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- W3011998156 abstract "With the advancement in science, nanotechnology is gaining importance in every aspect of life, specifically in medicine. Over the past decade research in nanomedicine has experienced constant growth. The demand for using nanotechnology in drug delivery system is constantly increasing and there is a need for development of more nano-based products. Often on packages, phrases such as nanocoatings, nanomaterials, and nanotechnology are seen but safety and toxicity remain a question to the consumers. When a product joins the category of the nano size, its safety information is expected to be there. However, such safety information provided with the product may not be sufficient or authentic. Also, there are no clear regulatory analytical methods and protocols notified for detecting its safety by the regulatory authorities. Hence, it becomes the role of regulatory agencies to ensure the safety of these nanoproducts prior to their launch in the market. This will avoid the safety concerns related to them. Nanotechnology has greatly advanced medicine. The unique advantages of nanotechnology cannot be denied. It is due to the complex properties of different nanomaterials as compared to that of micro materials. While nanomaterials demonstrate their advantages, the real information on the potential health and environmental hazards associated with this property are generally not available. Therefore, there is an immediate requirement to stop the unnecessary use of nanoformulations in drug development. This review focuses on the toxicity issues related to nanomedicine and corresponding regulatory concerns." @default.
- W3011998156 created "2020-03-23" @default.
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- W3011998156 date "2020-03-04" @default.
- W3011998156 modified "2023-09-30" @default.
- W3011998156 title "Toxicity and Regulatory Concerns for Nanoformulations in Medicine" @default.
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