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Feature · Product Review
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10.3390/ijms21145049 3 AgibalovaT.HempelA.MaurerH

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Dis Sci (1996) 41:178693

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Instead of classifying nanomedicines as a distinct category, regulatory bodies such as the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) emphasize a risk-based product-specific evaluation framework that calls for thorough physicochemical characterization, manufacturing reproducibility, biodistribution profiling, and safety assessment for drug products that contain nanomaterials

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They are one tool in the clinical toolbox

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4 German Breast Group (GBG) Forschungs GmbH, Neu-Isenburg, Germany

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The cells were subsequently treated with 0.5% Triton X-100 for a duration of 15 min to induce permeabilization

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