Casanova Fernando, Carney Paul R, Sarntinoranont Malisa
Department of Mechanical & Aerospace Engineering, University of Florida, Gainesville, FL, USA; Escuela de Ingeniería Mecánica, Universidad del Valle, Cali, Colombia.
Department of Pediatrics, Neurology, Neuroscience, and J. Crayton Pruitt Family Department of Biomedical Engineering, Wilder Center of Excellence for Epilepsy Research, Gainesville, FL, USA.
J Neurosci Methods. 2014 Nov 30;237:79-89. doi: 10.1016/j.jneumeth.2014.08.012. Epub 2014 Aug 20.
Convection enhanced delivery (CED) infuses drugs directly into brain tissue. Needle insertion is required and results in tissue damage which can promote flowback along the needle track and improper targeting. The goal of this study was to evaluate friction stress (calculated from needle insertion force) as a measure of tissue contact and damage during needle insertion for varying insertion speeds.
Forces and surface dimpling during needle insertion were measured in rat brain in vivo. Needle retraction forces were used to calculate friction stresses. These measures were compared to track damage from a previous study. Differences between brain tissues and soft hydrogels were evaluated for varying insertion speeds: 0.2, 2, and 10mm/s.
In brain tissue, average insertion force and surface dimpling increased with increasing insertion speed. Average friction stress along the needle-tissue interface decreased with insertion speed (from 0.58 ± 0.27 to 0.16 ± 0.08 kPa). Friction stress varied between brain regions: cortex (0.227 ± 0.27 kPa), external capsule (0.222 ± 0.19 kPa), and CPu (0.383 ± 0.30 kPa). Hydrogels exhibited opposite trends for dimpling and friction stress with insertion speed.
Previously, increasing needle damage with insertion speed has been measured with histological methods. Friction stress appears to decrease with increasing tissue damage and decreasing tissue contact, providing the potential for in vivo and real time evaluation along the needle track.
Force derived friction stress decreased with increasing insertion speed and was smaller within white matter regions. Hydrogels exhibited opposite trends to brain tissue.
对流增强递送(CED)将药物直接注入脑组织。需要插入针头,这会导致组织损伤,进而促进沿针道的回流和靶向不当。本研究的目的是评估摩擦应力(由针头插入力计算得出),以此作为不同插入速度下针头插入过程中组织接触和损伤的一种度量。
在大鼠脑内活体测量针头插入过程中的力和表面凹陷。用针头回缩力计算摩擦应力。将这些测量结果与先前一项研究中的针道损伤情况进行比较。针对不同的插入速度(0.2、2和10毫米/秒)评估脑组织和软水凝胶之间的差异。
在脑组织中,平均插入力和表面凹陷随插入速度增加而增大。沿针 - 组织界面的平均摩擦应力随插入速度降低(从0.58±0.27千帕降至0.16±0.08千帕)。摩擦应力在不同脑区有所不同:皮层(0.227±0.27千帕)、外囊(0.222±0.19千帕)和尾壳核(0.383±0.30千帕)。水凝胶在凹陷和摩擦应力随插入速度变化方面呈现相反趋势。
以前,用组织学方法测量了随着插入速度增加针头损伤情况。摩擦应力似乎随着组织损伤增加和组织接触减少而降低,这为沿针道进行体内实时评估提供了可能性。
由力得出的摩擦应力随插入速度增加而降低,在白质区域较小。水凝胶呈现出与脑组织相反的趋势。