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The work is devoted to the study of the theoretical value of destructive influence on normal tissues of an organism by infrared radiation that goes beyond the treated pathological focus. This situation is possible if the direct laser radiation on the tissues is extremely long-acting. The solution to this problem can be the uniform distribution of heat inside the volume through indirect heating of the liquid, which contributes to minimal damage to the perifocal structures. A non-stationary thermophysical model of the process of heat propagation in biological tissues is presented, allowing to carry out studies of energy transfer from internal liquid contents of Baker's cyst heated by infrared laser radiation of a given specific power through a certain thickness of its wall to surrounding biological tissues. Calculation of the spacetime temperature distribution in the cyst wall and surrounding fat tissue is carried out by the finite-difference method. The time of effective exposure to temperature on the entire thickness of the cyst wall was estimated to be 55 ° C on its outer surface. The safety procedure ensures the exposure duration of this value is not more than 10 seconds.

As a result of the calculations carried out, it is established that there are several operating modes of a surgical laser that meet all the safety requirements with a simultaneous effective procedure. Local one-sided hyperthermia of the synovial membrane and subsequent coagulation of the entire wall thickness due to heat transfer contributes to the elimination of the cavity neoplasm of the popliteal region. With a thickness of 3 mm, the heating mode is satisfactory, under which the exposure time lasts about 200 seconds, and the specific power of the laser radiation in the internal medium of the liquid contents of the Baker cyst is approximately 1.

This paper studies minimum volume elastoplastic bodies. One part of the boundary of every reviewed body is fixed to the same space points while stresses are set for the remaining part of the boundary surface (loaded surface). The shape of the loaded surface can change in space but the limit load factor calculated based on the assumption that the bodies are filled with elastoplastic medium must not be less than a fixed value. Besides, all varying bodies are supposed to have some type of a limited volume sample manifold inside of them.

The following problem has been set: what is the maximum number of cavities (or holes in a two-dimensional case) that a minimum volume body (plate) can have under the above limitations? It is established that in order to define a mathematically correct problem, two extra conditions have to be met: the areas of the holes must be bigger than the small constant while the total length of the internal hole contour lines within the optimum figure must be minimum among the varying bodies. Thus, unlike most articles on optimum design of elastoplastic structures where parametric analysis of acceptable solutions is done with the set topology, this paper looks for the topological parameter of the design connectivity.

The paper covers the case when the load limit factor for the sample manifold is quite large while the areas of acceptable holes in the varying plates are bigger than the small constant. The arguments are brought forward that prove the Maxwell and Michell beam system to be the optimum figure under these conditions. As an example, microphotographs of the standard biological bone tissues are presented. It is demonstrated that internal holes with large areas cannot be a part of the Michell system. At the same the Maxwell beam system can include holes with significant areas. The sufficient conditions are given for the hole formation within the solid plate of optimum volume. The results permit generalization for three-dimensional elastoplastic structures.

The paper concludes with the setting of mathematical problems arising from the new problem optimally designed elastoplastic systems.

Hemostasis system is one of the key body’s defense systems, which is presented in all the liquid tissues and especially important in blood. Hemostatic response is triggered as a result of the vessel injury. The interaction between specialized cells and humoral systems leads to the formation of the initial hemostatic clot, which stops bleeding. After that the slow process of clot dissolution occurs. The formation of hemostatic plug is a unique physiological process, because during several minutes the hemostatic system generates complex structures on a scale ranging from microns for microvessel injury or damaged endothelial cell-cell contacts, to centimeters for damaged systemic arteries. Hemostatic response depends on the numerous coordinated processes, which include platelet adhesion and aggregation, granule secretion, platelet shape change, modification of the chemical composition of the lipid bilayer, clot contraction, and formation of the fibrin mesh due to activation of blood coagulation cascade. Computer modeling is a powerful tool, which is used to study this complex system at different levels of organization. This includes study of intracellular signaling in platelets, modelling humoral systems of blood coagulation and fibrinolysis, and development of the multiscale models of thrombus growth. There are two key issues of the computer modeling in biology: absence of the adequate physico-mathematical description of the existing experimental data due to the complexity of the biological processes, and high computational complexity of the models, which doesn’t allow to use them to test physiologically relevant scenarios. Here we discuss some key unresolved problems in the field, as well as the current progress in experimental research of hemostasis and thrombosis. New findings lead to reevaluation of the existing concepts and development of the novel computer models. We focus on the arterial thrombosis, venous thrombosis, thrombosis in microcirculation and the problems of fibrinolysis and thrombolysis. We also briefly discuss basic types of the existing mathematical models, their computational complexity, and principal issues in simulation of thrombus growth in arteries.