International Journal of Biophysics

p-ISSN: 2168-4979    e-ISSN: 2168-4987

2015;  5(1): 18-23

doi:10.5923/j.biophysics.20150501.03

A Description of the Effect of Polarized Light as an Adjuvant Therapy on Wound Healing Process in Pediatrics

Samir M. Abdel-Mageed1, Ali Osman Selim2, Mohamed A. Abdel Ghafar3, Rania Reffat Ali4

1Physics Department, Faculty of Science, Alexandria University

2Physical Therapy for Surgery Department, Faculty of Physical Therapy, Cairo University

3Physical Therapy for Pediatrics Department, Faculty of Physical Therapy, October 6 University

4Basic science Department, Faculty of Physical Therapy, Cairo University

Correspondence to: Samir M. Abdel-Mageed, Physics Department, Faculty of Science, Alexandria University.

Email:

Copyright © 2015 Scientific & Academic Publishing. All Rights Reserved.

Abstract

Backgroundandpurpose: The ability of light to penetrate a tissue and deposit energy via the optical absorption properties of the tissue is the key to therapeutic applications. Birefringence which is an anisotropic property of dermal layer of skin, the blood flow in the tissue capillaries and the multi-scattering from the tissue static components affect the polarization of light. The goal of this study was to describe the healing process of deep partial thickness wound in pediatrics submitted (or not) to the excitation property or the polarization property of light.Subjects: Thirty children who suffered from deep partial thickness burn (20-30%) participated in this study (13 boys and 17 girls). Their ages ranged from 10 to18 years. They were classified randomly into two groups (study and control group) of equal numbers.Procedures: Group A (study) was treated using polarized light as an adjuvant therapy to the regular wound care (debridement, Local antimicrobial drug and beta dine) 5 sessions per week for 3 weeks. Group B (control) was treated using the regular wound care (debridement, Local antimicrobial drug and beta dine). Wound surface areas were measured before and after the treatment period by using wound tracing method. Results: The study showed a significant reduction in burn wound surface areas in both groups (P < 0.05) while there was no significant difference between both groups.Conclusion:it was concluded that polarized light has a limited effect as an adjuvant therapy on healing process of deep partial thickness burn wounds in children.

Keywords: Polarized light, Deep partial thickness burn, Wound healing, Paediatrics

Cite this paper: Samir M. Abdel-Mageed, Ali Osman Selim, Mohamed A. Abdel Ghafar, Rania Reffat Ali, A Description of the Effect of Polarized Light as an Adjuvant Therapy on Wound Healing Process in Pediatrics, International Journal of Biophysics , Vol. 5 No. 1, 2015, pp. 18-23. doi: 10.5923/j.biophysics.20150501.03.

1. Introduction

Burn is a coagulative necrosis of the skin caused by contact with fire, chemicals such as acids, hot liquids, hot air and hot gases, heated metals or electricity. Burn injuries remain one of the major health problems that can happen unexpectedly and have the potential to cause disability, lifelong disfigurement, prolonged hospitalization and/or death. [1, 2]
Unintentional and intentional burn injuries vary across age groups, gender, income and global region. The worldwide incidence of burn injuries was 1.3 per 100,000 populations in low and moderate income countries. Children under 5 and the elderly have the highest burn mortality worldwide. [3]
The repair of burn wound has long been a problem and this has come more into focus in recent times. Wound closure is undertaken as the most important advent preventing life threatening, infections, decreasing morbidity and mortality [7].
Wound healing is an intricate process in which the skin or any organ tissue repairs itself after injury [4]. Wound healing is a complex and dynamic process characterized by interaction of various cell types as lymphocytes, monocytes, epithelial cells and fibroblasts. Three main overlapping phases have been identified in tissue response to injury include inflammation, formation of granulation tissue and proliferation [5, 6].
Wound healing process is based on the vascular and cellular activity. Vasomotion is the periodic constriction and dilatation of small blood vessels. It is attributed to local metabolic needs, vascular myogenic responses and neurogenic controls. Besides the fibroblast and macrophage activity, human wound associated lymphocyte populations are modulated during a healing process. [4]
Polarized and non-polarized light from different sources in the spectral ranges of visible and near infrared (NIR) are widely used in clinical treatments and in medical research especially in the therapeutic field, such as Low Level Laser Therapy (LLLT), light phototherapy (lasers), quasi-monochromatic radiation (LEDs) and broadband light devices. [8] The most of laser types are polarized, where the electric field oscillates in a certain direction perpendicular to the propagation direction [9].
Light is a form of energy and has various colors with different wavelength; it has been used as a healing tool since ancient time. There is now better understanding of which component of natural light are useful in the stimulation of healing such as Biptron light therapy (BLT) which is a device emits a polarized light containing a range of wavelengths that correspond to visible light plus infrared radiation which have been reported to stimulate the biological reactions [10]. It was reported that polarized light causes enhancement of the cell membrane activities, acceleration of production of adenosine tri-phosphate (ATP) in mitochondria, stimulation of regeneration processes and acceleration of fibroblast proliferation and deposition of collagen [11, 12].
It was considered that polarized light rearrange the polar heads of a lipid bilayer in the cell membrane where enzyme reactions take place lead to structural changes occur in cell membranes in consequence the surface features and lipid protein connection can be modified [11]. Schindl et al. [13] stated that Biptron light therapy may significantly stimulate the faster epithelialization of the damaged skin, reducing the risk for the formation of the functionally and unacceptable scars.
However, the polarization point has never been experimentally proven and studies used polarized light in the treatment of wounds revealed conflicting data and studies in vivo are still scarce, with some studies reporting accelerated wound closure and increased tensile strength of scars while others have found no such improvement [14]. So, the purpose of this study was to evaluate the effect of polarized light in accelerating the healing rate in burn injuries in children.

2. Materials and Methods

Subjects:
Thirty children (13 boys and17 girls) participated in this study; their ages ranged from 10 to 18 years with a mean value of 15.2±2.6 years. The mean values for their body weight was 49.7±8.6 kg, and for their height was 160.6±7.6 cm, while it was 24.7±4.2 kg/cm2 for their body mass index (Table 1). A consent form was signed after the procedure and possible side effects had been explained under supervision of their guardians.
Table 1. Mean and Standard deviation of age, weight, height, and BMI
     
Inclusion criteria
Children with deep partial thickness bun affecting 20 to 30% of total body surface area (TBSA) with no relative contraindications for using of polarized light participated in this study.
Exclusion criteria
Children suffering from medical conditions that might affect burn healing were excluded. These conditions included diabetes mellitus, malignancy, inhalation injuries or any systemic diseases. Also children using drugs that can affect the skin and delay in healing, especially steroids, immunosuppressive agents, antineoplastic drugs and anticoagulants were excluded.
Children were randomly divided into two equal groups. Group A (study) was treated by polarized light as an adjuvant therapy to the regular wound care (debridement, local antimicrobial drug and beta dine) 5 sessions per week for 3 weeks. Group B (control) was treated by the regular wound care (debridement, local antimicrobial drug and beta dine) 5 sessions per week for 3 weeks.
Equipments:
1. Wound tracing method used to measure burn surface area (sterilized transparency film, fine tipped marker, white paper, carbon paper and metric graph paper 1mm2). [15]
2. Bioptron Compact III Light Therapy System (PAG-860) by (Bioptron AG, Switzerland) with the following technical characteristics was used: Wavelength 480-3400 nm, degree of polarization >95% (590-1550 nm), specific power density 40 mW/cm2, light energy per minute 2.4 J/cm2.
Procedures:
A. Measurement of wound surface area:
The burn wound outline was traced on a transparent film using a permanent marker. Each wound was traced twice to establish measurement reliability. Then the wound tracing was placed on a metric grid, and the number of square millimeters of the traced area were counted to determine the burn wound surface area, then the value was converted to cm2. The mean of the two trials was calculated and considered as a burn wound surface area (WSA). The wound surface area was measured before starting the study and after 3 weeks of treatment.
B. Treatment procedures:
The patient was placed in suitable position. Before the polarized light therapy all wounds were cleaned using 2% hydrogen peroxide. Polarized light therapy was performed for six min, at a distance of 10 cm, five times a week for three weeks. Patient was asked to note the erythema (when it begins and disappeared). If marked or painful erythema had occurred, therapy was stopped until erythema relieved and then the session time was decreased to the previous level and frequency.
Data analysis
Data was analyzed by using statistical package for social sciences (SPSS). Unpaired t-test was used to compare between the mean of wound surface area before and after the treatment for both groups. Level of significance was set at 0.05.

