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Preparation characterization and in vivo evaluation of a polymorphic form of valnemulin hydrogen tartrate

机译:酒石酸缬氨莫林多晶型物的制备表征和体内评价

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摘要

We prepared a polymorphic form of valnemulin hydrogen tartrate (Form I) to overcome the instability and irritating odor of valnemulin hydrochloride that affect its use in the production and application of veterinary drugs. The physicochemical properties of Form I were characterized by scanning electron microscopy, X-ray powder diffraction, infrared spectroscopy, differential scanning calorimetry, and thermogravimetric analysis. The results showed the crystal structure and thermal properties of Form I were very different from those of a commercially available form of valnemulin hydrogen tartrate (Form II). Form I and Form II were more stable than valnemulin hydrochloride after storage under irradiation and high humidity conditions, respectively. The solubility of Form I was 2.6 times that of Form II, and Form I was selected for use in pharmaceutical kinetics experiments in vivo. Compared to valnemulin hydrochloride, after oral administration at a dose of 10 mg/kg in pigs, Form I had similar pharmaceutical kinetic behavior but a slightly higher area under the concentration–time curve from time zero to the last measurable concentration. Consequently, Form I should be suitable for the development of simple formulations and be effective in the clinical application of veterinary drugs.
机译:我们制备了多形形式的酒石酸氢戊烯丙醇盐(晶型I),以克服盐酸缬氨菌灵盐酸盐的不稳定性和刺激性气味,这会影响其在兽药生产和应用中的用途。通过扫描电子显微镜,X射线粉末衍射,红外光谱,差示扫描量热法和热重分析来表征晶型I的物理化学性质。结果表明,晶型I的晶体结构和热性质与市售品形式的酒石酸缬氨莫林(晶型II)有很大不同。分别在辐射和高湿度条件下储存后,晶型I和晶型II比盐酸缬氨菌灵更稳定。形式I的溶解度是形式II的2.6倍,并且选择形式I用于体内药物动力学实验。与盐酸伐尼莫林相比,在猪中口服剂量为10 mg / kg时,晶型I具有相似的药物动力学行为,但在浓度-时间曲线上从零时到最后可测量浓度的面积略高。因此,晶型I应该适合开发简单的制剂,并在兽药的临床应用中有效。

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