Lipid-based nanoformulations for peptide delivery
Contribuinte(s) |
Micro et nanomédecines biomimétiques (MINT) ; Université d'Angers (UA) - Institut National de la Santé et de la Recherche Médicale (INSERM) Centre Hospitalier Universitaire d'Angers (CHU Angers) ; PRES Université Nantes Angers Le Mans [UNAM] |
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Data(s) |
2016
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Resumo |
International audience <p>Nanoformulations have attracted a lot of attention because of their size-dependent properties. Among the array of nanoformulations, lipid nanoformulations (LNFs) have evoked increasing interest because of the advantages of their high degree of biocompatibility and versatility. The performance of lipid nanoformulations is greatly influenced by their composition and structure. Therapeutic peptides represent a growing share of the pharmaceutical market. However, the main challenge for their development into commercial products is their inherent physicochemical and biological instability. Important peptides such as insulin, calcitonin and cyclosporin A have been incorporated into LNFs. The association or encapsulation of peptides within lipid-based carriers has shown to protect the labile molecules against enzymatic degradation. This review describes strategies used for the formulation of peptides and some methods used for the assessment of association efficiency. The advantages and drawbacks of such carriers are also described.</p> |
Identificador |
hal-01392463 https://hal.archives-ouvertes.fr/hal-01392463 DOI : 10.1016/j.ijpharm.2016.02.019 OKINA : ua14547 |
Idioma(s) |
en |
Publicador |
HAL CCSD |
Relação |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ijpharm.2016.02.019 |
Fonte |
ISSN: 1873-3476 International journal of pharmaceutics https://hal.archives-ouvertes.fr/hal-01392463 International journal of pharmaceutics, 2016, 502, pp.80-97. <10.1016/j.ijpharm.2016.02.019> |
Palavras-Chave | #drug delivery #Lipids #Nanoformulations #Peptides #[SDV] Life Sciences [q-bio] |
Tipo |
info:eu-repo/semantics/article Journal articles |