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一种基于可逆化学反应的新型提取方法,用于 LC/MS/MS 分析稳定的有机锗化合物 Ge-132。

A novel extraction method based on a reversible chemical conversion for the LC/MS/MS analysis of the stable organic germanium compound Ge-132.

机构信息

Department of Pharmaceutical Sciences, Tohoku University Hospital , 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.

出版信息

Anal Chem. 2015 Feb 17;87(4):2042-7. doi: 10.1021/ac504466u. Epub 2015 Jan 28.

Abstract

Poly trans-[(2-carboxyethyl)germasesquioxane] (IUPAC name) is the most common water-soluble organic germanium compound. This compound is known as bis(carboxyethyl)germaniumsesquioxide and it is commonly called Ge-132; it is hydrolyzed to 3-(trihydroxygermyl)propanoic acid (THGPA) in water. We have developed a method for the quantification of THGPA in rat plasma, using a novel extraction method based on a reversible chemical conversion. THGPA in plasma is converted to 3-(trichlorogermyl)propanoic acid (TCGPA) under acidic conditions using concentrated hydrochloride, which is followed by extraction with chloroform. TCGPA is then converted back to THGPA through hydrolysis. The extraction recovery of this method is approximately 100%. Moreover, we synthesized deuterated Ge-132, which was used as an internal standard in our experiments. This method covers a linearity range of 0.01-5 μg/mL for concentrations of THGPA in plasma. The intra-day and inter-day precisions of the analysis are about 4.1%, and the accuracy is within ±2.6% at THGPA concentrations of 0.025, 0.25, and 2.5 μg/mL. The total run time is 5 min. Our method was successfully applied to a pharmacokinetic investigation following oral administration of Ge-132.

摘要

聚[(2-羧乙基)锗倍半氧烷](IUPAC 名称)是最常见的水溶性有机锗化合物。这种化合物被称为双(羧乙基)锗倍半氧烷,通常称为 Ge-132;它在水中水解为 3-(三羟基锗基)丙酸(THGPA)。我们开发了一种用于定量测定大鼠血浆中 THGPA 的方法,该方法基于一种新的基于可逆化学转化的提取方法。在酸性条件下,用浓盐酸将血浆中的 THGPA 转化为 3-(三氯锗基)丙酸(TCGPA),然后用氯仿提取。然后通过水解将 TCGPA 转化回 THGPA。该方法的提取回收率约为 100%。此外,我们合成了氘代 Ge-132,用于实验中的内标。该方法的线性范围为 0.01-5μg/mL 时的血浆中 THGPA 浓度。分析的日内和日间精密度约为 4.1%,在 0.025、0.25 和 2.5μg/mL 的 THGPA 浓度下,准确度在±2.6%范围内。总运行时间为 5 分钟。我们的方法成功应用于口服 Ge-132 后的药代动力学研究。

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