SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "AMNE:(NATURAL SCIENCES Physical Sciences) ;lar1:(ki)"

Sökning: AMNE:(NATURAL SCIENCES Physical Sciences) > Karolinska Institutet

  • Resultat 1-10 av 297
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Sepehri, Sobhan, 1986, et al. (författare)
  • Characterization of Binding of Magnetic Nanoparticles to Rolling Circle Amplification Products by Turn-On Magnetic Assay
  • 2019
  • Ingår i: Biosensors-Basel. - : MDPI AG. ; 9:3
  • Tidskriftsartikel (refereegranskat)abstract
    • The specific binding of oligonucleotide-tagged 100 nm magnetic nanoparticles (MNPs) to rolling circle products (RCPs) is investigated using our newly developed differential homogenous magnetic assay (DHMA). The DHMA measures ac magnetic susceptibility from a test and a control samples simultaneously and eliminates magnetic background signal. Therefore, the DHMA can reveal details of binding kinetics of magnetic nanoparticles at very low concentrations of RCPs. From the analysis of the imaginary part of the DHMA signal, we find that smaller MNPs in the particle ensemble bind first to the RCPs. When the RCP concentration increases, we observe the formation of agglomerates, which leads to lower number of MNPs per RCP at higher concentrations of RCPs. The results thus indicate that a full frequency range of ac susceptibility observation is necessary to detect low concentrations of target RCPs and a long amplification time is not required as it does not significantly increase the number of MNPs per RCP. The findings are critical for understanding the underlying microscopic binding process for improving the assay performance. They furthermore suggest DHMA is a powerful technique for dynamically characterizing the binding interactions between MNPs and biomolecules in fluid volumes.
  •  
2.
  • Häbel, Henrike, 1987, et al. (författare)
  • Colloidal particle aggregation in three dimensions
  • 2019
  • Ingår i: Journal of Microscopy. - : Wiley. - 0022-2720 .- 1365-2818. ; 275:3, s. 149-158
  • Tidskriftsartikel (refereegranskat)abstract
    • Colloidal systems are of importance not only for everyday products, but also for the development of new advanced materials. In many applications, it is crucial to understand and control colloidal interaction. In this paper, we study colloidal particle aggregation of silica nanoparticles, where the data are given in a three-dimensional micrograph obtained by high-angle annular dark field scanning transmission electron microscopy tomography. We investigate whether dynamic models for particle aggregation, namely the diffusion limited cluster aggregation and the reaction limited cluster aggregation models, can be used to construct structures present in the scanning transmission electron microscopy data. We compare the experimentally obtained silica aggregate to the simulated postaggregated structures obtained by the dynamic models. In addition, we fit static Gibbs point process models, which are commonly used models for point patterns with interactions, to the silica data. We were able to simulate structures similar to the silica structures by using Gibbs point process models. By fitting Gibbs models to the simulated cluster aggregation patterns, we saw that a smaller probability of aggregation would be needed to construct structures similar to the observed silica particle structure.
  •  
3.
  • Skedung, Lisa, et al. (författare)
  • Feeling small : Exploring the Tactile Perception Limits
  • 2013
  • Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 3, s. 2617-
  • Tidskriftsartikel (refereegranskat)abstract
    • The human finger is exquisitely sensitive in perceiving different materials, but the question remains as to what length scales are capable of being distinguished in active touch. We combine material science with psychophysics to manufacture and haptically explore a series of topographically patterned surfaces of controlled wavelength, but identical chemistry. Strain-induced surface wrinkling and subsequent templating produced 16 surfaces with wrinkle wavelengths ranging from 300 nm to 90 mu m and amplitudes between 7 nm and 4.5 mu m. Perceived similarities of these surfaces (and two blanks) were pairwise scaled by participants, and interdistances among all stimuli were determined by individual differences scaling (INDSCAL). The tactile space thus generated and its two perceptual dimensions were directly linked to surface physical properties - the finger friction coefficient and the wrinkle wavelength. Finally, the lowest amplitude of the wrinkles so distinguished was approximately 10 nm, demonstrating that human tactile discrimination extends to the nanoscale.
  •  
4.
  • Ahrentorp, Fredrik, et al. (författare)
  • Sensitive magnetic biodetection using magnetic multi-core nanoparticles and RCA coils
  • 2017
  • Ingår i: Journal of Magnetism and Magnetic Materials. - : Elsevier BV. - 0304-8853 .- 1873-4766. ; 427, s. 14-18
  • Tidskriftsartikel (refereegranskat)abstract
    • We use functionalized iron oxide magnetic multi-core particles of 100 nm in size (hydrodynamic particle diameter) and AC susceptometry (ACS) methods to measure the binding reactions between the magnetic nanoparticles (MNPs) and bio-analyte products produced from DNA segments using the rolling circle amplification (RCA) method. We use sensitive induction detection techniques in order to measure the ACS response. The DNA is amplified via RCA to generate RCA coils with a specific size that is dependent on the amplification time. After about 75 min of amplification we obtain an average RCA coil diameter of about 1 mu m. We determine a theoretical limit of detection (LOD) in the range of 11 attomole (corresponding to an analyte concentration of 55 fM for a sample volume of 200 mu L) from the ACS dynamic response after the MNPs have bound to the RCA coils and the measured ACS readout noise. We also discuss further possible improvements of the LOD.
  •  
5.
  • Elmabsout, Ali Ateia, et al. (författare)
  • Cloning and Functional Studies of a Splice Variant of CYP26B1 Expressed in Vascular Cells
  • 2012
  • Ingår i: Plos One. - San Francisco, USA : Public Library of Science (PLoS). - 1932-6203. ; 7:5
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: All-trans retinoic acid (atRA) plays an essential role in the regulation of gene expression, cell growth and differentiation and is also important for normal cardiovascular development but may in turn be involved in cardiovascular diseases, i.e. atherosclerosis and restenosis. The cellular atRA levels are under strict control involving several cytochromes P450 isoforms (CYPs). CYP26 may be the most important regulator of atRA catabolism in vascular cells. The present study describes the molecular cloning, characterization and function of atRA-induced expression of a spliced variant of the CYP26B1 gene. Methodology/Principal Findings: The coding region of the spliced CYP26B1 lacking exon 2 was amplified from cDNA synthesized from atRA-treated human aortic smooth muscle cells and sequenced. Both the spliced variant and full length CYP26B1 was found to be expressed in cultured human endothelial and smooth muscle cells, and in normal and atherosclerotic vessel. atRA induced both variants of CYP26B1 in cultured vascular cells. Furthermore, the levels of spliced mRNA transcript were 4.5 times higher in the atherosclerotic lesion compared to normal arteries and the expression in the lesions was increased 20-fold upon atRA treatment. The spliced CYP26B1 still has the capability to degrade atRA, but at an initial rate one-third that of the corresponding full length enzyme. Transfection of COS-1 and THP-1 cells with the CYP26B1 spliced variant indicated either an increase or a decrease in the catabolism of atRA, probably depending on the expression of other atRA catabolizing enzymes in the cells. Conclusions/Significance: Vascular cells express the spliced variant of CYP26B1 lacking exon 2 and it is also increased in atherosclerotic lesions. The spliced variant displays a slower and reduced degradation of atRA as compared to the full-length enzyme. Further studies are needed, however, to clarify the substrate specificity and role of the CYP26B1 splice variant in health and disease.
  •  
6.
  • Sepehri, Sobhan, 1986, et al. (författare)
  • Homogeneous Differential Magnetic Assay
  • 2019
  • Ingår i: Acs Sensors. - : American Chemical Society (ACS). - 2379-3694. ; 4:9, s. 2381-2388
  • Tidskriftsartikel (refereegranskat)abstract
    • Assays are widely used for detection of various targets, including pathogens, drugs, and toxins. Homogeneous assays are promising for the realization of point-of-care diagnostics as they do not require separation, immobilization, or washing steps. For low concentrations of target molecules, the speed and sensitivity of homogeneous assays have hitherto been limited by slow binding kinetics, time-consuming amplification steps, and the presence of a high background signal. Here, we present a homogeneous differential magnetic assay that utilizes a differential magnetic readout that eliminates previous limitations of homogeneous assays. The assay uses a gradiometer sensor configuration combined with precise microfluidic sample handling. This enables simultaneous differential measurement sample containing a synthesized Vibrio cholerae target and a negative control sample, which reduces the background signal and increases the readout speed. Very low concentrations of targets down to femtomolar levels are thus detectable without any additional amplification of the number of targets. Our homogeneous differential magnetic assay method opens new possibilities for rapid and highly sensitive diagnostics at the point of care.
  •  
7.
