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Milk Transfer and Toxicokinetics of Valproic Acid in Lactating Cynomolgus Monkeys

机译:哺乳期食蟹猴中丙戊酸的乳汁转移和毒代动力学

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摘要

Studies on milk transfer of drugs in non-human primates (NHPs) are among the crucial components in the assessment of peri- and postnatal toxicity because of the similarity between NHPs and humans. To evaluate the milk transfer of valproic acid (VPA) in NHPs, the toxicokinetics of VPA, an antiepileptic drug, were studied in pregnant cynomolgus monkeys. VPA was administered once daily to pregnant cynomolgus monkeys at doses of 0, 30, 90, and 270 mg/kg by oral gavage from Day 100 of gestation (GD 100) to Day 31 of lactation (LD 31). Concentrations of VPA and its metabolite, 4-ene-VPA, in the maternal plasma on GD 100, GD 140, and LD 30, and concentrations of VPA and 4-ene-VPA in the offspring plasma and milk on LDs 30 and 31, respectively, were quantified using liquid chromatography tandem mass spectrometry (LC/MS/MS). After administration of a single oral dose of VPA to pregnant monkeys on GD 100, the concentrations of VPA and 4-ene-VPA were generally quantifiable in the plasma of all treatment groups up to 24 hr after administration, which showed that VPA was absorbed and that the monkeys were systemically exposed to VPA and 4-ene-VPA. After administration of multiple doses of VPA to the monkeys, VPA was detected in the pup’s plasma and in milk taken on LD 30 and LD 31, respectively, which showed that VPA was transferred via milk, and the pup was exposed to VPA. Further, the concentration of VPA in the milk increased with an increase in the dose. Extremely low concentrations of 4-ene VPA were detected in the milk and in the pup plasma. In conclusion, pregnant monkeys were exposed to VPA and 4-ene-VPA after oral administration of VPA at doses of 30, 90, and 270 mg/kg/day from GD 100 to LD 31. VPA was transferred via milk, and the VPA exposure to the pup increased with an increase in the dose of VPA. The metabolite, 4-ene VPA, was present in extremely low concentrations (< 0.5 μg/ml) in the milk and in the pup plasma. In this study, we established methods to confirm milk transfer in NHPs, such as mating and diagnosis of pregnancy by examining gestational sac with ultrasonography, collection of milk and pup plasma and determination of toxicokinetics, using cynomolgus monkeys.
机译:由于NHP与人类之间的相似性,对非人类灵长类动物(NHP)中药物的乳汁转移的研究是评估围产期和产后毒性的关键组成部分。为了评估丙戊酸(VPA)在NHPs中的乳汁转移,在怀孕的食蟹猕猴中研究了抗癫痫药VPA的毒代动力学。从妊娠的第100天(GD 100)到哺乳的第31天(LD 31),每天通过口服管饲法分别以0、30、90和270 mg / kg的剂量向怀孕的食蟹猴施用VPA。母体血浆中GD 100,GD 140和LD 30上VPA及其代谢物4-烯-VPA的浓度,后代血浆和LD 30和31中乳汁中VPA和4-烯-VPA的浓度,分别使用液相色谱串联质谱法(LC / MS / MS)进行定量。在以GD 100的剂量给怀孕的猴子单次口服VPA后,一般可在给药后24小时内量化所有治疗组血浆中VPA和4-烯-VPA的浓度,这表明VPA已被吸收和吸收。猴子全身暴露于VPA和4-ene-VPA。向猴子施用多剂量的VPA后,分别在幼犬血浆和LD 30和LD 31摄食的牛奶中检测到VPA,这表明VPA是通过牛奶转移的,并且幼犬暴露于VPA。此外,牛奶中VPA的浓度随剂量的增加而增加。在牛奶和幼犬血浆中检测到极低浓度的4-ene VPA。总之,以30、90和270 mg / kg /天的剂量从GD 100到LD 31口服VPA后,怀孕的猴子暴露于VPA和4-ene-VPA。VPA通过牛奶转移,VPA随着VPA剂量的增加,幼崽的暴露也增加。代谢产物4-烯VPA在牛奶和幼犬血浆中的浓度极低(<0.5μg/ ml)。在这项研究中,我们建立了方法来确认NHP中的乳汁转移,例如通过超声检查妊娠囊,收集乳汁和幼犬血浆以及使用食蟹猴确定毒物动力学来确认交配和妊娠的诊断。

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