Acta Scientific Pharmaceutical Sciences (ASPS)(ISSN: 2581-5423)

Opinion Volume 5 Issue 7

Guiding Aspects Translating Nanomedicine

Luiza Ianny de Lima and João Paulo Figueiró Longo*

Institute of Biological Science - IB, Genetics and Morphology Department, University of Brasília - UnB, Brazil

*Corresponding Author: João Paulo Figueiró Longo, Institute of Biological Science - IB, Genetics and Morphology Department, University of Brasília - UnB, Brazil.

Received: May 25, 2021; Published: June 03, 2021

Abstract

  As a prospect for the next years, we believe that nanomedicine could be widely translated to clinical practices based on chemotherapy reduction in toxicity provided by the technology. Oncology patients, who are the core point of all this process, can greatly benefit from adopting nanomedicines. In this way, several conventional chemotherapeutical drugs could be used in their nano-based generic form, with lower related toxicity, providing better results for patients. For this approach, doctors could adopt simple and easy production nanocarriers early to reduce the risks. During this process, new innovations with more complex technical structures could be added as confidence in nanomedicine advances.

Keywords: Nanomedicine; Toxicity; Clinical Translation

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Citation

Citation: Luiza Ianny de Lima and João Paulo Figueiró Longo. “Guiding Aspects Translating Nanomedicine". Acta Scientific Pharmaceutical Sciences 5.7 (2020): 30-33.




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Acceptance rate32%
Acceptance to publication20-30 days
Impact Factor0.759

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