In Vitro and In Vivo Models for Evaluating the Oral Toxicity of Nanomedicines
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DOI: 10.3390/nano10112177
Abstract: Toxicity studies for conventional oral drug formulations are standardized and well documented, as required by the guidelines of administrative agencies such as the US Food & Drug Administration (FDA), the European Medicines Agency (EMA) or… read more here.
Keywords: vitro vivo; models evaluating; vivo models; toxicity ... See more keywords