Andrea Zattoni

Prof. Andrea Zattoni

1. Department of Chemistry G. Ciamician, University of Bologna, Bologna, Italy
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orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

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

Representative Publications

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1 February 2021 in Journal of Chromatography A
Verified
Journal Article
Closed access
VMValentina Marassi
Valentina Marassi
SMSerena Maggio
Serena Maggio
MBMichela Battistelli
Michela Battistelli
VSVilberto Stocchi
Vilberto Stocchi
Andrea ZattoniAndrea Zattoni
Andrea Zattoni
BRBarbara Roda
Barbara Roda

1 June 2002 in Journal of Separation Science
Verified
Journal Article
Closed access
PDF file
PRPierluigi Reschiglian
Pierluigi Reschiglian
Barbara RodaBarbara Roda
Barbara Roda
Andrea ZattoniAndrea Zattoni
Andrea Zattoni
BMByung Ryul Min
Byung Ryul Min
MMMyeong Hee Moon
Myeong Hee Moon

8 June 2018 in Analytical and Bioanalytical Chemistry
Verified
Journal Article
Closed access
PDF file
Barbara RodaBarbara Roda
Barbara Roda
VMValentina Marassi
Valentina Marassi
Andrea ZattoniAndrea Zattoni
Andrea Zattoni
FBFrancesco Borghi
Francesco Borghi
RAResmi Anand
Resmi Anand
SMSandra Monti
Sandra Monti

4 January 2023 in Chemosensors
Verified
Journal Article
Open access
PDF file
AZAlessandro Zappi
Alessandro Zappi
VMValentina Marassi
Valentina Marassi
SGStefano Giordani
Stefano Giordani
NKNicholas Kassouf
Nicholas Kassouf
Barbara RodaBarbara Roda
Barbara Roda
Dora MelucciDora Melucci
Dora Melucci
Instrument automation, technological advancements and improved computational power made separation science an extremely data-rich approach, requiring the use of statistical and data analysis tools that are able to optimize processes and combine multiple outputs. The use of chemometrics is growing, greatly improving the ability to extract meaningful information. Separation–multidetection generates multidimensional data, whose elaboration should not be left to the discretion of the operator. However, some applications or techniques still suffer from the lack of method optimization through DoE and downstream multivariate analysis, limiting their potential. This review aims at summarizing how chemometrics can assist analytical chemists in terms of data elaboration and method design, focusing on what can be achieved by applying chemometric approaches to separation science. Recent applications of chemometrics in separation analyses, in particular in gas, liquid and size-exclusion chromatography, together with field flow fractionation, will be detailed to visualize the state of the art of separation chemometrics, encompassing volatile, soluble and solid (colloidal) analytes. The samples considered will range from food chemistry and environmental chemistry to bio/pharmaceutical science.

23 August 2023 in Molecules
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Journal Article
Open access
PDF file
SGStefano Giordani
Stefano Giordani
VMValentina Marassi
Valentina Marassi
APAnna Placci
Anna Placci
Andrea ZattoniAndrea Zattoni
Andrea Zattoni
Barbara RodaBarbara Roda
Barbara Roda
Pierluigi ReschiglianPierluigi Reschiglian
Pierluigi Reschiglian
Field-flow fractionation (FFF) is a family of single-phase separative techniques exploited to gently separate and characterize nano- and microsystems in suspension. These techniques cover an extremely wide dynamic range and are able to separate analytes in an interval between a few nm to 100 µm size-wise (over 15 orders of magnitude mass-wise). They are flexible in terms of mobile phase and can separate the analytes in native conditions, preserving their original structures/properties as much as possible. Molecular biology is the branch of biology that studies the molecular basis of biological activity, while biotechnology deals with the technological applications of biology. The areas where biotechnologies are required include industrial, agri-food, environmental, and pharmaceutical. Many species of biological interest belong to the operational range of FFF techniques, and their application to the analysis of such samples has steadily grown in the last 30 years. This work aims to summarize the main features, milestones, and results provided by the application of FFF in the field of molecular biology and biotechnology, with a focus on the years from 2000 to 2022. After a theoretical background overview of FFF and its methodologies, the results are reported based on the nature of the samples analyzed.

26 August 2022 in Molecules
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Journal Article
Open access
PDF file
VMValentina Marassi
Valentina Marassi
MMMarco Macis
Marco Macis
SGStefano Giordani
Stefano Giordani
LFLucia Ferrazzano
Lucia Ferrazzano
ATAlessandra Tolomelli
Alessandra Tolomelli
WCWalter Cabri
Walter Cabri
Aggregation is among the most critical parameters affecting the pharmacological and safety profile of peptide Active Pharmaceutical Ingredients (APIs). For this reason, it is of utmost importance to define the exact aggregation state of peptide drugs, particularly when the API is marketed as a ready-to-use solution. Consequently, appropriate non-destructive techniques able to replicate the peptide environment must be employed. In our work, we exploited Asymmetrical Flow Field-Flow Fractionation (AF4), connected to UV, dRI, fluorescence, and MALS detectors, to fully characterize the aggregation state of Liraglutide, a peptide API used for the treatment of diabetes type 2 and chronic obesity. In previous studies, Liraglutide was hypothesized to assemble into hexa-octamers in phosphate buffer, but no information on its behavior in the formulation medium was provided up to now. The method used allowed researchers to work using formulation as the mobile phase with excellent recoveries and LoQ/LoD, discerning between stable and degraded samples, and detecting, when present, aggregates up to 108 Da. The native state of Liraglutide was assessed and found to be an association into pentamers, with a non-spherical conformation. Combined to benchmark analyses, the sameness study was complete and descriptive, also giving insight on the aggregation process and covalent/non-covalent aggregate types.