George D, Miniter P, Andriole V T
Department of Medicine, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Antimicrob Agents Chemother. 1996 Jan;40(1):86-91. doi: 10.1128/AAC.40.1.86.
The efficacy of UK-109496, a new azole antifungal agent, was evaluated in an immunosuppressed, temporarily leukopenic rabbit model of invasive aspergillosis. Oral therapy with UK-109496 at a dosage of 10 or 15 mg/kg of body weight every 8 h was begun 24 h after a lethal or sublethal challenge, and results were compared with those for amphotericin B therapy and untreated controls. UK-109496 eliminated mortality and also reduced the tissue burden of Aspergillus fumigatus 10- to 100-fold in liver and kidney tissues and to a lesser degree in lung tissue, and at the higher dose, no viable organisms were recovered from brain tissue from these animals. Both dosages of UK-109496 decreased or eliminated circulating antigen. The half-life of UK-109496 in rabbits was 2.5 to 3 h, and no accumulation of drug was seen even after 15 doses in either uninfected or infected animals. Thus, UK-109496 shows activity in this rabbit model of invasive aspergillosis. Additional studies are needed to determine the potential of the drug for use in the treatment of this infection.
新型唑类抗真菌药物UK-109496的疗效在免疫抑制、暂时白细胞减少的侵袭性曲霉病兔模型中进行了评估。在致死性或亚致死性攻击24小时后,开始以每8小时10或15毫克/千克体重的剂量口服UK-109496进行治疗,并将结果与两性霉素B治疗组和未治疗的对照组进行比较。UK-109496消除了死亡率,还使肝脏和肾脏组织中烟曲霉的组织负荷降低了10至100倍,在肺组织中的降低程度较小,并且在较高剂量下,这些动物的脑组织中未检测到存活的生物体。UK-109496的两种剂量均降低或消除了循环抗原。UK-109496在兔体内的半衰期为2.5至3小时,即使在未感染或感染动物中给予15剂后也未观察到药物蓄积。因此,UK-109496在这种侵袭性曲霉病兔模型中显示出活性。需要进行更多研究以确定该药物用于治疗这种感染的潜力。