Ultraviolet-B phototherapy is a dosimetric therapy. The clinical outcome depends on delivering a defined radiant exposure, measured in millijoules per square centimetre, to a defined skin area within a defined time, and the difference between a therapeutic dose and a burning dose is often less than a factor of three. This white paper is written for medical device engineers and clinical engineering teams building UVB LED phototherapy equipment, and for component buyers who must judge whether an emitter is suitable for that role. It covers the dose-response relationship, spectral irradiance measurement, minimal erythema dose (MED) reference values, and the design discipline required to keep a UVB device safe. QUEENDOM’s J-14 3535 UVB (275/310 nm) and J-13 3 mm UVB emitters are used as the worked examples. The paper also draws a hard boundary between UVB phototherapy and UVA or 405 nm systems, which operate in a different biological regime and must not be substituted for one another.

1. Why UVB dosimetry is unforgiving

UVB occupies the 280–315 nm band. It is the portion of the solar spectrum that produces sunburn, stimulates cutaneous vitamin D synthesis, and — under controlled dosage — induces the immunomodulation that makes phototherapy effective in psoriasis, vitiligo, atopic dermatitis and several other conditions. Narrowband UVB, historically produced by fluorescent lamps with a peak near 311 nm, has become the clinical standard for many indications because it delivers therapeutic effect with less erythema than broadband UVB.

Two properties make UVB dosimetry harder than most lighting engineering tasks.

The erythema action spectrum is steep. The relative effectiveness of UVB for producing erythema peaks near 297 nm and falls sharply towards 315 nm. A small error in peak wavelength is a large error in biological effect.

The dose-response curve saturates. Therapeutic response increases with dose and then plateaus, while erythema continues to increase. The therapeutic window is the region between the minimum effective dose and the threshold erythema dose, and it is narrow.

BandWavelength rangePrimary biological effectRole in phototherapy
УФА (ультрафиолет А) / UVA315–400 nmPigmentation, dermal penetrationPUVA, UVA1 for scleroderma
УФБ (ультрафиолет Б) / UVB280–315 nmEpidermal DNA damage, immunomodulationNarrowband UVB phototherapy
Narrowband UVB310–313 nmOptimised therapeutic/erythema ratioStandard clinical phototherapy
UVB, short275–300 nmHigh erythema effectivenessEmerging LED platform, requires careful dosing
УФС (ультрафиолет С) / UVC200–280 nmGermicidal, superficial absorptionDisinfection, not phototherapy

2. The dose-response relationship

Phototherapy dose is expressed as radiant exposure:

“ H = E × t “

where H is dose in mJ/cm², E is irradiance in mW/cm² and t is exposure time in seconds. Because the response is not linear, the clinical protocol steps the dose along a protocol-specific ladder, typically starting at 50–70 % of the patient’s MED and increasing by 5–20 % per session depending on the response and the number of treatments per week.

Therapeutic response and erythema versus delivered UVB dose 0 250 500 750 1000 1250 0 25 50 75 100 Delivered UVB dose (mJ/cm²) Relative response (%) minimum effective dose MED (erythema threshold)
Figure. Therapeutic response and erythema versus delivered UVB dose. Green solid: therapeutic response, which plateaus above roughly 500 mJ/cm². Red dashed: erythema, which continues to rise. Blue marker: representative minimum effective dose. Amber marker: representative minimal erythema dose. Representative values, for engineering and clinical-protocol reference only. Not a certified clinical dataset.

2.1 Dose versus exposure time

Because dose is the product of irradiance and time, a device’s practical session length is set by the irradiance it can deliver at the treatment plane. The table below shows delivered dose against exposure time for three irradiance levels that correspond to typical LED panel and lamp-based systems.

Irradiance at skin30 s60 s120 s300 s
1 mW/cm²30 mJ/cm²60 mJ/cm²120 mJ/cm²300 mJ/cm²
3 mW/cm²90 mJ/cm²180 mJ/cm²360 mJ/cm²900 mJ/cm²
10 mW/cm²300 mJ/cm²600 mJ/cm²1,200 mJ/cm²3,000 mJ/cm²
30 mW/cm²900 mJ/cm²1,800 mJ/cm²3,600 mJ/cm²9,000 mJ/cm²

Clinical protocols for whole-body narrowband UVB commonly operate between 5 and 15 mW/cm² at the patient plane, producing session lengths of one to ten minutes. Higher irradiance shortens sessions but increases the consequence of a timer or shutter fault, which is why IEC 60601-2-83 places such emphasis on independent dose-limiting safeguards.

3. Spectral irradiance and why wavelength accuracy matters

The therapeutic and erythematous effectiveness of UVB depends on wavelength, and the two action spectra are not identical. The practical consequence is that the emitter’s peak wavelength and full-width half-maximum must be specified and verified, not assumed.

