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Journal articles on the topic 'Complex coacervate'

Author: Grafiati

Published: 29 June 2021

Last updated: 2 February 2022

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1

Kim, Sangsik, Jun Huang, Yongjin Lee, Sandipan Dutta, Hee Young Yoo, Young Mee Jung, YongSeok Jho, Hongbo Zeng, and Dong Soo Hwang. "Complexation and coacervation of like-charged polyelectrolytes inspired by mussels." Proceedings of the National Academy of Sciences 113, no. 7 (February 1, 2016): E847—E853. http://dx.doi.org/10.1073/pnas.1521521113.

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It is well known that polyelectrolyte complexes and coacervates can form on mixing oppositely charged polyelectrolytes in aqueous solutions, due to mainly electrostatic attraction between the oppositely charged polymers. Here, we report the first (to the best of our knowledge) complexation and coacervation of two positively charged polyelectrolytes, which provides a new paradigm for engineering strong, self-healing interactions between polyelectrolytes underwater and a new marine mussel-inspired underwater adhesion mechanism. Unlike the conventional complex coacervate, the like-charged coacervate is aggregated by strong short-range cation–π interactions by overcoming repulsive electrostatic interactions. The resultant phase of the like-charged coacervate comprises a thin and fragile polyelectrolyte framework and round and regular pores, implying a strong electrostatic correlation among the polyelectrolyte frameworks. The like-charged coacervate possesses a very low interfacial tension, which enables this highly positively charged coacervate to be applied to capture, carry, or encapsulate anionic biomolecules and particles with a broad range of applications.

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2

Furlani, Franco, Pietro Parisse, and Pasquale Sacco. "On the Formation and Stability of Chitosan/Hyaluronan-Based Complex Coacervates." Molecules 25, no. 5 (February 27, 2020): 1071. http://dx.doi.org/10.3390/molecules25051071.

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This contribution is aimed at extending our previous findings on the formation and stability of chitosan/hyaluronan-based complex coacervates. Colloids are herewith formed by harnessing electrostatic interactions between the two polyelectrolytes. The presence of tiny amounts of the multivalent anion tripolyphosphate (TPP) in the protocol synthesis serves as an adjuvant “point-like” cross-linker for chitosan. Hydrochloride chitosans at different viscosity average molar mass, M v ¯ , in the range 10,000–400,000 g/mol, and fraction of acetylated units, FA, (0.16, 0.46 and 0.63) were selected to fabricate a large library of formulations. Concepts such as coacervate size, surface charge and homogeneity in relation to chitosan variables are herein disclosed. The stability of coacervates in Phosphate Buffered Saline (PBS) was verified by means of scattering techniques, i.e., Dynamic Light Scattering (DLS) and Small-Angle X-ray Scattering (SAXS). The conclusions from this set of experiments are the following: (i) a subtle equilibrium between chitosan FA and M v ¯ does exist in ensuring colloidal stability; (ii) once diluted in PBS, osmotic swelling-driven forces trigger the enlargement of the polymeric mesh with an ensuing increase of coacervate size and porosity.

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3

Dompé, Marco, Francisco Javier Cedano-Serrano, Mehdi Vahdati, Dominique Hourdet, Jasper van der Gucht, Marleen Kamperman, and Thomas E. Kodger. "Hybrid Complex Coacervate." Polymers 12, no. 2 (February 4, 2020): 320. http://dx.doi.org/10.3390/polym12020320.

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Underwater adhesion represents a huge technological challenge as the presence of water compromises the performance of most commercially available adhesives. Inspired by natural organisms, we have designed an adhesive based on complex coacervation, a liquid–liquid phase separation phenomenon. A complex coacervate adhesive is formed by mixing oppositely charged polyelectrolytes bearing pendant thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) chains. The material fully sets underwater due to a change in the environmental conditions, namely temperature and ionic strength. In this work, we incorporate silica nanoparticles forming a hybrid complex coacervate and investigate the resulting mechanical properties. An enhancement of the mechanical properties is observed below the PNIPAM lower critical solution temperature (LCST): this is due to the formation of PNIPAM–silica junctions, which, after setting, contribute to a moderate increase in the moduli and in the adhesive properties only when applying an ionic strength gradient. By contrast, when raising the temperature above the LCST, the mechanical properties are dominated by the association of PNIPAM chains and the nanofiller incorporation leads to an increased heterogeneity with the formation of fracture planes at the interface between areas of different concentrations of nanoparticles, promoting earlier failure of the network—an unexpected and noteworthy consequence of this hybrid system.

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4

Lu, Tiemei, and Evan Spruijt. "Multiphase Complex Coacervate Droplets." Journal of the American Chemical Society 142, no. 6 (January 20, 2020): 2905–14. http://dx.doi.org/10.1021/jacs.9b11468.

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5

Voets, Ilja K., Arie de Keizer, and Martien A. Cohen Stuart. "Complex coacervate core micelles." Advances in Colloid and Interface Science 147-148 (March 2009): 300–318. http://dx.doi.org/10.1016/j.cis.2008.09.012.

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6

Nguyen Le, My Lan, Hang Nga Le Thi, and Vinh Tien Nguyen. "Hydrolyzed Karaya Gum: Gelatin Complex Coacervates for Microencapsulation of Soybean Oil and Curcumin." Journal of Food Quality 2021 (April 14, 2021): 1–10. http://dx.doi.org/10.1155/2021/5593065.

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This is the first report on utilizing hydrolyzed karaya gum (HKG) as a novel polyanion material for complex coacervation with gelatin A. With negative zeta potentials at pH > 2.5, HKG formed the complex coacervate with a maximum yield at pH 3.75 and 1 : 1 HKG:gelatin ratio. The optimal complex coacervates were used to encapsulate soybean oil containing curcumin using different shell:core ratios, homogenization speeds, concentrations of emulsifier, and drying techniques. Optical microscopy showed that increasing homogenization speed and Tween 80 concentration produced smaller and more uniform coacervate particles. Increasing the shell:core mass ratio from 1 to 4 resulted in a linear increase in encapsulation efficiencies for both soybean oil and curcumin. Accelerated peroxidation tests on the microcapsules showed enhanced protective effects against oil peroxidation when increasing shell:core ratios and using freeze-drying instead of oven-drying at 50 oC. In vitro release of curcumin in simulated gastric and intestinal fluids was faster when using freeze-drying and decreasing shell:core ratio. This study shows perspective novel applications of HKG in microencapsulating active ingredients for food and pharmaceutical industries.

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7

Hofs, B., A. de Keizer, S. van der Burgh, F. A. M. Leermakers, M. A. Cohen Stuart, P. E. Millard, and A. H. E. Müller. "Complex coacervate core micro-emulsions." Soft Matter 4, no. 7 (2008): 1473. http://dx.doi.org/10.1039/b802148a.

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8

Wang, Qifeng, and Joseph B. Schlenoff. "The Polyelectrolyte Complex/Coacervate Continuum." Macromolecules 47, no. 9 (April 28, 2014): 3108–16. http://dx.doi.org/10.1021/ma500500q.

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9

Mason, Alexander F., and Jan C. M. van Hest. "Multifaceted cell mimicry in coacervate-based synthetic cells." Emerging Topics in Life Sciences 3, no. 5 (September 4, 2019): 567–71. http://dx.doi.org/10.1042/etls20190094.

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Cells, the discrete living systems that comprise all life on Earth, are a boundless source of inspiration and motivation for many researchers in the natural sciences. In the field of bottom-up synthetic cells, researchers seek to create multifaceted, self-assembled, chemical systems that mimic the properties and behaviours of natural life. In this perspective, we will describe the relatively recent application of complex coacervates to synthetic cells, and how they have been used to model an expanding range of biologically relevant phenomena. Furthermore, we will explore the unique advantages and disadvantages of coacervate-based synthetic cells, and their potential impact on the field in the years to come.

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10

Dompé, Marco, Francisco J. Cedano-Serrano, Mehdi Vahdati, Ugo Sidoli, Olaf Heckert, Alla Synytska, Dominique Hourdet, et al. "Tuning the Interactions in Multiresponsive Complex Coacervate-Based Underwater Adhesives." International Journal of Molecular Sciences 21, no. 1 (December 21, 2019): 100. http://dx.doi.org/10.3390/ijms21010100.

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In this work, we report the systematic investigation of a multiresponsive complex coacervate-based underwater adhesive, obtained by combining polyelectrolyte domains and thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) units. This material exhibits a transition from liquid to solid but, differently from most reactive glues, is completely held together by non-covalent interactions, i.e., electrostatic and hydrophobic. Because the solidification results in a kinetically trapped morphology, the final mechanical properties strongly depend on the preparation conditions and on the surrounding environment. A systematic study is performed to assess the effect of ionic strength and of PNIPAM content on the thermal, rheological and adhesive properties. This study enables the optimization of polymer composition and environmental conditions for this underwater adhesive system. The best performance with a work of adhesion of 6.5 J/m2 was found for the complex coacervates prepared at high ionic strength (0.75 M NaCl) and at an optimal PNIPAM content around 30% mol/mol. The high ionic strength enables injectability, while the hydrated PNIPAM domains provide additional dissipation, without softening the material so much that it becomes too weak to resist detaching stress.

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11

Heo, Tae-Young, Inhye Kim, Liwen Chen, Eunji Lee, Sangwoo Lee, and Soo-Hyung Choi. "Effect of Ionic Group on the Complex Coacervate Core Micelle Structure." Polymers 11, no. 3 (March 10, 2019): 455. http://dx.doi.org/10.3390/polym11030455.

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Pairs of ionic group dependence of the structure of a complex coacervate core micelle (C3M) in an aqueous solution was investigated using DLS, cryo-TEM, and SANS with a contrast matching technique and a detailed model analysis. Block copolyelectrolytes were prepared by introducing an ionic group (i.e., ammonium, guanidinium, carboxylate, and sulfonate) to poly(ethylene oxide-b-allyl glycidyl ether) (NPEO = 227 and NPAGE = 52), and C3Ms were formed by simple mixing of two oppositely-charged block copolyelectrolyte solutions with the exactly same degree of polymerization. All four C3Ms are spherical with narrow distribution of micelle dimension, and the cores are significantly swollen by water, resulting in relatively low brush density of PEO chains on the core surface. With the pair of strong polyelectrolytes, core radius and aggregation number increases, which reflects that the formation of complex coacervates are significantly sensitive to the pairs of ionic groups rather than simple charge pairing.

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12

Blocher, Whitney C., and Sarah L. Perry. "Complex coacervate-based materials for biomedicine." Wiley Interdisciplinary Reviews: Nanomedicine and Nanobiotechnology 9, no. 4 (November 4, 2016): e1442. http://dx.doi.org/10.1002/wnan.1442.

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13

Dompé, Marco, Francisco J. Cedano‐Serrano, Olaf Heckert, Nicoline van den Heuvel, Jasper van der Gucht, Yvette Tran, Dominique Hourdet, Costantino Creton, and Marleen Kamperman. "Thermoresponsive Complex Coacervate‐Based Underwater Adhesive." Advanced Materials 31, no. 21 (March 29, 2019): 1808179. http://dx.doi.org/10.1002/adma.201808179.

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14

Burgess, D. J. "Practical analysis of complex coacervate systems." Journal of Colloid and Interface Science 140, no. 1 (November 1990): 227–38. http://dx.doi.org/10.1016/0021-9797(90)90338-o.

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15

Han, Juan, Yun Wang, Tong Chen, Xiaowei Hu, Lei Gu, Xu Tang, Lei Wang, and Liang Ni. "Heat-induced coacervation for purification of Lycium barbarum polysaccharide based on amphiphilic polymer–protein complex formation." Canadian Journal of Chemistry 95, no. 8 (August 2017): 837–44. http://dx.doi.org/10.1139/cjc-2017-0008.

