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The formation of host-guest complexes between surfactants and cyclodextrins.

Advances in colloid and interface science

Valente AJ, Söderman O.
PMID: 24011696
Adv Colloid Interface Sci. 2014 Mar;205:156-76. doi: 10.1016/j.cis.2013.08.001. Epub 2013 Aug 12.

Cyclodextrins are able to act as host molecules in supramolecular chemistry with applications ranging from pharmaceutics to detergency. Among guest molecules surfactants play an important role with both fundamental and practical applications. The formation of cyclodextrin/surfactant host-guest compounds leads...

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Valente AJ, Söderman O. The formation of host-guest complexes between surfactants and cyclodextrins. Adv Colloid Interface Sci. 2013;205:156-76doi: 10.1016/j.cis.2013.08.001.
Valente, A. J., & Söderman, O. (2014). The formation of host-guest complexes between surfactants and cyclodextrins. Advances in colloid and interface science, 205156-76. https://doi.org/10.1016/j.cis.2013.08.001
Valente, Artur J M, and Söderman, Olle. "The formation of host-guest complexes between surfactants and cyclodextrins." Advances in colloid and interface science vol. 205 (2014): 156-76. doi: https://doi.org/10.1016/j.cis.2013.08.001
Valente AJ, Söderman O. The formation of host-guest complexes between surfactants and cyclodextrins. Adv Colloid Interface Sci. 2014 Mar;205:156-76. doi: 10.1016/j.cis.2013.08.001. Epub 2013 Aug 12. PMID: 24011696.
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Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins.

The journal of physical chemistry. B

Favrelle A, Gouhier G, Guillen F, Martin C, Mofaddel N, Petit S, Mundy KM, Pitre SP, Wagner BD.
PMID: 26362021
J Phys Chem B. 2015 Oct 08;119(40):12921-30. doi: 10.1021/acs.jpcb.5b07157. Epub 2015 Sep 24.

Cyclodextrins (CDs) are the most widely used organic hosts for the inclusion of guest molecules. CDs can be readily modified through substitutions of the hydroxyl groups, and these modified CDs can have different host binding properties compared to those...

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Favrelle A, Gouhier G, Guillen F, et al. Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins. J Phys Chem B. 2015;119(40):12921-30doi: 10.1021/acs.jpcb.5b07157.
Favrelle, A., Gouhier, G., Guillen, F., Martin, C., Mofaddel, N., Petit, S., Mundy, K. M., Pitre, S. P., & Wagner, B. D. (2015). Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins. The journal of physical chemistry. B, 119(40), 12921-30. https://doi.org/10.1021/acs.jpcb.5b07157
Favrelle, Audrey, et al. "Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins." The journal of physical chemistry. B vol. 119,40 (2015): 12921-30. doi: https://doi.org/10.1021/acs.jpcb.5b07157
Favrelle A, Gouhier G, Guillen F, Martin C, Mofaddel N, Petit S, Mundy KM, Pitre SP, Wagner BD. Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins. J Phys Chem B. 2015 Oct 08;119(40):12921-30. doi: 10.1021/acs.jpcb.5b07157. Epub 2015 Sep 24. PMID: 26362021.
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Inclusion of fluorophores in cyclodextrins: a closer look at the fluorometric determination of association constants by linear and nonlinear fitting procedures.

Methods and applications in fluorescence

Hutterer R.
PMID: 28925371
Methods Appl Fluoresc. 2017 Dec 13;6(1):013001. doi: 10.1088/2050-6120/aa8d96.

The author discusses methods for the fluorometric determination of affinity constants by linear and nonlinear fitting methods. This is outlined in particular for the interaction between cyclodextrins and several anesthetic drugs including benzocaine. Special emphasis is given to the...

