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Journal articles on the topic 'Catanionic mixtures'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Pérez, Lourdes, Aurora Pinazo, M. C. Morán, and Ramon Pons. "Aggregation Behavior, Antibacterial Activity and Biocompatibility of Catanionic Assemblies Based on Amino Acid-Derived Surfactants." International Journal of Molecular Sciences 21, no. 23 (2020): 8912. http://dx.doi.org/10.3390/ijms21238912.

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The surface activity, aggregates morphology, size and charge characteristics of binary catanionic mixtures containing a cationic amino acid-derived surfactant N(π), N(τ)-bis(methyl)-L-Histidine tetradecyl amide (DMHNHC14) and an anionic surfactant (the lysine-based surfactant Nα-lauroyl-Nεacetyl lysine (C12C3L) or sodium myristate) were investigated for the first time. The cationic surfactant has an acid proton which shows a strong pKa shift irrespective of aggregation. The resulting catanionic mixtures exhibited high surface activity and low critical aggregation concentration as compared with

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2

Stenstam, Anna, Ali Khan, and Håkan Wennerström. "Lysozyme in Catanionic Surfactant Mixtures." Langmuir 20, no. 18 (2004): 7760–65. http://dx.doi.org/10.1021/la049508w.

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3

Bramer, Tobias, Noel Dew, and Katarina Edsman. "Pharmaceutical applications for catanionic mixtures." Journal of Pharmacy and Pharmacology 59, no. 10 (2007): 1319–34. http://dx.doi.org/10.1211/jpp.59.10.0001.

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4

Sakai, Hideki, Yuji Okabe, Koji Tsuchiya, Kenichi Sakai, and Masahiko Abe. "Catanionic Mixtures Forming Gemini-like Amphiphiles." Journal of Oleo Science 60, no. 11 (2011): 549–55. http://dx.doi.org/10.5650/jos.60.549.

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5

Pinazo, Aurora, Ramon Pons, Ana Marqués, Maribel Farfan, Anderson da Silva, and Lourdes Perez. "Biocompatible Catanionic Vesicles from Arginine-Based Surfactants: A New Strategy to Tune the Antimicrobial Activity and Cytotoxicity of Vesicular Systems." Pharmaceutics 12, no. 9 (2020): 857. http://dx.doi.org/10.3390/pharmaceutics12090857.

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Their stability and low cost make catanionic vesicles suitable for application as drug delivery systems. In this work we prepared catanionic vesicles using biocompatible surfactants: two cationic arginine-based surfactants (the monocatenary Nα-lauroyl-arginine methyl ester—LAM and the gemini Nα,Nϖ-bis(Nα-lauroylarginine) α, ϖ-propylendiamide—C3(CA)2) and three anionic amphiphiles (the single chain sodium dodecanoate, sodium myristate, and the double chain 8-SH). The critical aggregation concentration, colloidal stability, size, and charge density of these systems were comprehensively studied f

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6

Sanan, Reshu, Rajwinder Kaur, and Rakesh Kumar Mahajan. "Micellar transitions in catanionic ionic liquid–ibuprofen aqueous mixtures; effects of composition and dilution." RSC Adv. 4, no. 110 (2014): 64877–89. http://dx.doi.org/10.1039/c4ra10840j.

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Interactions between 1-dodecyl-3-methylimidazolium chloride and ibuprofen molecules in aqueous solution form catanionic mixtures, with morphologies of mixed micelles dependent on solution composition.

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7

Varde, D., D. Carriere, Laura Arriaga, et al. "On the origin of the stability of foams made from catanionic surfactant mixtures." Soft Matter 7 (June 17, 2011): 6557–70. https://doi.org/10.1039/c1sm05374d.

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8

Oliveira, Isabel S., Sandra G. Silva, Maria Luísa do Vale, and Eduardo F. Marques. "Model Catanionic Vesicles from Biomimetic Serine-Based Surfactants: Effect of the Combination of Chain Lengths on Vesicle Properties and Vesicle-to-Micelle Transition." Membranes 13, no. 2 (2023): 178. http://dx.doi.org/10.3390/membranes13020178.

