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本文引用的文献

1
Transferosomes as a transdermal drug delivery system: Dermal kinetics and recent developments.传递体作为一种经皮给药系统:皮肤动力学及最新进展
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2024 Jan-Feb;16(1):e1918. doi: 10.1002/wnan.1918. Epub 2023 Aug 1.
2
Pain management with transdermal drug administration: A review.经皮给药的疼痛管理:综述
Int J Pharm. 2022 Apr 25;618:121696. doi: 10.1016/j.ijpharm.2022.121696. Epub 2022 Mar 23.
3
Plasma concentrations of tramadol after transdermal application of a single metered dose of a compounded tramadol gel to cats.向猫经皮单次给予定量复方曲马多凝胶后血浆中的曲马多浓度。
Am J Vet Res. 2021 Oct;82(10):840-845. doi: 10.2460/ajvr.82.10.840.
4
Recent advances in transdermal drug delivery systems: a review.经皮给药系统的最新进展:综述
Biomater Res. 2021 Jul 28;25(1):24. doi: 10.1186/s40824-021-00226-6.
5
Enhancement in antinociceptive and anti-inflammatory effects of tramadol by transdermal proniosome gel.透皮前体脂质体凝胶增强曲马多的抗伤害感受和抗炎作用。
Asian J Pharm Sci. 2020 Nov;15(6):786-796. doi: 10.1016/j.ajps.2019.05.001. Epub 2019 Jun 19.
6
Evaluation of the thermal antinociceptive effects and pharmacokinetics after intramuscular administration of buprenorphine hydrochloride to cockatiels (Nymphicus hollandicus).盐酸丁丙诺啡肌肉注射给予鸡尾鹦鹉(虎皮鹦鹉)后的热镇痛效果及药代动力学评估。
Am J Vet Res. 2018 Dec;79(12):1239-1245. doi: 10.2460/ajvr.79.12.1239.
7
Preliminary pharmacokinetics of tramadol hydrochloride after administration via different routes in male and female B6 mice.盐酸曲马多在雄性和雌性B6小鼠中不同给药途径后的初步药代动力学研究。
Vet Anaesth Analg. 2018 Jan;45(1):111-122. doi: 10.1016/j.vaa.2016.09.007. Epub 2017 Aug 16.
8
Pharmacokinetics of tramadol following intravenous and oral administration in male rhesus macaques (Macaca mulatta).曲马多在雄性恒河猴(猕猴)静脉注射和口服给药后的药代动力学
J Vet Pharmacol Ther. 2015 Aug;38(4):375-82. doi: 10.1111/jvp.12194. Epub 2014 Dec 9.
9
Pharmacokinetics of tramadol and its primary metabolite O-desmethyltramadol in African penguins (Spheniscus demersus).曲马多及其主要代谢产物O-去甲基曲马多在非洲企鹅(斑嘴环企鹅)体内的药代动力学。
J Zoo Wildl Med. 2014 Mar;45(1):93-9. doi: 10.1638/2013-0190R.1.
10
Evaluation of thermal antinociceptive effects after oral administration of tramadol hydrochloride to American kestrels (Falco sparverius).对美洲隼(雀鹰)口服盐酸曲马多后热镇痛效果的评估。
Am J Vet Res. 2014 Feb;75(2):117-23. doi: 10.2460/ajvr.75.2.117.

盐酸曲马多经皮给药对禽类的热镇痛作用。

Thermal antinociceptive effect of transdermal tramadol hydrochloride in avian.

作者信息

Lim Chien Yee, Goh Soon Heng, Tan Li Peng, Veloo Krishna Veni, Ong Wee Kiat, Yong Shen Fung, Lim Chien Joo, Choong Siew Shean

机构信息

Wildlife Medicine & Conservation Research Group, Faculty of Veterinary Medicine, Universiti Malaysia Kelantan City Campus, Kelantan, Malaysia.

Faculty of Agro Based Industry, University Malaysia Kelantan Jeli Campus, Kelantan, Malaysia.

出版信息

J Vet Med Sci. 2025 Aug 1;87(8):947-953. doi: 10.1292/jvms.25-0009. Epub 2025 Jul 1.

DOI:10.1292/jvms.25-0009
PMID:40603067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12344297/
Abstract

Drug administration in avian species via the parenteral route tends to result in stress, as most often birds need to be handled and manipulated. The purpose of this study was to evaluate the potential of the transdermal administration route as an alternative for tramadol hydrochloride in avian. A total of 24 85-day-old broiler chickens were used as a model for avian species in this study. The chickens were divided into four equal groups of 6 animals each: i. Control, without intervention (C); ii. Intravenous at 5 mg/kg (IV); iii. Transdermal at 5 mg/kg (TD1); and iv. Transdermal at 10 mg/kg (TD2). The thermal antinociception effect was opted to simulate pain, by using a heating plate. The foot withdrawal response of each animal to a thermal stimulus was determined pre-administration (as baseline), followed by 30-, 60-, 120-, 240-, 360- and 480-min post-tramadol administration. All treatment groups showed significantly higher (P<0.05) foot withdrawal temperature threshold compared to the control group. Comparatively, there was a statistically significant higher temperature threshold than baseline at 60-, and 120-min post treatment for both TD1 and TD2 groups, while the IV group only at 60-min post treatment. Intravenous tramadol recorded the highest change in the foot withdrawal thermal threshold, while transdermal tramadol at 10 mg/kg recorded the longest effective time up to 240 min post-administration. This is the first study to evaluate the analgesic effectiveness of transdermal tramadol in avian, thus further investigation is required to confirm similar effects in other species.

摘要

禽类通过非肠道途径给药往往会导致应激,因为大多数情况下需要对鸟类进行处理和操作。本研究的目的是评估经皮给药途径作为禽类盐酸曲马多替代给药方式的潜力。本研究共使用24只85日龄的肉鸡作为禽类模型。将鸡分为四组,每组6只动物:i. 对照组,无干预(C);ii. 静脉注射5 mg/kg(IV);iii. 经皮给药5 mg/kg(TD1);iv. 经皮给药10 mg/kg(TD2)。通过使用加热板选择热抗伤害感受效应来模拟疼痛。在给药前(作为基线)测定每只动物对热刺激的足部退缩反应,随后在曲马多给药后30、60、120、240、360和480分钟测定。与对照组相比,所有治疗组的足部退缩温度阈值均显著更高(P<0.05)。相比之下,TD1组和TD2组在治疗后60分钟和120分钟时的温度阈值均显著高于基线,而IV组仅在治疗后60分钟时显著高于基线。静脉注射曲马多记录的足部退缩热阈值变化最大,而10 mg/kg经皮给药曲马多记录的最长有效时间长达给药后240分钟。这是第一项评估经皮曲马多对禽类镇痛效果的研究,因此需要进一步研究以证实其在其他物种中的类似效果。