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负载替米考星和氟苯尼考的氢化蓖麻油固体脂质纳米粒对猪的研究:联合抗菌活性和药代动力学

Tilmicosin- and florfenicol-loaded hydrogenated castor oil-solid lipid nanoparticles to pigs: Combined antibacterial activities and pharmacokinetics.

作者信息

Ling Z, Yonghong L, Junfeng L, Li Z, Xianqiang L

机构信息

College of Animal Science and Technology, Tarim University, Alar, Xinjiang, China.

Key Laboratory of Tarim Animal Husbandry Science and Technology of Xinjiang Production & Construction Corps, Alar, China.

出版信息

J Vet Pharmacol Ther. 2018 Apr;41(2):307-313. doi: 10.1111/jvp.12465. Epub 2017 Nov 15.

Abstract

The combined antibacterial effects of tilmicosin (TIL) and florfenicol (FF) against Actinobacillus pleuropneumoniae (APP) (n = 2), Streptococcus suis (S. suis) (n = 2), and Haemophilus parasuis (HPS) (n = 2) were evaluated by chekerboard test and time-kill assays. The pharmacokinetics (PKs) of TIL- and FF-loaded hydrogenated castor oil (HCO)-solid lipid nanoparticles (SLN) were performed in healthy pigs. The results indicated that TIL and FF showed synergistic or additive antibacterial activities against APP, S. suis and HPS with the fractional inhibitory concentration (FIC) ranging from 0.375 to 0.75. The time-kill assays showed that 1/2 minimum inhibitory concentration (MIC) TIL combined with 1/2 MIC FF had a stronger ability to inhibit the growth of APP, S. suis, and HPS than 1 MIC TIL or 1 MIC FF, respectively. After oral administration, plasma TIL and FF concentrations could maintain about 0.1 μg/ml for 192 and 176 hr. The SLN prolonged the last time point with detectable concentrations (T ), area under the concentration-time curve (AUC ), elimination half-life (T ), and mean residence time (MRT) by 3.1, 5.6, 12.7, 3.4-fold of the active pharmaceutical ingredient (API) of TIL and 11.8, 16.5, 18.1, 12.1-fold of the API of FF, respectively. This study suggests that the TIL-FF-SLN could be a useful oral formulation for the treatment of APP, S. suis, and HPS infection in pigs.

摘要

通过棋盘法和时间-杀菌试验评估了替米考星(TIL)和氟苯尼考(FF)联合对胸膜肺炎放线杆菌(APP)(n = 2)、猪链球菌(S. suis)(n = 2)和副猪嗜血杆菌(HPS)(n = 2)的抗菌效果。在健康猪身上进行了负载TIL和FF的氢化蓖麻油(HCO)-固体脂质纳米粒(SLN)的药代动力学(PKs)研究。结果表明,TIL和FF对APP、S. suis和HPS表现出协同或相加抗菌活性,其部分抑菌浓度(FIC)范围为0.375至0.75。时间-杀菌试验表明,1/2最低抑菌浓度(MIC)的TIL与1/2 MIC的FF联合对APP、S. suis和HPS生长的抑制能力分别强于1 MIC的TIL或1 MIC的FF。口服给药后,血浆中TIL和FF浓度可在192和176小时内维持在约0.1μg/ml。SLN使可检测浓度的最后时间点(T)、浓度-时间曲线下面积(AUC)、消除半衰期(T)和平均驻留时间(MRT)分别延长至替米考星活性药物成分(API)的3.1、5.6、12.7、3.4倍和氟苯尼考API的11.8、16.5、18.1、12.1倍。本研究表明,TIL-FF-SLN可能是治疗猪APP、S. suis和HPS感染的一种有用的口服制剂。

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