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Stable Nanoparticles sentence examples within Form Stable Nanoparticles
Upon simple mixing, MPI and F-PET would coassemble to form stable nanoparticles, which show greatly improved cross-membrane and transmucosal penetration capacities compared with MPI alone or nonfluorinated MPI/PEI nanoparticles.
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The synthesized dimer (IND-OE) could form stable nanoparticles (IND-OE/DOX) loaded with DOX via single emulsion method.
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Stable Nanoparticles sentence examples within Colloidally Stable Nanoparticles
These colloidally stable nanoparticles exhibit antibacterial properties against both Gram negative (Escherichia coli) and Gram positive (Staphylococcus epidermidis) bacteria due to the presence of the positively charged polylysine chains on their surface.
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Again, a neutral solution pH was critical for the synthesis of colloidally stable nanoparticles.
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Stable Nanoparticles sentence examples within Formed Stable Nanoparticles
SN-38 and CPT-11 formed stable nanoparticles without any other excipients, and showed potent cytotoxicity against PC cells in vitro, slowed tumor growth in vivo, namely subcutaneously and orthotopically xenografted mice, with minimal adverse effects, and prolonged their overall survival.
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Stable Nanoparticles sentence examples within Highly Stable Nanoparticles
The highly stable nanoparticles were characterized using UV–visible spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy and field emission scanning electron microscopy with EDAX.
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Cubosomes are highly stable nanoparticles formed from the lipid cubic phase and stabilized by a polymer based outer corona.
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Stable Nanoparticles sentence examples within Obtaining Stable Nanoparticles
A simple and environmentally safe method for obtaining stable nanoparticles of metal sulfides nanoparticles—NpAg2S, NpCdS, and NpZnS—was developed using different strains of microorganisms in an aqueous solution of metal salts and sulfur sources at the National Research Center Kurchatov Institute—GosNIIgenetika.
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Stable Nanoparticles sentence examples within stable nanoparticles formed
We found that the minimal TPGS:CCM ratio for producing nanoparticles was 5:1 (w/w): at or above this ratio, stable nanoparticles formed with an average particle diameter of 12 nm.
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Cubosomes are highly stable nanoparticles formed from the lipid cubic phase and stabilized by a polymer based outer corona.
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Stable Nanoparticles sentence examples within stable nanoparticles could
The stable nanoparticles could be dissociated to turn on NIRF due to the rift of embedded disulfide bonds by glutathione (GSH).
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Dynamic light scattering and zeta potential measurements revealed the mixing ratio ranges of the constituents where stable nanoparticles could be created.
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These colloidally stable nanoparticles exhibit antibacterial properties against both Gram negative (Escherichia coli) and Gram positive (Staphylococcus epidermidis) bacteria due to the presence of the positively charged polylysine chains on their surface.
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Again, a neutral solution pH was critical for the synthesis of colloidally stable nanoparticles.
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4-AAA(mPEG)2 formed stable nanoparticles and PLGA4.
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Results The CS-ES2-AF could self-assemble into stable nanoparticles in aqueous solution, which significantly enhances its anti-neovascularization activity, tumor targeting more explicit, and prolongs its half-life.
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Upon simple mixing, MPI and F-PET would coassemble to form stable nanoparticles, which show greatly improved cross-membrane and transmucosal penetration capacities compared with MPI alone or nonfluorinated MPI/PEI nanoparticles.
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SN-38 and CPT-11 formed stable nanoparticles without any other excipients, and showed potent cytotoxicity against PC cells in vitro, slowed tumor growth in vivo, namely subcutaneously and orthotopically xenografted mice, with minimal adverse effects, and prolonged their overall survival.
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In the present work, we decorated rod-shaped cellulose nanocrystals with magnetic nanoparticles and coated these with polydopamine and polyethylene glycol polymer brushes to obtain chemical and colloidal stable nanoparticles.
