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Evonik titanium dioxide tio2 nanoparticles
The compartmentalized enzyme‐photocatalyst system for sustainable coenzyme regeneration. (a) The glucose dehydrogenase‐loaded silica nanoparticles (GDH@SiNPs) and <t>TiO</t> <t>2</t> nanoparticle system complete the NAD + /NADH cycle, enabling continuous coenzyme regeneration while preventing enzyme inactivation by reactive oxygen species generated during photocatalysis. (b) Bare GDH is easily deactivated by the reaction of TiO 2 nanoparticles. (c) The silica matrix quenched ROS before reaching the enzyme core due to their short half‐life in an aqueous environment, effectively shielding GDH from oxidative inactivation.
Titanium Dioxide Tio2 Nanoparticles, supplied by Evonik, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/titanium+dioxide+tio2+nanoparticles/pmc13206201-136-0-7?v=Evonik
Average 86 stars, based on 1 article reviews
titanium dioxide tio2 nanoparticles - by Bioz Stars, 2026-08
86/100 stars

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1) Product Images from "Biomimetic Compartmentalization of Enzymes for Sustainable Coenzyme Recycling in Oxidative Photocatalysis"

Article Title: Biomimetic Compartmentalization of Enzymes for Sustainable Coenzyme Recycling in Oxidative Photocatalysis

Journal: Chembiochem

doi: 10.1002/cbic.70381

The compartmentalized enzyme‐photocatalyst system for sustainable coenzyme regeneration. (a) The glucose dehydrogenase‐loaded silica nanoparticles (GDH@SiNPs) and TiO 2 nanoparticle system complete the NAD + /NADH cycle, enabling continuous coenzyme regeneration while preventing enzyme inactivation by reactive oxygen species generated during photocatalysis. (b) Bare GDH is easily deactivated by the reaction of TiO 2 nanoparticles. (c) The silica matrix quenched ROS before reaching the enzyme core due to their short half‐life in an aqueous environment, effectively shielding GDH from oxidative inactivation.
Figure Legend Snippet: The compartmentalized enzyme‐photocatalyst system for sustainable coenzyme regeneration. (a) The glucose dehydrogenase‐loaded silica nanoparticles (GDH@SiNPs) and TiO 2 nanoparticle system complete the NAD + /NADH cycle, enabling continuous coenzyme regeneration while preventing enzyme inactivation by reactive oxygen species generated during photocatalysis. (b) Bare GDH is easily deactivated by the reaction of TiO 2 nanoparticles. (c) The silica matrix quenched ROS before reaching the enzyme core due to their short half‐life in an aqueous environment, effectively shielding GDH from oxidative inactivation.

Techniques Used: Generated

Oxidative stress resistance, and recycling of NAD + and NADH by alternating addition of glucose in the dark and irradiation with UV light. (a) NAD + and NADH conversion in this study. (b) Monitoring of GDH activity in the presence of ROS (generated by TiO 2 nanoparticles under UV light irradiation) ( n = 3). (c) Recycling of NAD + and NADH using GDH@SiNPs and TiO 2 nanoparticles ( n = 3). (d) Recycling of NAD + and NADH using native GDH and TiO 2 nanoparticles. For c and d, an increase in the y ‐axis value indicates NADH accumulation by GDH‐catalyzed reduction, while a decrease reflects NAD + regeneration by TiO 2 ‐mediated oxidation ( n = 3).
Figure Legend Snippet: Oxidative stress resistance, and recycling of NAD + and NADH by alternating addition of glucose in the dark and irradiation with UV light. (a) NAD + and NADH conversion in this study. (b) Monitoring of GDH activity in the presence of ROS (generated by TiO 2 nanoparticles under UV light irradiation) ( n = 3). (c) Recycling of NAD + and NADH using GDH@SiNPs and TiO 2 nanoparticles ( n = 3). (d) Recycling of NAD + and NADH using native GDH and TiO 2 nanoparticles. For c and d, an increase in the y ‐axis value indicates NADH accumulation by GDH‐catalyzed reduction, while a decrease reflects NAD + regeneration by TiO 2 ‐mediated oxidation ( n = 3).

Techniques Used: Irradiation, Activity Assay, Generated

Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of HeLa cells in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).
Figure Legend Snippet: Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of HeLa cells in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).

