• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1128/AAC.00758-17
PMID:28848022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5655053/
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/7481/5655053/96ba2bf937ca/zac0111766420004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/633ddbb4eeee/zac0111766420001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/1e21a52b7308/zac0111766420002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/5d6df16e483a/zac0111766420003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/96ba2bf937ca/zac0111766420004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/633ddbb4eeee/zac0111766420001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/1e21a52b7308/zac0111766420002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/5d6df16e483a/zac0111766420003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7481/5655053/96ba2bf937ca/zac0111766420004.jpg

相似文献

1
Pharmacological Basis of CD101 Efficacy: Exposure Shape Matters.CD101 疗效的药理学基础:暴露形状很重要。
Antimicrob Agents Chemother. 2017 Oct 24;61(11). doi: 10.1128/AAC.00758-17. Print 2017 Nov.
2
Pharmacodynamics of a Long-Acting Echinocandin, CD101, in a Neutropenic Invasive-Candidiasis Murine Model Using an Extended-Interval Dosing Design.长效棘白菌素 CD101 在延长给药间隔的中性粒细胞减少性侵袭性念珠菌病小鼠模型中的药效学研究。
Antimicrob Agents Chemother. 2018 Jan 25;62(2). doi: 10.1128/AAC.02154-17. Print 2018 Feb.
3
Overcoming the Resistance Hurdle: Pharmacokinetic-Pharmacodynamic Target Attainment Analyses for Rezafungin (CD101) against Candida albicans and Candida glabrata.克服耐药障碍:瑞他康唑(CD101)对白色念珠菌和光滑念珠菌的药代动力学-药效学目标达成分析。
Antimicrob Agents Chemother. 2018 May 25;62(6). doi: 10.1128/AAC.02614-17. Print 2018 Jun.
4
Structure-Activity Relationships of a Series of Echinocandins and the Discovery of CD101, a Highly Stable and Soluble Echinocandin with Distinctive Pharmacokinetic Properties.一系列棘白菌素的构效关系以及CD101的发现,CD101是一种具有独特药代动力学特性的高度稳定且可溶的棘白菌素。
Antimicrob Agents Chemother. 2017 Jan 24;61(2). doi: 10.1128/AAC.01541-16. Print 2017 Feb.
5
CD101: a novel long-acting echinocandin.CD101:一种新型长效棘白菌素。
Cell Microbiol. 2016 Sep;18(9):1308-16. doi: 10.1111/cmi.12640. Epub 2016 Jul 22.
6
Determination of Pharmacodynamic Target Exposures for Rezafungin against Candida tropicalis and Candida dubliniensis in the Neutropenic Mouse Disseminated Candidiasis Model.测定中性粒细胞减少症小鼠播散性念珠菌病模型中雷泽芬康唑对热带念珠菌和都柏林念珠菌的药效学靶标暴露量。
Antimicrob Agents Chemother. 2019 Oct 22;63(11). doi: 10.1128/AAC.01556-19. Print 2019 Nov.
7
Pharmacokinetics and Pharmacodynamics of APX001 against Candida spp. in a Neutropenic Disseminated Candidiasis Mouse Model.APX001 对中性粒细胞减少性播散性念珠菌病小鼠模型中念珠菌属的药代动力学和药效学研究。
Antimicrob Agents Chemother. 2018 Mar 27;62(4). doi: 10.1128/AAC.02542-17. Print 2018 Apr.
8
Pharmacodynamic Evaluation of Rezafungin (CD101) against Candida auris in the Neutropenic Mouse Invasive Candidiasis Model.抗真菌药物 Rezafungin(CD101)对中性粒细胞减少症小鼠侵袭性念珠菌病模型中念珠菌属的药效学评价。
Antimicrob Agents Chemother. 2018 Oct 24;62(11). doi: 10.1128/AAC.01572-18. Print 2018 Nov.
9
In vitro potency and fungicidal activity of CD101, a novel echinocandin, against recent clinical isolates of Candida spp.新型棘白菌素CD101对近期念珠菌属临床分离株的体外药效和杀菌活性
Diagn Microbiol Infect Dis. 2017 Nov;89(3):205-211. doi: 10.1016/j.diagmicrobio.2017.07.007. Epub 2017 Jul 21.
10
In vivo pharmacodynamic characterization of anidulafungin in a neutropenic murine candidiasis model.阿尼芬净在中性粒细胞减少小鼠念珠菌病模型中的体内药效学特征
Antimicrob Agents Chemother. 2008 Feb;52(2):539-50. doi: 10.1128/AAC.01061-07. Epub 2007 Dec 10.

引用本文的文献

1
Activity of rezafungin against Candida auris.瑞扎芬净对耳念珠菌的活性。
J Antimicrob Chemother. 2025 Apr 30;80(6):1482-93. doi: 10.1093/jac/dkaf124.
2
Successful rezafungin treatment of an azole-resistant vascular graft infection.瑞扎芬净成功治疗唑类耐药的血管移植物感染。
Rev Esp Quimioter. 2025 Apr 16;38(4):358-360. doi: 10.37201/req/028.2025.
3
Rezafungin: A Review in Invasive Candidiasis.瑞扎芬净:侵袭性念珠菌病综述

