An updated analysis of viral clearance unit operations for biotechnology manufacturing

OO Ajayi, SA Johnson, T Faison, N Azer… - Current Research in …, 2022 - Elsevier
Viral contamination is a potential risk of using biotechnology products derived from
mammalian cell lines. Therefore, to provide assurance of the safety of these products …

Nanofiltration as a robust method contributing to viral safety of plasma‐derived therapeutics: 20 yearsʼ experience of the plasma protein manufacturers

NJ Roth, HO Dichtelmüller, F Fabbrizzi, E Flechsig… - …, 2020 - Wiley Online Library
Background Nanofiltration entails the filtering of protein solutions through membranes with
pores of nanometric sizes that have the capability to effectively retain a wide range of …

Mille-feuille paper: A novel type of filter architecture for advanced virus separation applications

S Gustafsson, P Lordat, T Hanrieder, M Asper… - Materials …, 2016 - pubs.rsc.org
Mille-feuille (“a thousand leaves”) paper is the first non-woven, wet-laid filter paper,
composed of 100% native cellulose, which is capable of removal of the “worst-case” model …

Strategies for tailoring the pore-size distribution of virus retention filter papers

S Gustafsson, A Mihranyan - ACS applied materials & interfaces, 2016 - ACS Publications
The goal of this work is to demonstrate how the pore-size distribution of the nanocellulose-
based virus-retentive filter can be tailored. The filter paper was produced using cellulose …

[HTML][HTML] Recent advances in ultrafiltration and virus filtration for production of antibodies and related biotherapeutics

EM Goodrich, DM Bohonak, PW Genest… - Approaches to the …, 2020 - Elsevier
Virus filtration and ultrafiltration are critical technologies that play unique roles in all antibody
purification processes. The need to remove both retroviral as well as potential adventitious …

Characterization of non-infectious virus-like particle surrogates for viral clearance applications

S Johnson, KA Brorson, DD Frey, AK Dhar… - Applied Biochemistry …, 2017 - Springer
Viral clearance is a critical aspect of biopharmaceutical manufacturing process validation.
To determine the viral clearance efficacy of downstream chromatography and filtration steps …

Particle concentration measurement of virus samples using electrospray differential mobility analysis and quantitative amino acid analysis

KD Cole, LF Pease III, DH Tsai, T Singh, S Lute… - … of Chromatography A, 2009 - Elsevier
Virus reference materials are needed to develop and calibrate detection devices and
instruments. We used electrospray differential mobility analysis (ES-DMA) and quantitative …

[图书][B] Single-stranded RNA phages: From molecular biology to nanotechnology

P Pumpens - 2020 - taylorfrancis.com
This is a comprehensive guide to single-stranded RNA phages (family Leviviridae), first
discovered in 1961. These phages played a unique role in early studies of molecular …

Virus retentive filters

G Miesegaes, S Lute, H Aranha… - … , Bioseparation, and Cell …, 2009 - Wiley Online Library
Ensuring the absence of detectable viruses in biopharmaceutical products is imperative from
both a regulatory and patient safety standpoint. Biopharmaceutical viral safety is the result of …

[HTML][HTML] A novel high-throughput process development screening tool for virus filtration

A Tang, I Ramos, K Newell, KD Stewart - Journal of Membrane Science, 2020 - Elsevier
Virus filtration is used extensively in mammalian cell culture derived biopharmaceutical
manufacturing processes. This processing step relies on bench scale models that require …