By Ross J. Hunter, Victor R. Preedy
The nanosciences are a quickly increasing box of study with a large applicability to all components of healthiness and ailment prevention. This e-book, covers the law of nanomedicine, nanotubes, topical functions of nanoparticles, nanocrystals, antioxidant nanoparticles, lipid nanocapsules, nanotheragnostic colloids, nanotechnology within the keep an eye on of infectious affliction, virus-based nanoparticles and the security of nanoparticles. It additionally covers nanomedicine on the subject of pulmonary drug supply, the keep watch over of infectious disorder, radiation security, arthritis, melanoma nanomedicine, blood illnesses, neurodegenerative problems, and tissue and implant engineering.
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Additional resources for Nanomedicine in Health and Disease
Breggin, L. et al. 2009. Securing the Promise of Nanotechnologies—Towards Transatlantic Regulatory Cooperation. Report, Royal Institute of International Affairs. CHMP. 2006. Reflection paper on Nanotechnology-Based Medicinal Products for Human Use. Chowdhury, N. 2010. Regulation of nanomedicines in the EU: distilling lessons from the paediatric and the advanced therapy medicinal products approaches. Nanomedicine 5(1): 135–142. Communication from the Commission to the European Parliament, the Council and the European Economic and Social Committee—Regulatory aspects of nanomaterials, 2008.
Jones Valsami. 2008. The ecotoxicology of nanoparticles and nanomaterials: current status, knowledge gaps, challenges and future needs. Ecotoxicology 17: 315–325. Hardman, R. 2006. A toxicological review of quantum dots: Toxicity depends on physicochemical and environmental factors. Environ. Health Persp. 114(2): 165–172. , and R. Bawa. 2007. The carbon nanotube patent landscape in nanomedicine: an expert opinion. Expert Opin. Ther. Patents 17(9): 1–11. Harris, S. 2009. The regulation of nanomedicine: Will the existing regulatory scheme of the FDA suffice?
2010). With a wide array of definitions, finding a precise and feasible definition of nanomedicine and inter-related applications and devices is also likely to be a challenge. For example, the inclusion of a definition of “nanomaterials” in both the Cosmetics Regulation and the proposed Novel Foods Regulation will arguably have a significant impact. It will thus have to be seen whether such nano-specific aspects or definitions will be introduced in the nanomedical sphere in the future. With the advancement of nanomedicine, the borderline between medicines, devices and therapies is becoming increasingly blurred, which will in turn blur the demarcation between the regulatory systems.