dc.contributor.author
Feiner Gracia, Natalia
dc.contributor.author
Glinkowska Mares, Adrianna
dc.contributor.author
Buzhor, Marina
dc.contributor.author
Rodríguez Trujillo, Adriano
dc.contributor.author
Samitier i Martí, Josep
dc.contributor.author
Amir, Roey J.
dc.contributor.author
Pujals Riatós, Silvia
dc.contributor.author
Albertazzi, Lorenzo
dc.date.issued
2021-03-16T11:07:51Z
dc.date.issued
2021-03-16T11:07:51Z
dc.date.issued
2020-12-23
dc.date.issued
2021-03-16T11:07:51Z
dc.identifier
https://hdl.handle.net/2445/175181
dc.description.abstract
The performance of supramolecular nanocarriers as drug delivery systems depends on their stability in the complex and dynamic biological media. After administration, nanocarriers are challenged by physiological barriers such as shear stress and proteins present in blood, endothelial wall, extracellular matrix, and eventually cancer cell membrane. While early disassembly will result in a premature drug release, extreme stability of the nanocarriers can lead to poor drug release and low efficiency. Therefore, comprehensive understanding of the stability and assembly state of supramolecular carriers in each stage of delivery is the key factor for the rational design of these systems. One of the main challenges is that current 2D in vitro models do not provide exhaustive information, as they fail to recapitulate the 3D tumor microenvironment. This deficiency in the 2D model complexity is the main reason for the differences observed in vivo when testing the performance of supramolecular nanocarriers. Herein, we present a real-time monitoring study of self-assembled micelles stability and extravasation, combining spectral confocal microscopy and a microfluidic cancer-on-a-chip. The combination of advanced imaging and a reliable 3D model allows tracking of micelle disassembly by following the spectral properties of the amphiphiles in space and time during the crucial steps of drug delivery. The spectrally active micelles were introduced under flow and their position and conformation continuously followed by spectral imaging during the crossing of barriers, revealing the interplay between carrier structure, micellar stability, and extravasation. Integrating the ability of the micelles to change their fluorescent properties when disassembled, spectral confocal imaging and 3D microfluidic tumor blood vessel-on-a-chip resulted in the establishment of a robust testing platform suitable for real-time imaging and evaluation of supramolecular drug delivery carrier's stability.
dc.format
application/pdf
dc.publisher
American Chemical Society
dc.relation
Reproducció del document publicat a: https://doi.org/10.1021/acsabm.0c01209
dc.relation
ACS Applied Bio Materials, 2020, vol. 4, num. 1, p. 669-681
dc.relation
https://doi.org/10.1021/acsabm.0c01209
dc.relation
info:eu-repo/grantAgreement/EC/H2020/757397/EU//NANOSTORM
dc.relation
info:eu-repo/grantAgreement/EC/H2020/713673/EU//INPhINIT
dc.rights
cc-by-nc-nd (c) Feiner-Gracia, N. et al., 2020
dc.rights
http://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Enginyeria Electrònica i Biomèdica)
dc.subject
Química supramolecular
dc.subject
Nanopartícules
dc.subject
Supramolecular chemistry
dc.title
Real-time ratiometric imaging of micelles assembly state in a microfluidic cancer-on-a-chip
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion