MDI, Arlington, Heights, IL, USA; Argonne National Laboratory, Argonne, IL, USA.
Argonne National Laboratory, Argonne, IL, USA; Arizona State University, Tempe, AZ, USA.
Biochim Biophys Acta Gen Subj. 2017 Jan;1861(1 Pt B):3686-3692. doi: 10.1016/j.bbagen.2016.03.037. Epub 2016 Apr 6.
Many pipeline drugs have low solubility in their crystalline state and require compounding in special dosage forms to increase bioavailability for oral administration. The use of amorphous formulations increases solubility and uptake of active pharmaceutical ingredients. These forms are rapidly gaining commercial importance for both pre-clinical and clinical use.
Synthesis of amorphous drugs was performed using an acoustic levitation containerless processing method and spray drying. The structure of the products was investigated using in-situ high energy X-ray diffraction. Selected solvents for processing drugs were investigated using acoustic levitation. The stability of amorphous samples was measured using X-ray diffraction. Samples processed using both spray drying and containerless synthesis were compared.
We review methods for making amorphous pharmaceuticals and present data on materials made by containerless processing and spray drying. It was shown that containerless processing using acoustic levitation can be used to make phase-pure forms of drugs that are known to be difficult to amorphize. The stability and structure of the materials was investigated in the context of developing and making clinically useful formulations.
Amorphous compounds are emerging as an important component of drug development and for the oral delivery of drugs with low solubility. Containerless techniques can be used to efficiently synthesize small quantities of pure amorphous forms that are potentially useful in pre-clinical trials and for use in the optimization of clinical products.
Developing new pharmaceutical products is an essential enterprise to improve patient outcomes. The development and application of amorphous pharmaceuticals to increase absorption is rapidly gaining importance and it provides opportunities for breakthrough research on new drugs. There is an urgent need to solve problems associated with making formulations that are both stable and that provide high bioavailability. This article is part of a Special Issue entitled "Science for Life" Guest Editor: Dr. Austen Angell, Dr. Salvatore Magazù and Dr. Federica Migliardo.
许多候选药物在其晶态下溶解度较低,需要通过特殊的剂型来增加生物利用度以实现口服给药。无容器处理技术和喷雾干燥技术可用于制备无定形药物,以提高药物的溶解度和生物利用度。这些制剂形式在临床前和临床应用中都具有重要的商业价值。
采用声悬浮无容器处理方法和喷雾干燥法制备无定形药物。利用原位高能 X 射线衍射研究了产物的结构。采用声悬浮法研究了用于药物加工的溶剂。利用 X 射线衍射法测量了无定形样品的稳定性。对比了喷雾干燥和无容器合成两种方法加工的样品。
综述了制备无定形药物的方法,并介绍了采用无容器处理和声悬浮喷雾干燥法制备药物的相关数据。结果表明,采用声悬浮无容器处理法可以制备出已知难以形成无定形的纯药物相。在开发和制备具有临床应用价值的制剂过程中,研究了材料的稳定性和结构。
无定形化合物在药物开发中具有重要地位,对于提高低溶解度药物的口服生物利用度具有重要意义。无容器技术可以高效地合成小批量的纯无定形形式,这些形式可能在临床前试验和优化临床产品中具有重要作用。
开发新的药物产品对于改善患者的治疗效果至关重要。无定形药物的开发和应用可以提高药物的吸收度,具有重要意义,为新药的突破性研究提供了机会。目前迫切需要解决与制剂的稳定性和高生物利用度相关的问题。本文是一个特刊的一部分,主题为“科学为生命服务”,客座编辑为 Austen Angell 博士、Salvatore Magazù 博士和 Federica Migliardo 博士。