首页> 外文期刊>American journal of therapeutics >Mass balance study of (14C)M100240, a dual angiotensin-converting enzymeeutral endopeptidase inhibitor, in healthy male subjects.
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Mass balance study of (14C)M100240, a dual angiotensin-converting enzymeeutral endopeptidase inhibitor, in healthy male subjects.

机译:在健康男性受试者中进行双重血管紧张素转换酶/中性内肽酶抑制剂(14C)M100240的质量平衡研究。

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[4S-[4alpha,7alpha(R*),12bbeta]]-7[[2-(acetylthio)-1-oxo-3-phenylpropyl]am ino]-1,2,3,4,6,7,8,12b-octahydro-6-oxo-pyrido[2,1-a][2]benzazepine-4-carbo xylic acid (M100240) is an acetate thioester of MDL 100,173-a dual angiotensin-converting enzymeeutral endopeptidase inhibitor currently in phase II development. The mass balance of [(14)C]M100240 was assessed following oral administration of [(14)C]M100240. Healthy male subjects were given a single 25-mg dose of [(14)C]M100240 (50 microCi) as an oral solution under fasting conditions. Blood samples and excreta were collected postdose. (14)C-radioactivity was measured by liquid scintillation counting. Plasma concentrations of M100240 and MDL 100,173 were determined by LC/MS/MS methods. Pharmacokinetic parameters were calculated. About 98% of the total radioactive dose was recovered within 7 days of oral administration, with most of the radioactivity recovered within 72 hours. Of the recovered radioactive dose, 49.4% and 48.5% were recovered in the urineand feces, respectively. Unchanged M100240 and MDL 100,173 were not detected in the excreta. On average, 76% of the total radioactivity in the blood was associated with the plasma fraction. M100240 accounted for less than 0.06% of the (14)C-radioactivity in plasma and MDL 100,173 accounted for 15.8% (AUC( infinity )) of (14)C-radioactivity in plasma after oral dosing. These data suggest that the drug was absorbed but rapidly converted to its metabolites either presystemically or postsystemically. Up to 78% of the total radioactivity was identified as MDL 100,173. The apparent terminal elimination half-life of MDL 100,173 was longer than that of (14)C-radioactivity, attributable to assay sensitivity and the saturable binding phenomenon commonly associated with angiotensin-converting enzyme inhibitors. M100240 undergoes extensive metabolism in humans, and its metabolites are excreted relatively equally in feces and urine.
机译:[4S- [4alpha,7alpha(R *),12bbeta] -7 [[2-(乙酰硫基)-1-氧代-3-苯基丙基] am ino] -1,2,3,4,6,7,8 ,12b-八氢-6-氧代吡啶并[2,1-a] [2]苯并ze庚因-4-羰基木酸(M100240)是MDL 100,173的乙酸盐硫酯,是一种双重血管紧张素转换酶/中性内肽酶抑制剂第二阶段开发。口服[(14)C] M100240后评估[(14)C] M100240的质量平衡。健康的男性受试者在禁食条件下以口服溶液形式单次服用25毫克的[(14)C] M100240(50 microCi)。用药后收集血液样本和排泄物。 (14)C放射性通过液体闪烁计数测定。通过LC / MS / MS方法测定M100240和MDL 100,173的血浆浓度。计算了药代动力学参数。口服后7天内恢复了总放射性剂量的约98%,大部分放射性在72小时内恢复了。在回收的放射性剂量中,尿液和粪便中分别回收了49.4%和48.5%。在粪便中未检测到未改变的M100240和MDL 100,173。平均而言,血液中总放射性的76%与血浆分数有关。口服给药后,M100240占血浆(14)C放射性的不到0.06%,MDL 100,173占血浆(14)C放射性的15.8%(AUC(infinity))。这些数据表明该药物被吸收,但在系统前或系统后迅速转化为其代谢产物。最高总放射性的78%被确定为MDL 100,173。 MDL 100,173的表观末端消除半衰期比(14)C放射性更长,这归因于测定灵​​敏度和通常与血管紧张素转化酶抑制剂相关的可饱和结合现象。 M100240在人体内会广泛代谢,其代谢产物在粪便和尿液中的排泄量相对相等。

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