sepharose and Cadaver

The present study aimed to investigate the technical feasibility of percutaneous endoscopic mini-hemilaminectomy via a uniportal approach, and to evaluate the possibility of decompression and endoscopic examination of the thoracic and lumbar spinal canals in small dogs during such procedures. Fresh canine cadavers of mixed-breed dogs (n=7) were used in this study. Following injection of a barium and agarose mixture (BA-gel) to stimulate intervertebral disc herniation, percutaneous endoscopic mini-hemilaminectomy was performed using a lateral approach to the thoracic and lumbar vertebrae. BA-gel was removed to decompress the spinal cord using an elevator and rongeurs after mini-hemilaminectomy. Pre and post-operative computed tomography (CT) scans were obtained to evaluate surgical outcomes. Intra-operative complications, incision length, and procedure time were recorded. All procedures were completed with clear visualization of the spinal cord and floor of the spinal canal. The mean total operating time was 58.00 ± 18.06 min. Lengths of incision were under 1 cm in all dogs. Intra-operative complications included iatrogenic nerve root injuries caused by the micro-rongeur in two dogs. CT imaging revealed that removal of BA-gel resulted in sufficient spinal cord decompression. Our findings indicated that percutaneous endoscopic thoracolumbar mini-hemilaminectomy is feasible for spinal cord decompression and allows for adequate observation of the spinal canal. Thus, this technique may be an alternative surgical option for treatment of thoracolumbar disk disease in dogs.

Topics: Animals; Barium Sulfate; Cadaver; Disease Models, Animal; Dog Diseases; Dogs; Endoscopy; Feasibility Studies; Intervertebral Disc Displacement; Laminectomy; Neuroendoscopy; Sepharose; Tomography, X-Ray Computed

Descriptive anatomical study on ovine and human cadaveric lumbar spinal segments.. To describe the alternative transpedicular approach to deliver therapeutic agents into intervertebral disc (IVD).. The present delivery approach of therapeutic agents (growth factors/cells/hydrogels) within the IVD is through injection, via the annulus fibrosus (AF). However, it has recently been demonstrated that small needle puncture of the AF leads to further degeneration and disc herniation. In addition, the injected material has a high chance to be extruded through the AF injury.. Lumbar ovine and human spinal segments were used. Under fluoroscopy, a 2-mm Kirschner wire was introduced in the caudal vertebra through the pedicle and the inferior endplate to the nucleus pulposus. Gross anatomy analysis and high-resolution peripheral quantitative computed tomography (HR-pQCT) were performed to assess the right position of the wire in pedicles. Discography and nucleotomy were performed using a 14G cannula insertion or a 2-mm arthroscopic shaver blade, respectively. Nucleoplasty was also performed with agarose gel/contrast agent and imaged with HR-pQCT.. Gross anatomy, fluoroscopy, and HR-pQCT images showed that the nucleus pulposus could be approached through the endplate via the pedicle without affecting the spinal canal and the neural foramina. The contrast agent was delivered into the IVD and nucleus pulposus was removed from the disc and filled with agarose gel.. This study describes how a transpedicular approach can be used as an alternative route to deliver therapeutic agents to the disc without disruption of the AF showing the potential use of this technique in preclinical research and highlighting its clinical relevance for IVD regeneration.

Topics: Animals; Cadaver; Contrast Media; Drug Delivery Systems; Fluoroscopy; Gels; Humans; Intervertebral Disc; Lumbar Vertebrae; Regeneration; Reproducibility of Results; Sepharose; Sheep; Tomography, X-Ray Computed

The purpose of this article is to compare in vitro T1rho measurements in agarose phantoms and articular cartilage specimens using 2D multislice spiral and 3D magnetization prepared partitioned k-space spoiled gradient-echo snapshot MRI sequences.. Six phantoms (agarose concentration, 2%, 3%, and 4%; n = 2 each) and 10 axially sliced patellar specimens from five cadaveric donors were scanned at 3 T. T1rho-weighted images were acquired using 2D spiral and 3D magnetization prepared partitioned k-space spoiled gradient-echo snapshot sequences. Regions of interest were analyzed to measure T1rho values centrally within phantoms, to evaluate effects of pulse sequence and agarose concentration. In patellar specimens, regions of interest were analyzed to measure T1rho values with respect to anatomic location (the medial and lateral facets and the median ridge in deep and superficial halves of the cartilage) as well as location that exhibited magic angle effect in proton density-weighted images, to evaluate the effects of pulse sequence, anatomic location, and magic angle.. In phantoms, T1rho values were similar (p = 0.9) between sequences but decreased significantly (p < 0.001), from ∼55 to ∼29 milliseconds, as agarose concentration increased from 2% to 4%. In cartilage specimens, T1rho values were also similar between sequences (p = 0.3) but were significantly higher (p < 0.001) in the superficial layer (95-120 milliseconds) compared with the deep layer (45-75 milliseconds).. T1rho measurements of human patellar cartilage specimens and agarose phantoms using 2D spiral and 3D magnetization prepared partitioned k-space spoiled gradient-echo snapshot sequences gave similar values. Lower T1rho values for phantoms with higher agarose concentrations and proteoglycan concentrations that are higher in deeper layers of cartilage than in superficial layers suggest that our method is sensitive to concentration of macromolecules in biologic tissues.

Topics: Cadaver; Cartilage, Articular; Humans; Imaging, Three-Dimensional; Magnetic Resonance Imaging; Patella; Phantoms, Imaging; Sepharose

To determine the effects of transplantable substrates on canine chondrocytes grown in three-dimensional culture.. 3 canine cadavers.. Articular cartilage harvested from canine cadavers was used to obtain chondrocytes for primary culture. Subcultured chondrocytes were grown in agarose alone (AG), or in agarose on canine cancellous bone (CB), polypropylene mesh, or oxidized regenerated cellulose substrate. Cell proliferation, proteoglycan and glycosaminoglycan (GAG) production, and collagen production were assessed on days 3, 6, 10, 15 and 20.. Chondrocytes from groups AG and CB proliferated and produced matrix over the entire 20-day study period. Group-CB chondrocytes had significantly more GAG than did chondrocytes of all other groups on days 6 (P = 0.0297) and 15 (P = 0.00272). Those of groups AG and CB contained significantly (P = 0.0235) more GAG on day 20. Chondrocytes of the polypropylene mesh group proliferated and produced matrix through day 10 in culture, but were no longer viable and had no matrix production on days 15 and 20. Regenerated cellulose appeared to be toxic to canine chondrocytes during all stages of in vitro three-dimensional culture.. Three-dimensional culture of canine chondrocytes in agarose appears to produce favorable results with respect to chondrocyte proliferation and matrix production. Canine CB appears to have beneficial effects with regard to early GAG synthesis. Polypropylene mesh and oxidized regenerated cellulose had detrimental effects on cellular proliferation and matrix production.

Topics: Analysis of Variance; Animals; Bone and Bones; Cadaver; Cartilage, Articular; Cell Culture Techniques; Cell Division; Cells, Cultured; Cellulose; Collagen; Dogs; Female; Glycosaminoglycans; Polypropylenes; Proteoglycans; Sepharose; Time Factors

Topics: Adult; Bacterial Proteins; Cadaver; Chromatography, Affinity; Female; Humans; Immunosorbent Techniques; Isoantibodies; Kidney Transplantation; Living Donors; Plasmapheresis; Sepharose; Tissue Donors