Köppel C, Kristinsson J, Wagemann A, Tenczer J, Martens F
Reanimationszentrum, Klinikum Rudolf Virchow, Freie Universität Berlin, Germany.
Eur J Drug Metab Pharmacokinet. 1991 Jan-Mar;16(1):43-7. doi: 10.1007/BF03189873.
Chlormezanone plasma concentrations were determined in 5 volunteers (group 1) after a single oral dose of 200 mg of chlormezanone with high performance liquid chromatography. A plasma elimination half-life of 23 +/- 2.3 h was calculated. The mean peak chlormezanone plasma level was 1.86 +/- 0.2 micrograms/ml, 1 h after ingestion. Additionally, chlormezanone plasma levels were determined after repeated oral doses of chlormezanone recommended for treatment of muscular spasms due to degenerative skeletal disease. After 5 days of repeated daily doses of 3 x 200 mg (group 2; 12 patients) or 3 x 400 mg (group 3; 10 patients) of chlormezanone, mean predose chlormezanone plasma levels were 12.0 +/- 2.0 micrograms/ml (group 2) and 22.7 +/- 4.0 micrograms/ml (group 3), respectively. Comparable plasma concentrations were determined after 10 days of repeated doses of 3 x 200 mg or 3 x 400 mg of chlormezanone in 3 patients from each of these 2 groups. In 7 patients of group 3, chlormezanone had to be discontinued on the 5th day due to increasing muscular weakness, ataxia and exercise-inducible tachycardia. After a loading dose of 800 mg and repeated doses of 3 x 200 mg chlormezanone to 5 patients (group 4), plasma levels of 6.5 +/- 2.1 micrograms/ml, 8.9 +/- 2.2 micrograms/ml, 12.7 +/- 2.0 micrograms/ml, and 10.4 +/- 2.4 micrograms/ml were determined after 2, 8, 16, and 36 h, respectively. Trace amounts of a degradation product of the acid-labile chlormezanone could be detected in plasma besides the unchanged drug after administration of repeated oral doses.(ABSTRACT TRUNCATED AT 250 WORDS)
采用高效液相色谱法,对5名志愿者(第1组)单次口服200毫克氯美扎酮后的血浆浓度进行了测定。计算得出血浆消除半衰期为23±2.3小时。服药1小时后,氯美扎酮血浆平均峰值水平为1.86±0.2微克/毫升。此外,还对因退行性骨骼疾病导致的肌肉痉挛推荐的氯美扎酮重复口服剂量后的血浆水平进行了测定。在第2组(12名患者)每日重复服用3×200毫克或第3组(10名患者)每日重复服用3×400毫克氯美扎酮5天后,服药前氯美扎酮血浆平均水平分别为12.0±2.0微克/毫升(第2组)和22.7±4.0微克/毫升(第3组)。在这两组中各选取3名患者,重复服用3×200毫克或3×400毫克氯美扎酮10天后,测定了可比的血浆浓度。在第3组的7名患者中,由于肌肉无力、共济失调和运动诱发性心动过速加重,氯美扎酮在第5天不得不停药。对5名患者(第4组)给予800毫克负荷剂量并重复服用3×200毫克氯美扎酮后,分别在2、8、16和36小时测定血浆水平为6.5±2.1微克/毫升、8.9±2.2微克/毫升、12.7±2.0微克/毫升和10.4±2.4微克/毫升。重复口服给药后,除未改变的药物外,血浆中还可检测到痕量的酸不稳定氯美扎酮降解产物。(摘要截断于250字)