Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Karol M Łącki"'
Autor:
Frank Riske, Karol M Łącki
Publikováno v:
Biotechnology journal. 15(1)
Affinity chromatography (AC) has been used in large-scale bioprocessing for almost 40 years and is considered the preferred method for primary capture in downstream processing of various types of biopharmaceuticals. The objective of this mini-review
Autor:
Mattias Ahnfelt, Umay Saplakoglu, Mary Beth Switzer, Kristina Nilsson-Välimaa, Brad Evans, Eggert Brekkan, Karol M Łącki, Ranga Godavarti, Jeff Salm, Ziawei Fung, Alex Berrill, Jessika Feliciano
Publikováno v:
Engineering in Life Sciences. 16:169-178
This chapter provides an overview of alternative separation methods in order to help the reader decide if such methods are of interest, how they compare with other methods, and what particular approaches may suit specific process challenges. Alternat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6579d674d53962d1d707408405f6ce88
https://doi.org/10.1016/b978-0-08-100623-8.00010-4
https://doi.org/10.1016/b978-0-08-100623-8.00010-4
The most common alternative separation methods used in bioprocessing are flocculation and precipitation. They are proven, readily scaled, do not require overt energy input or capital investment, and can offer significant selectivity. They have the ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d48e8819af6e889fa8083d011b6a6e36
https://doi.org/10.1016/b978-0-08-100623-8.00011-6
https://doi.org/10.1016/b978-0-08-100623-8.00011-6
As with many other alternative separations methods, crystallization and aqueous polymer two-phase extraction (ATPE) have been well-studied academically and are amenable to predictive and process modeling. Their solution nature allows them to be optim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cacb8f9baad1b8479097bfe1c1ede2ee
https://doi.org/10.1016/b978-0-08-100623-8.00012-8
https://doi.org/10.1016/b978-0-08-100623-8.00012-8
Autor:
Karol M. Łącki, Günter Jagschies
“Process capability” is the process’s ability to deliver product of the required quality in the quantity necessary for each step in the life cycle of the product. In order to be of any practical value, a process intended to make biopharmaceutic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e39f6ae6ec9b122b7246d3933aebe646
https://doi.org/10.1016/b978-0-08-100623-8.00004-9
https://doi.org/10.1016/b978-0-08-100623-8.00004-9
Autor:
John W. Armando, E. Morrey Atkinson, Peter Bernhardt, Torbjörn S. Blank, Yvonne A. Brady, Eggert Brekkan, Andrea Buchacher, Karolina Busson, Maire H. Caparon, Enrique N. Carredano, Jeffrey R. Carter, Andreas Castan, Shuang Chen, Kenneth P. Clapp, Scott A. Cook, John T. Cundy, John M. Curling, Åke Danielsson, Kjell O. Eriksson, Alain Fairbank, Suzanne S. Farid, Simon Fischer, Kine A.-K. Frej, Parrish M. Galliher, Klaus Gebauer, Glen S. Giese, Alan Gilbert, Anna Grönberg, Albrecht Gröner, Robert S. Gronke, Martin Hall, Kim R. Hejnaes, Rachel S. Hendricks, Rolf A. Hjorth, Geoff Hodge, Matt H. Hutchinson, Günter Jagschies, Michael J. Jenkins, Mikael I. Johansson, John Joseph, Oliver Kaltenbrunner, Gautam Kapoor, Tomas M. Karlsson, Brian D. Kelley, Annika Kleinjans, Jashwant Kumar, Karol M. Łącki, Philip Lester, Jakob Liderfelt, Xin Xin Lin, Eva K. Lindskog, Mats Lundgren, Ratish Mangalath-Illam, Trevor J. Marshall, Joseph P. Martin, Krunal K. Mehta, Brian Montgomery, Daniel Nelson, Roger Nordberg, Dana A. Olson, Martin Östling, John P. Pieracci, David J. Pollard, Alain Pralong, Hari Pujar, Joost P. Quaadgras, Tom C. Ransohoff, Anurag S. Rathore, Craig Robinson, Jonathan Royce, Michael A. Rubacha, Henrik Sandegren, Andreas Schaubmar, Patrick Schulz, Sumit K. Singh, Stephen E. Sobacke, Sriram Srinivasan, Matthew J. Stork, Bruce S. Tangarone, Jorg Thommes, Matthew J. Traylor, Johan Tschöp, James M. Van Alstine, Johnson Varghese, Ganesh Vedantham, Thomas von Hirschheydt, William B. Wellborn, Till Wenger, Susanne Westin, David G. Westman, Matthew Westoby, William G. Whitford, Ambrose J. Williams, John M. Woodgate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ab37a02755962071e60b3fe89a67442
https://doi.org/10.1016/b978-0-08-100623-8.09990-4
https://doi.org/10.1016/b978-0-08-100623-8.09990-4
Autor:
Karol M. Łącki
Over the years chromatography has proven itself as the work horse for purification of biologics. General rules and considerations for chromatographic separations are well defined and understood. They are briefly discussed in this chapter. The discuss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64a6f75c3aa0d3bfbcd63150fe92ef07
https://doi.org/10.1016/b978-0-08-100623-8.00016-5
https://doi.org/10.1016/b978-0-08-100623-8.00016-5
The chapter provides the reader with the basic understanding of process design and discusses few concepts important for consideration during this stage of the product lifecycle. The main focus of the chapter is on the downstream purification part of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0abb4f2a535bfef03bb7af7cb270fb41
https://doi.org/10.1016/b978-0-08-100623-8.00032-3
https://doi.org/10.1016/b978-0-08-100623-8.00032-3
Autor:
Karol M Łącki
Publikováno v:
Current Opinion in Chemical Engineering. 6:25-32
A brief overview of the high throughput process development field as related to biopharmaceutical manufacturing is provided. The overview outlines available high-throughput techniques used during process development of upstream and downstream unit op