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Bifunctional Submicron Colloidosomes Coassembled from Fluorescent and Superparamagnetic Nanoparticles
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Tobias Bollhorst Shakiba Shahabi Katharina Wörz Charlotte Petters Prof. Ralf Dringen Dr. Michael Maas Prof. Kurosch Rezwan 《Angewandte Chemie (International ed. in English)》2015,54(1):118-123
Colloidosomes are microcapsules consisting of nanoparticle shells. These microcarriers can be self‐assembled from a wide range of colloidal particles with selective chemical, physical, and morphological properties and show promise for application in the field of theranostic nanomedicine. Previous studies have mainly focused on fairly large colloidosomes (>1 μm) based on a single kind of particle; however, the intrinsic building‐block nature of this microcarrier has not been exploited so far for the introduction of tailored functionality at the nanoscale. We report a synthetic route based on interfacial shear rheology studies that allows the simultaneous incorporation of different nanoparticles with distinct physical properties, that is, superparamagnetic iron oxide and fluorescent silica nanoparticles, in a single submicron colloidosome. These tailor‐made microcapsules can potentially be used in various biomedical applications, including magnetic hyperthermia, magnetic particle imaging, drug targeting, and bioimaging. 相似文献
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Lee S Müller M Rezwan K Spencer ND 《Langmuir : the ACS journal of surfaces and colloids》2005,21(18):8344-8353
We have investigated the influence of pH and ionic strength on the conformation of porcine gastric mucin (PGM) in bulk aqueous solution, its adsorption behavior onto poly(dimethylsiloxane) (PDMS) surfaces, and its lubricating behavior upon the self-mated sliding contact of a PDMS tribopair by means of circular dichroism (CD) spectroscopy, optical waveguide lightmode spectroscopy (OWLS), and pin-on-disk tribometry, respectively. In a low-concentration regime (1 mg/mL), where the formation of a mucus-gel is generally excluded, PGM is still observed to exhibit effective aqueous lubricating properties under specific conditions of acidic pH and low ionic strength. This behavior was closely correlated with specific conformations in the bulk solution as well as specific adsorption behavior at the water/PDMS interface. The lubrication mechanism of the self-mated sliding contact of PDMS by means of surface modification with PGM is discussed in terms of isoviscous-elastic/soft-elastohydrodynamic lubrication (soft-EHL). 相似文献
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Supramolecular Interactions of Nonsteroidal Anti‐inflammatory Drug in Nanochannels of Molecular Containers: A Spectroscopic,Thermogravimetric and Microscopic Investigation
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Banibrata Maity Aninda Chatterjee Sayeed Ashique Ahmed Dr. Debabrata Seth 《Chemphyschem》2014,15(16):3502-3514
Supramolecular host–guest complexation between the nonsteroidal anti‐inflammatory drug indomethacin (IMC) and molecular containers were investigated. The weakly fluorescent drug molecule becomes highly fluorescent on complexation with different molecular containers, and time‐resolved fluorescence emission spectroscopy reveals that the lifetime components of IMC significantly increase in the presence of molecular containers, compared with the lifetimes in neat water. The respective solid host–guest complexes were synthesised and characterised by Fourier transform infrared and 1H nuclear magnetic resonance spectroscopic analysis. Microscopy techniques were used to analyse modifications of the surface morphology, owing to the formation of supramolecular complexes. The effect of the molecular container on the optical properties of IMC has also been investigated to determine the effect of nanochannels of different size and structure. 相似文献
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Rezwan K Studart AR Vörös J Gauckler LJ 《The journal of physical chemistry. B》2005,109(30):14469-14474
The amounts of negatively charged bovine serum albumin and positively charged lysozyme adsorbed on alumina, silica, titania, and zirconia particles (diameters 73 to 271 nm) in aqueous suspensions are measured. The adsorbed proteins change the zeta potentials and the isoelectric points (IEP) of the oxide particles. The added to adsorbed protein ratios at pH 7.5 are compared with the protein treated particle zeta potentials. It is found that the amounts of adsorbed proteins on the alumina, silica, and titania (but not on the zirconia) particle surfaces are highly correlated with the zeta potential. For the slightly less hydrophilic zirconia particles high amounts of protein adsorption are observed even under repulsive electrostatic conditions. One reason could be that the hydrophobic effect plays a more important role for zirconia than electrostatic interaction. 相似文献
