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Showing 1 to 12 of 30 entries
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Materials science. Diffusion of a polymer 'pancake'.

Nature

Sukhishvili SA, Chen Y, Muller JD, Gratton E, Schweizer KS, Granick S.
PMID: 10910345
Nature. 2000 Jul 13;406(6792):146. doi: 10.1038/35018166.

No abstract available.

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Sukhishvili SA, Chen Y, Muller JD, et al. Materials science. Diffusion of a polymer 'pancake'. Nature. 2000;406(6792):146doi: 10.1038/35018166.
Sukhishvili, S. A., Chen, Y., Muller, J. D., Gratton, E., Schweizer, K. S., & Granick, S. (2000). Materials science. Diffusion of a polymer 'pancake'. Nature, 406(6792), 146. https://doi.org/10.1038/35018166
Sukhishvili, et al. "Materials science. Diffusion of a polymer 'pancake'." Nature vol. 406,6792 (2000): 146. doi: https://doi.org/10.1038/35018166
Sukhishvili SA, Chen Y, Muller JD, Gratton E, Schweizer KS, Granick S. Materials science. Diffusion of a polymer 'pancake'. Nature. 2000 Jul 13;406(6792):146. doi: 10.1038/35018166. PMID: 10910345.
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Ionically Paired Layer-by-Layer Hydrogels: Water and Polyelectrolyte Uptake Controlled by Deposition Time.

Gels (Basel, Switzerland)

Selin V, Ankner JF, Sukhishvili SA.
PMID: 30674783
Gels. 2018 Jan 11;4(1). doi: 10.3390/gels4010007.

Despite intense recent interest in weakly bound nonlinear ("exponential") multilayers, the underlying structure-property relationships of these films are still poorly understood. This study explores the effect of time used for deposition of individual layers of nonlinearly growing layer-by-layer (LbL)...

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Selin V, Ankner JF, Sukhishvili SA. Ionically Paired Layer-by-Layer Hydrogels: Water and Polyelectrolyte Uptake Controlled by Deposition Time. Gels. 2018;4(1)doi: 10.3390/gels4010007.
Selin, V., Ankner, J. F., & Sukhishvili, S. A. (2018). Ionically Paired Layer-by-Layer Hydrogels: Water and Polyelectrolyte Uptake Controlled by Deposition Time. Gels (Basel, Switzerland), 4(1), . https://doi.org/10.3390/gels4010007
Selin, Victor, et al. "Ionically Paired Layer-by-Layer Hydrogels: Water and Polyelectrolyte Uptake Controlled by Deposition Time." Gels (Basel, Switzerland) vol. 4,1 (2018). doi: https://doi.org/10.3390/gels4010007
Selin V, Ankner JF, Sukhishvili SA. Ionically Paired Layer-by-Layer Hydrogels: Water and Polyelectrolyte Uptake Controlled by Deposition Time. Gels. 2018 Jan 11;4(1). doi: 10.3390/gels4010007. PMID: 30674783; PMCID: PMC6321383.
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New Family of Water-Soluble Sulfo-Fluoro Polyphosphazenes and Their Assembly within Hemocompatible Nanocoatings.

ACS applied bio materials

Albright V, Marin A, Kaner P, Sukhishvili SA, Andrianov AK.
PMID: 35021324
ACS Appl Bio Mater. 2019 Sep 16;2(9):3897-3906. doi: 10.1021/acsabm.9b00485. Epub 2019 Aug 28.

In this work, novel sulfo-fluoro polyphosphazenes (PPzs) were synthesized via macromolecular substitution of polydichlorophosphazene utilizing "non-covalent protection" methodology by converting acid functionalities into hydrophobic alkylammonium salts. Resulting PPzs showed excellent solubility in aqueous solutions over a broad pH range...

