Nonclinical regulatory immunotoxicity testing of nanomedicinal products: Proposed strategy and possible pitfalls-Reference-Cited by-同舟云学术

Nonclinical regulatory immunotoxicity testing of nanomedicinal products: Proposed strategy and possible pitfalls

Published:2020-04-07 Issue:5 Volume:12 Page:
ISSN:1939-5116
Container-title:WIREs Nanomedicine and Nanobiotechnology
language:en
Short-container-title:WIREs Nanomed Nanobiotechnol

Author:

Giannakou Christina¹^ORCID,Park Margriet V. D. Z.²^ORCID,Bosselaers Irene E. M.³^ORCID,Jong Wim H.²^ORCID,Laan Jan Willem³^ORCID,Loveren Henk⁴^ORCID,Vandebriel Rob J.²^ORCID,Geertsma Robert E.²

Affiliation:

1. Triskelion B.V. Zeist Netherlands

2. RIVM Bilthoven Netherlands

3. CBG‐MEB Utrecht Netherlands

4. Department of Toxicogenomics Maastricht University Maastricht Netherlands

Funder

European Union's Horizon 2020 Research and Innovation Programme

Onderzoeksprogramma Geneesmiddelenketen

Publisher

Wiley

Subject

Biomedical Engineering,Medicine (miscellaneous),Bioengineering

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/wnan.1633

Reference74 articles.

1. Risk Assessment and Risk Minimization in Nanomedicine: A Need for Predictive, Alternative, and 3Rs Strategies

2. A decision-making framework for the grouping and testing of nanomaterials (DF4nanoGrouping)

3. Nanomedicinal products: a survey on specific toxicity and side effects

4. Translational Studies of Phenotypic Probes for the Mononuclear Phagocyte System and Liposomal Pharmacology

5. Systemic and immunotoxicity of silver nanoparticles in an intravenous 28 days repeated dose toxicity study in rats

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