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采用柱上进样的毛细管气相色谱法测定皮克级硝酸甘油血浆浓度。

Determination of picogram nitroglycerin plasma concentrations using capillary gas chromatography with on-column injection.

作者信息

Noonan P K, Kanfer I, Riegelman S, Benet L Z

出版信息

J Pharm Sci. 1984 Jul;73(7):923-7. doi: 10.1002/jps.2600730715.

Abstract

A specific, sensitive, and precise capillary gas chromatographic (GC) assay capable of analyzing picogram concentrations of nitroglycerin in human plasma was developed. The analytical procedure involves a double extraction of 1 mL of plasma with pentane, after the addition of internal standard (1 ng of 2,6-dinitrotoluene), followed by evaporation and reconstitution in 50 microL of heptane. The extract (1 microL) was injected onto a capillary column using the on-column injection technique. The GC oven temperature was programmed from 120 degrees C to 180 degrees C at a rate of 5 degrees C/min. The oven temperature was then programmed to 250 degrees C and was maintained for 10 min. The nitroglycerin and internal standard retention times were 8.6 and 11.4 min, respectively. The position of the end of the capillary column inside the detector is a critical determinant of sensitivity: the column exit must be positioned such that nitroglycerin adsorption to the detector is minimized (i.e., sensitivity maximized). The assay limit of quantitation was 25 pg/mL (CV = 7.6%) using 1 mL of plasma. This GC assay, specific for nitroglycerin in the presence of its metabolites, isosorbide dinitrate, and several other drugs, may be used to quantitate plasma levels obtained after therapeutic nitroglycerin doses.

摘要

已开发出一种特异性强、灵敏度高且精确的毛细管气相色谱(GC)分析法,可用于分析人血浆中皮克浓度的硝酸甘油。分析过程包括在加入内标(1 ng 2,6-二硝基甲苯)后,用戊烷对1 mL血浆进行两次萃取,然后蒸发并复溶于50 μL庚烷中。使用柱上进样技术将1 μL萃取液注入毛细管柱。GC柱温箱温度以5℃/min的速率从120℃程序升温至180℃。然后将柱温箱温度程序升温至250℃并保持10分钟。硝酸甘油和内标的保留时间分别为8.6分钟和11.4分钟。毛细管柱末端在检测器内的位置是灵敏度的关键决定因素:柱出口的位置必须使硝酸甘油在检测器上的吸附最小化(即灵敏度最大化)。使用1 mL血浆时,定量分析下限为25 pg/mL(CV = 7.6%)。这种GC分析法对硝酸甘油及其代谢物异山梨醇二硝酸酯和其他几种药物具有特异性,可用于定量治疗剂量硝酸甘油后获得的血浆水平。

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