Lelievre-Pegorier M, Sakly R, Meulemans A, Merlet-Benichou C
Antimicrob Agents Chemother. 1985 Oct;28(4):565-9. doi: 10.1128/AAC.28.4.565.
Nonpregnant and pregnant guinea pigs in the last third of gestation were injected intramuscularly with 4 mg of gentamicin per kg, and drug concentrations in plasma were determined by radioimmunoassay at several intervals after injection. The maximum gentamicin concentration was lower in pregnant than in nonpregnant animals (14.6 +/- 0.7 micrograms/ml versus 21.6 +/- 0.7 micrograms/ml), and the peak time occurred significantly later (0.57 +/- 0.12 h versus 0.13 +/- 0.02 h). Four hours after gentamicin injection, drug concentrations in plasma were 2.1 +/- 0.8 and 0.3 +/- 0.1 micrograms/ml in pregnant and nonpregnant animals, respectively. Pregnant animals therefore eliminated the drug from their plasma more slowly. These data provide good evidence that the kinetics of plasma gentamicin varies in pregnant females because its volume of distribution was larger in pregnant than in nonpregnant animals. Detectable but small amounts of gentamicin (less than or equal to 0.50 microgram/ml) were found in the plasma of 46 of 57 fetuses. However, no net variations in these concentrations were observed during the period between 15 min and 6 h after injection to the mother. Gentamicin concentrations were also determined in the kidneys, liver, lungs, heart, and brain of fetal guinea pigs after administration to their mothers of one daily injection of 4 mg/kg for 7 days. Gentamicin was present in all these fetal organs; however, as in the adult organs, the kidneys contained far more than any of the others. Gentamicin concentrations were not significantly different in the kidney cortex and medulla (1.79 +/- 0.16 versus 1.48 +/- 0.92 micrograms/g), indicating that, contrary to what is observed for adults, renal accumulation of gentamicin in the fetus does not occur preferentially in the cortex.
对妊娠晚期的非妊娠和妊娠豚鼠每千克肌肉注射4毫克庆大霉素,并在注射后的几个时间间隔通过放射免疫分析法测定血浆中的药物浓度。妊娠动物的庆大霉素最大浓度低于非妊娠动物(14.6±0.7微克/毫升对21.6±0.7微克/毫升),且峰值出现时间明显更晚(0.57±0.12小时对0.13±0.02小时)。庆大霉素注射4小时后,妊娠和非妊娠动物血浆中的药物浓度分别为2.1±0.8和0.3±0.1微克/毫升。因此,妊娠动物从血浆中消除药物的速度较慢。这些数据充分证明,妊娠雌性动物血浆中庆大霉素的动力学有所不同,因为其在妊娠动物中的分布容积大于非妊娠动物。在57只胎儿中的46只胎儿的血浆中发现了可检测到但含量很少的庆大霉素(小于或等于0.50微克/毫升)。然而,在给母体注射后15分钟至6小时期间,这些浓度未观察到净变化。在给母体每日注射4毫克/千克,持续7天后,还测定了胎儿豚鼠的肾脏、肝脏、肺、心脏和大脑中的庆大霉素浓度。所有这些胎儿器官中均存在庆大霉素;然而,与成年器官一样,肾脏中的含量远远超过其他任何器官。肾皮质和髓质中的庆大霉素浓度无显著差异(1.79±0.16对1.48±0.92微克/克),这表明与成年动物不同,胎儿体内庆大霉素在肾脏中的蓄积并非优先发生在皮质。