A sandwich ELISA for the quantification of the anticancer peptide CIGB-552 in human plasma

CIGB-552 is a synthetic anticancer peptide that has been evaluated in vitro and in vivo in lung and colon cancer models. To optimize therapy in the clinic, pharmacokinetic studies are necessary. Previously, a sandwich-type enzyme-linked immunosorbent assay (ELISA) had been developed by our working group for the quantification of CIGB-552 in biological matrices. The objective of this work was to carry out the full validation of the ELISA to support its application in clinical trials. First, we obtained a polyclonal antibody specific for CIGB-552 and with purity greater than 95 %. The lower limit of quantification and the upper limit of quantification were 3125 ng/ml and 200 ng/ml, respectively. The method is exact and precise in the quantification of the peptide with relative error and coefficient of variation values less than 20 %. The ELISA is specific in the presence of CIGB-552 metabolites in the sample, and also presents robustness to certain protocol variations. In summary, the validated ELISA meets the requirements for its application in upcoming clinical trials as part of pharmacokinetic studies.

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Publication Details

Journal
Analytical Biochemistry
Published
2024-11-27
DOI
https://doi.org/10.1016/j.ab.2024.115725
Citations
4
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
1.62

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article

A sandwich ELISA for the quantification of the anticancer peptide CIGB-552 in human plasma

Antonio Guardia, Julio R. Fernández, Ania Cabrales, Norlan Bressler Hernández et al.
4 citations
Analytical Biochemistry
Monoclonal and Polyclonal Antibodies Research
1.62
article

A sandwich ELISA for the quantification of the anticancer peptide CIGB-552 in human plasma

Antonio Guardia, Julio R. Fernández, Ania Cabrales, Norlan Bressler Hernández, Hilda Garay, Gilda Lemos, A Arteaga, Brizaida Oliva Arguellez
article en
4 citations

Abstract

CIGB-552 is a synthetic anticancer peptide that has been evaluated in vitro and in vivo in lung and colon cancer models. To optimize therapy in the clinic, pharmacokinetic studies are necessary. Previously, a sandwich-type enzyme-linked immunosorbent assay (ELISA) had been developed by our working group for the quantification of CIGB-552 in biological matrices. The objective of this work was to carry out the full validation of the ELISA to support its application in clinical trials. First, we obtained a polyclonal antibody specific for CIGB-552 and with purity greater than 95 %. The lower limit of quantification and the upper limit of quantification were 3125 ng/ml and 200 ng/ml, respectively. The method is exact and precise in the quantification of the peptide with relative error and coefficient of variation values less than 20 %. The ELISA is specific in the presence of CIGB-552 metabolites in the sample, and also presents robustness to certain protocol variations. In summary, the validated ELISA meets the requirements for its application in upcoming clinical trials as part of pharmacokinetic studies.

Analytical BiochemistryVol. 698
Centro de Ingeniería Genética y Biotecnología (CU)
Ministerio de Ciencia, Tecnología y Medio Ambiente
Good health and well-being
Openalex Percentile: Top 15%
Monoclonal and Polyclonal Antibodies Research
1.62
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A sandwich ELISA for the quantification of the anticancer peptide CIGB-552 in human plasma — Antonio Guardia, Julio R. Fernández, et al. · Analytical Biochemistry (2024) | TGRS Research Map | TGRS