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5-(4-硝基苯基)-2,4-戊二烯醛(Spydust)的吸收与代谢

Absorption and metabolism of 5-(4-nitrophenyl)-2,4-pentadienal (Spydust).

作者信息

Burka L T, Sanders J M, Kool C P, Kim Y C, Matthews H B

出版信息

Toxicol Appl Pharmacol. 1987 Jan;87(1):121-6. doi: 10.1016/0041-008x(87)90090-1.

Abstract

5-(4-Nitrophenyl)-2,4-pentadienal (NPPD) was recently alleged to have been used as a tracking agent to monitor the activities of U.S. citizens in the Soviet Union. In order to better assess human risk from possible exposure to this compound the absorption and metabolism of [14C]NPPD has been investigated in male F344 rats. These studies have revealed that NPPD was readily and quantitatively absorbed from the gastrointestinal tract, distributed throughout the tissues, metabolized, and rapidly excreted primarily in urine. NPPD was sparingly absorbed following dermal administration of 0.01, 0.1, and 1.0 mg/cm2. The amount absorbed increased as the dose increased but the percentage of the dose absorbed decreased as the dose increased, e.g., 50% (5 of 10 micrograms applied) of the low dose was absorbed but only 5% (50 of 100 micrograms applied) of the high dose was absorbed. The material absorbed after dermal administration was rapidly excreted and the distribution and metabolism of the dermally administered compound was no different from oral administration. A total of five metabolites, 4-nitrocinnamic acid, 4-acetamidobenzoic acid, 4-nitrohippuric acid, 4-acetamidocinnamic acid, and 4-nitrobenzoic acid, were identified by cochromatography with authentic standards and comparison of UV spectra. These metabolites are formed by oxidative metabolism of the pentadienal side chain, reduction of the nitro group, and/or conjugation of the resulting amino group with acetate or carboxylic acid with glycine.

摘要

5-(4-硝基苯基)-2,4-戊二烯醛(NPPD)最近被指曾被用作追踪剂,以监测苏联境内美国公民的活动。为了更好地评估因可能接触该化合物而对人体产生的风险,已对雄性F344大鼠体内[14C]NPPD的吸收和代谢情况进行了研究。这些研究表明,NPPD很容易从胃肠道被定量吸收,分布于全身组织,进行代谢,并主要通过尿液迅速排泄。经皮给予0.01、0.1和1.0mg/cm2的NPPD后,吸收量较少。吸收量随剂量增加而增加,但吸收剂量的百分比随剂量增加而降低,例如,低剂量的50%(施用10微克中的5微克)被吸收,而高剂量的仅5%(施用100微克中的50微克)被吸收。经皮给药后吸收的物质迅速排泄,经皮给药化合物的分布和代谢与口服给药无异。通过与标准品共色谱分析和紫外光谱比较,共鉴定出五种代谢产物,即4-硝基肉桂酸、4-乙酰氨基苯甲酸、4-硝基马尿酸、4-乙酰氨基肉桂酸和4-硝基苯甲酸。这些代谢产物是由戊二烯醛侧链的氧化代谢、硝基的还原和/或所得氨基与乙酸或羧酸与甘氨酸的结合形成的。

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