Relevant bibliographies by topics / Saponine

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Saponine'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Saponine"

1

van Der Haar, A. W. "Untersuchungen Ueber die Saponine." Recueil des Travaux Chimiques des Pays-Bas 42, no. 12 (September 3, 2010): 1080–83. http://dx.doi.org/10.1002/recl.19230421211.

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Schenkel, Eloir, Wolfgang Werner, and Karl Schulte. "Die Saponine ausThinouia coriacea." Planta Medica 57, no. 05 (October 1991): 463–67. http://dx.doi.org/10.1055/s-2006-960152.

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Glombitza, Karl-Werner, and Hermann Kurth. "Saponine aus Anagallis arvensis L. (Primulaceae)." Archiv der Pharmazie 320, no. 10 (October 1987): 1083–87. http://dx.doi.org/10.1002/ardp.198700012.

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van der Haar, A. W. "Untersuchungen über die Saponine und Verwandte Körper." Recueil des Travaux Chimiques des Pays-Bas 43, no. 8 (September 3, 2010): 542–45. http://dx.doi.org/10.1002/recl.19240430804.

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van der Haar, A. W. "Untersuchungen über die Saponine und Verwandte Körper." Recueil des Travaux Chimiques des Pays-Bas 43, no. 8 (September 3, 2010): 546–47. http://dx.doi.org/10.1002/recl.19240430805.

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van der Haar, A. W. "Untersuchungen über die Saponine und Verwandte Körper." Recueil des Travaux Chimiques des Pays-Bas 43, no. 8 (September 3, 2010): 548–49. http://dx.doi.org/10.1002/recl.19240430806.

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van Der Haar, A. W. "Untersuchungen über die Saponine und Verwandte Körper." Recueil des Travaux Chimiques des Pays-Bas 46, no. 11 (September 3, 2010): 775–92. http://dx.doi.org/10.1002/recl.19270461103.

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van der Haar, A. W. "Untersuchungen über die Saponine und verwandte Körper." Recueil des Travaux Chimiques des Pays-Bas 48, no. 7 (September 3, 2010): 726–42. http://dx.doi.org/10.1002/recl.19290480709.

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Reznicek, G., J. Jurenitsch, M. Freiler, S. Korhammer, E. Haslinger, K. Hiller, and W. Kubelka. "Isolierung und Struktur weiterer neuer Saponine ausSolidago canadensis." Planta Medica 58, no. 01 (February 1992): 94–98. http://dx.doi.org/10.1055/s-2006-961398.

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Kronabel, Dieter. "Antileukämisch wirksame Saponine und Sapogenine aus Asparagus officinalis L." Deutsche Zeitschrift für Onkologie 46, no. 02 (June 25, 2014): 62–65. http://dx.doi.org/10.1055/s-0033-1357646.

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Dissertations / Theses on the topic "Saponine"

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Guo, Shengjun. "Structural studies of saponins from Quillaja saponaria Molina /." Uppsala : Swedish Univ. of Agricultural Sciences (Sveriges lantbruksuniv.), 2000. http://epsilon.slu.se/avh/2000/91-576-5786-6.pdf.

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Nord, Lars. "Structural analysis of saponins from Quillaja saponaria Molina and methods for structure-property relationship studies /." Uppsala : Swedish Univ. of Agricultural Sciences (Sveriges lantbruksuniv.), 2000. http://epsilon.slu.se/avh/2000/91-576-5769-6.pdf.

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Nazabadioko, Serge. "Synthese d'oligosaccharides pour l'hemisynthese de saponines." Reims, 1996. http://www.theses.fr/1996REIMP202.

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Nguyen, Duc Hung. "Valorisation des produits médicamenteux naturels : de l'extraction à l'encapsulation." Thesis, Bourgogne Franche-Comté, 2020. http://www.theses.fr/2020UBFCJ003.

