Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Kinetic modeling”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 55 records · Page 3Linked to original sources

Simulation of linear compartment models with application to nuclear medicine kinetic modeling.

Several techniques are evaluated for solving the linear ordinary differential equations arising from compartment models. The methods involve approximating the matrix exponential of the state matrix (i.e. the transition matrix). The computational efficiencies of these techniques, together with that of a general purpose differential equation solver, are compared for several models arising from radiopharmacokinetic studies. The matrix exponential calculations are performed using both Ward's Padé approximation method and an eigenvalue-eigenvector decomposition (QR factorization) of the matrix A. These two algorithms have been incorporated as simulation options into the programs of the ADAPT package. ADAPT consists of a set of high-level programs for simulation, parameter estimation and experiment design, developed primarily for basic and clinical research modeling and data analysis applications involving pharmacokinetic and pharmacodynamic processes. The advantages and disadvantages of these simulation strategies for solving linear kinetic models within a parameter estimation setting are illustrated and discussed.

Algorithms↗

Effect of wall growth on the kinetic modeling of nitrite oxidation in a CSTR.

A simple kinetic model was developed for describing nitrite oxidation by autotrophic aerobic nitrifiers in a continuous stirred tank reactor (CSTR), in which mixed (suspended and attached) growth conditions prevail. The CSTR system was operated under conditions of constant nitrite feed concentration and varying volumetric flow rates. Experimental data from steady-state conditions in the CSTR system and from batch experiments were used for the determination of the model's kinetic parameters. Model predictions were verified against experimental data obtained under transient operating conditions, when volumetric flow rate and nitrite feed concentration disturbances were imposed on the CSTR. The presented kinetic modeling procedure is quite simple and general and therefore can also be applied to other mixed growth biological systems.

Bacteria, Aerobic↗

PET kinetic modeling of 11C-acetate from projections.

Positron emission tomography (PET) image reconstruction techniques inevitably introduce inaccuracies in images. To avoid these inaccuracies in PET kinetic modeling, kinetic parameters can directly be obtained from the projections. The present work describes modeling 11C-acetate in the sinograms measured in normal and ischemic rats with the Sherbrooke small animal PET scanner. Each bin of the dynamic sinograms was decomposed in its basis functions using spectral analysis technique in conjunction with the 11C-acetate kinetic model. Homogeneous structures were clearly separated and reconstructed as well as the kinetic model parameters. Rate constants were well correlated to those obtained by means of curve fitting from images.

Acetates↗

Models for computer simulation studies of input functions for tracer kinetic modeling with positron emission tomography.

In tracer kinetic modeling with Positron Emission Tomography (PET), the direct measurement (piecewise linear approximation) of plasma time-activity curve of tracer (PTAC) is often used as the input function to estimate regional physiological parameters. However, no explicit general model is available for PTAC itself, which limits the further study of the effects of PTAC, such as PTAC measurement noise or PTAC sampling schedules, on the physiological parameters estimation. A PTAC model is proposed in this paper and compared with other four possible candidates. Eight sets of [18F]-fluoro-2-deoxy-D-glucose (FDG) experimental data were used to test the models and several statistical criteria were used to validate their adequacy. An application of the model to improve the estimation of local cerebral metabolic rate of glucose (LCMRGlc) is presented. This model is also expected to be useful for generating realistic PTAC curves in computer simulation studies of other tracers and their kinetic modeling characteristics.

Animals↗

Urea kinetic modeling for CRRT.

Urea kinetic modeling (UKM) for dialysis quantification and prescription, although widely used in chronic renal failure (CRF), has been largely absent in the acute setting. A quantitative approach to prescription of continuous renal replacement therapies (CRRTs) for acute renal failure (ARF) based on UKM is presented. For patients with a relatively constant urea generation rate, G, who are receiving a fixed dose of CRRT, blood urea nitrogen (BUN) falls in an exponential fashion, approaching a plateau level after 3 to 4 days of continuous treatment. The CRRT clearance, K, necessary to achieve a desired plateau value of BUN, Cgoal, may be computed as G/Cgoal x K for all but predilutional CRRT modalities may be calculated as equal to the effluent (dialysate plus ultrafiltrate) flow rate from the filter. Urea mass balance equations are proposed for the determination of patient G value either during the pretreatment rise in BUN or during the decline in BUN with CRRT. In the absence of a reliable estimate of patient G, a reasonable CRRT starting prescription is to set the filter effluent rate in liters per hour (approximately K) to 1.2 times the patient's body weight in kilograms divided by the desired Cgoal in milligrams per deciliter. This relationship assumes moderate hypercatabolism (normalized protein catabolic rate = 2.0 g/kg/d) and patient urea distribution volume equal to 60% of body weight. For Cgoal = 60 mg/dL, this reduces to an easily remembered formula for K (in L/hr) of twice the patient's body weight divided by 100.

Acute Kidney Injury↗

Thermodynamically feasible kinetic models of reaction networks.

The dynamics of biological reaction networks are strongly constrained by thermodynamics. An holistic understanding of their behavior and regulation requires mathematical models that observe these constraints. However, kinetic models may easily violate the constraints imposed by the principle of detailed balance, if no special care is taken. Detailed balance demands that in thermodynamic equilibrium all fluxes vanish. We introduce a thermodynamic-kinetic modeling (TKM) formalism that adapts the concepts of potentials and forces from irreversible thermodynamics to kinetic modeling. In the proposed formalism, the thermokinetic potential of a compound is proportional to its concentration. The proportionality factor is a compound-specific parameter called capacity. The thermokinetic force of a reaction is a function of the potentials. Every reaction has a resistance that is the ratio of thermokinetic force and reaction rate. For mass-action type kinetics, the resistances are constant. Since it relies on the thermodynamic concept of potentials and forces, the TKM formalism structurally observes detailed balance for all values of capacities and resistances. Thus, it provides an easy way to formulate physically feasible, kinetic models of biological reaction networks. The TKM formalism is useful for modeling large biological networks that are subject to many detailed balance relations.

Cell Physiological Phenomena↗

Gaussian kinetic model for granular gases.

A kinetic model for the Boltzmann equation is proposed and explored as a practical means to investigate the properties of a dilute granular gas. It is shown that all spatially homogeneous initial distributions approach a universal "homogeneous cooling solution" after a few collisions. The homogeneous cooling solution (HCS) is studied in some detail and the exact solution is compared with known results for the hard sphere Boltzmann equation. It is shown that all qualitative features of the HCS, including the nature of overpopulation at large velocities, are reproduced by the kinetic model. It is also shown that all the transport coefficients are in excellent agreement with those from the Boltzmann equation. Also, the model is specialized to one having a velocity independent collision frequency and the resulting HCS and transport coefficients are compared to known results for the Maxwell model. The potential of the model for the study of more complex spatially inhomogeneous states is discussed.

Journal Article↗

Combined kinetic analysis of solid-state reactions: a powerful tool for the simultaneous determination of kinetic parameters and the kinetic model without previous assumptions on the reaction mechanism.

The combined kinetic analysis implies a simultaneous analysis of experimental data representative of the forward solid-state reaction obtained under any experimental conditions. The analysis is based on the fact that when a solid-state reaction is described by a single activation energy, preexponetial factor and kinetic model, every experimental T-alpha-dalpha/dt triplet should fit the general differential equation independently of the experimental conditions used for recording such a triplet. Thus, only the correct kinetic model would fit all of the experimental data yielding a unique activation energy and preexponential factor. Nevertheless, a limitation of the method should be considered; thus, the proposed solid-state kinetic models have been derived by supposing ideal conditions, such as unique particle size and morphology. In real systems, deviations from such ideal conditions are expected, and therefore, experimental data might deviate from ideal equations. In this paper, we propose a modification in the combined kinetic analysis by using an empirical equation that fits every f(alpha) of the ideal kinetic models most extensively used in the literature and even their deviations produced by particle size distributions or heterogeneities in particle morphologies. The procedure here proposed allows the combined kinetic analysis of data obtained under any experimental conditions without any previous assumption about the kinetic model followed by the reaction. The procedure has been verified with simulated and experimental data.

Journal Article↗

WebCell: a web-based environment for kinetic modeling and dynamic simulation of cellular networks.

SUMMARY: WebCell is a web-based environment for managing quantitative and qualitative information on cellular networks and for interactively exploring their steady-state and dynamic behaviors in response to systemic perturbations. It is designed as a user-friendly web interface, allowing users to efficiently construct, visualize, analyze and store reaction network models, thereby facilitating kinetic modeling and in silico simulation of biological systems of interest. A collected model library is also available to provide comprehensive implications for cellular dynamics of the published models.

Cell Physiological Phenomena↗

Adsorption of Cu(II) and Pb(II) onto a grafted silica: isotherms and kinetic models.

The isotherms and kinetics of adsorption of lead(II) and copper(II) onto a grafted silica are studied at 20 degrees C. A commercial silica is grafted with an ethylediamine derivative, N-[3-(trimethoxysilyl)propyl]-ethylenediamine. From the Langmuir isotherms, maximum adsorption capacities of the grafted silica towards Pb(II) and Cu(II) are determined (0.184 mmol Pb(II)g-1 and 0.261 mmol Cu(II)g-1) and compared to those of non-modified silica (respectively, 0.019 and 0.036 mmol g-1). Four kinetic models, i.e., pseudo-first order, pseudo-second order, Langmuir and double-exponential are applied to fit the experimental kinetic data. The kinetic parameters are determined which allow to calculate the theoretical metal uptake as a function of time. The results are discussed and indicate the best fit is obtained with the double-exponential model. A discussion on the adsorption mechanism with respect to the double-exponential model leads to two possible interpretations: the metal uptake may follow a diffusion-controlled mechanism or a two-site adsorption process.

Adsorption↗

Equivalence of the microscopic and macroscopic models of chromatography: stochastic-dispersive versus lumped kinetic model.

The microscopic model of chromatography is a stochastic model that consists of two fundamental processes: (i) the random migration of the molecules in the mobile phase, and (ii) the random adsorption-desorption of molecules on the stationary phase contained in a chromatographic column. The diffusion and drift of the molecules in the mobile phase is described with a simple one-dimensional random walk. The adsorption-desorption process is modeled by a Poisson process that assumes exponential sojourn times of the molecules in both the mobile and the stationary phases. The microscopic, or molecular model of chromatography studied here turns out to be identical to the macroscopic lumped kinetic model of chromatography, whose solution is well known in chromatography. A complete equivalence of the two models is established via the identical expressions they provide for the band profiles.

Chromatography↗

Delayed fluorescence induction transients: mathematical modelling based on the chosen kinetic models.

The paper deals with mathematical modelling of the transients obtained by fitting of delayed fluorescence (DF) induction trace. The transients are in certain, doubtless connection with electrochemical gradient (ECG) formed across thylakoid membranes upon illumination. The fitting of the C and D transients by using consecutive model for first-order reactions (A --> B --> C) showed that they might play a role of the intermediate (B), according to scheme down bellow: ("A1 state")ECG (k1(C transient))--> C transient (k2(C transient))--> products, ("A2 state")ECG (k1(D transient))--> D transient (k2(D transient))--> products. The two ECG controlled "states" (A1 & A2) are not the same, which does not exclude some sort of proportionality. On the other hand, the E band, contributing mainly to the stationary level of DF induction trace, may be fitted by parallel model of at least two first-order reactions.

Electrochemistry↗

Efficient chemical kinetic modeling through neural network maps.

An approach to modeling nonlinear chemical kinetics using neural networks is introduced. It is found that neural networks based on a simple multivariate polynomial architecture are useful in approximating a wide variety of chemical kinetic systems. The accuracy and efficiency of these ridge polynomial networks (RPNs) are demonstrated by modeling the kinetics of H(2) bromination, formaldehyde oxidation, and H(2)+O(2) combustion. RPN kinetic modeling has a broad range of applications, including kinetic parameter inversion, simulation of reactor dynamics, and atmospheric modeling.

Algorithms↗

Theoretical approach and clinical application of kinetic modelling in dialysis.

Using kinetic modelling for shaping profile dialysis, we present a promising approach to improve the cardiovascular stability of patients during dialysis treatment. In order to obtain an insight into the physiological mechanisms of increased stability, a model considering alterations of electrolytes and water distribution and of acid-base status was developed. This algorithm was used for the evaluation of 114 dialysis sessions, which were performed with highly individualised profiles. Each profile was developed for one patient by trying empirically to prevent episodes of hypotension as well as other clinical problems throughout dialysis. The main advantage of profile dialysis compared to standard bicarbonate dialysis, for example, is a reduced water influx into the cell during the treatment. According to our clinical and theoretical results a correlation between water influx into the cell and time of occurrence of hypotensive episodes in individuals can be assumed. Hypotension usually starts after 0.5 litres of water have entered the intracellular space, regardless of the time necessary for this fluid shift.

Acid-Base Equilibrium↗

Kinetic modeling of teboroxime using dynamic SPECT imaging of a canine model.

