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晶型技术对咖啡因/草酸 2:1 共晶压缩性能的影响。

Effect of cocrystallization techniques on compressional properties of caffeine/oxalic acid 2:1 cocrystal.

机构信息

Poona College of Pharmacy, Bharati Vidyapeeth University, Erandwane, Pune, India.

出版信息

Pharm Dev Technol. 2013 Feb;18(1):55-60. doi: 10.3109/10837450.2011.618950. Epub 2011 Oct 10.

Abstract

CONTEXT

Caffeine/oxalic acid 2:1 cocrystal exhibited superior stability to humidity over caffeine, but compressional behavior is not studied yet.

OBJECTIVE

To compare compressional properties of caffeine/oxalic acid 2:1 cocrystal obtained by different cocrystallization techniques.

MATERIALS AND METHODS

Cocrystal was obtained by solvent precipitation and ultrasound assisted solution cocrystallization (USSC) and characterized by X-ray powder diffraction and scanning electron microscopy. Compaction study was carried out at different compaction forces. Compact crushing strength, thickness and elastic recovery were determined.

RESULTS AND DISCUSSION

Compaction was in order, caffeine > solvent precipitation cocrystal > USSC cocrystal. Caffeine exhibited sticking and lamination, where solvent precipitation compacts showed advantage. Caffeine and solvent precipitation compacts showed sudden drop in compactability, higher elastic recovery with severe lamination at 20,000 N. This was due to overcompaction. Crystal habit of two cocrystal products was same, but USSC cocrystals were difficult to compact. Uniform needle shaped USSC cocrystals must be difficult to orient in different direction and fracture during compression. Elastic recovery of USSC cocrystals was also more compared to other powders indicating less fracture and poor bonding between particles resulting in poor compaction.

CONCLUSION

Cocrystal formation did not improve compressional property of caffeine. Cocrystals exposed to different crystallization environments in two techniques may have resulted in generation of different surface properties presenting different compressional properties.

摘要

背景

咖啡因/草酸 2:1 共晶在抗湿性方面优于咖啡因,但尚未研究其压缩性能。

目的

比较不同共晶技术制备的咖啡因/草酸 2:1 共晶的压缩性能。

材料与方法

通过溶剂沉淀法和超声辅助溶液共晶化(USSC)法获得共晶,并通过 X 射线粉末衍射和扫描电子显微镜进行表征。在不同的压缩力下进行压实研究。测定了压缩强度、厚度和弹性恢复。

结果与讨论

压缩顺序为咖啡因>溶剂沉淀共晶>USSC 共晶。咖啡因表现出粘聚和层积,而溶剂沉淀共晶则具有优势。咖啡因和溶剂沉淀共晶的压缩性突然下降,弹性恢复高,在 20000N 时出现严重的层积现象。这是由于过度压实造成的。两种共晶产物的晶体形态相同,但 USSC 共晶较难压实。均匀的针状 USSC 共晶在压缩过程中必须难以在不同方向上取向和断裂。与其他粉末相比,USSC 共晶的弹性恢复也更高,这表明颗粒之间的断裂和结合不良,导致压实不良。

结论

共晶的形成并没有改善咖啡因的压缩性能。两种技术中暴露于不同结晶环境的共晶可能会产生不同的表面性质,从而表现出不同的压缩性能。

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