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The highly stable nanoparticles were characterized using UV–visible spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy and field emission scanning electron microscopy with EDAX.
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Conclusion: Critical formulation and process parameters affected size of PLGA, chitosan and silica nanoparticles and protein encapsulation, while silica produced the smallest and most stable nanoparticles.
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We found that the minimal TPGS:CCM ratio for producing nanoparticles was 5:1 (w/w): at or above this ratio, stable nanoparticles formed with an average particle diameter of 12 nm.
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The obtained supported silver nanoparticles were acidified using various methods until we got stable nanoparticles.
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The micelles were subjected to physico-chemical characterizations, including hydrodynamic radius and polydispersity index (PDI) to assess formation of stable nanoparticles, zeta potential to measure the surface charge, encapsulation efficiency and drug loading to check effectivity of the nanocarrier system to carry the payload.
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The synthesized dimer (IND-OE) could form stable nanoparticles (IND-OE/DOX) loaded with DOX via single emulsion method.
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These multifunctional pH-sensitive amino lipids exhibited structurally dependent formulation of stable nanoparticles with the DNA plasmids of CRISPR/Cas9 system with the sizes ranging from 100 to 200 nm.
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Our data indicated that the HR9/DNA, MPG/DNA, M918/protein, and penetratin/protein complexes formed the stable nanoparticles that were effectively delivered in HEK‐293T cell line at certain ratios.
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With a high CMCS concentration up to 7 mg/mL, stable nanoparticles were successfully prepared.
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Results: Our data confirmed the formation of stable nanoparticles through non-covalent bonds with a diameter of less than 200 nm.
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The interaction between the nanoemulsion core and the polymer shell is critical to forming stable nanoparticles.
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Two formulation processes, nanoprecipitation and emulsion-evaporation, allowed the formation of stable nanoparticles.
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A post-synthetic purification strategy has been implemented in order to separate discrete nanoparticles from aggregates and unstable nanoparticles, leading to USPIONs that preserve chemical and colloidal stability for extended periods of time.
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Electrostatic complexation between the different ELP derivatives and nucleic acids was studied to determine the stoichiometry of ELPS/nucleic acids complex formation, and to find optimal conditions leading to stable nanoparticles with controlled size and surface potential.
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Fabrication of essential oil loaded-chitosan nanoparticles using electrospraying technique appears to be a novel strategy to develop thermally stable nanoparticles possessing higher encapsulation efficiency and particle stability.
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Results The carrier PP could efficiently condense Dz13 into stable nanoparticles at mass ratios of >1.
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Overall, there is a consensus that using colloidally stable nanoparticles is crucial for understanding and controlling cellular uptake, because materials that are prone to aggregation show higher non-specific interactions with biological fluids and cell membranes [18,19].
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Our results indicated that the designed DNA and peptide constructs could form non-covalent stable nanoparticles at certain ratios as observed by scanning electron microscope (SEM) and Zetasizer.
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The polymers aggregated into stable nanoparticles for a range of processing parameters.
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Dex-DOX prodrugs were able to self-assemble into stable nanoparticles in phosphate buffered saline (PBS).
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In this study, we developed a chlorin e6-conjugated methoxy-poly(ethylene glycol)-poly(d,l-lactide) (mPEG-PLA-Ce6) amphiphilic polymer, which self-assembled to form stable nanoparticles.
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The mean particle sizes and ζ-potential indicated that stable nanoparticles can be produced around pH 7–9 where native gliadin particles were unstable.
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Physicochemically stable nanoparticles were obtained with a particle size within the 300–400 nm range and surface potential higher than +30 mV for the 1F/1C ratio nanoparticle and around −30 mV for the 3F/1C and 5F/1C ratios nanoparticles.
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The photosensitizers could form stable nanoparticles in aqueous solution.
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Moreover, the atomic force microscopy and dynamic light scattering experiments revealed a formation of stable nanoparticles from these complexes in the solution and the solid state.
