Abstract

Ultraviolet (UV) rays have been identified as a carcinogen with long-term irradiation and are an important risk factor for skin cancer. Here, we report the use of optical coherence tomography/optical coherence tomography angiography (OCT/OCTA) to study acute UV-induced effects on skin in vivo. To understand the relationship between the acute effects and irradiated UV power density, three groups were irradiated with different power densities in our experiments. Furthermore, the same skin area was repeatedly scanned with OCT during UV irradiation to investigate the progress of the induced acute effects and after irradiation for observation of skin recovery. Subsequently, the OCT/OCTA results were quantitatively analyzed to acquire skin thickness and blood-vessel density for comparison. UV-induced acute effects on morphology and microcirculation can be identified from OCT/OCTA results, which showed the increases in the skin thickness and blood-vessel density and even severe damage types such as blisters. The results of quantitative analyses also illustrated that the severity of damage induced by UV irradiation can be distinguished and the skin recovery can be monitored with OCT. Our results indicate that OCT can be a promising tool for early detection of UV-induced acute skin damage.

Highlights

  • Previous reports have indicated that exposure to solar radiation has a high risk of deleterious effects on skin, which may further result in skin cancers such as basal/squamous-cell carcinoma (BCC/SCC) and cutaneous malignant melanoma [1,2,3]

  • Ultraviolet (UV) rays have been identified as a carcinogen with long-term irradiation and are an important risk factor for skin cancer

  • We report the use of optical coherence tomography/optical coherence tomography angiography (OCT/OCTA) to study acute UV-induced effects on skin in vivo

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Summary

Introduction

Previous reports have indicated that exposure to solar radiation has a high risk of deleterious effects on skin, which may further result in skin cancers such as basal/squamous-cell carcinoma (BCC/SCC) and cutaneous malignant melanoma [1,2,3]. Excessive UV exposure induces genetic mutants as a result of damage to the cellular DNA of skin, and it is a key factor in nonmelanoma skin cancers and BCC/SCC [4]. The UV spectrum ranges from 10 to 400 nm and can be roughly divided into three sub-bands: UVA, UVB, and UVC. Long-term exposure to UVA rays makes skin cells age faster and causes damages to DNA. UVB rays cause DNA damage and may further result in skin cancer with long-term irradiation. The UVC component in solar light is blocked by the atmosphere

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