Publications by authors named "Mp Krafft"

Droplet-based microfluidics is leading the development of miniaturized, rapid, and sensitive version of enzyme-linked immunosorbent assays (ELISAs), a central method for protein detection. These assays involve the use of a functionalized surface able to selectively capture the desired analyte. Using the droplet's oil water interface as a capture surface requires designing custom-perfluorinated fluorosurfactants bearing azide-containing polar groups, which spontaneously react when forming the droplet with strain-alkyne-functionalized antibodies solubilized in the aqueous phase.

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Article Synopsis
  • Microbubbles can be used to deliver drugs and genes, with their release being triggered by ultrasound applied inside blood vessels.
  • Research shows that when a microbubble with a DMPC shell is exposed to pulsed ultrasound, the amount of DMPC molecules that detach reaches up to 70%.
  • The study also indicates that the intensity of the bubble's vibrations correlates with the rate of molecular desorption, suggesting that ultrasound can effectively control this process.
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  • Under non-equilibrium conditions, liquid droplets can dynamically interact with their environment, creating systems that exhibit self-organizing functions similar to living organisms.
  • The study highlights the importance of pairing and eruptive behaviors in cells for collective activity and function maintenance, but these have been difficult to replicate in artificial systems.
  • The researchers developed a droplet system using hydrophobic oils on water, which can autonomously form moving structures and display cyclic behaviors, mimicking complex cellular dynamics through the interaction of their interfacial properties.
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Polyhedral molecules are appealing for their eye-catching architecture and distinctive chemistry. Perfluorination of such, often greatly strained, compounds is a momentous challenge. It drastically changes the electron distribution, structure and properties.

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The oscillation of shelled microbubbles during exposure to ultrasound is influenced by the mechanical properties of the shell components. The oscillation behavior of bubbles coated with various phospholipids and other amphiphiles has been studied. However, there have been few investigations of how the adsorption conditions of the shell molecules relate to the viscoelastic properties of the shell and influence the oscillation behavior of the bubbles.

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Perfluorination gives cubane the capacity to host an extra electron in its inner structure.

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Graphene oxide (GO), single-walled carbon nanohorn (CNHox), and nitrogen-doped CNH (N-CNH) were functionalized with fluorinated poly(ethylene glycol) (-PEG) and/or with a fluorinated dendrimer (-DEN) to prepare a series of assembled nanocomposites (GO/-PEG, CNHox/-PEG, N-CNH/-PEG, N-CNH/-DEN, and N-CNH/-DEN/-PEG) that provide effective multisite O reservoirs. In all cases, the O uptake increased with time and saturated after 10-20 min. When graphitic carbons (GO and CNHox) were coated with -PEG, the O uptake doubled.

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  • Nitric oxide (NO) gas nanocarrier materials were created by assembling poly(amido amine) dendrimers with fluorocarbon binding sites and fluorinated poly(ethylene glycol) on nitrogen-doped carbon nanohorns (NCNHs).
  • The nitrogen doping in CNH and the hierarchical arrangement of the materials improved their ability to load NO gas, outperforming similar graphene-based materials.
  • The sustained release of NO gas from these nanocarriers demonstrates potential for effective biomedical therapies against bacteria and parasites.
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After the protocol-related indecisive clinical trial of Oxygent, a perfluorooctylbromide/phospholipid nanoemulsion, in cardiac surgery, that often unduly assigned the observed untoward effects to the product, the development of perfluorocarbon (PFC)-based O nanoemulsions ("blood substitutes") has come to a low. Yet, significant further demonstrations of PFC O-delivery efficacy have continuously been reported, such as relief of hypoxia after myocardial infarction or stroke; protection of vital organs during surgery; potentiation of O-dependent cancer therapies, including radio-, photodynamic-, chemo- and immunotherapies; regeneration of damaged nerve, bone or cartilage; preservation of organ grafts destined for transplantation; and control of gas supply in tissue engineering and biotechnological productions. PFC colloids capable of augmenting O delivery include primarily injectable PFC nanoemulsions, microbubbles and phase-shift nanoemulsions.

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Ligand-targeted microbubbles are focusing interest for molecular imaging and delivery of chemotherapeutics. Lipid-peptide conjugates (lipopeptides) that feature alternating serine-glycine (SG) segments rather than classical poly(oxyethylene) linkers between the lipid polar head and a targeting ligand were proposed for the liposome-mediated, selective delivery of anticancer drugs. Here, we report the synthesis of perfluoroalkylated lipopeptides (-lipopeptides) bearing two hydrophobic chains (C F , = 6, 7, 8, -) grafted through a lysine moiety on a hydrophilic chain composed of a lysine-serine-serine (KSS) sequence followed by 5 SG sequences.

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Hypothesis: Fluorocarbon gases introduced above monolayers of phospholipids at the air/water interface were recently found to promote the adsorption of diverse molecular compounds, with potential application in drug-loaded microbubble design. Quantitative determination of the fluorocarbon present in the monolayers is strongly needed for the development of such applications. We hypothesized that neutron reflectometry (NR) and ellipsometry experiments would allow quantification of the fluorocarbon trapped in the monolayers.

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Background: Ex vivo lung perfusion (EVLP) is a technology that allows the re-evaluation of questionable donor lung before implantation and it has the potential to repair injured donor lungs that are otherwise unsuitable for transplantation. We hypothesized that perfluorocarbon-based oxygen carrier, a novel reconditioning strategy instilled during EVLP would improve graft function.

