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Grant support
This research was funded by Universidad Politecnica de Madrid (Programa Propio UPM 2020-contratos predoctorales), Asociacion para la Difusion de Avances Oncologicos (ADAO), the Spanish Ministry of Science, Innovation and Universities (MICIU) (PID2021-122711NB-C21), Comunidad de Madrid-Doctorados industriales (IND2022/BMD-23595 and IND2023/BMD-28759) and Asociacion Espanola contra el Cancer (2022-AYUDA-33655). Nageru S.L. had no role in the design of the study; in the collection, analysis, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
Analysis of institutional authors
Sanchez-Diez, MartaCorresponding AuthorGavira-O'Neill, Clara EAuthorQuiroz-Troncoso, JosefaAuthorGonzalez-Martos, RaquelAuthorRamirez-Castillejo, CarmenCorresponding AuthorPastor, Juan ManuelAuthorAssessment of Cell Viability in Drug Therapy: IC50 and Other New Time-Independent Indices for Evaluating Chemotherapy Efficacy
Publicated to:Pharmaceutics. 17 (2): 247- - 2025-02-01 17(2), DOI: 10.3390/pharmaceutics17020247
Authors: Sanchez-Diez, Marta; Romero-Jimenez, Paula; Alegria-Aravena, Nicolas; Gavira-O'Neill, Clara E; Vicente-Garcia, Elena; Quiroz-Troncoso, Josefa; Gonzalez-Martos, Raquel; Ramirez-Castillejo, Carmen; Pastor, Juan Manuel
Affiliations
Abstract
Background/Objectives: Cell viability assays play a crucial role in cancer research and the development of effective treatments. Evaluating the efficacy of conventional treatments across different tumor profiles is essential for understanding patient resistance to chemotherapy and relapse. The IC50 index has been commonly used as a guide in these assays. The idea behind the IC50 index is to compare cell proliferation under treatment with respect to a control population exposed to the same treatment. The index requires normalization to a control and is time dependent. These aspects are disadvantages, as small variations yield different results. In this article, we propose a new method to analyze cell viability assays. Methods: This method involves calculating the effective growth rate for both control (untreated) cells and cells exposed to a range of drug doses for short times, during which exponential proliferation can be assumed. The concentration dependence of the effective growth rate gives a real estimate of the treatment on cell proliferation. A curve fit of the effective growth rate related to concentration yields the concentration corresponding to a given effective growth rate. Results: We use this estimation to calculate the IC50 index and introduce two new parameters (ICr0 and ICrmed) to compare treatment efficacy under different culture conditions or cell lines. Conclusions: In summary, this study presents a new method to analyze cell viability assays and introduces two more precise parameters, improving the comparison and evaluation of efficacy under different conditions.
Keywords
Quality index
Bibliometric impact. Analysis of the contribution and dissemination channel
The work has been published in the journal Pharmaceutics due to its progression and the good impact it has achieved in recent years, according to the agency WoS (JCR), it has become a reference in its field. In the year of publication of the work, 2025, it was in position 46/354, thus managing to position itself as a Q1 (Primer Cuartil), in the category Pharmacology & Pharmacy.
Impact and social visibility
Leadership analysis of institutional authors
There is a significant leadership presence as some of the institution’s authors appear as the first or last signer, detailed as follows: First Author (SANCHEZ DIEZ, MARTA) and Last Author (PASTOR RUIZ, JUAN MANUEL).
the authors responsible for correspondence tasks have been SANCHEZ DIEZ, MARTA and RAMIREZ CASTILLEJO, MARIA DEL CARMEN.