Cristiana Boi

Prof. Cristiana Boi

Department of Civil, Chemical, Environmental and Materials Engineering, Alma Mater Studiorum-Università di Bologna, via Terracini 34, 40131 Bologna, Italy
orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2007 in Journal of Chromatography B
Verified
Journal Article
Closed access
Cristiana BoiCristiana Boi
Cristiana Boi

3 January 2023 in Biotechnology Advances
Verified
Journal Article
Closed access
SGSara Giancaterino
Sara Giancaterino
Cristiana BoiCristiana Boi
Cristiana Boi

1 February 2020 in Journal of Chromatography A
Verified
Journal Article
Closed access
Cristiana BoiCristiana Boi
Cristiana Boi
AMAndrea Malavasi
Andrea Malavasi
RCRuben G. Carbonell
Ruben G. Carbonell
GGGary Gilleskie
Gary Gilleskie

1 August 2007 in Journal of Chromatography A
Verified
Journal Article
Closed access
Cristiana BoiCristiana Boi
Cristiana Boi
SDSimone Dimartino
Simone Dimartino
Giulio SartiGiulio Sarti
Giulio Sarti

1 May 2008 in Biotechnology Progress
Verified
Journal Article
Closed access
PDF file
Cristiana BoiCristiana Boi
Cristiana Boi
SDSimone Dimartino
Simone Dimartino
Giulio SartiGiulio Sarti
Giulio Sarti
Recovery of antibodies with Protein A affinity chromatography columns has become the standard for the biotechnology industry. Membrane affinity chromatography has not yet experienced extensive application due to the lower capacity of membrane supports compared to chromatographic beads. In this work, new affinity membranes endowed with an interesting binding capacity for human IgG are studied in view of their application in the capturing step of a monoclonal antibody production process. The membranes have been extensively tested with pure IgG solutions and with a cell culture supernatant containing IgG1. The effects of feed flow rate and IgG concentration on the separation performances have been studied in detail, considering in particular binding capacity, selectivity and recovery. These new high capacity affinity membranes appear good candidates to avoid the throughput limitations and other well‐known drawbacks of traditional bead‐based chromatographic columns.

24 December 2019 in Membranes
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Journal Article
Open access
PDF file
ELEleonora Lalli
Eleonora Lalli
JSJouciane S. Silva
Jouciane S. Silva
Cristiana BoiCristiana Boi
Cristiana Boi
Giulio SartiGiulio Sarti
Giulio Sarti
Affinity capture represents an important step in downstream processing of proteins and it is conventionally performed through a chromatographic process. The performance of this step highly depends on the type of matrix employed. In particular, resin beads and convective materials, such as membranes and monoliths, are the commonly available supports. The present work deals with non-competitive binding of bovine serum albumin (BSA) on different chromatographic media functionalized with Cibacron Blue F3GA (CB). The aim is to set up the development of the purification process starting from the lab-scale characterization of a commercially available CB resin, regenerated cellulose membranes and polymeric monoliths, functionalized with CB to identify the best option. The performance of the three different chromatographic media is evaluated in terms of BSA binding capacity and productivity. The experimental investigation shows promising results for regenerated cellulose membranes and monoliths, whose performance are comparable with those of the packed column tested. It was demonstrated that the capacity of convective stationary phases does not depend on flow rate, in the range investigated, and that the productivity that can be achieved with membranes is 10 to 20 times higher depending on the initial BSA concentration value, and with monoliths it is approximately twice that of beads, at the same superficial velocity.