Talaczynska Alicja, Mizera Mikolaj, Szybowicz Miroslaw, Nowicka Ariadna B, Garbacki Piotr, Paczkowska Magdalena, Zalewski Przemyslaw, Kozak Maciej, Oszczapowicz Irena, Jelinska Anna, Cielecka-Piontek Judyta
Acta Pol Pharm. 2016 Sep;73(5):1299-1309.
Amorphous and crystalline forms of cefuroxime axetil were identified and characterized using DSC, XRPD, SEM, FT-IR and Raman spectroscopy. Based on the results of chromatographic studies, changes in the kinetic mechanism and rate of degradation of the crystalline form of cefuroxime axetil in binary systems with excipients were also evaluated. The findings suggest that the mechanism of degradation of cefuroxime axetil in such systems depends on two factors: the applied excipient and storage conditions. Cefuroxime axetil in combination with magnesium stearate, croscarmellose sodium and crospovidone, microcrystalline cellulose, aerosil is decomposed according to the first-order reaction model in dry air as well as at an increased relative air humidity, which may be associated with non-catalytic interactions between the active pharmaceutical ingredient and the excipients. However, in the presence of mannitol, under elevated humidity conditions (RH - 76%), the degradation of cefuroxime axetil follows the autocatalytic model. According to ESP maps, computed binding energies and HOMO - LUMO gaps, differences of degradation curves between cefuroxime axetil - mannitol and other investigated systems were explained. This study of the polymorphic transformation of the crystalline form of cefuroxime axetil and its binary systems with excipients after exposure to increased temperature and humidity indicated a conversion towards the amorphous form or the coexistence of both forms.
采用差示扫描量热法(DSC)、X射线粉末衍射法(XRPD)、扫描电子显微镜法(SEM)、傅里叶变换红外光谱法(FT-IR)和拉曼光谱法对头孢呋辛酯的无定形和结晶形式进行了鉴定和表征。基于色谱研究结果,还评估了头孢呋辛酯结晶形式在与辅料的二元体系中降解动力学机制和降解速率的变化。研究结果表明,头孢呋辛酯在这些体系中的降解机制取决于两个因素:所用辅料和储存条件。头孢呋辛酯与硬脂酸镁、交联羧甲基纤维素钠和交联聚维酮、微晶纤维素、气相二氧化硅组合时,在干燥空气中以及相对空气湿度增加时,按照一级反应模型分解,这可能与活性药物成分和辅料之间的非催化相互作用有关。然而,在甘露醇存在下,在高湿度条件(相对湿度-76%)下,头孢呋辛酯的降解遵循自催化模型。根据静电势(ESP)图、计算的结合能和最高占据分子轨道-最低未占据分子轨道(HOMO-LUMO)能隙,解释了头孢呋辛酯-甘露醇与其他研究体系之间降解曲线的差异。对头孢呋辛酯结晶形式及其与辅料的二元体系在温度和湿度升高后多晶型转变的研究表明,会向无定形形式转变或两种形式共存。