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Efficacy of DA-7218 a New Oxazolidinone Prodrug in the Treatment of Experimental Actinomycetoma Produced by Nocardia brasiliensis

机译:新型恶唑烷酮前药DA-7218在治疗巴西诺卡氏菌产生的放线菌病中的功效

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摘要

Two recently synthesized oxazolidinones: (R)-3-(4-(2-(2-methyltetrazol-5-yl)-pyridin-5-yl)-3-fluorophenyl)-5-hydroxymethyloxazolidin-2-one (DA-7157) and its corresponding pro-drug (R)-3-(4-(2-(2-methyltetrazol-5-yl)-pyridin-5-yl)-3-fluorophenyl)-2-oxo-5-oxazolidinyl) methyl disodium phosphate (DA-7218), have shown very good activity against several Gram positive bacteria, including Nocardia and Mycobacterium. In the present work we evaluated the therapeutic in vivo effects of DA-7218 on Nocardia brasiliensis. We first determined the plasma concentration of the prodrug in BALB/c mice using several doses and then tested its activity in an in vivo experimental actinomycetoma murine model. At the end of treatment, there was a statistically significant difference between the three drug receiving groups (25, 12.5 and 5 mg/kg) and the control group (saline solution) (p=0.001), proving that DA-7218 is effective for the treatment of experimental murine actinomycetoma. This compound could be a potential option for patients affected with mycetoma by Nocardia brasiliensis.
机译:最近合成的两种恶唑烷酮:(R)-3-(4-(2-(2-(2-甲基四唑-5-基)-吡啶基-5-基)-3-氟苯基)-5-羟基甲基恶唑烷酮-2-一(DA-7157 )及其相应的前药(R)-3-(4-(2-(2-(2-甲基四唑-5-基)-吡啶基-5-基)-3-氟苯基)-2-氧代-5-恶唑烷基)甲基磷酸二钠(DA-7218)对多种革兰氏阳性细菌(包括诺卡氏菌和分枝杆菌)表现出非常好的活性。在本工作中,我们评估了DA-7218对巴西诺卡氏菌的体内治疗作用。我们首先使用几种剂量确定BALB / c小鼠中前药的血浆浓度,然后在体内实验放线菌素小鼠模型中测试其活性。在治疗结束时,三个药物接受组(25、12.5和5 mg / kg)与对照组(盐溶液)之间存在统计学差异(p = 0.001),证明DA-7218对实验性小鼠放线菌素瘤的治疗。对于由巴西诺卡氏菌感染的菌丝瘤的患者,该化合物可能是潜在的选择。

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