Center for Chemical Toxicology Research and Pharmacokinetics, College of Veterinary Medicine, North Carolina State University, 4700 Hillsborough Street, Raleigh, NC 27606, USA.
Environ Toxicol Pharmacol. 2008 May;25(3):373-9. doi: 10.1016/j.etap.2007.12.001. Epub 2007 Dec 7.
The experimental objectives were to identify a vehicle which produces a homogenous formulation when combined with the anesthetic solution sevoflurane and understand the dermal absorption of sevoflurane in silastic membranes and amphibian skin in vitro utilizing a flow-through diffusion system. Seven vehicles were evaluated in varying ratios with 5 formulations resulting in the desired homogenous consistency for practical application. Sevoflurane diffusion across silastic membranes was influenced by pluronic/lecithin organogel (PLO), pluronic F 127 20% gel, and sterile lube. Flux and permeability across silastic membranes were significantly greater in sterile lube than in the other formulations. While no significant vehicle effects were observed in bullfrog skin, the flux-time profiles suggest that sevoflurane diffusion in bullfrog skin may be positively influenced by PLO. Future in vivo studies are required to assess sevoflurane retention after removal of these formulations to more accurately control the plane of anesthesia in amphibians.
实验目的是确定一种与麻醉剂七氟醚混合时能产生均匀制剂的载体,并利用流动扩散系统,在体外的硅橡胶膜和两栖动物皮肤上了解七氟醚的经皮吸收。评估了 7 种不同比例的载体,其中 5 种制剂达到了实际应用所需的均匀稠度。七氟醚在硅橡胶膜中的扩散受到泊洛沙姆/卵磷脂有机凝胶(PLO)、20%泊洛沙姆 F127 凝胶和无菌润滑剂的影响。无菌润滑剂中七氟醚的通量和渗透性明显大于其他制剂。虽然在牛蛙皮中没有观察到明显的载体效应,但通量-时间曲线表明,PLO 可能会对七氟醚在牛蛙皮中的扩散产生积极影响。需要进行未来的体内研究,以评估这些制剂去除后七氟醚的保留情况,以便更准确地控制两栖动物的麻醉平面。