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伊维菌素浇泼剂在韩国韩牛中的比较药代动力学与生物等效性研究

Comparative Pharmacokinetics and Bioequivalence of Pour-On Ivermectin Formulations in Korean Hanwoo Cattle.

作者信息

Kim Suyoung, Chae HyunYoung, Lee Eon-Bee, Lee Gayeong, Park Seung-Chun, Kang Jeongwoo

机构信息

Laboratory of Veterinary Pharmacokinetics and Pharmacodynamics, Institute for Veterinary Biomedical Science, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Republic of Korea.

Animal Disease Diagnosis Division, Animal and Plant Quarantine Agency (APQA), Ministry of Agriculture, Food and Rural Affairs, 177, Hyeoksin 8-ro, Gimcheon-si 39660, Republic of Korea.

出版信息

Antibiotics (Basel). 2023 Dec 19;13(1):3. doi: 10.3390/antibiotics13010003.

Abstract

This study aimed to conduct a bioequivalence study of applying three pour-on ivermectin formulations at a dose of 1 mg/kg on the back of Korean native beef cattle (Hanwoo). To conduct bioequivalence testing, the pharmacokinetics of three groups (control Innovator, test Generic A, and test Generic B) of five clinically healthy Korean Hanwoo cattle (average weight 500 kg) were studied. After topical application to the skin, blood samples were drawn at the indicated times. These blood samples were analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The time required to reach the maximum concentration (T), the maximum concentration (C), and the area under the curve (AUC) of each pharmacokinetic parameter were compared for bioequivalence. The results showed that the control had a T of 41 ± 1.24 h, a C of 0.11 ± 0.01 μg/mL, and an AUC of 9.33 ± 0 hμg/mL). The comparator Generic A had a T of 40 ± 1.14 h, a C of 0.10 ± 0.01 (μg/mL, and an AUC of 9.41 ± 0.57 hμg/mL, while Generic B had a T of 40 ± 2.21 h, a C of 0.10 ± 0.01 μg/mL, and an AUC of 9 h*μg/mL. The values of the bioequivalence indicators C, T, and AUC were all within the range of 80% to 120%, confirming that all three tested formulations were bioequivalent. In conclusion, the study showed that the two generic products were bioequivalent to the original product in Hanwoo cattle.

摘要

本研究旨在对三种剂量为1毫克/千克的浇泼剂伊维菌素制剂在韩国本土肉牛(韩牛)背部进行生物等效性研究。为进行生物等效性测试,对五头临床健康的韩国韩牛(平均体重500千克)分三组(对照创新药、试验仿制药A和试验仿制药B)进行了药代动力学研究。皮肤局部用药后,在指定时间采集血样。这些血样采用液相色谱 - 串联质谱法(LC - MS/MS)进行分析。比较各药代动力学参数达到最大浓度所需时间(T)、最大浓度(C)和曲线下面积(AUC)以确定生物等效性。结果显示,对照组的T为41±1.24小时,C为0.11±0.01微克/毫升,AUC为9.33±0小时微克/毫升)。对照仿制药A的T为40±1.14小时,C为0.10±0.01(微克/毫升,AUC为9.41±0.57小时微克/毫升,而仿制药B的T为40±2.21小时,C为0.10±0.01微克/毫升,AUC为9小时*微克/毫升。生物等效性指标C、T和AUC的值均在80%至120%范围内,证实所有三种受试制剂具有生物等效性。总之,该研究表明两种仿制药产品在韩牛中与原产品具有生物等效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1260/10812518/a92cb2ca3085/antibiotics-13-00003-g001.jpg

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