Brodfuehrer J I, Powis G
Department of Pharmacology, Mayo Clinic & Foundation, Rochester, MN 55905.
J Chromatogr. 1988 Jun 3;427(2):247-55. doi: 10.1016/0378-4347(88)80127-0.
A sensitive gas chromatographic assay with electron-capture detection has been developed for sulfamic acid diester (sulfamic acid 1,7-heptanediyl ester, NSC 329680) based on its conversion to 1,7-diiodoheptane in the presence of excess sodium iodide. The assay is linear up to 1 microgram/ml sulfamic acid diester and has a lower limit of detection of 25 ng/ml from 0.5 ml plasma. The coefficient of variation of the assay is 6.4% at 1 microgram/ml and 8.0% at 100 ng/ml. Sulfamic acid diester is relatively stable in 0.9% sodium chloride and 0.1 M sodium phosphate buffers, pH 7.0-9.0, with half-lives greater than 38 h. The major breakdown product of sulfamic acid diester is sulfamic acid 1,7-heptane-monoyl ester. When added to whole blood sulfamic acid diester shows concentration-dependent breakdown. At 50 and 100 micrograms/ml sulfamic acid diester, the half-time in whole blood is 6.9 h and 65% of the drug is sequestered by the blood cells. At 10 micrograms/ml sulfamic acid diester in blood, there is no detectable breakdown of the drug over 24 h and all of the drug is sequestered by the blood cells. Protein binding of sulfamic acid diester in human plasma is 82% at 10 micrograms/ml and 68% at 100 micrograms/ml.
已开发出一种灵敏的气相色谱法并采用电子捕获检测,用于测定氨基磺酸二酯(氨基磺酸1,7 - 庚二醇酯,NSC 329680),其原理是在过量碘化钠存在下将其转化为1,7 - 二碘庚烷。该测定法在氨基磺酸二酯浓度高达1微克/毫升时呈线性,从0.5毫升血浆中检测的下限为25纳克/毫升。该测定法的变异系数在1微克/毫升时为6.4%,在100纳克/毫升时为8.0%。氨基磺酸二酯在0.9%氯化钠和pH值7.0 - 9.0的0.1 M磷酸钠缓冲液中相对稳定,半衰期大于38小时。氨基磺酸二酯的主要分解产物是氨基磺酸1,7 - 庚烷单酯。当添加到全血中时,氨基磺酸二酯呈现浓度依赖性分解。在氨基磺酸二酯浓度为50和100微克/毫升时,在全血中的半衰期为6.9小时,65%的药物被血细胞隔离。在血液中氨基磺酸二酯浓度为10微克/毫升时,24小时内未检测到药物分解,所有药物都被血细胞隔离。在人血浆中,氨基磺酸二酯在10微克/毫升时的蛋白结合率为82%,在100微克/毫升时为68%。