本文引用的文献

1
Pharmacokinetics of the Novel Echinocandin CD101 in Multiple Animal Species.新型棘白菌素CD101在多种动物物种中的药代动力学
Antimicrob Agents Chemother. 2017 Mar 24;61(4). doi: 10.1128/AAC.01626-16. Print 2017 Apr.
2
Safety and Pharmacokinetics of CD101 IV, a Novel Echinocandin, in Healthy Adults.新型棘白菌素CD101静脉注射剂在健康成年人中的安全性和药代动力学
Antimicrob Agents Chemother. 2017 Jan 24;61(2). doi: 10.1128/AAC.01627-16. Print 2017 Feb.
3
Preclinical Evaluation of the Stability, Safety, and Efficacy of CD101, a Novel Echinocandin.
Drugs. 2025 Mar;85(3):415-423. doi: 10.1007/s40265-024-02134-0. Epub 2025 Feb 6.
4
New Perspectives on Antimicrobial Agents: Rezafungin.抗微生物药物的新视角:瑞扎芬净
Antimicrob Agents Chemother. 2025 Jan 31;69(1):e0064623. doi: 10.1128/aac.00646-23. Epub 2024 Dec 12.
5
The distinctive pharmacokinetic profile of rezafungin, a long-acting echinocandin developed in the era of modern pharmacometrics.瑞扎芬净独特的药代动力学特征,这是一种在现代药物计量学时代研发的长效棘白菌素。
J Antimicrob Chemother. 2025 Jan 3;80(1):18-28. doi: 10.1093/jac/dkae415.
6
Treatment Outcomes Among Patients With a Positive Candida Culture Close to Randomization Receiving Rezafungin or Caspofungin in the ReSTORE Study.在 ReSTORE 研究中,接近随机分组时,接受瑞他康唑或卡泊芬净治疗的阳性念珠菌培养患者的治疗结局。
Clin Infect Dis. 2024 Sep 26;79(3):672-681. doi: 10.1093/cid/ciae363.
7
The Role of Novel Antifungals in the Management of Candidiasis: A Clinical Perspective.新型抗真菌药物在念珠菌病治疗中的作用:临床视角。
Mycopathologia. 2023 Dec;188(6):937-948. doi: 10.1007/s11046-023-00759-5. Epub 2023 Jul 20.
8
Rezafungin: First Approval.雷沙康唑:首次批准。
Drugs. 2023 Jun;83(9):833-840. doi: 10.1007/s40265-023-01891-8.
9
Pharmacodynamics, Mechanisms of Action and Resistance, and Spectrum of Activity of New Antifungal Agents.新型抗真菌药物的药效学、作用机制与耐药性以及活性谱
J Fungi (Basel). 2022 Aug 16;8(8):857. doi: 10.3390/jof8080857.
10
Therapeutic Approaches for Combating Associated Infection.对抗相关感染的治疗方法。
Curr Drug Targets. 2022;23(16):1465-1488. doi: 10.2174/1389450123666220623164548.
新型棘白菌素CD101的稳定性、安全性及有效性的临床前评估
Antimicrob Agents Chemother. 2016 Oct 21;60(11):6872-6879. doi: 10.1128/AAC.00701-16. Print 2016 Nov.
4
Activity of a long-acting echinocandin, CD101, determined using CLSI and EUCAST reference methods, against Candida and Aspergillus spp., including echinocandin- and azole-resistant isolates.使用临床和实验室标准协会(CLSI)及欧洲抗微生物药敏试验委员会(EUCAST)参考方法测定的长效棘白菌素CD101对念珠菌和曲霉属的活性,包括对棘白菌素和唑类耐药的分离株。
J Antimicrob Chemother. 2016 Oct;71(10):2868-73. doi: 10.1093/jac/dkw214. Epub 2016 Jun 10.
5
Single or 2-Dose Micafungin Regimen for Treatment of Invasive Candidiasis: Therapia Sterilisans Magna!单剂或 2 剂米卡芬净方案治疗侵袭性念珠菌病:伟大的杀菌治疗!
Clin Infect Dis. 2015 Dec 1;61 Suppl 6:S635-42. doi: 10.1093/cid/civ715.
6
In vivo activity of oritavancin in animal infection models and rationale for a new dosing regimen in humans.替加环素在动物感染模型中的体内活性及在人体中采用新的给药方案的原理。
Clin Infect Dis. 2012 Apr;54 Suppl 3:S220-8. doi: 10.1093/cid/cis001.
7
Comparison of the efficacy and safety of oritavancin front-loaded dosing regimens to daily dosing: an analysis of the SIMPLIFI trial.比较奥沙万古霉素前负荷剂量方案与每日剂量方案的疗效和安全性:SIMPLIFI 试验分析。
Antimicrob Agents Chemother. 2011 Jul;55(7):3476-84. doi: 10.1128/AAC.00029-11. Epub 2011 May 2.
8
Pharmacokinetic-pharmacodynamic considerations in the design of hospital-acquired or ventilator-associated bacterial pneumonia studies: look before you leap!在设计医院获得性或呼吸机相关性细菌性肺炎研究时的药代动力学-药效学考虑因素:三思而后行!
Clin Infect Dis. 2010 Aug 1;51 Suppl 1:S103-10. doi: 10.1086/653057.
9
Echinocandin pharmacodynamics: review and clinical implications.棘白菌素类药物的药效动力学:综述及临床意义。
J Antimicrob Chemother. 2010 Jun;65(6):1108-18. doi: 10.1093/jac/dkq081. Epub 2010 Mar 23.
10
Time-kill kinetics of oritavancin and comparator agents against Staphylococcus aureus, Enterococcus faecalis and Enterococcus faecium.奥利万星及对照药物对金黄色葡萄球菌、粪肠球菌和屎肠球菌的时间杀菌动力学
J Antimicrob Chemother. 2009 Jun;63(6):1191-9. doi: 10.1093/jac/dkp126. Epub 2009 Apr 15.