Luo Yong, Zou MingYang, Zhang XinTao, Ye SuFen, Huang XianCheng, Li JiaTong, You Tian
Sports Medicine and Rehabilitation Center Peking University Shenzhen Hospital Shenzhen China.
Southern University of Science and Technology Shenzhen China.
J Exp Orthop. 2024 Dec 3;11(4):e70104. doi: 10.1002/jeo2.70104. eCollection 2024 Oct.
In this study, we aimed to characterize the elution profile of the ligament augmentation and reconstruction system (LARS) immersed in different concentrations of vancomycin using different immersion methods and determine whether the amount of vancomycin released was lower than the toxic concentrations for osteoblasts and chondroblasts.
The LARS was presoaked with 5, 2.5 or 1.25 mg/mL vancomycin solutions or wrapped in presoaked sterile gauze. After 10 min, the rinsed and unrinsed LARS samples were eluted in 100 mL agitated 37°C phosphate-buffered saline. An ultraviolet spectrophotometer was used to analyze 1 mL samples taken after 10 min and 0.5, 1, 6, 12, 24h.
Initially, no hysteresis was observed with vancomycin release into the solution at the tested conditions. The LARS elution profiles for different concentrations of the vancomycin solutions varied significantly. The amount of vancomycin released after 24 h was 9.10 ± 1.21, 5.29 ± 0.63 and 2.28 ± 0.59 mg for the 5, 2.5 and 1.25 mg/mL solutions, respectively. The amount of vancomycin released in the soaked group was significantly higher than in the rinsed and wrapped groups. The released amounts of vancomycin were below the toxic concentrations for osteoblasts and chondrocytes.
Soaked LARS can act as a reservoir for vancomycin, with the amount released and the elution profile dependent on rinsing, soaking solution concentration and soaking method. The eluted concentrations of vancomycin were lower than those previously reported for osteoblast and chondrocyte toxicity and higher than the minimal inhibitory concentrations for .
N/A.
在本研究中,我们旨在通过不同的浸泡方法,描绘浸泡于不同浓度万古霉素中的韧带增强与重建系统(LARS)的洗脱曲线,并确定万古霉素的释放量是否低于对成骨细胞和软骨细胞的毒性浓度。
将LARS用5、2.5或1.25mg/mL的万古霉素溶液预浸泡,或用预浸泡过的无菌纱布包裹。10分钟后,将冲洗过和未冲洗过的LARS样本在100mL 37°C搅拌的磷酸盐缓冲盐水中洗脱。使用紫外分光光度计分析在10分钟以及0.5、1、6、12、24小时后采集的1mL样本。
最初,在测试条件下,未观察到万古霉素释放到溶液中的滞后现象。不同浓度万古霉素溶液的LARS洗脱曲线差异显著。对于5、2.5和1.25mg/mL的溶液,24小时后万古霉素的释放量分别为9.10±1.21、5.29±0.63和2.28±0.59mg。浸泡组万古霉素的释放量显著高于冲洗并包裹组。万古霉素的释放量低于对成骨细胞和软骨细胞的毒性浓度。
浸泡过的LARS可作为万古霉素的储存库,释放量和洗脱曲线取决于冲洗、浸泡溶液浓度和浸泡方法。万古霉素的洗脱浓度低于先前报道的对成骨细胞和软骨细胞毒性的浓度,且高于……的最低抑菌浓度。
无。