Pruñonosa J, Obach R, Vallès J M
J Chromatogr. 1986 Apr 25;377:253-60. doi: 10.1016/s0378-4347(00)80780-x.
A sensitive, selective and rapid high-performance liquid chromatographic procedure was developed for the determination of cyanamide in plasma. The procedure involved extraction with ethyl acetate, derivatization with 5-(dimethylamino)naphthalene-1-sulphonyl chloride and posterior analysis by high-performance liquid chromatography on a mu Bondapak C18 column with fluorimetric detection. Linearity ranged from 5 to 500 ng/ml and the lower limit of sensitivity of the assay was 4 ng/ml of cyanamide in plasma. The precision of the method was 3.0-8.9%, expressed as relative standard deviation over the linear range. This method has been used to elucidate the time course of the cyanamide concentration in the plasma of humans, following oral administration of cyanamide at therapeutic doses.
建立了一种灵敏、选择性好且快速的高效液相色谱法,用于测定血浆中的氰胺。该方法包括用乙酸乙酯萃取、用5-(二甲氨基)萘-1-磺酰氯衍生化,然后在μ Bondapak C18柱上进行高效液相色谱分析并采用荧光检测。线性范围为5至500 ng/ml,该测定方法的灵敏度下限为血浆中氰胺4 ng/ml。该方法的精密度为3.0 - 8.9%,以线性范围内的相对标准偏差表示。该方法已用于阐明治疗剂量口服氰胺后人体血浆中氰胺浓度的时间进程。