Academic literature on the topic 'Dextran'

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Journal articles on the topic "Dextran"

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Barrowcliffe, M. P., G. D. Zanelli, D. Ellison, and J. G. Jones. "Clearance of charged and uncharged dextrans from normal and injured lungs." Journal of Applied Physiology 68, no. 1 (1990): 341–47. http://dx.doi.org/10.1152/jappl.1990.68.1.341.

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To examine how molecular charge affects the transfer of molecules across the alveolar-capillary barrier, we prepared the following dextrans of equivalent molecular size (mol wt 10,000) but varying molecular charge: neutral dextran, cationic DEAE dextran, and anionic dextran sulfate. These were labeled with 99mTc. The lungs of three groups of anesthetized rabbits were insufflated with dextran aerosols, with six rabbits receiving each type, and the half-time pulmonary clearance (t1/2) was measured. Control t1/2's (95% confidence limits) were 95 (74-120), 227 (192-268), and 291 (246-345) min for
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Whiteside, C. I., and C. J. Lumsden. "Transglomerular cationic macromolecular flux is mediated by a convection-binding mechanism." American Journal of Physiology-Renal Physiology 256, no. 5 (1989): F882—F893. http://dx.doi.org/10.1152/ajprenal.1989.256.5.f882.

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Glomerular polyanion function was explored using charged and neutral [3H]dextrans in the multiple indicator-dilution experiment. Anesthetized dogs received an intrarenal bolus of 125I-labeled albumin (plasma reference), [14C]inulin (glomerular reference) and [3H]dextran (test solute), followed by rapid serial sampling of the renal venous and urine outflows. Reduced urinary recovery of cationic diethylaminoethyl dextrans (DEAE) [3H]dextrans [19.0– to 31.5–A Stokes-Einstein radius (SER)], compared with neutral [3H]dextran indicated intrarenal binding reversed by excess unlabeled cationic dextran
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Schmid, Jonas, Daniel Wefers, Rudi F. Vogel, and Frank Jakob. "Analysis of Structural and Functional Differences of Glucans Produced by the Natively Released Dextransucrase of Liquorilactobacillus hordei TMW 1.1822." Applied Biochemistry and Biotechnology 193, no. 1 (2020): 96–110. http://dx.doi.org/10.1007/s12010-020-03407-6.

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AbstractThe properties of the glucopolymer dextran are versatile and linked to its molecular size, structure, branching, and secondary structure. However, suited strategies to control and exploit the variable structures of dextrans are scarce. The aim of this study was to delineate structural and functional differences of dextrans, which were produced in buffers at different conditions using the native dextransucrase released by Liquorilactobacillus (L.) hordei TMW 1.1822. Rheological measurements revealed that dextran produced at pH 4.0 (MW = 1.1 * 108 Da) exhibited the properties of a viscoe
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Beck-Candanedo, Stephanie, David Viet, and Derek G. Gray. "Partitioning of charged and neutral dextran-dye derivatives in biphasic cellulose nanocrystal suspensions." Canadian Journal of Chemistry 86, no. 6 (2008): 503–11. http://dx.doi.org/10.1139/v08-005.

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The partitioning behaviour of dye-labeled dextrans of high molecular weight in aqueous suspensions of native cellulose nanocrystals was studied. Cellulose concentrations lie in the isotropic–nematic coexistence region. Blue dextrans of various molecular weights and degrees of substitution of dye molecules (anionic Cibacron blue 3G-A) were investigated. Increasing the total concentration of blue dextran and degree of dye substitution led to increasing partition coefficients. Increasing dextran molecular weight resulted in higher partition coefficients, in agreement with theory. Partition coeffi
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Newman, B. A., and E. A. Kabat. "An immunochemical study of the combining site specificities of C57BL/6J monoclonal antibodies to alpha (1----6)-linked dextran B512." Journal of Immunology 135, no. 2 (1985): 1220–31. http://dx.doi.org/10.4049/jimmunol.135.2.1220.

