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benchtop magnetic resonance imaging mri system  (Niumag Corporation)

 
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    Niumag Corporation benchtop magnetic resonance imaging mri system
    Benchtop Magnetic Resonance Imaging Mri System, supplied by Niumag Corporation, 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/benchtop+magnetic+resonance+imaging+mri+system/benchtop+imaging+magnetic+mri+resonance+system/pmc12993413-241-11-18
    Average 86 stars, based on 1 article reviews
    benchtop magnetic resonance imaging mri system - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Magnetic Resonance Imaging:

    Article Title: Effect of ultrasonic-assisted hot-air drying on the quality and drying kinetics of Taraxacum mongolicum
    Article Snippet: .. The internal water distribution within TMHM sample was visualized using a benchtop magnetic resonance imaging (MRI) system (MesoMR23-060H-I, Niumag Electric Co., Ltd., Shanghai, China) equipped with a 0.5 T permanent magnet and a 60 mm diameter radiofrequency coil. ..

    Article Title: Effect of ultrasonic-assisted hot-air drying on the quality and drying kinetics of Taraxacum mongolicum.
    Article Snippet: .. The internal water distribution within TMHM sample was visualized using a benchtop magnetic resonance imaging (MRI) system (MesoMR23-060H-I, Niumag Electric Co., Ltd., Shanghai, China) equipped with a 0.5 T permanent magnet and a 60 mm diameter radiofrequency coil. ..



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    benchtop magnetic resonance imaging mri system  (Niumag Corporation)
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    Niumag Corporation benchtop magnetic resonance imaging mri system
    Benchtop Magnetic Resonance Imaging Mri System, supplied by Niumag Corporation, 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/benchtop+magnetic+resonance+imaging+mri+system/benchtop+imaging+magnetic+mri+resonance+system/pmc12993413-241-11-18
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    benchtop icon magnetic-resonance imaging instrument (mri  (Bruker Corporation)
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    Dual-mode detection of MagSiNs. Vibrating sample magnetometry was used to measure magnetization as a function of magnetic field of ( A ) CoFe 2 O 4 nanoparticles, and ( B ) MagSiNs in a reversible magnetic field at 300 K. T 1 and T 2 averaged <t>MRI</t> scans w.r.t the concentration of CoFe 2 O 4 nanoparticles were taken. ( C ) As expected CoFe 2 O 4 nanoparticles showed a T 2 -weighted effect with higher negative contrast at higher concentrations. ( D ) MagSiNs with the silica shell showed a T 2 -weighted, negative contrast effect only till 3 mM. However, it still demonstrated the efficacy of MagSiNs as MRI contrast agents. ( E ) Ratio of transverse/longitudinal relaxivity ( r 2 / r 1 ) for iron-oxide NPs and commercially available T 2 contrast agent RESOVIST when compared to the CoFe 2 O 4 nanoparticles and MagSiNs. MRI measurements were carried out in a <t>1T</t> <t>benchtop</t> MRI. ( F ) Fluorophores embedded in the silica shell of MagSiNs to impart ( i ) green fluorescence from FITC or ( ii ) red fluorescence from RITC.
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    icon 1 t benchtop magnetic resonance imaging (mri) system  (Bruker Corporation)
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    Dual-mode detection of MagSiNs. Vibrating sample magnetometry was used to measure magnetization as a function of magnetic field of ( A ) CoFe 2 O 4 nanoparticles, and ( B ) MagSiNs in a reversible magnetic field at 300 K. T 1 and T 2 averaged <t>MRI</t> scans w.r.t the concentration of CoFe 2 O 4 nanoparticles were taken. ( C ) As expected CoFe 2 O 4 nanoparticles showed a T 2 -weighted effect with higher negative contrast at higher concentrations. ( D ) MagSiNs with the silica shell showed a T 2 -weighted, negative contrast effect only till 3 mM. However, it still demonstrated the efficacy of MagSiNs as MRI contrast agents. ( E ) Ratio of transverse/longitudinal relaxivity ( r 2 / r 1 ) for iron-oxide NPs and commercially available T 2 contrast agent RESOVIST when compared to the CoFe 2 O 4 nanoparticles and MagSiNs. MRI measurements were carried out in a <t>1T</t> <t>benchtop</t> MRI. ( F ) Fluorophores embedded in the silica shell of MagSiNs to impart ( i ) green fluorescence from FITC or ( ii ) red fluorescence from RITC.
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    Dual-mode detection of MagSiNs. Vibrating sample magnetometry was used to measure magnetization as a function of magnetic field of ( A ) CoFe 2 O 4 nanoparticles, and ( B ) MagSiNs in a reversible magnetic field at 300 K. T 1 and T 2 averaged MRI scans w.r.t the concentration of CoFe 2 O 4 nanoparticles were taken. ( C ) As expected CoFe 2 O 4 nanoparticles showed a T 2 -weighted effect with higher negative contrast at higher concentrations. ( D ) MagSiNs with the silica shell showed a T 2 -weighted, negative contrast effect only till 3 mM. However, it still demonstrated the efficacy of MagSiNs as MRI contrast agents. ( E ) Ratio of transverse/longitudinal relaxivity ( r 2 / r 1 ) for iron-oxide NPs and commercially available T 2 contrast agent RESOVIST when compared to the CoFe 2 O 4 nanoparticles and MagSiNs. MRI measurements were carried out in a 1T benchtop MRI. ( F ) Fluorophores embedded in the silica shell of MagSiNs to impart ( i ) green fluorescence from FITC or ( ii ) red fluorescence from RITC.

