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Journal of the Korean Institute of Illuminating and Electrical Installation Engineers

ISO Journal TitleJ Korean Inst. IIIum. Electr. Install. Eng.

  1. (Researcher, KOPTI, Korea)
  2. (Principal Researcher, KOPTI, Korea)
  3. (Director, R&D Center, Optoelec Co., Ltd., Korea)



Color rendering (Ra, Rf, Rf_skin), Cyanosis color-difference index (CCDI), Cyanosis observation, Medical lighting, Tunable correlated color temperature (CCT)

1. Introduction

Cyanosis is a clinical condition characterized by bluish or purplish discoloration of the skin and mucous membranes due to reduced arterial oxygen saturation and serves as a critical visual indicator for rapid patient assessment in emergency, respiratory, and cardiovascular care[1]. Although it can be measured with specialized equipment, visual inspection by medical personnel remains a vital basis for clinical judgment in emergencies and during initial consultations[2]. Because the perceived skin color depends strongly on the spectral characteristics of the lighting, the lighting conditions directly affect detection accuracy; in particular, the 450–500nm range strongly influences cyanosis contrast[3, 4]. However, hospital wards commonly use conventional white LEDs optimized mainly for a high General Color Rendering Index (Ra), which may distort skin color perception[5]. To quantify such distortion, the AS/NZS 1680.2.5 standard defines the Cyanosis Observation Index (COI) with a recommended criterion of 3.3 or lower[6].

Previous studies have largely focused on improving color reproduction and optimizing spectra for cyanosis observation at specific correlated color temperatures (CCTs) [7– 9]. Since the 450–500nm region favors cyanosis contrast while the red region favors natural skin-color reproduction, and warm and cool-white LEDs differ markedly in these bands, a fixed spectrum cannot simultaneously optimize both. Moreover, the optimal spectral conditions vary with the patient's condition and observation environment, so fixed-CCT lighting cannot adequately accommodate diverse clinical situations. These facts motivate the development of tunable-CCT lighting that actively controls the spectral power distribution (SPD); LED sources are well suited to such medical lighting owing to their wavelength selectivity and flexible control of illuminance and CCT[10].

In this study, a dual-channel LED lighting system for cyanosis observation is designed by combining 3000 K and 5000 K LEDs with distinct spectral characteristics. Using lookup table (LUT)-based current control, optical and colorimetric performance under CCT-tunable operation are quantitatively evaluated through an integrated analysis of color quality metrics—Ra, the Color Fidelity Index (Rf), the Skin Color Fidelity Index (Rf_skin), and a cyanosis color-difference index (CCDI, the color difference between normal and cyanotic skin)—together with illuminance and uniformity.

2. System Design

2.1. Design Requirements for Medical Lighting

Medical lighting must provide sufficient and uniformly distributed illuminance. Here, the average illuminance is defined as the arithmetic mean over the observation plane, and uniformity is defined as the ratio of minimum to average illuminance on that plane. EN 12464-1 and KS A 3011 specify at least 200 lx with a uniformity of 0.6 or higher for hospital wards[11, 12]. The proposed system is intended as ceiling-mounted lighting for general wards and inpatient observation rather than for high-illuminance treatment or emergency use; its design parameters were therefore set to meet general-ward requirements across the entire tunable CCT range, while higher levels may be required in environments such as emergency or treatment rooms. To ensure accurate perception of skin and mucous membrane color changes, an Ra of 90 or higher was adopted as the baseline. Ra, Rf, and Rf_skin were used to assess general color rendering, color fidelity, and skin-color reproduction, respectively, with Rf and Rf_skin evaluated by the ANSI/IES TM-30 method[13]. In addition, cyanosis observation performance was assessed using the CIEDE2000-based CCDI, which quantifies the perceptual difference between normal and cyanotic skin rather than applying the fixed COI threshold of the AS/NZS standard.

2.2. Spectral and Color Characteristics of LED Light Sources

The Luminus MP-3030-21C2 LED package was employed in this research. The main specifications of the LED package, including package size, nominal CCT, Color Rendering Index (CRI), and relevant optical characteristics, are summarized in Table 1, which is based on the manufacturer’s datasheet[14].

Table 1. Main specifications of the LED light source used in this study

Item Specification
Manufacturer Luminus Devices
Model MP-3030-21C2
Package type 3030 SMD LED
Package size 3.0 mm × 3.0 mm
Nominal CCT 3000 K / 5000 K
CRI ≥ 90
Major spectral feature 3000 K: red region dominant / 5000 K: blue–cyan region dominant

To implement the dual-channel configuration, 3000 K and 5000 K LEDs were utilized as they exhibit distinct spectral characteristics. The selected LED package provides high color rendering performance (CRI ≥ 90) and broad spectral characteristics, which are important for perceiving subtle color changes in the skin and mucous membrane.

