Tange Mio, Hattori Yusuke, Otsuka Makoto, Yoshida Miyako, Haginaka Jun, Uchida Takahiro
School of Pharmaceutical Sciences, Mukogawa Women's University.
Chem Pharm Bull (Tokyo). 2013;61(11):1121-9. doi: 10.1248/cpb.c13-00428. Epub 2013 Aug 16.
This study aimed to compare the dissolution rate of eight different formulations of ceftriaxone sodium preparation for injection, the original product and seven generic versions. The dissolution time was measured precisely as the point at which the freeze-dried ceftriaxone sodium preparation became a transparent solution on the addition of 0.9% sodium chloride solution. To investigate whether differences in the crystalline structure may explain the differences in dissolution rates, the eight products were subjected to X-ray diffraction (XRD) and differential scanning calorimetry (DSC). Powder surface characteristics were examined, including surface area, amount of water adsorbed, water interactions and morphology. The measurement of near-infrared spectroscopy of powder preparations was conducted, and we predicted dissolution time by partial least squares (PLS). The dissolution time of the eight products were different. There were no differences in XRD and DSC findings between the original and generic products, surface characteristics, i.e., surface area, morphology etc., were different between preparations. On near-infrared (NIR) spectroscopy, a good relationship was demonstrated between the actual and predicted dissolution time for each ceftriaxone preparation. The difference in dissolution time between the eight products was due to differences in powder surface characteristics, such as water interaction and crystal shape. Finally, it was shown that the dissolution rates of the products could be predicted by NIR analysis.
本研究旨在比较注射用头孢曲松钠制剂的8种不同配方(原研产品和7种仿制药)的溶出速率。溶出时间精确测量为冻干的头孢曲松钠制剂加入0.9%氯化钠溶液后变为透明溶液的时间点。为研究晶体结构差异是否可解释溶出速率差异,对这8种产品进行了X射线衍射(XRD)和差示扫描量热法(DSC)分析。检查了粉末表面特性,包括表面积、吸附水量、水相互作用和形态。对粉末制剂进行了近红外光谱测量,并通过偏最小二乘法(PLS)预测溶出时间。这8种产品的溶出时间各不相同。原研产品和仿制药之间在XRD和DSC结果上没有差异,但制剂之间的表面特性,即表面积、形态等存在差异。在近红外(NIR)光谱分析中,每种头孢曲松制剂的实际溶出时间和预测溶出时间之间呈现出良好的相关性。这8种产品溶出时间的差异是由于粉末表面特性的差异,如水相互作用和晶体形状。最后表明,通过近红外分析可以预测产品的溶出速率。