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Biomedical subjects

F T Lindstrom

Publications and source records attributed to F T Lindstrom.

11 recordsLinked to original sources
PubMed1985

Waste disposal technologies for polychlorinated biphenyls.

Improper practices in the disposal of polychlorinated biphenyl (PCB) wastes by land burial, chemical means and incineration distribute these chemicals and related compounds such as polychlorinated dibenzofurans (PCDFs) and polychlorinated dibenzodioxins (PCDDs) throughout the environment. The complete range of methods for disposal that have been proposed and are in use are examined and analyzed, with emphasis given to the two most commonly used methods: land burial and incineration. The understanding of aquifer contamination caused by migration of PCBs from subsurface burial sites requires a description of the physical, chemical and biological processes governing transport in unsaturated and saturated soils. For this purpose, a model is developed and solved for different soil conditions and external driving functions. The model couples together the fundamental transport phenomena for heat, mass, and moisture flow within the soil. To rehabilitate a contaminated aquifer, contaminated groundwaters are withdrawn through drainage wells, PCBs are extracted with solvents or activated carbon and treated by chemical, photochemical or thermal methods. The chemical and photochemical methods are reviewed, but primary emphasis is devoted to the use of incineration as the preferred method of disposal. After discussing the formation of PCDFs and PCDDs during combustion from chloroaromatic, chloroaliphatic, as well as organic and inorganic chloride precursors, performance characteristics of different thermal destructors are presented and analyzed. To understand how this information can be used, basic design equations are developed from governing heat and mass balances that can be applied to the construction of incinerators capable of more than 99.99% destruction with minimal to nondetectable levels of PCDFs and PCDDs.

Benzofurans↗
PubMed1985

A mathematical model for the transport and fate of organic chemicals in unsaturated/saturated soils.

A mathematical model, simulating the transport and fate of nonionizable organic compounds in unsaturated/saturated porous media (soils) in a terrestrial microcosm has been developed. Using the principles of water mass, momentum, heat energy and chemical mass balance, the three fields: moisture, temperature, and liquid phase chemical concentration are solved for simultaneously by coupling the soil slab to an environmentally realistic air-soil interface (a dynamic free boundary) conditions and a prescribed height water table. The environmental conditions at the soil surface-air chamber interface are easily changed, via geometric scaling factors, to simulate either an open agricultural field or a landfill type of situation. Illustrative simulation runs examine the effects of different soil-chemical characteristics on hydrological and chemical concentration profiles.

Biodegradation, Environmental↗
PubMed1984

Estimation of population pharmacokinetic parameters using destructively obtained experimental data: a simulation study of the one-compartment open model.

A simulation study of the one-compartment open pharmacokinetic model has been made. The population pharmacokinetic parameters which characterize the population of drug residues over time are assumed to be stochastic. A general theoretical model framework for parameter estimation via the method of extended least squares is presented. Formulas approximating the required mean and variance time functions are developed and subsequently used in the simulation study. The effects of four different designs in four different animal populations are presented. The simulated data are those of the single observation per animal per time point type. The characterizing population pharmacokinetic parameters have been analyzed for bias and reliability in both a naive and second-order mean model. Recommendations for choosing an appropriate sampling design are included.

Analysis of Variance↗
PubMed1980

In vitro binding of 14C-labeled acidic compounds to serum albumin and their tissue distribution in the rat.

The acidic compounds, such as phenoxyacetic acids, substituted benzoic acids, or acetylsalicylic acid, were found to bind to bovine serum albumin (BSA). Among phenoxyacetic acids, the binding affinity to BSA was highest for 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), which was approximately 4-, 24-, and 160-fold greater than those for 2,4-dichlorophenoxyacetic acid (2,4-D), o-chlorophenoxyacetic acid (CPA), and phenoxyacetic acid (PAA), respectively. There were two bound to serum albumins of other mammalian species. The binding affinity varied among species and also depended on the chemicals. However, the order of binding affinity in the albumin of each species remained the same as observed in BSA with few exceptions. Blood/tissue ratios of 14C from rats dosed with these 14C-labeled acids were highly correlated with the logarithm of the binding affinity constantsaffinity constants.

Animals↗
PubMed1977

Diffusion model for drug release from suspensions I: theoretical considerations.

A new mathematical model based on physicochemical principles is presented; it does not require a "diffusion layer" for the release of a suspended drug from a semisolid vehicle. This general model has wide range application to systems where release is controlled by the diffusion rate or dissolution rate of a drug. The appropriate mathematical relationships are derived and evaluated. Theoretical drug concentration distributions in the vehicle and a membrane and the predicted cumulative drug mass uptake by blood under specified conditions are presented. The dissolution rate of solid drug in the vehicle markedly influences predicted drug release using the model presented. It is anticipated that the model will stimulate further research to confirm or reject the assumption that the dissolution rate may be slow enough to be important in the systems studied.

Biological Transport↗
PubMed1977

Diffusion model for drug release from suspensions II: release to a perfect sink.

Numerical mathematical methods are applied to a diffusion model based on physicochemical principles to predict drug release from suspensions of drug in semisolid vehicles. The predicted mass of drug released versus time curves using this model are in agreement with some reported experimental data but differ from predictions using the classical model for semisolid suspensions. The differences are discussed in relation to the drug dissolution rate and diffusion rate in the vehicle.

Biological Transport↗
PubMed1976

Distribution of HEOD (dieldrin) in mammals: III. Transport--transfer.

A mathematical model simulating the blood transport and tissue residue distributions of the highly toxic and highly lipid soluble pesticide dieldrin in mammals is presented. This model is a significant improvement over our previously published preliminary model for dieldrin distribution in mammals. The assumptions and working hypotheses of the model are presented and used in generating a set of differential equations based upon mass balance principles. Two simulation cases are examined. The first simply demonstrates the gross features of: 1) Transport limiting conditions; 2) equal transport-equal membrane transfer conditions, and 3) membrane transfer limit conditions. The second studies a single tissue (the blood-brain barrier case) example of the above mentioned conditions. All simulations made were conducted for a hypothetical mature male rate of the average Wistar type eating food ad lib.

Animals↗
PubMed1975

Distribution of HEOD (dieldrin) in mammals: II. some applications of the preliminary model.

The preliminary model of the lipid-phase pharmacokinetics of dieldrin in mammals is applied to evaluation of the probable role of auto-induction, the effect(s) of growth, and the role of compartmentalization. Realistic simulations and comparison to actual data permit the conclusion to be drawn that induction of its own metabolism plays a relatively monor role in the distribution and level of dieldrin residues. Although some of the effects of growth are resonably well simulated, the model as constructed does not permit compartmentalization. It was concluded that the model should be revised to include aspects of the as-yet quantitatively unknown intracellular binding and membrane transport within the flow-limited model.

Adipose Tissue↗