首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >A new combined flow-cytometry-based assay reveals excellent activity against Toxoplasma gondii and low toxicity of new bisphosphonates in vitro and in vivo.
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A new combined flow-cytometry-based assay reveals excellent activity against Toxoplasma gondii and low toxicity of new bisphosphonates in vitro and in vivo.

机译:一种新的基于流式细胞仪的组合测定法显示了对弓形虫的优异活性,并且在体外和体内都显示出新的双膦酸盐的低毒性。

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OBJECTIVES: The aim of this study was to investigate the antiparasitic activity and toxicity of bisphosphonates using a new combined flow cytometry assay. METHODS: Using Toxoplasma gondii tachyzoites carrying the green-fluorescent protein (GFP), we established a new flow cytometry assay combining testing of in vitro and in vivo activity plus toxicity of newly synthesized bisphosphonates against T. gondii. Toxicity as determined by this assay was compared with toxicity as determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) test. RESULTS: In vivo, therapeutic efficacy was 100% for bisphosphonates 2F, 3B, 18A, 22A and 30B at 490, 1000, 512, 44.05 and 47.6 microM concentrations, respectively. Toxicity at 100% inhibitory concentrations was 20% for 2F and 3B, 60% for 22A and 30B, and 75% for 18A. In vitro, 6 (91A, 203A, 200C, 210A, 204A and 282A) of 15 newly synthesized bisphosphonates (12 nitrogen-containing and 3 n-alkyl) inhibited parasite replication by >50% at a concentration of 100 microM. Whereas substances 91A and 282A (high efficacy) showed moderate and low toxicity (cell viability between 70% and 100%), respectively, toxicities of 203A, 200C, 210A and 204A were 70%, 65%, 80% and 70%, respectively, as determined by flow cytometry. Compounds 290A, 218A, 214A, 266A and 219A inhibited parasite replication by between 20% and 50% at a concentration of 100 microM. CONCLUSIONS: Newly synthesized bisphosphonates 2F, 3B, 91A and 282A showed excellent therapeutic activity and low toxicity. These antiparasitic drugs may therefore be promising compounds for use in patients with acute and reactivated toxoplasmosis. The new flow cytometry assay allowed simultaneous determination of therapeutic efficacy and toxicity.
机译:目的:本研究的目的是使用一种新的联合流式细胞术来研究双膦酸盐的抗寄生虫活性和毒性。方法:使用携带绿色荧光蛋白(GFP)的弓形虫速殖子,我们建立了一种新的流式细胞术,结合体外和体内活性测试以及新合成的双膦酸盐对弓形虫的毒性。将通过该测定法确定的毒性与通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)测试确定的毒性进行比较。结果:在体内,分别以490、1000、512、44.05和47.6 microM的浓度对双膦酸酯2F,3B,18A,22A和30B的治疗效果为100%。在100%抑制浓度下,2F和3B的毒性为20%,22A和30B的毒性为60%,18A的毒性为75%。在体外,在100 microM的浓度下,15种新合成的双膦酸酯(12种含氮和3个正烷基)中的6种(91A,203A,200C,210A,204A和282A)抑制寄生虫复制> 50%。物质91A和282A(高效)分别显示出中度和低度毒性(细胞活力在70%和100%之间),而203A,200C,210A和204A的毒性分别为70%,65%,80%和70% (通过流式细胞仪确定)。化合物290A,218A,214A,266A和219A在100 microM的浓度下可抑制寄生虫复制20%至50%。结论:新合成的双膦酸酯2F,3B,91A和282A具有出色的治疗活性和低毒性。因此,这些抗寄生虫药物可能是用于急性和再活化弓形体病患者的有前途的化合物。新的流式细胞术可以同时测定治疗效果和毒性。

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