Fig. 1. Chromaticity coordinates and spectral power distributions of 3000 K and 5000 K LED light sources

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Fig. 1 illustrates the CIE color coordinates and SPDs of the two LEDs. The 3000 K LED exhibits high radiant intensity near 630nm, emphasizing the red spectral region. In contrast, the 5000 K LED shows pronounced spectral components around 450nm and 490nm, highlighting the blue–cyan spectral range.

Specifically, in the 450–500nm range, the radiant intensity of the 5000 K LED is approximately 2 to 3 times higher than that of the 3000 K LED, which contributes to enhancing the reflection contrast between oxygenated and deoxygenated blood. Conversely, the 3000 K LED shows a relatively high radiant intensity in the red spectral region, making it advantageous for reproducing the red components of the skin and mucous membrane.

Table 2 summarizes the color quality metrics for the two LEDs. The measured CCTs were 2991 K and 4827 K, respectively, which are close to the target CCTs. Furthermore, the Ra of both light sources satisfies the standards for medical lighting, and the Rf and Rf_skin also exhibit similar levels.

Table 2. Optical and color quality metrics of the 3000 K and 5000 K LEDs

Target CCT (K) Measured CCT (K) Ra Rf Rf_skin
3000 2991 93.9 88.3 90.4
5000 4827 93.2 91.2 94.6

As such, the two light sources exhibit complementary spectral characteristics in the blue–cyan and red regions. Their combined operation provides a foundation for supporting both cyanosis contrast perception and skin color reproduction across the tunable CCT range.

2.3. Dual-Channel LED Panel Design

Fig. 2 illustrates the dual-channel LED panel and the simulation configuration. The proposed light source is designed with a panel structure of 594mm × 594mm × 31mm and consists of a total of 140 LEDs.

Fig. 2. Configuration of the dual-channel LED panel and simulation setup, including panel dimensions, LED array (3000 K and 5000 K), and observation plane geometry

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The optical and electrical characteristics of the dual-channel LED panel, based on the MP-3030-21C2 LED package, are summarized in Table 3. The LED package specifications were obtained from the manufacturer’s datasheet[14], and the panel-level driving conditions were determined based on the LUT-based current control used in the simulation.

Table 3. Optical and electrical characteristics of the dual-channel LED panel based on the MP-3030-21C2 LED package

Item 3000 K channel 5000 K channel Condition
Typical luminous flux 33lm 38lm If = 45mA, Tc = 25°C
Forward voltage 5.3 V Typ., If = 45mA
Reference current 45 mA Tc = 25°C
Maximum forward current 120 mA
Maximum power dissipation 0.8 W
Calculated luminous efficacy 138lm/W 159lm/W Calculated at If = 45mA
Number of LEDs 70 LEDs 70 LEDs Total 140 LEDs
Channel driving current range 0–1286mA 0–1054mA LUT-based control

The 3000 K and 5000 K LEDs are arranged in an alternating pattern to ensure uniform distribution across the panel surface. This layout is intended to achieve illuminance uniformity through the spatial mixing of the two light sources during tunable CCT operation. The same configuration is applied as the simulation conditions for the subsequent optical performance evaluation, where the observation plane is defined as a 2.12m × 2.12m area located 2m below the panel.

2.4. Lookup Table (LUT)-Based CCT Control and Current Configuration

Table 4 presents the LUT summarizing the driving currents for the 3000 K and 5000 K channels according to the target CCT, along with the resulting simulated CCT and the corresponding error (ΔCCT).

Table 4. LUT-based channel currents, simulated CCT, and CCT deviation for target correlated color temperatures. ΔCCT was calculated as the simulated CCT minus the target CCT

Target CCT (K) LED current (mA) Simulated CCT (K) ΔCCT (K)
3000 K 5000 K
3000 1286 0 3090 90
3200 1163 101 3216 16
3500 866 345 3540 40
3800 615 550 3846 46
4000 469 669 4041 41
4200 368 747 4184 -16
4300 276 828 4328 28
4500 180 910 4485 -15
4600 108 966 4612 12
4800 32 1043 4753 -47
5000 0 1054 4815 -185

As the CCT increases, the driving current for the 3000 K channel decreases from 1286mA to 0mA, while the current for the 5000 K channel increases from 0mA to 1054mA. In the intermediate CCT range, both channels are driven simultaneously; for example, at a target CCT of 4000 K, the current is distributed as 469mA and 669mA for each channel, respectively. The simulated CCT exhibits an error ranging from -185 K to +90 K relative to the target values, which corresponds to a relative error of 0.26– 3.7%. This LUT-based current control was implemented to compensate for the nonlinear spectral mixing characteristics associated with CCT variations and to achieve stable operation across a wide CCT range.

