98%
921
2 minutes
20
Fluorescent polymer cubosomes and hexosomes with aggregation-induced emission (AIE) were prepared from amphiphilic block copolymers PEG--PTPEMA where the hydrophobic block PTPEMA was a polymethacrylate with tetraphenylethene (TPE) as the AIE side group. Four highly asymmetric block copolymers with hydrophilic block weight ratio ≤ 20% were synthesized. Cubosomes and hexosomes with strong fluorescence emission were obtained by nanoprecipitation of polymers with < 9% in dioxane/water and THF/water systems. Their ordered internal structures were studied by electron microscopy (cryo-EM, SEM and TEM) and the X-ray scattering technique (SAXS). To elucidate the formation mechanisms of these inverted colloids, other parameters influencing the morphologies, like the water content during self-assembly and the organic solvent composition, were also investigated. This study not only inspires people to design novel building blocks for the preparation of functional cubosomes and hexosomes, but also presents the first AIE fluorescent polymer cubosome and hexosome with potential applications in bio-related fields.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179552 | PMC |
http://dx.doi.org/10.1039/d1sc00270h | DOI Listing |
J Colloid Interface Sci
August 2025
School of Science, STEM College, RMIT University, Victoria 3001, Australia. Electronic address:
Lipid nanocarrier (NC)-mediated delivery of antibiotics (including liposomes, cubosomes and hexosomes) is a promising strategy in dealing with the global issue of antimicrobial resistance and has been shown to improve the efficacy of currently available antibiotics. However, our understanding of the effect of lipid nanostructure on interactions of NCs with bacteria is lacking. Herein, we investigate the interactions of four different lipid NCs (including both cubosomes and hexosomes) with a simple bacterial supported lipid bilayer (SLB) mimicking the lipid bilayer of Escherichia coli (E.
View Article and Find Full Text PDFAdv Pharm Bull
April 2025
Department of Pharmaceutics, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Purpose: This study aimed to develop sustained-release triamcinolone acetonide (TA) formulations using lipid liquid crystals (LLCs) for ocular drug delivery and to characterize the designed formulations.
Methods: Eighteen dispersed LLC formulations were prepared through a top-down approach, incorporating varying concentrations of TA and different proportions of glyceryl monooleate, deionized water, and pluronic F127. An additional formulation comprising TA: hydroxypropyl beta-cyclodextrin (HPβCD) complex was also developed to investigate the influence of HPβCD on the properties of the formulations.
Expert Opin Drug Deliv
September 2025
School of Science, STEM College, RMIT University, Melbourne, Victoria, Australia.
Introduction: Lyotropic liquid crystalline lipid nanoparticles (LNPs) are a platform technology with broad-ranging potential in bioactive agent delivery applications. Their biomimetic properties impart the capacity to encapsulate large biomolecules and to overcome biological barriers.
Areas Covered: The properties of lyotropic liquid crystalline LNPs can vary significantly between phases.
Small
May 2025
School of Science, STEM College, RMIT University, Melbourne, Victoria, 3000, Australia.
Lipid nanoparticles have emerged as critical platforms for bioactive agent delivery, with their success in COVID-19 vaccines highlighting the urgent need to address gaps in understanding their biological interactions. Lyotropic liquid crystalline nanoparticles (LLCNPs) represent promising nanocarriers for bioactive agent delivery. In this study, it is revealed for the first time how internal nanostructures of LLCNPs - liposomes, cubosomes, hexosomes, and micellar cubosomes - influence their cellular uptake pathways.
View Article and Find Full Text PDFChemphyschem
July 2025
Department of Chemistry, Northwestern University, Evanston, IL, 60208, USA.
This study investigates the dynamic behavior of lyotropic liquid crystal nanoparticles (LCNPs), which are widely recognized for their applications in drug delivery. By employing nanosecond near-infrared laser pulse-induced temperature jump (T-jump) and time-resolved X-ray solution scattering, the structural dynamics of phase transitions in phytantriol-based cubosomes and hexosomes are revealed. Both cubosome and hexosome LCNPs undergo phase transitions into noncrystalline phases at high temperatures.
View Article and Find Full Text PDF