• 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

吡喹酮

Praziquantel.

作者信息

Cioli Donato, Pica-Mattoccia Livia

机构信息

Institute of Cell Biology, C.N.R., 32 Via Ramarini, 00016 Monterotondo (RM), Italy.

出版信息

Parasitol Res. 2003 Jun;90 Supp 1:S3-9. doi: 10.1007/s00436-002-0751-z. Epub 2002 Nov 22.

DOI:10.1007/s00436-002-0751-z
PMID:12811543
Abstract

Praziquantel is the drug of choice for the treatment of all forms of schistosomiasis. This review summarizes the main features of the drug, with special attention being given to those aspects that may be of interest to the practicing physician. After a brief mention of the history, the chemistry, the major available brands and their costs, doses and administration schedules are reviewed. Pharmacokinetics and drug interactions are analyzed and the low toxicity and mild side effects are stressed. A major weakness of praziquantel is its relative inefficacy against recent infections, a factor that may occasionally result in low cure rates in hyperendemic areas. Recent findings of schistosome isolates with a decreased sensitivity to praziquantel are discussed in the broader context of a possible emergence of drug resistance.

摘要

吡喹酮是治疗各种类型血吸虫病的首选药物。本综述总结了该药物的主要特点,特别关注执业医师可能感兴趣的那些方面。在简要提及该药的历史、化学结构、主要现有品牌及其成本后,对剂量和给药方案进行了综述。分析了药代动力学和药物相互作用,并强调了其低毒性和轻微副作用。吡喹酮的一个主要缺点是其对近期感染相对无效,这一因素可能偶尔导致高流行地区的治愈率较低。在可能出现耐药性的更广泛背景下,讨论了对吡喹酮敏感性降低的血吸虫分离株的最新研究结果。

相似文献

1
Praziquantel.吡喹酮
Parasitol Res. 2003 Jun;90 Supp 1:S3-9. doi: 10.1007/s00436-002-0751-z. Epub 2002 Nov 22.
2
[Study progress on the mode of action of praziquantel against schistosomes].[吡喹酮抗血吸虫作用机制的研究进展]
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2007 Dec;25(6):492-502.
3
Schistosomiasis: challenges for control, treatment and drug resistance.血吸虫病:控制、治疗及耐药性方面的挑战
Curr Opin Infect Dis. 2006 Dec;19(6):577-82. doi: 10.1097/01.qco.0000247591.13671.6a.
4
Praziquantel: its use in control of schistosomiasis in sub-Saharan Africa and current research needs.吡喹酮:在撒哈拉以南非洲控制血吸虫病中的应用及其当前研究需求。
Parasitology. 2009 Nov;136(13):1825-35. doi: 10.1017/S0031182009000493. Epub 2009 Mar 13.
5
Schistosomiasis control: keep taking the tablets.血吸虫病防治:持续服用药片。
Trends Parasitol. 2004 Feb;20(2):92-7. doi: 10.1016/j.pt.2003.11.010.
6
Praziquantel for the treatment of schistosomiasis: its use for control in areas with endemic disease and prospects for drug resistance.吡喹酮治疗血吸虫病:其在地方病流行地区的防控应用及耐药性前景
Expert Rev Anti Infect Ther. 2006 Apr;4(2):199-210. doi: 10.1586/14787210.4.2.199.
7
[Drug therapy of mansoni schistosomiasis].
Arq Gastroenterol. 1980 Apr-Jun;17(2):88-95.
8
Schistosomiasis control: praziquantel forever?血吸虫病防治:吡喹酮会一直使用吗?
Mol Biochem Parasitol. 2014 Jun;195(1):23-9. doi: 10.1016/j.molbiopara.2014.06.002. Epub 2014 Jun 21.
9
[Research progress of the evaluation methods on the resistance of schistosome to praziquantel].[血吸虫对吡喹酮耐药性评估方法的研究进展]
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2005 Jun 30;23(3):182-4.
10
Praziquantel: mechanisms of action, resistance and new derivatives for schistosomiasis.吡喹酮:血吸虫病的作用机制、耐药性及新衍生物
Curr Opin Infect Dis. 2008 Dec;21(6):659-67. doi: 10.1097/QCO.0b013e328318978f.

