Elena Dreassi

Prof. Elena Dreassi

Dipartimento Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, 53100 Siena, Italy
orcid

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

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

Representative Publications

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12 January 2017 in Lipids
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Journal Article
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Elena DreassiElena Dreassi
Elena Dreassi
ACAnnarita Cito
Annarita Cito
AZAssunta Zanfini
Assunta Zanfini
LMLara Materozzi
Lara Materozzi
MBMaurizio Botta
Maurizio Botta
VFValeria Francardi
Valeria Francardi

1 January 2010 in LWT
Verified
Journal Article
Closed access
AZAssunta Zanfini
Assunta Zanfini
GCGianfranco Corbini
Gianfranco Corbini
CRCaterina La Rosa
Caterina La Rosa
Elena DreassiElena Dreassi
Elena Dreassi

28 March 2011 in Journal of Medicinal Chemistry
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Journal Article
Closed access
MRMarco Radi
Marco Radi
Elena DreassiElena Dreassi
Elena Dreassi
Chiara BrulloChiara Brullo
Chiara Brullo
Emmanuele CrespanEmmanuele Crespan
Emmanuele Crespan
CTCristina Tintori
Cristina Tintori
MBMaurizio Botta
Maurizio Botta

Verified
Journal Article
Open access
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ABAnnalaura BRAI
Annalaura BRAI
Federica PoggialiniFederica Poggialini
Federica Poggialini
CVChiara Vagaggini
Chiara Vagaggini
Claudia PasqualiniClaudia Pasqualini
Claudia Pasqualini
Sauro SimoniSauro Simoni
Sauro Simoni
Elena DreassiElena Dreassi
Elena Dreassi
The progression of drugs into clinical phases requires proper toxicity assessment in animals and the correct identification of possible metabolites. Accordingly, different animal models are used to preliminarily evaluate toxicity and biotransformations. Rodents are the most common models used to preliminarily evaluate the safety of drugs; however, their use is subject to ethical consideration and elevated costs, and strictly regulated by national legislations. Herein, we developed a novel, cheap and convenient toxicity model using Tenebrio molitor coleoptera (TMC). A panel of 15 drugs—including antivirals and antibacterials—with different therapeutic applications was administered to TMC and the LD50 was determined. The values are comparable with those already determined in mice and rats. In addition, a TMC model was used to determine the presence of the main metabolites and in vivo pharmacokinetics (PK), and results were compared with those available from in vitro assays and the literature. Taken together, our results demonstrate that TMC can be used as a novel and convenient preliminary toxicity model to preliminarily evaluate the safety of experimental compounds and the formation of main metabolites, and to reduce the costs and number of rodents, according to 3R principles.

1 June 1996 in Journal of Pharmaceutical and Biomedical Analysis
Verified
Journal Article
Closed access
SPS. Pinzauti
S. Pinzauti
Paola GratteriPaola Gratteri
Paola Gratteri
SFS. Furlanetto
S. Furlanetto
Paola Angela MuraPaola Angela Mura
Paola Angela Mura
Elena DreassiElena Dreassi
Elena Dreassi
RPR. Phan-Tan-Luu
R. Phan-Tan-Luu

9 June 2022 in Food Chemistry
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Journal Article
Closed access
ABAnnalaura Brai
Annalaura Brai
CTClaudia Immacolata Trivisani
Claudia Immacolata Trivisani
CVChiara Vagaggini
Chiara Vagaggini
RSRoberto Stella
Roberto Stella
RARoberto Angeletti
Roberto Angeletti
Elena DreassiElena Dreassi
Elena Dreassi