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Synthesis and Characterization of Chiral Fe 3 O 4 /GelMA Hydrogels. (A) Synthesis procedure of chiral Fe 3 O 4 /GelMA hydrogels. (B) SEM image (scale bar: 30 μm, 30 nm) of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (C) UV-vis, (D) XRD spectra, and (E) CD spectra of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. FT-IR spectra of (F1) L-cysteine and D-cysteine, and (F2) bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (G1-3) Fe 2p XPS spectra of bare Fe₃O₄, D‑Fe₃O₄, and L‑Fe₃O₄ <t>nanoparticles.</t> (H) Zeta potential of Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (I) Loading content of Fe 3 O 4 SPs in FG, D-FG and L-FG groups. (J1-2) General view and SEM cross-section view of the GelMA, Fe 3 O 4 /GelMA, D-Fe 3 O 4 /GelMA, L-Fe 3 O 4 /GelMA hydrogel (scale bar: 100 μm). (K1-2) Elemental spectrum analysis of chiral Fe 3 O 4 /GelMA hydrogel shows the presence of carbon (C), nitrogen (N), oxygen (O), sulfur (S), and iron (Fe). (L)The photocurable property of chiral hydrogels. (M) Degradation profile and (N) Swelling rate of the chiral Fe 3 O 4 /GelMA hydrogel. (O) Maximum compressive strength of chiral hydrogels. (P1-2) pH value and Zeta potential during degradation. (Q) Storage modulus (G′) and loss modulus (G″) versus frequency of chiral hydrogels. (n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001). Abbreviation: SPs, superparticles; SEM, scanning electron microscopy; UV–vis, ultraviolet–visible; XRD, X-ray diffraction; CD, circular dichroism; FT-IR, Fourier-transform infrared spectroscopy.
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Synthesis and Characterization of Chiral Fe 3 O 4 /GelMA Hydrogels. (A) Synthesis procedure of chiral Fe 3 O 4 /GelMA hydrogels. (B) SEM image (scale bar: 30 μm, 30 nm) of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (C) UV-vis, (D) XRD spectra, and (E) CD spectra of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. FT-IR spectra of (F1) L-cysteine and D-cysteine, and (F2) bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (G1-3) Fe 2p XPS spectra of bare Fe₃O₄, D‑Fe₃O₄, and L‑Fe₃O₄ <t>nanoparticles.</t> (H) Zeta potential of Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (I) Loading content of Fe 3 O 4 SPs in FG, D-FG and L-FG groups. (J1-2) General view and SEM cross-section view of the GelMA, Fe 3 O 4 /GelMA, D-Fe 3 O 4 /GelMA, L-Fe 3 O 4 /GelMA hydrogel (scale bar: 100 μm). (K1-2) Elemental spectrum analysis of chiral Fe 3 O 4 /GelMA hydrogel shows the presence of carbon (C), nitrogen (N), oxygen (O), sulfur (S), and iron (Fe). (L)The photocurable property of chiral hydrogels. (M) Degradation profile and (N) Swelling rate of the chiral Fe 3 O 4 /GelMA hydrogel. (O) Maximum compressive strength of chiral hydrogels. (P1-2) pH value and Zeta potential during degradation. (Q) Storage modulus (G′) and loss modulus (G″) versus frequency of chiral hydrogels. (n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001). Abbreviation: SPs, superparticles; SEM, scanning electron microscopy; UV–vis, ultraviolet–visible; XRD, X-ray diffraction; CD, circular dichroism; FT-IR, Fourier-transform infrared spectroscopy.
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Synthesis and Characterization of Chiral Fe 3 O 4 /GelMA Hydrogels. (A) Synthesis procedure of chiral Fe 3 O 4 /GelMA hydrogels. (B) SEM image (scale bar: 30 μm, 30 nm) of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (C) UV-vis, (D) XRD spectra, and (E) CD spectra of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. FT-IR spectra of (F1) L-cysteine and D-cysteine, and (F2) bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (G1-3) Fe 2p XPS spectra of bare Fe₃O₄, D‑Fe₃O₄, and L‑Fe₃O₄ <t>nanoparticles.</t> (H) Zeta potential of Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (I) Loading content of Fe 3 O 4 SPs in FG, D-FG and L-FG groups. (J1-2) General view and SEM cross-section view of the GelMA, Fe 3 O 4 /GelMA, D-Fe 3 O 4 /GelMA, L-Fe 3 O 4 /GelMA hydrogel (scale bar: 100 μm). (K1-2) Elemental spectrum analysis of chiral Fe 3 O 4 /GelMA hydrogel shows the presence of carbon (C), nitrogen (N), oxygen (O), sulfur (S), and iron (Fe). (L)The photocurable property of chiral hydrogels. (M) Degradation profile and (N) Swelling rate of the chiral Fe 3 O 4 /GelMA hydrogel. (O) Maximum compressive strength of chiral hydrogels. (P1-2) pH value and Zeta potential during degradation. (Q) Storage modulus (G′) and loss modulus (G″) versus frequency of chiral hydrogels. (n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001). Abbreviation: SPs, superparticles; SEM, scanning electron microscopy; UV–vis, ultraviolet–visible; XRD, X-ray diffraction; CD, circular dichroism; FT-IR, Fourier-transform infrared spectroscopy.