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Heat-induced coacervation of triblock copolymer solution was described, and its application in the purification of Lycium barbarum polysaccharide (LBP) was investigated. The formation of coacervate micelles–protein complex combined with the incompatibility between coacervate micelles and polysaccharide made it an ideal system for the separation of protein and LBP. This separation process was governed by a series of parameters including polymer concentration, amount of crude LBP solution, and pH. In the primary coacervation extraction process, LBP was preferentially distributed to dilute phase with a high recovery ratio of 82%, whereas 87% of protein was partitioned to the coacervate phase. The coacervate micelles–protein interaction and the interphase potential was regulated by temperature and electrolytes, respectively, which contributed to the recovery and recycling of the polymer. After phase separation, LBP was precipitated with the addition of ethanol. The FTIR spectrum was used to identify LBP. In addition, the antioxidant activity of LBP was measured.

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16

Khan, Nasreen, Nadia Z. Zaragoza, Carly E. Travis, Monojoy Goswami, and Blair K. Brettmann. "Polyelectrolyte Complex Coacervate Assembly with Cellulose Nanofibers." ACS Omega 5, no. 28 (July 7, 2020): 17129–40. http://dx.doi.org/10.1021/acsomega.0c00977.

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17

Rumyantsev, Artem M., Ekaterina B. Zhulina, and Oleg V. Borisov. "Scaling Theory of Complex Coacervate Core Micelles." ACS Macro Letters 7, no. 7 (June 22, 2018): 811–16. http://dx.doi.org/10.1021/acsmacrolett.8b00316.

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18

Cohen Stuart, M. A., N. A. M. Besseling, and R. G. Fokkink. "Formation of Micelles with Complex Coacervate Cores." Langmuir 14, no. 24 (November 1998): 6846–49. http://dx.doi.org/10.1021/la980778m.

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19

Bourouina, Nadia, Martien A. Cohen Stuart, and J. Mieke Kleijn. "Complex coacervate core micelles as diffusional nanoprobes." Soft Matter 10, no. 2 (2014): 320–31. http://dx.doi.org/10.1039/c3sm52245h.

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20

Qin, Jian, Dimitrios Priftis, Robert Farina, Sarah L. Perry, Lorraine Leon, Jonathan Whitmer, Kyle Hoffmann, Matthew Tirrell, and Juan J. de Pablo. "Interfacial Tension of Polyelectrolyte Complex Coacervate Phases." ACS Macro Letters 3, no. 6 (May 30, 2014): 565–68. http://dx.doi.org/10.1021/mz500190w.

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21

Balchunas, Andrew, and Sarah Veatch. "Complex Coacervate Formation on a Heterogeneous Membrane." Biophysical Journal 116, no. 3 (February 2019): 79a. http://dx.doi.org/10.1016/j.bpj.2018.11.467.

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22

Lv, Kangle, Adam W. Perriman, and Stephen Mann. "Photocatalytic multiphase micro-droplet reactors based on complex coacervation." Chemical Communications 51, no. 41 (2015): 8600–8602. http://dx.doi.org/10.1039/c5cc01914a.

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23

Marianelli, A. M., B. M. Miller, and C. D. Keating. "Impact of macromolecular crowding on RNA/spermine complex coacervation and oligonucleotide compartmentalization." Soft Matter 14, no. 3 (2018): 368–78. http://dx.doi.org/10.1039/c7sm02146a.

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24

Nolles, A., N. J. E. van Dongen, A. H. Westphal, A. J. W. G. Visser, J. M. Kleijn, W. J. H. van Berkel, and J. W. Borst. "Encapsulation into complex coacervate core micelles promotes EGFP dimerization." Physical Chemistry Chemical Physics 19, no. 18 (2017): 11380–89. http://dx.doi.org/10.1039/c7cp00755h.

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High packaging densities are obtained by encapsulation of EGFP and mEGFP in complex coacervate core micelles (C3Ms) resulting in noticeable spectral differences between EGFP and mEGFP. We address these changes to dimerization of EGFP whereas mEGFP mainly remains monomeric in C3Ms.

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25

Arfin, Najmul, V. K. Aswal, and H. B. Bohidar. "Overcharging, thermal, viscoelastic and hydration properties of DNA–gelatin complex coacervates: pharmaceutical and food industries." RSC Adv. 4, no. 23 (2014): 11705–13. http://dx.doi.org/10.1039/c3ra46618c.

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26

Magana, Jose Rodrigo, Christian C. M. Sproncken, and Ilja K. Voets. "On Complex Coacervate Core Micelles: Structure-Function Perspectives." Polymers 12, no. 9 (August 28, 2020): 1953. http://dx.doi.org/10.3390/polym12091953.

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The co-assembly of ionic-neutral block copolymers with oppositely charged species produces nanometric colloidal complexes, known, among other names, as complex coacervates core micelles (C3Ms). C3Ms are of widespread interest in nanomedicine for controlled delivery and release, whilst research activity into other application areas, such as gelation, catalysis, nanoparticle synthesis, and sensing, is increasing. In this review, we discuss recent studies on the functional roles that C3Ms can fulfil in these and other fields, focusing on emerging structure–function relations and remaining knowledge gaps.

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27

Nolles, Antsje, Adrie H. Westphal, Jacob A. de Hoop, Remco G. Fokkink, J. Mieke Kleijn, Willem J. H. van Berkel, and Jan Willem Borst. "Encapsulation of GFP in Complex Coacervate Core Micelles." Biomacromolecules 16, no. 5 (April 16, 2015): 1542–49. http://dx.doi.org/10.1021/acs.biomac.5b00092.

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28

Fares, Hadi M., Yara E. Ghoussoub, Jose D. Delgado, Jingcheng Fu, Volker S. Urban, and Joseph B. Schlenoff. "Scattering Neutrons along the Polyelectrolyte Complex/Coacervate Continuum." Macromolecules 51, no. 13 (June 18, 2018): 4945–55. http://dx.doi.org/10.1021/acs.macromol.8b00699.

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29

Zhu, Yanhui, Qiaojie Luo, Hongjie Zhang, Qiuquan Cai, Xiaodong Li, Zhiquan Shen, and Weipu Zhu. "A shear-thinning electrostatic hydrogel with antibacterial activity by nanoengineering of polyelectrolytes." Biomaterials Science 8, no. 5 (2020): 1394–404. http://dx.doi.org/10.1039/c9bm01386e.

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30

Moreau, Nicolette G., Nicolas Martin, Pierangelo Gobbo, T. Y. Dora Tang, and Stephen Mann. "Spontaneous membrane-less multi-compartmentalization via aqueous two-phase separation in complex coacervate micro-droplets." Chemical Communications 56, no. 84 (2020): 12717–20. http://dx.doi.org/10.1039/d0cc05399f.

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31

Hynes, Russell K., Paulos B. Chumala, Daniel Hupka, and Gary Peng. "A Complex Coacervate Formulation for Delivery of Colletotrichum truncatum 00-003B1." Weed Technology 24, no. 2 (June 2010): 185–92. http://dx.doi.org/10.1614/wt-d-09-00008.1.

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A complex coacervate formulation was developed for Colletotrichum truncatum 00-003B1 (Ct), a bioherbicidal fungus against scentless chamomile, and tested in the greenhouse. A two-step process was developed to formulate Ct conidia: (1) invert emulsion preparation—emulsify an aqueous suspension of Ct conidia in nonrefined vegetable oil with the aid of a surfactant, and (2) encapsulate the Ct conidia invert emulsion by complex coacervation. Formulation ingredients, including nonrefined vegetable oils, surfactants, proteins, and carbohydrates, and formulation-processing parameters, including mixing speed and the amount of oil added to invert emulsions, were examined for maximum retention of Ct conidia in the formulation. Most formulation ingredients considered and tested in this study were compatible with Ct, with no significant reduction in conidial germination and mycelial growth. The surfactant soya lecithin promoted the greatest retention of Ct conidia (88%) in the invert emulsion, followed by sorbitan monooleate (82%), glycerol monooleate (70%), and sorbitan trioleate (55%). Optimal retention of Ct conidia in the invert emulsion was observed with a water : oil ratio of 1 : 1.8 to 1 : 3.7, and an overhead paddle stirring speed of 300 rpm when preparing the emulsion. Complex coacervate wall ingredients of 1% gelatin and 2% gum arabic were most effective for Ct conidia retention. In greenhouse studies, scentless chamomile disease rating, following a 24-h dew period, was higher on plants sprayed with the Ct conidia complex coacervate formulation than on plants with Ct conidia suspended in 0.1% Tween 80.

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32

Ghasemi, Mohsen, Sean Friedowitz, and Ronald G. Larson. "Overcharging of polyelectrolyte complexes: an entropic phenomenon." Soft Matter 16, no. 47 (2020): 10640–56. http://dx.doi.org/10.1039/d0sm01466d.

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33

Facciotti, Camilla, Vittorio Saggiomo, Anton Bunschoten, Remco Fokkink, Jan Bart ten Hove, Junyou Wang, and Aldrik H. Velders. "Cyclodextrin-based complex coacervate core micelles with tuneable supramolecular host–guest, metal-to-ligand and charge interactions." Soft Matter 14, no. 47 (2018): 9542–49. http://dx.doi.org/10.1039/c8sm01504j.

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34

Tsung, Mei, and Diane J. Burgess. "Preparation and Stabilization of Heparin/Gelatin Complex Coacervate Microcapsules." Journal of Pharmaceutical Sciences 86, no. 5 (May 1997): 603–7. http://dx.doi.org/10.1021/js9603257.

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35

Rumyantsev, Artem M., Ekaterina B. Zhulina, and Oleg V. Borisov. "Complex Coacervate of Weakly Charged Polyelectrolytes: Diagram of States." Macromolecules 51, no. 10 (May 9, 2018): 3788–801. http://dx.doi.org/10.1021/acs.macromol.8b00342.

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36

Facciotti, Camilla, Vittorio Saggiomo, Simon van Hurne, Anton Bunschoten, Rebecca Kaup, and Aldrik H. Velders. "Oxidant-responsive ferrocene-based cyclodextrin complex coacervate core micelles." Supramolecular Chemistry 32, no. 1 (November 5, 2019): 30–38. http://dx.doi.org/10.1080/10610278.2019.1685094.

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37

Danial, Maarten, Harm-Anton Klok, Willem Norde, and Martien A. Cohen Stuart. "Complex Coacervate Core Micelles with a Lysozyme-Modified Corona." Langmuir 23, no. 15 (July 2007): 8003–9. http://dx.doi.org/10.1021/la700573j.

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38

Wang, Junyou, Arie de Keizer, Remco Fokkink, Yun Yan, Martien A. Cohen Stuart, and Jasper van der Gucht. "Complex Coacervate Core Micelles from Iron-Based Coordination Polymers." Journal of Physical Chemistry B 114, no. 25 (July 2010): 8313–19. http://dx.doi.org/10.1021/jp1003209.

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39

Lindhoud, Saskia, and Mireille M. A. E. Claessens. "Accumulation of small protein molecules in a macroscopic complex coacervate." Soft Matter 12, no. 2 (2016): 408–13. http://dx.doi.org/10.1039/c5sm02386f.

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By mixing the aqueous solutions of poly acrylic acid, poly-(N,N dimethylaminoethyl methacrylate) and lysozyme, complex coacervates with a protein concentration as high as 200 g L⁻¹ are obtained.

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40

Zhao, Mengmeng, Xuhui Xia, Jingyi Mao, Chao Wang, Mahesh B. Dawadi, David A. Modarelli, and Nicole S. Zacharia. "Composition and property tunable ternary coacervate: branched polyethylenimine and a binary mixture of a strong and weak polyelectrolyte." Molecular Systems Design & Engineering 4, no. 1 (2019): 110–21. http://dx.doi.org/10.1039/c8me00069g.