Techniques Used: CCK-8 Assay, Irradiation



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Fig. 3. FTIR-spectra of DA, ADA and PADA precipitated from solution (top) and cut-off from fingerprint region of the FTIR spectra of PADA precipitated from solution, PADA film on <t>TiO2</t> nanoparticles after washing and neat TiO2 nanoparticles (bottom).
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The compartmentalized enzyme‐photocatalyst system for sustainable coenzyme regeneration. (a) The glucose dehydrogenase‐loaded silica nanoparticles (GDH@SiNPs) and TiO 2 nanoparticle system complete the NAD + /NADH cycle, enabling continuous coenzyme regeneration while preventing enzyme inactivation by reactive oxygen species generated during photocatalysis. (b) Bare GDH is easily deactivated by the reaction of TiO 2 nanoparticles. (c) The silica matrix quenched ROS before reaching the enzyme core due to their short half‐life in an aqueous environment, effectively shielding GDH from oxidative inactivation.

Journal: Chembiochem

Article Title: Biomimetic Compartmentalization of Enzymes for Sustainable Coenzyme Recycling in Oxidative Photocatalysis

doi: 10.1002/cbic.70381

Figure Lengend Snippet: The compartmentalized enzyme‐photocatalyst system for sustainable coenzyme regeneration. (a) The glucose dehydrogenase‐loaded silica nanoparticles (GDH@SiNPs) and TiO 2 nanoparticle system complete the NAD + /NADH cycle, enabling continuous coenzyme regeneration while preventing enzyme inactivation by reactive oxygen species generated during photocatalysis. (b) Bare GDH is easily deactivated by the reaction of TiO 2 nanoparticles. (c) The silica matrix quenched ROS before reaching the enzyme core due to their short half‐life in an aqueous environment, effectively shielding GDH from oxidative inactivation.

Article Snippet: Titanium dioxide (TiO2) nanoparticles were purchased from EVONIK (Essen, Germany).

Techniques: Generated

Oxidative stress resistance, and recycling of NAD + and NADH by alternating addition of glucose in the dark and irradiation with UV light. (a) NAD + and NADH conversion in this study. (b) Monitoring of GDH activity in the presence of ROS (generated by TiO 2 nanoparticles under UV light irradiation) ( n = 3). (c) Recycling of NAD + and NADH using GDH@SiNPs and TiO 2 nanoparticles ( n = 3). (d) Recycling of NAD + and NADH using native GDH and TiO 2 nanoparticles. For c and d, an increase in the y ‐axis value indicates NADH accumulation by GDH‐catalyzed reduction, while a decrease reflects NAD + regeneration by TiO 2 ‐mediated oxidation ( n = 3).

Journal: Chembiochem

Article Title: Biomimetic Compartmentalization of Enzymes for Sustainable Coenzyme Recycling in Oxidative Photocatalysis

doi: 10.1002/cbic.70381

Figure Lengend Snippet: Oxidative stress resistance, and recycling of NAD + and NADH by alternating addition of glucose in the dark and irradiation with UV light. (a) NAD + and NADH conversion in this study. (b) Monitoring of GDH activity in the presence of ROS (generated by TiO 2 nanoparticles under UV light irradiation) ( n = 3). (c) Recycling of NAD + and NADH using GDH@SiNPs and TiO 2 nanoparticles ( n = 3). (d) Recycling of NAD + and NADH using native GDH and TiO 2 nanoparticles. For c and d, an increase in the y ‐axis value indicates NADH accumulation by GDH‐catalyzed reduction, while a decrease reflects NAD + regeneration by TiO 2 ‐mediated oxidation ( n = 3).

Article Snippet: Titanium dioxide (TiO2) nanoparticles were purchased from EVONIK (Essen, Germany).

Techniques: Irradiation, Activity Assay, Generated

Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of HeLa cells in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).

Journal: Chembiochem

Article Title: Biomimetic Compartmentalization of Enzymes for Sustainable Coenzyme Recycling in Oxidative Photocatalysis

doi: 10.1002/cbic.70381

Figure Lengend Snippet: Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of HeLa cells in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).

Article Snippet: Titanium dioxide (TiO2) nanoparticles were purchased from EVONIK (Essen, Germany).

Techniques: CCK-8 Assay, Irradiation

Fig. 3. FTIR-spectra of DA, ADA and PADA precipitated from solution (top) and cut-off from fingerprint region of the FTIR spectra of PADA precipitated from solution, PADA film on TiO2 nanoparticles after washing and neat TiO2 nanoparticles (bottom).

Journal: Polymer

Article Title: Polymer coating by oxidative polymerization of a new dopamine analogue with two amino groups

doi: 10.1016/j.polymer.2024.127630

Figure Lengend Snippet: Fig. 3. FTIR-spectra of DA, ADA and PADA precipitated from solution (top) and cut-off from fingerprint region of the FTIR spectra of PADA precipitated from solution, PADA film on TiO2 nanoparticles after washing and neat TiO2 nanoparticles (bottom).

Article Snippet: Dopamine (DA) and Titanium dioxide nanoparticles (TiO2) have been measured with Vertex 70 V spectrometer from Bruker Optics GmbH, Germany equipped with a Platinum diamond ATR unit.

Techniques: