Department of Small Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Res Vet Sci. 2011 Jun;90(3):480-3. doi: 10.1016/j.rvsc.2010.07.010. Epub 2010 Aug 14.
Buprenorphine plasma concentrations were measured after administering buprenorphine (20 μg/kg) into the lumbosacral epidural space of conscious cats chronically instrumented with an epidural catheter. Blood was collected from a jugular vein before injection and 15, 30, 45 and 60 min and 2, 3, 4, 5, 6, 8, 12 and 24 h after administration. Plasma buprenorphine concentrations were measured using ELISA. Background concentration (before injection) was 1.27 ± 0.27 ng/mL (mean ± SD). Including background concentration, the mean peak plasma concentration was obtained 15 min after injection (5.82 ± 3.75 ng/mL), and ranged from 3.79 to 2.20 ng/mL (30 min-3 h), remaining between 1.93 and 1.77 ng/mL (4-12 h), and declined to 1.40 ± 0.62 ng/mL at 24h. Elimination half-life was 58.8 ± 40.2 min and clearance 56.7 ± 21.5 mL/min. Results indicate early rapid systemic uptake of buprenorphine from epidural administration with plasma concentrations similar to using buccal or IM routes by 15 min postinjection.
在对长期接受硬膜外导管置管的意识猫进行腰骶硬膜外腔注射丁丙诺啡(20μg/kg)后,测量丁丙诺啡的血浆浓度。在注射前和注射后 15、30、45 和 60 分钟以及 2、3、4、5、6、8、12 和 24 小时从颈静脉采集血液。使用 ELISA 测量血浆丁丙诺啡浓度。背景浓度(注射前)为 1.27±0.27ng/mL(平均值±SD)。包括背景浓度在内,注射后 15 分钟时获得的平均血浆峰浓度为 5.82±3.75ng/mL,范围为 3.79-2.20ng/mL(30 分钟-3 小时),在 4-12 小时之间保持在 1.93-1.77ng/mL 之间,在 24 小时下降至 1.40±0.62ng/mL。消除半衰期为 58.8±40.2 分钟,清除率为 56.7±21.5mL/min。结果表明,丁丙诺啡从硬膜外给药后早期迅速全身吸收,在注射后 15 分钟时的血浆浓度与经颊或肌内途径相似。