Xinle Zhu, Li Zhang, Jian Li, Hui Zhao, Jinhua Gu, Hejia Wang
Department of Safety Assessment, China Institute of Veterinary Drug Control, Beijing, 100081, China.
Curr Drug Deliv. 2025;22(6):798-809. doi: 10.2174/0115672018289236240530095059.
In the present study, a valnemulin hydrogen fumarate prodrug was characterized, its stability was compared with valnemulin hydrochloride, and the efficacy was evaluated in controlling pneumonia among mice experimentally infected with Actinobacillus pleuropneumoniae.
Optical microscopy, X-ray powder diffraction, infrared spectroscopy, and hydrogen nuclear magnetic resonance spectroscopy were used to study the physical and chemical properties of the prodrug. The thermal stability was investigated in comparison with valnemulin hydrochloride to improve the preparation process of valnemulin hydrogen fumarate soluble powder and maximize its drug effect. Additionally, the efficacy of valnemulin hydrogen fumarate was evaluated in a challenge-treatment trial in mice using an infection test in vivo.
Valnemulin hydrogen fumarate had high crystallinity. After light irradiation for 20 days, valnemulin hydrogen fumarate did not degrade, whereas valnemulin hydrochloride did. These results showed that the valnemulin hydrogen fumarate was stable. At the same dose in drinking water, the valnemulin hydrogen fumarate was more effective than the reference drug of tiamulin fumarate in an challenge-treatment trial.
Valnemulin hydrogen fumarate shows excellent potential for application as a veterinary drug.
在本研究中,对富马酸沃尼妙林前药进行了表征,将其稳定性与盐酸沃尼妙林进行了比较,并在实验感染胸膜肺炎放线杆菌的小鼠中评估了其控制肺炎的疗效。
采用光学显微镜、X射线粉末衍射、红外光谱和氢核磁共振光谱研究前药的理化性质。与盐酸沃尼妙林相比,研究了其热稳定性,以改进富马酸沃尼妙林可溶性粉的制备工艺并使其药效最大化。此外,在小鼠体内感染试验的攻毒-治疗试验中评估了富马酸沃尼妙林的疗效。
富马酸沃尼妙林具有高结晶度。光照20天后,富马酸沃尼妙林未降解,而盐酸沃尼妙林降解了。这些结果表明富马酸沃尼妙林是稳定的。在饮水相同剂量下,在攻毒-治疗试验中,富马酸沃尼妙林比延胡索酸泰妙菌素参比药物更有效。
富马酸沃尼妙林作为兽药具有优异的应用潜力。