Fig. 1. Structure of PMC16 (cyclohexyl(C₆₀)porphyrin), Me²⁺ — carrying and releasing nanoparticles with the marked membranotropic/amphiphilic properties [1]

Fig. 2. The NP uptake selectivity prediction in a complete accessibility of intracellular ligands. P — [NP] uptaken, units per cell; P₀ — intracellular initial concentration of NP-ligands; K_S — Gompertz equation vectoral K; K₁ — an NP uptake steady state constant; K₂ — an efficient constant of saturation of a cellular ligand pool at [NP] → 0.5 P_max

Fig. 3. Probabilistic model for NPs distribution between RB and the neighboring RT cells as a function of the discriminative cell cycle turnover. Z-elimination coefficient for malignant and the RB-surrounding normal cells (RT) estimated for the drug efficiency duration time (σ) and the drug-free cell functioning time interval (ω). σ is normally distributed within a variation range of σ = σ/10, where remain constant while the inner rate of the “newborn” cell appearance is λ = 2, for a starting population size x(0) = 5