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Biomedical subjects

A M Lenhoff

Publications and source records attributed to A M Lenhoff.

23 records · Page 2Linked to original sources

The effects of axial diffusion and permeability barriers on the transient response of tissue cylinders. II. Solution in time domain.

A mathematical description of transient mass transfer in a Krogh tissue cylinder, for which a solution in transform space was presented previously, is solved in the time domain. The solution is found in the form of an expansion in terms of the eigenfunctions of a non-self-adjoint differential operator, with the eigenvalues being found by way of a computational scheme which makes use of the known characteristics of the constitutive compartments of the system. The solution is compared with previous solutions of both a complete and an approximate nature, and two modifications of the single-phase axial dispersion model are found to be especially useful: the previously-used flow-limited approximation is satisfactory for highly permeable solutes, while the apparently novel barrier-limited approximation is accurate for poorly permeable solutes at the early times of most experimental interest. Although the neglect of axial diffusion does not affect the qualitative nature of the solution, e.g. in predicting a bimodal response curve, significant discrepancies shed doubt on this practice when truly impulsive inputs are used. The results obtained raise several questions regarding existing approaches to interpretation of indicator dilution experiments. These include the use of extraction ratios and of exponential extrapolation of the tails of response curves.

Capillary Permeability↗

Microcirculatory mass transfer.

The dynamics of Krogh tissue cylinders and related structures are critically reviewed to determine the roles of underlying transport and reaction processes, and the interactions between them. Emphasis is put on the gaining of insight through efficient scaling procedures, and discussion is organized about the time constants characteristic of these structures and the processes occurring in them. The basis of discussion is a new analytic solution technique which provides a formal description of indefinitely large arrays of parallel interacting elements and which includes both axial diffusion and uniform convection as well as first or zero order reaction within each element. The solution has the form of an expansion in the eigenfunctions of a non-self-adjoint differential operator. Comparison of model predictions with previously available results identifies the useful parameter ranges of analytic approximations and determines the accuracy of existing numerical procedures.

Biological Transport, Active↗

Correlation between the osmotic second virial coefficient and the solubility of proteins.

A correlation between the osmotic second virial coefficient and the solubility of proteins is derived from classical thermodynamics to support an empirical relation previously found by Wilson and co-workers (1). The model is based on the equality of fugacities of the protein in the equilibrium phases, with the details of the model depending on the standard state used. The parameters in this model have been fitted to data for several systems, mainly with lysozyme as the protein. The model is found to describe experimental data, with variations in protein concentration, salt type and concentration, temperature, and pH, both qualitatively and quantitatively. Agreement between the model and the experimental data is very good for protein solubilities up to 30 mg/mL. Above this value the model underpredicts the experimental data, probably as a result of multibody interactions that are not included in the model here. Variations of the model parameters with protein type, temperature, pH, and salt type are discussed.

Hydrogen-Ion Concentration↗

STM and AFM in biotechnology.

Scanning tunneling microscopy (STM) and atomic force microscopy (AFM) are capable of providing atomic-scale images, as well as insights into functional characteristics, of surfaces. Biological materials can be studied by depositing them on appropriate substrates, and samples have been imaged with varying degrees of resolution. In this review, the principles of STM and AFM are summarized, and practical aspects of implementing them for studies relevant to biotechnology are discussed, with the emphasis on investigations of biological macromolecules such as DNA and proteins. Items covered include samples, surfaces, medium, tips, and typical operating conditions. Finally, prospects are discussed for potential future applications to biotechnology.

Biotechnology↗