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Albright V, Marin A, Kaner P, et al. New Family of Water-Soluble Sulfo-Fluoro Polyphosphazenes and Their Assembly within Hemocompatible Nanocoatings. ACS Appl Bio Mater. 2019;2(9):3897-3906doi: 10.1021/acsabm.9b00485.
Albright, V., Marin, A., Kaner, P., Sukhishvili, S. A., & Andrianov, A. K. (2019). New Family of Water-Soluble Sulfo-Fluoro Polyphosphazenes and Their Assembly within Hemocompatible Nanocoatings. ACS applied bio materials, 2(9), 3897-3906. https://doi.org/10.1021/acsabm.9b00485
Albright, Victoria, et al. "New Family of Water-Soluble Sulfo-Fluoro Polyphosphazenes and Their Assembly within Hemocompatible Nanocoatings." ACS applied bio materials vol. 2,9 (2019): 3897-3906. doi: https://doi.org/10.1021/acsabm.9b00485
Albright V, Marin A, Kaner P, Sukhishvili SA, Andrianov AK. New Family of Water-Soluble Sulfo-Fluoro Polyphosphazenes and Their Assembly within Hemocompatible Nanocoatings. ACS Appl Bio Mater. 2019 Sep 16;2(9):3897-3906. doi: 10.1021/acsabm.9b00485. Epub 2019 Aug 28. PMID: 35021324.
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Selective hydrogen bonding controls temperature response of layer-by-layer upper critical solution temperature micellar assemblies.

Soft matter

Aliakseyeu A, Albright V, Yarbrough D, Hernandez S, Zhou Q, Ankner JF, Sukhishvili SA.
PMID: 33458733
Soft Matter. 2021 Mar 04;17(8):2181-2190. doi: 10.1039/d0sm01997f.

This work establishes a correlation between the selectivity of hydrogen-bonding interactions and the functionality of micelle-containing layer-by-layer (LbL) assemblies. Specifically, we explore LbL films formed by assembly of poly(methacrylic acid) (PMAA) and upper critical solution temperature block copolymer micelles...

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Aliakseyeu A, Albright V, Yarbrough D, et al. Selective hydrogen bonding controls temperature response of layer-by-layer upper critical solution temperature micellar assemblies. Soft Matter. 2021;17(8):2181-2190doi: 10.1039/d0sm01997f.
Aliakseyeu, A., Albright, V., Yarbrough, D., Hernandez, S., Zhou, Q., Ankner, J. F., & Sukhishvili, S. A. (2021). Selective hydrogen bonding controls temperature response of layer-by-layer upper critical solution temperature micellar assemblies. Soft matter, 17(8), 2181-2190. https://doi.org/10.1039/d0sm01997f
Aliakseyeu, Aliaksei, et al. "Selective hydrogen bonding controls temperature response of layer-by-layer upper critical solution temperature micellar assemblies." Soft matter vol. 17,8 (2021): 2181-2190. doi: https://doi.org/10.1039/d0sm01997f
Aliakseyeu A, Albright V, Yarbrough D, Hernandez S, Zhou Q, Ankner JF, Sukhishvili SA. Selective hydrogen bonding controls temperature response of layer-by-layer upper critical solution temperature micellar assemblies. Soft Matter. 2021 Mar 04;17(8):2181-2190. doi: 10.1039/d0sm01997f. PMID: 33458733.
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Hydrogen-Bonded, Mechanically Strong Nanofibers with Tunable Antioxidant Activity.

ACS applied materials & interfaces

Gaikwad A, Hlushko H, Karimineghlani P, Selin V, Sukhishvili SA.
PMID: 32048504
ACS Appl Mater Interfaces. 2020 Mar 04;12(9):11026-11035. doi: 10.1021/acsami.9b23212. Epub 2020 Feb 24.

We report on mechanically strong, water-insoluble hydrogen-bonded nanofiber mats composed of a hydrophilic polymer and a natural polyphenol that exhibit prolonged antioxidant activity. The high performance of fibrous mats resulted from the formation of a network of hydrogen bonds...

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Gaikwad A, Hlushko H, Karimineghlani P, et al. Hydrogen-Bonded, Mechanically Strong Nanofibers with Tunable Antioxidant Activity. ACS Appl Mater Interfaces. 2020;12(9):11026-11035doi: 10.1021/acsami.9b23212.
Gaikwad, A., Hlushko, H., Karimineghlani, P., Selin, V., & Sukhishvili, S. A. (2020). Hydrogen-Bonded, Mechanically Strong Nanofibers with Tunable Antioxidant Activity. ACS applied materials & interfaces, 12(9), 11026-11035. https://doi.org/10.1021/acsami.9b23212
Gaikwad, Adwait, et al. "Hydrogen-Bonded, Mechanically Strong Nanofibers with Tunable Antioxidant Activity." ACS applied materials & interfaces vol. 12,9 (2020): 11026-11035. doi: https://doi.org/10.1021/acsami.9b23212
Gaikwad A, Hlushko H, Karimineghlani P, Selin V, Sukhishvili SA. Hydrogen-Bonded, Mechanically Strong Nanofibers with Tunable Antioxidant Activity. ACS Appl Mater Interfaces. 2020 Mar 04;12(9):11026-11035. doi: 10.1021/acsami.9b23212. Epub 2020 Feb 24. PMID: 32048504.
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Cationic Fluoropolyphosphazenes: Synthesis and Assembly with Heparin as a Pathway to Hemocompatible Nanocoatings.

ACS applied bio materials

Marin A, Brito J, Sukhishvili SA, Andrianov AK.
PMID: 35014813
ACS Appl Bio Mater. 2021 Dec 27; doi: 10.1021/acsabm.1c01099. Epub 2021 Dec 27.

The development of state-of-the-art blood-contacting devices can be advanced through integrating hemocompatibility, durability, and anticoagulant functionalities within engineered nanoscale coatings. To enable all-aqueous assembly of nanocoatings combining omniphobic fluorinated features with the potent anticoagulant activity of hydrophilic heparin, two...

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Marin A, Brito J, Sukhishvili SA, et al. Cationic Fluoropolyphosphazenes: Synthesis and Assembly with Heparin as a Pathway to Hemocompatible Nanocoatings. ACS Appl Bio Mater. 2021;doi: 10.1021/acsabm.1c01099.
Marin, A., Brito, J., Sukhishvili, S. A., & Andrianov, A. K. (2021). Cationic Fluoropolyphosphazenes: Synthesis and Assembly with Heparin as a Pathway to Hemocompatible Nanocoatings. ACS applied bio materials, . https://doi.org/10.1021/acsabm.1c01099
Marin, Alexander, et al. "Cationic Fluoropolyphosphazenes: Synthesis and Assembly with Heparin as a Pathway to Hemocompatible Nanocoatings." ACS applied bio materials vol. (2021). doi: https://doi.org/10.1021/acsabm.1c01099
Marin A, Brito J, Sukhishvili SA, Andrianov AK. Cationic Fluoropolyphosphazenes: Synthesis and Assembly with Heparin as a Pathway to Hemocompatible Nanocoatings. ACS Appl Bio Mater. 2021 Dec 27; doi: 10.1021/acsabm.1c01099. Epub 2021 Dec 27. PMID: 35014813.
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Biocompatible Nanocoatings of Fluorinated Polyphosphazenes through Aqueous Assembly.

ACS applied materials & interfaces

Selin V, Albright V, Ankner JF, Marin A, Andrianov AK, Sukhishvili SA.
PMID: 29505245
ACS Appl Mater Interfaces. 2018 Mar 21;10(11):9756-9764. doi: 10.1021/acsami.8b02072. Epub 2018 Mar 12.

Nonionic fluorinated polyphosphazenes, such as poly[bis(trifluoroethoxy)phosphazene] (PTFEP), display superb biocompatibility, yet their deposition to surfaces has been limited to solution casting from organic solvents or thermal molding. Herein, hydrophobic coatings of fluorinated polyphosphazenes are demonstrated through controlled deposition of...

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Selin V, Albright V, Ankner JF, et al. Biocompatible Nanocoatings of Fluorinated Polyphosphazenes through Aqueous Assembly. ACS Appl Mater Interfaces. 2018;10(11):9756-9764doi: 10.1021/acsami.8b02072.
Selin, V., Albright, V., Ankner, J. F., Marin, A., Andrianov, A. K., & Sukhishvili, S. A. (2018). Biocompatible Nanocoatings of Fluorinated Polyphosphazenes through Aqueous Assembly. ACS applied materials & interfaces, 10(11), 9756-9764. https://doi.org/10.1021/acsami.8b02072
Selin, Victor, et al. "Biocompatible Nanocoatings of Fluorinated Polyphosphazenes through Aqueous Assembly." ACS applied materials & interfaces vol. 10,11 (2018): 9756-9764. doi: https://doi.org/10.1021/acsami.8b02072
Selin V, Albright V, Ankner JF, Marin A, Andrianov AK, Sukhishvili SA. Biocompatible Nanocoatings of Fluorinated Polyphosphazenes through Aqueous Assembly. ACS Appl Mater Interfaces. 2018 Mar 21;10(11):9756-9764. doi: 10.1021/acsami.8b02072. Epub 2018 Mar 12. PMID: 29505245.
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Functional Surfaces through Controlled Assemblies of Upper Critical Solution Temperature Block and Star Copolymers.

Langmuir : the ACS journal of surfaces and colloids

Albright V, Palanisamy A, Zhou Q, Selin V, Sukhishvili SA.
PMID: 30346775
Langmuir. 2019 Aug 20;35(33):10677-10688. doi: 10.1021/acs.langmuir.8b02535. Epub 2018 Oct 31.

Endowing surfaces with multiple advanced functionalities, such as temperature-controlled swelling or the triggered release of functional small molecules, is attractive for a large variety of applications ranging from smart textiles to advanced biomedical applications. This Invited Feature Article summarizes...

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Albright V, Palanisamy A, Zhou Q, et al. Functional Surfaces through Controlled Assemblies of Upper Critical Solution Temperature Block and Star Copolymers. Langmuir. 2018;35(33):10677-10688doi: 10.1021/acs.langmuir.8b02535.
Albright, V., Palanisamy, A., Zhou, Q., Selin, V., & Sukhishvili, S. A. (2019). Functional Surfaces through Controlled Assemblies of Upper Critical Solution Temperature Block and Star Copolymers. Langmuir : the ACS journal of surfaces and colloids, 35(33), 10677-10688. https://doi.org/10.1021/acs.langmuir.8b02535
Albright, Victoria, et al. "Functional Surfaces through Controlled Assemblies of Upper Critical Solution Temperature Block and Star Copolymers." Langmuir : the ACS journal of surfaces and colloids vol. 35,33 (2019): 10677-10688. doi: https://doi.org/10.1021/acs.langmuir.8b02535
Albright V, Palanisamy A, Zhou Q, Selin V, Sukhishvili SA. Functional Surfaces through Controlled Assemblies of Upper Critical Solution Temperature Block and Star Copolymers. Langmuir. 2019 Aug 20;35(33):10677-10688. doi: 10.1021/acs.langmuir.8b02535. Epub 2018 Oct 31. PMID: 30346775.
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Hydrogen-bonded polymer complexes and nanocages of weak polyacids templated by a Pluronic® block copolymer.

Soft matter

Wang Y, Sukhishvili SA.
PMID: 27722711
Soft Matter. 2016 Oct 26;12(42):8744-8754. doi: 10.1039/c6sm01869f.

We investigate the phase behavior, morphology, and temperature response of hydrogen-bonded assemblies formed by a triblock copolymer Pluronic® F127 (F127) and polycarboxylic acids of varied hydrophobicity and chain lengths. As confirmed by FTIR, the complexes of poly(acrylic acid) (PAA)...

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Wang Y, Sukhishvili SA. Hydrogen-bonded polymer complexes and nanocages of weak polyacids templated by a Pluronic® block copolymer. Soft Matter. 2016;12(42):8744-8754doi: 10.1039/c6sm01869f.
Wang, Y., & Sukhishvili, S. A. (2016). Hydrogen-bonded polymer complexes and nanocages of weak polyacids templated by a Pluronic® block copolymer. Soft matter, 12(42), 8744-8754. https://doi.org/10.1039/c6sm01869f
Wang, Yuhao, and Sukhishvili, Svetlana A. "Hydrogen-bonded polymer complexes and nanocages of weak polyacids templated by a Pluronic® block copolymer." Soft matter vol. 12,42 (2016): 8744-8754. doi: https://doi.org/10.1039/c6sm01869f
Wang Y, Sukhishvili SA. Hydrogen-bonded polymer complexes and nanocages of weak polyacids templated by a Pluronic® block copolymer. Soft Matter. 2016 Oct 26;12(42):8744-8754. doi: 10.1039/c6sm01869f. PMID: 27722711.
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Determination of film thickness and refractive index in one measurement of phase-modulated ellipsometry.

Journal of the Optical Society of America. A, Optics, image science, and vision

Pristinski D, Kozlovskaya V, Sukhishvili SA.
PMID: 16985548
J Opt Soc Am A Opt Image Sci Vis. 2006 Oct;23(10):2639-44. doi: 10.1364/josaa.23.002639.

Ellipsometry is often used to determine the refractive index and/or the thickness of a polymer layer on a substrate. However, simultaneous determination of these parameters from a single-wavelength single-angle measurement is not always possible. The present study determines the...

