Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Gregory S. Blank"'
Autor:
Qi Chen, Gregory S. Blank, Scott Lute, Bin Yang, Daniel Strauss, Douglas D. Frey, Cintia Ho, Kurt Brorson, Zinaida Tebaykina
Publikováno v:
Biotechnology and Bioengineering. 104:371-380
During production of therapeutic monoclonal antibodies (mAbs) in mammalian cell culture, it is important to ensure that viral impurities and potential viral contaminants will be removed during downstream purification. Anion exchange chromatography pr
Publikováno v:
Biotechnology Progress. 25:1194-1197
Retrovirus-like particles (RVLPs) that are expressed during the production of monoclonal antibodies in Chinese hamster ovary (CHO) cell cultures must be removed during product recovery. Anion exchange chromatography (AEX) performed in product flow-th
Publikováno v:
Biotechnology and Bioengineering. 102:168-175
The mammalian cell-lines used to produce biopharmaceutical products are known to produce endogenous retrovirus-like particles and have the potential to foster adventitious viruses as well. To ensure product safety and regulatory compliance, recovery
Publikováno v:
Journal of Chromatography A. 830:127-134
Acetonitrile is used as an eluent for reversed-phase chromatography. However, because it is a flammable solvent, using acetonitrile on a large scale requires expensive equipment and facilities specially designed for flammable solvents. Using a non-fl
Publikováno v:
Journal of Chromatography A. 827:37-43
During preparative reversed-phase chromatography of recombinant human insulin-like growth factor-I (IGF), the separation of IGF from IGF aggregates cannot be determined using UV absorbance. An on-line reversed-phase chromatographic assay was develope
Publikováno v:
Biotechnology and Bioengineering. 45:149-157
There are three major methods for buffer exchange of proteins at industrial scale: size exclusion chromatography (SEC), tangential flow filtration (TFF), and countercurrent dialysis (CCD). In order to determine the optimal technology for a given proc
Autor:
Daniel Strauss, Tony Cano, Daniel Coleman, Qi Chen, Gregory S. Blank, Nick Cai, Magdalena Plancarte, Bin Yang, Heather Delucchi
Publikováno v:
Biotechnology progress. 26(3)
The quality-by-design (QbD) regulatory initiative promotes the development of process design spaces describing the multidimensional effects and interactions of process variables on critical quality attributes of therapeutic products. However, because
Publikováno v:
Biotechnology and bioengineering. 84(2)
The potential of viral contamination is a regulatory concern for continuous cell line-derived pharmaceutical proteins. Complementary and redundant safety steps, including an evaluation of the viral clearance capacity of unit operations in the purific
Publikováno v:
Scale-Up and Optimization in Preparative Chromatography: Principles and Biopharmaceutical Applications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35cdeded5cbc2f8201d5b214f6b58362
https://doi.org/10.1201/9780203909287.ch7
https://doi.org/10.1201/9780203909287.ch7
Autor:
Gregory S. Blank, Robert L. Fahrner
Publikováno v:
Methods for Affinity-Based Separations of Enzymes and Proteins ISBN: 9783764363055
Perfusion chromatography is an important tool for rapid separations of biomolecules. Introduced more than a decade ago [1-3], perfusion chromatography media are polymeric (polystyrene-divinylbenzene) and contain large through-pores that completely pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bd14a3748cb704345af3798405b7540
https://doi.org/10.1007/978-3-0348-8127-2_4
https://doi.org/10.1007/978-3-0348-8127-2_4