Paul A. Valle

Dr. Paul A. Valle

Instituto Tecnológico de Tijuana, Tijuana, Baja California, Mexico
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

View All Publications
1 November 2016 in Communications in Nonlinear Science and Numerical Simulation
Verified
Journal Article
Closed access
Paul A. VallePaul A. Valle
Paul A. Valle
KSKonstantin E. Starkov
Konstantin E. Starkov
LCLuis N. Coria
Luis N. Coria

1 July 2019 in Bulletin of Mathematical Biology
Verified
Journal Article
Closed access
PDF file
Paul A. VallePaul A. Valle
Paul A. Valle
LCLuis N. Coria
Luis N. Coria
YSYolocuauhtli Salazar
Yolocuauhtli Salazar

1 February 2021 in Applied Mathematical Modelling
Verified
Journal Article
Closed access
Paul A. VallePaul A. Valle
Paul A. Valle
LCLuis N. Coria
Luis N. Coria
KCKarla D. Carballo
Karla D. Carballo

1 February 2017 in Journal of Physics: Conference Series
Verified
Conference Paper
Open access
PDF file
AKAndrei Korobeinikov
Andrei Korobeinikov
KSKonstantin E Starkov
Konstantin E Starkov
Paul A. VallePaul A. Valle
Paul A. Valle

22 April 2021 in Cancers
Verified
Journal Article
Open access
PDF file
Paul A. VallePaul A. Valle
Paul A. Valle
LCLuis N. Coria
Luis N. Coria
CPCorina Plata
Corina Plata
This paper is devoted to exploring personalized applications of cellular immunotherapy as a control strategy for the treatment of chronic myelogenous leukemia described by a dynamical system of three first-order ordinary differential equations. The latter was achieved by applying both the Localization of Compact Invariant Sets and Lyapunov’s stability theory. Combination of these two approaches allows us to establish sufficient conditions on the immunotherapy treatment parameter to ensure the complete eradication of the leukemia cancer cells. These conditions are given in terms of the system parameters and by performing several in silico experimentations, we formulated a protocol for the therapy application that completely eradicates the leukemia cancer cells population for different initial tumour concentrations. The formulated protocol does not dangerously increase the effector T cells population. Further, complete eradication is considered when solutions go below a finite critical value below which cancer cells cannot longer persist; i.e., one cancer cell. Numerical simulations are consistent with our analytical results.

11 August 2021 in Symmetry
Verified
Journal Article
Open access
PDF file
BGBlanca E. Garcia
Blanca E. Garcia
ETEmmanuel Rodríguez Talavera
Emmanuel Rodríguez Talavera
YSYolocuauhtli Salazar
Yolocuauhtli Salazar
Paul A. VallePaul A. Valle
Paul A. Valle
Adriana Carolina Flores-GallegosAdriana Carolina Flores-Gallegos
Adriana Carolina Flores-Gallegos
RRRaul Rodriguez
Raul Rodriguez
Predictive models may be considered a tool to ensure food quality as they provide insights that support decision making on the design of processes, such as fermentation. Objective: To formulate a mathematical model that describes the growth of lactic acid bacteria (LAB) in batch fermentation. Methodology: Based on real-life experimental data from eight LAB strains, we formulated a primary model in the form of a third-degree polynomial function that successfully describes the four phases observed in LAB growth, i.e., lag, exponential, stationary, and death. Our cubic mathematical model allows us to understand the fundamental nonlinear dynamics of LAB as well as its time-variant dependencies. Parameters of the model are written in terms of initial biomass, maximum biomass, maximum growth rate, and lag phase duration. Further, a statistical analysis was performed to compare our cubic primary model with the ones proposed by Gompertz, Baranyi, and Vázquez-Murado by computing the coefficient of determination R2, the residual sum of squares RSS, and the Akaike Information Criterion AIC. Results: The average statistical results from the cubic model are as follows: R2=0.820 providing a better fit than the other three models, RSS=0.658 and AIC=−6.499, where both values are lower than the other models considered in this study. Conclusion: The cubic primary model formulated in this work describes the behavior of biomass as it accurately represents the four phases of biomass growth in batch fermentation process.