Morgan D J, Campbell G A, Crankshaw D P
Victorian College of Pharmacy, Parkville, Melbourne, Victoria, Australia.
Br J Clin Pharmacol. 1990 Jul;30(1):144-8. doi: 10.1111/j.1365-2125.1990.tb03755.x.
We have previously shown with i.v. bolus studies that the elimination of propofol is much slower than previously reported. Now we have studied the implications of this for prolonged i.v. infusion of propofol in seven patients who received continuous infusions of propofol for up to 9 h. Values of elimination half-life ranged from 13.1 to 44.7 h, systemic clearance from 1.02 to 1.63 l h-1 and volume of distribution from 1390 to 3940 l and these were similar to those obtained with bolus administration. The large volume of distribution is consistent with the high octanol/blood partition coefficient, which was found to be 72.0. Despite the very long elimination half-life, blood propofol concentrations appeared to approach steady state within 20 min rather than the 4-5 half-lives normally expected. This is because for this drug, which displays multicompartment pharmacokinetics, the rate of initial rise of blood concentrations is governed primarily by the very short distribution half-life of the drug. Therefore, the long elimination half-life of propofol is probably of little significance in designing infusions regimens, but the lower systemic clearance should be taken into account to avoid unwanted accumulation.
我们之前通过静脉推注研究表明,丙泊酚的消除比之前报道的要慢得多。现在我们研究了这一情况对7例接受丙泊酚持续输注长达9小时的患者长时间静脉输注丙泊酚的影响。消除半衰期的值在13.1至44.7小时之间,全身清除率在1.02至1.63升/小时之间,分布容积在1390至3940升之间,这些与静脉推注给药时获得的值相似。较大的分布容积与高辛醇/血液分配系数一致,该系数为72.0。尽管消除半衰期非常长,但丙泊酚血药浓度似乎在20分钟内接近稳态,而不是通常预期的4至5个半衰期。这是因为对于这种呈现多室药代动力学的药物,血药浓度的初始上升速率主要由药物非常短的分布半衰期决定。因此,丙泊酚长的消除半衰期在设计输注方案时可能意义不大,但较低的全身清除率应予以考虑以避免不必要的蓄积。