3. Optical Performance Evaluation

3.1. Illuminance Distribution and Uniformity Characteristics

Optical performance evaluation was performed using LightTools ray-tracing analysis based on the simulation conditions presented in Fig. 2. The luminous intensity characteristics and SPDs of the LEDs were based on datasheet values, and the light output for each CCT condition was calculated by reflecting the LUT-based current settings from Table 4.

Fig. 3 shows the ray-tracing results, luminous intensity distribution, and illuminance distribution at the 4000 K condition. The luminous intensity distribution exhibits a diffusive characteristic of 113°; consequently, the emitted rays are distributed across the entire observation plane. The illuminance distribution on the observation plane shows high values at the center and decreases towards the periphery.

Fig. 3. Ray-tracing visualization, angular light distribution, and spatial illuminance distribution of the dual-channel LED module at 4000 K on the observation plane

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Fig. 4 illustrates the variations in average illuminance and uniformity across the entire target CCT range (3000–5000 K) based on the LUT. The average illuminance is maintained within the range of 215.2–224.1lx, exhibiting a variation of 4.06% throughout the CCT range. Uniformity is maintained between 0.754 and 0.760, showing a minimal variation of 0.79%. This indicates that the light output and spatial distribution are stably preserved as the currents of the two channels are complementarily adjusted in response to CCT changes.

Fig. 4. Average illuminance and uniformity as a function of correlated color temperature (CCT) under LUT-based current control

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In addition, the optical performance values at representative CCT conditions (3000 K, 4000 K, and 5000 K) are summarized in Table 5. The average illuminance was calculated at 215lx, 223lx, and 215lx, respectively, satisfying the hospital lighting requirement of 200lx or higher. The uniformity ranged from 0.754 to 0.760, exceeding the 0.6 criterion specified by EN 12464-1 and KS A 3011.

Table 5. Summary of optical performance at representative CCT conditions

Target CCT (K) Average illuminance (lx) Max (lx) Min (lx) Uniformity
3000 215 273 162 0.754
4000 223 283 170 0.759
5000 215 277 162 0.755
Requirements ≥200 - - ≥0.6

3.2. Evaluation of Color Quality and Cyanosis Observation Performance

Fig. 5 shows the variations in the color quality metrics and the CCDI across the tunable CCT range.

Fig. 5. Variation of color quality indices (Ra, Rf, Rf_skin) and the cyanosis color-difference index (CCDI) as a function of correlated color temperature (CCT) under LUT-based current control

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Rather than computing the AS/NZS COI directly, a CIEDE2000-based CCDI was designated to quantify how perceptibly cyanotic skin differs from normal skin under each test SPD. The spectral reflectances of normal (oxygenated) and cyanotic (deoxygenated) skin were generated with a single-layer Kubelka–Munk model[3, 4] over 400–700nm at 5nm intervals. The absorption coefficient combined hemoglobin (oxygenated and deoxygenated molar extinction from Prahl[15]; blood volume fraction 8%, oxygen saturation 98% for normal and 70% for cyanotic skin), melanin (3%), and a baseline tissue term following Jacques[3], with a skin reduced-scattering power law[3]; the diffuse reflectance followed the Kubelka–Munk relation. For each SPD, both skin conditions were rendered under the same illuminant (no external reference), and the CIEDE2000 difference between them was computed[16]:

(1)
$CCDI(SPD) = \Delta E_{00} (Lab_{normal}, Lab_{cyanotic})$

where Lab_normal and Lab_cyanotic are the CIELAB coordinates of the modeled normal and cyanotic skin under the test SPD. A larger CCDI indicates a greater perceptual difference, i.e., more readily observable cyanosis; unlike the AS/NZS COI (lower = less distortion), it is a contrast measure for which larger values are favorable, so the 3.3 criterion does not apply.

Under tunable operation, Ra, Rf, and Rf_skin remained stable, with variations of 1.6% (92.3–93.8), 0.81% (89.5–90.2), and 2.16% (91.3–93.3), respectively. The CCDI increased monotonically from 0.86 at 3000 K to 1.54 at 5000 K, indicating that cyanosis is least perceptible at 3000 K and most at 5000 K, consistent with the higher 450–500 nm content of the 5000 K channel. Conversely, skin redness a* (evaluated against each SPD’s own white point) decreased from 15.4 to 12.4, indicating more natural skin-color reproduction at a lower CCT. Since the two move in opposite directions, no single fixed CCT maximizes both; the dual-channel tunable configuration—combining the cyanosis-contrast advantage of the 5000 K channel with the skin-color advantage of the 3000 K channel—lets the operator select the CCT best suited to each clinical situation. Table 6 summarizes the representative results.