  • Tuvblad, Catherine, 1968-, et al. (författare)
  • Physical and verbal aggressive behavior and COMT genotype : Sensitivity to the environment
  • 2016
  • Ingår i: American Journal of Medical Genetics Part B. - Hoboken, USA : John Wiley & Sons. - 1552-4841 .- 1552-485X. ; 171:5, s. 708-718
  • Tidskriftsartikel (refereegranskat)abstract
    • Catechol-O-methyltransferase (COMT) genotype has been implicated as a vulnerability factor for several psychiatric diseases as well as aggressive behavior, either directly, or in interaction with an adverse environment. The present study aimed at investigating the susceptibility properties of COMT genotype to adverse and favorable environment in relation to physical and verbal aggressive behavior. The COMT Val158Met polymorphism was genotyped in a Swedish population-based cohort including 1,783 individuals, ages 20-24 years (47% males). A significant three-way interaction was found, after correction for multiple testing, between COMT genotype, exposure to violence, and parent-child relationship in association with physical but not verbal aggressive behavior. Homozygous for the Val allele reported lower levels of physical aggressive behavior when they were exposed to violence and at the same time experienced a positive parent-child relationship compared to Met carriers. Thus, susceptibility properties of COMT genotype were observed in relation to physical aggressive behavior supporting the hypothesis that COMT genotypes are modifying the sensitivity to environment that confers either risk or protection for aggressive behavior. As these are novel findings, they warrant further investigation and replication in independent samples.
  •  
8.
  • Ravichandran, Ranjithkumar, et al. (författare)
  • Functionalised type-I collagen as a hydrogel building block for bio-orthogonal tissue engineering applications
  • 2016
  • Ingår i: Journal of materials chemistry. B. - : ROYAL SOC CHEMISTRY. - 2050-750X .- 2050-7518. ; 4:2, s. 318-326
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, we derivatized type I collagen without altering its triple helical conformation to allow for facile hydrogel formation via the Michael addition of thiols to methacrylates without the addition of other crosslinking agents. This method provides the flexibility needed for the fabrication of injectable hydrogels or pre-fabricated implantable scaffolds, using the same components by tuning the modulus from Pa to kPa. Enzymatic degradability of the hydrogels can also be easily fine-tuned by variation of the ratio and the type of the crosslinking component. The structural morphology reveals a lamellar structure mimicking native collagen fibrils. The versatility of this material is demonstrated by its use as a pre-fabricated substrate for culturing human corneal epithelial cells and as an injectable hydrogel for 3-D encapsulation of cardiac progenitor cells.
  •  
9.
  • Eriksson, Lars, et al. (författare)
  • Design Considerations of Phoswich Detectors for High Resolution Positron Emission Tomography
  • 2009
  • Ingår i: IEEE Transactions on Nuclear Science. - 0018-9499 .- 1558-1578. ; 56:1, s. 182-188
  • Tidskriftsartikel (refereegranskat)abstract
    • A way to improve the spatial resolution in positron emission tomography (PET) is to determine the depth-of-interaction (DOI) in the detector. A way to achieve this is to use the phoswich approach, a detector with two or more layers of different scintitlators. The layer identification is done by using differences in scintillation decay time and pulse shape discrimination techniques. The advantages of the concept have been demonstrated in the HRRT high resolution PET system using a LSO/LYSO combination giving a high spatial resolution uniformity of around 2.5 mm within a larger part of the imaged volume. A phoswich combination that lately has received attention is LuAP/LSO or LuYAP/LSO. The suggestions come from the Crystal Clear Collaboration and there is a patent application for its use in PET. This particular combination of phoswich may, however, have a complication since both LuAP and LuYAP emit in the excitation band of LSO, thus making the functionality more complex. In the present paper we have looked into this and suggested different ways to overcome potential drawbacks.
  •  
10.
  • Liamsuwan, Thiansin, et al. (författare)
  • A Monte Carlo track structure simulation code for the full-slowing-down carbon projectiles of energies 1 keV u-1–10 MeV u-1 in water
  • 2013
  • Ingår i: Physics in Medicine and Biology. - : IOP Publishing. - 0031-9155 .- 1361-6560. ; 58:3, s. 673-702
  • Tidskriftsartikel (refereegranskat)abstract
    • The paper presents a new Monte Carlo track structure code (KURBUC_carbon) for simulations of full slowing down carbon projectiles C0–C6+ of energies 1 keV/u–10 MeV/u in water vapour. The code facilitates investigation of spatial resolution effect for scoring track parameters under the Bragg peak of carbon ion beam. Interactions of carbon projectiles and secondary electrons were followed event-by-event down to 1 keV/u cutoff for primary ions, and down to 10 eV for electrons. Electronic interactions and nuclear elastic scattering were taken into account, including charge exchange reactions and double electronic interactions for the carbon projectiles. The reliability of the code was tested for radial dose, range, and W-value. The calculated results were compared with the published experimental data, and other model calculations. The results obtained showed good agreement in most cases where comparisons could be made. Depth dose profiles for 1-10 MeV/u C6+ were used to form an SOBP of 0.35 mm width in water. At all depths of the SOBP, the energy distributions of the carbon projectiles varied appreciably with the change in the scoring volume. The corresponding variation was nearly negligible for the track average LET, except at the distal end of the SOBP. By varying the scoring slab thickness from 1 to 100 µm, the maximum track average LET decreased by ~30%. The Monte Carlo track structure simulation in the full slowing down mode is a powerful tool for investigation of biophysical properties of radiation tracks under the Bragg peak and SOBP of carbon ion beam. For estimation of radiation effectiveness under the Bragg peak the new Monte Carlo track structure code provides yet another accurate and effective dosimetry tool at a single cell level. This is because radiobiology within tissue elements can only be understood with dosimetry at cellular and subcellular level.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 297
Typ av publikation
tidskriftsartikel (285)
forskningsöversikt (7)
konferensbidrag (2)
bokkapitel (2)
doktorsavhandling (1)
Typ av innehåll
refereegranskat (279)
övrigt vetenskapligt/konstnärligt (18)
Författare/redaktör
Brismar, Hjalmar (30)
Toma-Daşu, Iuliana (17)
Ureba, Ana (10)
Widengren, Jerker (9)
Dasu, Alexandru (9)
Sonesson, Andreas (8)
visa fler...
Siegbahn, Albert (8)
Iacobaeus, C (8)
Elofsson, Ulla (8)
Mavroidis, Panayioti ... (7)
Schneiderman, Justin ... (7)
Andreo, Pedro (7)
Fu, Ying (7)
Peskov, V. (6)
Patera, V (6)
Winkler, Dag, 1957 (6)
Callisen, Thomas H. (6)
Eriksson, Lars (5)
Jesorka, Aldo, 1967 (5)
Kalaboukhov, Alexei, ... (5)
Danielsson, Mats (5)
Xu, Hao (5)
Herland, Anna (5)
Gudowska, Irena (5)
Böhlen, Till Tobias (5)
Stathakis, Sotirios (5)
Gubanski, Michael (5)
Lind, Pehr A. (5)
Ödén, Jakob (5)
Brahme, A (4)
Jardemark, Kent Eric ... (4)
Klamra, Wlodzimierz (4)
Spiriti, E. (4)
Battistoni, G (4)
Landreh, Michael (4)
Brahme, Anders (4)
Lind, Bengt K (4)
Ågren, Hans (4)
Li, Li (4)
Griffith, May (4)
Fadeel, Bengt (4)
van der Marel, J. (4)
Önfelt, Björn (4)
Nordén, Bengt, 1945 (4)
Pfeiffer, Christoph, ... (4)
Molnár, J. (4)
Novak, D. (4)
Kerek, Andras (4)
Cooray, Gerald (4)
Papanikolaou, Nikos (4)
visa färre...
Lärosäte
Stockholms universitet (113)
Kungliga Tekniska Högskolan (112)
Uppsala universitet (58)
Lunds universitet (34)
Chalmers tekniska högskola (30)
visa fler...
Göteborgs universitet (27)
RISE (22)
Linköpings universitet (18)
Örebro universitet (6)
Sveriges Lantbruksuniversitet (5)
Umeå universitet (3)
Luleå tekniska universitet (2)
Mälardalens universitet (2)
Södertörns högskola (2)
Linnéuniversitetet (2)
Högskolan i Halmstad (1)
Högskolan i Gävle (1)
Jönköping University (1)
Högskolan i Skövde (1)
Karlstads universitet (1)
Högskolan Dalarna (1)
visa färre...
Språk
Engelska (297)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (294)
Medicin och hälsovetenskap (103)
Teknik (40)
Samhällsvetenskap (5)
Humaniora (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy