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    Dispersion of Intradiscally Injected Particles is Limited by Size

    Source: Journal of Biomechanical Engineering:;2026:;volume( 148 ):;issue:008::page 2356
    Author:
    Boie, Austin J.
    ,
    Michalek, Arthur J.
    DOI: 10.1115/1.4071977
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Abstract. Due to its avascular nature, treatment of degeneration of the intervertebral disc (IVD) is typically carried out via needle injection into the inner nucleus pulposus (NP) of the disc. Proposed treatments range from small peptides with nanometer-scale diameters to hydrogel-encapsulated stem cell constructs in the hundreds of nanometers. While low permeability of the NP has been implicated as a limiting factor in fluid injection capacity, the effect on suspended particles is largely unknown. This study tested the hypothesis that increasing particle size decreases intradiscal injectate dispersion by injecting saline carrying fluorescent markers representing small molecules (SM: 1 nm diameter) along with either small beads (SB: 45–53 μm diameter) or large beads (LB: 125–150 μm diameter) into bovine caudal IVDs. Following injection, the discs were transected and imaged. While SM dispersion was consistent and covered a median of 26% of the NP area, bead behavior was varied. While discs in the SB group showed dispersion to a median of 3.8% of the NP area, LB beads were localized mostly to the needle track and covered only 0.66% of NP area. In 20% of the SB-injected discs and 30% of LB, no fluorescent beads were found in the NP. These results suggest that while small molecule treatments may be practically delivered to the NP by injection, larger (>50 μm) particles are restricted by NP pore size and will remain localized to the track left by the delivery needle.
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      Dispersion of Intradiscally Injected Particles is Limited by Size

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    contributor authorBoie, Austin J.
    contributor authorMichalek, Arthur J.
    date accessioned2026-08-23T07:25:43Z
    date available2026-08-23T07:25:43Z
    date copyright2026/08/01
    date issued2026
    identifier issn0148-0731
    identifier otherbio-25-1351.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4315080
    description abstractAbstract. Due to its avascular nature, treatment of degeneration of the intervertebral disc (IVD) is typically carried out via needle injection into the inner nucleus pulposus (NP) of the disc. Proposed treatments range from small peptides with nanometer-scale diameters to hydrogel-encapsulated stem cell constructs in the hundreds of nanometers. While low permeability of the NP has been implicated as a limiting factor in fluid injection capacity, the effect on suspended particles is largely unknown. This study tested the hypothesis that increasing particle size decreases intradiscal injectate dispersion by injecting saline carrying fluorescent markers representing small molecules (SM: 1 nm diameter) along with either small beads (SB: 45–53 μm diameter) or large beads (LB: 125–150 μm diameter) into bovine caudal IVDs. Following injection, the discs were transected and imaged. While SM dispersion was consistent and covered a median of 26% of the NP area, bead behavior was varied. While discs in the SB group showed dispersion to a median of 3.8% of the NP area, LB beads were localized mostly to the needle track and covered only 0.66% of NP area. In 20% of the SB-injected discs and 30% of LB, no fluorescent beads were found in the NP. These results suggest that while small molecule treatments may be practically delivered to the NP by injection, larger (>50 μm) particles are restricted by NP pore size and will remain localized to the track left by the delivery needle.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleDispersion of Intradiscally Injected Particles is Limited by Size
    typeJournal Paper
    journal volume148
    journal issue8
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4071977
    journal fristpage2356
    journal lastpage2367
    page12
    treeJournal of Biomechanical Engineering:;2026:;volume( 148 ):;issue:008
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
    نرم افزار کتابخانه دیجیتال "دی اسپیس" فارسی شده توسط یابش برای کتابخانه های ایرانی | تماس با یابش
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