Suppr超能文献

含单体两性霉素B、5-氟胞嘧啶及用于补充钠的生理盐水的静脉制剂的抗真菌疗效。

Antifungal Efficacy of an Intravenous Formulation Containing Monomeric Amphotericin B, 5-Fluorocytosine, and Saline for Sodium Supplementation.

作者信息

Alvarez Celeste, Andes David R, Kang Jeong Yeon, Krug Carmen, Kwon Glen S

机构信息

Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, Wisconsin, 53705-2222, USA.

Section of Infectious Diseases, Department of Medicine, University of Wisconsin-Madison, Madison, Wisconsin, 53705-2281, USA.

出版信息

Pharm Res. 2017 May;34(5):1115-1124. doi: 10.1007/s11095-017-2121-7. Epub 2017 Feb 15.

Abstract

PURPOSE

Amphotericin B (AmB) and 5-fluorocytosine (5-FC) exhibit additive to synergistic activity against systemic mycoses. Incompatibility of prescribed formulations precludes concomitant IV administration, a route with distinct advantages. Previously, we used PEG-DSPE micelles to produce a reformulation of Fungizone (AmB-SD), AmB solubilized by sodium deoxycholate, called mAmB-90. Herein, we describe a second reformulation that facilitates co-delivery of mAmB-90 and 5-FC, and evaluate the effect of PEG-DSPE micelles on the combination's activity against Candida albicans.

METHODS

We assessed the effect of 5-FC addition on the stability, in vitro toxicity, and antifungal efficacy of mAmB-90. The aggregation state and particle size of mAmB-90 combined with 5-FC (FmAmB-90) was evaluated over 48 h. Hemolytic activity was measured in vitro. Antifungal activity was determined in vitro against C. albicans. The efficacy of monotherapy and combination treatment was evaluated in a neutropenic mouse model of disseminated candidiasis.

RESULTS

The aggregation state, particle size, and hemolytic activity of mAmB-90 were unaffected by 5-FC. While antifungal activity was similar in vitro, mAmB-90 alone and combined with 5-FC was more potent than AmB-SD in vivo.

CONCLUSIONS

Short-term stability and in vivo efficacy of our formulation suggest potential to simultaneously deliver AmB and 5-FC for potent antifungal efficacy.

摘要

目的

两性霉素B(AmB)和5-氟胞嘧啶(5-FC)对系统性真菌病表现出相加至协同的活性。规定制剂之间的不相容性排除了静脉联合给药,而静脉给药具有明显优势。此前,我们使用聚乙二醇-二硬脂酰磷脂酰乙醇胺(PEG-DSPE)胶束对两性霉素B脱氧胆酸钠溶解的两性霉素B(AmB-SD,商品名Fungizone)进行了重新配方,称为mAmB-90。在此,我们描述了第二种重新配方,其有助于mAmB-90和5-FC的共同递送,并评估PEG-DSPE胶束对该组合抗白色念珠菌活性的影响。

方法

我们评估了添加5-FC对mAmB-90的稳定性、体外毒性和抗真菌疗效的影响。在48小时内评估mAmB-90与5-FC组合(FmAmB-90)的聚集状态和粒径。体外测量溶血活性。体外测定对白色念珠菌的抗真菌活性。在中性粒细胞减少的播散性念珠菌病小鼠模型中评估单药治疗和联合治疗的疗效。