UNLABELLED: The tomographic utility of 99mTc-labeled teboroxime has been limited because of its fast washout from the heart, which requires rapid data acquisitions that have not been feasible until the recent development of multidetector SPECT systems. METHODS: Using a three-detector SPECT system to acquire dynamic tomographic data every 10.2 sec, we investigated the potential of modeling the kinetics of teboroxime to develop a sensitive and quantitative measure of cardiac perfusion. Seven studies were performed on four dogs; in three of the studies the LAD artery was occluded. The three-dimensional activity distributions were reconstructed and were corrected for attenuation using a transmission scan. Time-activity curves from the blood and tissue were fit to a two-compartment model with two-way exchange. RESULTS: Performing attenuation correction during the reconstruction process affected the washin parameter k21 significantly (p < 0.0001). The washin parameter k21 also decreased significantly (p < 0.002) when the LAD was occluded. CONCLUSIONS: The results indicate that the washin of teboroxime in myocardial tissue (k21) measured using dynamic SPECT imaging and kinetic modeling is an indicator of myocardial blood flow.

Algorithms↗

Adequacy of dialysis: marker molecules and kinetic modeling.

The effective use of kinetic modeling to assess adequacy of dialysis, based upon marker molecules, is in its infancy. However, for the patient, perhaps the most identifiable benefit of modeling is that the technical parameters of the therapy are at least being measured and monitored. With regard to choice of marker molecules, the National Dialysis Cooperative Study (NCDS) group, in choosing urea as the reference molecule, has given a useful impetus to its wider use. Since urea is directly connected with dietary protein intake and its net generation is also directly correlated with that of other metabolites, its application as a marker molecule makes good sense. Analysis of the NCDS data has permitted identification of a very useful quantitative parameter of minimal dialysis therapy based on urea clearance and distribution volume and dialysis time. For thrice-weekly dialysis, normalized whole body urea clearance (Kt/V) should be greater than or equal to 1.0 and less than approximately 1.5. Although this alone does not guarantee adequate dialysis, it does alert the dialysis staff to the potential for both under- and over-dialysis. It would thus appear that currently the most reliable and useful means by which to apply modeling techniques to dialysis therapy is urea kinetics. In time, the application of more broad-based modeling techniques to dialysis therapy will provide more clearly identifiable clinical benefits, as well as the already realizable economic benefits.

Acetates↗

New kinetic models for the hepatitis C virus.

Viral kinetic modeling has played an important role in the analysis of HCV RNA decay after the initiation of antiviral therapy. Models have provided a means of evaluating the antiviral effectiveness of therapy, of estimating parameters such as the rate of virion clearance and the rate of clearance of hepatitis C virus (HCV)-infected cells, and they have suggested mechanisms of action for both interferon and ribavirin. Nevertheless, the models that were originally formulated were unable to explain all of the observed HCV RNA profiles. We provide an update on the state of HCV kinetic modeling and discuss new models that have taken into consideration the different pharmacokinetics of standard and pegylated forms of interferon, allow for changes in drug effectiveness as drug concentrations fall between dosing intervals, and that have incorporated alanine aminotransferase kinetics and aspects of immune responses to provide a more comprehensive picture of the biology underlying changes in HCV RNA during therapy.

Antiviral Agents↗

Kinetic modeling of continuous flow peritoneal dialysis.

Kinetic models have been derived for analysis of the effects on peritoneal urea clearance (Kp) of continuous single-pass flow of fresh peritoneal dialysate and continuous flow of peritoneal dialysate recirculating through an external dialyzer. Generalized solution of the models shows that both predict Kp to be a well-defined function of the peritoneal mass transfer coefficient (MTC) and the dialysance (D) of the external dialyzer, while the MTC is a function of the rate and distribution of dialysate flow. Thus the models should be useful to guide studies to optimize CFPD. Analysis of reported in vivo data indicate that with dialysate flow rate and D both in the range of 200 ml/min, MTC levels of 60-70 ml/min and Kp levels of 50 ml/min can be achieved. If the model predictions are verified in vivo, 8-hour overnight CFPD 6 nights/week could provide the average-size anephric patient a weekly stdKt/V of 3.2 which is competitive with daily hemodialysis. Kinetic modeling of ultrafiltration indicated ultrafiltration rates 0.2-0.3 L/hr should be achieved with 1.0-1.25% dextrose dialysate. The model shows average rates of glucose absorption can theoretically be reduced by 33% compared to CAPD with the same amount of fluid removal.

Absorption↗