Microscopic and flow cytophotometric analysis of parasitemia in cultures of Plasmodium falciparum vitally stained with Hoechst 33342--application to studies of antimalarial agents.

R M Franklin, R Brun, A Grieder
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引用次数: 20

Abstract

Conditions for rapid vital staining of Plasmodium falciparum infected human erythrocytes were 1 microgram/ml of the dye Hoechst 33342 for 15 min in the standard culture medium at 37 degrees C. Fixed and stained cultures were analyzed by fluorescence microscopy and flow cytophotometry. The usefulness of this type of analysis for in vitro studies of antimalarial agents was demonstrated using three such agents--cyclosporin A, chloroquine, and pyrimethamine.

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Hoechst 33342染色恶性疟原虫培养物中寄生虫病的显微镜和流式细胞光度分析——在抗疟药物研究中的应用
恶性疟原虫感染人红细胞的快速活体染色条件为:标准培养基中加入1微克/毫升的Hoechst 33342染料,37℃下染色15 min,荧光显微镜和流式细胞光度法分析固定和染色培养物。使用环孢素A、氯喹和乙胺嘧啶三种抗疟药体外研究证明了这类分析的有用性。
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Studies on the sequence of variable antigen types in ponies infected with a clone of Trypanosoma evansi. Microscopic and flow cytophotometric analysis of parasitemia in cultures of Plasmodium falciparum vitally stained with Hoechst 33342--application to studies of antimalarial agents. Trypanosoma cruzi: inhibition of host cell uptake of infective bloodstream forms by alpha-2-macroglobulin. Species-specific monoclonal antibodies for a membrane antigen(s) in all developmental forms of Trypanosoma cruzi. Isolation of specific antigens from Angiostrongylus cantonensis. 2. By affinity chromatography.
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