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Synthesis and Characterization of Chiral Fe 3 O 4 /GelMA Hydrogels. (A) Synthesis procedure of chiral Fe 3 O 4 /GelMA hydrogels. (B) SEM image (scale bar: 30 μm, 30 nm) of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (C) UV-vis, (D) XRD spectra, and (E) CD spectra of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. FT-IR spectra of (F1) L-cysteine and D-cysteine, and (F2) bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (G1-3) Fe 2p XPS spectra of bare Fe₃O₄, D‑Fe₃O₄, and L‑Fe₃O₄ <t>nanoparticles.</t> (H) Zeta potential of Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (I) Loading content of Fe 3 O 4 SPs in FG, D-FG and L-FG groups. (J1-2) General view and SEM cross-section view of the GelMA, Fe 3 O 4 /GelMA, D-Fe 3 O 4 /GelMA, L-Fe 3 O 4 /GelMA hydrogel (scale bar: 100 μm). (K1-2) Elemental spectrum analysis of chiral Fe 3 O 4 /GelMA hydrogel shows the presence of carbon (C), nitrogen (N), oxygen (O), sulfur (S), and iron (Fe). (L)The photocurable property of chiral hydrogels. (M) Degradation profile and (N) Swelling rate of the chiral Fe 3 O 4 /GelMA hydrogel. (O) Maximum compressive strength of chiral hydrogels. (P1-2) pH value and Zeta potential during degradation. (Q) Storage modulus (G′) and loss modulus (G″) versus frequency of chiral hydrogels. (n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001). Abbreviation: SPs, superparticles; SEM, scanning electron microscopy; UV–vis, ultraviolet–visible; XRD, X-ray diffraction; CD, circular dichroism; FT-IR, Fourier-transform infrared spectroscopy.
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Synthesis and Characterization of Chiral Fe 3 O 4 /GelMA Hydrogels. (A) Synthesis procedure of chiral Fe 3 O 4 /GelMA hydrogels. (B) SEM image (scale bar: 30 μm, 30 nm) of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (C) UV-vis, (D) XRD spectra, and (E) CD spectra of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. FT-IR spectra of (F1) L-cysteine and D-cysteine, and (F2) bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (G1-3) Fe 2p XPS spectra of bare Fe₃O₄, D‑Fe₃O₄, and L‑Fe₃O₄ <t>nanoparticles.</t> (H) Zeta potential of Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (I) Loading content of Fe 3 O 4 SPs in FG, D-FG and L-FG groups. (J1-2) General view and SEM cross-section view of the GelMA, Fe 3 O 4 /GelMA, D-Fe 3 O 4 /GelMA, L-Fe 3 O 4 /GelMA hydrogel (scale bar: 100 μm). (K1-2) Elemental spectrum analysis of chiral Fe 3 O 4 /GelMA hydrogel shows the presence of carbon (C), nitrogen (N), oxygen (O), sulfur (S), and iron (Fe). (L)The photocurable property of chiral hydrogels. (M) Degradation profile and (N) Swelling rate of the chiral Fe 3 O 4 /GelMA hydrogel. (O) Maximum compressive strength of chiral hydrogels. (P1-2) pH value and Zeta potential during degradation. (Q) Storage modulus (G′) and loss modulus (G″) versus frequency of chiral hydrogels. (n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001). Abbreviation: SPs, superparticles; SEM, scanning electron microscopy; UV–vis, ultraviolet–visible; XRD, X-ray diffraction; CD, circular dichroism; FT-IR, Fourier-transform infrared spectroscopy.
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Synthesis and Characterization of Chiral Fe 3 O 4 /GelMA Hydrogels. (A) Synthesis procedure of chiral Fe 3 O 4 /GelMA hydrogels. (B) SEM image (scale bar: 30 μm, 30 nm) of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (C) UV-vis, (D) XRD spectra, and (E) CD spectra of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. FT-IR spectra of (F1) L-cysteine and D-cysteine, and (F2) bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (G1-3) Fe 2p XPS spectra of bare Fe₃O₄, D‑Fe₃O₄, and L‑Fe₃O₄ nanoparticles. (H) Zeta potential of Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (I) Loading content of Fe 3 O 4 SPs in FG, D-FG and L-FG groups. (J1-2) General view and SEM cross-section view of the GelMA, Fe 3 O 4 /GelMA, D-Fe 3 O 4 /GelMA, L-Fe 3 O 4 /GelMA hydrogel (scale bar: 100 μm). (K1-2) Elemental spectrum analysis of chiral Fe 3 O 4 /GelMA hydrogel shows the presence of carbon (C), nitrogen (N), oxygen (O), sulfur (S), and iron (Fe). (L)The photocurable property of chiral hydrogels. (M) Degradation profile and (N) Swelling rate of the chiral Fe 3 O 4 /GelMA hydrogel. (O) Maximum compressive strength of chiral hydrogels. (P1-2) pH value and Zeta potential during degradation. (Q) Storage modulus (G′) and loss modulus (G″) versus frequency of chiral hydrogels. (n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001). Abbreviation: SPs, superparticles; SEM, scanning electron microscopy; UV–vis, ultraviolet–visible; XRD, X-ray diffraction; CD, circular dichroism; FT-IR, Fourier-transform infrared spectroscopy.