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Mixtures of cationic and anionic surfactants often originate bilayer structures, such as vesicles and lamellar liquid crystals, that can be explored as model membranes for fundamental studies or as drug and gene nanocarriers. Here, we investigated the aggregation properties of two catanionic mixtures containing biomimetic surfactants derived from serine. The mixtures are designated as 12Ser/8-8Ser and 14Ser/10-10Ser, where mSer is a cationic, single-chained surfactant and n-nSer is an anionic, double-chained one (m and n being the C atoms in the alkyl chains). Our goal was to investigate the e

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9

Kowalczyk, Iwona, Anna Koziróg, Adrianna Szulc, Anna Komasa, and Bogumił Brycki. "Antimicrobial Properties of Monomeric and Dimeric Catanionic Surfactant System." Molecules 30, no. 1 (2025): 164. https://doi.org/10.3390/molecules30010164.

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Cationic gemini surfactants are used due to their broad spectrum of activity, especially surface, anticorrosive and antimicrobial properties. Mixtures of cationic and anionic surfactants are also increasingly described. In order to investigate the effect of anionic additive on antimicrobial activity, experimental studies were carried out to obtain MIC (minimal inhibitory concentration) against E. coli and S. aureus bacteria. Two gemini surfactants (12-6-12 and 12-O-12) and two single quaternary ammonium salts (DTAB and DDAC) were analyzed. The most commonly used commercial compounds of this cl

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10

Maurer, Eva, Luc Belloni, Thomas Zemb, and David Carrière. "Ion Exchange in Catanionic Mixtures: From Ion Pair Amphiphiles to Surfactant Mixtures." Langmuir 23, no. 12 (2007): 6554–60. http://dx.doi.org/10.1021/la070184w.

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11

Lin, Yi-An, Andrew G. Cheetham, Pengcheng Zhang, et al. "Multiwalled Nanotubes Formed by Catanionic Mixtures of Drug Amphiphiles." ACS Nano 8, no. 12 (2014): 12690–700. http://dx.doi.org/10.1021/nn505688b.

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12

Coldren, Bret A., Heidi Warriner, Ryan van Zanten, Joseph A. Zasadzinski, and Eric B. Sirota. "Lamellar Gels and Spontaneous Vesicles in Catanionic Surfactant Mixtures." Langmuir 22, no. 24 (2006): 10296. http://dx.doi.org/10.1021/la068001d.

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13

Mel'nikov, Sergey M., Rita Dias, Yuliya S. Mel'nikova, Eduardo F. Marques, Maria G. Miguel, and Björn Lindman. "DNA conformational dynamics in the presence of catanionic mixtures." FEBS Letters 453, no. 1-2 (1999): 113–18. http://dx.doi.org/10.1016/s0014-5793(99)00699-7.

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14

Coldren, Bret A., Heidi Warriner, Ryan van Zanten, Joseph A. Zasadzinski, and Eric B. Sirota. "Lamellar Gels and Spontaneous Vesicles in Catanionic Surfactant Mixtures." Langmuir 22, no. 6 (2006): 2465–73. http://dx.doi.org/10.1021/la052447x.

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15

Šegota, Suzana, Stanka Heimer, and Đurđica Težak. "New catanionic mixtures of dodecyldimethylammonium bromide/sodium dodecylbenzenesulphonate/water." Colloids and Surfaces A: Physicochemical and Engineering Aspects 274, no. 1-3 (2006): 91–99. http://dx.doi.org/10.1016/j.colsurfa.2005.08.051.

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16

Tieke, Bernd. "Polymerisation of styrene in microemulsion with catanionic surfactant mixtures." Colloid and Polymer Science 283, no. 4 (2004): 421–30. http://dx.doi.org/10.1007/s00396-004-1168-2.

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17

Sohrabi, Beheshteh, Samira Eivazzadeh, Ali Sharifi, and Reza Azadbakht. "Self-assembled catanionic surfactant mixtures in aqueous/ionic liquid systems." Journal of Molecular Liquids 211 (November 2015): 754–60. http://dx.doi.org/10.1016/j.molliq.2015.07.025.

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18

Mundhada, D. R., and A. V. Chandewar. "Evaluation Study of in-situ Gel Using Catanionic Surfactant Mixtures." Research Journal of Science and Technology 8, no. 4 (2016): 165. http://dx.doi.org/10.5958/2349-2988.2016.00025.5.

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19

Vlachy, N., D. Touraud, J. Heilmann, and W. Kunz. "Determining the cytotoxicity of catanionic surfactant mixtures on HeLa cells." Colloids and Surfaces B: Biointerfaces 70, no. 2 (2009): 278–80. http://dx.doi.org/10.1016/j.colsurfb.2008.12.038.

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20

Tajik, Behnoosh, Beheshteh Sohrabi, Reza Amani, and S. Majid Hashemianzadeh. "The study of polymer–surfactant interaction in catanionic surfactant mixtures." Colloids and Surfaces A: Physicochemical and Engineering Aspects 436 (September 2013): 890–97. http://dx.doi.org/10.1016/j.colsurfa.2013.07.026.

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21

Esposito, Rodolfo, Noemi Gallucci, Marcella Niccoli, et al. "Synergism and molecular mismatch in rhamnolipid/CTAC catanionic surfactant mixtures." Colloids and Surfaces A: Physicochemical and Engineering Aspects 674 (October 2023): 131931. http://dx.doi.org/10.1016/j.colsurfa.2023.131931.

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22

Gavrilko, T., I. Gnatyuk, V. Styopkin, N. Shcherban, J. Baran, and M. Drozd. "FTIR and DSC Studies of Binary Mixtures of Long-Chain Aliphatic Compounds: Lauric Acid – Cetyl-trimethylammonium Bromide." Ukrainian Journal of Physics 63, no. 5 (2018): 413. http://dx.doi.org/10.15407/ujpe63.5.413.

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Structural and thermal properties of a solid-state binary mixture of long-chain cationic and anionic surfactants (so-called catanionic complexes) composed of cetyltrimethyl-ammonium bromide, [H3C–(CH2)15–N+(CH3)3]Br−(CTAB), and saturated fatty acid (FA), CH3(CH2)12COOH (lauric acid, kC12), are studied. To clarify the effect of intermolecular interactions on the crystalline structure and phase transitions in this class of supramolecular compounds, the 1 : 1 kC12-CTAB binary mixture is investigated by means of X-ray diffraction, differential scanning calorimetry (DSC), and temperature-variable F

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23

Bhattacharjee, Jayita, V. K. Aswal, P. A. Hassan, Ravi Pamu, Janaky Narayanan, and Jayesh Bellare. "Structural evolution in catanionic mixtures of cetylpyridinium chloride and sodium deoxycholate." Soft Matter 8, no. 39 (2012): 10130. http://dx.doi.org/10.1039/c2sm25460c.

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24

Javadian, Soheila, Ali Motaee, Maryam Sharifi, Hasti Aghdastinat, and Fariba Taghavi. "Dispersion stability of multi-walled carbon nanotubes in catanionic surfactant mixtures." Colloids and Surfaces A: Physicochemical and Engineering Aspects 531 (October 2017): 141–49. http://dx.doi.org/10.1016/j.colsurfa.2017.07.081.

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25

Li, Hongguang, and Jingcheng Hao. "Reverse Vesicles of Salt-free Catanionic Surfactants in Toluene/Water Mixtures." Chemistry Letters 36, no. 6 (2007): 702–3. http://dx.doi.org/10.1246/cl.2007.702.

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26

Li, Hongguang, Stefan A. Wieczorek, Xia Xin, et al. "Phase Transition in Salt-Free Catanionic Surfactant Mixtures Induced by Temperature." Langmuir 26, no. 1 (2010): 34–40. http://dx.doi.org/10.1021/la902069w.

