Migration of plasticizers from PVC medical devices: Development of an infusion model

Affiliation auteurs!!!! Error affiliation !!!!
TitreMigration of plasticizers from PVC medical devices: Development of an infusion model
Type de publicationJournal Article
Year of Publication2015
AuteursBernard L., Cueff R., Chagnon M.C, Abdoulouhab F., Decaudin B., Breysse C., Kauffmann S., Cosserant B., Souweine B., Sautoua V., Grp ARMEDStudy Grou
JournalINTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume494
Pagination136-145
Date PublishedOCT 15
Type of ArticleArticle
ISSN0378-5173
Mots-clésClinical conditions, Infusion, Migration, Model, Plasticizers, PVC
Résumé

Alternatives to DEHP plasticizers are used in various PVC medical devices (MD) for infusion. As they are able to migrate from these MDs into infused solutions, they may come into contact with patient. Different and specific clinical parameters influence their migration in at-risk situations such as infusion. In contrast to the regulations for Food Contact Materials (MCDA), there is currently no acceptable migration limits for the use of these plasticizers in clinical situations. In order to assess their migration, and thus control the risks linked to these MDs, we developed a migration model for the plasticizers in MDs. To this end, we applied a cross-disciplinary methodological process similar to that used in the food-processing industry, taking into account the MDs' conditions of use in clinical practice. The simulation model is simple and includes the following conditions: MD should be tested with a dynamic method that respects our established clinical assumption (2 L of infused solutions via 13 dm(2) of plasticized PVC), at a temperature of 25 degrees C and during 24 h of contact, using a 50/50 (v/v) ethanol/water simulant. This model could be proposed as a tool for the safety evaluation of the patients' exposure risk to plasticizers from PVC medical devices for infusions. (C) 2015 Elsevier B.V. All rights reserved.

DOI10.1016/j.ijpharm.2015.08.033