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Cette thèse s’inscrit dans la cadre de la thématique du Laboratoire de Pharmacognosie et du Laboratoire de Pharmacie Galénique de l’UFR Sciences de Santé, circonscription Pharmacie, au sein de l’Université de Bourgogne Franche-Comté, afin de trouver de nouvelles molécules naturelles bioactives à encapsuler. D’une part, nous nous sommes concentrés sur la recherche de saponines naturelles de plantes issues de la biodiversité vietnamienne et de l’horticulture française du genres Dracaena, Cordyline (Asparagaceae) et Weigela (Caprifoliaceae). Les travaux menés ont conduit à isolement de 42 saponines naturelles en utilisant différentes techniques chromatographiques. Les structures on été déterminées par des méthodes de spectrométrie de masse en source ESI et de spectroscopie RMN. Parmi les 17 composés purs obtenus des 3 espèces appartenant au genre Weigela, 9 sont des glycosides de l’acide oléanolique et de l’hédéragénine de structure nouvelle. A partir des espèces Dracaena braunii et Cordyline fruticosa “Fairchild red”, nous avons isolé et caractérisé 18 saponines stéroïdiques dont 7 nouvelles de type spirostane et 6 nouvelles de type furostane. Les activités cytotoxiques de la majorité des saponines isolées ont été évaluées sur trois lignées cellulaires : CT26 (cellules tumorales coliques murines), B16 (cellules de mélanome murin) et HepG2 (cellules d’hépatocarcinome) par le test de prolifération cellulaire MTS. Des relations structure/ activité ont ainsi été proposées.D’autre part, nous avons sélectionné une molécule naturelle bien connue afin de mettre au point les essais d’encapsulation. La curcumine possède des propriétés thérapeutiques très intéressantes mais elle présente à la fois une faible solubilité et une faible biodisponibilité, limitant l'administration par voie orale. Dans cette partie de la thèse, nous avons cherché à améliorer la stabilité et la biodisponibilité de la curcumine ainsi qu’une libération contrôlée dans le tractus gastro-intestinal. Des billes de pectinate de calcium ont été préparées en utilisant la gélification ionique en présence de différents tensioactifs. Elles ont été caractérisées grâce à leurs propriétés physico-chimiques et leurs profils de dissolution in vitro. Leur activité antioxydante a été évaluée par le test DPPH. Le Kolliphor HS15® est le tensioactif le plus prometteur pour optimiser les propriétés de la curcumine
This thesis was carried out at the Laboratory of Pharmacognosy and the Laboratory of Pharmaceutical technology, at the UFR Sciences de Santé, circonscription Pharmacy, in the University of Burgundy Franche-Comté, to find new natural molecules to encapsulate. First of all, we focused on the natural saponins from plants of the Vietnam biodiversity and the french horticulture, belonging to the three genera Dracaena, Cordyline (Asparagaceae) and Weigela (Caprifoliaceae). The work led to the successful isolation and elucidation of 42 natural saponins using various chromatographic techniques. The structures were determined by ESI mass spectrometry and NMR spectroscopy. Among the 17 pure compounds obtained from three species of the Weigela genus, 9 oleanolic acid and hederagenin glycosides are previously undescribed ones. From the two species Dracaena braunii and Cordyline fruticosa “Fairchild red”, we isolated and characterized 18 steroidal saponins including 7 new spirostane-types and 6 new furostane-types ones. The cytotoxic activities of the majority of isolated saponins were evaluated against mouse colon cancer (CT26 cells), mouse melanoma (B16 cells) and human liver cancer (HepG2 cells) by MTS assays. The structure / activity relationships were also proposed.On the other hand, we selected a well-known natural molecule to develop encaspulation tests. Among the natural products, curcumin has very interesting therapeutic properties but exhibits both a poor solubility and a low bioavailability, limiting the administration by the oral route. The purpose of this study was to improve the solubility and bioavailability of curcumin as well as simultaneously achieve controlled release in gastrointestinal tract. Pectinate gel beads were prepared based on ionotropic gelation method with the presence of vaious surfactants. After drying, these beads were investigated for physicochemical characteristics (morphological aspects, encapsulation efficiency, stability, physical state) and dissolution kinetics (in vitro release). Antioxidant activity was also determined with DPPH assay. Kolliphor HS15® seems to be the best promising surfactant to increase stability and bioavailability of curcumin
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Wina, Elizabeth. "The utilization of Sapindus rarak DC. saponins to improve ruminant production through rumen manipulation." Beuren Stuttgart Grauer, 2005. http://d-nb.info/989872629/04.

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Dijoux, Marie-Geneviève. "Saponines et flavonoides de beta vulgaris l." Reims, 1993. http://www.theses.fr/1993REIMP206.