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Abstract This is the first report of an immunochemical study of the combining site specificities of a set of monoclonal antibodies to dextran B512 from C57BL/6J mice. The results confirm previous observations on antidextran combining sites and reveal specificities not seen earlier extending the observed repertoire of antibody combining sites to the single alpha (1----6)-linked glucosyl antigenic determinant. Eight C57BL/6J anti-dextran B512 hybridomas, four IgM,kappa and four IgA,kappa, were produced by PEG fusion of immune spleen cells with the nonproducer myeloma cell line P3X63Ag8 6.5.3. An
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Pène, J., V. Rousseau, H. Zaghouani, P. Paroutaud, A. D. Strosberg, and M. Stanislawski. "Monoclonal anti-alpha (1----3) dextran antibodies of Igha BALB/c and Ighb C.B20 mice display striking similarities." Journal of Immunology 137, no. 7 (1986): 2319–24. http://dx.doi.org/10.4049/jimmunol.137.7.2319.

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Abstract Allotype Ighb congenic C.B20 mice when immunized with dextran B1355S are unable to produce anti-alpha (1----3) dextran antibodies that express the VH-associated cross-reactive IdX idiotype. This intrastrain-specific idiotype is normally associated only with the anti-dextran response of Igha mice of which BALB/c is a prototype strain. In this study we have obtained monoclonal hybridoma antibodies specific for the alpha (1----3) glucosidic linkage of dextran from C.B20 mice that were presensitized with rabbit anti-IdX antibodies. These antibodies display the light chain isotype distribu
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Zou, Qing Song, Yuan Yuan Pu, Su Xia Li, Qing Wang, Xiao Wang, and Shan Chen. "Ultrasonic Degradation of Dextran in Aqueous Solution." Advanced Materials Research 396-398 (November 2011): 1624–27. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.1624.

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An ultrasonic device with frequency of 20 kHz was used to investigate the effect of different operational parameters such as ultrasonic power, temperature and initial molecular weight on dextran degradation. Results show that the molecular weight of dextran can be controlled by ultrasonic treatment. Higher the ultrasonic power and lower the temperature could increase the degradation rate (R).The initial molecular weight plays an important role in at the initial stage of dextran degradation (within 20 minutes). A smilar limiting molecular weight (Mw≈8.7×104) was obtained after 2 hours ultrasoni
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Gokcan, Hande, Duygu Ozmen, Meral Yildirim Yalcin, Enes Dertli, Omer Said Toker, and Monika Sujka. "Determination of Viscoelastic and Physicochemical Interactions of Dextran Type Exopolysaccharides (EPS) with Different Starch Samples." Sustainability 15, no. 6 (2023): 4934. http://dx.doi.org/10.3390/su15064934.

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In this study, the rheological properties of three distinct dextrans with different levels of (1 → 6)-linked α-D-glucose/(1 → 3)-linked α-D-glucose units from three lactic acid bacteria (LAB) strains were determined. Dextran PDER21 was further selected following the rheological measurements and its interactions with maize, wheat and waxy maize starches were determined by characterizing the viscoelastic and pasting properties of the dextran–starch mixtures. Fourier transform infrared (FTIR) spectroscopy analysis was also applied to unveil this interaction. The presence of dextran PDER21 in the
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Suheil, Saad Shalawy, and Asmaa Sabah Ahmaed. "Production of Dextran from Domestic Weissella cibaria Isolated." IOP Conference Series: Earth and Environmental Science 1262, no. 6 (2023): 062012. http://dx.doi.org/10.1088/1755-1315/1262/6/062012.

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Abstract Dextran is an exopolysaccharide (EPS) of bacterial origin that is readily available in the commercial market. that is used in various industrial applications as an adjuvant, emulsifier, carrier, and stabilizer in the food and biomedical industries. Industrial production of dextran is carried out by fermentation in sucrose-rich media. Studies to optimize dextran production have shown that dextran yield varies depending on specific production conditions. This study aimed to generate dextrans Lactobacillus species were obtained from the vaginal and stool samples of healthy infants. The m
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Nielsen, Thorbjørn Terndrup, Catherine Amiel, Laurent Duroux та ін. "Formation of nanoparticles by cooperative inclusion between (S)-camptothecin-modified dextrans and β-cyclodextrin polymers". Beilstein Journal of Organic Chemistry 11 (21 січня 2015): 147–54. http://dx.doi.org/10.3762/bjoc.11.14.