3. Results

The statistical analysis of the mean values of wound surface area (WSA) in control group before treatment was (105.7±20.96) and after treatment was (17.2±11.49) revealed a significant statistical reduction of mean values of WSA(P<0.05). Also the percentage of reduction was calculated to be 88.3% after treatment, when compared to the pretreatment value as shown in figure 1.
Figure 1. The statistical analysis of mean values of WSA pre treatment after post treatment in control and study groups
The statistical analysis of the mean values of wound surface area (WSA) in study group before treatment (104.9±24.22) and after treatment (12.3±9.45) revealed a significant statistical reduction of mean values of WSA (P<0.05). Also the percentage of reduction was calculated to be 88.3% after treatment, when compared to the pretreatment value as shown in figure 1.
The statistical analysis of the mean values of wound surface area (WSA) pre treatment for control group and study group revealed no statistical significant differences as shown in figure 2.
Figure 2. The Mean values of WSA (cm2) post treatment for both control and study groups
The statistical analysis of the mean values of wound surface area (WSA) post treatment for control group and study group revealed no statistical significant differences as shown in figure 3.
Figure 3. The Mean values of WSA (cm2) post treatment for both control and study groups

4. Discussion

The analysis of the results indicated that both groups showed significant statistical difference between pre and post experiment measurements, but there was no statistically significant difference between the study and the control groups.
Results of the current study came in agreement with those of Schlager et al. [16] who reported that irradiation of burns with a 250-mW/670-nm laser light produced no beneficial effects on wound-healing processes. Also it is supported by Cambier et al. [17] who found no improvement in the wound-healing process after irradiation with low-power lasers or polarized light.
These results can be explained as the therapeutic effect of polarized light may be due to either the polarization or the excitation property of the light. Once the polarized lights penetrate the tissues it starts to lose their polarization direction. The polarization loss in the tissue may be mainly due to many reasons; the blood flow in the tissue capillaries, the birefringent properties of the medium and the multi-scattering from the tissue static components [18].
First of all, according to the work of Fixler et al. [19] the polarization loss is directly proportional to the volumetric flow rate. Higher flow rate produces lower polarization values especially when the polarization direction is perpendicular to the direction of flow. The dermis layer of the skin - first layer encountered by the polarized light during second degree burn wound contains blood vessels and capillaries where the blood is flowing in many directions carrying its components. Accordingly, the polarized light beam necessarily hits the fluid flow through the tissue perpendicular to its polarization direction and this cause a polarization loss.
Secondly, the randomization of linear polarization during transmission through a tissue is more rapid in birefringent tissues than in non-birefringent tissues [20]. Birefringence is a polarization specific electromagnetic property of materials. Collagen fiber is the main components of the dermis layer (70% in dry weight) has a heterogeneous distribution in the skin, and commonly refer to as birefringent tissue [21]. There are two types of birefringence have been reported for collagen fibers, particularly intrinsic [22] and Form birefringence which is caused by asymmetrical alignment of chemical bonds or ions within the rod shaped triple chain collagen molecules and the next arises from the nonlinear optical property of the medium [23]. Therefore, Collagen’s rod like triple helix conformation results in both linear and circular anisotropic properties [24]. The most rapid depolarization occurred in rich collagen tissues of the skin [20].
Finally, on the cellular level, the mismatches of refractive indices between cellular components result in scattering [25]. The scattering properties of the cellular level elements also vary with their sizes. Therefore, the reduced scattering coefficient of the dermis as a function of the light wavelength can be described well as a combination of Mie and Rayleigh scattering. The former occur when the size of the element is comparable to the wavelength of the incident light such as scattering by mitochondria, nuclei and collagen fibers can be explained by Mie scattering. Contrary, when the size of the element is much smaller than the wavelength, its scattering property can be explained by Rayleigh scattering such as scattering include membranes and the banded ultra-structures of collagen fibrils fibers [26]. Therefore; light with long wavelength has more penetration power in skin. Rayleigh scattering dominates in the spectral range below 650 nm while Mie scattering plays a major role above 650nm. As the main scatterers in the dermis are the collagen fibers which are densely packed [27]. As a result, the orientation of polarization becomes randomized by multiple scattering events from these collagen fibers and the polarization value reduced [28].
Based on the three facts discussed above ; the dermis static components such as collagen fibers exhibit optical birefringent properties which acts as a strong multiple scatterers for linear polarized light, also the blood flow in the tissue capillaries and the blood dynamic components act as a scatterers. Consequently, linear polarization of radiation randomized through the dermis layer and polarization lost. So there are no additional benefits in using polarized light as an excitation source without maintaining the excitation direction.
The slight improvement in the group treated by polarized light compared to the control group comes in agreement with Ribeiro [29] who reported that the relative direction of the laser polarization plays an important role in the wound healing process when highly coherent He-Ne laser is used. Also these results confirmed by the clinical results of Monstrey et al. [30] that polarized light therapy was effective in the treatment of burn wounds.
These results may be attributed to the excitation property of the light despite of its polarization property. The light interaction with the biological tissue is not an intrinsic property of the light. Where the first law of photochemistry states that light must be absorbed before photochemistry can occur.
It was stated that mitochondria thought to be a likely site for the initial effects of light; absorption of photons by chromosphere molecules such as cytochrome c that proposed as the primary photoacceptor for the red-NIR range in mammalian cells leads to electronically excited states and consequently acceleration of electron transfer reactions in the mitochondria membrane respiratory chain [31]. A further electron transport automatically leads to increasing of ATP production rate [32], alteration of reactive oxygen species and induction of transcription factors which increasing the activity of the Na+ /H+ and Ca2+/Na+ antiporters and of all the ATP driven carriers for ions, such as Na+ /K+ ATPase and Ca2+ pumps. ATP is the substrate for adenyl cyclase, and therefore the ATP level controls the level of cAMP. Both Ca2+ and cyclic adenosine mono-phosphate cAMP are very important second messengers. Ca2+ adjusts most of the biological process in the human body [31].
The positive effect of light on wound healing can be explained by many biological mechanisms including modulation in levels of cytokines and growth factors which are responsible for the different stages of wound healing. It was reported that cytokines responsible for the initial inflammatory phase, fibroblast proliferation and migration in wound healing [33]. Also it was confirmed that light can increase growth factors responsible for the neovascularization and inducing collagen synthesis from fibroblasts which necessary for wound healing [34]. Light can incite fibroblasts transformation to myofibloblasts which has the phenotype of contractile cells that accelerate wound contraction [35].

