Schell W A, De Almeida G M, Dodge R K, Okonogi K, Perfect J R
Division of Infectious Diseases, Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.
Antimicrob Agents Chemother. 1998 Oct;42(10):2630-2. doi: 10.1128/AAC.42.10.2630.
Multiple isolates of Cryptococcus neoformans, including those with fluconazole resistance, were tested to assess the in vitro activity of the new triazole TAK-187. MICs of TAK-187 were at least eightfold lower than those of fluconazole, and fungicidal concentrations for most isolates were 4 microg/ml or less. TAK-187 also was evaluated as intermittent therapy using two dosages in a rabbit model of experimental cryptococcal meningitis. Compared to daily treatment with fluconazole, as little as two doses of TAK-187 given 7 days apart were found to be effective. Plasma and cerebrospinal fluid TAK-187 concentrations were many times higher than MICs and fungicidal concentrations. Based upon its therapeutic efficacy and long half-life in the rabbit model, TAK-187 should be investigated for intermittent dosing in treatment or suppression of cryptococcal infections in humans.
对新型隐球菌的多个分离株,包括那些对氟康唑耐药的分离株进行了测试,以评估新型三唑类药物TAK-187的体外活性。TAK-187的最低抑菌浓度(MIC)比氟康唑至少低八倍,大多数分离株的杀菌浓度为4微克/毫升或更低。在实验性隐球菌性脑膜炎的兔模型中,还使用两种剂量对TAK-187进行了间歇性治疗评估。与氟康唑每日治疗相比,发现每隔7天给予低至两剂TAK-187是有效的。血浆和脑脊液中TAK-187的浓度比MIC和杀菌浓度高许多倍。基于其在兔模型中的治疗效果和长半衰期,应该对TAK-187进行研究,以确定其在治疗或抑制人类隐球菌感染时的间歇性给药方案。