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Hutterer R. Inclusion of fluorophores in cyclodextrins: a closer look at the fluorometric determination of association constants by linear and nonlinear fitting procedures. Methods Appl Fluoresc. 2017;6(1):013001doi: 10.1088/2050-6120/aa8d96.
Hutterer, R. (2017). Inclusion of fluorophores in cyclodextrins: a closer look at the fluorometric determination of association constants by linear and nonlinear fitting procedures. Methods and applications in fluorescence, 6(1), 013001. https://doi.org/10.1088/2050-6120/aa8d96
Hutterer, Rudi. "Inclusion of fluorophores in cyclodextrins: a closer look at the fluorometric determination of association constants by linear and nonlinear fitting procedures." Methods and applications in fluorescence vol. 6,1 (2017): 013001. doi: https://doi.org/10.1088/2050-6120/aa8d96
Hutterer R. Inclusion of fluorophores in cyclodextrins: a closer look at the fluorometric determination of association constants by linear and nonlinear fitting procedures. Methods Appl Fluoresc. 2017 Dec 13;6(1):013001. doi: 10.1088/2050-6120/aa8d96. PMID: 28925371.
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Environmental Gas Sensing with Cavitands.

Chemistry (Weinheim an der Bergstrasse, Germany)

Pinalli R, Pedrini A, Dalcanale E.
PMID: 28949043
Chemistry. 2018 Jan 24;24(5):1010-1019. doi: 10.1002/chem.201703630. Epub 2017 Oct 26.

Environmental gas sensing needs stringent sensor requirements in terms of sensitivity, selectivity and ruggedness. One of the major issues to be addressed is combining in a single device the conflicting requirements of molecular-level selectivity and low-ppb sensitivity. The exploitation...

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Pinalli R, Pedrini A, Dalcanale E. Environmental Gas Sensing with Cavitands. Chemistry. 2017;24(5):1010-1019doi: 10.1002/chem.201703630.
Pinalli, R., Pedrini, A., & Dalcanale, E. (2018). Environmental Gas Sensing with Cavitands. Chemistry (Weinheim an der Bergstrasse, Germany), 24(5), 1010-1019. https://doi.org/10.1002/chem.201703630
Pinalli, Roberta, et al. "Environmental Gas Sensing with Cavitands." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 24,5 (2018): 1010-1019. doi: https://doi.org/10.1002/chem.201703630
Pinalli R, Pedrini A, Dalcanale E. Environmental Gas Sensing with Cavitands. Chemistry. 2018 Jan 24;24(5):1010-1019. doi: 10.1002/chem.201703630. Epub 2017 Oct 26. PMID: 28949043.
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Optimized methods for preparation of 6(I)-(ω-sulfanyl-alkylene-sulfanyl)-β-cyclodextrin derivatives.

Beilstein journal of organic chemistry

Bednářová E, Hybelbauerová S, Jindřich J.
PMID: 26977195
Beilstein J Org Chem. 2016 Feb 24;12:349-52. doi: 10.3762/bjoc.12.38. eCollection 2016.

A general high-yielding method for the preparation of monosubstituted β-cyclodextrin derivatives which have attached a thiol group in position 6 is described. The thiol group is attached through linkers of different lengths and repeating units (ethylene glycol or methylene)....

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Bednářová E, Hybelbauerová S, Jindřich J. Optimized methods for preparation of 6(I)-(ω-sulfanyl-alkylene-sulfanyl)-β-cyclodextrin derivatives. Beilstein J Org Chem. 2016;12:349-52doi: 10.3762/bjoc.12.38.
Bednářová, E., Hybelbauerová, S., & Jindřich, J. (2016). Optimized methods for preparation of 6(I)-(ω-sulfanyl-alkylene-sulfanyl)-β-cyclodextrin derivatives. Beilstein journal of organic chemistry, 12349-52. https://doi.org/10.3762/bjoc.12.38
Bednářová, Eva, et al. "Optimized methods for preparation of 6(I)-(ω-sulfanyl-alkylene-sulfanyl)-β-cyclodextrin derivatives." Beilstein journal of organic chemistry vol. 12 (2016): 349-52. doi: https://doi.org/10.3762/bjoc.12.38
Bednářová E, Hybelbauerová S, Jindřich J. Optimized methods for preparation of 6(I)-(ω-sulfanyl-alkylene-sulfanyl)-β-cyclodextrin derivatives. Beilstein J Org Chem. 2016 Feb 24;12:349-52. doi: 10.3762/bjoc.12.38. eCollection 2016. PMID: 26977195; PMCID: PMC4778511.
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Binding Selectivity of Macrocycle Ionophores in Ionic Liquids versus Aqueous Solution and Solvent-free Conditions.

