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泊沙康唑的药代动力学/药效学特征。

Pharmacokinetic/pharmacodynamic profile of posaconazole.

机构信息

Department of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, USA.

出版信息

Clin Pharmacokinet. 2010 Jun;49(6):379-96. doi: 10.2165/11319340-000000000-00000.

Abstract

Posaconazole is a recently approved lipophilic triazole antifungal agent that exhibits potent and broad-spectrum antifungal activity in vitro and in vivo against most Candida spp., Cryptococcus neoformans, Aspergillus spp., many Zygomycetes, endemic fungi and dermatophytes. It has been documented that posaconazole has potency and spectrum of activity similar to those of itraconazole and superior to those of fluconazole against clinically important isolates of Candida spp., C. neoformans and Aspergillus spp. This new triazole has been developed for the treatment of fungal infections, which most often occur in severely immunocompromised patients, such as organ transplant patients or cancer patients undergoing chemotherapy. Since posanconazole has low solubility in aqueous and acidic media, its absorption is dose limited and significantly dependent upon food intake. The time to reach the maximum plasma concentration has been reported to be 5-8 hours following oral administration of a single dose. The relative bioavailability of posaconazole has been estimated to be significantly different among regimens and has been observed to be significantly increased by administration in divided doses. Posaconazole binds predominantly to albumin, and the extent of protein binding is high (>98%). Posaconazole has a large mean apparent volume of distribution after oral administration (V(d)/F), which is approximately 5-25 L/kg, suggesting extensive extravascular distribution and penetration into intracellular spaces. The V(d)/F is influenced by the dosage regimen. Since food significantly increases its bioavailability, posaconazole should be administered with a full meal whenever possible, to ensure optimal absorption. Posaconazole primarily circulates in plasma and then is widely distributed to the tissues and is slowly eliminated. Posaconazole is not metabolized to a significant extent through the cytochrome P450 (CYP) enzyme system and also has no effect on the CYP isoenzymes of 1A2, 2C8, 2C9, 2D6 and 2E1. The limited metabolism of posaconazole is mediated predominantly through phase 2 biotransformations via uridine diphosphate glucuronosyltransferase enzyme pathways. Therefore, inhibitors or inducers of these clearance pathways may affect posaconazole plasma concentrations. Since posaconazole is an inhibitor primarily of CYP3A4, plasma concentrations of drugs that are predominantly metabolized by CYP3A4 may be increased by posaconazole. Posaconazole has a median terminal elimination half-life of 15-35 hours. The renal elimination of posaconazole is less than 1 mL/h, which is negligible compared with the mean total oral clearance of 16.3 L/h. Posaconazole shows potent in vitro activity against yeasts such as Candida spp. and C. neoformans, and against a range of moulds such as Aspergillus spp., as well as many dimorphic fungi and dermatophytes. Posaconazole has been shown to improve survival and/or to reduce the fungal tissue burden in animals infected with Blastomyces dermatitidis, C. neoformans, Aspergillus fumigatus, Aspergillus flavus, Aspergillus terreus, Coccidioides immitis or Pseudallescheria boydii. The predictive pharmacokinetic/pharmacodynamic parameter for posaconazole treatment efficacy--the ratio between the mean free-drug area under the plasma concentration-time curve from 0 to 24 hours and the minimum inhibitory concentration (AUC(24)/MIC)--is about 17, which is similar to the value observed for other azoles in this infection model of disseminated Candida albicans infection.

摘要

泊沙康唑是一种新型的亲脂性三唑类抗真菌药物,具有强大而广泛的体外和体内抗真菌活性,可对抗大多数念珠菌属、新型隐球菌、曲霉菌属、许多接合菌、地方性真菌和皮肤真菌。已有文献证明,泊沙康唑对临床上重要的念珠菌属、新型隐球菌和曲霉菌属分离株的活性和谱与伊曲康唑相似,优于氟康唑。这种新型三唑类药物是为治疗真菌感染而开发的,真菌感染通常发生在严重免疫功能低下的患者中,如器官移植患者或正在接受化疗的癌症患者。由于泊沙康唑在水和酸性介质中的溶解度低,其吸收剂量受限,并且非常依赖于食物摄入。据报道,口服单剂量后,达到最大血浆浓度的时间为 5-8 小时。泊沙康唑的相对生物利用度在不同方案中估计有显著差异,并观察到分剂量给药时显著增加。泊沙康唑主要与白蛋白结合,蛋白结合程度高(>98%)。泊沙康唑口服后表观分布容积较大(V(d)/F),约为 5-25 L/kg,提示其广泛分布于血管外,并渗透到细胞内空间。V(d)/F 受给药方案的影响。由于食物显著增加了其生物利用度,因此应尽可能在进餐时服用泊沙康唑,以确保最佳吸收。泊沙康唑主要在血浆中循环,然后广泛分布到组织中,并缓慢消除。泊沙康唑通过细胞色素 P450(CYP)酶系统代谢的程度不大,也不会对 1A2、2C8、2C9、2D6 和 2E1 的 CYP 同工酶产生影响。泊沙康唑的有限代谢主要通过尿苷二磷酸葡萄糖醛酸转移酶酶途径的相 2 生物转化来介导。因此,这些清除途径的抑制剂或诱导剂可能会影响泊沙康唑的血浆浓度。由于泊沙康唑主要是 CYP3A4 的抑制剂,因此主要由 CYP3A4 代谢的药物的血浆浓度可能会被泊沙康唑增加。泊沙康唑的终末消除半衰期中位数为 15-35 小时。泊沙康唑的肾脏清除率低于 1 mL/h,与 16.3 L/h 的总口服清除率相比可以忽略不计。泊沙康唑对念珠菌属和新型隐球菌等酵母以及曲霉菌属等多种霉菌具有强大的体外活性,以及许多二相真菌和皮肤真菌。泊沙康唑已被证明可提高患有皮炎芽生菌、新型隐球菌、烟曲霉、黄曲霉、土曲霉、粗球孢子菌或拟青霉感染的动物的存活率和/或降低真菌组织负担。泊沙康唑治疗疗效的预测药代动力学/药效学参数-从 0 到 24 小时的游离药物平均药时曲线下面积与最低抑菌浓度(AUC(24)/MIC)之比-约为 17,与其他唑类药物在这种播散性白色念珠菌感染的感染模型中观察到的值相似。

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