引用本文的文献

1
A genome-scale drug discovery pipeline uncovers therapeutic targets and a unique p97 allosteric binding site in .一个全基因组规模的药物发现流程揭示了治疗靶点以及(此处文本不完整,缺少具体所指内容中的)一个独特的p97变构结合位点。
Proc Natl Acad Sci U S A. 2025 Sep 2;122(35):e2505710122. doi: 10.1073/pnas.2505710122. Epub 2025 Aug 29.
2
Pluronic P123/L64 Mixed Micelles as Immediate Release Systems to Enhance the Bioavailability of Praziquantel in Rats.普朗尼克P123/L64混合胶束作为速释系统以提高大鼠体内吡喹酮的生物利用度
Int J Nanomedicine. 2025 Jul 7;20:8861-8871. doi: 10.2147/IJN.S520910. eCollection 2025.
3
Tranylcypromine-Based LSD1 Inhibitors as Useful Agents to Reduce Viability of .
基于反苯环丙胺的赖氨酸特异性去甲基化酶1(LSD1)抑制剂作为降低……活力的有效药物
ACS Infect Dis. 2025 Aug 8;11(8):2178-2189. doi: 10.1021/acsinfecdis.5c00224. Epub 2025 Jul 2.
4
Advances in Mechanochemical Methods for One-Pot Multistep Organic Synthesis.一锅多步有机合成的机械化学方法进展
Chemistry. 2025 Jun 17;31(34):e202500798. doi: 10.1002/chem.202500798. Epub 2025 May 24.
5
Prevention and control of schistosomiasis in the Philippines from a health education perspective.从健康教育角度看菲律宾血吸虫病的防治
Front Public Health. 2025 Apr 9;13:1558564. doi: 10.3389/fpubh.2025.1558564. eCollection 2025.
6
A genome-scale drug discovery pipeline uncovers new therapeutic targets and a unique p97 allosteric binding site in .一个全基因组规模的药物发现流程揭示了新的治疗靶点以及……中一个独特的p97变构结合位点。
bioRxiv. 2025 Mar 15:2025.03.14.643303. doi: 10.1101/2025.03.14.643303.
7
UPLC-MS/MS method for simultaneous determination of pyrantel, praziquantel, febantel, fenbendazole and oxfendazole in dog plasma and its application to a bioequivalence study.超高效液相色谱-串联质谱法同时测定犬血浆中噻嘧啶、吡喹酮、非班太尔、芬苯达唑和奥芬达唑及其在生物等效性研究中的应用
Front Pharmacol. 2025 Feb 13;16:1544215. doi: 10.3389/fphar.2025.1544215. eCollection 2025.
8
Design and Process Considerations for Preparation of Modified Release Ivermectin and Praziquantel Tablets by Wet Granulation.采用湿法制粒制备伊维菌素和吡喹酮缓释片的设计与工艺考量
AAPS PharmSciTech. 2025 Jan 22;26(1):43. doi: 10.1208/s12249-024-03030-2.
9
Amorphous Solid Dispersion Formation for Enhanced Release Performance of Racemic and Enantiopure Praziquantel.无定形固体分散体形成增强消旋和对映纯吡喹酮的释放性能。
Mol Pharm. 2024 Oct 7;21(10):5285-5296. doi: 10.1021/acs.molpharmaceut.4c00711. Epub 2024 Sep 18.
10
Mechanochemical Synthesis of New Praziquantel Cocrystals: Solid-State Characterization and Solubility.新型吡喹酮共晶体的机械化学合成:固态表征与溶解度
Cryst Growth Des. 2024 May 11;24(11):4668-4681. doi: 10.1021/acs.cgd.4c00296. eCollection 2024 Jun 5.