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x ray diffraction xrd patterns  (Bruker Corporation)
99
Bruker Corporation x ray diffraction xrd patterns
Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
X Ray Diffraction Xrd Patterns, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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x ray diffraction xrd patterns - by Bioz Stars, 2026-06
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x ray diffraction  (Bruker Corporation)
99
Bruker Corporation x ray diffraction
Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
X Ray Diffraction, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/x ray diffraction/product/Bruker Corporation
Average 99 stars, based on 1 article reviews
x ray diffraction - by Bioz Stars, 2026-06
99/100 stars
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x ray diffraction  (Malvern Panalytical)
86
Malvern Panalytical x ray diffraction
Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
X Ray Diffraction, supplied by Malvern Panalytical, 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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x ray diffraction patterns  (Bruker Corporation)
99
Bruker Corporation x ray diffraction patterns
Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
X Ray Diffraction Patterns, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/x ray diffraction patterns/product/Bruker Corporation
Average 99 stars, based on 1 article reviews
x ray diffraction patterns - by Bioz Stars, 2026-06
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wide angle x ray diffraction xrd  (Bruker Corporation)
99
Bruker Corporation wide angle x ray diffraction xrd
Comprehensive physicochemical characterization of HMS-derived nanocarriers. <t>(A)</t> <t>Wide-angle</t> <t>XRD</t> patterns of HMS. (B) Small-angle XRD profiles of HMS confirming mesostructural ordering. (C) FTIR spectra of HMS, HMS-NH2, HMS-DTX, HMS-DTX-SH, and PEG-HMS-DTX, illustrating the stepwise surface functionalization of HMS-based nanocarriers. (D) Nitrogen adsorption–desorption isotherms of HMS, HMS–NH₂, HMS–NH₂–DTX, and HMS–NH₂–DTX–SiSS revealing porosity changes. (E) Representative TEM images of HMS-DTX and PEG-HMS-DTX nanoparticles at low and high magnifications. (Scale bar = 100 nm). (F) Hydrodynamic size distributions of HMS–DTX and PEG–HMS–DTX obtained by DLS. (G) Zeta potential analysis of HMS–DTX and PEG–HMS–DTX. (H) Temporal particle size evolution of HMS–DTX and PEG–HMS–DTX in PBS or FBS containing 0 or 10 mM GSH. (I) Cumulative DTX release behavior of HMS–DTX and PEG–HMS–DTX in PBS with or without 10 mM GSH at 37 °C.
Wide Angle X Ray Diffraction Xrd, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) Energy-dispersive X-ray spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).

Journal: Bioactive Materials

Article Title: Smart microenvironment-adaptive nanocatalytic hydrogel for sequential antibacterial, anti-inflammatory, and regenerative therapy of biofilm-infected wounds

doi: 10.1016/j.bioactmat.2026.02.043

Figure Lengend Snippet: Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) Energy-dispersive X-ray spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).

Article Snippet: X-ray diffraction (XRD) patterns were conducted on a Bruker D8 ADVANCE X-ray diffractometer using Cu-Kα radiation (λ = 1.5418 Å).

Techniques: Spectroscopy, Concentration Assay

Comprehensive physicochemical characterization of HMS-derived nanocarriers. (A) Wide-angle XRD patterns of HMS. (B) Small-angle XRD profiles of HMS confirming mesostructural ordering. (C) FTIR spectra of HMS, HMS-NH2, HMS-DTX, HMS-DTX-SH, and PEG-HMS-DTX, illustrating the stepwise surface functionalization of HMS-based nanocarriers. (D) Nitrogen adsorption–desorption isotherms of HMS, HMS–NH₂, HMS–NH₂–DTX, and HMS–NH₂–DTX–SiSS revealing porosity changes. (E) Representative TEM images of HMS-DTX and PEG-HMS-DTX nanoparticles at low and high magnifications. (Scale bar = 100 nm). (F) Hydrodynamic size distributions of HMS–DTX and PEG–HMS–DTX obtained by DLS. (G) Zeta potential analysis of HMS–DTX and PEG–HMS–DTX. (H) Temporal particle size evolution of HMS–DTX and PEG–HMS–DTX in PBS or FBS containing 0 or 10 mM GSH. (I) Cumulative DTX release behavior of HMS–DTX and PEG–HMS–DTX in PBS with or without 10 mM GSH at 37 °C.

Journal: International Journal of Pharmaceutics: X

Article Title: Tumor-responsive PEGylated mesoporous nanoparticles achieve enhanced chemotherapy and reduced toxicity in prostate cancer

doi: 10.1016/j.ijpx.2026.100492

Figure Lengend Snippet: Comprehensive physicochemical characterization of HMS-derived nanocarriers. (A) Wide-angle XRD patterns of HMS. (B) Small-angle XRD profiles of HMS confirming mesostructural ordering. (C) FTIR spectra of HMS, HMS-NH2, HMS-DTX, HMS-DTX-SH, and PEG-HMS-DTX, illustrating the stepwise surface functionalization of HMS-based nanocarriers. (D) Nitrogen adsorption–desorption isotherms of HMS, HMS–NH₂, HMS–NH₂–DTX, and HMS–NH₂–DTX–SiSS revealing porosity changes. (E) Representative TEM images of HMS-DTX and PEG-HMS-DTX nanoparticles at low and high magnifications. (Scale bar = 100 nm). (F) Hydrodynamic size distributions of HMS–DTX and PEG–HMS–DTX obtained by DLS. (G) Zeta potential analysis of HMS–DTX and PEG–HMS–DTX. (H) Temporal particle size evolution of HMS–DTX and PEG–HMS–DTX in PBS or FBS containing 0 or 10 mM GSH. (I) Cumulative DTX release behavior of HMS–DTX and PEG–HMS–DTX in PBS with or without 10 mM GSH at 37 °C.

Article Snippet: The crystalline phase composition was examined by wide-angle X-ray diffraction (XRD) on a Bruker D8 Advance diffractometer equipped with Cu Kα radiation (λ = 1.5406 Å, 40 kV, 40 mA).

Techniques: Derivative Assay, Adsorption, Zeta Potential Analyzer