Current hurdles to the translation of nanomedicines from bench to the clinic.
Drug Deliv Transl Res
; 12(3): 500-525, 2022 03.
Article
en En
| MEDLINE
| ID: mdl-34302274
ABSTRACT
The field of nanomedicine has significantly influenced research areas such as drug delivery, diagnostics, theranostics, and regenerative medicine; however, the further development of this field will face significant challenges at the regulatory level if related guidance remains unclear and unconsolidated. This review describes those features and pathways crucial to the clinical translation of nanomedicine and highlights considerations for early-stage product development. These include identifying those critical quality attributes of the drug product essential for activity and safety, appropriate analytical methods (physical, chemical, biological) for characterization, important process parameters, and adequate pre-clinical models. Additional concerns include the evaluation of batch-to-batch consistency and considerations regarding scaling up that will ensure a successful reproducible manufacturing process. Furthermore, we advise close collaboration with regulatory agencies from the early stages of development to assure an aligned position to accelerate the development of future nanomedicines.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Sistemas de Liberación de Medicamentos
/
Nanomedicina
Tipo de estudio:
Guideline
/
Prognostic_studies
Idioma:
En
Revista:
Drug Deliv Transl Res
Año:
2022
Tipo del documento:
Article
País de afiliación:
España