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151.
Marie-Alexandrine Bolzinger Stéphanie Briançon Jocelyne Pelletier Yves Chevalier 《Current Opinion in Colloid & Interface Science》2012,17(3):156-165
Penetration of molecules and particles inside and through skin has long been well documented but it now merits renewed attention as a result of new areas of concern such as transdermal therapies, safety of cosmetic products, penetration of environmental compounds and skin decontamination.The topic is complex as skin structure is heterogeneous and because there are a number of penetration routes through the stratum corneum barrier: the intercellular, intracellular and follicular pathways. Recent advances in the study of penetration mechanisms deal with the control of the intercellular penetration route by the crystalline state of lipids, and the penetration through skin appendages (the follicular pathway) that appears to contribute much more than was previously thought.Applications dependent on skin penetration that have received special attention include transdermal delivery of nano- and microparticles by hair follicles, targeting of the skin immune system in order to develop new vaccination strategies, and problems relating to the risk assessment of nanoparticles and skin decontamination. 相似文献
152.
Marquez M Patel K Carswell AD Schmidtke DW Grady BP 《Langmuir : the ACS journal of surfaces and colloids》2006,22(19):8010-8016
A novel method for the formation of nanometer-scale polymer structures via template assisted admicellar polymerization (TAAP) is described. Admicellar polymerization uses a surfactant layer adsorbed on a surface to localize monomer to the surface prior to polymerization of the monomer. Nanostructures are formed by restricting adsorption to the uncovered sites of an already-templated surface, in this case to the interstitial sites between adsorbed latex spheres. Unlike most other process that form polymer nanostructures, polymer dimensions can be significantly smaller than the interstitial size because of sphere-surfactant interactions. Protein adsorption in the interstitial sites of colloidal arrays was also studied for three different proteins, and the results were compared with those obtained via admicellar polymerization. 相似文献
153.
Mixing the dipyrido[24]crown-8 derivatives carrying one or two formyl group(s) on the 4 position(s) of their pyridine ring(s) with a 3-fold symmetrical trisammonium ion template in a 3:1 ratio in CD3NO2 results in the formation of thermodynamically stable [4]pseudorotaxanes which, upon addition of a 1,3,5-trisaminobenzene cap, form mechanically interlocked molecular bundles with one and two caps, respectively, by virtue of dynamic imine bond formation. 相似文献
154.
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156.
Nigel J. Brookes Dr. Alireza Ariafard Dr. Robert Stranger Prof. Brian F. Yates Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(27):8117-8132
The experimentally known reduction of carbon monoxide using a 3‐coordinate [Ta(silox)3] (silox=OSi(tBu)3) complex initially forms a ketenylidene [(silox)3Ta? CCO], followed by a dicarbide [(silox)3Ta? CC? Ta(silox)3] structure. The mechanism for this intricate reaction has finally been revealed by using density functional theory, and importantly a likely structure for the previously unknown intermediate [(silox)3Ta? CO]2 has been identified. The analysis of the reaction pathway and the numerous intermediates has also uncovered an interesting pattern that results in CO cleavage, that being scission from a structure of the general form [(silox)3Ta? CnO] in which n is even. When n is odd, cleavage cannot occur. The mechanism has been extended to consider the effect of altering both the metal species and the ligand environment. Specifically, we predict that introducing electron‐rich metals to the right of Ta in the periodic table to create mixed‐metal dinuclear intermediates shows great promise, as does the ligand environment of the Cummins‐style 3‐coordinate amide structure. This latter environment has the added complexity of improved electron donation from amide rotation that can significantly increase the reaction exothermicity. 相似文献
157.
Alexander N. Zaykov Brian V. Popp Dr. Zachary T. Ball Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(22):6651-6659
The use of carboxylate side chains to induce peptide helicity upon binding to dirhodium centers is examined through experimental and computational approaches. Dirhodium binding efficiently stabilizes α helicity or induces α helicity in otherwise unstructured peptides for peptides that contain carboxylate side chains with i, i+4 spacing. Helix induction is furthermore possible for sequences with i, i+3 carboxylate spacing, though in this case the length of the side chains is crucial: ligating to longer glutamate side chains is strongly helix inducing, whereas ligating the shorter aspartate side chains destabilizes the helical structure. Further studies demonstrate that a dirhodium metallopeptide complex persists for hours in cellular media and exhibits low toxicity toward mammalian cells, enabling exploitation of these metallopeptides for biological applications. 相似文献
158.
Dalvit C Flocco M Veronesi M Stockman BJ 《Combinatorial chemistry & high throughput screening》2002,5(8):605-611
High-throughput ligand-based NMR screening with competition binding experiments is extended to (19)F detection. Fluorine is a favorable nucleus for these experiments because of the significant contribution of the Chemical Shift Anisotropy (CSA) to the (19)F transverse relaxation of the ligand signal when bound to a macromolecular target. A low to moderate affinity ligand containing a fluorine atom is used as a reference molecule for the detection and characterization of new ligands. Titration NMR experiments with the selected reference compound are performed for finding the optimal set-up conditions for HTS and for deriving the binding constants of the identified NMR hits. Rapid HTS of large chemical mixtures and plant or fungi extracts against the receptor of interest is possible due to the high sensitivity of the (19)F nucleus and the absence of overlap with the signals of the mixtures to be screened. Finally, a novel approach for HTS using a reference molecule in combination with a control molecule is presented. 相似文献
159.
Plumb RS Stumpf CL Gorenstein MV Castro-Perez JM Dear GJ Anthony M Sweatman BC Connor SC Haselden JN 《Rapid communications in mass spectrometry : RCM》2002,16(20):1991-1996
The application of liquid chromatography/mass spectrometry (LC/MS) followed by principal components analysis (PCA) has been successfully applied to the screening of rat urine following the administration of three candidate pharmaceuticals. With this methodology it was possible to differentiate the control samples from the dosed samples and to identify the components of the mass spectrum responsible for the separation. These data clearly show that LC/MS is a viable alternative, or complementary, technique to proton NMR for metabonomics applications in drug discovery and development. 相似文献
160.
The reaction of the cluster complex HCC[Co2(CO)6]CCo3(CO)9 with (or without) BrCCo3(CO)9 under Cadiot-Chodkiewicz coupling conditions gave the unusual alkynyl carboxamide complex C2H5N(H)C(O)CC[Co2(CO)6]CCo3(CO)9 rather than a coupled product containing two tricobalt cluster units. Steric demands imposed by the Co3 cluster allow attack at the least hindered alkyne carbon and stabilise the formed ynamine, so allowing subsequent CO insertion. The product has been characterised by X-ray crystallography. 相似文献