Chemphyschem : a European journal of chemical physics and physical chemistry

Gámez F, Hortal AR, Hurtado P, Avilés-Moreno JR, Hamad S, Martínez-Haya B.
PMID: 26346407
Chemphyschem. 2015 Dec 01;16(17):3672-80. doi: 10.1002/cphc.201500477. Epub 2015 Sep 30.

The understanding of supramolecular recognition in room-temperature ionic liquids (RTILs) is key to develop the full potential of these materials. In this work, we provide insights into the selectivity of the binding of alkali metal cations by standard cyclodextrin...

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Gámez F, Hortal AR, Hurtado P, et al. Binding Selectivity of Macrocycle Ionophores in Ionic Liquids versus Aqueous Solution and Solvent-free Conditions. Chemphyschem. 2015;16(17):3672-80doi: 10.1002/cphc.201500477.
Gámez, F., Hortal, A. R., Hurtado, P., Avilés-Moreno, J. R., Hamad, S., & Martínez-Haya, B. (2015). Binding Selectivity of Macrocycle Ionophores in Ionic Liquids versus Aqueous Solution and Solvent-free Conditions. Chemphyschem : a European journal of chemical physics and physical chemistry, 16(17), 3672-80. https://doi.org/10.1002/cphc.201500477
Gámez, Francisco, et al. "Binding Selectivity of Macrocycle Ionophores in Ionic Liquids versus Aqueous Solution and Solvent-free Conditions." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 16,17 (2015): 3672-80. doi: https://doi.org/10.1002/cphc.201500477
Gámez F, Hortal AR, Hurtado P, Avilés-Moreno JR, Hamad S, Martínez-Haya B. Binding Selectivity of Macrocycle Ionophores in Ionic Liquids versus Aqueous Solution and Solvent-free Conditions. Chemphyschem. 2015 Dec 01;16(17):3672-80. doi: 10.1002/cphc.201500477. Epub 2015 Sep 30. PMID: 26346407.
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Inclusion of trans-resveratrol in methylated cyclodextrins: synthesis and solid-state structures.

Beilstein journal of organic chemistry

Trollope L, Cruickshank DL, Noonan T, Bourne SA, Sorrenti M, Catenacci L, Caira MR.
PMID: 25670983
Beilstein J Org Chem. 2014 Dec 29;10:3136-51. doi: 10.3762/bjoc.10.331. eCollection 2014.

The phytoalexin trans-resveratrol, 5-[(1E)-2-(4-hydroxyphenyl)ethenyl]-1,3-benzenediol, is a well-known, potent antioxidant having a variety of possible biomedical applications. However, its adverse physicochemical properties (low stability, poor aqueous solubility) limit such applications and its inclusion in cyclodextrins (CDs) has potential for addressing...

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Trollope L, Cruickshank DL, Noonan T, et al. Inclusion of trans-resveratrol in methylated cyclodextrins: synthesis and solid-state structures. Beilstein J Org Chem. 2014;10:3136-51doi: 10.3762/bjoc.10.331.
Trollope, L., Cruickshank, D. L., Noonan, T., Bourne, S. A., Sorrenti, M., Catenacci, L., & Caira, M. R. (2014). Inclusion of trans-resveratrol in methylated cyclodextrins: synthesis and solid-state structures. Beilstein journal of organic chemistry, 103136-51. https://doi.org/10.3762/bjoc.10.331
Trollope, Lee, et al. "Inclusion of trans-resveratrol in methylated cyclodextrins: synthesis and solid-state structures." Beilstein journal of organic chemistry vol. 10 (2014): 3136-51. doi: https://doi.org/10.3762/bjoc.10.331
Trollope L, Cruickshank DL, Noonan T, Bourne SA, Sorrenti M, Catenacci L, Caira MR. Inclusion of trans-resveratrol in methylated cyclodextrins: synthesis and solid-state structures. Beilstein J Org Chem. 2014 Dec 29;10:3136-51. doi: 10.3762/bjoc.10.331. eCollection 2014. PMID: 25670983; PMCID: PMC4311586.
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Probing the common alkali metal affinity of native and variously methylated β-cyclodextrins by combining electrospray-tandem mass spectrometry and molecular modeling.

Physical chemistry chemical physics : PCCP

Przybylski C, Bonnet V, Cézard C.
PMID: 26138713
Phys Chem Chem Phys. 2015 Jul 15;17(29):19288-305. doi: 10.1039/c5cp02895g.

