| Literature DB >> 35565029 |
Na Cao1, Hongtao Liang1, Ruoyu Zhang1, Yanhua Li1, Hui Cao1.
Abstract
The development of appropriate photothermal detection of skin diseases to meet complex clinical demands is an urgent challenge for the prevention and therapy of skin cancer. An extensive body of literature has ignored all high-order harmonics above the second order and their influences on low-order harmonics. In this paper, a new iterative numerical method is developed for solving the nonlinear thermal diffusion equation to improve nonlinear photothermal detection for the noninvasive assessment of the thickness of port-wine stain (PWS). First, based on the anatomical and structural properties of skin tissue of PWS, a nonlinear theoretical model for photothermal detection is established. Second, a corresponding nonlinear thermal diffusion equation is solved by using the new iterative numerical method and taking into account harmonics above the second-order and their effects on lower-order harmonics. Finally, the thickness and excitation light intensity of PWS samples are numerically simulated. The simulation results show that the numerical solution converges fasterand the physical meaning of the solution is clearerwith the new method than with the traditional perturbation method. The rate of change in each harmonic with the sample thickness for the new method is higher than that for the conventional perturbation method, suggesting that the proposed numerical method may provide greater detection sensitivity. The results of the study provide a theoretical basis for the clinical treatment of PWS.Entities:
Keywords: new numerical iterative method; nonlinear thermal diffusion equation; port-wine stain; sensitivity
Mesh:
Year: 2022 PMID: 35565029 PMCID: PMC9104969 DOI: 10.3390/ijerph19095637
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 4.614
Figure 1(a) Schematic of multilayered skin; (b) schematic of skin with different growth phases of a cancerous lesion; (c) theoretical model for photoacoustic detection of skin tissue.
Thickness, optical and thermal parameters of the skin model at 840 nm [11,25,26,27].
| Layers | d (mm) | β (mm−1) | σ (mm−1) | g | ρ (g/cm−3) | C (J/(g. K)) | K0 (mW/(cm. K)) |
|---|---|---|---|---|---|---|---|
| Stratum corneum | 0.01 | 0.00091 | 18.95 | 0.8 | 1.2 | 3.59 | 2.4 |
| Living epidermis | 0.08 | 0.13 | 18.95 | 0.8 | 1.2 | 3.59 | 2.4 |
| Papillary dermis | 0.10 | 0.105 | 11.65 | 0.8 | 1.09 | 3.35 | 4.2 |
| Upper blood plexus | 0.08 | 0.15875 | 15.485 | 0.818 | 1.09 | 3.35 | 4.2 |
| Reticular dermis | 1.50 | 0.105 | 11.65 | 0.8 | 1.09 | 3.35 | 4.2 |
| Deep blood plexus | 0.07 | 0.4443 | 46.165 | 0.962 | 1.09 | 3.35 | 4.2 |
| Dermis | 0.16 | 0.105 | 11.65 | 0.8 | 1.09 | 3.35 | 4.2 |
| Hypodermis | 3.00 | 0.009 | 11.44 | 0.9 | 1.21 | 2.24 | 1.97 |
| Muscle tissues | 3.00 | 0.029 | 7.13 | 0.9 | 1.075 | 3.5 | 4.5 |
| PWS | 0.001~1.5 | 0.15875 | 46.7 | 0.99 | 1.0 | 3.6 | 5.3 |
Figure 2Variation in the amplitude with frequency on the posterior surface of a wine−discolored sample when the sample thickness varies: (a) fundamental frequency wave; (b) second harmonic (low frequency).
Figure 3Variation in the amplitude of the posterior surface of the wine−discolored samples with frequency for different sample thicknesses: (a) fundamental frequency wave; (b) second harmonic (high frequency).
Figure 4Variation in the harmonic amplitude with frequency for each order of harmonic for different sample thicknesses.
Figure 5Variation in the harmonic amplitude with light energy for different sample thicknesses. (a) Fundamental frequency wave; (b) second harmonic; (c) third harmonic; (d) fourth harmonic.
Figure 6Variation in the fundamental frequency wave and second harmonic with frequency.
Figure 7Variation in the second harmonic with frequency for different sample thicknesses.
Figure 8The variation in the second harmonic amplitude with number of iterations for different light energies.