Byron Jacobs

Prof. Byron Jacobs

University of Johannesburg, Johannesburg, Gauteng, South Africa
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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1 February 2016 in Journal of Computational Physics
Verified
Journal Article
Closed access
CAChristopher Angstmann
Christopher Angstmann
IDI.C. Donnelly
I.C. Donnelly
Bruce HenryBruce Henry
Bruce Henry
Byron JacobsByron Jacobs
Byron Jacobs
TLT.A.M. Langlands
T.A.M. Langlands
JNJ.A. Nichols
J.A. Nichols

1 September 2017 in Chaos, Solitons & Fractals
Verified
Journal Article
Closed access
CAChristopher Angstmann
Christopher Angstmann
Bruce HenryBruce Henry
Bruce Henry
Byron JacobsByron Jacobs
Byron Jacobs
AMA.V. McGann
A.V. McGann


1 January 2015 in Abstract and Applied Analysis
Verified
Journal Article
Open access
PDF file
Byron JacobsByron Jacobs
Byron Jacobs
A novel derivation of a second-order accurate Grünwald-Letnikov-type approximation to the fractional derivative of a function is presented. This scheme is shown to be second-order accurate under certain modifications to account for poor accuracy in approximating the asymptotic behavior near the lower limit of differentiation. Some example functions are chosen and numerical results are presented to illustrate the efficacy of this new method over some other popular choices for discretizing fractional derivatives.

1 March 2019 in Communications in Nonlinear Science and Numerical Simulation
Verified
Journal Article
Closed access
CAChristopher Angstmann
Christopher Angstmann
Bruce HenryBruce Henry
Bruce Henry
Byron JacobsByron Jacobs
Byron Jacobs
AMAnna V. McGann
Anna V. McGann

4 May 2017 in Bioengineering
Verified
Journal Article
Open access
PDF file
OEOluwaseun Egbelowo
Oluwaseun Egbelowo
CHCharis Harley
Charis Harley
Byron JacobsByron Jacobs
Byron Jacobs
We extend the nonstandard finite difference method of solution to the study of pharmacokinetic–pharmacodynamic models. Pharmacokinetic (PK) models are commonly used to predict drug concentrations that drive controlled intravenous (I.V.) transfers (or infusion and oral transfers) while pharmacokinetic and pharmacodynamic (PD) interaction models are used to provide predictions of drug concentrations affecting the response of these clinical drugs. We structure a nonstandard finite difference (NSFD) scheme for the relevant system of equations which models this pharamcokinetic process. We compare the results obtained to standard methods. The scheme is dynamically consistent and reliable in replicating complex dynamic properties of the relevant continuous models for varying step sizes. This study provides assistance in understanding the long-term behavior of the drug in the system, and validation of the efficiency of the nonstandard finite difference scheme as the method of choice.