Submitted:
01 July 2026
Posted:
02 July 2026
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Abstract
Keywords:
1. Introduction
2. Characteristics and Generation Mechanisms of Medical Radioactive Wastewater
2.1. Medical Radionuclides
2.2. Sources of Medical Radioactive Wastewater
- In the course of diagnostic and therapeutic procedures in nuclear medicine, excretions produced after patients have ingested or been injected with radioisotopes—such as sweat, saliva, urine, faeces and vomit [36].This type of wastewater is one of the major sources of medical radioactive wastewater; its radioactivity is closely related to the dose of the radionuclide received by the patient, the half-life of the radionuclide, and the metabolic rate—radioactive isotopes not absorbed or utilised by the patient are excreted through metabolic processes and subsequently enter the wastewater system. Table 2 shows the typical proportion of therapeutic radionuclides discharged via metabolic pathways [34].
- 2.
- Wash water generated from the cleaning of patient medication cups, syringes and pipettes used during the dispensing of high-activity radioisotopes [37]. During diagnostic and therapeutic procedures and drug preparation in the Department of Nuclear Medicine, trace amounts of radionuclides remain on the surfaces of various vessels that have come into contact with radioisotopes. To prevent cross-contamination and ensure the safety of diagnosis and treatment, these vessels must be washed repeatedly; the wastewater generated during this process carries residual radioactive substances, forming radioactive washwater. Although the radioactivity of this wastewater is lower than that of wastewater generated from patient excreta, the high frequency of vessel cleaning and the large volume of water used result in a relatively significant volume of wastewater. Furthermore, as the distribution of nuclide residues is uniform, this represents one of the key areas requiring strict control in wastewater reduction efforts.
- 3.
- Radioactive wastewater discharged from the preparation of medical labelled compounds and the disposal of excess radioactive isotopes [38]. During the preparation of radiopharmaceuticals, operations such as the synthesis and purification of medical labelled compounds are required, which generate small quantities of waste liquid containing radionuclides. Furthermore, to ensure precise therapeutic dosing and prevent excessive radionuclides from entering the patient’s body, surplus radioactive isotopes generated during preparation must be disposed of in accordance with regulations; such disposal waste liquid also directly constitutes a component of medical radioactive wastewater. The wastewater generated by this process has relatively high radioactivity, with a single nuclide component and concentrated concentrations. If not subject to targeted control measures, it can easily cause local radioactive contamination and increase the difficulty of subsequent treatment.
3. Source-Oriented Reduction Strategies
3.1. Measures for the Reduction of Medical Radionuclides
3.1.1. Innovations in Imaging Equipment and Detection Technology: Enhancing Sensitivity and Reducing Counting Requirements
a. High-Sensitivity Detector Materials and Structural Optimisation
b. Clinical Applications of TOF Technology
3.1.2. Optimisation of Image Reconstruction Algorithms: Compensating for Insufficient Counts at Low Doses and Improving Image Quality
a. Optimisation and Application of Iterative Reconstruction Algorithms
b. Breakthroughs in DLR
3.1.3. Individualised Acquisition and Administration Protocols: Precise Matching of Requirements to Avoid Dose Waste
3.1.4. Radiopharmaceutical Modifications: Improving the Target-to-Background Ratio and Increasing Nuclide Utilisation
3.2. Measures to Reduce the Volume of Medical Radioactive Wastewater
3.2.1. Water Conservation at Source: Reducing Unnecessary Water Use and Controlling Volume at the Point of Generation
3.2.2. Separate Collection: Avoiding Mixing and Reducing Inert Wastewater
3.2.3. System Optimisation: Optimising the Drainage System to Improve Flow Control Efficiency
4. Treatment Technologies: From Decay to Process Intensification
4.1. Decay Tanks
4.1.1. Pulsed-Flow Decay Tanks
4.1.2. Intermittent Decay Tank
4.1.3. Intelligent Decay Tanks
4.2. Decontamination Technologies
4.2.1. Chemical Precipitation Method
4.2.2. Adsorption Method
4.2.3. Ion Exchange
4.2.4. Electrochemical Methods
4.2.5. Membrane Separation Method
4.2.6. Biological Methods
4.2.7. Comparison of Methods
5. Management and Discharge: From Compliance to Risk-Based Control
5.1. Management Standards
5.2. Discharge Standards
6. End-to-End Framework for Sustainable Management of Medical Radioactive Wastewater
7. Future Perspectives
8. Conclusion
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
Abbreviations
| PET/CT | Positron Emission Tomography/ Computed Tomography |
| SPECT/CT | Single-Photon Emission Computed Tomography/ Computed Tomography |
| MIBG | Meta-Iodobenzylguanidine |
| TOF | Time-of-Flight |
| DLR | Deep Learning Reconstruction |
| SNR | Signal-to-Noise Ratio |
| LSO | Lutetium Oxyorthosilicate |
| LYSO | Lutetium Yttrium Oxyorthosilicate |
| SiPMs | Silicon Photomultiplier Tubes |
| LAFOV | Long Axial Field of View |
| OSEM | Ordered Subsets Expectation Maximization |
| PSF | Point Spread Function |
| FDG | Fluorodeoxyglucose |
| FBP | Filtered Backprojection |
| AUC | Area Under the Curve |
| BSREM | Block Sequential Regularised Expectation Maximisation |
| AI | Artificial Intelligence |
| DPR | Deep Progressive Reconstruction |
| BSA | Body Surface Area |
| BMI | Body Mass Indices |
| TBR | Target-to-Background Ratio |
| EB | Evans Blue |
| RJ | Radioactivity Judgement |
| IoT | Internet of Things |
| MOF | Metal-Organic Framework |
| MSBP | Melamine-Styrene-Based Polymer |
| N-AF | Alkaline Anion-Exchange Fibres |
| CDI | Capacitive Deionisation |
| FCDI | Flow-Electrode Capacitive Deionisation |
| PPy | Polypyrrole |
| NiHCF | Nickel Hexacyanoferrate |
| MF | Microfiltration |
| UF | Ultrafiltration |
| NF | Nanofiltration |
| RO | Reverse Osmosis |
| ALARA | As Low As Reasonably Achievable |
| FO | Forward Osmosis |
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| Radionuclide | Half-life | Main radiation type | Clinical application | Category |
|---|---|---|---|---|
| ⁹⁹mTc | 6.02 h | γ-ray | SPECT imaging of multiple organs (most widely used) | Diagnostic |
| ¹⁸F | 109.8 min | β⁺ (positron) | PET/CT imaging for tumours, the brain and the myocardium | Diagnostic |
| ⁶⁸Ga | 67.7 min | β⁺ (positron) | PET/CT imaging for prostate cancer and neuroendocrine tumours | Diagnostic |
| ¹²³I | 13.2 h | γ-ray | Thyroid function and nodule diagnosis | Diagnostic |
| ¹³¹I | 8.02 days | β⁻ + γ | Hyperthyroidism, differentiated thyroid cancer (therapy + imaging) | Theranostic |
| ¹⁷⁷Lu | 6.64 d | β⁻ + γ | Targeted therapy for neuroendocrine tumours, prostate cancer | Therapeutic |
| ⁹⁰Y | 64.1 h | β⁻ | Liver cancer microspheres, tumour-targeted therapy | Therapeutic |
| ²²³Ra | 11.4 days | α-ray | Treatment of bone metastases in prostate cancer | Therapeutic |
| ²²⁵Ac | 10.0 days | α-ray | Targeted alpha therapy for advanced solid tumours | Therapeutic |
| ⁸⁹Sr | 50.5 d | β⁻ | Palliative analgesia for bone metastases | Therapeutic |
| ¹⁵³Sm | 46.3 h | β⁻ + γ | Pain relief and lesion inhibition in bone metastases | Therapeutic |
| ³²P | 14.3 days | β⁻ | Haematological diseases, cutaneous haemangioma | Therapeutic |
| ¹²⁵I | 59.4 days | γ-ray | In vitro assay, brachytherapy seed implantation | Adjuvant/ Therapeutic |
| Nuclide and form | Disease or condition treated | Proportion of activity discharged to sewers (%) |
|---|---|---|
| 198 Au colloid | Malignant disease | 0 |
| 131 I | Hyperthyroidism | 54 |
| 131 I | Thyroid carcinoma | 84-90 |
| 131 I MIBG1 | Pheochromocytoma | 89 |
| 32 P phosphate | Polycythaemia, etc. | 42 |
| 89 Sr chloride | Bone metastases | 92 |
| Radioactive Contaminants | Require collection or Not | Treatment Method | |
|---|---|---|---|
| WHO standard | Radioactive wastewater | Required | Stored in a secure area and discharged after decay to background levels |
| ICRP Publication 25 | Liquids spilled during laboratory operations and normal cleaning solutions for glassware | Not required | Treated via the drainage and sewage systems |
| Blood and excreta from patients undergoing radionuclide therapy | Not required | Discharged via bathroom drains | |
| ICRP Publication 105 | Excreta from patients undergoing radionuclide therapy | Not recommended | Discharged into the sewage system |
| IAEA | Excreta from patients undergoing diagnostic imaging | Not required | Discharged via the toilet drain |
| Excreta from patients undergoing therapy | Not required | Discharged after dilution in a continuous wastewater treatment system | |
| China | Radioactive liquid and solid waste | Required | a) Radioactive liquid waste containing nuclides with a half-life of less than 24 hours may be released directly after a storage period exceeding 30 days; b) Radioactive liquid waste containing nuclides with a half-life of more than 24 hours may be released after a storage period exceeding 10 times the longest half-life (including a storage period exceeding 180 days for waste containing iodine-131) |
| Italy | Radioactive waste liquids discharged by patients | Generally required | Stored in a dedicated septic tank for approximately 10 hours |
| UK | Radioactive liquid and solid waste | Subject to the limits specified by the wastewater treatment operator | If the discharge limits are not exceeded, the waste may be discharged into the sewage system; however, radioactive barium sulphate must not be discharged |
| Spain | Excreta from patients treated in the nuclear medicine department | Not required | Discharged via the toilet drain |
| France | Urine from patients treated with short-lived radioactive elements | Must | Collected in a shielded room and connected to a septic tank to delay and allow the decay |
| Urine from patients treated with radioactive elements having a long half-life | - | Handled by a designated facility | |
| USA | Excreta from patients undergoing medical diagnosis or treatment with radioactive substances | Not required | Discharged directly into the municipal sewerage system |
| Oman | Radioactive wastewater | Recommended | In areas lacking a centralised sewage system, decay tanks are still recommended as a safe disposal method. |
| Country | Regulations and Standards | Control Method | Standard Values |
|---|---|---|---|
| China | GB 18466-2005 | Concentration | Total α activity at the total discharge outlet for radioactive waste liquid ≤ 1 Bq/L, total β activity ≤ 10 Bq/L, and the activity concentration of 131I ≤ 10 Bq/L |
| HJ 1188—2021 | Concentration | Total α ≤ 1 Bq/L and total β ≤ 10 Bq/L at the total discharge outlet for radioactive waste liquid; the activity concentration of 131I shall not exceed 10 Bq/L | |
| GB 18871-2002 | Concentration and total | Firstly, discharges must not exceed the discharge limits approved by the regulatory authority, including both total discharge limits and concentration limits; Secondly, for waste liquid meeting the criteria for low-level radioactive waste, the discharge requirements are as follows: 1) The total activity discharged per month shall be ≤ 10 ALImin; 2) The activity of each discharge shall be ≤ 1 ALImin, and the discharge point shall be flushed with a volume of water not less than three times the discharge volume after each discharge. |
|
| USA | 10 CFR Part 20 - Standards for Protection Against Radiation | Monthly average concentration and annual total | The monthly average concentration must not exceed the specified limit; the total annual amount of radioactive material must not exceed 185 GBq for 3H and 37 GBq for 14C, and the total amount of other radioactive materials must not exceed 37 GBq |
| France | ASN Position Papers & Technical Instructions | Concentration | The total radioactivity level in wastewater discharged by healthcare facilities into the municipal sewer system must be below 10 Bq/L; the discharge limit for 131I may be relaxed to 100 Bq/L |
| UK | The Environmental Permitting (England and Wales) Regulations 2016 | Monthly average concentration and annual total | Must not exceed the prescribed concentration and total quantity limits |
| India | AERB/NRF/SG/RW-10 | Annual total, daily total and monthly average concentration | The total annual discharge shall not exceed 37 GBq; for 131I, the daily discharge shall not exceed 3.7 MBq and the monthly average concentration shall not exceed 22.2 MBq/m³ |
| Oman | Ministerial Decree No.249/97 | Daily total and monthly average concentration |
131I daily emission limit: 3.7 MBq, Monthly average concentration limit: 22.2 MBq/m³ |
| Slovenia | 96/29/Euratom of 13 May | Annual total and quarterly total | Annual total 200 GBq, quarterly total 80 GBq |
| Brazil | Resolução CNEN 167/14 | Monthly average concentration and annual total | For 131I in liquid waste, the total monthly activity released must not exceed 1.9×10⁴ Bq/m³, and the total annual amount of 131I discharged into the sanitary sewer system must not exceed 1×10⁷ Bq |
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