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The formation of a composition- and property-tunable complex ternary coacervate was achieved by combining branched polyethylenimine (BPEI) and a binary mixture of polyacrylic acid (PAA) and poly(4-styrenesulfonic acid) (SPS).

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41

Lindhoud, Saskia, Renko de Vries, Willem Norde, and Martien A. Cohen Stuart. "Structure and Stability of Complex Coacervate Core Micelles with Lysozyme." Biomacromolecules 8, no. 7 (July 2007): 2219–27. http://dx.doi.org/10.1021/bm0700688.

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42

Sureka, Hursh V., Allie C. Obermeyer, Romeo J. Flores, and Bradley D. Olsen. "Catalytic Biosensors from Complex Coacervate Core Micelle (C3M) Thin Films." ACS Applied Materials & Interfaces 11, no. 35 (August 23, 2019): 32354–65. http://dx.doi.org/10.1021/acsami.9b08478.

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43

Yan, Yun, Arie de Keizer, Martien A. Cohen Stuart, Markus Drechsler, and Nicolaas A. M. Besseling. "Stability of Complex Coacervate Core Micelles Containing Metal Coordination Polymer." Journal of Physical Chemistry B 112, no. 35 (September 4, 2008): 10908–14. http://dx.doi.org/10.1021/jp8044059.

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44

Son, Chaeyeon, Sun Young Kim, So Yeong Bahn, Hyung Joon Cha, and Yoo Seong Choi. "CaCO3 thin-film formation mediated by a synthetic protein-lysozyme coacervate." RSC Advances 7, no. 25 (2017): 15302–8. http://dx.doi.org/10.1039/c6ra28808a.

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A thin film was formed through in vitro CaCO₃ crystallization in the presence of complex coacervates, which was expected to be planar and poorly crystalline CaCO₃ guided at the interface of two immiscible liquid phases upon complex coacervation.

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45

Nolles, Antsje, Adrie Westphal, J. Kleijn, Willem van Berkel, and Jan Borst. "Colorful Packages: Encapsulation of Fluorescent Proteins in Complex Coacervate Core Micelles." International Journal of Molecular Sciences 18, no. 7 (July 19, 2017): 1557. http://dx.doi.org/10.3390/ijms18071557.

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46

Matthew, Howard W., Steven O. Salley, Ward D. Peterson, and Michael D. Klein. "Complex coacervate microcapsules for mammalian cell culture and artificial organ development." Biotechnology Progress 9, no. 5 (September 1993): 510–19. http://dx.doi.org/10.1021/bp00023a010.

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47

Kembaren, Riahna, Remco Fokkink, Adrie H. Westphal, Marleen Kamperman, J. Mieke Kleijn, and Jan Willem Borst. "Balancing Enzyme Encapsulation Efficiency and Stability in Complex Coacervate Core Micelles." Langmuir 36, no. 29 (June 29, 2020): 8494–502. http://dx.doi.org/10.1021/acs.langmuir.0c01073.

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Aloi, Antonio, Clément Guibert, Luuk L. C. Olijve, and Ilja K. Voets. "Morphological evolution of complex coacervate core micelles revealed by iPAINT microscopy." Polymer 107 (December 2016): 450–55. http://dx.doi.org/10.1016/j.polymer.2016.08.002.

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Sproncken, Christian C. M., Romà Surís-Valls, Hande E. Cingil, Christophe Detrembleur, and Ilja K. Voets. "Complex Coacervate Core Micelles Containing Poly(vinyl alcohol) Inhibit Ice Recrystallization." Macromolecular Rapid Communications 39, no. 17 (April 10, 2018): 1700814. http://dx.doi.org/10.1002/marc.201700814.

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Xiao, Jun-Xia, Lu-Hui Wang, Tong-Cheng Xu, and Guo-Qing Huang. "Complex coacervation of carboxymethyl konjac glucomannan and chitosan and coacervate characterization." International Journal of Biological Macromolecules 123 (February 2019): 436–45. http://dx.doi.org/10.1016/j.ijbiomac.2018.11.086.

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