Department of Radiology, Thomas Jefferson University, 132 S. 10th Street, Philadelphia, PA 19107, USA.
School of Biomedical Engineering, Science and Health Systems, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104, USA.
Acta Biomater. 2019 Jul 15;93:12-24. doi: 10.1016/j.actbio.2019.02.041. Epub 2019 Feb 28.
Despite aggressive peri-operative antibiotic treatments, up to 10% of patients undergoing instrumented spinal surgery develop an infection. Like most implant-associated infections, spinal infections persist through colonization and biofilm formation on spinal instrumentation, which can include metal screws and rods for fixation and an intervertebral cage commonly comprised of polyether ether ketone (PEEK). We have designed a PEEK antibiotic reservoir that would clip to the metal fixation rod and that would achieve slow antibiotic release over several days, followed by a bolus release of antibiotics triggered by ultrasound (US) rupture of a reservoir membrane. We have found using human physiological fluid (synovial fluid), that higher levels (100-500 μg) of vancomycin are required to achieve a marked reduction in adherent bacteria vs. that seen in the common bacterial medium, trypticase soy broth. To achieve these levels of release, we applied a polylactic acid coating to a porous PEEK puck, which exhibited both slow and US-triggered release. This design was further refined to a one-hole or two-hole cylindrical PEEK reservoir that can clip onto a spinal rod for clinical use. Short-term release of high levels of antibiotic (340 ± 168 μg), followed by US-triggered release was measured (7420 ± 2992 μg at 48 h). These levels are sufficient to prevent adhesion of Staphylococcus aureus to implant materials. This study demonstrates the feasibility of an US-mediated antibiotic delivery device, which could be a potent weapon against spinal surgical site infection. STATEMENT OF SIGNIFICANCE: Spinal surgical sites are prone to bacterial colonization, due to presence of instrumentation, long surgical times, and the surgical creation of a dead space (≥5 cm) that is filled with wound exudate. Accordingly, it is critical that new approaches are developed to prevent bacterial colonization of spinal implants, especially as neither bulk release systems nor controlled release systems are available for the spine. This new device uses non-invasive ultrasound (US) to trigger bulk release of supra-therapeutic doses of antibiotics from materials commonly used in existing surgical implants. Thus, our new delivery system satisfies this critical need to eradicate surviving bacteria, prevent resistance, and markedly lower spinal infection rates.
尽管进行了积极的围手术期抗生素治疗,但仍有多达 10%接受器械性脊柱手术的患者发生感染。与大多数植入物相关的感染一样,脊柱感染持续存在于脊柱器械上的定植和生物膜形成中,这些器械包括用于固定的金属螺钉和棒以及通常由聚醚醚酮 (PEEK) 制成的椎间笼。我们设计了一种 PEEK 抗生素储库,可以夹在金属固定杆上,并在数天内实现缓慢释放抗生素,然后通过超声 (US) 破坏储库膜触发抗生素突释。我们发现,使用人体生理液(滑液)时,需要更高水平(100-500μg)的万古霉素才能显著减少与常见细菌培养基(胰蛋白酶大豆肉汤)相比附着的细菌。为了达到这些释放水平,我们将聚乳酸涂层应用于多孔 PEEK 药盘,该药盘表现出缓慢和 US 触发的释放。该设计进一步细化为一个单孔或两孔圆柱形 PEEK 储库,可以夹在脊柱棒上用于临床使用。测量到短期释放高水平抗生素(340±168μg),然后是 US 触发的释放(48 小时时为 7420±2992μg)。这些水平足以防止金黄色葡萄球菌附着在植入物材料上。本研究证明了超声介导的抗生素递送装置的可行性,这可能是对抗脊柱手术部位感染的有力武器。意义声明:由于器械的存在、手术时间长以及手术造成的充满伤口渗出物的死腔(≥5cm),脊柱手术部位容易发生细菌定植。因此,开发新方法来防止脊柱植入物的细菌定植至关重要,特别是因为既没有用于脊柱的散装释放系统也没有控释系统。这种新装置使用非侵入性超声 (US) 从现有手术植入物中常用的材料中触发超治疗剂量抗生素的批量释放。因此,我们的新递送系统满足了消除残留细菌、防止耐药性和显著降低脊柱感染率的这一关键需求。