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- W3024043480 endingPage "2000673" @default.
- W3024043480 startingPage "2000673" @default.
- W3024043480 abstract "The rate of translational effort of nanomedicine requires strategic planning of nanosafety research in order to enable clinical trials and safe use of nanomedicine in patients. Herein, the experiences that have emerged based on the safety data of classic liposomal formulations in the space of oncology are discussed, along with a description of the new challenges that need to be addressed according to the rapid expansion of nanomedicine platform beyond liposomes. It is valuable to consider the combined use of predictive toxicological assessment supported by deliberate investigation on aspects such as absorption, distribution, metabolism, and excretion (ADME) and toxicokinetic profiles, the risk that may be introduced during nanomanufacture, unique nanomaterials properties, and nonobvious nanosafety endpoints, for example. These efforts will allow the generation of investigational new drug-enabling safety data that can be incorporated into a rational infrastructure for regulatory decision-making. Since the safety assessment relates to nanomaterials, the investigation should cover the important physicochemical properties of the material that may lead to hazards when the nanomedicine product is utilized in humans." @default.
- W3024043480 created "2020-05-21" @default.
- W3024043480 creator A5011975977 @default.
- W3024043480 creator A5019473289 @default.
- W3024043480 creator A5057974208 @default.
- W3024043480 creator A5063209705 @default.
- W3024043480 date "2020-05-14" @default.
- W3024043480 modified "2023-10-12" @default.
- W3024043480 title "Safety Considerations of Cancer Nanomedicine—A Key Step toward Translation" @default.
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