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Novel (S)-camptothecin–dextran polymers were obtained by “click” grafting of azide-modified (S)-camptothecin and alkyne-modified dextrans. Two series based on 10 kDa and 70 kDa dextrans were prepared with a degree of substitution of (S)-camptothecin between 3.1 and 10.2%. The binding properties with β-cyclodextrin and β-cyclodextrin polymers were measured by isothermal titration calorimetry and fluorescence spectroscopy, showing no binding with β-cyclodextrin but high binding with β-cyclodextrin polymers. In aqueous solution nanoparticles were formed from association between the (S)-camptothec
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Dissertations / Theses on the topic "Dextran"

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Dijk-Wolthuis, Welmoed van. "Biodegradable dextran hydrogels for pharmaceutical applications = Bioafbreekbare dextraan-hydrogelen voor farmaceutische toepassingen /." [S.l. : s.n.], 1997. http://www.gbv.de/dms/bs/toc/238021521.pdf.

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Piazza, Rodolfo Debone [UNESP]. "Modificação da superfície de óxidos de ferro por dextrana derivatizada para aplicações em liberação de fármaco." Universidade Estadual Paulista (UNESP), 2014. http://hdl.handle.net/11449/110705.

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Piazza, Rodolfo Debone. "Modificação da superfície de óxidos de ferro por dextrana derivatizada para aplicações em liberação de fármaco /." Araraquara, 2014. http://hdl.handle.net/11449/139300.

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Orientador: Miguel Jafelicci Junior<br>Banca: Marcio José Tiera<br>Banca: Carolina Vautier Teixeira Giongo<br>Resumo: A modificação da superfície de nanopartículas de óxido de ferro tem atraído interesse da comunidade científica devido às várias aplicações deste material em diferentes áreas do conhecimento. A biomedicina é uma área em crescente avanço no uso das nanopartículas, pois a sinergia entre as propriedades magnéticas e a biocompatibilidade da superfície modificada permite o uso destes materiais em diagnóstico e tratamento de doenças, como na liberação controlada de drogas. A aplicação
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Faivre, Béatrice. "Un transporteur d'oxygène a visée transfusionnelle : l'hémoglobine-dextran 10-benzène-tetracarboxylate évaluation préclinique chez le cobaye." Vandoeuvre-les-Nancy, INPL, 1993. http://www.theses.fr/1993INPL086N.

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L'hémoglobine conjuguée au dextran-benzène-tetracarboxylate (hb-dex-btc) est un transporteur d'O2 dont les objectifs sont de se substituer, de façon temporaire, à la fonction oxyphorique des hématies et de contribuer à la restauration de la volémie. Notre travail consiste à réaliser l'évaluation pharmaco-toxicologique de cette hémoglobine. Tout d'abord, nous présentons l'historique de la recherche sur les substituts du sang, la physiologie de l'hémoglobine dans le globule rouge et dans le plasma (structure, mécanismes d'oxygénation, d'oxydation, de réduction, catabolisme) ainsi que les princip
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Landon, Robert Stephen. "Optimisation of the dextran fermentation." Thesis, University of Manchester, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.333270.

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Delattre, Cécilia. "Mise au point et évaluation de nouveaux revêtements de stents pour application cardio-vasculaire." Thesis, Sorbonne Paris Cité, 2015. http://www.theses.fr/2015USPCD061/document.

