Nanosafety is a critical facet of ensuring the responsible development and application of nanotechnology-based drugs and products. With the increasing integration of nanomaterials in pharmaceutical formulations, concerns about potential adverse effects on human health and the environment have grown. Rigorous safety assessments are essential to address these concerns, encompassing aspects such as toxicity, biodistribution, and biocompatibility of nanomaterials. Comprehensive studies are conducted to understand the interactions between nanoparticles and biological systems, evaluating their potential to induce cellular damage or trigger immune responses.
Regulatory bodies and industry stakeholders collaborate to establish guidelines that govern the safe use of nanomaterials in pharmaceuticals, aiming to mitigate risks and enhance patient safety. Moreover, ongoing research endeavors focus on developing innovative nanosafety assessment methods and predictive models to streamline the evaluation process. As the pharmaceutical landscape continues to advance with nanotechnology, prioritizing nanosafety remains paramount to harness the full therapeutic potential of these novel formulations while safeguarding public health.
Vladlen Slepak
University of Miami Miller School of Medicine, United States
Yong Xiao Wang
Albany Medical College, United States
Consolato M Sergi
Universities of Alberta and Ottawa, Canada
Huiqin Yang
ICON Clinical Research Ltd, United KingdomSubmit your abstract Today
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