    Journal: Pharmaceuticals

    Article Title: Biocompatible, Multi-Mode, Fluorescent, T 2 MRI Contrast Magnetoelectric-Silica Nanoparticles (MagSiNs), for On-Demand Doxorubicin Delivery to Metastatic Cancer Cells

    doi: 10.3390/ph15101216

    Figure Lengend Snippet: Dual-mode detection of MagSiNs. Vibrating sample magnetometry was used to measure magnetization as a function of magnetic field of ( A ) CoFe 2 O 4 nanoparticles, and ( B ) MagSiNs in a reversible magnetic field at 300 K. T 1 and T 2 averaged MRI scans w.r.t the concentration of CoFe 2 O 4 nanoparticles were taken. ( C ) As expected CoFe 2 O 4 nanoparticles showed a T 2 -weighted effect with higher negative contrast at higher concentrations. ( D ) MagSiNs with the silica shell showed a T 2 -weighted, negative contrast effect only till 3 mM. However, it still demonstrated the efficacy of MagSiNs as MRI contrast agents. ( E ) Ratio of transverse/longitudinal relaxivity ( r 2 / r 1 ) for iron-oxide NPs and commercially available T 2 contrast agent RESOVIST when compared to the CoFe 2 O 4 nanoparticles and MagSiNs. MRI measurements were carried out in a 1T benchtop MRI. ( F ) Fluorophores embedded in the silica shell of MagSiNs to impart ( i ) green fluorescence from FITC or ( ii ) red fluorescence from RITC.

    Article Snippet: The longitudinal relaxation time ( r 1 ) and transverse relaxation time ( r 2 ) were determined for cobalt ferrite nanoparticles, and MagSiNs using a 1T Bruker Benchtop Icon magnetic-resonance imaging instrument (MRI) in order to assess their suitability as MRI image contrast agents.

    Techniques: Concentration Assay, Fluorescence

    Assessing the biodistribution of MagSiNs to determine the usefulness of MagSiNs as drug nanocarriers. ( A ) Representative ex vivo T 2 -weighted, negative contrast, MRI scans of the mouse organs from the different time cohorts using the Bruker 1T benchtop MRI. The T 2 -weighted images were used to quantify the integrated intensity of the mouse organs from each time cohort. Di water and 10 mg/mL MagSiNs were used as control samples. ( B ) The ratio of the T 2 -weighted, integrated intensity of the signal from control mouse organs to that of the T 2 -weighted, integrated intensity of the signal from MagSiNs injected mouse organs was used to determine biodistribution kinetics over 48 h. There was no non-specific accumulation of the MagSiNs in any organs. ( C ) ICP-OES of the fecal pellets determined the control mice (no MagSiNs exposure) had a baseline signal of 10.7 ± 2.0 Fe (ppb) per milligram of sample. There was a statistically significant increased amount of Fe in the fecal pellet of mice injected with MagSiNs at the 4 h (36.2% higher) and 24 h (50.4% higher) post-injection mark. This indicated that the MagSiNs are indeed being cleared out through the G-I tract and not accumulating in vivo. The MagSiNs exhibited T 2 -MRI contrast and possessed favorable biodistribution, which made them suitable as drug nanocarriers.

    Journal: Pharmaceuticals

    Article Title: Biocompatible, Multi-Mode, Fluorescent, T 2 MRI Contrast Magnetoelectric-Silica Nanoparticles (MagSiNs), for On-Demand Doxorubicin Delivery to Metastatic Cancer Cells

    doi: 10.3390/ph15101216

    Figure Lengend Snippet: Assessing the biodistribution of MagSiNs to determine the usefulness of MagSiNs as drug nanocarriers. ( A ) Representative ex vivo T 2 -weighted, negative contrast, MRI scans of the mouse organs from the different time cohorts using the Bruker 1T benchtop MRI. The T 2 -weighted images were used to quantify the integrated intensity of the mouse organs from each time cohort. Di water and 10 mg/mL MagSiNs were used as control samples. ( B ) The ratio of the T 2 -weighted, integrated intensity of the signal from control mouse organs to that of the T 2 -weighted, integrated intensity of the signal from MagSiNs injected mouse organs was used to determine biodistribution kinetics over 48 h. There was no non-specific accumulation of the MagSiNs in any organs. ( C ) ICP-OES of the fecal pellets determined the control mice (no MagSiNs exposure) had a baseline signal of 10.7 ± 2.0 Fe (ppb) per milligram of sample. There was a statistically significant increased amount of Fe in the fecal pellet of mice injected with MagSiNs at the 4 h (36.2% higher) and 24 h (50.4% higher) post-injection mark. This indicated that the MagSiNs are indeed being cleared out through the G-I tract and not accumulating in vivo. The MagSiNs exhibited T 2 -MRI contrast and possessed favorable biodistribution, which made them suitable as drug nanocarriers.

    Article Snippet: The longitudinal relaxation time ( r 1 ) and transverse relaxation time ( r 2 ) were determined for cobalt ferrite nanoparticles, and MagSiNs using a 1T Bruker Benchtop Icon magnetic-resonance imaging instrument (MRI) in order to assess their suitability as MRI image contrast agents.

    Techniques: Ex Vivo, Injection, In Vivo