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L’objectif de ce travail est d’évaluer la biocompatibilité d’un copolymère de Dextrane- Polybutylmethacrylate utilisé comme revêtement de stent métallique en Cobalt-Chrome. L’étude s’est déroulée en trois phase : 1/La production du polymère et la caractérisation physico-chimique, 2/L’évaluation in vitro et 3/L’évaluation in vivo dans plusieurs modèles. Dans un premier temps deux copolymères de concentrations distinctes ont été synthétisés et mis en forme pour les différentes expériences. Leur caractérisation par FTIR, mesure d’angle de contact et une première implantation in vivo évaluant la r
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Bhambra, Kalwant S. "The fractionation of dextran using ethanol." Thesis, Aston University, 1985. http://publications.aston.ac.uk/10231/.

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Faucher-Sivera, Nadine. "Contribution à l'étude d'un nouveau dextran de poids moléculaire 40 000 (plasmacair R) : pharmacocinétique et effets rhéologiques." Montpellier 1, 1988. http://www.theses.fr/1988MON11068.

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Claverie, Marion. "GH70 dextransucases : Insights on the molecular determinants of dextran molar mass control." Thesis, Toulouse, INSA, 2017. http://www.theses.fr/2017ISAT0037/document.

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Les glucane-saccharases (GS) de la famille GH70 sont des enzymes produites par certaines bactéries lactiques. A partir de saccharose, substrat renouvelable et peu coûteux, elles sont capables de catalyser la synthèse d’α-glucanes, homopolysaccharides dont les propriétés diffèrent suivant la spécificité de l’enzyme (taille, type de liaisons α-osidiques, degrés de branchement). Les glucanes contenant une très grande majorité de liaisons α-(1,6), appelés dextranes, présentent de nombreuses applications industrielles qui dépendent principalement de leur taille. Cependant, la synthèse directe de de
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Crepon, Bertrand. "Dérivés du dextrane : substituts de plasma sanguin." Paris 13, 1988. http://www.theses.fr/1988PA132001.

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Books on the topic "Dextran"

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Rakshit, D. End-modification reactions of Dextran. University of Birmingham, 1987.

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Bhambra, Kalwant Singh. The fractionation of dextran using ethanol. Aston University. Department of Chemical Engineering, 1985.

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Asghar, M. A. Alkaline degradations of carbohydrates, particularly Dextran. University of Birmingham, 1990.

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D, Klemm, and Heinze Thomas 1958-, eds. Polysaccharides II. Springer, 2006.

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Sibson, S. J. Solvent extraction of dextran from fermentation products. UMIST, 1994.

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Sibson, S. J. Solvent extraction of dextran from fermentation products. UMIST, 1989.

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Till, Andrew. The production of clinical dextran using membrane processes.. Aston University. Department of Chemical Engineering and Applied chemistry, 1988.

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Butera, Geoffrey. A study of iron Dextran complexes by liquid chromatography. University of Salford, 1990.

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Poland, Keith Robert. The fractionation of dextran polymer by ultrafiltration to yield clinical products. Aston University. Department of Chemical Engineering, 1986.

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Kind, Clive Nicholas. Biochemical aspects of the fate of imferon (iron-dextran) in the body. Leicester Polytechnic, 1991.

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Book chapters on the topic "Dextran"

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Bährle-Rapp, Marina. "Dextran." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2818.

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Petroianu, Georg, and Peter Michael Osswald. "Dextran." In Anästhesie in Frage und Antwort. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-05715-5_19.

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Petroianu, Georg, and Peter Michael Osswald. "Dextran." In Anästhesie in Frage und Antwort. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-662-05717-9_26.

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Beyer, Karl-Heinz. "Dextran." In Biotransformation der Arzneimittel. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74386-3_99.

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Steiner, G., and C. Zimmerer. "Dextran." In Polymer Solids and Polymer Melts – Definitions and Physical Properties I. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32072-9_36.

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Wang, Rong, Pieter J. Dijkstra, and Marcel Karperien. "Dextran." In Biomaterials from Nature for Advanced Devices and Therapies. John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119126218.ch18.

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Bährle-Rapp, Marina. "Carboxymethyl Dextran." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1670.

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Bährle-Rapp, Marina. "Dextran Sulfate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2820.

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Tsai, Sheung-Pun, and J. Tze-Fei Wong. "Dextran-Hemoglobin." In Advances in Blood Substitutes. Birkhäuser Boston, 1997. http://dx.doi.org/10.1007/978-1-4612-1976-7_12.

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Bährle-Rapp, Marina. "Dextran Hydroxypropyltrimonium Chloride." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2819.

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Conference papers on the topic "Dextran"

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Bizios, R., F. A. Blumenstock, P. J. Del Vecchio, and A. B. Malik. "PERMSELECTIVITY OF CULTURED ENDOTHELIAL MONOLAYERS: EFFECT OF SIZE AND CHARGE OF THE TRANSPORTED MOLECULES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643351.

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Known molecular size neutral dextrans (molecular weight (MW) range ∼6,000-∼500,000), anionic (dextran sulfate, ∼500,000 MW), and cationic (DEAE-dextran, ∼500,000 MW) were used to determine the permselectivity characteristics of bovine pulmonary arterial endothelial monolayers. The experimental system consisted of two compartments separated by a gelatinized polycarbonate membrane (0.8 μm pore size) on one side of which endothelial monolayers were grown to confluence. Dextran solutions (1 gram %) were prepared in phosphate buffered saline buffer (containing 0.5 gram % serum albumin) and placed o
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Saldeen, T., R. Moalli, F. M. Hasan, A. Carvalho, and M. Eriksson. "EFFECT OF DEXTRAN ON PLASMINOGEN ACTIVATOR INHIBITOR (PAI)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644445.

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Adult respiratory distress syndrome (ARDS) is often associated with impaired fibrinolysis and appearance of microemboli in the lung. Increased production of PAI, associated with acute lung injury, may contribute to this process. In patients at risk of developing microembolic complications, aeteinistration of dextran reduced the incidence of ARDS. Accordingly, we studied the effect of dextran adninistration on plasma PAI levels in a rabbit model of endotoxin-induced lung injury and in patients. E coli endotoxin (500 μg/kg bw, infused over 5 min) was administrered to three groups of anesthetized
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Kutsevol, N., R. Soushko, J. M. Guenet, et al. "BIOHYBRID BRANCHED COPOLYMERS OF CONTROLLED NANOSTRUCTURE BASED ON POLYACRYLAMIDE GRAFTED TO DEXTRAN OR DEXTRAN SULPHATE BACKBONE." In IV INTERNATIONAL CONFERENCE TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2008. http://dx.doi.org/10.1063/1.2989043.

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van den Broek, Chantal N., Marcel C. M. Rutten, Ole Frøbert, and Frans N. van de Vosse. "Culture Medium With Blood Analog Mechanical Properties." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176336.

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Culture of arteries has become increasingly important in studying atherosclerosis and the effect of clinical interventions [1]. Ideally, arterial culturing should imitate in vivo conditions within an ex vivo environment. Physiological wall shear stresses are important as they induce an atheroprotective endothelial phenotype [2], which is relevant for maintaining arterial wall integrity. The arteries in such ex vivo studies, however, are perfused with culture medium, which has a viscosity lower than blood. Previously, the culture medium has been supplemented with dextran to obtain physiological
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Hu, Song-Qing, Sha-Sha Guo, Hai-Liu Wei, et al. "Preparation of Dextran-PAB Carrier for Affinity Ultrafiltration." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5515856.

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Predoi, D., S. L. Iconaru, N. Buton, et al. "Antimicrobial studies on iron oxide-dextran colloidal suspension." In 9TH INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2018. http://dx.doi.org/10.1063/1.5045967.

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CHEN, SHAN, SIYUAN GUO, LIN LI, DASHENG LIU, JIAJIONG LU, and HAITAO MO. "SEPARATION AND PURIFICATION OF DEXTRAN BY EUSOC TECHNOLOGY." In Proceedings of the 4th International Conference. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702623_0119.