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Voutquenne-Nazabadioko, Laurence. "Saponines et activite hemolytique : saponines et glycosides de cinq especes de sapindaceae." Reims, 1997. http://www.theses.fr/1997REIMP208.

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Francis, George. "Effects of low dietary levels of saponins on two common culture fish - common carp (Cyprinus carpio L.) and Nile tilapia (Oreochromis niloticus (L.))." [S.l. : s.n.], 2001. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB10316339.

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Benkhaled, Mohammed. "Determination de structures de saponines de medicago." Reims, 1992. http://www.theses.fr/1992REIMP206.

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Schmid, Christian [Verfasser]. "Geschmacksaktive Saponine in Süßholz (Glycyrrhiza glabra L.): Strukturaufklärung, Psychophysik und Aktivierung von Süß- und Bittergeschmacksrezeptoren / Christian Schmid." München : Verlag Dr. Hut, 2019. http://d-nb.info/1198542969/34.

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Books on the topic "Saponine"

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1953-, Marston A., ed. Saponins. Cambridge: Cambridge University Press, 1995.

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Koh, Rani. Saponins: Properties, applications, and health benefits. Hauppauge, N.Y: Nova Science Publishers, 2011.

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Waller, George R., and Kazuo Yamasaki, eds. Saponins Used in Food and Agriculture. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0413-5.

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Oleszek, W., and A. Marston. Saponins in food, feedstuffs, and medicinal plants. Dordrecht: Springer, 2011.

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1934-, Pierantoni Ruggero, ed. Sapone, Sapey. Milano: Electa, 2009.

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Waller, George R., and Kazuo Yamasaki, eds. Saponins Used in Traditional and Modern Medicine. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1367-8.

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Oleszek, Wieslaw, and Andrew Marston, eds. Saponins in Food, Feedstuffs and Medicinal Plants. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-015-9339-7.

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Miceli, Monica. Bolle di sapone. Torino: Edizioni San Paolo, 1995.

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Bócsa, Iván. Nemesítés a lucerna antinutritív anyagai ellen: Akadémiai székfoglaló, 1991. szeptember 10. Budapest: Akadémiai Kiadó, 1994.

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Haithcock, Richard L. Occaneechi, Saponi, and Tutelo of the Saponi Nation: The Piedmont Catawaba. 9th ed. [United States: R.L. Haithcock and V.L. Haithcock, 1995.

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Book chapters on the topic "Saponine"

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Bährle-Rapp, Marina. "Saponine." In Springer Lexikon Kosmetik und Körperpflege, 490. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_9116.

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Pengelly, Andrew. "Triterpenoids and saponins." In The constituents of medicinal plants, 95–111. 3rd ed. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0006.

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Abstract This chapter focuses on the various classes of triterpenoids (free triterpenes, triterpenoid saponins, steroidal saponins, cardiac glycosides, phytosterols, phytoecdysteroids, curcurbitacins and quassinoids), which occur in the free state within plants or as aglycones of glycosides. Information on the chemical structures and pharmacological actions of these triterpenoids and saponins are also presented.
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Bährle-Rapp, Marina. "Saponins." In Springer Lexikon Kosmetik und Körperpflege, 490. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_9117.

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Makkar, Harinder P. S., P. Siddhuraju, and Klaus Becker. "Saponins." In Plant Secondary Metabolites, 93–100. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-425-4_16.

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Mahato, S. B., and S. Garai. "Triterpenoid Saponins." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, 1–196. Vienna: Springer Vienna, 1998. http://dx.doi.org/10.1007/978-3-7091-6496-9_1.

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Sahu, N. P., S. Banerjee, N. B. Mondal, and D. Mandal. "Steroidal Saponins." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, 45–141. Vienna: Springer Vienna, 2008. http://dx.doi.org/10.1007/978-3-211-74019-4_2.

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Oleszek, Marta, and Wieslaw Oleszek. "Saponins in Food." In Handbook of Dietary Phytochemicals, 1–40. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1745-3_34-1.

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Bomford, R. "Saponins as Immunoadjuvants." In Immunological Adjuvants and Vaccines, 43–46. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0283-5_6.

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Seigler, David S. "Saponins and Cardenolides." In Plant Secondary Metabolism, 456–72. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4913-0_24.