5. Conclusions

The effects of polarized light as an adjuvant therapy for deep partial thickness second degree burn were not satisfactory and statistically non-significant. But it showed a very slight improvement in the wound healing process.

References

[1]  Peck MD, Kruger GE, Van Der Merwe AE, Godakumbura W, Ahuja RB. Burns and fires from non electric domestic appliances in low and middle income countries Part1. The scope of the problem. Burns 2008; 34(3):303-311.
[2]  Peck M and Pressman MA. The correlation between burn mortality rates from the flame and economic status of countries. Burns 2013; 39(6):1054-9.
[3]  World health Organization (WHO) Global Burden of Disease 2008.www.who.int/healthinfo/global_burden_disease/estimates_regional/en/index.html (Accessed on September 20, 2011).
[4]  Nguyen DT, Orgill DP and Murphy GF. The Pathophysiologic Basis for Wound Healing and Cutaneous Regeneration. Biomaterials for Treating Skin Loss. CRC Press (US) & Woodhead Publishing (UK/Europe), Boca Raton/Cambridge 2009, 25-57.
[5]  Morison MJ, Ovington LG and Wilki K. Chronic wound care: a problem based learning approach. Edinburgh: Mosby, 2004.
[6]  Nienartowicz A, Sobaniec-Lotowska ME, Jarocka-Cytra E and Lemancewicz D. Mast cells in neoangiogenesis. Med Sci Monit 2006; 12(3): 53-56.
[7]  Desanti L. Pathophysiology and current managment of burn injury. Adv skin wound care. 2005; 18(6):323-332.
[8]  Sankaran V, Everett MJ, Maitland DJ et al .Comparison of polarized light propagation in biological tissue and phantoms. Optics Letters 2003; 24(15): 1044-46.
[9]  Lin JF, Lo YL. Measurement of optical rotation and phase retardance of optical samples with depolarization effects using linearly and circularly polarized probe lights. Opt Laser Eng 2009; 47(9):948–55.
[10]  Depuydl K, Monstrey S and Hoeksema H. The use of polarized light in the treatment of burn wounds. Abstract. Presented at the 10th annual EURAPS meeting. Madrid. Spain 2001.
[11]  Monstrey SA, Hoeksema HG and Depuydt KA. The effect of polarized light on wound healing. European Jornal of plastic surgery; 2004, 24(8): 304-310.
[12]  Medenica LA and Lens MA.the use of polarized polychromatic non coherent light alone as a therapy for venous leg ulceration. Journal of wound care; 2004, 12(1), 37-40.
[13]  Schindl A, Schindl M, Pernerstorfer-Schon H and Schindl L. Low intensity laser therapy: a review. J Investing Med.2000, 48(5): 312-326.
[14]  Samoilova KA, Obolenskaya KD and Vologdina AV. Proceedings of EUROPTO conference on low power light on biological systems. Stockholm Sweden, Sep 2008: 90-103.
[15]  Bohannon RE and Pfaller BV. "Documentation of wound surface area from tracing of wound perimeters: Clinical report of three techniques". Phys.there 1983; 63(10): 1622-1628.
[16]  Schlager A, Oehler K, Huebner K-U, Schmuth M, Spoetl L. Healing of burns after treatment with 670-nanometer low-power laser light. Plast Reconstr Surg 2000; 105(5): 1635–9.
[17]  Cambier DC, Vanderstraeten GG, Mussen MJ, van der Spank JT. Low-power laser and healing of burns: a preliminary assay. Plast Reconstr Surg 1996; 97(3): 555–8.
