SIST EN ISO 13304-1:2023 PDF
Radiological protection - Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation - Part 1: General principles (ISO 13304-1:2020)
Radiological protection - Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation - Part 1: General principles (ISO 13304-1:2020)
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 27
- Дата публикации:
- 30 января 2023 г.
- Издание:
- ISO 13304-1:2020
- ICS:
- 13.280
The primary purpose of this document is to provide minimum acceptable criteria required to establish a procedure for retrospective dosimetry by electron paramagnetic resonance spectroscopy and to report the results. The second purpose is to facilitate the comparison of measurements related to absorbed dose estimation obtained in different laboratories. This document covers the determination of absorbed dose in the measured material. It does not cover the calculation of dose to organs or to the body. It covers measurements in both biological and inanimate samples, and specifically: a) based on inanimate environmental materials like glass, plastics, clothing fabrics, saccharides, etc., usually made at X-band microwave frequencies (8 GHz to 12 GHz); b) in vitro tooth enamel using concentrated enamel in a sample tube, usually employing X-band frequency, but higher frequencies are also being considered; c) in vivo tooth dosimetry, currently using L-band (1 GHz to 2 GHz), but higher frequencies are also being considered; d) in vitro nail dosimetry using nail clippings measured principally at X-band, but higher frequencies are also being considered; e) in vivo nail dosimetry with the measurements made at X-band on the intact finger or toe; f) in vitro measurements of bone, usually employing X-band frequency, but higher frequencies are also being considered. For biological samples, in vitro measurements are carried out in samples after their removal from the person or animal and under laboratory conditions, whereas the measurements in vivo are carried out without sample removal and may take place under field conditions. NOTE The dose referred to in this document is the absorbed dose of ionizing radiation in the measured materials.
Abstract
Overview
EN ISO 13304-1:2022 (ISO 13304-1:2020) - "Radiological protection - Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation - Part 1: General principles" - defines the minimum criteria for establishing and reporting retrospective dosimetry by EPR spectroscopy. Its primary aim is to ensure reliable determination of the absorbed dose in measured materials and to facilitate meaningful comparison of dose estimates between laboratories. This European adoption by CEN aligns with the ISO international text.
Key topics and technical requirements
The standard sets out general principles and minimum acceptable criteria across the EPR retrospective dosimetry workflow, including:
-
Scope and limitations
- Covers absorbed dose in the measured material only - does not provide conversion to organ or whole-body dose.
- Applies to both biological (tooth enamel, nails, bone) and inanimate materials (glass, plastics, clothing, saccharides).
-
Sample types and measurement modes
- Inanimate environmental materials: typically X‑band (8–12 GHz).
- In vitro tooth enamel and bone: usually X‑band, with higher frequencies under consideration.
- In vivo tooth dosimetry: typically L‑band (1–2 GHz).
- In vitro and in vivo nail dosimetry: X‑band for clippings and intact fingers/toes respectively.
-
Laboratory and field requirements
- Safety (magnetic field, electromagnetic exposure, biohazards).
- Sample collection, identification, transport and storage procedures.
- Sample preparation and resonator/sample loading practices.
-
Instrumentation and measurement
- Principles of EPR spectrometers and resonator requirements.
- Optimization of measurement parameters (microwave, magnetic field, signal channels).
- Background signal measurement, spectrometer stability, baseline drift control.
- Use of standard samples/field markers, reproducibility monitoring and coding of spectra.
-
Data handling and quality
- Determination of radiation-induced signal intensity and conversion to absorbed dose.
- Measurement uncertainty estimation.
- Investigation procedures for questioned doses.
- Quality assurance (QA) / Quality control (QC) and minimum documentation requirements for traceability and inter-laboratory comparability.
Applications and users
EN ISO 13304-1 is intended for professionals and organizations involved in:
- Radiation protection and emergency response (triage after radiological incidents)
- EPR diagnostics laboratories and dosimetry service providers
- Forensic radiology and public health dose reconstruction
- Research institutions developing retrospective dosimetry methods
- Regulatory bodies and accreditation assessors
Using this standard helps ensure consistent, comparable EPR-based absorbed dose estimates across laboratories, improving the reliability of retrospective dose reconstruction and supporting clinical, epidemiological, forensic, and emergency decision-making.
Related standards
- ISO 13304 series (see ISO 13304-2 referenced informatively in the document) for additional technical guidance and complementary parts of the series.
Технические детали
- Технический комитет
- I13 - Imaginarni 13
- SKU
- SIST EN ISO 13304-1:2023
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