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Massiot, Georges, Marie-Geneviève Dijoux, and Catherine Lavaud. "Saponins and Artifacts." In Advances in Experimental Medicine and Biology, 183–92. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0413-5_15.

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Conference papers on the topic "Saponine"

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Nakashima, S., T. Tohmatsu, H. Hattori, A. Suganuma, and Y. Nozawa. "EVIDENCE FOR INVOLVEMENT OF GTP-BINDING PROTEIN IN ARACKIDONIC ACID RELEASE BY PHOSPHOLIPASE A2 IN PERMEABILIZED HUMAN PLATELETS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644631.

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Platelet activation is accompanied by the active metabolism of membrane phospholipids. Phosphoinositide breakdown by phospholipase C generates second messengers; inositol trisphosphate and diacylglycerol. Recently, it is suggested that GTP-binding protein is linked to the activation of phospholipase C as is true for adenylate cyclase. Although it is known that the receptor stimulation by agonists leads to generation of arachidonic acid, its molecular mechanism has not yet been clear. However, several studies in neutrophils and mast cells using pertussis toxin, have shown the possibility that a GTP-binding protein may act as an intermediary unit component between the receptor and phospholipase A2. The present study was therefore designed to examine the effect of GTP and its analogue GTPγS on the arachidonic acid release in saponin-permeabilized human platelets. GTP or GTPγS alone caused a small but significant liberation of arachidonic acid in permeabilized cells but not in intact cells. GTP or GTPγS was found to enhance thrombin-induced [3H]arachidonic acid release in saponi n-permeabi li zed human platelets. The release of arachidonic acid has been ascribed to activity of phospholipase A2 and/or to sequential action of phospholipase C and diacylglycerol lipase. Inhibitors of phospholipase C (neomycin)/ diacylglycerol lipase (RHC 80267) pathway of arachidonate liberation did not reduce the level of the [3H]arachidonic acid release. The loss of [3H]arachidonate radioactivity from phosphatidylcholine was almost complementary to the increment of released [3H]arachidonic acid, suggesting thrombin-induced hydrolysis of phosphatidylcholine by phospholipase A2. Although phospholipase A2 usually are described as having a requirement for calcium, the effect of GTPγS was more evident at lower calcium concentrations (buffer>0.1 mM>1.0 mM). These data thus indicate that release of arachidonic acid by phospholipase A2 in saponin-treated platelets is closely linked to GTP-binding protein which may decrease the calcium requirement for phospholipase A2 activation.
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Authi, K. S., B. J. Evenden, and N. Crawford. "ACTION OF GTPγS [GUANOSINE 5∲-0-(3-THIOPHOSPHATE)] ON SAPONIN-PERMEABILISED PLATELETS: INVOLVEMENT OF 'G' PROTEINS IN PLATELET ACTIVATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644514.

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Certain ligand-receptor interactions at cell surfaces lead to the phospholipase-C (PLC) hydrolysis of phosphatidyl inositol (4.5) bisphosphate (PIP2). The products serve as intracellular second messengers, e.g. inositol (1.4.5) trisphosphate (IP3) releases Ca2+ from intracellular stores and diacylglycerol activates protein kinase-C. From studies using GTP and analogues (e.g. GTPγS) there is evidence of a key role for a guanine nucleotide binding protein(s) as a link between receptors and PIP2 hydrolysis. We report the actions of GTPγS on washed human platelets permeabilised with saponin (12-14 μg/ml) to allow penetration of low MWt polar substances. The responses to GTPγS are dose dependent (range 9-60 μM) and at 60 μM the agent induces shape change, aggregation and the secretion of 50% of previously incorporated [14C]-5HT. No effect of GTPγS is seen with intact cells. Shape change occurs 25-30 sec after GTPγS; aggregation and secretion is complete after 3 min. When GTP was used (up to 135 μM) with similarly permeabilised platelets no responses were initiated. Phosphatidylinositol turnover was monitored using 32P-labelling before permeabilisation. The addition of 90 μM GTPγS resulted in a 143 ± 23% (n=4) increase in 32P-phosphatidic acid (PA) with respect to the basal levels of “saponised control” cells. These findings suggest that GTPγS stimulates PLC activity through a ‘G’ protein interaction. The GDP analogue (GDPβS) produced no activation responses in saponised platelets but inhibited responses induced by GTPγS in a dose dependent manner (0-480 μM, max inhibition 480 μM). At 960 μM, GDPβS totally inhibited aggregation and secretion initiated by low doses of thrombin (0.1 U/ml) and collagen (1 μg/ml). Identical inhibition by GDPβS of thrombin and collagen-induced activation of intact platelets was observed indicating membrane penetration of this analogue. Shape change effects were not inhibited by GDPSS. The inhibitory effects of GDPSS towards thrombin and collagen induced secretion could be progressively overcome at higher doses of thrombin (0.2 U/ml - 2 U/ml) and collagen (5 μg/ml - 60 μg/ml) suggesting that at higher concentrations these agonists may exert effects through 'G' protein-independent mechanisms.
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Shiga, Hirokazu, S. Takashige, A. Hermawan Dwi, A. Sultana, Shuji Adachi, and Hidefumi Yoshii. "Encapsulation of krill oil by spray drying." In 21st International Drying Symposium. Valencia: Universitat Politècnica València, 2018. http://dx.doi.org/10.4995/ids2018.2018.7323.