Spectral irradiance of UVB emitters against the erythema action spectrum 270 290 310 330 350 0 25 50 75 100 Wavelength (nm) Relative spectral irradiance (%) erythema action spectrum (peak ~297 nm)
Figure. Relative spectral irradiance of two UVB emitters against the erythema action spectrum. Blue solid: 275 nm emitter, FWHM ≈ 12 nm. Green solid: 310 nm emitter, FWHM ≈ 14 nm. Red dashed: erythema action spectrum, normalised, peaking near 297 nm. Note the substantial overlap of the 275 nm emitter with the erythema peak. Representative values, for engineering reference only. Not a certified test report.

The figure carries the central engineering warning of this paper. A 275 nm emitter lies close to the peak of the erythema action spectrum and is therefore intrinsically more erythemogenic per unit dose than a 310 nm emitter. It is useful where superficial, high-potency action is wanted, but its therapeutic window is narrower and its dosing must be more conservative. A 310 nm emitter sits further from the erythema peak and closer to the therapeutic optimum that made narrowband UVB successful with fluorescent lamps.

PropertyJ-14 3535 UVBJ-13 3 mm UVB
Peak wavelength options275 nm / 310 nm275 nm / 310 nm
FWHM≤ 12 nm (275 nm) / ≤ 14 nm (310 nm)≤ 12 nm / ≤ 15 nm
Radiant flux8–18 mW @ 350 mA (270–320 nm total)2–5 mW @ 20 mA
Forward voltage5.5–7.0 V @ 350 mA5.0–6.5 V @ 20 mA
Viewing angle120°20°–30° (lensed)
Package3.5 × 3.5 mm ceramic, quartz window3 mm through-hole, metal can
Thermal resistance~15 K/W~180 K/W
Targeted functionPanel array, high-irradiance devicesPoint treatment, targeted applicator
Erythema-band overlapHigh at 275 nmHigh at 275 nm

4. Minimal erythema dose and the dosing ladder

MED is defined as the lowest radiant exposure that produces a just-perceptible erythema, assessed 24 hours after exposure. It is patient-specific and depends on Fitzpatrick skin type, prior UV exposure, medication and the anatomical site. Published reference values are used to set the starting dose; they are not a substitute for individual determination.

Fitzpatrick skin typeОписаниеTypical MED at 311 nm (mJ/cm²)Typical whole-body starting dose (mJ/cm²)
IVery fair, always burns200–300130–200
IIFair, burns easily300–500200–350
IIIMedium, sometimes burns500–700350–500
IVOlive, rarely burns700–900500–650
VBrown, very rarely burns900–1,200650–850
VIDeeply pigmented, never burns> 1,200850–1,000+

These values are given for engineering context only. Clinical protocols, starting doses and dose increments are the responsibility of the treating clinician and must follow the applicable national guidance and the device’s cleared indications.

Design considerationRequirementRationale
Dose accuracy±10 % of set pointClinical protocols assume delivered dose
Independent timerSeparate from control firmwarePrevents overexposure on control failure
Irradiance calibrationBefore first use and at defined intervalsLED output drifts with age and temperature
Shutter or enableFail-safe to offDose must stop when the session ends
Uniformity over treatment area≤ 1.3:1 max-to-minAvoids hot spots above MED
Eye protectionMandatory gogglesUVB is a significant ocular hazard

4.1 Dose uniformity and the hot-spot problem

In a multi-emitter panel, dose non-uniformity is the most common source of unexpected erythema. If the maximum-to-minimum irradiance ratio is 1.5:1 and the protocol sets the mean dose at 60 % of MED, the hottest point receives 90 % of MED, and a slightly photosensitive patient will burn. Panels should be designed and validated for a uniformity ratio no worse than 1.3:1 across the treatment area.

Irradiance uniformity across a treatment panel at three emitter pitches 0 200 400 600 800 0 2 4 6 8 Position across panel (mm) Irradiance at 150 mm (mW/cm²) mean irradiance
Figure. Irradiance profile across an 800 mm treatment panel at 150 mm. Red dashed: 60 mm emitter pitch, uniformity 3.6:1 — unusable. Amber solid: 30 mm pitch, uniformity 1.6:1 — marginal. Green solid: 20 mm pitch with diffuser, uniformity 1.08:1 — suitable for clinical use. Representative values, for engineering reference only. Not a certified test report.

5. Product mapping

The two UVB families cover different device architectures. The J-14 3535 ceramic package with a quartz window is designed for panel arrays in whole-body or large-area devices, where its lower thermal resistance and higher per-emitter flux support the irradiance levels clinical protocols require. The J-13 3 mm device, with its lensed narrow beam and through-hole mounting, suits targeted applicators and hand-held point-treatment devices.

Device architectureRecommended partКоличествоWhy
Whole-body treatment panelJ-14 3535 UVB (310 nm)200–600Flux density with manageable thermal load
Targeted plaque therapyJ-13 3 mm UVB (310 nm)5–30Narrow beam, small spot
Hand-held point applicatorJ-13 3 mm UVB (275/310 nm)1–10Lensed output, low current
High-potency superficial deviceJ-14 3535 UVB (275 nm)50–200Short-wavelength action, careful dosimetry
Research / spectroscopic sourceJ-14 3535 UVB10–50Narrow FWHM, quartz window

5.1 Distinguishing UVB from UVA and 405 nm systems

A recurring failure in procurement documents is the conflation of UVB phototherapy devices with UVA or 405 nm systems. They are different therapies with different indications, different action spectra and different safety profiles, and the emitters are not interchangeable.

