Jallad N S, Garg D C, Martinez J J, Mroszczak E J, Weidler D J
Division of Clinical Pharmacology, University of Miami School of Medicine, FL 33101.
J Clin Pharmacol. 1990 Jan;30(1):76-81. doi: 10.1002/j.1552-4604.1990.tb03442.x.
The elderly are likely candidates to receive analgesics for pain from a variety of etiologies. Ketorolac tromethamine is a nonsteroidal, analgesic, anti-inflammatory, antipyretic investigational drug with anti-prostaglandin synthetase activity. Sixteen healthy, young men (mean age 30 years and mean weight 75 kg) and 13 healthy, elderly subjects (11 men and two women; mean age 72 years and mean weight 75 kg) participated in an open-label, parallel single-dose study. On each day of ketorolac tromethamine administration the subjects fasted overnight and for 2 hours post-dose. A single intramuscular (IM) dose of 30 mg of ketorolac tromethamine was administered followed by an oral dose (PO) of 10 mg after a 1 week washout period for the elderly subjects. Plasma samples were taken from 0 through 48 hours post-dose and analyzed for ketorolac by HPLC. The elimination of ketorolac was decreased slightly in the elderly following both doses, as evidenced by a prolongation in half-life (4.7 to 6.1 hours for PO and 4.5 to 7.0 hours for IM) and a reduced total plasma clearance compared to the young adult subjects. These differences were statistically significant (P less than .001). Considerable overlap frequently was observed when comparing the range of values obtained for the young and elderly for plasma half-life, clearance, AUC, Tmax and Cmax. The absorption of ketorolac tromethamine was not altered substantially in the elderly following either dose route. Ketorolac plasma protein binding was not altered substantially in the elderly. The present results show that the elderly may need slightly less frequent dosing of ketorolac than young adults to maintain similar plasma levels.(ABSTRACT TRUNCATED AT 250 WORDS)
老年人因各种病因导致疼痛时很可能需要使用镇痛药。酮咯酸氨丁三醇是一种具有抗前列腺素合成酶活性的非甾体类、镇痛、抗炎、解热的研究用药物。16名健康青年男性(平均年龄30岁,平均体重75千克)和13名健康老年受试者(11名男性和2名女性;平均年龄72岁,平均体重75千克)参与了一项开放标签、平行单剂量研究。在给予酮咯酸氨丁三醇的每一天,受试者需空腹过夜并在给药后禁食2小时。给予老年受试者30毫克酮咯酸氨丁三醇的单次肌内注射剂量,1周洗脱期后再给予10毫克口服剂量。给药后0至48小时采集血浆样本,采用高效液相色谱法分析酮咯酸。与年轻成年受试者相比,老年受试者在两种给药剂量后酮咯酸的消除均略有减少,表现为半衰期延长(口服给药从4.7小时延长至6.1小时,肌内注射给药从4.5小时延长至7.0小时)以及总血浆清除率降低。这些差异具有统计学意义(P小于0.001)。在比较青年和老年受试者血浆半衰期、清除率、药时曲线下面积、达峰时间和峰浓度的取值范围时,经常观察到相当大的重叠。老年受试者经任一给药途径后,酮咯酸氨丁三醇的吸收均未发生实质性改变。老年受试者的酮咯酸血浆蛋白结合率也未发生实质性改变。目前的结果表明,与年轻成年人相比,老年人可能需要稍低的酮咯酸给药频率以维持相似的血浆水平。(摘要截选至250字)