Importance of Combining Advanced Particle Size Analysis Techniques To Characterize Cell-Penetrating Peptide-Ferrocifen Self-Assemblies.


Journal

The journal of physical chemistry letters
ISSN: 1948-7185
Titre abrégé: J Phys Chem Lett
Pays: United States
ID NLM: 101526034

Informations de publication

Date de publication:
07 Nov 2019
Historique:
pubmed: 15 10 2019
medline: 21 11 2019
entrez: 15 10 2019
Statut: ppublish

Résumé

The design of a simple platform to target the delivery of notably hydrophobic drugs into cancer cells is an ultimate goal. Here, three strategies were combined in the same nanovector, in limiting the use of excipients: cell-penetrating peptides, an amphiphilic prodrug, and self-assembly. Light scattering and cryogenic transmission electron microscopy revealed one size population of objects around 100 nm with a narrow size distribution. However, in-depth analysis of the suspension by nanoparticle tracking analysis, small-angle X-ray scattering, and nuclear magnetic resonance (NMR) diffusometry demonstrated the presence of another population of small objects (<2 nm). It has been shown that these small self-assemblies represented >99% of the matter! This presence was clearly and unambiguously demonstrated by NMR diffusometry experiments. The study highlights the importance and the complementary contribution of each characterization method to reflect the reality of the studied nanoassembly.

Identifiants

pubmed: 31609118
doi: 10.1021/acs.jpclett.9b01493
doi:

Substances chimiques

Cell-Penetrating Peptides 0
Ferrous Compounds 0
ferrocifen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6613-6620

Auteurs

Léna Guyon (L)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.

Elise Lepeltier (E)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.

Jean-Christophe Gimel (JC)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.

Brice Calvignac (B)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.

Florence Franconi (F)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.
PRISM Plate-forme de recherche en imagerie et spectroscopie multi-modales, PRISM-Icat , Angers et PRISM-Biosit CNRS UMS 3480, INSERM UMS 018, Rennes, UBL Universite Bretagne , 35000 Rennes , France.

Nolwenn Lautram (N)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.

Aurélien Dupont (A)

Univ Rennes , CNRS , Inserm, BIOSIT-UMS 3480, US_S 018, F-35000 Rennes , France.

Claudie Bourgaux (C)

Institut Galien Paris-Sud, UMR CNRS 8612, Faculté de Pharmacie , Université Paris-Sud XI , 92290 Châtenay-Malabry , France.

Pascal Pigeon (P)

Sorbonne Université , UPMC Université Paris 06, UMR 8232, IPCM and PSL Chimie Paris Tech , 75005 Paris , France.

Patrick Saulnier (P)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.

Gérard Jaouen (G)

Sorbonne Université , UPMC Université Paris 06, UMR 8232, IPCM and PSL Chimie Paris Tech , 75005 Paris , France.

Catherine Passirani (C)

Micro et Nanomédecines Translationnelles, MINT , UNIV Angers , UMR INSERM 1066, UMR CNRS 6021, 49000 Angers , France.

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Classifications MeSH