The solid-state continuum: a perspective on the interrelationships between different solid-state forms in drug substance and drug product

被引:25
作者
Elder, David P. [1 ]
Patterson, James E. [2 ]
Holm, Rene [3 ]
机构
[1] GlaxoSmithKline, Ware SG12 0DP, Herts, England
[2] GlaxoSmithKline, Global Mfg & Supply, Melbourne, Vic, Australia
[3] H Lundbeck & Co AS, Biol & Pharmaceut Sci, Valby, Denmark
关键词
cocrystals; polymorphism; salts; solid form; solid-state nomenclature; RANITIDINE HYDROCHLORIDE POLYMORPHS; ACTIVE PHARMACEUTICAL INGREDIENT; HIGH-THROUGHPUT CRYSTALLIZATION; INTRAMOLECULAR PROTON-TRANSFER; ACID SUPRAMOLECULAR COMPOUNDS; SITE-SELECTIVE PROCESSES; PHYSICAL STABILITY; CRYSTAL-STRUCTURE; PHYSICOCHEMICAL PROPERTIES; MECHANICAL-PROPERTIES;
D O I
10.1111/jphp.12293
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
ObjectiveThe objective of the review is to provide an overview of the nomenclature used in the solid-state continuum and relate these to the development of drug substances and drug products. Key findingsThe importance of a rational approach to solid-state form selection, including integrated decision making (ensuring equal weight is given to the needs of the drug substance and the drug product), is vital for the effective development of a drug candidate. For example, how do secondary processing considerations influence the selection of drug substance solid-state form and resulting formulation, and how can drug substance solid-state form be used to optimise secondary processing? Further, the potential use of crystal' engineering to optimise stability, purity and optical resolutions, and the linked regulatory requirements, will be discussed. SummaryThe nomenclature used in the solid-state continuum, which contains a large number of different crystalline and non-crystalline forms, for example, amorphous systems, was reviewed. Further, the significant role of the drug substance within the solid oral dose form from a physicochemical perspective was covered.
引用
收藏
页码:757 / 772
页数:16
相关论文
共 178 条
[1]   Cocrystal or salt:: Does it really matter? [J].
Aakeroy, Christer B. ;
Fasulo, Meg E. ;
Desper, John .
MOLECULAR PHARMACEUTICS, 2007, 4 (03) :317-322
[2]   Current Computational Approaches to Support Pharmaceutical Solid Form Selection [J].
Abramov, Yuriy A. .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2013, 17 (03) :472-485
[3]  
Aguiar AJ, 1969, J PHARM SCI, V56, P847
[4]   Polymorphs, Salts, and Cocrystals: What's in a Name? [J].
Aitipamula, Srinivasulu ;
Banerjee, Rahul ;
Bansal, Arvind K. ;
Biradha, Kumar ;
Cheney, Miranda L. ;
Choudhury, Angshuman Roy ;
Desiraju, Gautam R. ;
Dikundwar, Amol G. ;
Dubey, Ritesh ;
Duggirala, Nagakiran ;
Ghogale, Preetam P. ;
Ghosh, Soumyajit ;
Goswami, Pramod Kumar ;
Goud, N. Rajesh ;
Jetti, Ram R. K. R. ;
Karpinski, Piotr ;
Kaushik, Poonam ;
Kumar, Dinesh ;
Kumar, Vineet ;
Moulton, Brian ;
Mukherjee, Arijit ;
Mukherjee, Gargi ;
Myerson, Allan S. ;
Puri, Vibha ;
Ramanan, Arunachalam ;
Rajamannar, T. ;
Reddy, C. Malla ;
Rodriguez-Hornedo, Nair ;
Rogers, Robin D. ;
Row, T. N. Guru ;
Sanphui, Palash ;
Shan, Ning ;
Shete, Ganesh ;
Singh, Amit ;
Sun, Changquan C. ;
Swift, Jennifer A. ;
Thaimattam, Ram ;
Thakur, Tejender S. ;
Thaper, Rajesh Kumar ;
Thomas, Sajesh P. ;
Tothadi, Srinu ;
Vangala, Venu R. ;
Variankaval, Narayan ;
Vishweshwar, Peddy ;
Weyna, David R. ;
Zaworotko, Michael J. .
CRYSTAL GROWTH & DESIGN, 2012, 12 (05) :2147-2152
[5]   COMPARATIVE STUDIES ON THE BIOAVAILABILITY OF AMPICILLIN ANHYDRATE AND TRIHYDRATE [J].
ALI, AA ;
FAROUK, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1981, 9 (03) :239-243
[6]  
Alkorta I, 2007, NATL ACAD SCI LETT, V30, P139
[7]   Towards Effective Solid Form Screening [J].
Alleso, Morten ;
Tian, Fang ;
Cornett, Claus ;
Rantanen, Jukka .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 99 (09) :3711-3718
[8]   High-throughput surveys of crystal form diversity of highly polymorphic pharmaceutical compounds [J].
Almarsson, Ö ;
Hickey, MB ;
Peterson, ML ;
Morissette, SL ;
Soukasene, S ;
McNulty, C ;
Tawa, M ;
MacPhee, JM ;
Remenar, JF .
CRYSTAL GROWTH & DESIGN, 2003, 3 (06) :927-933
[9]  
[Anonymous], 1965, PHYS CHEM ORGANIC SO
[10]  
[Anonymous], 2009, PHARM DEV