Yokoi Yukiko, Yonemochi Etsuo, Terada Katsuhide
Chemistry, Manufacturing and Control Research Laboratories, Pharmaceutical Development Department, Meiji Seika Kaisha Ltd., 760 Morooka-cho, Kohoku-ku, Yokohama 222-8567, Japan.
Int J Pharm. 2005 Feb 16;290(1-2):91-9. doi: 10.1016/j.ijpharm.2004.11.020. Epub 2005 Jan 8.
The improvement in physicochemical stability of amorphous cefditoren pivoxil (CDTR-PI) in aqueous suspensions by addition of sugar ester (SE) and hydroxypropyl methylcellulose (HPMC) was explained by prolonging the induction period prior to crystallization and the reduction in crystal peak intensity. Furthermore, the stabilizing effect of these additives in a multiple additive system was greater than in a single additive system. To determine the mechanism, by which these additives stabilized the amorphous CDTR-PI, we evaluated the surface states of CDTR-PI in suspension by measuring Raman spectra and zeta potential. The change in Raman spectra demonstrated that SE and HPMC interacted with CDTR-PI at the same interaction sites on CDTR-PI. The zeta potential reflected the adsorption phenomena of the additives and indicated that both SE and HPMC adsorbed onto particles of CDTR-PI with no apparent competitive interaction and the response was complementary. It was considered, based on this study, that HPMC and SE would stabilize amorphous CDTR-PI by different mechanisms; HPMC would mainly inhibit crystal growth by small amount of adsorption and SE would inhibit both crystal growth and nucleation by large amount of adsorption. This was considered to result in the hybrid effect in the multiple additive system.
通过添加糖酯(SE)和羟丙基甲基纤维素(HPMC)提高了非晶态头孢妥仑匹酯(CDTR-PI)水悬浮液的物理化学稳定性,这可通过延长结晶前的诱导期和降低晶体峰强度来解释。此外,这些添加剂在多重添加剂体系中的稳定作用大于单一添加剂体系。为了确定这些添加剂稳定非晶态CDTR-PI的机制,我们通过测量拉曼光谱和zeta电位评估了悬浮液中CDTR-PI的表面状态。拉曼光谱的变化表明,SE和HPMC在CDTR-PI上的相同相互作用位点与CDTR-PI相互作用。zeta电位反映了添加剂的吸附现象,表明SE和HPMC均吸附到CDTR-PI颗粒上,没有明显的竞争相互作用,且响应是互补的。基于这项研究,认为HPMC和SE将通过不同机制稳定非晶态CDTR-PI;HPMC主要通过少量吸附抑制晶体生长,而SE将通过大量吸附抑制晶体生长和成核。这被认为导致了多重添加剂体系中的混合效应。