Nahoul K, Dehennin L, Scholler R
J Steroid Biochem. 1987 Feb;26(2):241-9. doi: 10.1016/0022-4731(87)90078-1.
A 200 mg dose of micronized progesterone (P) was administered orally to six healthy volunteers. Serial blood samples were collected and plasma P was assayed according to three methods of different specificity. The results were compared to those obtained with a reference technique based on gas chromatography-mass spectrometry. The interference of P metabolites particularly 5 alpha- and 5 beta-dihydroprogesterone was shown to be important when no or inadequate chromatography was included in the method. Radioimmunoassay after chromatography on a Celite column yielded results similar to those of the reference method. After oral administration, plasma P reached a peak at 3.00 +/- 0.44 h (mean +/- SEM; range: 1-4 h). The mean peak level 4.70 +/- 1.15 ng/ml (mean +/- SEM; range: 2.40-10.10 ng/ml) was at the lower limit of the range defined for a normal functional corpus luteum. The levels returned to initial values by 24 h after the single oral dose. The separation of P from its metabolites by an adequate chromatographic system appears mandatory after oral administration of micronized P.
对6名健康志愿者口服200毫克微粉化孕酮(P)。采集系列血样,并根据三种特异性不同的方法测定血浆P。将结果与基于气相色谱 - 质谱法的参考技术所获得的结果进行比较。当方法中未包含色谱法或色谱法不充分时,P代谢物尤其是5α - 和5β - 二氢孕酮的干扰作用显著。在硅藻土柱上进行色谱分离后进行放射免疫测定,其结果与参考方法相似。口服给药后,血浆P在3.00 +/- 0.44小时(平均值 +/- 标准误;范围:1 - 4小时)达到峰值。平均峰值水平为4.70 +/- 1.15纳克/毫升(平均值 +/- 标准误;范围:2.40 - 10.10纳克/毫升),处于正常功能黄体所定义范围的下限。单次口服给药后24小时,水平恢复到初始值。口服微粉化P后,通过适当的色谱系统将P与其代谢物分离似乎是必要的。