Abstract:In myopia, diabetes and aging, fibrous vitreous liquefaction and degeneration is associated with the formation of opacities within the vitreous body that cast shadows on the retina, appearing as 'floaters' to the patient. Vitreous opacities degrade contrast sensitivity function and can cause significant impairment in vision-related quality-of-life. This study introduces 'nanobubble ablation' for safe destruction of vitreous opacities. Following intravitreal injection, hyaluronic acid coated gold nanoparticles … Show more
“…Given the high mRNA delivery efficiency of CADosomes in PBCECs, we next aimed to investigate mRNA delivery in an in vivo rabbit eye model [ [62] , [63] , [64] ]. Many ophthalmic diseases, such as trauma and dry eyes, are due to malfunctions at the level of the cornea, leading to severe visual impairment.…”
Section: Resultsmentioning
confidence: 99%
“…7 D) and a Terminal deoxynucleotidyl transferase dUTP Nick End Labeling (TUNEL) assay (Fig. S8B) indicated that tissue morphology remained intact [ 62 ]. To conclude, this proof-of-concept in vivo data showed the potential of mRNA CADosomes for local nucleic acid delivery towards the cornea.…”
“…Given the high mRNA delivery efficiency of CADosomes in PBCECs, we next aimed to investigate mRNA delivery in an in vivo rabbit eye model [ [62] , [63] , [64] ]. Many ophthalmic diseases, such as trauma and dry eyes, are due to malfunctions at the level of the cornea, leading to severe visual impairment.…”
Section: Resultsmentioning
confidence: 99%
“…7 D) and a Terminal deoxynucleotidyl transferase dUTP Nick End Labeling (TUNEL) assay (Fig. S8B) indicated that tissue morphology remained intact [ 62 ]. To conclude, this proof-of-concept in vivo data showed the potential of mRNA CADosomes for local nucleic acid delivery towards the cornea.…”
“…Bubble implosion comprises bubble topological changes, shock wave emissions, phase transition through supercritical states 1 , and intense pressure and temperature peaks, respectively 2 . Although such effects are traditionally considered to be responsible for damage on material surfaces [3][4][5][6] , cavitation is also exploited in several applications, many of which are in the field of biomedicine, such as drug delivery 7,8 , kidney stones fragmentation 9 , ophthalmic microsurgery 10,11 , eye floaters treatment 12 , and in the field of botany 13,14 . The trend, especially in biomedicine, is to push the technological limit towards the nanoscale.…”
In the present work, a diffuse interface model has been used to numerically investigate the laser-induced cavitation of nano/microbubbles. The mesoscale approach is able to describe the cavitation process in its entirety, starting from the vapor bubble formation due to the focused laser energy deposition, up to its macroscopic motion.In particular, the simulations show a complete and detailed description of the bubble formation and the subsequent breakdown wave emission with a precise estimation of the energy partition between the shockwave radiating in the liquid and the internal energy of the bubble. The scaling of the ratio between the energy stored in the bubble at its maximum radius and the one deposited by the laser is found in agreement with experimental observation on macroscopic bubbles.
“…[7,8] As such, GNPs have the potential for extensive medical applications in diagnosis and treatment. In pre-clinical settings, the use of GNPs includes point-of-care diagnostics [9,10] (lateral flow assays such as pregnancy tests and rapid COVID-19 tests), in vivo imaging [11,12] (photoacoustic and computerised tomography), and therapeutics [13][14][15] (photothermal therapy, radiotherapy, catalytic therapy, and drug delivery). Although GNPs treatment designs and applications are rapidly developing with some having reached clinical trials, [16][17][18] none has yet been approved for clinical use primarily because it is hard to predict the changes that nanoparticles undergo and how they behave in complex biological systems.…”
Gold nanoparticles (GNPs) are promising materials for many
bioapplications. However, upon contacting with biological media, GNPs
undergo changes. The interaction with proteins results in the so-called
protein corona (PC) around GNPs, leading to the new bioidentity and
optical properties. Understanding the mechanisms of PC formation and its
functions can help us to utilise its benefits and avoid its drawbacks.
To date, most of the previous works aimed to understand the mechanisms
governing PC formation and focused on the spherical nanoparticles
although non-spherical nanoparticles are designed for a wide range of
applications in biosensing. In this work, we investigated the
differences in PC formation on spherical and anisotropic GNPs (nanostars
in particular) from the joint experimental (extinction spectroscopy,
zeta potential and surface enhanced Raman scattering [SERS]) and
computational methods (the finite element method and molecular dynamics
[MD] simulations). We discovered that protein does not fully cover
the surface of anisotropic nanoparticles, leaving SERS hot-spots at the
tips and high curvature edges “available” for analyte binding (no SERS
signal after pre-incubation with protein) while providing
protein-induced stabilization (indicated by extinction spectroscopy) of
the GNPs by providing a protein layer around the particle’s core. The
findings are confirmed from our MD simulations, the adsorption energy
significantly decreases with the increased radius of curvature, so that
tips (adsorption energy: 2762.334 kJ/mol) would be the least
preferential binding site compared to core (adsorption energy: 11819.263
kJ/mol). These observations will help the development of new
nanostructures with improved sensing and targeting ability.
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