The biocompatibility and toxicity of magnetic particles
This chapter looks into the characteristics of nano- and micro-particles that may affect their toxicity profile. It also provides insight on the different available in vitro toxicity tests and assesses the suitability of each, and give examples of their evaluation both in vitro and in vivo. In vitro...
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Published in | Laboratory Techniques in Biochemistry and Molecular Biology Vol. 32; pp. 163 - 223 |
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Main Authors | , , |
Format | Book Chapter |
Language | English |
Published |
The Netherlands
Elsevier Science & Technology
2007
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Subjects | |
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Abstract | This chapter looks into the characteristics of nano- and micro-particles that may affect their toxicity profile. It also provides insight on the different available in vitro toxicity tests and assesses the suitability of each, and give examples of their evaluation both in vitro and in vivo. In vitro studies are superseding most in vivo studies, due to their ease of use, accessibility, cost effectiveness, and lack of ethical restrictions. The chapter also deals with the immunogenicity of biological targeting reagents and discusses issues around allergic reactions or complement activation. As toxicity determinations are a crucial part of any drug approval process, an overview of the legal aspects of the process according to the regulatory bodies in the United States, Europe, and Japan have been provided. Although in vitro tests are only one, and generally the first one, of the required stages in biocompatibility testing, they are valuable in providing an initial toxicity profile, before the materials become further developed or require more costly testing procedures. In vitro tests can help to determine mechanisms of cell toxicity and general suitability of the particles. |
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AbstractList | This chapter looks into the characteristics of nano- and micro-particles that may affect their toxicity profile. It also provides insight on the different available in vitro toxicity tests and assesses the suitability of each, and give examples of their evaluation both in vitro and in vivo. In vitro studies are superseding most in vivo studies, due to their ease of use, accessibility, cost effectiveness, and lack of ethical restrictions. The chapter also deals with the immunogenicity of biological targeting reagents and discusses issues around allergic reactions or complement activation. As toxicity determinations are a crucial part of any drug approval process, an overview of the legal aspects of the process according to the regulatory bodies in the United States, Europe, and Japan have been provided. Although in vitro tests are only one, and generally the first one, of the required stages in biocompatibility testing, they are valuable in providing an initial toxicity profile, before the materials become further developed or require more costly testing procedures. In vitro tests can help to determine mechanisms of cell toxicity and general suitability of the particles. |
Author | Damani, Jaime Häfeli, Urs O. Aue, Jennifer |
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CitedBy_id | crossref_primary_10_1021_mp900083m crossref_primary_10_1016_j_mtcomm_2021_102333 crossref_primary_10_1088_1361_6528_ab0124 crossref_primary_10_1039_c2dt30853c crossref_primary_10_1088_0022_3727_46_12_125006 crossref_primary_10_4155_tde_11_12 |
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Snippet | This chapter looks into the characteristics of nano- and micro-particles that may affect their toxicity profile. It also provides insight on the different... |
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Title | The biocompatibility and toxicity of magnetic particles |
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