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instron 4411 test device  (Instron Corp)

 
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    Instron Corp instron 4411 test device
    Instron 4411 Test Device, supplied by Instron Corp, 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/result/instron 4411 test device/product/Instron Corp
    Average 86 stars, based on 1 article reviews
    instron 4411 test device - by Bioz Stars, 2026-05
    86/100 stars

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    Image Search Results


    Analysis of nerve sensory and motor function recovery. (A) Latency at different time points of the injured hindlimb paw in response to hot radiation stimulation measured by a Hargreaves test (n=4, 60 s is the threshold). (For IM+DNH/PLGA@BLZ, ***p < 0.001 vs. Sham, US+DNH/PLGA, and US+DNH/PLGA@BLZ; &p< 0.05 vs. Crush; For IM+DNH/PLGA, *p< 0.05 vs. Sham); (B) Withdrawal threshold at different time points of the injured hindlimb paw measured by the von Frey test (n=4, 2 g is the threshold). (For US+DNH/PLGA@BLZ, ###p < 0.001 vs. all other groups; For US+DNH/PLGA, *p < 0.05 vs. US+DNH/PLGA@BLZ and Sham; &&&p < 0.001: US+DNH/PLGA@BLZ and Sham vs. Crush and IM+DNH/PLGA@BLZ); (C) Representative images of mouse footprints recorded while the mice were on a walking apparatus; (D-F) Quantitative data analysis for (n=4) (D) foot pressure, (E) stance duration, and (F) swing duration based on the ratio related to the injury foot (left hind in system, LH) to the healthy foot (right hind in system, RH). (ns = no significant difference, *p < 0.05, **p < 0.01, ***p < 0.001).

    Journal: Journal of controlled release : official journal of the Controlled Release Society

    Article Title: Ultrasound-guided nanocomposite hydrogel injection to enhance nerve repair via temporal delivery of a colony-stimulating factor 1 receptor inhibitor

    doi: 10.1016/j.jconrel.2026.114797

    Figure Lengend Snippet: Analysis of nerve sensory and motor function recovery. (A) Latency at different time points of the injured hindlimb paw in response to hot radiation stimulation measured by a Hargreaves test (n=4, 60 s is the threshold). (For IM+DNH/PLGA@BLZ, ***p < 0.001 vs. Sham, US+DNH/PLGA, and US+DNH/PLGA@BLZ; &p< 0.05 vs. Crush; For IM+DNH/PLGA, *p< 0.05 vs. Sham); (B) Withdrawal threshold at different time points of the injured hindlimb paw measured by the von Frey test (n=4, 2 g is the threshold). (For US+DNH/PLGA@BLZ, ###p < 0.001 vs. all other groups; For US+DNH/PLGA, *p < 0.05 vs. US+DNH/PLGA@BLZ and Sham; &&&p < 0.001: US+DNH/PLGA@BLZ and Sham vs. Crush and IM+DNH/PLGA@BLZ); (C) Representative images of mouse footprints recorded while the mice were on a walking apparatus; (D-F) Quantitative data analysis for (n=4) (D) foot pressure, (E) stance duration, and (F) swing duration based on the ratio related to the injury foot (left hind in system, LH) to the healthy foot (right hind in system, RH). (ns = no significant difference, *p < 0.05, **p < 0.01, ***p < 0.001).

    Article Snippet: Thermal hypersensitivity was induced by focusing infrared radiation onto the plantar skin of the hind limb paw using the Hargreaves device (Ugo Basile Thermal Plantar Test Instrument).

    Techniques: