THE EFFECT OFWATER CONTENT ON DAMAGE DEPTH IN TISSUE SUBJECTED TO CO2 LASER, AN EXPERMANTEL AND THEORITCAL STUDY.

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Presentation transcript:

THE EFFECT OFWATER CONTENT ON DAMAGE DEPTH IN TISSUE SUBJECTED TO CO2 LASER, AN EXPERMANTEL AND THEORITCAL STUDY

The aim of the study: This study aims to evaluate the damage depth produced by subjecting CO2 laser on different types of tissue (muscle, brain and lung). Studied the thermal damage using two methods, thermal Dose (CEM43) and Arrhenius’ equation . find the effect of water content on damage depth

introduction Carbon dioxide CO2 (10600 nm) laser is widely used as a scalpel in surgical operation and in other medical fields[1] .For CW CO2 laser the photons that absorb are the essential part of induced laser photons which cause a rapid increase in the temperature of tissue where many phenomenon may happen such as hyperthermia, denaturation of proteins, coagulation, and cells necrosis until the limit of water evaporation is reached[2]. The percentage of the water in different tissue, which is (muscle, brain and lung), had been determined by measuring the weight of each fresh tissue before and after drying in oven, it was found that brain tissue has water content more than muscle and lung tissue[3] . Each tissue sample was subjecting to different power CO2 laser for 20 s, after that the tissue was prepared for examination under light microscope by fixation of the tissue on glass slide using (paraffin) embedding section method to determine damage depth using scaled optics[4] .This result was used in computer program to find the average thermal dose that was used in Thermal Dose (CEM43) equation and Arrhenius’ equation to determine the damage depth theoretically.

Theory 1.Temperature distribution in tissue cut by CO2 laser

2.Methods of predication thermal damage depth

Experiment Work 1. Measurement the percentage of water in tissues The samples were prepared by cutting the sheep tissue samples into a small piece as shown: The cutting step followed by calculating the weight of each sample by using electrical sensitive balance (Mettler). Then the samples were placed in the oven in temperature 50°C for 10 min. and then the weight of each sample was calculated to determine the difference in weight that represents the weight of the water. This step was repeated several times until the weight of tissue was fixed[3].

2.Experimental Measurement of damage depth 2.1Set up of the work CW CO2 laser Pieces of tissue from the sheep Holder Power meter. Microscope Scaled optics

2.2Experimental work In this work different sheep organs (age 6 months)was used(Brain ,Lung ,Muscle)and the tissues of these organs were prepared by cutting them in to pieces each with the same dimension . The tissues exposed to CO2 laser for 20 seconds with different power laser. The power and the spot diameter of laser was (5 to 14Watt) and (2mm) respectively, as shown: Then each tissue was prepared for examination under light microscope by fixation of the tissue on glass slide using (paraffin) embedding section method.

RESULTS 1. Measurements the percentage of water in different tissues Samples Weight before dehydration Weight after dehydration Percentage of water Muscle 0.72 0.15 79 Lung 0.77 0.11 85 Liver 1.16 0.22 81 Heart 1.19 0.16 86 Brain 1.29 0.14 89

2. Measurements of damage depth in tissues 2  2. Measurements of damage depth in tissues 2.1 Damage depth of muscle tissues Thermal damage in muscle tissue under the microscope caused by CO2 laser after20 s with power of: (a) 5w and damage depth of 4.4010-4 m. (b) 10w and damage depth of 2.3010-4 m. (c) 14w and damage depth of 1.3510-4 m. (a) (b) (c)

The theoretical Dose, Arrhenius and experimental variation of damage depth with power in muscle tissue, it is found that the damage depth in tissue decrease as the CW CO2 power (intensity) increase .

2.2 Damage depth of lung tissues Thermal damage in tissue of lung under the microscope caused by CO2 laser after20 s with power of: (a) 5w and damage depth of 3.810-4m. (b)9w and damage depth of 2.010-4 m. (c) 10w and damage depth of 1.6010-4m. (a) (b) ( c)

The theoretical Dose, Arrhenius and experimental variation of damage depth with power in the tissue of lung, it is found that the damage depth in tissue decrease as the CW CO2 power (intensity) increase .

2.3 Damage depth of brain tissues Thermal damage in tissue of brain under the microscope caused by CO2 laser after20 s with power of : (a)7w and damage depth of 2.410-4 m. (b)9w and damage depth of 1.9010-4 m. (c)10w and damage depth of 1.510-4 m. (a) (b) (c)

The theoretical Dose, Arrhenius and experimental variation of damage depth with power in the brain tissue , it is found that the damage depth in tissue decrease as the CW CO2 power (intensity) increase .

3.Effect of water content on damage depth The damage depths of tissue with different water content, for muscle(79%),lung(85%),brain(89%),it is found that as power increased damage depth is decreased, also it is found that as water content increased damage depth is decreased. This is due to increase in cutting speed where heat is not allowed to accumulate to cause large damage. The variation of laser power with damage depth at 20 s in the muscle, lung and brain.

CONCLUSIONS Water content in tissue has big effect on thermal damage depth, where as water content increases the damage depth decreases. The damage depth of thermal damage can be calculated by two model of method, which is CEM43 and Arrhenius model. In addition, it is found that Arrhenius equation is more accurate than thermal dose in obtaining thermal damage depth, Comparing with theoretical and experimental finding. It is found that as power intensity is increased, thermal damage is reduced but it is limited by phenomena of photo disruption. CW CO2 laser can be used successfully to cut or ablate bio- tissue, which result thermal damage.

References [1] Shibib,K.S., Hubeatir,K.A., One dimensional Finite Element Solution of Moving Boundaries in Far IR Laser Tissue Ablation, Iraqi J. Laser,1(2012),11,pp.13-19. [2] Cox, B. T., Introduction to Laser-Tissue Interactions, Report No.4886, Optics in Medicine, 2007. [3] Reinoso, F., Telfer, A., Rowland,M., Tissue water content in rats measured by desiccation, Pharmacological and Toxicological Methods ,38(1997),2,pp.87-92 [4] https://science.vla.gov.uk/tse-lab-net/documents/tse-oie-rl-prp.pdf [5] Holman, J., Heat Transfer (McGraw-Hill Series in Mechanical Engineering), McGraw-Hill Education, 2009. [6] Tzu-Ching Shih, Thermal Models Of Biohat Transfer Equations In Living Tissue and Thermal Dose Equivalence Due To Hyperthermia, Biomedical Engineering Applicants. Basis & Commnications,14(2002),2,pp. 68-50 [7] Chang, I. A., Considerations for Thermal Injury Analysis for RF Ablation Devices, The Open Biomedical Engineering Journal,4(2010),pp.3-12 [8] Romero ,L.F., Trelles, O., Trelles, M.A., Real-Time Simulation for Laser-Tissue Interaction Model, John von Neumann Institute for Computing NIC Series, 33(2006), pp. 415-422 [9] Salavati,M. E., A Three-Dimensional Finite Element Model to Study Dynamic Changes of Tissue during Laser Interstitial Thermotherapy,American Journal of Biomedical Engineering,5 (2015),3,pp.86-93, doi:10.5923/j.ajbe.20150503.02.

Thank you