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Pristinski D, Kozlovskaya V, Sukhishvili SA. Determination of film thickness and refractive index in one measurement of phase-modulated ellipsometry. J Opt Soc Am A Opt Image Sci Vis. 2006;23(10):2639-44doi: 10.1364/josaa.23.002639.
Pristinski, D., Kozlovskaya, V., & Sukhishvili, S. A. (2006). Determination of film thickness and refractive index in one measurement of phase-modulated ellipsometry. Journal of the Optical Society of America. A, Optics, image science, and vision, 23(10), 2639-44. https://doi.org/10.1364/josaa.23.002639
Pristinski, Denis, et al. "Determination of film thickness and refractive index in one measurement of phase-modulated ellipsometry." Journal of the Optical Society of America. A, Optics, image science, and vision vol. 23,10 (2006): 2639-44. doi: https://doi.org/10.1364/josaa.23.002639
Pristinski D, Kozlovskaya V, Sukhishvili SA. Determination of film thickness and refractive index in one measurement of phase-modulated ellipsometry. J Opt Soc Am A Opt Image Sci Vis. 2006 Oct;23(10):2639-44. doi: 10.1364/josaa.23.002639. PMID: 16985548.
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Large-amplitude, reversible, pH-triggered wetting transitions enabled by layer-by-layer films.

ACS applied materials & interfaces

Lu Y, Sarshar MA, Du K, Chou T, Choi CH, Sukhishvili SA.
PMID: 24191775
ACS Appl Mater Interfaces. 2013 Dec 11;5(23):12617-23. doi: 10.1021/am403944m. Epub 2013 Nov 19.

We report on the use of layer-by-layer (LbL) hydrogels, composed of amphiphilic polymers that undergo reversible collapse-dissolution transition in solutions as a function of pH, to induce sharp, large-amplitude wetting transition at microstructured surfaces. Surface hydrogels were composed of...

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Lu Y, Sarshar MA, Du K, et al. Large-amplitude, reversible, pH-triggered wetting transitions enabled by layer-by-layer films. ACS Appl Mater Interfaces. 2013;5(23):12617-23doi: 10.1021/am403944m.
Lu, Y., Sarshar, M. A., Du, K., Chou, T., Choi, C. H., & Sukhishvili, S. A. (2013). Large-amplitude, reversible, pH-triggered wetting transitions enabled by layer-by-layer films. ACS applied materials & interfaces, 5(23), 12617-23. https://doi.org/10.1021/am403944m
Lu, Yiming, et al. "Large-amplitude, reversible, pH-triggered wetting transitions enabled by layer-by-layer films." ACS applied materials & interfaces vol. 5,23 (2013): 12617-23. doi: https://doi.org/10.1021/am403944m
Lu Y, Sarshar MA, Du K, Chou T, Choi CH, Sukhishvili SA. Large-amplitude, reversible, pH-triggered wetting transitions enabled by layer-by-layer films. ACS Appl Mater Interfaces. 2013 Dec 11;5(23):12617-23. doi: 10.1021/am403944m. Epub 2013 Nov 19. PMID: 24191775.
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Hydrogen-bonded layer-by-layer temperature-triggered release films.

Langmuir : the ACS journal of surfaces and colloids

Zhuk A, Pavlukhina S, Sukhishvili SA.
PMID: 19572503
Langmuir. 2009 Dec 15;25(24):14025-9. doi: 10.1021/la901478v.

A hydrogen-bonded layer-by-layer (LbL) technique was used to build multilayers of neutral, temperature-responsive polymers such as poly(N-isopropylacrylamide) (PNIPAM), poly(N-vinylcaprolactam) (PVCL), poly(vinyl methyl ether) (PVME), or poly(acrylamide) (PAAm) with a polycarboxylic acid such as poly(acrylic acid) (PAA), poly(methacrylic acid) (PMAA),...

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Zhuk A, Pavlukhina S, Sukhishvili SA. Hydrogen-bonded layer-by-layer temperature-triggered release films. Langmuir. 2009;25(24):14025-9doi: 10.1021/la901478v.
Zhuk, A., Pavlukhina, S., & Sukhishvili, S. A. (2009). Hydrogen-bonded layer-by-layer temperature-triggered release films. Langmuir : the ACS journal of surfaces and colloids, 25(24), 14025-9. https://doi.org/10.1021/la901478v
Zhuk, Aliaksandr, et al. "Hydrogen-bonded layer-by-layer temperature-triggered release films." Langmuir : the ACS journal of surfaces and colloids vol. 25,24 (2009): 14025-9. doi: https://doi.org/10.1021/la901478v
Zhuk A, Pavlukhina S, Sukhishvili SA. Hydrogen-bonded layer-by-layer temperature-triggered release films. Langmuir. 2009 Dec 15;25(24):14025-9. doi: 10.1021/la901478v. PMID: 19572503.
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Showing 1 to 12 of 30 entries