Optimization of protein solution by a novel experimental design method using thermodynamic properties-Reference-Cited by-同舟云学术

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Optimization of protein solution by a novel experimental design method using thermodynamic properties

Published:2012-09 Issue:9 Volume:35 Page:1609-1619
ISSN:0253-6269
Container-title:Archives of Pharmacal Research
language:en
Short-container-title:Arch. Pharm. Res.

Author:

Kim Nam Ah,An In Bok,Lee Sang Yeol,Park Eun-Seok,Jeong Seong Hoon

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12272-012-0912-2.pdf

Reference35 articles.

1. Bloomfield, M. S. and Butler, W. C., Robustness testing, using experimental design, of a flow-through dissolution method for a product where the actives have markedly differing solubility properties. Int. J. Pharm., 206, 55–61 (2000).

2. Bolton, S., Experimental design in clinical trials (Reprinted from Pharmaceutical Statistics Practical and Clinical Applications, vol 80, pg 384–443, 1997). Clin. Res. Regul. Aff., 17, 285–344 (2000).

3. Box, G., Bisgaard, S., and Fung, C., An Explanation and critique of Taguchi’s contributions to quality Engineering. Qual. Reliab. Eng. Int., 4, 123–131 (1988).

4. Chi, E. Y., Krishnan, S., Kendrick, B. S., Chang, B. S., Carpenter, J. F., and Randolph, T. W., Roles of conformational stability and colloidal stability in the aggregation of recombinant human granulocyte colony-stimulating factor. Protein Sci., 12, 903–913 (2003a).

5. Chi, E. Y., Krishnan, S., Randolph, T. W., and Carpenter, J. F., Physical stability of proteins in aqueous solution: Mechanism and driving forces in nonnative protein aggregation. Pharm. Res., 20, 1325–1336 (2003b).

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