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Neil Vasdev Raman Chirakal Rezwan Ashique Gary J. Schrobilgen Karen Gulenchyn 《Journal of fluorine chemistry》2003,121(1):9-14
The detection of 3-nitro-l-tyrosine has been used as a biomarker of “reactive nitrogen species” in biological matrices and has been an ongoing challenge in analytical chemistry. In this work, fluorine-18 labelled 5-fluoro-3-nitro-l-tyrosine (FNT) was synthesized as a potential radiotracer to probe the biological fate of 3-nitro-l-tyrosine. The synthesis of []FNT was carried out by reaction of []3-fluoro-l-tyrosine with NaNO3 in TFA solvent for 5 min at 4 °C. The radiochemical yield (RCY) of []FNT was 96±2% and []3-fluoro-l-tyrosine, was 29±1%, relative to []3-fluoro-l-tyrosine and []F2, respectively. The syntheses of []FNT were also accomplished by direct fluorination of 3-nitro-l-tyrosine with []F2 and by nitration of l-tyrosine with NaNO3, followed by fluorination, in TFA (4 °C) or anhydrous HF (−65 °C) solvent. The latter two synthetic routes produced []FNT in 13.5±1.5% RCY, within 1 h. Products were characterized by use of , and NMR spectroscopy and mass spectrometry. 相似文献
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Shaheen M. Sarkar Md. Nazmul Alam Md. Rezwan Miah 《Reaction Kinetics and Catalysis Letters》2009,96(1):175-183
A palladium (Pd) catalyst was prepared by immobilization of a 1,2-diaminocyclohexane based Pd-complex onto amorphous silica
gel and its applications as a heterogeneous catalyst for Suzuki-Miyaura and Sonogashira coupling reactions are described.
The catalyst was highly efficient, reusable and air-stable.
An erratum to this article is available at . 相似文献
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Sepay Nayim Sepay Nadir Al Hoque Ashique Mondal Rina Halder Umesh Chandra Muddassir Mohd. 《Structural chemistry》2020,31(5):1831-1840
Structural Chemistry - Novel coronavirus, 2019-nCoV is a danger to the world and is spreading rapidly. Very little structural information about 2019-nCoV make this situation more difficult for drug... 相似文献
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Adsorption and reduction of glutathione disulfide on α-Al2O3 nanoparticles: experiments and modeling
Dringen R Koehler Y Derr L Tomba G Schmidt MM Treccani L Colombi Ciacchi L Rezwan K 《Langmuir : the ACS journal of surfaces and colloids》2011,27(15):9449-9457
Glutathione disulfide (GSSG; γ-GluCysGly disulfide) was used as a physiologically relevant model molecule to investigate the fundamental adsorption mechanisms of polypeptides onto α-alumina nanoparticles. Its adsorption/desorption behavior was studied by enzymatic quantification of the bound GSSG combined with zeta potential measurements of the particles. The adsorption of GSSG to alumina nanoparticles was rapid, was prevented by alkaline pH, was reversed by increasing ionic strength, and followed a nearly ideal Langmuir isotherm with a standard Gibbs adsorption energy of -34.7 kJ/mol. Molecular dynamics simulations suggest that only one of the two glutathionyl moieties contained in GSSG binds stably to the nanoparticle surface. This was confirmed experimentally by the release of GSH from the bound GSSG upon reducing its disulfide bond with dithiothreitol. Our data indicate that electrostatic interactions via the carboxylate groups of one of the two glutathionyl moieties of GSSG are predominantly responsible for the binding of GSSG to the alumina surface. The results and conclusions presented here can provide a base for further experimental and modeling studies on the interactions of biomolecules with ceramic materials. 相似文献
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Mostak Ahmed Mubarak A. Khan Md. Rezwan Miah Syed Abdul Monim M. Anwar H. Khan 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(11):927-936
Polyethyleneterephthalate (PET) based proton exchange membrane for using in fuel cells was successfully prepared by gamma radiation-induced graft copolymerization of styrene monomer onto PET film and the consequent selective sulfonation of the grafting chain in the film state using chlorosulfonic acid (ClSO3H). The effects of grafting conditions (e.g., monomer concentration, irradiation dose) on the degree of grafting and sulfonation condition (e.g., optimum concentration of ClSO3H) on the degree of sulfonation were studied. The degree of grafting, the degree of sulfonation and the physico-chemical properties (such as, water uptake, mechanical strength, thermal durability, hydrolytic stability, oxidative stability) of the gamma radiation-induced grafted membrane were found to be better when compared to those of the UV-radiation grafted membrane. The membrane shows higher ion exchange capacity (0.9 mmol g?1) and higher proton conductivity (0.075 S cm?1), similar to those of Nafion membrane. 相似文献