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81.
Kristian Bonderup Pedersen David Benning Peter Kjær Kristensen Vladimir N. Popok Kjeld Pedersen 《Journal of Materials Science: Materials in Electronics》2014,25(7):2863-2871
In this paper the microscopical structure of wedge bonded interfaces is investigated, with a focus on what effect the power in the ultrasonic bonding and the initial microscopical structure of the \(Al\) wire have on the quality of the bonding. The quality evaluation is based on mapping the microscopical restructuring of the wire grains during bonding and thereby assessing the effective bonding area. Three approaches are utilized in the interface characterization: mechanical shear test, optical microscopy combined with micro-sectioning, and scanning electron microscopy assisted by focused ion beam milling. The shear test is applied to quantify the strength of the bonded interfaces, while the other methods are used to map the grain reconstruction caused by the bonding. From the results it is possible to map a 3D image of the wire deformation, and the grain refinement region which is the dominating parameter with respect to fatigue related cracking of the interfaces. It is found that the bonding power, as well as the initial wire structure directly affects the refinement region and thereby the strength of the interface. 相似文献
82.
Indoloazepinone‐Constrained Oligomers as Cell‐Penetrating and Blood–Brain‐Barrier‐Permeating Compounds 下载免费PDF全文
Olivier Van der Poorten Dr. Baptiste Legrand Dr. Lubomir L. Vezenkov Dr. Júlia García‐Pindado Dr. Nadir Bettache Dr. Astrid Knuhtsen Prof. Dr. Daniel Sejer Pedersen Dr. Macarena Sánchez‐Navarro Prof. Dr. Jean Martinez Dr. Meritxell Teixidó Dr. Marcel Garcia Prof. Dr. Dirk Tourwé Dr. Muriel Amblard Dr. Steven Ballet 《Chembiochem : a European journal of chemical biology》2018,19(7):696-705
Non‐cationic and amphipathic indoloazepinone‐constrained (Aia) oligomers have been synthesized as new vectors for intracellular delivery. The conformational preferences of the [l ‐Aia‐Xxx]n oligomers were investigated by circular dichroism (CD) and NMR spectroscopy. Whereas Boc‐[l ‐Aia‐Gly]2,4‐OBn oligomers 12 and 13 and Boc‐[l ‐Aia‐β3‐h‐l ‐Ala]2,4‐OBn oligomers 16 and 17 were totally or partially disordered, Boc‐[l ‐Aia‐l ‐Ala]2‐OBn ( 14 ) induced a typical turn stabilized by C5‐ and C7‐membered H‐bond pseudo‐cycles and aromatic interactions. Boc‐[l ‐Aia‐l ‐Ala]4‐OBn ( 15 ) exhibited a unique structure with remarkable T‐shaped π‐stacking interactions involving the indole rings of the four l ‐Aia residues forming a dense hydrophobic cluster. All of the proposed FITC‐6‐Ahx‐[l ‐Aia‐Xxx]4‐NH2 oligomers 19 – 23 , with the exception of FITC‐6‐Ahx‐[l ‐Aia‐Gly]4‐NH2 ( 18 ), were internalized by MDA‐MB‐231 cells with higher efficiency than the positive references penetratin and Arg8. In parallel, the compounds of this series were successfully explored in an in vitro blood–brain barrier (BBB) permeation assay. Although no passive diffusion permeability was observed for any of the tested Ac‐[l ‐Aia‐Xxx]4‐NH2 oligomers in the PAMPA model, Ac‐[l ‐Aia‐l ‐Arg]4‐NH2 ( 26 ) showed significant permeation in the in vitro cell‐based human model of the BBB, suggesting an active mechanism of cell penetration. 相似文献
83.
Alveolar hypoxia causes pulmonary vasoconstriction; we investigated whether hypoxia could also impair pulmonary vasodilation. We found in the isolated perfused rat lung a delay in vasodilation following agonist-induced vasoconstriction. The delay was not due to erythrocyte or plasma factors, or to alterations in base-line lung perfusion pressure. Pretreating lungs with arachidonic acid abolished hypoxic vasoconstriction, but did not influence the hypoxia-induced impairment of vasodilation after angiotensin II, bradykinin, or serotonin pressor responses. Progressive slowing of vasodilation followed angiotensin II-induced constriction as the lung oxygen tension fell progressively below 60 Torr. KCl, which is not metabolized by the lung, caused vasoconstriction; the subsequent vasodilation time was delayed during hypoxia. However, catecholamine depletion in the lungs abolished this hypoxic vasodilation delay after KCl-induced vasoconstriction. In lungs from high altitude rats, the hypoxia-induced vasodilation impairment after an angiotensin II pressor response was markedly less than it was in lungs from low altitude rats. We conclude from these studies that (a) hypoxia impairs vasodilation of rat lung vessels following constriction induced by angiotensin II, serotonin, bradykinin, or KCl, (b) hypoxia slows vasodilation following KCl-induced vasoconstriction probably by altering lung handling of norepinephrine, (c) the effect of hypoxia on vasodilation is not dependent on its constricting effect on lung vessels, (d) high altitude acclimation moderates the effect of acute hypoxia on vasodilation, and (e) the hypoxic impairment of vasodilation is possibly the result of an altered rate of dissociation of agonists from their membrane receptors on the vascular smooth muscle. 相似文献
84.
85.
