Formation of mannitol hemihydrate in freeze-dried protein formulations-A design of experiment approach

被引:24
作者
Larsen, Helena Marie Lindholm [1 ]
Trnka, Hjalte [1 ]
Grohganz, Holger [1 ]
机构
[1] Univ Copenhagen, Dept Pharm, DK-2100 Copenhagen, Denmark
关键词
Mannitol hemihydrate; Freeze-drying; Design of experiments; Solid state; XRPD; Protein formulation; RAMAN-SPECTROSCOPY; PHYSICAL STATE; BEHAVIOR; HYDRATE; CRYSTALLIZATION; LYOPHILIZATION; STABILITY; SURFACE; BINARY;
D O I
10.1016/j.ijpharm.2013.11.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Since the discovery of mannitol hemihydrate, this form of mannitol has been seen as potentially negative with regard to the stability of pharmaceutical formulations. The formation of mannitol hemihydrate is reported in several case studies; however, no systematic investigation has been performed so far. In this study, design of experiments was applied for response surface modelling of mannitol hemihydrate formation. The formulation parameters investigated in a composite face-centred design were the overall solid content, protein concentration, protein type and the ratio between mannitol and sucrose. Additionally, annealing as process parameter was included in a full factorial mixed design. For two proteins, models with a high goodness of fit (R-2: 0.82 and 0.93) and goodness of prediction (Q(2): 0.78 and 0.89) were achieved. Inclusion of the process parameter annealing resulted in models of similar quality. The successful application of design of experiments showed that the most prominent factors enhancing the formation of hemihydrate were a high protein concentration, low relative mannitol content and annealing at -20 degrees C. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 52
页数:8
相关论文
共 36 条
[1]   High-throughput measurement of protein stability in microtiter plates [J].
Aucamp, JP ;
Cosme, AM ;
Lye, GJ ;
Dalby, PA .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 89 (05) :599-607
[2]  
Cannon AJ, 2000, PDA J PHARM SCI TECH, V54, P13
[3]   Differentiation and quantitative determination of surface and hydrate water in lyophilized mannitol using NIR spectroscopy [J].
Cao, Wenjin ;
Mao, Chen ;
Chen, Wendy ;
Lin, Hong ;
Krishnan, Sampathkumar ;
Cauchon, Nina .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 95 (09) :2077-2086
[4]  
Carpenter John F, 2002, Pharm Biotechnol, V13, P109
[5]  
Cavatur R K, 1998, Pharm Dev Technol, V3, P579, DOI 10.3109/10837459809028642
[6]   Crystallization behavior of mannitol in frozen aqueous solutions [J].
Cavatur, RK ;
Vemuri, NM ;
Pyne, A ;
Chrzan, Z ;
Toledo-Valasquez, D ;
Suryanarayanan, R .
PHARMACEUTICAL RESEARCH, 2002, 19 (06) :894-900
[7]   Mechanisms of Protein Stabilization in the Solid State [J].
Chang, Liuquan ;
Pikal, Michael J. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (09) :2886-2908
[8]   Detecting phase separation of freeze-dried binary amorphous systems using pair-wise distribution function and multivariate data analysis [J].
Chieng, Norman ;
Trnka, Hjalte ;
Boetker, Johan ;
Pikal, Michael ;
Rantanen, Jukka ;
Grohganz, Holger .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 454 (01) :167-173
[9]   Implementation of a process analytical technology system in a freeze-drying process using Raman Spectroscopy for in-line process monitoring [J].
De Beer, T. R. M. ;
Alleso, M. ;
Goethals, F. ;
Coppens, A. ;
Heyden, Y. Vander ;
De Diego, H. Lopez ;
Rantanen, J. ;
Verpoort, F. ;
Vervaet, C. ;
Remon, J. P. ;
Baeyens, W. R. G. .
ANALYTICAL CHEMISTRY, 2007, 79 (21) :7992-8003
[10]   Optimization of a pharmaceutical freeze-dried product and its process using an experimental design approach and innovative process analyzers [J].
De Beer, T. R. M. ;
Wiggenhorn, M. ;
Hawe, A. ;
Kasper, J. C. ;
Almeida, A. ;
Quinten, T. ;
Friess, W. ;
Winter, G. ;
Vervaet, C. ;
Remon, J. P. .
TALANTA, 2011, 83 (05) :1623-1633