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本文引用的文献

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Development of halofantrine resistance and determination of cross-resistance patterns in Plasmodium falciparum.恶性疟原虫中卤泛群抗性的产生及交叉抗性模式的确定
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Plasmodium falciparum and Plasmodium vivax: lactate dehydrogenase activity and its application for in vitro drug susceptibility assay.恶性疟原虫和间日疟原虫:乳酸脱氢酶活性及其在体外药物敏感性测定中的应用。
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The effect of (S)-9-(3-hydroxy-2-phosphonylmethoxypropyl) adenine on nuclear and organellar DNA synthesis in erythrocytic schizogony in malaria.(S)-9-(3-羟基-2-膦酰甲氧基丙基)腺嘌呤对疟原虫红细胞裂体增殖中细胞核和细胞器DNA合成的影响
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Plasmodium falciparum: modifications of the in vitro culture conditions improving parasitic yields.恶性疟原虫:改善体外培养条件以提高寄生虫产量的方法。
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Susceptibility of Plasmodium falciparum to five drugs: an in vitro study of isolates mainly from Thailand.恶性疟原虫对五种药物的敏感性:一项主要针对泰国分离株的体外研究
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A simple, rapid, and sensitive DNA assay procedure.一种简单、快速且灵敏的DNA检测程序。
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An improved technique for the cultivation of Plasmodium falciparum in vitro without daily medium change.
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A new technique for drug susceptibility tests for Plasmodium falciparum by ethidium bromide fluoroassay.一种通过溴化乙锭荧光测定法进行恶性疟原虫药物敏感性试验的新技术。
Trans R Soc Trop Med Hyg. 1986;80(1):47-9. doi: 10.1016/0035-9203(86)90192-6.
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Fluorometric assay of DNA in cartilage explants using Hoechst 33258.使用Hoechst 33258对软骨外植体中的DNA进行荧光测定。
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用于在24孔悬浮培养物中测定恶性疟原虫药物敏感性的简单、快速且准确的荧光测定法。

Simple, fast, and accurate fluorometric method to determine drug susceptibility of Plasmodium falciparum in 24-well suspension cultures.

作者信息

Smeijsters L J, Zijlstra N M, Franssen F F, Overdulve J P

机构信息

Department of Parasitology and Tropical Veterinary Medicine, Faculty of Veterinary Medicine, Utrecht University, The Netherlands.

出版信息

Antimicrob Agents Chemother. 1996 Apr;40(4):835-8. doi: 10.1128/AAC.40.4.835.

DOI:10.1128/AAC.40.4.835
PMID:8849236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC163215/
Abstract

An in vitro test which quantifies drug inhibition of Plasmodium falciparum replication by measuring the fluorescence intensity of Hoechst 33258 dye bound to DNA is described. The procedure does not require expensive reagents or equipment and can be completed in less than 10 min. The assay was highly accurate and sensitive: cultures with as few as 0.4% schizont-infected erythrocytes could reliably be analyzed. The method was not biased by the actual parasite stage used; i.e., the amount of fluorescence detected in a sample of a culture of mature schizonts equaled the amount detected with the ring form culture derived from these schizonts. Even the presence of large proportions of free merozoites, which are easily neglected in microscopic estimates, did not bias the results. Furthermore, measurement of the chloroquine susceptibility of the multidrug-resistant K1 strain and the chloroquine-susceptible NF54 strain showed that the method is most suitable for quantifying the drug resistance of P. falciparum.

摘要

本文描述了一种体外试验,该试验通过测量与DNA结合的Hoechst 33258染料的荧光强度来量化药物对恶性疟原虫复制的抑制作用。该方法不需要昂贵的试剂或设备,且可在不到10分钟内完成。该检测方法具有高度准确性和敏感性:感染裂殖体的红细胞比例低至0.4%的培养物也能得到可靠分析。该方法不受所使用的实际寄生虫阶段的影响;也就是说,在成熟裂殖体培养物样本中检测到的荧光量与从这些裂殖体衍生的环状体培养物中检测到的荧光量相等。即使存在大量易在显微镜评估中被忽略的游离裂殖子,也不会影响结果。此外,对多药耐药K1株和氯喹敏感NF54株的氯喹敏感性测量表明,该方法最适合于量化恶性疟原虫的耐药性。