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本文引用的文献

1
The determination of treatment effect of chitosan oligosaccharide in lambs with experimentally cryptosporidiosis.壳寡糖对实验性隐孢子虫病羔羊治疗效果的测定
Small Rumin Res. 2019 Nov;180:27-34. doi: 10.1016/j.smallrumres.2019.09.021. Epub 2019 Sep 27.
2
Infection: Epidemiology, Pathogenesis, and Differential Diagnosis.感染:流行病学、发病机制与鉴别诊断
Eur J Microbiol Immunol (Bp). 2019 Oct 22;9(4):119-123. doi: 10.1556/1886.2019.00019. eCollection 2019 Dec 25.
3
Effect of Nitazoxanide, Artesunate Loaded Polymeric Nano Fiber and Their Combination on Experimental Cryptosporidiosis.硝唑尼特、青蒿琥酯负载的聚合物纳米纤维及其组合对实验性隐孢子虫病的影响。
Iran J Parasitol. 2019 Apr-Jun;14(2):240-249.
4
Inhibitory activity of chitosan nanoparticles against Cryptosporidium parvum oocysts.壳聚糖纳米粒子对微小隐孢子虫卵囊的抑制活性。
Parasitol Res. 2019 Jul;118(7):2053-2063. doi: 10.1007/s00436-019-06364-0. Epub 2019 Jun 11.
5
Efficacy of chitosan, a natural polysaccharide, against Cryptosporidium parvum in vitro and in vivo in neonatal mice.天然多糖壳聚糖对新生小鼠体内外微小隐孢子虫的疗效
Exp Parasitol. 2018 Nov;194:1-8. doi: 10.1016/j.exppara.2018.09.003. Epub 2018 Sep 17.
6
Risk factors for Cryptosporidium infection in low and middle income countries: A systematic review and meta-analysis.中低收入国家隐孢子虫感染的危险因素:系统评价和荟萃分析。
PLoS Negl Trop Dis. 2018 Jun 7;12(6):e0006553. doi: 10.1371/journal.pntd.0006553. eCollection 2018 Jun.
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Assessment of spiramycin-loaded chitosan nanoparticles treatment on acute and chronic toxoplasmosis in mice.评估载有螺旋霉素的壳聚糖纳米颗粒对小鼠急性和慢性弓形虫病的治疗效果。
J Parasit Dis. 2018 Mar;42(1):102-113. doi: 10.1007/s12639-017-0973-8. Epub 2017 Dec 15.
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Applications of nanoparticle systems in drug delivery technology.纳米颗粒系统在药物递送技术中的应用。
Saudi Pharm J. 2018 Jan;26(1):64-70. doi: 10.1016/j.jsps.2017.10.012. Epub 2017 Oct 25.
9
Atorvastatin repurposing for the treatment of cryptosporidiosis in experimentally immunosuppressed mice.阿托伐他汀用于治疗实验性免疫抑制小鼠隐孢子虫病的新用途。
Exp Parasitol. 2017 Oct;181:57-69. doi: 10.1016/j.exppara.2017.07.010. Epub 2017 Jul 29.
10
Effect of Egyptian propolis on cryptosporidiosis in immunosuppressed rats with special emphasis on oocysts shedding, leukogram, protein profile and ileum histopathology.埃及蜂胶对免疫抑制大鼠隐孢子虫病的影响,特别关注卵囊排出、白细胞计数、蛋白质谱和回肠组织病理学。
Asian Pac J Trop Med. 2017 Mar;10(3):253-262. doi: 10.1016/j.apjtm.2017.03.004. Epub 2017 Mar 6.

壳聚糖纳米颗粒对硝唑尼特治疗免疫抑制和免疫健全小鼠模型隐孢子虫病疗效的改善评估。

Assessment of chitosan nanoparticles in improving the efficacy of nitazoxanide on cryptosporidiosis in immunosuppressed and immunocompetent murine models.

作者信息

Moawad Howayda Said Fouad, Hegab Mohamed Hegab Abd El-Hady, Badawey Maha Saber Reda, Ashoush Shaimaa Elsayed, Ibrahim Shereen Mahmoud, Ali Amira Abd El-Lateef Saleh

机构信息

Faculty of Medicine, Zagazig University, Zagazig, Egypt.

出版信息

J Parasit Dis. 2021 Sep;45(3):606-619. doi: 10.1007/s12639-020-01337-y. Epub 2021 Jan 6.

DOI:10.1007/s12639-020-01337-y
PMID:34475640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8368908/
Abstract

Cryptosporidiosis is one of the major causes of diarrhea in immunocompetent and immunocompromised patients. It is self-limited in immunocompetent individuals. However, in the immunocompromised it can cause life-threatening diarrhea and results in chronic malabsorption of fluids, vitamins and electrolytes resulting in wasting. Our study is concerned with assessing and comparing the efficacy of nitazoxanide (NTZ) alone and NTZ loaded chitosan nanoparticles (NTZ loaded CS NPs) in the treatment of experimental cryptosporidiosis using parasitological and histopathological parameters. One hundred mice were divided into 5 groups (20 mice each). Each group was divided into 2 subgroups according to the immune status [a-immunocompetent, b-immunosuppressed]. group 1: control (healthy), group 2: control infected by oocysts, group 3: infected treated by NTZ, group 4: infected then treated by NTZ loaded CS NPs and group 5: infected then treated by chitosan nanoparticles (CS NPs) alone. Treatment of infected mice with NTZ loaded on CS NPs resulted in the highest significant reduction in oocysts shedding in both immunocompetent and immunosuppressed groups followed by treatment with NTZ form then by treatment with CS NPs alone. The treatment with NTZ loaded CS NPs displayed a remarkable improvement of the histopathological changes of the intestine, liver and lung while NTZ treated group showed some improvement. Treatment with NTZ loaded CS NPs in murine cryptosporidiosis gave the best results as it caused marked reduction in fecal oocysts counts and improvement of histopathological changes in immunocompetent and immunosuppressed groups.

摘要

隐孢子虫病是免疫功能正常和免疫功能低下患者腹泻的主要原因之一。在免疫功能正常的个体中,它是自限性的。然而,在免疫功能低下的患者中,它可导致危及生命的腹泻,并导致液体、维生素和电解质的慢性吸收不良,从而导致消瘦。我们的研究关注于使用寄生虫学和组织病理学参数评估和比较硝唑尼特(NTZ)单独使用以及负载硝唑尼特的壳聚糖纳米颗粒(负载NTZ的CS NPs)在治疗实验性隐孢子虫病中的疗效。将100只小鼠分为5组(每组20只)。根据免疫状态,每组又分为2个亚组[a - 免疫功能正常,b - 免疫抑制]。第1组:对照组(健康),第2组:受卵囊感染的对照组,第3组:感染后用NTZ治疗,第4组:感染后用负载NTZ的CS NPs治疗,第5组:感染后仅用壳聚糖纳米颗粒(CS NPs)治疗。用负载NTZ的CS NPs治疗感染小鼠,在免疫功能正常和免疫抑制组中,卵囊排出量的显著减少最为明显,其次是用NTZ剂型治疗,然后是仅用CS NPs治疗。用负载NTZ的CS NPs治疗使肠道、肝脏和肺的组织病理学变化有显著改善,而用NTZ治疗的组有一定改善。在鼠隐孢子虫病中,用负载NTZ的CS NPs治疗效果最佳,因为它能显著减少粪便中卵囊计数,并改善免疫功能正常和免疫抑制组的组织病理学变化。