PF McKay N Imami M Johns DA Taylor-Fishwick LM Sedibane NF Totty JJ Hsuan DB Palmer AJ George BM Foxwell MA Ritter 《Canadian Metallurgical Quarterly》1998,28(12):4071-4083
The human gp200-MR6 molecule has previously been shown to have either an antagonistic or agonistic effect on IL-4 function, demonstrated by inhibition of IL-4-induced proliferation of T cells or mimicking of IL-4-induced maturation of epithelium, respectively. We now show that gp200-MR6 ligation can also mimic IL-4 and have an anti-proliferative pro-maturational influence within the immune system, causing up-regulation of co-stimulatory molecules on B lymphocytes. Biochemical analysis and cDNA cloning reveal that gp200-MR6 belongs to the human macrophage mannose receptor family of multidomain molecules. It comprises 1722 amino acids in toto (mature protein, 1695 amino acids; signal sequence, 27 amino acids) organized into 12 external domains (an N-terminal cysteine-rich domain, a fibronectin type II domain and 10 C-type carbohydrate recognition domains), a transmembrane region and a small cytoplasmic C terminus (31 amino acids) containing a single tyrosine residue (Y1679), but no obvious kinase domain. Strong amino acid sequence identity (77%) suggests that gp200-MR6 is the human homologue of the murine DEC-205, indicating that this molecule has much wider functional activity than its classical endocytic role. We also show that the gp200-MR6 molecule is closely associated with tyrosine kinase activity; the link between gp200-MR6 and the IL-4 receptor may therefore be via intracellular signaling pathways, with multifunctionality residing in its extracellular multidomain structure. 相似文献
86.
G. Sørensen A.L. Nielsen Morten Møller Pedersen S. Poulsen H. Nissen M. Poulsen S.D. Nygaard 《Progress in Organic Coatings》2010
Porous microparticles represent an attractive encapsulation platform as they provide a feasible route to a wide range of encapsulated chemical compounds. This assures an increased lifetime of the encapsulated compound by protecting it from the surrounding environment as well as providing a way to control the release rate. Porous microparticles encapsulating the commonly used biocide for wood protection, 3-iodoprop-2-ynyl N-butylcarbamate (IPBC), have been synthesized. The microparticles are spherical with an average size distribution of roughly 1 μm as determined by scanning electron microscopy (SEM). Determination of the release rate of the biocide from microcapsules incorporated into the paint film has been performed under diluted conditions. These experiments show that a slower release of the biocide can be obtained by encapsulation. Additionally, the microparticles have been shown to prolong the biocidal effect of the fungicide under accelerated weathering tests by protecting the biocide from UV-induced chemical degradation. 相似文献
87.
88.
M. Stuber M. A. Spiegel S. E. Fischer M. B. Scheidegger P. G. Danias E. M. Pedersen P. Boesiger 《Magma (New York, N.Y.)》1999,9(1-2):85-91
Myocardial tagging has shown to be a useful magnetic resonance modality for the assessment and quantification of local myocardial
function. Many myocardial tagging techniques suffer from a rapid fading of the tags, restricting their application mainly
to systolic phases of the cardiac cycle. However, left ventricular diastolic dysfunction has been increasingly appreciated
as a major cause of heart failure. Subtraction based slice-following CSPAMM myocardial tagging has shown to overcome limitations
such as fading of the tags. Remaining impediments, to this technique, however, are extensive scanning times (∼10 min), the
requirement of repeated breath-holds using a coached breathing pattern, and the enhanced sensitivity of artifacts related
to poor patient compliance or inconsistent depths of end-expiratory breath-holds. We therefore propose a combination of slice-following
CSPAMM myocardial tagging with a segmented EPI imaging sequence. Together with an optimized RF excitation scheme, this enables
to acquire as many as 20 systolic and diastolic grid-tagged images per cardiac cycle with a high tagging contrast during a
short period of sustained respiration. 相似文献
89.
90.
We have compared the effects of three different margarines, one based on palm oil (PALM-margarine), one based on partially
hydrogenated soybean oil (TRANS-margarine) and one with a high content of polyunsaturated fatty acids (PUFA-margarine), on serum lipids in 27 young women.
The main purpose of the study was to test if replacement of trans fatty acids in margarine by palmitic acid results in unfavorable effects on serum lipids. The sum of saturated fatty acids
(12∶0, 14∶0, 16∶0) was 36.3% of total fatty acids in the PALM-diet, the same as the sum of saturated (12∶0, 14∶0, 16∶0) (12.5%)
and trans (23.1%) fatty acids in the TRANS-diet. This sum was 20.7% in the PUFA-diet. The content of oleic acid was 37.9, 35.2, and 38.6%, respectively, in the three
diets, whereas linoleic acid amounted to 16, 13.5, and 27.3%, respectively. Total fat provided 30–31% and the test margarines
26% of total energy in all three diets. The subjects consumed each of the diets for 17 d in a Latin-square crossover design.
There were no significant differences in total cholesterol, low density lipoprotein (LDL)-cholesterol and apolipoprotein B
(apoB) between the TRANS-and the PALM-diets. High density lipoprotein (HDL)-cholesterol and apoA-I were significantly higher on the PALM-diet compared
to the TRANS-diet whereas the ratio of LDL-cholesterol to HDL-cholesterol was lower, although not significantly (P=0.077) on the PALM-diet. Total cholesterol, LDL-cholesterol, and apoB were significantly lower on the PUFA-diet compared
to the two other diets. HDL-cholesterol was not different on the PALM-and the PUFA-diets but it was significantly lower on
the TRANS-diet compared to the PUFA diet. Compared to the PUFA-diet the ratio of LDL-to HDL-cholesterol was higher on both the PALM-
and the TRANS-diets whereas apoA-I was not different. Triglycerides and lipoprotein (a) were not significantly different among the three
diets. We concluded that nutritionally, palmitic acid from palm oil may be a reasonable alternative to trans fatty acids from partially hydrogenated soybean oil in margarine if the aim is to avoid trans fatty acids. A palm oil-based margarine is, however, less favorable than one based on a more polyunsaturated vegetable oil. 相似文献