Sheokand Sneha, Modi Sameer R, Bansal Arvind K
Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), SAS Nagar, Punjab 160062, India.
Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), SAS Nagar, Punjab 160062, India.
J Pharm Sci. 2014 Nov;103(11):3364-3376. doi: 10.1002/jps.24160. Epub 2014 Sep 11.
It is well established that pharmaceutical processing can cause disruption of the crystal structure, leading to generation of amorphous content in crystalline materials. The presence of even a small amount of amorphous form, especially on the surface of crystalline material, can affect processing, performance, and stability of a drug product. This necessitates the need to quantify, monitor, and control the amorphous form. Numerous analytical techniques have been reported for the quantification of amorphous phase, but issues of sensitivity, suitability, limit of detection, and quantitation pose significant challenges. The present review focuses on use of dynamic vapor sorption (DVS) for quantification of amorphous content in predominantly crystalline materials. The article discusses (1) theoretical and experimental considerations important for developing a quantification method, (2) methods used for quantification of amorphous content, (3) basis for selecting a suitable methodology depending on the properties of a material, and (4) role of various instrument and sample-related parameters in designing a protocol for quantification of amorphous content. Finally, DVS-based hyphenated techniques have been discussed as they can offer higher sensitivity for quantification of amorphous content.
众所周知,药物加工会导致晶体结构破坏,从而使结晶材料中产生无定形成分。即使存在少量无定形形式,尤其是在结晶材料表面,也会影响药品的加工、性能和稳定性。这就需要对无定形形式进行量化、监测和控制。已有许多分析技术用于无定形相的量化,但灵敏度、适用性、检测限和定量等问题带来了重大挑战。本综述重点关注动态蒸汽吸附(DVS)在主要为结晶材料中无定形含量量化方面的应用。本文讨论了:(1)开发量化方法时重要的理论和实验考量;(2)用于无定形含量量化的方法;(3)根据材料特性选择合适方法的依据;(4)各种仪器和样品相关参数在设计无定形含量量化方案中的作用。最后,对基于DVS的联用技术进行了讨论,因为它们在无定形含量量化方面可提供更高的灵敏度。