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Items: 1 to 20 of 100

1.

Model-based design space determination of peptide chromatographic purification processes.

Gétaz D, Butté A, Morbidelli M.

J Chromatogr A. 2013 Apr 5;1284:80-7. doi: 10.1016/j.chroma.2013.01.117. Epub 2013 Feb 8.

PMID:
23466201
2.

Model-based design of peptide chromatographic purification processes.

Gétaz D, Stroehlein G, Butté A, Morbidelli M.

J Chromatogr A. 2013 Apr 5;1284:69-79. doi: 10.1016/j.chroma.2013.01.118. Epub 2013 Feb 9.

PMID:
23465131
3.

Information Processing: Rate-Based Investigation of Cell Physiological Changes along Design Space Development.

Sagmeister P, Wechselberger P, Herwig C.

PDA J Pharm Sci Technol. 2012 Nov-Dec;66(6):526-41. doi: 10.5731/pdajpst.2012.00889.

PMID:
23183649
4.

Modeling of mixed-mode chromatography of peptides.

Bernardi S, Gétaz D, Forrer N, Morbidelli M.

J Chromatogr A. 2013 Mar 29;1283:46-52. doi: 10.1016/j.chroma.2013.01.054. Epub 2013 Jan 22.

PMID:
23433883
5.

Effect of high pH column regeneration on the separation performances in reversed phase chromatography of peptides.

Gétaz D, Gencoglu M, Forrer N, Morbidelli M.

J Chromatogr A. 2010 May 21;1217(21):3531-7. doi: 10.1016/j.chroma.2010.03.042. Epub 2010 Mar 27.

PMID:
20382392
6.

A novel approach to establishing the design space for the oral formulation manufacturing process.

Norioka T, Hayashi Y, Onuki Y, Andou H, Tsunashima D, Yamashita K, Takayama K.

Chem Pharm Bull (Tokyo). 2013;61(1):39-49.

7.

Establishment of a design space for biopharmaceutical purification processes using DoE.

Amadeo I, Mauro L, Ortí E, Forno G.

Methods Mol Biol. 2014;1129:11-27. doi: 10.1007/978-1-62703-977-2_2.

PMID:
24648063
8.

A model for predicting slopes S in the basic equation for the linear-solvent-strength theory of peptide separation by reversed-phase high-performance liquid chromatography.

Vu H, Spicer V, Gotfrid A, Krokhin OV.

J Chromatogr A. 2010 Jan 22;1217(4):489-97. doi: 10.1016/j.chroma.2009.11.065. Epub 2009 Nov 27.

PMID:
20004401
9.

Model-based risk analysis of coupled process steps.

Westerberg K, Broberg-Hansen E, Sejergaard L, Nilsson B.

Biotechnol Bioeng. 2013 Sep;110(9):2462-70. doi: 10.1002/bit.24909. Epub 2013 Apr 22.

PMID:
23532926
11.

Bypass chromatography--design and analysis of an improved strategy for operating batch chromatography processes.

Siitonen J, Sainio T, Rajendran A.

J Chromatogr A. 2012 Mar 23;1230:77-92. doi: 10.1016/j.chroma.2012.01.071. Epub 2012 Jan 31.

PMID:
22342182
12.

Influence of the pore size of reversed phase materials on peptide purification processes.

Gétaz D, Dogan N, Forrer N, Morbidelli M.

J Chromatogr A. 2011 May 20;1218(20):2912-22. doi: 10.1016/j.chroma.2011.03.008. Epub 2011 Mar 12.

PMID:
21450297
14.

Defining process design space for a hydrophobic interaction chromatography (HIC) purification step: application of quality by design (QbD) principles.

Jiang C, Flansburg L, Ghose S, Jorjorian P, Shukla AA.

Biotechnol Bioeng. 2010 Dec 15;107(6):985-97. doi: 10.1002/bit.22894.

PMID:
20683852
15.

Model-based rational strategy for chromatographic resin selection.

Nfor BK, Zuluaga DS, Verheijen PJ, Verhaert PD, van der Wielen LA, Ottens M.

Biotechnol Prog. 2011 Nov-Dec;27(6):1629-43.

PMID:
22238769
16.

Investigation of design space for freeze-drying: use of modeling for primary drying segment of a freeze-drying cycle.

Koganti VR, Shalaev EY, Berry MR, Osterberg T, Youssef M, Hiebert DN, Kanka FA, Nolan M, Barrett R, Scalzo G, Fitzpatrick G, Fitzgibbon N, Luthra S, Zhang L.

AAPS PharmSciTech. 2011 Sep;12(3):854-61. doi: 10.1208/s12249-011-9645-7. Epub 2011 Jun 28.

17.

Optimal design of batch and simulated moving bed chromatographic separation processes.

Jupke A, Epping A, Schmidt-Traub H.

J Chromatogr A. 2002 Jan 25;944(1-2):93-117.

PMID:
11831767
18.

Characterization of a monoclonal antibody cell culture production process using a quality by design approach.

Horvath B, Mun M, Laird MW.

Mol Biotechnol. 2010 Jul;45(3):203-6. doi: 10.1007/s12033-010-9267-4.

PMID:
20300882
19.

Strategies for developing design spaces for viral clearance by anion exchange chromatography during monoclonal antibody production.

Strauss DM, Cano T, Cai N, Delucchi H, Plancarte M, Coleman D, Blank GS, Chen Q, Yang B.

Biotechnol Prog. 2010 May-Jun;26(3):750-5. doi: 10.1002/btpr.385.

PMID:
20306523
20.

A slow gradient approach for the purification of synthetic polypeptides by reversed phase high performance liquid chromatography.

Harris PW, Lee DJ, Brimble MA.

J Pept Sci. 2012 Sep;18(9):549-55. doi: 10.1002/psc.2432. Epub 2012 Jul 25.

PMID:
22833387
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