h, positive UBTs were demonstrated for three E. coli strains for up to 12 h, for the K. pneumoniae (KPC) strain for up to 8 h, and for the P. aeruginosa (VIM-1 plus AmpC) strain for up to only 4 h. The minimal bactericidal concentrations (MBCs) of the E. coli (NDM-1) strain and the K. pneumoniae (WT) strain correlated well between broth and urine but did not correlate well for the two P. aeruginosa strains. exhibits positive UBTs for 24 h even after a dosage of 1 g administered i.v. q.d. for 5 of 7 Enterobacteriaceae strains and after 2 g administered i.v. t.i.d. for all strains except one P. aeruginosa strain (50% of the time). In general, the UBTs correlated well with the MICs of the Enterobacteriaceae but were lower for P. aeruginosa. The clinical efficacy with a dosage regimen of of 2 g administered i.v. t.i.d. should be evaluated in the treatment of complicated UTI.
机译:这项附件研究属于1期研究,旨在将健康受试者中新型铁载体一磺内酰胺的尿液浓度和杀菌滴度(UBT)相关联,以评估在复杂尿路感染(UTI)的临床研究中应研究哪种剂量的尿嘧啶)。共有19名健康男性受试者的3个队列被纳入附加研究,并接受以下剂量。第一组在第1天每天(q.d.)静脉(i.v.)每天1 g(第1小时),第2天每天(t.i.d)每天1 g三次,第2组q.d。 i.v. (第1天)(1小时)和第2天g.i.d.在第2天,第3组接受了1 gq.d。 i.v. (第4天输注)(第4小时)。在给药后24小时内收集尿液。确定了7种大肠埃希菌分离株(3种野生型[WT],CTX-M-15,TEM-3,TEM-5,NDM-1),2种肺炎克雷伯菌肺炎分离株(WT,KPC),1种奇异变形杆菌( WT)和两个铜绿假单胞菌分离株(WT,VIM-1加AmpC)。尿液药物浓度通过液相色谱-串联质谱法(LC-MS / MS)测定。中位数尿液排泄介于38%和46%之间(3个队列)。 i.v.之后的UBT中位数每天1或2克并在1或2 g t.i.d.在7株肠杆菌科细菌中,有5剂的最低剂量(1 g q.d.d.)和高剂量的2 g静脉内给药后24小时显示UBT呈阳性。 t.i.d.对于所有测试的菌株。在i.v.之后在4小时内输注1 g,三个大肠杆菌菌株长达12 h,肺炎克雷伯菌(KPC)菌株长达8 h,铜绿假单胞菌(VIM-1 plus AmpC)应变仅持续4小时。大肠杆菌(NDM-1)菌株和肺炎克雷伯氏菌(WT)菌株的最低杀菌浓度(MBC)在肉汤和尿液之间具有很好的相关性,但与两种铜绿假单胞菌菌株却没有很好的相关性。即使在静脉内施用1 g的剂量后,在24小时内仍显示阳性UBT。 q.d.用于7个肠杆菌科菌株中的5个,并在静脉内施用2g后。 t.i.d.除一种铜绿假单胞菌菌株外(50%的时间)。通常,UBT与肠杆菌科的MIC密切相关,但对于铜绿假单胞菌则较低。静脉内给予2 g剂量方案的临床疗效t.i.d.在治疗复杂的尿路感染时应进行评估。

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