Biomedical Engineering Reference
In-Depth Information
11. Hutchinson N, Chhatre S, Baldascini H, Davies JL, Bracewell DG, Hoare M (2009) Ultra
scale-down approach to correct dispersive and retentive effects in small-scale columns when
predicting larger scale elution profiles. Biotechnol Progr 25:1103-1110
12. Jin J, Chhatre S, Titchener-Hooker NJ, Bracewell DG (2010) Evaluation of the impact of
lipid
fouling
during
the
chromatographic
purification
of
virus-like
particles
from
Saccharomyces cerevisiae. J Chem Technol Biotechnol 85:209-215
13. Kelley BD, Switzer M, Bastek P, Kramarczyk JK, Molnar K, Yu T, Coffman J (2008a) High-
throughput screening of chromatographic separations: IV ion-exchange. Biotechnol Bioeng
100:950-963
14. Kelley BD, Tobler SA, Brown P, Coffman J, Godavarti R, Iskra T, Switzer M, Vunnum S
(2008b) Weak partitioning chromatography for anion exchange purification of monoclonal
antibodies. Biotechnol Bioeng 101:553-566
15. Lye GJ, Ayazi Shamlou P, Baganz F, Dalby PA, Woodley JM (2003) Accelerated design of
bioconversion processes using automated microscale processing techniques. Trends Biotechnol
21:29-37
16. Micheletti M, Lye G (2006) Microscale bioprocess optimisation. Curr Opin. Biotech 17:
611-618
17. Staby A, Jensen RH, Bensch M, Hubbuch J, Dünweber DL, Krarup J et al (2007) Comparison
of chromatographic ion-exchange resins VI weak anion-exchange resins. J Chromatogr A
1164:82-94
18. Nfor BK, Ahamed T, van Dedem GWK, van der Wielen LAM, van de Sandt EJAX,
Eppink MHM, Ottens M (2008) Review: design strategies for integrated protein purification
processes: challenges, progress and outlook. J Chem Technol Biotechnol 83:124-132
19. Nfor BK, Verhaert PDEM, van der Wielen LAM, Hubbuch J, Ottens M (2009) Rational and
systematic protein purification process development: the next generation. Trends Biotechnol
27:673-679
20. Nfor BK, Noverraz M, Chilamkurthi S, Verhaert PDEM, van der Wielen LAM, Ottens M
(2010) High-throughput isotherm determination and thermodynamic modeling of protein
adsorption on mixed mode adsorbents. J Chromatogr A 1217:6829-6850
21. Ngiam S-H, Zhou Y, Turner MK, Titchener-Hooker NJ (2001) Graphical method for the
calculation of chromatographic performance in representing the trade-off between purity and
recovery. J Chromatogr A 937:1-11
22. Przybycien TM, Pujar NS, Steele LM (2004) Alternative bioseparation operations: life
beyond packed-bed chromatography. Curr Opin Biotechnol 15:469-478
23. Rege K, Pepsin M, Falcon B, Steele L, Heng M (2006) High-throughput process development
for recombinant protein purification. Biotechnol Bioeng 93:618-630
24. Shapiro M, Haswell S, Lye G, Bracewell D (2009) Design and characterization of a
microfluidic packed bed system for protein breakthrough and dynamic binding capacity
determination. Biotechnol Progr 25:277-285
25. Shapiro M, Haswell S, Lye G, Bracewell D (2011) Microfluidic chromatography for early
stage evaluation of biopharmaceutical binding and separation conditions. Separ Sci Technol
46:185-194
26. Shukla AK, Shukla MM and Shukla AM (2007) Incision-based filtration/separation pipette
tip. US Patent 7276158
27. Stein A, Kiesewetter A (2007) Cation exchange chromatography in antibody purification: pH
screening for optimised binding and HCP removal. J Chromatogr B 848:151-158
28. Siu SC, Boushaba R, Topoyassakul V, Graham A, Choudhury S, Moss G, Titchener-Hooker
NJ (2006) Visualising fouling of a chromatographic matrix using confocal scanning laser
microscopy. Biotechnol Bioeng 95:714-723
29. Susanto A, Knieps-Grünhagen E, von Lieres E, Hubbuch J (2008) High throughput screening
for
the
design
and
optimization
of
chromatographic
processes:
assessment
of
model
parameter
determination
from
high
throughput
compatible
data.
Chem
Eng
Technol
31:1846-1855
Search WWH ::
Custom Search