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首页> 外文期刊>Oligonucleotides >In Vitro Metabolic Stabilities and Metabolism of 2 '-O-(Methoxyethyl) Partially Modified Phosphorothioate Antisense Oligonucleotides in Preincubated Rat or Human Whole Liver Homogenates
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In Vitro Metabolic Stabilities and Metabolism of 2 '-O-(Methoxyethyl) Partially Modified Phosphorothioate Antisense Oligonucleotides in Preincubated Rat or Human Whole Liver Homogenates

机译:预培养大鼠或人全肝匀浆中2'-O-(甲氧乙基)部分修饰的硫代磷酸酯反义寡核苷酸的体外代谢稳定性和代谢

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摘要

In vitro metabolic stability testing of phosphorothioate 2'-O-methoxyethyl (2'-MOE) partially modified antisense oligonucleotides (ASOs) is not routinely performed to help screen discovery compounds (eg, predict in vivo half-lives), as no suitable in vitro test system currently exists. The aims of this work were to develop, optimize, and evaluate an in vitro whole liver homogenate (rat or human) test system. The test system was used to evaluate in vitro metabolic stabilities (intrinsic clearance) of selected ASOs, with results compared to reported in vivo half-lives, and generated metabolites also identified. Test system optimization involved preincubating whole liver homogenates at 37 degrees C for >= 24 hours, which increased in vitro ASO metabolism rate. From calculated in vitro intrinsic clearance (CLint) values in preincubated rat or human whole liver homogenates, metabolic stabilities of fully phosphorothioated 2'-MOE ASOs (ISIS 104838 and ISIS 301012) were, as expected, greater (ie, lower CLint) than a 2'-MOE ASO containing a single phosphodiester substitution (ISIS 104838PO10). However, comparable-to-lower in vitro metabolic stability for ISIS 301012 was seen compared to ISIS 104838, in contrast to reported similar to 2-fold longer in vivo tissue elimination half-lives for ISIS 301012. Identified in vitro metabolic products of ISIS 301012 were consistent with previously reported in vivo observations.
机译:常规不进行硫代磷酸酯2'-O-甲氧基乙基(2'-MOE)部分修饰的反义寡核苷酸(ASO)的体外代谢稳定性测试,以帮助筛选发现的化合物(例如,预测体内半衰期),因为不适合用于当前存在体外测试系统。这项工作的目的是开发,优化和评估体外全肝匀浆(大鼠或人)测试系统。该测试系统用于评估所选ASO的体外代谢稳定性(内在清除率),其结果与已报道的体内半衰期进行了比较,并且还鉴定了生成的代谢产物。测试系统优化涉及将全肝匀浆在37摄氏度下预孵育> = 24小时,这会增加体外ASO代谢率。根据预培养的大鼠或人全肝匀浆的体外固有清除率(CLint)值,完全磷酸化2'-MOE ASO(ISIS 104838和ISIS 301012)的代谢稳定性比预期的要大(即,较低的CLint)。包含单个磷酸二酯取代的2'-MOE ASO(ISIS 104838PO10)。但是,与ISIS 104838相比,可以看到ISIS 301012的体外代谢稳定性相当低,与之相比,ISIS 301012的体内组织消除半衰期延长了2倍。ISIS 301012的体外代谢产物与先前报道的体内观察结果一致。

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