Nuevo nanotransportador para liberar fármacos en el interior de las células
Un nuevo estudio de la Universidad de Barcelona ha analizado la viabilidad de una nueva nanomolécula como vehículo de liberación
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Autor: Adrià Botet-Carreras
On the uptake of cationic liposomes by cells: From changes in elasticity to internalization
In this study, we assessed the capacity of a previously reported engineered liposomal formulation, which had been tested against model
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Studying Lipid Membrane Interactions of a Super-Cationic Peptide in Model Membranes and Living Bacteria.
The super-cationic peptide dendrimers (SCPD) family is a valuable class of antimicrobial peptide candidates for the future development of antibacterial
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Engineering and development of model lipid membranes mimicking the HeLa cell membrane.
Cells are complex systems whose interaction with nanocarriers, i.e., liposomes, are continuously under investigation to improve drug uptake. Model membranes
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Characterization of monolayers and liposomes that mimic lipid composition of HeLa cells.
In this work, based on several studies, we develop an artificial lipid membrane to mimic the HeLa cell membrane using
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Planar lipid bilayers formed from thermodynamically-optimized liposomes as new featured carriers for drug delivery systems through human skin.
The fundamental objective pursued in this work is to investigate how liposomes formed with a thermo- dynamically optimized molar composition
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