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27

Michina, Youlia, David Carrière, Thibault Charpentier, et al. "Absence of Lateral Phase Segregation in Fatty Acid-Based Catanionic Mixtures." Journal of Physical Chemistry B 114, no. 5 (2010): 1932–38. http://dx.doi.org/10.1021/jp910267v.

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28

Kovalchuk, N. M., A. Barton, A. Trybala, and V. Starov. "Mixtures of catanionic surfactants can be superspreaders: Comparison with trisiloxane superspreader." Journal of Colloid and Interface Science 459 (December 2015): 250–56. http://dx.doi.org/10.1016/j.jcis.2015.08.024.

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29

Li, Chen, Xiao Jin-Xin, and Ma Ji-Ming. "Aqueous Two-phase System of Catanionic Surfactant Mixtures Formed by Adding Salts." Acta Physico-Chimica Sinica 19, no. 07 (2003): 577–79. http://dx.doi.org/10.3866/pku.whxb20030701.

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30

Pucci, Carlotta, Lourdes Pérez, Camillo La Mesa, and Ramon Pons. "Characterization and stability of catanionic vesicles formed by pseudo-tetraalkyl surfactant mixtures." Soft Matter 10, no. 48 (2014): 9657–67. http://dx.doi.org/10.1039/c4sm01575d.

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31

Dias, Rita S., Björn Lindman, and Maria G. Miguel. "Compaction and Decompaction of DNA in the Presence of Catanionic Amphiphile Mixtures." Journal of Physical Chemistry B 106, no. 48 (2002): 12608–12. http://dx.doi.org/10.1021/jp020392r.

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32

Wang, Ce, Xu-Long Cao, Lan-Lei Guo, et al. "Effect of adsorption of catanionic surfactant mixtures on wettability of quartz surface." Colloids and Surfaces A: Physicochemical and Engineering Aspects 509 (November 2016): 564–73. http://dx.doi.org/10.1016/j.colsurfa.2016.09.057.

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33

Wang, Ce, Xu-Long Cao, Lan-Lei Guo, et al. "Effect of molecular structure of catanionic surfactant mixtures on their interfacial properties." Colloids and Surfaces A: Physicochemical and Engineering Aspects 509 (November 2016): 601–12. http://dx.doi.org/10.1016/j.colsurfa.2016.09.069.

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34

Frenning, Göran, Johan Gråsjö, and Per Hansson. "The release of catanionic mixtures embedded in gels: An approximate analytical analysis." AIChE Journal 57, no. 6 (2010): 1402–8. http://dx.doi.org/10.1002/aic.12368.

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35

Li, Hongguang, Jingcheng Hao, and Zhonghua Wu. "Phase Behavior and Properties of Reverse Vesicles in Salt-Free Catanionic Surfactant Mixtures." Journal of Physical Chemistry B 112, no. 12 (2008): 3705–10. http://dx.doi.org/10.1021/jp7112329.

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36

Varade, D., D. Carriere, L. R. Arriaga, et al. "On the origin of the stability of foams made from catanionic surfactant mixtures." Soft Matter 7, no. 14 (2011): 6557. http://dx.doi.org/10.1039/c1sm05374d.

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37

Blanco, Elena, Carlos Rodriguez-Abreu, Pablo Schulz, and Juan M. Ruso. "Effect of alkyl chain asymmetry on catanionic mixtures of hydrogenated and fluorinated surfactants." Journal of Colloid and Interface Science 341, no. 2 (2010): 261–66. http://dx.doi.org/10.1016/j.jcis.2009.09.062.

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38

Emelyanova, Ksenia A., Polina O. Sorina, and Alexey I. Victorov. "Transmembrane potential in vesicles formed by catanionic surfactant mixtures in an aqueous salt solution." Physical Chemistry Chemical Physics 22, no. 45 (2020): 26438–51. http://dx.doi.org/10.1039/d0cp05248e.

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39

Vlachy, Nina, Marcus Drechsler, Didier Touraud, and Werner Kunz. "Anion specificity influencing morphology in catanionic surfactant mixtures with an excess of cationic surfactant." Comptes Rendus Chimie 12, no. 1-2 (2009): 30–37. http://dx.doi.org/10.1016/j.crci.2008.10.010.

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40

Iampietro, Daniel J., Laura L. Brasher, Eric W. Kaler, Anna Stradner, and Otto Glatter. "Direct Analysis of SANS and SAXS Measurements of Catanionic Surfactant Mixtures by Fourier Transformation." Journal of Physical Chemistry B 102, no. 17 (1998): 3105–13. http://dx.doi.org/10.1021/jp973326b.

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41

O'Driscoll, Benjamin M. D., E. Anne Nickels, and Karen J. Edler. "Formation of robust, free-standing nanostructured membranes from catanionic surfactant mixtures and hydrophilic polymers." Chem. Commun., no. 10 (2007): 1068–70. http://dx.doi.org/10.1039/b614224a.

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42

Yang, Mei, Jingcheng Hao, and Hongguang Li. "Synergism and formation of vesicle gels in salt-free catanionic hydrocarbon/fluorocarbon surfactant mixtures." RSC Adv. 4, no. 76 (2014): 40595–605. http://dx.doi.org/10.1039/c4ra07794f.

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43

Wang, Yujie, and Eduardo F. Marques. "Mesophase formation and thermal behavior of catanionic mixtures of gemini surfactants with sodium alkylsulfates." Journal of Thermal Analysis and Calorimetry 100, no. 2 (2010): 501–8. http://dx.doi.org/10.1007/s10973-009-0653-8.

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44

Bramer, Tobias, Göran Frenning, Johan Gråsjö, Katarina Edsman, and Per Hansson. "Implications of regular solution theory on the release mechanism of catanionic mixtures from gels." Colloids and Surfaces B: Biointerfaces 71, no. 2 (2009): 214–25. http://dx.doi.org/10.1016/j.colsurfb.2009.02.008.

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45

Blanco, Elena, Ulf Olsson, Juan M. Ruso, Pablo C. Schulz, Gerardo Prieto, and Félix Sarmiento. "Phase behavior of semifluorinated catanionic mixtures: Head group dependence and spontaneous formation of vesicles." Journal of Colloid and Interface Science 331, no. 2 (2009): 522–31. http://dx.doi.org/10.1016/j.jcis.2008.12.009.

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46

Rojewska, Monika, Anna Olejnik, Joanna Rychlik, and Krystyna Prochaska. "Adsorption properties and biological activity of catanionic mixtures containing derivatives of quaternary lysosomotropic substances." Colloids and Surfaces A: Physicochemical and Engineering Aspects 441 (January 2014): 890–98. http://dx.doi.org/10.1016/j.colsurfa.2013.01.062.

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47

Shen, Yuwen, Heinz Hoffmann, Lihua Jiang, Haitao Lin, Jingcheng Hao, and Li Yang. "Lamellar phase formation in catanionic mixtures of hydrogenated and fluorinated surfactants: a comparative study." Colloid and Polymer Science 292, no. 1 (2013): 67–75. http://dx.doi.org/10.1007/s00396-013-3040-8.

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48

di Gregorio, Maria Chiara, Emilia Severoni, Leana Travaglini, et al. "Bile acid derivative-based catanionic mixtures: versatile tools for superficial charge modulation of supramolecular lamellae and nanotubes." Physical Chemistry Chemical Physics 20, no. 28 (2018): 18957–68. http://dx.doi.org/10.1039/c8cp02745e.

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49

Edlund, Håkan, Alireza Sadaghiani, and Ali Khan. "Phase Behavior and Phase Structure for Catanionic Surfactant Mixtures: Dodecyltrimethylammonium Chloride−Sodium Nonanoate−Water System." Langmuir 13, no. 19 (1997): 4953–63. http://dx.doi.org/10.1021/la9621372.

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50

Wang, Ce, Hongbo Fang, Qingtao Gong, et al. "Roles of Catanionic Surfactant Mixtures on the Stability of Foams in the Presence of Oil." Energy & Fuels 30, no. 8 (2016): 6355–64. http://dx.doi.org/10.1021/acs.energyfuels.6b01112.

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