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Trastuzumab quantification in serum: a new,rapid, robust ELISA assay based on a mimetic peptide that specifically recognizes trastuzumab
Authors:Barbara Cardinali  Gianluigi Lunardi  Enrico Millo  Andrea Armirotti  Gianluca Damonte  Aldo Profumo  Stefania Gori  Giuseppina Iacono  Alessia Levaggi  Lucia Del Mastro
Affiliation:1. Development of Innovative Therapies Unit, IRCCS AOU San Martino-IST, 16132, Genoa, Italy
2. Medical Oncology Unit, Sacro Cuore Don Calabria Hospital, Via Sempreboni, 5, 37024, Negrar, Verona, Italy
3. Department of Experimental Medicine (DIMES), Section of Biochemistry, University of Genoa, 16132, Genoa, Italy
4. Center of Excellence for Biomedical Research, University of Genoa, 16132, Genoa, Italy
6. Drug Discovery and Development, Italian Institute for Technology (IIT), 16163, Genoa, Italy
5. Biopolymers and Proteomics Unit, IRCCS AOU San Martino-IST, 16132, Genoa, Italy
Abstract:Trastuzumab, a humanized monoclonal antibody directed against the epidermal growth factor receptor 2 (HER2), is a milestone in the treatment of HER2-overexpressing breast cancer patients. An enzyme-linked immunosorbent assay (ELISA) for trastuzumab has been developed for routine use in the laboratory to support clinical and pharmacokinetic studies to optimize therapy. The method relies on an antigen peptide linked to a 96-well plate via the streptavidin/biotin system. The peptide sequence mimics the extracellular portion of the HER2 receptor that is recognized by trastuzumab. The calibration range of the assay is 10 to 360 ng/mL per well, corresponding to a trastuzumab serum concentration from 5 to 180 μg/mL with a lower limit of quantification of 10 μg/mL. Validation results demonstrate that trastuzumab can be accurately and precisely quantified in human serum using this assay. The procedure was also tested in sera obtained from breast cancer patients to evaluate trastuzumab serum levels, confirming the applicability of method that could be a valid assay to use in daily laboratory practice.
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