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Dow Corning polydimethylsiloxane pdms base resin
Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate <t>PDMS</t> and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.
Polydimethylsiloxane Pdms Base Resin, supplied by Dow Corning, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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polydimethylsiloxane pdms base resin - by Bioz Stars, 2026-05
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1) Product Images from "An embolism-free nonfouling hydrogel coating with high toughness and lubricity for intravascular medical devices via chain-entanglement mediated topological gelation"

Article Title: An embolism-free nonfouling hydrogel coating with high toughness and lubricity for intravascular medical devices via chain-entanglement mediated topological gelation

Journal: Bioactive Materials

doi: 10.1016/j.bioactmat.2025.11.033

Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate PDMS and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.
Figure Legend Snippet: Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate PDMS and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.

Techniques Used: Polymer, Lyophilization

Lubrication and stability of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Quantitative analysis of the friction coefficient of coatings prepared at different monomer concentrations rubbed for 900 s at a pressure of 10 kPa ( n = 3). b) The friction coefficients of the substrate PDMS, CHC, and THC under pressures of 10 kPa, 50 kPa, and 100 kPa ( n = 3). c) Friction coefficient versus time curves for PDMS, CHC, and THC under a pressure of 100 kPa. d) SEM and EDS images of PDMS, CHC, and THC after friction for 900 s under a pressure of 100 kPa. e) The thickness of the THC prepared at 30 wt% monomer concentration did not change after 12 h of ultrasonication or PBS washing for 30 days. f,g) The structural stability of two coatings (CHC and THC) under tensile tests (f) and extreme bending tests (g) . Data presented as mean ± SD and analyzed using a one-way ANOVA with Tukey's post hoc test in (b) , ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ns: no significant difference at P > 0.05.
Figure Legend Snippet: Lubrication and stability of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Quantitative analysis of the friction coefficient of coatings prepared at different monomer concentrations rubbed for 900 s at a pressure of 10 kPa ( n = 3). b) The friction coefficients of the substrate PDMS, CHC, and THC under pressures of 10 kPa, 50 kPa, and 100 kPa ( n = 3). c) Friction coefficient versus time curves for PDMS, CHC, and THC under a pressure of 100 kPa. d) SEM and EDS images of PDMS, CHC, and THC after friction for 900 s under a pressure of 100 kPa. e) The thickness of the THC prepared at 30 wt% monomer concentration did not change after 12 h of ultrasonication or PBS washing for 30 days. f,g) The structural stability of two coatings (CHC and THC) under tensile tests (f) and extreme bending tests (g) . Data presented as mean ± SD and analyzed using a one-way ANOVA with Tukey's post hoc test in (b) , ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ns: no significant difference at P > 0.05.

Techniques Used: Concentration Assay



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Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate <t>PDMS</t> and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.
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Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate <t>PDMS</t> and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.
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Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate <t>PDMS</t> and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.
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Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate <t>PDMS</t> and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.
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Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate PDMS and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.

Journal: Bioactive Materials

Article Title: An embolism-free nonfouling hydrogel coating with high toughness and lubricity for intravascular medical devices via chain-entanglement mediated topological gelation

doi: 10.1016/j.bioactmat.2025.11.033

Figure Lengend Snippet: Formation and the characterizations of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Schematic illustration of the formation of the chain-entangled hydrogel coating. b) Representative SEM images of the substrate PDMS and coatings prepared at different monomer concentrations. c) Molecular weights of the dissolved polymer coating. Coated samples undergo substrate degradation, dialysis, lyophilization, and GPC testing. d) Statistical thickness data of the coatings in dry and swollen states prepared at different monomer concentrations ( n = 3), where a polymer brush's theoretical swollen thickness limit is calculated based on the molecular weights, assuming the polymer chains are fully extended. e) Schematic illustration of the coating structure prepared at different monomer concentrations.

Article Snippet: Polydimethylsiloxane (PDMS) base resin and a curing agent Sylgard 184 kit were purchased from Dow Corning (Hangzhou, China).

Techniques: Polymer, Lyophilization

Lubrication and stability of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Quantitative analysis of the friction coefficient of coatings prepared at different monomer concentrations rubbed for 900 s at a pressure of 10 kPa ( n = 3). b) The friction coefficients of the substrate PDMS, CHC, and THC under pressures of 10 kPa, 50 kPa, and 100 kPa ( n = 3). c) Friction coefficient versus time curves for PDMS, CHC, and THC under a pressure of 100 kPa. d) SEM and EDS images of PDMS, CHC, and THC after friction for 900 s under a pressure of 100 kPa. e) The thickness of the THC prepared at 30 wt% monomer concentration did not change after 12 h of ultrasonication or PBS washing for 30 days. f,g) The structural stability of two coatings (CHC and THC) under tensile tests (f) and extreme bending tests (g) . Data presented as mean ± SD and analyzed using a one-way ANOVA with Tukey's post hoc test in (b) , ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ns: no significant difference at P > 0.05.

Journal: Bioactive Materials

Article Title: An embolism-free nonfouling hydrogel coating with high toughness and lubricity for intravascular medical devices via chain-entanglement mediated topological gelation

doi: 10.1016/j.bioactmat.2025.11.033

Figure Lengend Snippet: Lubrication and stability of the chain entanglement-mediated zwitterionic physical hydrogel coatings. a) Quantitative analysis of the friction coefficient of coatings prepared at different monomer concentrations rubbed for 900 s at a pressure of 10 kPa ( n = 3). b) The friction coefficients of the substrate PDMS, CHC, and THC under pressures of 10 kPa, 50 kPa, and 100 kPa ( n = 3). c) Friction coefficient versus time curves for PDMS, CHC, and THC under a pressure of 100 kPa. d) SEM and EDS images of PDMS, CHC, and THC after friction for 900 s under a pressure of 100 kPa. e) The thickness of the THC prepared at 30 wt% monomer concentration did not change after 12 h of ultrasonication or PBS washing for 30 days. f,g) The structural stability of two coatings (CHC and THC) under tensile tests (f) and extreme bending tests (g) . Data presented as mean ± SD and analyzed using a one-way ANOVA with Tukey's post hoc test in (b) , ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ns: no significant difference at P > 0.05.

Article Snippet: Polydimethylsiloxane (PDMS) base resin and a curing agent Sylgard 184 kit were purchased from Dow Corning (Hangzhou, China).

Techniques: Concentration Assay