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CD101 疗效的药理学基础:暴露形状很重要。

Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters.

机构信息

Institute for Clinical Pharmacodynamics (ICPD), Schenectady, New York, USA

Institute for Clinical Pharmacodynamics (ICPD), Schenectady, New York, USA.

出版信息

Antimicrob Agents Chemother. 2017 Oct 24;61(11). doi: 10.1128/AAC.00758-17. Print 2017 Nov.

Abstract

CD101 is a novel echinocandin with concentration-dependent fungicidal activity and a long half-life (∼133 h in humans, ∼70 to 80 h in mice). Given these characteristics, it is likely that the shape of the CD101 exposure (i.e., the time course of CD101 concentrations) influences efficacy. To test this hypothesis, doses which produce the same total area under the concentration-time curve (AUC) were administered to groups of neutropenic ICR mice infected with R303 using three different schedules. A total CD101 dose of 2 mg/kg was administered as a single intravenous (i.v.) dose or in equal divided doses of either 1 mg/kg twice weekly or 0.29 mg/kg/day over 7 days. The studies were performed using a murine disseminated candidiasis model. Animals were euthanized at 168 h following the start of treatment. Fungi grew well in the no-treatment control group and showed variable changes in fungal density in the treatment groups. When the CD101 AUC from 0 to 168 h (AUC) was administered as a single dose, a >2 log CFU reduction from the baseline at 168 h was observed. When twice-weekly and daily regimens with similar AUC values were administered, net fungal stasis and a >1 log CFU increase from the baseline were observed, respectively. These data support the hypothesis that the shape of the CD101 AUC influences efficacy. Thus, CD101 administered once per week demonstrated a greater degree of fungal killing than the same dose divided into twice-weekly or daily regimens.

摘要

CD101 是一种新型棘白菌素,具有浓度依赖性杀菌活性和较长的半衰期(在人体中约为 133 小时,在小鼠中约为 70 至 80 小时)。鉴于这些特性,CD101 暴露的形状(即 CD101 浓度的时间过程)很可能会影响疗效。为了验证这一假设,使用三种不同方案,给感染了 R303 的中性粒细胞减少 ICR 小鼠组施用产生相同总浓度-时间曲线下面积(AUC)的剂量。总剂量为 2 毫克/千克的 CD101 单次静脉(i.v.)给药,或每周两次给予相等的 1 毫克/千克剂量,或连续 7 天每天给予 0.29 毫克/千克。这些研究使用了一种鼠播散性念珠菌病模型。动物在治疗开始后 168 小时安乐死。未治疗对照组中的真菌生长良好,而治疗组中的真菌密度则发生了变化。当 0 至 168 小时的 CD101 AUC(AUC)作为单次剂量给药时,在 168 小时时观察到从基线的 >2 对数 CFU 减少。当给予每周两次和每日方案且 AUC 值相似时,观察到净真菌停滞和从基线的 >1 对数 CFU 增加。这些数据支持这样的假设,即 CD101 AUC 的形状影响疗效。因此,每周一次给予 CD101 比将相同剂量分为每周两次或每日方案给药显示出更大程度的真菌杀伤作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/633ddbb4eeee/zac0111766420001.jpg

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