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本文引用的文献

1
Therapeutic agents and biocides for ocular infections by free-living amoebae of Acanthamoeba genus.用于治疗棘阿米巴属自由生活阿米巴引起的眼部感染的治疗剂和杀菌剂。
Surv Ophthalmol. 2017 Mar-Apr;62(2):203-218. doi: 10.1016/j.survophthal.2016.10.009. Epub 2016 Nov 9.
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Isolation and identification of Acanthamoeba species from natural water sources in the northeastern part of Thailand.从泰国东北部天然水源中分离和鉴定棘阿米巴属物种。
Parasitol Res. 2016 Apr;115(4):1705-9. doi: 10.1007/s00436-016-4911-y. Epub 2016 Jan 16.
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Phylogenetic analysis and the evolution of the 18S rRNA gene typing system of Acanthamoeba.棘阿米巴18S rRNA基因分型系统的系统发育分析与进化
J Eukaryot Microbiol. 2015 Jan-Feb;62(1):69-84. doi: 10.1111/jeu.12186.
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Biology and pathogenesis of Acanthamoeba.棘阿米巴的生物学和发病机制。
Parasit Vectors. 2012 Jan 10;5:6. doi: 10.1186/1756-3305-5-6.
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Weak cytotoxic activity of miltefosine against clinical isolates of Acanthamoeba spp.米替福新对棘阿米巴属临床分离株的细胞毒性活性较弱。
J Parasitol. 2011 Jun;97(3):538-40. doi: 10.1645/GE-2669.1. Epub 2010 Oct 28.
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Resistance of Acanthamoeba cysts to disinfection treatments used in health care settings.棘阿米巴包囊对医疗机构中使用的消毒处理的抗性。
J Clin Microbiol. 2010 Aug;48(8):2689-97. doi: 10.1128/JCM.00309-10. Epub 2010 Jun 2.
7
Molecular identification of t4 and t5 genotypes in isolates from acanthamoeba keratitis patients.棘阿米巴角膜炎患者分离株中t4和t5基因型的分子鉴定
J Clin Microbiol. 2009 May;47(5):1458-62. doi: 10.1128/JCM.02365-08. Epub 2009 Mar 25.
8
Variable responses of Acanthamoeba strains to three multipurpose lens cleaning solutions.棘阿米巴菌株对三种多功能镜片清洁溶液的不同反应。
Optom Vis Sci. 2007 Mar;84(3):202-7. doi: 10.1097/OPX.0b013e3180339f81.
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In-vitro activity of miltefosine and voriconazole on clinical isolates of free-living amebas: Balamuthia mandrillaris, Acanthamoeba spp., and Naegleria fowleri.米替福新和伏立康唑对自由生活阿米巴临床分离株的体外活性:曼氏巴贝斯虫、棘阿米巴属和福氏耐格里阿米巴。
J Eukaryot Microbiol. 2006 Mar-Apr;53(2):121-6. doi: 10.1111/j.1550-7408.2005.00082.x.
10
Acanthamoeba genotype T4 from the UK and Iran and isolation of the T2 genotype from clinical isolates.来自英国和伊朗的棘阿米巴基因型T4以及从临床分离株中分离出T2基因型。
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米替福新对[具体物种]的体外杀囊活性研究

Investigation of the in vitro cysticidal activity of miltefosine against spp.

作者信息

Chao Malin, Thongseesuksai Thaksaporn, Boonmars Thidarut, Laummaunwai Porntip

机构信息

Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Neglected, Zoonosis and Vector-Borne Disease Research Group, Khon Kaen University, Khon Kaen, Thailand.

出版信息

J Parasit Dis. 2020 Jun;44(2):491-495. doi: 10.1007/s12639-020-01204-w. Epub 2020 Feb 17.

DOI:10.1007/s12639-020-01204-w
PMID:32508430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7244662/
Abstract

The present study evaluated the in vitro efficacy of miltefosine against cysts of spp. belonging to genotypes T3, T4 and T5. Each genotype was incubated with miltefosine at the concentration of 2.42, 4.84, 9.68, 19.36, 38.72 and 77.44 mM for different periods; 1, 3, 5, 7 d at 37 °C. The viability was assessed by staining with 0.4% trypan blue and culturing on NNA medium at 30 °C for 1 month. The results showed 100% eradication of cyst stage of all concentrations, but exhibited a different degree of activity against different genotypes. The MCC of 38.72 mM could kill genotype T4 and T5 after 1 d of incubation, whereas the killing of T3 needed MCC of 77.44 mM at the same incubation time. Miltefosine showed statistically highly significant difference (< 0.001) in comparison to non-treated control. Although our finding needs to confirm in animal models, this information may be the guideline for optimizing therapy or considered to combine with the other drugs for effective treatment.

摘要

本研究评估了米替福新对属于T3、T4和T5基因型的 种囊肿的体外疗效。将每种基因型与米替福新在浓度为2.42、4.84、9.68、19.36、38.72和77.44 mM的条件下孵育不同时间;在37°C下分别孵育1、3、5、7天。通过用0.4%台盼蓝染色并在30°C的NNA培养基上培养1个月来评估活力。结果显示,所有浓度均能100%根除囊肿阶段,但对不同基因型表现出不同程度的活性。38.72 mM的最低杀菌浓度在孵育1天后可杀死T4和T5基因型,而在相同孵育时间下,杀死T3基因型需要77.44 mM的最低杀菌浓度。与未处理的对照相比,米替福新显示出统计学上的高度显著差异(<0.001)。尽管我们的发现需要在动物模型中得到证实,但这些信息可能是优化治疗的指导原则,或者可考虑与其他药物联合用于有效治疗。