Houghton G W, Dennis M J, Rigler E D, Parsons R L
Biopharm Drug Dispos. 1984 Jul-Sep;5(3):203-9. doi: 10.1002/bdd.2510050302.
Nine healthy male volunteers took part in a crossover study to compare the pharmacokinetics of ketoprofen after administration of a single oral dose (200 mg) of ketoprofen as 'Orudis' capsules or encapsulated sustained-release pellets, 'Oruvail'. The mean +/- standard deviation values for highest observed plasma ketoprofen concentrations were determined by high performance liquid chromatography to be 23 +/- 11 micrograms ml-1 at 0.82 +/- 0.18 h after dosing with ketoprofen capsules and 3.5 +/- 1.0 micrograms ml-1 at 4.9 +/- 1.0 h after dosing with sustained-release pellets. The apparent ketoprofen elimination half-lives after these treatments were 3.3 +/- 1.2 h and 8.4 +/- 3.4 h, respectively. The systemic availability of ketoprofen was essentially the same after each treatment. Administration of sustained-release pellets (containing 200 mg ketoprofen) once every 24 h is predicted to produce similar average and markedly higher minimum plasma ketoprofen concentrations than are produced by ketoprofen capsules (100 mg) every 12 h, and similar minimum plasma ketoprofen concentrations to those achieved by dosing ketoprofen capsules (50 mg) every 6 h. Once-daily administration of a non-steroidal anti-inflammatory agent has an obvious therapeutic advantage over more frequent dosing. This study suggests that the sustained-release pellet formulation described herein is a suitable formulation for once-daily administration of ketoprofen.
九名健康男性志愿者参与了一项交叉研究,以比较单次口服200毫克酮洛芬作为“奥鲁地”胶囊或缓释微丸“奥鲁韦尔”后酮洛芬的药代动力学。通过高效液相色谱法测定,服用酮洛芬胶囊后0.82±0.18小时观察到的最高血浆酮洛芬浓度的平均值±标准差为23±11微克/毫升,服用缓释微丸后4.9±1.0小时为3.5±1.0微克/毫升。这些治疗后酮洛芬的表观消除半衰期分别为3.3±1.2小时和8.4±3.4小时。每次治疗后酮洛芬的全身可用性基本相同。预计每24小时服用一次缓释微丸(含200毫克酮洛芬)产生的平均血浆酮洛芬浓度与每12小时服用酮洛芬胶囊(100毫克)相似,但最低血浆酮洛芬浓度明显更高,且最低血浆酮洛芬浓度与每6小时服用酮洛芬胶囊(50毫克)所达到的浓度相似。每日一次服用非甾体抗炎药比更频繁给药具有明显的治疗优势。本研究表明,本文所述的缓释微丸制剂是酮洛芬每日一次给药的合适制剂。