首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Evaluation of T-3811ME (BMS-284756) a New Des-F(6)-Quinolone for Treatment of Meningitis Caused by Penicillin-Resistant Streptococcus pneumoniae in Rabbits
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Evaluation of T-3811ME (BMS-284756) a New Des-F(6)-Quinolone for Treatment of Meningitis Caused by Penicillin-Resistant Streptococcus pneumoniae in Rabbits

机译:新型Des-F(6)-喹诺酮类药物T-3811ME(BMS-284756)治疗抗青霉素耐药性肺炎链球菌引起的脑膜炎的评价

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摘要

T-3811ME (BMS-284756) is a new des-F(6)-quinolone with high levels of activity against gram-positive bacteria, including penicillin-resistant Streptococcus pneumoniae (PRSP) strains. T-3811, the free base of T-3811ME, exhibited potent activity against 28 clinical strains of PRSP isolated clinically (MIC at which 90% of the isolates tested are inhibited, 0.0625 μg/ml). After the intravenous dosing of T-3811ME (20 mg/kg of body weight as T-3811) in rabbits with meningitis caused by PRSP, the area under the concentration-time curve (AUC) of T-3811 in cerebrospinal fluid (CSF) was 5.79 μg · h/ml and was 4.5-fold higher than that of T-3811in the CSF of rabbits without meningitis. In addition, the AUC/MIC for T-3811ME (20 mg/kg as T-3811) in CSF was 185, which was 4.3-fold higher than that for ceftriaxone (administered intravenously at 100 mg/kg). After the administration of any dose of T-3811ME (5, 10, and 20 mg/kg as T-3811), the viable cell counts in CSF decreased in a dose-dependent manner. In particular, after dosing of 20 mg/kg (as T-3811), the viable cell counts in CSF were significantly less than those in the nontreated group (P < 0.01). By histopathological evaluation, 6 h after the administration of T-3811ME (20 mg/kg as T-3811), the thickening of the cerebral meninx and the infiltration of neutrophils into the cerebral meninx were less severe in the treated group than in the nontreated group. T-3811ME (BMS-284756) may be expected to be evaluated for the management of meningitis caused by highly penicillin-resistant pneumococci.
机译:T-3811ME(BMS-284756)是一种新型的des-F(6)-喹诺酮,对革兰氏阳性细菌(包括耐青霉素的肺炎链球菌(PRSP)菌株)具有很高的活性。 T-3811,T-3811ME的游离碱,对临床分离出的28种PRSP临床菌株表现出有效的活性(MIC抑制了90%的分离株,0.0625μg/ ml)。对PRSP引起的脑膜炎的兔静脉给药T-3811ME(体重为20 mg / kg,作为T-3811)后,脑脊液(CSF)中T-3811的浓度-时间曲线下面积(AUC)在没有脑膜炎的兔子的脑脊液中,其为5.79μg·h / ml,比T-3811高4.5倍。此外,CSF中T-3811ME(20 mg / kg,T-3811)的AUC / MIC为185,比头孢曲松(静脉注射100 mg / kg)高4.3倍。施用任何剂量的T-3811ME(T-3811为5、10和20 mg / kg)后,CSF中的活细胞计数均呈剂量依赖性降低。特别地,在以20 mg / kg的剂量给药(作为T-3811)之后,CSF中的活细胞计数显着低于未治疗组(P <0.01)。通过组织病理学评估,在施用T-3811ME(20 mg / kg,作为T-3811)后6小时,与未治疗组相比,治疗组的脑膜增厚和嗜中性粒细胞向脑膜的浸润程度较轻。组。可以预期对T-3811ME(BMS-284756)进行评估,以控制由高度耐青霉素的肺炎球菌引起的脑膜炎。

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