Marion duPont Scott Equine Medical Center, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Tech, Leesburg, Virginia, USA.
Equine Vet J. 2013 Mar;45(2):148-53. doi: 10.1111/j.2042-3306.2012.00633.x. Epub 2012 Sep 26.
Use of a novel, biodegradable, antimicrobial-impregnated gel provides an alternative method of local treatment of infections in horses.
To determine in vivo elution of antimicrobial medications from antimicrobial-impregnated cross-linked dextran gel and to evaluate the effect on wound healing when implanted subcutaneously in horses.
Amikacin-, vancomycin- or amikacin/clindamycin-impregnated gel was placed subcutaneously in 11 horses' necks, using 6 replicates with a 3 month washout between experiments. Capillary ultrafiltration probes for collection of interstitial fluid were placed 0 cm and 1.5 cm from the gel-filled incisions. Samples were collected at 0, 4, 8 and 12 h, and on Days 1-10. Blood was collected on Days 0, 1 and 7. Amikacin and vancomycin samples were analysed via fluorescence polarisation immunoassay, and clindamycin samples via high-performance liquid chromatography. Histology of biopsy samples was performed at the completion of the study. Differences in mean histomorphological scores between groups were assessed using Wilcoxon's signed ranks test.
Maximum antimicrobial concentrations were detected at 4 h (amikacin), and 8 h (vancomycin, and amikacin and clindamycin from the combination gel). Mean ± s.d. peak concentrations for amikacin, vancomycin, amikacin (amikacin/clindamycin) and clindamycin were 6133 ± 1461, 7286 ± 2769, 3948 ± 317 and 985 ± 960, respectively. Median number of days for which antimicrobial concentration remained above minimum inhibitory concentration for target microorganisms at implantation was ≥10 days for vancomycin, 9 days (± 1) for amikacin and 8 days (± 1) for clindamycin. Mean plasma amikacin and vancomycin concentrations were lower than detectable limits; mean serum clindamycin concentrations were 0.52 µg/ml and 0.63 µg/ml at 24 h and 7 days, respectively. There were no significant differences in histomorphological scores between treatment and control incisions (P≥0.22).
Cross-linked dextran gel is a safe, effective alternative local antimicrobial delivery method.
使用新型可生物降解的载抗菌药物凝胶提供了一种治疗马匹感染的局部治疗方法。
确定载抗菌药物的交联葡聚糖凝胶的体内洗脱情况,并评估其在马皮下植入时对伤口愈合的影响。
将阿米卡星、万古霉素或阿米卡星/克林霉素载药凝胶植入 11 匹马的颈部,每个实验有 6 个重复,每个实验之间间隔 3 个月。在充满凝胶的切口 0cm 和 1.5cm 处放置毛细管超滤探头以收集间质液。分别在 0、4、8 和 12 小时以及第 1-10 天采集样本。在第 0、1 和 7 天采集血液样本。通过荧光偏振免疫测定法分析阿米卡星和万古霉素样本,通过高效液相色谱法分析克林霉素样本。研究结束时进行活检样本的组织学检查。使用 Wilcoxon 符号秩检验评估组间平均组织形态学评分的差异。
在 4 小时(阿米卡星)和 8 小时(万古霉素和组合凝胶中的阿米卡星和克林霉素)检测到最大抗菌浓度。阿米卡星、万古霉素、阿米卡星(阿米卡星/克林霉素)和克林霉素的平均峰值浓度±标准差分别为 6133±1461、7286±2769、3948±317 和 985±960。在植入时抗菌药物浓度保持在目标微生物最低抑菌浓度以上的中位数天数,万古霉素为≥10 天,阿米卡星为 9 天(±1),克林霉素为 8 天(±1)。平均血浆阿米卡星和万古霉素浓度低于检测限;在 24 小时和 7 天时,血清克林霉素的浓度分别为 0.52µg/ml 和 0.63µg/ml。治疗切口和对照切口的组织形态学评分无显著差异(P≥0.22)。
交联葡聚糖凝胶是一种安全有效的局部抗菌药物递送方法。