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头孢噻吩钠的冷冻干燥:冷冻过程中的颗粒状团聚结晶。I

Freeze-drying of cephalothin sodium: granularly agglomerated crystallization during freezing. I.

作者信息

Suzuki Y, Takeda T, Inazu K, Sakamoto T

机构信息

Research Laboratories, Shionogi & Co., Ltd., Hyogo, Japan.

出版信息

Biol Pharm Bull. 1993 Apr;16(4):402-6. doi: 10.1248/bpb.16.402.

Abstract

Optimal conditions for the crystallization and subsequent freeze-drying of an aqueous cephalothin sodium (CET-Na) solution of supersaturated concentrations to obtain granular crystalline CET-Na have been discussed, as have the qualities of the product thus obtained. In general, CET-Na in supersaturated aqueous solution is barely recrystallized, even when in its frozen stage. Our previous report revealed that when the solution is kept at low temperatures for a long duration, the molecules begin to change structurally to as condensed a state as that of liquid crystals, and such change facilitates a spontaneous nucleation and seed-independent crystal growth in the frozen solution. These findings prompted the authors to investigate optimal CET-Na concentrations and thermal histories during the crystallization and subsequent freeze-drying process without seeding. It has subsequently been found out that optimization of the latter conditions gives granular agglomerated crystalline CET-Na contaminated with neither the amorphous nor the quasi-crystalline form. The optimized conditions are: 25-28% CET-Na concentrations; storage before the freezing process at 0 degrees C for 2 h, and subsequent storage at 20-25 degrees C for 1 h; cooling in the freezing process at a rate not faster than 0.5 degrees C/min; warming of the solution for facilitating crystallization prior to vacuum application for drying at -4 degrees C. Under these conditions, the freeze-dried product of CET-Na in granular form has been successfully obtained in a shorter freeze-drying cycle, exhibiting a faster reconstitution time than those of CET-Na prepared according to seeded crystallization followed by a conventional freeze-drying.

摘要

已经讨论了将过饱和浓度的头孢噻吩钠(CET-Na)水溶液结晶并随后冷冻干燥以获得颗粒状结晶CET-Na的最佳条件,以及由此获得的产品质量。一般来说,过饱和水溶液中的CET-Na即使在冷冻阶段也几乎不会重结晶。我们之前的报告显示,当溶液在低温下长时间保存时,分子开始在结构上转变为液晶那样的凝聚态,这种变化促进了冷冻溶液中的自发成核和无晶种晶体生长。这些发现促使作者研究在不接种晶种的结晶和随后的冷冻干燥过程中的最佳CET-Na浓度和热历史。随后发现,优化后一种条件可得到既不含有无定形也不含有准晶形式的颗粒状团聚结晶CET-Na。优化条件为:CET-Na浓度为25-28%;在冷冻过程前于0℃储存2小时,随后在20-25℃储存1小时;在冷冻过程中以不超过0.5℃/分钟的速率冷却;在真空干燥前于-4℃加热溶液以促进结晶。在这些条件下,已成功在较短的冷冻干燥周期内获得了颗粒状的CET-Na冷冻干燥产品,其复溶时间比按照接种结晶后进行常规冷冻干燥制备的CET-Na更快。

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