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Journal articles on the topic 'Sorbitan esters'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Fiume, Monice M., Wilma F. Bergfeld, Donald V. Belsito, et al. "Safety Assessment of Sorbitan Esters as Used in Cosmetics." International Journal of Toxicology 38, no. 2_suppl (2019): 60S—80S. http://dx.doi.org/10.1177/1091581819871877.

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The Cosmetic Ingredient Review Expert Panel (Panel) assessed the safety of 20 sorbitan esters; this report included sorbitan esters that were reviewed in 1985 and 2002, as well as 3 previously unreviewed sorbitan esters (sorbitan undecylenate, sorbitan sesquicaprylate, and sorbitan palmate). Most of the sorbitan esters are reported to function in cosmetics as surfactant-emulsifying agents. The Panel reviewed the data from previous sorbitan ester reports, as well as additional data included in this report, to determine the safety of these ingredients. The Panel concluded that the sorbitan ester

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2

MAŁYSA, Anna. "TRIBOLOGICAL PROPERTIES OF BLACKBERRY WASTE SEED EXTRACT OBTAINED UNDER SUPERCRITICAL CO2 CONDITIONS WITH SORBITAN ESTERS COMPOSITONS." Tribologia 278, no. 2 (2018): 89–93. http://dx.doi.org/10.5604/01.3001.0012.6980.

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This paper presents results of tribological research of a composition containing as a base, extract of waste blackberry seeds obtained by extraction under supercritical carbon dioxide conditions with sorbitan esters as additives (sorbitan trioleate (STO) sorbitan monolaurate (MLS) and etoxylated sorbitan monolaurate (EO20MLS)). The influence of the concentration of surfactants on the motion resistance, wear and anti-seize properties of the obtained lubricants was analysed. Two types of tests were performed: seizure, with linear load increase and constant load (four-ball device T02). The obtain

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3

Nilsson, Emelie J., Tania K. Lind, Dieter Scherer, et al. "Mechanisms of crystallisation in polysorbates and sorbitan esters." CrystEngComm 22, no. 22 (2020): 3840–53. http://dx.doi.org/10.1039/d0ce00236d.

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4

Lim, Wen Huei, and Salmiah Ahmad. "Dishwashing performance of mixed palm stearin sulfonated methyl esters and polyoxyethylene sorbitan esters." Journal of Surfactants and Detergents 5, no. 1 (2002): 33–38. http://dx.doi.org/10.1007/s11743-002-0202-4.

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5

Giacometti, Jasminka, Čedomila Milin, Nikola Wolf, and Fabio Giacometti. "Process for Preparing Nonionic Surfactant Sorbitan Fatty Acid Esters with and without Previous Sorbitol Cyclization." Journal of Agricultural and Food Chemistry 44, no. 12 (1996): 3950–54. http://dx.doi.org/10.1021/jf950314j.

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6

Rajpoot, Kuldeep. "Acyclovir-loaded sorbitan esters-based organogel: development and rheological characterization." Artificial Cells, Nanomedicine, and Biotechnology 45, no. 3 (2016): 551–59. http://dx.doi.org/10.3109/21691401.2016.1161639.

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7

Sonwai, Sopark, Pawitchaya Podchong, and Dérick Rousseau. "Crystallization kinetics of cocoa butter in the presence of sorbitan esters." Food Chemistry 214 (January 2017): 497–506. http://dx.doi.org/10.1016/j.foodchem.2016.07.092.

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8

Gombač, Zala, Ilja Gasan Osojnik Črnivec, Mihaela Skrt, et al. "Stabilisation of Lutein and Lutein Esters with Polyoxyethylene Sorbitan Monooleate, Medium-Chain Triglyceride Oil and Lecithin." Foods 10, no. 3 (2021): 500. http://dx.doi.org/10.3390/foods10030500.

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Lutein is a challenging compound to incorporate into food, as it is poorly soluble and unstable in aqueous solutions. In this study, the aim was to prepare stable encapsulates of lutein and lutein esters using feasible and straightforward techniques. Fine suspensions based on polyoxyethylene sorbitan monooleate and medium-chain triglyceride oil micelle-like units with 3.45% lutein esters or 1.9% lutein equivalents provided high encapsulation efficiencies of 79% and 83%, respectively. Lutein encapsulated in fine suspensions showed superior stability, as 86% was retained within the formulation o

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9

Omidian, H., M. J. Zohuriaan-Mehr, and H. Bouhendi. "Polymerization of sodium acrylate in inverse-suspension stabilized by sorbitan fatty esters." European Polymer Journal 39, no. 5 (2003): 1013–18. http://dx.doi.org/10.1016/s0014-3057(02)00352-x.