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Thermostable nanoparticles have numerous applications in catalysis and in the oil/gas industry.
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Results indicate that by increasing the PAC to CHT ratio 10:1 to 30:1 formed stable nanoparticles with diameters of 122.
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Using our developed PUFAylation technology, the GEM prodrug was able to spontaneously self-assemble into colloidal-stable nanoparticles with sub-100 nm size on covalent attachment of hydrophobic linoleic acid via amide linkage.
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Our data showed that HR9 and Cady-2 could form stable nanoparticles with DNA and proteins, respectively and enhance their delivery into HEK-293 T cells in a non-covalent approach.
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It was also shown that the most unstable nanoparticles (microporous silicon ones) could be protected from dissolution via interaction with the polysaccharide molecules (dextrane) into the solution.
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POD-PEG can self-assemble into stable nanoparticles (POD-PEG NPs).
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The introduction of TEG can improve the water solubility of borondipyrromethene (BODIPY) and facilitate the assembly of TBDP to form stable nanoparticles.
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LMs employed in cancer treatment suffer from high surface tension, thereby yielding unstable nanoparticles (NPs).
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The SEM data confirmed the formation of stable nanoparticles with a size below 250 nm.
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Cubosomes are highly stable nanoparticles formed from the lipid cubic phase and stabilized by a polymer based outer corona.
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For one thing, PgEMC could self-assemble into stable nanoparticles with PEG shell and optimizing diameters of 60 nm to simultaneously facilitate long blood circulation and deep tumor penetration.
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Green chemistry is beneficial for the production of eco-friendly and stable nanoparticles using biological agents.
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Achieving uniformly dispersed and stable nanoparticles of gold on oxide supports is a challenge in heterogeneous catalysis.
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This work may provide a universal modification method for obtaining stable nanoparticles.
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In this regard, there is a growing need for the development of cost-effective, reliable, and scalable experimental protocols to synthesize stable nanoparticles with desired morphologies and controlled sizes.
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We attained more stable nanoparticles with better size-uniformity (25–50 nm diameter), having a smooth surface with Entrapment efficiency (E.
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Stable nanoparticles were observed after the addition of aqueous root extract into the silver nitrate solution.
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The rationale behind this strategy is to generate colloidally stable nanoparticles and avoid the nonspecific protein adsorption due to ZW groups insertion, while the effective interaction with biosystems is guaranteed by the BAGs presence.
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rROPISA led to stable nanoparticles in all cases, ranging from 40 to 500 nm in diameter, depending on the experimental conditions, as assessed by dynamic light scattering and transmission electron microscopy.
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The stable nanoparticles could be dissociated to turn on NIRF due to the rift of embedded disulfide bonds by glutathione (GSH).
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Simply flipping the orientation of one coiled-coil results in either self-assembling or colloidally stable nanoparticles.
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A simple and environmentally safe method for obtaining stable nanoparticles of metal sulfides nanoparticles—NpAg2S, NpCdS, and NpZnS—was developed using different strains of microorganisms in an aqueous solution of metal salts and sulfur sources at the National Research Center Kurchatov Institute—GosNIIgenetika.
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The results show that there are significant changes of microstructure and properties in the samples with CT and TCT, especially due to the precipitation of metastable nanoparticles $${\text{W}}_{x} {\text{Co}}_{y} {\text{C}}_{z}$$WxCoyCz in the binder during the heat treatments of CT and TCT.
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By dialysis of QxPVP-PBA polymers dissolved in HCl against MOPS buffer, we prepared stable nanoparticles at neutral pH, mostly stabilized by positive charges and by chains likely interconnected through cyclic PBA structures termed boroxines.
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> 10 mol%), crystallization of PAN was decreased and consequently stable nanoparticles in the size range of 80–250 nm were achieved.
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Dynamic light scattering and zeta potential measurements revealed the mixing ratio ranges of the constituents where stable nanoparticles could be created.
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