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An oil from Pacific krill (Euphausia pacifica) has a high content of PUFAs and phospholipids. The sediment was formed with homogenization of krill oil and maltodextrin (MD; dextrose equivalent (DE) = 19) solution using sodium caseinate, gum arabic, hydrolyzed whey protein or modified starch as a surfactant. Quillaja saponin could form the emulsion without the sediment. MD (28.5 wt%) was solubilized with distiller water (50 wt%) and mixed with krill oil (20wt%) and Quillaja saponin (1.5 wt%). The homogenized solution was spray-dried using Okawara-L8 spray dryer with a centrifugal atomizer. Spray-dried powder was evaluated in the oil-droplet size and surface-oil content. Keywords: krill oil, emulsion, Quillaja saponin, spray drying, PUFAs
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Tian, Jing, Sen Zhao, Bin Zhai, and Longquan Xu. "Biotransformation of Group B Soybean Saponins." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5515692.

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Barriga Medina, elia. "Saponin determination, expression analysis and functional characterization of saponin biosynthetic genes in Chepodium quia leaves." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1383205.

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Segaran, Abirame, and Lee Suan Chua. "Saponins Rich Fractions From Eurycoma longifolia Extract." In Third International Conference on Separation Technology 2020 (ICoST 2020). Paris, France: Atlantis Press, 2020. http://dx.doi.org/10.2991/aer.k.201229.008.

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Prabhudesai, S. A., V. K. Sharma, D. Chakrabarty, Miguel A. Vicente, S. Mitra, R. Mukhopadhyay, Alka B. Garg, R. Mittal, and R. Mukhopadhyay. "Dynamics of Water Confined in Synthetic Saponite Clays." In SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3606198.

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Nechaeva, M. V., and I. F. Golovatskaya. "The effect of sodium selenite on the secondary metabolism of cell culture Lychnis chalcedonica in vitro." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.181.

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We studied the effect of sodium selenite (Se) on the secondary metabolism of Lychnis chalcedonica L. cell culture in vitro. It was found that low concentrations of Se reduce the flavonoid content, but do not change the content of saponins.
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Cui, Shuling. "Qualitative and Quantitative Analysis of Bu-Gong Saponin." In 2014 International Conference on Materials Science and Energy Engineering (CMSEE 2014). WORLD SCIENTIFIC, 2015. http://dx.doi.org/10.1142/9789814678971_0093.

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Li, Jian, Shujuan Chen, Ning Liu, Yan Huang, and Xin Liu. "Hypoglycemic and Hypolipidemic Activity of Total Saponins in Cinnamon." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2010). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5516306.

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Reports on the topic "Saponine"

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Guven, N., D. J. Panfil, and L. L. Carney. Evaluation of saponite and saponite/sepiolite fluids for geothermal drilling. Office of Scientific and Technical Information (OSTI), February 1991. http://dx.doi.org/10.2172/5908401.

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Popov, Georgi, Aleksander Shkondrov, Magdalena Kondeva-Burdina, Vasil Manov, and Irena Krasteva. Effect of a Purified Saponins Mixture from Astragalus glycyphylloides on Rat Hepatocytes. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, May 2021. http://dx.doi.org/10.7546/crabs.2021.05.09.

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