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Bezugly, N., N. Kutsevol, S. Filipchenko, Alberto D’Amore, Domenico Acierno, and Luigi Grassia. "BRANCHED POLYELECTROLYTES BASED ON HYDROLYZED DEXTRAN-GRAFT-POLYACRYLAMIDE." In IV INTERNATIONAL CONFERENCE TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2008. http://dx.doi.org/10.1063/1.2989061.

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Liu, Sijia, Jonathan S. Lindsey, and Masahiko Taniguchi. "Chlorin–dextran conjugates for brightness enhancement in water." In Reporters, Markers, Dyes, Nanoparticles, and Molecular Probes for Biomedical Applications XV, edited by Ramesh Raghavachari and Mikhail Y. Berezin. SPIE, 2024. http://dx.doi.org/10.1117/12.3000409.

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Yu, Miao, and Alisa Morss Clyne. "Dextran and PEG Coating Reduced Nanoparticle Toxicity to Cells." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80819.

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Iron oxide nanoparticles are of interest for drug delivery, since they can be targeted using a magnetic field. However, prior to using nanoparticles in vivo, they must be shown as relatively non-toxic to cells. We and others have shown that bare iron oxide nanoparticles are readily taken up by cells, where they catalyze production of highly toxic reactive oxygen species (ROS). This oxidative stress disrupts the cell cytoskeleton and alters cell mechanics. [1] Iron oxide nanoparticles under current development for in vivo biomedical applications are often coated with a polysaccharide (eg. dextr
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Reports on the topic "Dextran"

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Dubick, Michael A., Gary M. Zaucha, Don W. Korte, Wade Jr., and Charles E. Acute and Subacute Toxicity of 7.5% Hypertonic Saline/6% Dextran-70 (HSD) in Dogs. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada244808.

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Dubick, M. A., J. J. Summary, J. Y. Greene, J. W. Holcroft, and C. E. Wade. Assessment of 7.5% NaCl /6% Dextran-70 (HSD) Effects on Serum or Plasma Protein Determinations. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada232833.

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Lin, Yi-En, and Mei-Chun Chen. Dextran-40 administration may reduce partial flap failure rates: A systematic review and meta-analysis protocol. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.12.0013.

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Dubick, Michael A., and Charles E. Wade. Prekallikrein and Protease Inhibitor Levels in Plasma from Conscious, Hemorrhaged and Euvolemic Swine Infused with 7.5% NaCl/6% Dextran-70. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada211966.

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Dubick, M. A., A. F. Kilani, J. J. Summary, J. Y. Greene, and C. E. Wade. Further Evaluation of the Effects of 7.5% NaCl/6% Dextran-70 (HSD) administration on Coagulation and Platelet Aggregation in Hemorrhaged and Euvolemic Swine. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada266477.

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Schwartz, Bertha, Vaclav Vetvicka, Ofer Danai, and Yitzhak Hadar. Increasing the value of mushrooms as functional foods: induction of alpha and beta glucan content via novel cultivation methods. United States Department of Agriculture, 2015. http://dx.doi.org/10.32747/2015.7600033.bard.

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Abstract:
During the granting period, we performed the following projects: Firstly, we differentially measured glucan content in several pleurotus mushroom strains. Mushroom polysaccharides are edible polymers that have numerous reported biological functions; the most common effects are attributed to β-glucans. In recent years, it became apparent that the less abundant α-glucans also possess potent effects in various health conditions. In our first study, we explored several Pleurotus species for their total, β and α-glucan content. Pleurotuseryngii was found to have the highest total glucan concentrati
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Norris, D. K. Tectonic Developments and Major Dextral Faults. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1987. http://dx.doi.org/10.4095/126942.

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Struik, L. C. Dextral strike-slip through Wells Gray Provincial Park, British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1985. http://dx.doi.org/10.4095/120056.

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Grasby, S. E., and E. W. Mountjoy. Compressional and Dextral Motion Along the Chatter Creek Fault, Main Ranges, British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1991. http://dx.doi.org/10.4095/132622.

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Yeo, G. M. Late Carboniferous Dextral Movement On the CobequidHollow Fault System, Nova Scotia : Evidence and Implications. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/120392.

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