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Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators

BACKGROUND: The purpose of this work was to design, validate and implement a media-fill test combined with fluorescein (MFT-F) for the specific qualification and training of radiopharmacy operators, in accordance with United States Pharmacopeia General Chapter 797 and European Good Manufacturing Pra...

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Autores principales: Fersing, Cyril, Deshayes, Emmanuel, Langlet, Sarah, Calas, Laurence, Lisowski, Vincent, Kotzki, Pierre Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7790972/
https://www.ncbi.nlm.nih.gov/pubmed/33411035
http://dx.doi.org/10.1186/s41181-020-00117-6
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author Fersing, Cyril
Deshayes, Emmanuel
Langlet, Sarah
Calas, Laurence
Lisowski, Vincent
Kotzki, Pierre Olivier
author_facet Fersing, Cyril
Deshayes, Emmanuel
Langlet, Sarah
Calas, Laurence
Lisowski, Vincent
Kotzki, Pierre Olivier
author_sort Fersing, Cyril
collection PubMed
description BACKGROUND: The purpose of this work was to design, validate and implement a media-fill test combined with fluorescein (MFT-F) for the specific qualification and training of radiopharmacy operators, in accordance with United States Pharmacopeia General Chapter 797 and European Good Manufacturing Practices. MFT-F was embedded in the quality management system of our radiopharmacy unit. Its validation involved fluorescein concentration choice, media growth promotion test and evaluation protocol controls (with or without intentional aseptic mistakes). Each operator was evaluated following a three-part evaluation form. Evaluation criteria related to garbing and hygiene, fluorescent contamination and bacteriological contamination (pre- and post-evaluation environment controls and MFT-F samples). Combined MFT-F allowed the assessment of aseptic compounding skills and non-contamination of the working area through a single evaluation. It was also designed to fit the constraints of radiopharmacy common practice related to radiation protection equipment and to the small volumes handled. RESULTS: A 0.01% fluorescein concentration was chosen to prepare MFT-F. Addition of fluorescein in the culture medium did not jeopardize its growth properties according to growth promotion test. Eleven operators were evaluated and carried out 3 MFT-F over 3 successive days. Pre- and post-evaluation bacteriological controls of every session showed no CFU of microbiological contaminant above 5. All operators validated the garbing and hygiene evaluation, with an average score of 92.7%. All operators validated the fluorescent contamination evaluation, with an average score of 29.4 out of 30. None of the MFT-F samples showed any visible bacterial growth after incubation. CONCLUSIONS: Combined MFT-F, as a part of a comprehensive sterile compounding training program, appeared as a convenient and promising tool to increase both the sterile compounding safety and awareness of radioactive contamination in radiopharmacy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41181-020-00117-6.
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spelling pubmed-77909722021-01-19 Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators Fersing, Cyril Deshayes, Emmanuel Langlet, Sarah Calas, Laurence Lisowski, Vincent Kotzki, Pierre Olivier EJNMMI Radiopharm Chem Guideline Article BACKGROUND: The purpose of this work was to design, validate and implement a media-fill test combined with fluorescein (MFT-F) for the specific qualification and training of radiopharmacy operators, in accordance with United States Pharmacopeia General Chapter 797 and European Good Manufacturing Practices. MFT-F was embedded in the quality management system of our radiopharmacy unit. Its validation involved fluorescein concentration choice, media growth promotion test and evaluation protocol controls (with or without intentional aseptic mistakes). Each operator was evaluated following a three-part evaluation form. Evaluation criteria related to garbing and hygiene, fluorescent contamination and bacteriological contamination (pre- and post-evaluation environment controls and MFT-F samples). Combined MFT-F allowed the assessment of aseptic compounding skills and non-contamination of the working area through a single evaluation. It was also designed to fit the constraints of radiopharmacy common practice related to radiation protection equipment and to the small volumes handled. RESULTS: A 0.01% fluorescein concentration was chosen to prepare MFT-F. Addition of fluorescein in the culture medium did not jeopardize its growth properties according to growth promotion test. Eleven operators were evaluated and carried out 3 MFT-F over 3 successive days. Pre- and post-evaluation bacteriological controls of every session showed no CFU of microbiological contaminant above 5. All operators validated the garbing and hygiene evaluation, with an average score of 92.7%. All operators validated the fluorescent contamination evaluation, with an average score of 29.4 out of 30. None of the MFT-F samples showed any visible bacterial growth after incubation. CONCLUSIONS: Combined MFT-F, as a part of a comprehensive sterile compounding training program, appeared as a convenient and promising tool to increase both the sterile compounding safety and awareness of radioactive contamination in radiopharmacy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41181-020-00117-6. Springer International Publishing 2021-01-07 /pmc/articles/PMC7790972/ /pubmed/33411035 http://dx.doi.org/10.1186/s41181-020-00117-6 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Guideline Article
Fersing, Cyril
Deshayes, Emmanuel
Langlet, Sarah
Calas, Laurence
Lisowski, Vincent
Kotzki, Pierre Olivier
Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators
title Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators
title_full Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators
title_fullStr Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators
title_full_unstemmed Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators
title_short Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators
title_sort implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators
topic Guideline Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7790972/
https://www.ncbi.nlm.nih.gov/pubmed/33411035
http://dx.doi.org/10.1186/s41181-020-00117-6
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