AttributeUVB (J-14 / J-13)UVA 365/385 nm (J-12)UVA 405 nm (J-10 / J-11)
Wavelength band275 / 310 nm365 / 375 / 385 nm405 nm
Penetration depth in skinEpidermis, 20–100 µmDermis, 100–300 µmDermis, 300–700 µm
Primary therapy usePsoriasis, vitiligo, atopic dermatitisPUVA, UVA1 protocolsPhotodynamic activation, sensing
Erythema potency per unit doseHighLowVery low
Ocular hazardHigh — goggles mandatoryModerateLower
Typical device power for therapyLow (mW/cm² at patient)ModerateModerate to high
Interchangeable with UVB?—NoNo

6. Common mistakes and how to avoid them

MistakeConsequenceCorrection
Treating 405 nm as a substitute for UVBNo therapeutic effect at required doseSpecify UVB emitters for UVB therapy
Assuming published MED applies to every patientErythema or underdosingDetermine MED individually or use conservative starting doses
Quoting emitter flux instead of patient-plane irradianceDelivered dose unknownCalibrate irradiance at the treatment plane
Uniformity ratio above 1.3:1Hot spots exceeding MEDIncrease emitter density or add a diffuser
Relying on firmware timing aloneOverexposure if firmware faultsFit an independent hardware dose limit
No periodic recalibrationDose drifts as emitters ageRecalibrate at defined intervals against a reference meter
Standard silicone encapsulation on a UVB partRapid optical degradationUse a quartz-window emitter such as J-14
Ignoring ocular protectionCorneal and lens injuryMandatory goggles; IEC 62471 classification

7. Verification and test methods

  1. Spectral irradiance measurement — measure the device’s spectral irradiance at the treatment plane with a calibrated spectroradiometer, and report peak wavelength, FWHM and total UVB irradiance. This single measurement underpins dose accuracy.
  2. Irradiance uniformity scan — map the treatment plane on a grid of at least 5 × 5 points and report the maximum-to-minimum ratio. Repeat at the minimum and maximum working distances specified.
  3. Dose timing verification — measure actual delivered dose for each programmed dose level using a calibrated radiometer with dose integration, and confirm it within ±10 % of set point.
  4. Emitter aging and calibration interval — run an LM-80-style maintenance test on the emitter family at rated current, then set the device’s recalibration interval from the resulting depreciation rate.
  5. Photobiological safety assessment — classify the complete device against IEC 62471, including reflected and scattered ultraviolet within the treatment room.
  6. Fault-mode testing — verify that timer failure, shutter failure and firmware crash all result in termination of exposure rather than continuation.

8. Conclusion and selection guidance

UVB phototherapy devices should be designed around dose, not around emitter count or flux. For whole-body and large-area panels, J-14 3535 UVB at 310 nm delivers the wavelength and irradiance that clinical narrowband protocols assume, in a ceramic package with a quartz window that tolerates continuous UV operation. For targeted and hand-held applicators, J-13 3 mm UVB provides a compact, lensed source. Where a 275 nm variant of either part is chosen, treat the device as a higher-potency system with a narrower therapeutic window, and reduce starting doses accordingly: 275 nm sits substantially closer to the erythema action spectrum peak than 310 nm does. In all cases, verify spectral irradiance at the treatment plane, keep uniformity at or below 1.3:1, provide an independent hardware dose limit, and recalibrate at defined intervals. Never substitute UVA or 405 nm emitters into a UVB therapy device.

9. Referenced standards

  • IEC 60601-1 — Medical electrical equipment: general requirements for basic safety and essential performance
  • IEC 60601-2-83 — Particular requirements for the basic safety and essential performance of home light therapy equipment
  • IEC 62471 — Photobiological safety of lamps and lamp systems
  • ISO 15858 — UV-C devices: safety information — permissible human exposure
  • IES LM-80 — Approved method: measuring luminous flux maintenance of LED light sources
  • IES TM-21 — Projecting long-term lumen maintenance of LED light sources
  • CIE S 007 / CIE 174 — Erythema reference action spectrum and standard erythema dose

10. Contact us

QUEENDOM supplies the J-14 3535 UVB (275/310 nm) and J-13 3 mm UVB emitters from stock, with spectral characterization data, binning statements and reference panel layouts for medical device development. Our component engineering group can provide spectral irradiance files and uniformity design guidance on request. Where devices require visible-spectrum sources for photodynamic or sensing functions, our J-12 3535 UVA (365/375/385 nm) and J-10 3 mm UVA (405 nm) parts are available separately. Contact us for samples and application support.

Related products and applications

The UV-B emitters referenced in this dosimetry paper are available in the following families.