Aerosolized L-693,989 for Pneumocystis carinii prophylaxis in rats

Author:

Powles M A1,McFadden D C1,Liberator P A1,Anderson J W1,Vadas E B1,Meisner D1,Schmatz D M1

Affiliation:

1. Merck Research Laboratories, Rahway, New Jersey 07065.

Abstract

Water-soluble pneumocandin L-693,989, a potent antipneumocystis agent in the rat model for Pneumocystis carinii pneumonia (PCP), inhibits P. carinii cyst development and effectively prevents the development of PCP when used as a prophylactic agent (D. M. Schmatz, M. A. Powles, D. C. McFadden, L. Pittarelli, J. Balkovec, M. Hammond, R. Zambias, P. Liberator, and J. Anderson, Antimicrob. Agents Chemother. 36:1964-1970, 1992). However, because of limited oral bioavailability, this compound would likely be restricted to parenteral use in humans. As an alternative, the aerosol delivery of L-693,989 was explored to determine the dosing regimen required to prevent the onset of PCP. Rats with latent P. carinii infections were immunosuppressed continuously with dexamethasone to promote the onset of PCP. During the 6-week immunosuppression period, L-693,989 was delivered to rats as a nebulized solution (volume median diameter of 3.8 microns) via a nose exposure inhalation chamber. The efficiency of aerosol delivery to the lungs and the rate of clearance were determined by using radiolabelled compound. It was found that a daily dose of 0.7 micrograms of L-693,989 per lung or a weekly dose of 77.9 micrograms/lung effectively prevented the development of P. carinii cysts and trophozoites as well as the associated pneumonia commonly seen in rats with acute P. carinii infections. These results demonstrate that L-693,989 is potentially useful as an aerosol prophylactic agent for PCP.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference19 articles.

1. Bilateral upperlobe Pneumocystis cannii pneu- monia in a patient receiving inhaled pentamidine prophylaxis;Abd A. G.;Chest,1988

2. Abruzzo G. K. A. M. Flattery C. J. Gill J. G. Smith H. Kropp and K. Bartizal. 1993. Evaluation of water-soluble lipopeptides L-733 560 L-705 589 and L-731 373 in a mouse model of disseminated aspergillosis abstr. 355. Program Abstr. 33rd Intersci. Conf. Antimicrob. Agents Chemother. New Orleans La.

3. Synthesis, stability and biological evaluation of water-soluble prodrugs of a new echinocandin lipopeptide. Discovery of a potential clinical agent for the treatment of systemic candidiasis and Pneumocystis caninii pneumonia (PCP);Balkovec J. M.;J. Med. Chem.,1992

4. Bartizal K. G. K. Abruzzo A. M. Flattery C. J. Gill J. G. Smith L. Lynch C. Pacholok T. Scott L. Kong and H. Kropp. 1993. Anti-Candida in vivo efficacy of water-soluble lipopeptides L-705 589 L-731 373 and L-733 560 abstr. 353. Program Abstr. 33rd Intersci. Conf. Antimicrob. Agents Chemother. New Orleans La.

5. Biodistribution, tissue reaction and Iung retention of pentamidine aerosolized as three different salts;Debs R.;Am. Rev. Respir. Dis.,1990

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3