Journal: Bioactive Materials

Article Title: Chiral Fe 3 O 4 /GelMA hydrogels regulate the osteoimmune microenvironment via Itgb3-mediated macrophage polarization to combat peri-implantitis

doi: 10.1016/j.bioactmat.2026.03.055

Figure Lengend Snippet: Synthesis and Characterization of Chiral Fe 3 O 4 /GelMA Hydrogels. (A) Synthesis procedure of chiral Fe 3 O 4 /GelMA hydrogels. (B) SEM image (scale bar: 30 μm, 30 nm) of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (C) UV-vis, (D) XRD spectra, and (E) CD spectra of bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. FT-IR spectra of (F1) L-cysteine and D-cysteine, and (F2) bare Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (G1-3) Fe 2p XPS spectra of bare Fe₃O₄, D‑Fe₃O₄, and L‑Fe₃O₄ nanoparticles. (H) Zeta potential of Fe 3 O 4 SPs, D-Fe 3 O 4 SPs and L-Fe 3 O 4 SPs. (I) Loading content of Fe 3 O 4 SPs in FG, D-FG and L-FG groups. (J1-2) General view and SEM cross-section view of the GelMA, Fe 3 O 4 /GelMA, D-Fe 3 O 4 /GelMA, L-Fe 3 O 4 /GelMA hydrogel (scale bar: 100 μm). (K1-2) Elemental spectrum analysis of chiral Fe 3 O 4 /GelMA hydrogel shows the presence of carbon (C), nitrogen (N), oxygen (O), sulfur (S), and iron (Fe). (L)The photocurable property of chiral hydrogels. (M) Degradation profile and (N) Swelling rate of the chiral Fe 3 O 4 /GelMA hydrogel. (O) Maximum compressive strength of chiral hydrogels. (P1-2) pH value and Zeta potential during degradation. (Q) Storage modulus (G′) and loss modulus (G″) versus frequency of chiral hydrogels. (n = 3, ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001). Abbreviation: SPs, superparticles; SEM, scanning electron microscopy; UV–vis, ultraviolet–visible; XRD, X-ray diffraction; CD, circular dichroism; FT-IR, Fourier-transform infrared spectroscopy.

Article Snippet: Surface potentials of the three nanoparticle types were determined using a nanoparticle size and zeta potential analyzer (ZS90, Malvern Zetasizer Nano, UK).

Techniques: Circular Dichroism, Zeta Potential Analyzer, Electron Microscopy, Fourier Transform Infrared Spectroscopy, Spectroscopy