排序方式: 共有23条查询结果,搜索用时 218 毫秒
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Bart J. Crielaard Cristianne J. F. Rijcken Lingdong Quan Steffen vanderWal Isil Altintas Martin vanderPot John A. W. Kruijtzer Rob M. J. Liskamp Raymond M. Schiffelers Cornelus F. vanNostrum Wim E. Hennink Dong Wang Twan Lammers Gert Storm 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2012,124(29):7366-7370
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Jimmy Weterings Cristianne J. F. Rijcken Harald Veldhuis Tommi Meulemans Darya Hadavi Matt Timmers Maarten Honing Hans Ippel Rob M. J. Liskamp 《Chemical science》2020,11(33):9011
We describe the development of TMTH-SulfoxImine (TMTHSI) as a superior click reagent. This reagent combines a great reactivity, with small size and low hydrophobicity and compares outstandingly with existing click reagents. TMTHSI can be conveniently functionalized with a variety of linkers allowing attachment of a diversity of small molecules and (peptide, nucleic acid) biologics.TMTHSI was developed as new reagent for strain-promoted azide–alkyne cycloaddition reactions, enabling connection of a diversity of small to large molecular constructs. 相似文献
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The technique of ferromagnetic resonance at 23 GHz has been used to determine the first three anisotropy constants of pure Ni down to 4.2K. A temperature and orientation dependent linewidth has also been observed. 相似文献
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Cristianne J. F. Rijcken Mark Leemhuis Theo F. J. Veldhuis Wim E. Hennink Cornelus F. van Nostrum 《Macromolecular rapid communications》2006,27(16):1312-1316
Summary: This paper describes the facile step‐by‐step synthesis to graft lactic acid or lactoyl lactate onto primary as well as secondary alcohol derivatives of methacrylamides via esterification. Elongation of the chains is achieved by repeating the coupling reactions with either hydroxyl‐protected monolactate or hydroxyl‐protected dilactate, followed by mild deprotection using tetrabutylammonium fluoride. This versatile synthesis route generates, on a multi‐gram scale, monodisperse oligolactates of predetermined lengths with functional end groups. The products can be used, for example, as building blocks for biodegradable polymeric materials.
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Crielaard BJ Rijcken CJ Quan L van der Wal S Altintas I van der Pot M Kruijtzer JA Liskamp RM Schiffelers RM van Nostrum CF Hennink WE Wang D Lammers T Storm G 《Angewandte Chemie (International ed. in English)》2012,51(29):7254-7258
Polymerizable and hydrolytically cleavable dexamethasone (DEX, red dot in picture) derivatives were covalently entrapped in core-cross-linked polymeric micelles that were prepared from a thermosensitive block copolymer (yellow and gray building block). By varying the oxidation degree of the thioether in the drug linker, the release rate of DEX could be controlled. The DEX-loaded micelles were used for efficient treatment of inflammatory arthritis in two animal models. 相似文献
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Ramzi A Rijcken CJ Veldhuis TF Schwahn D Hennink WE van Nostrum CF 《The journal of physical chemistry. B》2008,112(3):784-792
The structure of assemblies of block copolymers composed of thermosensitive, biodegradable poly(N-(2-hydroxypropyl) methacrylamide-dilactate) and poly(ethylene glycol) (pHPMAmDL-b-PEG) has been studied by small-angle neutron scattering (SANS). Three amphiphilic copolymers with a fixed PEG of 5 kDa and a partially deuterated pHPMAmDL(d) block of 6700, 10400, or 21200 Da were used to form micelles in aqueous media by heating the polymeric solution from below to above the cloud point temperature (around 10 degrees C) of the thermosensitive block. Simultaneous and quantitative analysis of the scattering cross sections obtained at three different solvent contrasts is expedited using core-shell model, which assumed a homogeneous core of uniform scattering length density. The mean core radius increased from 13 to 18.5 nm with the molecular weight of the pHPMAmDL(d) block, while the thickness of the stabilizing PEG layer was around 8 nm for the three investigated assemblies. In addition, the volume fraction values of the stabilizing PEG chains in the shell are low and decreased from 31% to 14% with increasing the size of pHPMAmDL(d) block which shows that the shell layer of the assemblies is highly hydrated. The corresponding PEG chain grafting densities decreased from 0.22 to 0.11 nm-2 and the distance between PEG chains on the nanoparticles surface increased from 2.4 to 3.4 nm. The pHPMAmDL-b-PEG micelles showed a controlled instability due to hydrolysis of the lactic acid side groups in the thermosensitive block; that is, an increase of the degradation time leads to an increase of the size of the core which becomes less hydrophobic and consequently more hydrated. Neutron experiments supplied accurate information on how the size of the core and the micelle's aggregation number changed with the incubation time. This feature and the initially small size and dense structure in aqueous solution make the polymeric micelles suitable as carriers for hydrophobic drugs. 相似文献