In the study herein, we investigated the solution and gas phase affinity of native and variously methylated β-cyclodextrins (CDs) as hosts towards three common alkali metals as guests namely lithium, sodium and potassium. For this purpose, two complementary approaches...

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Przybylski C, Bonnet V, Cézard C. Probing the common alkali metal affinity of native and variously methylated β-cyclodextrins by combining electrospray-tandem mass spectrometry and molecular modeling. Phys Chem Chem Phys. 2015;17(29):19288-305doi: 10.1039/c5cp02895g.
Przybylski, C., Bonnet, V., & Cézard, C. (2015). Probing the common alkali metal affinity of native and variously methylated β-cyclodextrins by combining electrospray-tandem mass spectrometry and molecular modeling. Physical chemistry chemical physics : PCCP, 17(29), 19288-305. https://doi.org/10.1039/c5cp02895g
Przybylski, Cédric, et al. "Probing the common alkali metal affinity of native and variously methylated β-cyclodextrins by combining electrospray-tandem mass spectrometry and molecular modeling." Physical chemistry chemical physics : PCCP vol. 17,29 (2015): 19288-305. doi: https://doi.org/10.1039/c5cp02895g
Przybylski C, Bonnet V, Cézard C. Probing the common alkali metal affinity of native and variously methylated β-cyclodextrins by combining electrospray-tandem mass spectrometry and molecular modeling. Phys Chem Chem Phys. 2015 Jul 15;17(29):19288-305. doi: 10.1039/c5cp02895g. PMID: 26138713.
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Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives - their stability, complexation ability in solution or when deposited on solid anionic surface.

Beilstein journal of organic chemistry

Popr M, Filippov SK, Matushkin N, Dian J, Jindřich J.
PMID: 25815069
Beilstein J Org Chem. 2015 Feb 02;11:192-9. doi: 10.3762/bjoc.11.20. eCollection 2015.

The thermal stability of the monosubstituted cationic cyclodextrin (CD) derivatives PEMEDA-β-CD and PEMPDA-β-CD, which differ in their substituent linker length (ethylene and propylene, respectively), was studied via (1)H NMR experiments. PEMPDA-β-CD exhibited higher resistance towards the Hofmann degradation and...

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Popr M, Filippov SK, Matushkin N, et al. Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives - their stability, complexation ability in solution or when deposited on solid anionic surface. Beilstein J Org Chem. 2015;11:192-9doi: 10.3762/bjoc.11.20.
Popr, M., Filippov, S. K., Matushkin, N., Dian, J., & Jindřich, J. (2015). Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives - their stability, complexation ability in solution or when deposited on solid anionic surface. Beilstein journal of organic chemistry, 11192-9. https://doi.org/10.3762/bjoc.11.20
Popr, Martin, et al. "Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives - their stability, complexation ability in solution or when deposited on solid anionic surface." Beilstein journal of organic chemistry vol. 11 (2015): 192-9. doi: https://doi.org/10.3762/bjoc.11.20
Popr M, Filippov SK, Matushkin N, Dian J, Jindřich J. Properties of cationic monosubstituted tetraalkylammonium cyclodextrin derivatives - their stability, complexation ability in solution or when deposited on solid anionic surface. Beilstein J Org Chem. 2015 Feb 02;11:192-9. doi: 10.3762/bjoc.11.20. eCollection 2015. PMID: 25815069; PMCID: PMC4362307.
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Self-healing polymer materials constructed by macrocycle-based host-guest interactions.

Soft matter

Yang X, Yu H, Wang L, Tong R, Akram M, Chen Y, Zhai X.
PMID: 25614350
Soft Matter. 2015 Feb 04;11(7):1242-52. doi: 10.1039/c4sm02372b.

Self-healing polymers, which can spontaneously recover themselves after being ruptured, result in enhanced lifetimes for materials and open up a fascinating direction in material science. Macrocycle-based host-guest interactions, one of the most crucial non-covalent interactions, play a key role...

