Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois at Champaign-Urbana, Urbana, IL.
A. Watson Armour III Center for Animal Health and Welfare, John G. Shedd Aquarium, Chicago, IL.
Am J Vet Res. 2022 Dec 9;84(1):ajvr.22.08.0138. doi: 10.2460/ajvr.22.08.0138.
To evaluate the pharmacokinetics of terbinafine administered to western pond turtles (Actinemys marmorata) via oral gavage and bioencapsulated in earthworms.
7 western pond turtles.
A randomized complete crossover single-dose pharmacokinetic study was performed. Compounded terbinafine (25 mg/mL; 30 mg/kg) was administered through oral gavage (OG) directly into the stomach or bioencapsulated (BEC) into an earthworm vehicle. Blood (0.2 mL) was drawn from the jugular vein at 0, 0.5, 1, 2, 4, 8, 12, 24, 48, 72, and 120 hours after administration. Plasma terbinafine levels were measured using high-performance liquid chromatography.
Peak plasma terbinafine concentrations of 786.9 ± 911 ng/mL and 1,022.2 ± 911 were measured at 1.8 ± 2.8 and 14.1 ± 12.3 hours after OG and BEC administration, respectively. There was a significant (P = .031) increase in area under the curve with BEC compared to OG. Using steady-state predictions, with once-daily terbinafine administration, 3/7 and 7/7 turtles had plasma concentrations persistently greater than the minimum inhibitory concentration (MIC) for Emydomyces testavorans for the OG and BEC administration routes of administration, respectively. With administration every 48 hours, 3/7 turtles for the OG phase and 6/7 turtles for the BEC phase had concentrations greater than the E. testavorans MIC throughout the entire dosing interval.
Administration of terbinafine (30 mg/kg) every 24 or 48 hours via earthworm bioencapsulation in western pond turtles may be appropriate for the treatment of shell lesions caused by E. testavorans. Clinical studies are needed to assess the efficacy of treatment.
评估通过口服灌胃和生物包封在蚯蚓体内给予西部锦龟(Actinemys marmorata)特比萘芬的药代动力学。
7 只西部锦龟。
进行了一项随机完全交叉单剂量药代动力学研究。将配制的特比萘芬(25 mg/mL;30 mg/kg)通过口服灌胃(OG)直接灌胃到胃中或生物包封(BEC)到蚯蚓载体中。在给药后 0、0.5、1、2、4、8、12、24、48、72 和 120 小时,从颈静脉抽取 0.2 mL 血液。使用高效液相色谱法测量血浆特比萘芬水平。
OG 和 BEC 给药后 1.8 ± 2.8 和 14.1 ± 12.3 小时,分别测量到特比萘芬的峰血浆浓度为 786.9 ± 911 ng/mL 和 1022.2 ± 911 ng/mL。与 OG 相比,BEC 时 AUC 显著增加(P =.031)。使用稳态预测,每天一次给予特比萘芬,3/7 和 7/7 只龟的血浆浓度持续高于 Emydomyces testavorans 的最小抑菌浓度(MIC),用于 OG 和 BEC 给药途径。每隔 48 小时给药时,3/7 只 OG 期龟和 6/7 只 BEC 期龟在整个给药间隔内的浓度均高于 E. testavorans MIC。
每隔 24 或 48 小时通过西部锦龟的蚯蚓生物包封给予特比萘芬(30 mg/kg),可能适用于治疗 E. testavorans 引起的壳病变。需要进行临床研究来评估治疗效果。