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10

Smidrkal, Jan, Radka Cervenkova, and Vladimir Filip. "Two-stage synthesis of sorbitan esters, and physical properties of the products." EUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY 106, no. 12 (2004): 851–55. http://dx.doi.org/10.1002/ejlt.200401003.

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11

Amim, Jorge, Leandro S. Blachechen, and Denise F. S. Petri. "Effect of sorbitan-based surfactants on glass transition temperature of cellulose esters." Journal of Thermal Analysis and Calorimetry 107, no. 3 (2011): 1259–65. http://dx.doi.org/10.1007/s10973-011-1796-y.

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12

Ueda, Kumiko, Masanori Fujimoto, Hiromi Noto, Yuriko Kawaguchi, Toshiyuki Sakaeda, and Seigo Iwakawa. "Effect of oxyethylene moiety in polyoxyethylene sorbitan esters on the pharmacokinetics of menatetrenone incorporated in O/W lipid emulsions prepared with polyoxyethylene sorbitan esters and soybean oil in rats." Journal of Pharmacy and Pharmacology 54, no. 10 (2002): 1357–63. http://dx.doi.org/10.1211/002235702760345437.

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13

Noudeh, G. Dehghan, P. Khazaeli, S. Mirzaei, F. Sharififar, and S. Nasrollaho. "Determination of the Toxicity Effect of Sorbitan Esters Surfactants Group on Biological Membrane." Journal of Biological Sciences 9, no. 5 (2009): 423–30. http://dx.doi.org/10.3923/jbs.2009.423.430.

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14

Ye, M., R. Walkup, and K. Hill. "Separation of T-MAZ ethoxylated sorbitan fatty acid esters by reverse phase chromatography." Chromatographia 38, no. 5-6 (1994): 337–41. http://dx.doi.org/10.1007/bf02269777.

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15

Ye, Ming Y., Kim D. Hill, and Ron G. Walkup. "Separation of T-MAZ ethoxylated sorbitan fatty acid esters by supercritical fluid chromatography." Journal of Chromatography A 662, no. 2 (1994): 323–27. http://dx.doi.org/10.1016/0021-9673(94)80519-9.

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16

Pensado, Andrea, Manuel Martín-Pastor, Giovanni K. Zorzi, Edison S. Carvalho, and Alejandro Sanchez. "Structural analysis of nanosystems: Solid Sorbitan esters Nanoparticles (SSN) as a case study." European Journal of Pharmaceutics and Biopharmaceutics 104 (July 2016): 189–99. http://dx.doi.org/10.1016/j.ejpb.2016.05.002.

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17

Liu, Yali, and Dominique Jasmin Lunter. "Systematic Investigation of the Effect of Non-Ionic Emulsifiers on Skin by Confocal Raman Spectroscopy—A Comprehensive Lipid Analysis." Pharmaceutics 12, no. 3 (2020): 223. http://dx.doi.org/10.3390/pharmaceutics12030223.

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Non-ionic emulsifiers are commonly found in existing pharmaceutical and cosmetic formulations and have been widely employed to enhance the penetration and permeation of active ingredients into the skin. With the potential of disrupting skin barrier function and increasing fluidity of stratum corneum (SC) lipids, we herein examined the effects of two kinds of non-ionic emulsifiers on intercellular lipids of skin, using confocal Raman spectroscopy (CRS) with lipid signals on skin CRS spectrum. Non-ionic emulsifiers of polyethylene glycol alkyl ethers and sorbitan fatty acid esters were studied t

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18

Dehghan No, Gholamreza, Payam Khazaeli, and Pedram Rahmani. "Study of the Effects of Polyethylene Glycol Sorbitan Esters Surfactants Group on Biological Membranes." International Journal of Pharmacology 4, no. 1 (2007): 27–33. http://dx.doi.org/10.3923/ijp.2008.27.33.

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19

Fontenele Domingues, Maria Aliciane, Ana Paula Badan Ribeiro, Ming Chih Chiu, and Lireny Aparecida Guaraldo Gonçalves. "Sorbitan and sucrose esters as modifiers of the solidification properties of zero trans fats." LWT - Food Science and Technology 62, no. 1 (2015): 122–30. http://dx.doi.org/10.1016/j.lwt.2015.01.008.

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20

Kabir-ud-Din and Zahid Yaseen. "Formulation of amphiphilic drug amitriptyline hydrochloride by polyoxyethylene sorbitan esters in aqueous electrolytic solution." Colloids and Surfaces B: Biointerfaces 93 (May 2012): 208–14. http://dx.doi.org/10.1016/j.colsurfb.2012.01.007.

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21

Suliga, Justyna, and Paweł Śliwa. "Micellar-mediated extraction of green tea containing Chrysanthemum morifolium flowers." Science, Technology and Innovation 1, no. 1 (2017): 49–52. http://dx.doi.org/10.5604/01.3001.0010.7557.

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Micellar mediated extraction (MME) is a new and alternative method of obtaining biologically active substances, such as flavones, flavanones, anthocyanins, triterpene from plant material. In this study a series of polyethoxylated sorbitan esters of fatty acids (Tween 20, 40, 60 and 80) have been applied for the extraction of green tea containing Chrysanthemum morifolium flowers. Results showed that all tested surfactants were effective in the solubilisation of flavonoids and phenolic compounds. Probably, because of too high hydrophilicity, Tween 20 was not sufficient to obtain antioxidants, in

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22

Prouzet, Eric, Frederic Cot, Georges Nabias, André Larbot, Patricia Kooyman, and Thomas J. Pinnavaia. "Assembly of Mesoporous Silica Molecular Sieves Based on Nonionic Ethoxylated Sorbitan Esters as Structure Directors." Chemistry of Materials 11, no. 6 (1999): 1498–503. http://dx.doi.org/10.1021/cm9810281.

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23

Sarney, Douglas B., Mark J. Barnard, Mailo Virto, and Evgeny N. Vulfson. "Enzymatic synthesis of sorbitan esters using a low-boiling-point azeotrope as a reaction solvent." Biotechnology and Bioengineering 54, no. 4 (1997): 351–56. http://dx.doi.org/10.1002/(sici)1097-0290(19970520)54:4<351::aid-bit8>3.0.co;2-j.

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24

Rehman, Nuzhat, Mohammad Amin Mir, Musarat Jan, Adil Amin, Aijaz Ahmad Dar, and Ghulam Mohammad Rather. "Mixed Micellization and Interfacial Properties of Polyoxyethylene Sorbitan Esters with Cetylpyridinium Chloride: A Tensiometric Study." Journal of Surfactants and Detergents 12, no. 4 (2009): 295–304. http://dx.doi.org/10.1007/s11743-009-1123-9.

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25

Grant, Justin, Helen Lee, Roger C. W. Liu, and Christine Allen. "Intermolecular Interactions and Morphology of Aqueous Polymer/Surfactant Mixtures Containing Cationic Chitosan and Nonionic Sorbitan Esters." Biomacromolecules 9, no. 8 (2008): 2146–52. http://dx.doi.org/10.1021/bm800219m.

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26

Ishibashi, Chinami, Hironori Hondoh, and Satoru Ueno. "Influence of Fatty Acid Moieties of Sorbitan Esters on Polymorphic Occurrence of the Palm Mid-Fraction." Journal of the American Oil Chemists' Society 95, no. 6 (2018): 709–20. http://dx.doi.org/10.1002/aocs.12062.

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27

Sonwai, Sopark, Pawitchaya Podchong, and Dérick Rousseau. "Crystallization Kinetics of Coconut Oil in the Presence of Sorbitan Esters with Different Fatty Acid Moieties." Journal of the American Oil Chemists' Society 93, no. 6 (2016): 849–58. http://dx.doi.org/10.1007/s11746-016-2828-3.

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28

Cheong, Jean Ne, Hamed Mirhosseini, and Chin Ping Tan. "Effect of polyoxyethylene sorbitan esters and sodium caseinate on physicochemical properties of palm-based functional lipid nanodispersions." International Journal of Food Sciences and Nutrition 61, no. 4 (2010): 417–24. http://dx.doi.org/10.3109/09637481003591574.

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29

Al-Juaid, Salih Salem. "Inhibition of carbon steel corrosion in hydrochloric acid solutions using polyoxyethylene sorbitan fatty acid esters (tween compounds)." Chemistry and Technology of Fuels and Oils 48, no. 4 (2012): 313–20. http://dx.doi.org/10.1007/s10553-012-0374-8.

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30

Demand, Sarah, Simon Egger, Patrick Degen, et al. "New Approach to Structure–Property Correlations of Different Films of Sorbitan Esters and Their Self‐Assembly into Viscoelastic Monolayers." Journal of Surfactants and Detergents 22, no. 3 (2019): 597–611. http://dx.doi.org/10.1002/jsde.12261.

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31

Mohajeri, Ehsan, and Gholamreza Dehghan Noudeh. "Effect of Temperature on the Critical Micelle Concentration and Micellization Thermodynamic of Nonionic Surfactants: Polyoxyethylene Sorbitan Fatty Acid Esters." E-Journal of Chemistry 9, no. 4 (2012): 2268–74. http://dx.doi.org/10.1155/2012/961739.

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In this study, non-ionic surfactants, polyoxyethylene sorbitan fatty acid esters (polysorbate) are chosen to examine the temperature effect on the CMC over a wide temperature range. The enthalpy and entropy of micelle formation are evaluated according to the phase separation model. The surface tension of solutions was determined by means of Du Nöuys ring. The CMC values were taken from the sharp breaks in the surface tension vs. logarithms of surfactant concentration plots. As the surfactants' chain length increases the CMC at a constant temperature decreases, which is directly related to the

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32

Delgado-Magnero, Karelia H., Pedro A. Valiente, Miriam Ruiz-Peña, Aurora Pérez-Gramatges, and Tirso Pons. "Unraveling the binding mechanism of polyoxyethylene sorbitan esters with bovine serum albumin: A novel theoretical model based on molecular dynamic simulations." Colloids and Surfaces B: Biointerfaces 116 (April 2014): 720–26. http://dx.doi.org/10.1016/j.colsurfb.2013.11.018.

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33

Freixeiro, Paula, Andrea Pensado, Lauren Allen, et al. "Solid sorbitan esters nanoparticles are efficient and low-cost vehicles for subunit vaccines: Proof of concept with Neisseria meningitidis protein Mip." Journal of Drug Delivery Science and Technology 42 (December 2017): 299–306. http://dx.doi.org/10.1016/j.jddst.2017.04.031.

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34

Elmowafy, Enas, Marwa O. El-Derany, Francesca Biondo, Mattia Tiboni, Luca Casettari, and Mahmoud E. Soliman. "Quercetin Loaded Monolaurate Sugar Esters-Based Niosomes: Sustained Release and Mutual Antioxidant—Hepatoprotective Interplay." Pharmaceutics 12, no. 2 (2020): 143. http://dx.doi.org/10.3390/pharmaceutics12020143.

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Flavonoids possess different interesting biological properties, including antibacterial, antiviral, anti-inflammatory and antioxidant activities. However, unfortunately, these molecules present different bottlenecks, such as low aqueous solubility, photo and oxidative degradability, high first-pass effect, poor intestinal absorption and, hence, low systemic bioavailability. A variety of delivery systems have been developed to circumvent these drawbacks, and among them, in this work niosomes have been selected to encapsulate the hepatoprotective natural flavonoid quercetin. The aim of this stud

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35

Grant, J., J. Cho, and C. Allen. "Self-Assembly and Physicochemical and Rheological Properties of a Polysaccharide−Surfactant System Formed from the Cationic Biopolymer Chitosan and Nonionic Sorbitan Esters." Langmuir 22, no. 9 (2006): 4327–35. http://dx.doi.org/10.1021/la060017g.

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36

Grant, J., J. Cho, and C. Allen. "Self-Assembly and Physicochemical and Rheological Properties of a Polysaccharide−Surfactant System Formed from the Cationic Biopolymer Chitosan and Nonionic Sorbitan Esters." Langmuir 23, no. 8 (2007): 4688. http://dx.doi.org/10.1021/la7004166.

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37

Kamel, Rabab, Mona Basha, and Sameh H. Abd El-Alim. "Development of a novel vesicular system using a binary mixture of sorbitan monostearate and polyethylene glycol fatty acid esters for rectal delivery of rutin." Journal of Liposome Research 23, no. 1 (2012): 28–36. http://dx.doi.org/10.3109/08982104.2012.727422.

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38

Yeh, Daniel H., Kurt D. Pennell, and Spyros G. Pavlostathis. "Toxicity and biodegradability screening of nonionic surfactants using sediment-derived methanogenic consortia." Water Science and Technology 38, no. 7 (1998): 55–62. http://dx.doi.org/10.2166/wst.1998.0277.

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The objective of this study was to screen and select biologically-compatible surfactants for subsequent use in enhancing the bioavailability and reductive dechlorination of sorbed-phase chlorinated organic contaminants. Sixteen surfactants commonly used in surfactant-enhanced bioavailability experiments were examined: polyoxyethylene (POE) alcohols (Brij 30/35, Witconol SN-70/90/120), POE sorbitan fatty acid esters (Tween 20/21/40/60/61/65/80/81/85), the octylphenol ethoxylate Triton X-100, and the anionic sodium dodecyl sulfate. Two hexachlorobenzene-dechlorinating, mixed enrichment cultures

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39

Kakiuchi, Takashi, Yoshikazu Teranishi, and Katsumi Niki. "Adsorption of sorbitan fatty acid esters and a sucrose mono-alkanoate at the nitrobenzene-water interface and its effect on the rate of ion transfer across the interface." Electrochimica Acta 40, no. 18 (1995): 2869–74. http://dx.doi.org/10.1016/0013-4686(95)00215-z.

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40

Yeh, Carol Kuei-Jyum, Su-Lan Peng, and I. Yuang Hsu. "Co-surfactant of ethoxylated sorbitan ester and sorbitan monooleate for enhanced flushing of tetrachloroethylene." Chemosphere 49, no. 4 (2002): 421–30. http://dx.doi.org/10.1016/s0045-6535(02)00274-6.

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41

Upadhyay, Kamal K., Chandraprabha Tiwari, Ajay J. Khopade, Himadri B. Bohidar, and Sanjay K. Jain. "Sorbitan Ester Organogels for Transdermal Delivery of Sumatriptan." Drug Development and Industrial Pharmacy 33, no. 6 (2007): 617–25. http://dx.doi.org/10.1080/03639040701199266.

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42

Wu, Y., S. Iglauer, P. Shuler, Y. Tang, and W. A. Goddard. "Alkyl Polyglycoside-Sorbitan Ester Formulations for Improved Oil Recovery." Tenside Surfactants Detergents 47, no. 5 (2010): 280–87. http://dx.doi.org/10.3139/113.110078.

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43

Shukla, Prateek, Tandra Nandi, and Rajinder Palsingh. "Synthesis of Sorbitan Ester Stabilized Uniform Spherical Silver Nanoparticles." Oriental Journal of Chemistry 32, no. 6 (2016): 2947–55. http://dx.doi.org/10.13005/ojc/320614.

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44

Sagiri, Sai S., Kunal Pal, Piyali Basak, Usman Ali Rana, Imran Shakir, and Arfat Anis. "Encapsulation of Sorbitan Ester-Based Organogels in Alginate Microparticles." AAPS PharmSciTech 15, no. 5 (2014): 1197–208. http://dx.doi.org/10.1208/s12249-014-0147-2.

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45

Arcos, Jose A., Manuel Bernabé, and Cristina Otero. "Quantitative enzymatic production of 1,6-diacyl sorbitol esters." Biotechnology and Bioengineering 60, no. 1 (1998): 53–60. http://dx.doi.org/10.1002/(sici)1097-0290(19981005)60:1<53::aid-bit6>3.0.co;2-#.

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46

Fraile, José M., and Carlos J. Saavedra. "Synthesis of Isosorbide Esters from Sorbitol with Heterogeneous Catalysts." ChemistrySelect 2, no. 3 (2017): 1013–18. http://dx.doi.org/10.1002/slct.201601866.

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47

Wang, Zhendi, and Merv Fingas. "Analysis of sorbitan ester surfactants. Part I: High performance liquid chromatography." Journal of High Resolution Chromatography 17, no. 1 (1994): 15–19. http://dx.doi.org/10.1002/jhrc.1240170104.

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48

Wang, Zhendi, and Merv Fingas. "Analysis of sorbitan ester surfactants. Part II: Capillary supercritical fluid chromatography." Journal of High Resolution Chromatography 17, no. 2 (1994): 85–90. http://dx.doi.org/10.1002/jhrc.1240170208.

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49

Piątek-Hnat, Marta, Kuba Bomba, and Jakub Pęksiński. "Synthesis and Selected Properties of Ester Elastomer Containing Sorbitol." Applied Sciences 10, no. 5 (2020): 1628. http://dx.doi.org/10.3390/app10051628.

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The aim of this work was synthesizing ester elastomers, using sorbitol as a monomer obtainable from renewable sources. Three polymers were synthesized, utilizing three different polycondensation times. Their mechanical and thermal properties were examined and compared. Poly(sorbitol sebacate-co-butylene sebacate) elastomers were synthesized as a result of polycondensation reaction, using sebacic acid, butylene glycol and sorbitol as monomers. Resulting materials had good mechanical properties and a cross-linked structure. Such elastomers are susceptible to hydrolytic degradation which has been

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50

Kim, Jung-Ho, Shashi Kant Bhatia, Dongwon Yoo, et al. "Lipase-Catalyzed Production of 6-O-cinnamoyl-sorbitol from D-sorbitol and Cinnamic Acid Esters." Applied Biochemistry and Biotechnology 176, no. 1 (2015): 244–52. http://dx.doi.org/10.1007/s12010-015-1570-x.

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