Methods: We utilized perfluorocarbon-based oxygen carrier (PFCOC) during EVLP to recondition and improve lung graft function in a pig model of EVLP and lung transplantation.

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Hypoxia is a major impediment to many foremost cancer treatments that require O for generation of tumoricidal reactive oxygen species. Liquid perfluorocarbons (PFCs) are inert gas solvents that help alleviate this oxygen deficit situation. PFC nanoemulsions have demonstrated oxygen delivery to tissues.

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We found that monolayers of dipalmitoylphosphatidylcholine (DPPC) and semi-fluorinated tetrablock di(F10H16) self-assemble to form a new type of large, complex flower-like patterns on the surface of water and on solid substrates. The hierarchical organization of these unusual self-assemblies was investigated using compression and surface potential isotherms, in situ fluorescence and Brewster angle microscopies, and atomic force microscopy after transfer.

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Nanomaterials have great potential for the prevention and treatment of cancer. Circulating tumor cells (CTCs) are cancer cells of solid tumor origin entering the peripheral blood after detachment from a primary tumor. The occurrence and circulation of CTCs are accepted as a prerequisite for the formation of metastases, which is the major cause of cancer-associated deaths.

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Article Synopsis
  • Semifluorinated alkanes form small surface domains called hemimicelles at the air/water interface, which are important for stabilizing lipid-coated microbubbles used in ultrasound imaging.
  • Research has shown that these hemimicelles affect the phase behavior and mechanical properties of phospholipid monolayers, leading to enhanced stability in microbubbles.
  • The combination of semifluorinated alkanes and phospholipids can improve the viscoelastic properties of the microbubble coatings, making them a promising approach for better ultrasound contrast agents.
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Dendrons consisting of two phosphonate functions and three oligo(ethylene glycol) (OEG) chains grafted on a central phenoxyethylcarbamoylphenoxy group were synthesized and investigated as Langmuir monolayers at the surface of water. The OEG chain in the position was grafted with a -Bu end-group, a hydrocarbon chain, or a partially fluorinated chain. These dendrons are models of structurally related OEG dendrons that were found to significantly improve the stability of aqueous dispersions of iron oxide nanoparticles when grafted on their surface.

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Dendrons fitted with three oligo(ethylene glycol) (OEG) chains, one of which contains a fluorinated or hydrogenated end group and bears a bisphosphonate polar head (C X OEGDen, X = F or H; = 2 or 4), were synthesized and grafted on the surface of iron oxide nanoparticles (IONPs) for microbubble-mediated imaging and therapeutic purposes. The size and stability of the dendronized IONPs (IONP@C X OEGDen) in aqueous dispersions were monitored by dynamic light scattering. The investigation of the spontaneous adsorption of IONP@C X OEGDen at the interface between air or air saturated with perfluorohexane and an aqueous phase establishes that exposure to the fluorocarbon gas markedly increases the rate of adsorption of the dendronized IONPs to the gas/water interface and decreases the equilibrium interfacial tension.

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Microbubbles shelled with soft materials are expected to find applications as ultrasound-sensitive drug delivery systems, including through sonoporation. Microbubbles with specific vibrational characteristics and long intravascular persistence are required for clinical uses. To achieve this aim, the kinetics of the microbubble shell components at the gas/liquid interface while being subjected to ultrasound need to be better understood.

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In view of preparing effective nitric oxide gas carriers, a fluorinated poly(ethylene glycol) (-PEG) was noncovalently conjugated with acid-treated graphene oxide (GO) to prepare the composite of -PEG@GO. When the persistence of NO gas doped on GO and -PEG@GO was investigated for 3 h, the conserved NO gas decreased from 49.00 ± 7.

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Semifluorinated alkanes FnHm self-assemble into nanometer-sized surface micelles at the air-water interface. In this study, we investigated how an atmosphere enriched with perfluorohexane (PFH) influences the interfacial viscoelasticity and structural order of a monolayer of FnHm by the combination of dilational rheology and grazing-incidence small-angle X-ray scattering (GISAXS). The monolayers behaved predominantly elastic which can be attributed to the strong dipole repulsions of the surface domains.

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Microbubbles have potential for applications as drug and gene delivery systems, in which the release of a substance is triggered by an ultrasonic pulse. In this paper, we discuss the adsorption and desorption of a film of phospholipid on the surface of a single microbubble under ultrasound irradiation. Our optical observation system consisted of a high-speed camera, a laser Doppler vibrometer, and an ultrasound cell; 1,2-dimyristoyl--glycero-3-phosphocholine (DMPC) was used as the surfactant.

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The structure and lateral correlation of fluorocarbon-hydrocarbon tetrablock di(F10Hm) domains at the air/water interface have been determined by quantitative analysis of grazing incidence small-angle X-ray scattering (GISAXS) data. The measured GISAXS signals can be well represented by the full calculation of the form and structure factors. The form factor suggests that di(F10Hm) domains take a hemiellipsoid shape.

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Although most phospholipid-shelled microbubbles (MBs) investigated for medical applications are stabilized by a fluorocarbon (C) gas, information on the interactions between the phospholipid and C molecules at the gas/water interface remains scarce. We report that the procedure of introduction of perfluorohexane (-hexane), that is, either in the gas phase above dimyristoylphosphatidylcholine (DMPC) or dipalmitoylphosphatidylcholine (DPPC) Langmuir monolayers, or in the aqueous subphase, radically affects the compression isotherms. When introduced in the gas phase, -hexane is rapidly incorporated in the interfacial film, but is also readily desorbed upon compression and eventually totally expelled from the phospholipid monolayers.

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