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Yang X, Yu H, Wang L, et al. Self-healing polymer materials constructed by macrocycle-based host-guest interactions. Soft Matter. 2015;11(7):1242-52doi: 10.1039/c4sm02372b.
Yang, X., Yu, H., Wang, L., Tong, R., Akram, M., Chen, Y., & Zhai, X. (2015). Self-healing polymer materials constructed by macrocycle-based host-guest interactions. Soft matter, 11(7), 1242-52. https://doi.org/10.1039/c4sm02372b
Yang, Xianpeng, et al. "Self-healing polymer materials constructed by macrocycle-based host-guest interactions." Soft matter vol. 11,7 (2015): 1242-52. doi: https://doi.org/10.1039/c4sm02372b
Yang X, Yu H, Wang L, Tong R, Akram M, Chen Y, Zhai X. Self-healing polymer materials constructed by macrocycle-based host-guest interactions. Soft Matter. 2015 Feb 04;11(7):1242-52. doi: 10.1039/c4sm02372b. PMID: 25614350.
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Ring Shuttling Controls Macroscopic Motion in a Three-Dimensional Printed Polyrotaxane Monolith.

Angewandte Chemie (International ed. in English)

Lin Q, Hou X, Ke C.
PMID: 28326657
Angew Chem Int Ed Engl. 2017 Apr 10;56(16):4452-4457. doi: 10.1002/anie.201612440. Epub 2017 Mar 22.

Amplification of molecular motions into the macroscopic world has great potential in the development of smart materials. Demonstrated here is an approach that integrates mechanically interlocked molecules into complex three-dimensional (3D) architectures by direct-write 3D printing. The design and...

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Lin Q, Hou X, Ke C. Ring Shuttling Controls Macroscopic Motion in a Three-Dimensional Printed Polyrotaxane Monolith. Angew Chem Int Ed Engl. 2017;56(16):4452-4457doi: 10.1002/anie.201612440.
Lin, Q., Hou, X., & Ke, C. (2017). Ring Shuttling Controls Macroscopic Motion in a Three-Dimensional Printed Polyrotaxane Monolith. Angewandte Chemie (International ed. in English), 56(16), 4452-4457. https://doi.org/10.1002/anie.201612440
Lin, Qianming, et al. "Ring Shuttling Controls Macroscopic Motion in a Three-Dimensional Printed Polyrotaxane Monolith." Angewandte Chemie (International ed. in English) vol. 56,16 (2017): 4452-4457. doi: https://doi.org/10.1002/anie.201612440
Lin Q, Hou X, Ke C. Ring Shuttling Controls Macroscopic Motion in a Three-Dimensional Printed Polyrotaxane Monolith. Angew Chem Int Ed Engl. 2017 Apr 10;56(16):4452-4457. doi: 10.1002/anie.201612440. Epub 2017 Mar 22. PMID: 28326657.
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Chitosan-myristate nanogel as an artificial chaperone protects neuroserpin from misfolding.

Advanced biomedical research

Nazem H, Mohsenifar A, Majdi S.
PMID: 27995109
Adv Biomed Res. 2016 Oct 26;5:170. doi: 10.4103/2277-9175.190942. eCollection 2016.

BACKGROUND: Molecular chaperon-like activity for protein refolding was studied using nanogel chitosan-myristic acid (CMA) and the protein neuroserpin (NS), a member of the serine proteinase inhibitor superfamily (serpin).MATERIALS AND METHODS: Recombinant his-tag fusion NS was expressed in RESULTS: Heating...

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Nazem H, Mohsenifar A, Majdi S. Chitosan-myristate nanogel as an artificial chaperone protects neuroserpin from misfolding. Adv Biomed Res. 2016;5:170doi: 10.4103/2277-9175.190942.
Nazem, H., Mohsenifar, A., & Majdi, S. (2016). Chitosan-myristate nanogel as an artificial chaperone protects neuroserpin from misfolding. Advanced biomedical research, 5170. https://doi.org/10.4103/2277-9175.190942
Nazem, Habib, et al. "Chitosan-myristate nanogel as an artificial chaperone protects neuroserpin from misfolding." Advanced biomedical research vol. 5 (2016): 170. doi: https://doi.org/10.4103/2277-9175.190942
Nazem H, Mohsenifar A, Majdi S. Chitosan-myristate nanogel as an artificial chaperone protects neuroserpin from misfolding. Adv Biomed Res. 2016 Oct 26;5:170. doi: 10.4103/2277-9175.190942. eCollection 2016. PMID: 27995109; PMCID: PMC5137230.
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Showing 1 to 12 of 1193 entries