Table 6. Summary of color quality indices, CCDI (ΔE₀₀), and skin redness a* for 3000 K, 4000 K, and 5000 K

Target CCT (K) Ra Rf Rf_skin CCDI (ΔE₀₀) a*_normal
3000 93.8 89.6 91.5 0.86 15.4
4000 93.0 89.5 91.3 1.27 13.7
5000 92.3 90.2 93.3 1.54 12.4
Requirements ≥90 - - - -

To relate the LED sources to the panel-level simulation, the measured color quality indices were compared with the simulated values at representative CCTs (Table 7).

Table 7. Comparison between measured LED source characteristics and simulated LED panel performance

Target CCT (K) Metric Measured LED source Simulated LED panel
3000 CCT (K) 2991 3090
Ra 93.9 93.8
Rf 88.3 89.6
Rf_skin 90.4 91.5
5000 CCT (K) 4827 4815
Ra 93.2 92.3
Rf 91.2 90.2
Rf_skin 94.6 93.3

The measured and simulated Ra, Rf, and Rf_skin agreed closely at both 3000 K and 5000 K, indicating that the source characteristics were well reflected in the panellevel simulation and that the proposed tunable system can flexibly select CCT through active SPD control.

4. Conclusion

In this study, a dual-channel CCT-tunable LED lighting system for cyanosis observation was designed and evaluated through simulation. LUT-based current control of combined 3000 K and 5000 K LEDs achieved continuous CCT variation over the entire range.

Across the full range, the average illuminance (215.2–224.1lx) and uniformity (0.754–0.760) satisfied the hospital requirements of ≥200lx and ≥0.6, with variations limited to 4.06% and 0.79%, respectively, confirming stable light output and spatial distribution. Color quality also remained stable (Ra 92.3–93.8, with steady Rf and Rf_skin), preserving skin and mucous-membrane color reproduction despite CCT variation.

The CIEDE2000-based CCDI increased monotonically from 0.86 (3000 K) to 1.54 (5000 K), indicating greater cyanosis perceptibility at higher CCT—consistent with the stronger 450–500nm emission of the 5000 K channel—whereas skin redness a* decreased from 15.4 to 12.4. Because these two requirements are favored at opposite ends of the range, the tunable dual-channel design allows the appropriate CCT to be selected depending on the clinical situation. As the CCDI is a simulation-based relative measure rather than the AS/NZS COI, it does not by itself establish clinical effectiveness; experimental validation, together with comparisons against various LED spectra and conventional hospital lighting, remains as future work.

Overall, the proposed system maintains stable optical and colorimetric performance under tunable CCT operation, indicating its potential for LED-based medical lighting.

Acknowledgements

This work was supported by the Technology Innovation Program (No. 2410015585, Development and demonstration of high color light ICT lighting system with cyanosis diagnosis and sterilization to enter the global market) funded By the Ministry of Trade, Industry and Resources (MOTIR, Korea)

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Biography

Seung-Wan Park
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He received his B.S. degree from the School of Optical Engineering, Chosun University, Gwangju, South Korea, in Feb. 2023. He is a research engineer at the Korea Photonics Technology Institute, specializing in Design and Development of Mobility Convergence Product Lighting Optics. He is interested in mobility lighting systems.

Yu-Rim Kang
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She received her M.S. degree from the School of Mechanical System Engineering, Chosun University, Gwangju, South Korea, in Feb. 2023. She is a researcher at the Korea Photonics Technology Institute, specializing in thermal design and the analysis of mobility convergence products. She is interested in thermal management systems.

Yoon-Chul Lee
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He completed his Ph.D. coursework in Physics at Chonnam National University, Gwangju, South Korea, in Feb. 2013. He is a Principal Research Engineer at the Korea Photonics Technology Institute, specializing in optic system design. He is interested in mobility lighting systems and Human-Central Lighting.

Yong Woo Kim
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He received his M.E. degree in Optical Engineering from Sejong University, Seoul, South Korea, in August 2003. He is currently a Director with Optoelec Co., Ltd., specializing in R&D of wafer-level optics and various applied optical solutions. He is interested in Micro & Nano optics and advanced lighting systems.

Hyeon Woo Kim
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He is a researcher specializing in urology and biomedical engineering. He holds an M.D. from Pusan National University School of Medicine (2008) and obtained Ph.D. degrees from the Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Korea (2017) and Pusan National University School of Medicine (2025). His research focuses on functional urology, endourology, and medical device development, aimed at bridging the gap between engineering technology and clinical applications.

Chang-Ju Park
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He is a researcher specializing in optical sensors and actuators. He received his Ph.D. in Medical System Engineering from the Gwangju Institute of Science and Technology (GIST), Gwangju, Republic of Korea, in August 2016. His research interests include optical and spectroscopic sensing technologies, as well as bio-medical systems.