结果

mAmB-90的聚集状态、粒径和溶血活性不受5-FC影响。虽然体外抗真菌活性相似,但单独的mAmB-90以及与5-FC联合使用时在体内比AmB-SD更有效。

结论

我们制剂的短期稳定性和体内疗效表明其有潜力同时递送AmB和5-FC以获得强效抗真菌疗效。

相似文献

2
Reformulation of Fungizone by PEG-DSPE Micelles: Deaggregation and Detoxification of Amphotericin B.
Pharm Res. 2016 Sep;33(9):2098-106. doi: 10.1007/s11095-016-1948-7. Epub 2016 May 19.
3
Combination antifungal therapy involving amphotericin B, rapamycin and 5-fluorocytosine using PEG-phospholipid micelles.
Pharm Res. 2008 Sep;25(9):2056-64. doi: 10.1007/s11095-008-9588-1. Epub 2008 Apr 16.
4
Efficacy and toxicity evaluation of new amphotericin B micelle systems for brain fungal infections.
Int J Pharm. 2015 Oct 15;494(1):17-22. doi: 10.1016/j.ijpharm.2015.08.003. Epub 2015 Aug 6.
6
Pharmacokinetics and Renal Toxicity of Monomeric Amphotericin B in Rats after a Multiple Dose Regimen.
Pharm Nanotechnol. 2016;4(1):16-23. doi: 10.2174/2211738504666160301233754.
7
Optimization, stabilization, and characterization of amphotericin B loaded nanostructured lipid carriers for ocular drug delivery.
Int J Pharm. 2019 Dec 15;572:118771. doi: 10.1016/j.ijpharm.2019.118771. Epub 2019 Oct 26.
9
Lipoamino acid-based micelles as promising delivery vehicles for monomeric amphotericin B.
Int J Pharm. 2016 Jan 30;497(1-2):23-35. doi: 10.1016/j.ijpharm.2015.11.034. Epub 2015 Nov 23.
10
Preparation, characterization, and evaluation of amphotericin B-loaded MPEG-PCL-g-PEI micelles for local treatment of oral .
Int J Nanomedicine. 2017 Jun 6;12:4269-4283. doi: 10.2147/IJN.S124264. eCollection 2017.

引用本文的文献

3
Antifungal Combinations against Species: From Bench to Bedside.
J Fungi (Basel). 2022 Oct 13;8(10):1077. doi: 10.3390/jof8101077.
4
Amphotericin B and Curcumin Co-Loaded Porous Microparticles as a Sustained Release System against .
Molecules. 2022 May 11;27(10):3079. doi: 10.3390/molecules27103079.
5
Current and promising pharmacotherapeutic options for candidiasis.
Expert Opin Pharmacother. 2021 May;22(7):867-887. doi: 10.1080/14656566.2021.1873951. Epub 2021 Feb 4.

本文引用的文献

1
Reformulation of Fungizone by PEG-DSPE Micelles: Deaggregation and Detoxification of Amphotericin B.
Pharm Res. 2016 Sep;33(9):2098-106. doi: 10.1007/s11095-016-1948-7. Epub 2016 May 19.
2
Clinical Practice Guideline for the Management of Candidiasis: 2016 Update by the Infectious Diseases Society of America.
Clin Infect Dis. 2016 Feb 15;62(4):e1-50. doi: 10.1093/cid/civ933. Epub 2015 Dec 16.
3
Flucytosine antagonism of azole activity versus Candida glabrata: role of transcription factor Pdr1 and multidrug transporter Cdr1.
Antimicrob Agents Chemother. 2013 Nov;57(11):5543-7. doi: 10.1128/AAC.02394-12. Epub 2013 Aug 26.
4
Amphotericin primarily kills yeast by simply binding ergosterol.
Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):2234-9. doi: 10.1073/pnas.1117280109. Epub 2012 Jan 17.
7
Antifungal therapeutic drug monitoring: established and emerging indications.
Antimicrob Agents Chemother. 2009 Jan;53(1):24-34. doi: 10.1128/AAC.00705-08. Epub 2008 Oct 27.
8
Antifungal serum concentration monitoring: an update.
J Antimicrob Chemother. 2008 Jan;61(1):17-25. doi: 10.1093/jac/dkm389. Epub 2007 Nov 12.
9
Flucytosine therapeutic monitoring: 15 years experience from the UK.
J Antimicrob Chemother. 2007 Apr;59(4):791-3. doi: 10.1093/jac/dkl550. Epub 2007 Mar 5.
10
Oral versus intravenous flucytosine in patients with human immunodeficiency virus-associated cryptococcal meningitis.
Antimicrob Agents Chemother. 2007 Mar;51(3):1038-42. doi: 10.1128/AAC.01188-06. Epub 2006 Dec 28.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验