• 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

载吡喹酮壳聚糖纳米粒对小鼠体内曼氏血吸虫童虫的治疗效果。

Therapeutic efficacy of praziquantel loaded-chitosan nanoparticles on juvenile Schistosoma mansoni worms in murine model.

机构信息

Zoology Department, Faculty of Science, Alexandria University, Egypt.

Parasitology Department, Medical Research Institute, Alexandria University, Egypt.

出版信息

Exp Parasitol. 2024 Nov;266:108843. doi: 10.1016/j.exppara.2024.108843. Epub 2024 Oct 5.

DOI:10.1016/j.exppara.2024.108843
PMID:39369770
Abstract

Praziquantel (PZQ) is the standard treatment for schistosomiasis; however, it is poorly effective on immature and juvenile worms. The present study aimed to evaluate the therapeutic efficacy of praziquantel loaded-chitosan nanoparticles (PZQ-CSNPs) on the 25 days old juvenile Schistosoma mansoni worms compared to PZQ and chitosan nanoparticles (CSNPs). It was conducted on 60 Swiss albino mice, including 20 control and 40 experimental mice. The control groups included healthy uninfected and infected non-treated mice. The experimental groups included mice infected treated on the 25th day with 400 mg/kg PZQ, 30 mg/kg CSNPs, 100 mg/kg, and 400 mg/kg PZQ-CSNPs. The results revealed that PZQ-CSNPs (100, 400 mg/kg) gave the best results substantiated by a remarkable decrease in worm burden, egg count, granuloma count and size compared to the other treatments. Moreover, it induced severe deformations of worm morphology regarding oral and ventral suckers, tegument, spines distribution, and male gynaecophoric canal. Liver enzymes and oxidative stress markers were significantly decreased while antioxidant activities were increased compared to control and other treated groups. In conclusion, a single dose of PZQ-CSNPs had significant antischistosomal therapeutic effects during the early maturation phase.

摘要

吡喹酮(PZQ)是血吸虫病的标准治疗方法;然而,它对未成熟和幼年虫的效果很差。本研究旨在评估载吡喹酮壳聚糖纳米粒(PZQ-CSNPs)对 25 日龄曼氏血吸虫幼体的治疗效果,与 PZQ 和壳聚糖纳米粒(CSNPs)进行比较。该研究在 60 只瑞士白化病小鼠上进行,包括 20 只对照组和 40 只实验组。对照组包括健康未感染和未治疗感染的小鼠。实验组包括在第 25 天用 400mg/kg PZQ、30mg/kg CSNPs、100mg/kg 和 400mg/kg PZQ-CSNPs 治疗感染的小鼠。结果表明,PZQ-CSNPs(100、400mg/kg)的效果最佳,其依据是与其他治疗方法相比,蠕虫负荷、虫卵计数、肉芽肿计数和大小显著减少。此外,它诱导了蠕虫形态的严重变形,涉及口腔和腹吸盘、表皮、棘分布和雄性生殖孔道。与对照组和其他治疗组相比,肝酶和氧化应激标志物显著降低,而抗氧化活性增加。总之,单次剂量的 PZQ-CSNPs 在早期成熟阶段具有显著的抗血吸虫治疗效果。

相似文献

1
Therapeutic efficacy of praziquantel loaded-chitosan nanoparticles on juvenile Schistosoma mansoni worms in murine model.载吡喹酮壳聚糖纳米粒对小鼠体内曼氏血吸虫童虫的治疗效果。
Exp Parasitol. 2024 Nov;266:108843. doi: 10.1016/j.exppara.2024.108843. Epub 2024 Oct 5.
2
Enhancement of the therapeutic efficacy of praziquantel in murine Schistosomiasis mansoni using silica nanocarrier.利用硅纳米载体增强吡喹酮治疗曼氏血吸虫病的疗效。
Parasitol Res. 2019 Dec;118(12):3519-3533. doi: 10.1007/s00436-019-06475-8. Epub 2019 Oct 31.
3
In vivo assessment of the antischistosomal activity of curcumin loaded nanoparticles versus praziquantel in the treatment of Schistosoma mansoni.载姜黄素纳米粒抗曼氏血吸虫作用的体内评价与吡喹酮治疗曼氏血吸虫病的比较。
Sci Rep. 2020 Sep 25;10(1):15742. doi: 10.1038/s41598-020-72901-y.
4
Pharmacodynamics of mefloquine and praziquantel combination therapy in mice harbouring juvenile and adult Schistosoma mansoni.青蒿琥酯和吡喹酮联合治疗感染曼氏血吸虫幼、成虫小鼠的药效学研究。
Mem Inst Oswaldo Cruz. 2011 Nov;106(7):814-22. doi: 10.1590/s0074-02762011000700006.
5
Parasitological, hematological and ultrastructural study of the effect of COX-2 inhibitor, pyocyanin pigment and praziquantel, on S. mansoni infected mice.COX-2抑制剂、绿脓菌素和吡喹酮对曼氏血吸虫感染小鼠影响的寄生虫学、血液学及超微结构研究
J Egypt Soc Parasitol. 2006 Apr;36(1):197-220.
6
Anthelmintic activity in vitro and in vivo of Baccharis trimera (Less) DC against immature and adult worms of Schistosoma mansoni.三齿苦荬菜(Less)DC 对曼氏血吸虫未成熟和成虫的体内外驱虫活性。
Exp Parasitol. 2014 Apr;139:63-72. doi: 10.1016/j.exppara.2014.02.010. Epub 2014 Mar 3.
7
Evaluation of prophylactic efficacy and safety of praziquantel-miltefosine nanocombination in experimental Schistosomiasis mansoni.评价吡喹酮-米替福新纳米复方在实验性曼氏血吸虫病中的预防效果和安全性。
Acta Trop. 2020 Dec;212:105714. doi: 10.1016/j.actatropica.2020.105714. Epub 2020 Sep 17.
8
Therapeutic efficacy of candidate antischistosomal drugs in a murine model of schistosomiasis mansoni.候选抗血吸虫药物在曼氏血吸虫病小鼠模型中的治疗效果。
Parasitol Res. 2024 May 21;123(5):215. doi: 10.1007/s00436-024-08236-8.
9
Adult worm tegumental damage and egg-granulomas in praziquantel-resistant and -susceptible Schistosoma mansoni treated in vivo.体内治疗的抗吡喹酮和敏感曼氏血吸虫的成虫体表损伤及虫卵肉芽肿
J Helminthol. 2002 Dec;76(4):327-33. doi: 10.1079/JOH2002135.
10
Potential antifibrotic effects of AT1 receptor antagonist, losartan, and/or praziquantel on acute and chronic experimental liver fibrosis induced by Schistosoma mansoni.血管紧张素 II 受体拮抗剂氯沙坦和/或吡喹酮对曼氏血吸虫诱导的急性和慢性实验性肝纤维化的潜在抗纤维化作用。
Clin Exp Pharmacol Physiol. 2011 Oct;38(10):695-704. doi: 10.1111/j.1440-1681.2011.05575.x.

引用本文的文献

1
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.