Takeuchi Y, Takebayashi Y, Sunagawa M, Isobe Y, Hamazume Y, Uemura A, Noguchi T
Research Laboratories, Sumitomo Pharmaceuticals Co., Ltd., Osaka, Japan.
Chem Pharm Bull (Tokyo). 1993 Nov;41(11):1998-2002. doi: 10.1248/cpb.41.1998.
A formulation of meropenem, a novel carbapenem antibiotic for injection, was developed as a vial filled with a mixture of meropenem and dried sodium carbonate. During the design phase, we studied the effect of water in the formulation on the stability of meropenem in the solid state. Meropenem is obtained as trihydrate, whose moisture content is 12.35% and is nonhygroscopic. Dehydrated meropenem, whose moisture content was 3.4%, took up moisture quickly even under low humidity (33% RH). Also, the chemical stability of dehydrated meropenem was poor compared with that of untreated meropenem, which is quite stable. Degradation of meropenem by free water was considered as a possible cause of the poor stability. Degradation of meropenem due to liberation of its crystal water to free water was also observed when meropenem was micronized by pneumatic pulverization. Crystal water of meropenem was found to stay bound and to be almost inert in the formulation. Thus, meropenem injection formulation is stable for long time at room temperature.
美罗培南是一种新型注射用碳青霉烯类抗生素,其制剂是将美罗培南与干燥碳酸钠的混合物填充于小瓶中制成。在设计阶段,我们研究了制剂中的水分对美罗培南固态稳定性的影响。美罗培南以三水合物形式获得,其含水量为12.35%,且不吸湿。含水量为3.4%的脱水美罗培南即使在低湿度(33%相对湿度)下也会迅速吸湿。此外,与未经处理的美罗培南相比,脱水美罗培南的化学稳定性较差,而未经处理的美罗培南相当稳定。美罗培南因游离水导致的降解被认为是稳定性差的一个可能原因。当通过气流粉碎对美罗培南进行微粉化时,还观察到美罗培南因结晶水释放为游离水而发生降解。发现美罗培南的结晶水在制剂中保持结合状态且几乎无活性。因此,美罗培南注射制剂在室温下长时间稳定。