[18]  Hoeksema HG, Monstrey SA and Saelens HU. Efficacy of polarized light therapy in the conservative treatment of deep dermal burns. Br J Plastic Surg; 2002; 55(5):420-426.
[19]  Fixler D, Ankri R, Duadi H, Lubart R, and Zalevsky Z, Depolarization of light in biological tissues, Optics and Lasers in Engineering 2012; 50(6): 850–854
[20]  Steven L. Jacques, Jessica R. Roman, and Ken Lee, Imaging Superficial Tissues With Polarized Light, Lasers in Surgery and Medicine 2000; 26:119–129.
[21]  Maitland DJ and Walsh JT. Quantitative Measurements of Linear Birefringence during Heating of Native Collagen Lasers in Surgery and Medicine1997; 20(3):310–318.
[22]  Bennett HS. The microscopical investigation of biological materials with polarized light. In: Jones RM (ed.) McClung’s Handbook of Microscopical Technique. New York: Hafner Publ. Co. 1967; 591–766.
[23]  Vidal BC. Form birefringence as applied to biopolymer and inorganic material supraorganization. Biotech Histochem 2010; 85(6): 365–378.
[24]  Yoshioka K, O’Konski CT. Electric properties of macromolecules. IX. Dipole moment, polarizability, and optical anisotropy factor of collagen in solution from electric birefringence. Biopolymers 1966; 4(5):499–507.
[25]  Guzlksu N, Federici J.F, Lim H.C, Chauhdry H.R, Ritter A.B, and Findley T. Measurement of skin stretch via light reflection. Journal of Biomedical Optics 2003; 8:80–86.
[26]  Mobley J and Dinh TV. Biomedical Photonics Handbook. CRC Press, 2003.
[27]  Jacques S.L. Origins of tissue optical properties in the UVA, visible, and NIR regions. Trends in Optics and Photonics: Advances in Optical Imaging and Photon Migration. 1996; 2:364–371.
[28]  Drezek R, Dunn A, and Kortum R.R. Light scattering from cells: finite-difference time-domain simulations and goniometric measurements. Applied Optics 1999, 38(16):3651–3661.
[29]  Ribeiro MS1, Da Silva Dde F, De Araújo CE, De Oliveira SF, Pelegrini CM, Zorn TM, Zezell DM. Effects of low-intensity polarized visible laser radiation on skin burns: a light microscopy study. J Clin Laser Med Surg. 2004; 22(1):59-66
[30]  Monstrey S, Hoeksema H, Saelens H, Depuydt K, Hamdi M, Van Landuyt K, et al. A conservative approach for deep dermal burn wounds using polarised-light therapy. Br J Plast Surg 2002; 55(5): 420–6.
[31]  W. Yu, J.O. Naim, M. McGowan, K. Ippolito and R.J. Lanzafame. Photomodulation of oxidative metabolism and electron chain enzymes in rat liver mitochondria, Photochem Photobiol 1997; 66(6): 866-71.
[32]  Passarella S. He-Ne laser irradiation of isolated mitochondria, J Photochem Photobiol B 1989; 3(16): 642-3.
[33]  Poon VK, Huang L, and Burd A. Biostimulation of dermal fibroblast by sublethal Q-switched Nd: YAG 532 nm laser: collagen remodeling and pigmentation, J Photochem Photobiol B 2005; 81(1): 1-8.
[34]  Kipshidze N, Nikolaychik V, Keelan MH, Shankar LR, Khanna A, Kornowski R, Leon M and Moses J. Low-power helium: neon laser irradiation enhances production of vascular endothelial growth factor and promotes growth of endothelial cells in vitro, Lasers Surg Med 2001; 28(4): 355-64.
[35]  Medrado AR, Pugliese LS, Reis SR and Andrade ZA, Influence of low level laser therapy on wound healing and its biological action upon myofibroblasts, Lasers Surg Med 2003; 32(3): 239-44.