超声辅助浆液共晶法制备诺氟沙星-尿素共晶的溶解度及放大效能

Fikri Alatas, Dery Stiawan, Nur Achsan Al-Hakim
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摘要

诺氟沙星是一种治疗低水溶性尿路感染的抗菌药物。本研究旨在了解超声辅助浆液共晶法制备诺氟沙星-尿素共晶对诺氟沙星溶解度的影响及放大的潜力。用粉末x射线衍射仪(PXRD)对乙醇-丙酮(1:1)混合溶剂湿磨法生成诺氟沙星-尿素(1:1)共晶的筛选结果进行了鉴定。采用超声辅助浆液共晶法,将诺氟沙星和尿素的重量提高到湿磨法的5倍。对超声辅助浆料共晶法制备的共晶产物进行了晶体形貌观察,并用PXRD和差示扫描量热仪(DSC)对其进行了表征。在水和pH 4.0的醋酸缓冲溶液中进行溶解度和溶解试验,评价其理化性质。通过PXRD对共晶进行筛选,发现诺氟沙星-尿素共晶的形成。超声辅助浆料共晶法制备的诺氟沙星-尿素共晶产物的PXRD谱图与湿磨法相似。诺氟沙星-尿素共晶的熔点和晶体形态与纯诺氟沙星和尿素不同。与纯诺氟沙星相比,诺氟沙星-尿素共晶在水中的溶解度和溶出率较高,在pH 4.0的醋酸缓冲液中差异不显著。研究表明,诺氟沙星-尿素共晶可以提高诺氟沙星在水中的溶解度,超声辅助浆液共晶法制备诺氟沙星具有扩大规模的潜力。
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Solubility and Scale-Up Potency of Norfloxacin-Urea Co-Crystal Prepared by Ultrasound-Assisted Slurry Co-Crystallization Method
Norfloxacin is an antimicrobial in treating urinary tract infections with low water solubility. This study aims to know the effect of norfloxacin-urea co-crystal formation on the solubility of norfloxacin and the potential for scale-up when prepared by ultrasound-assisted slurry co-crystallization method. Identification of the screening result of the norfloxacin-urea (1 : 1) co-crystal formation by a wet grinding method using an ethanol-acetone (1 : 1) solvent mixture was performed by powder X-ray diffractometer (PXRD). The ultrasound-assisted slurry co-crystallization method was used for co-crystal formation with five-fold the weight of norfloxacin and urea than the wet grinding method. The co-crystal product prepared by the ultrasound-assisted slurry co-crystallization method was observed for its crystal morphology and characterized by PXRD and differential scanning calorimeter (DSC). Solubility and dissolution tests in water and acetate buffer solution pH 4.0 were used to evaluate the physicochemical properties. Identification of co-crystal screening by PXRD revealed the formation of norfloxacin-urea co-crystal. The PXRD pattern of the norfloxacin-urea co-crystal product prepared by the ultrasound-assisted slurry co-crystallization method was similar to the wet grinding method. Norfloxacin-urea co-crystal has a different melting point and crystal morphology from pure norfloxacin and urea. The solubility and dissolution rate of norfloxacin-urea co-crystal was higher in water and not significantly different in acetate buffer solution pH 4.0 compared to pure norfloxacin. This study showed that the norfloxacin-urea co-crystal formation could enhance the solubility of norfloxacin in water and had the potential for scale-up when prepared using the ultrasound-assisted slurry co-crystallization method.
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