Concentric Analgesics, San Francisco, California, USA.
ToxStrategies, Inc., Cary, North Carolina, USA.
J Orthop Res. 2022 Oct;40(10):2281-2293. doi: 10.1002/jor.25271. Epub 2022 Feb 6.
Vocacapsaicin is a novel prodrug of trans-capsaicin (trans-8-methyl-N-vanillyl-6-nonenamide) being developed as a nonopioid, long-lasting, site-specific treatment for postsurgical pain management. The objective of these studies was to examine the safety and tolerability of vocacapsaicin in an osteotomy model in two animal species and to evaluate bone healing parameters. Rats undergoing unilateral femoral osteotomy received a single perioperative administration (by instillation) of vocacapsaicin (vehicle, 0.15, 0.3, and 0.6 mg/kg). Rabbits undergoing unilateral ulnar osteotomy received a single perioperative administration (by infiltration and instillation) of vocacapsaicin (vehicle, 0.256 and 0.52 mg) alone or in combination with 0.5% ropivacaine. Clinical signs, body weights, food consumption, radiography, histopathologic examinations, ex vivo bone mineral density measurements (rats only), and biomechanical testing were evaluated at 4 and 8 weeks in rats and at 2 and 10 weeks in rabbits. Plasma samples were also collected in rabbits. There were no vocacapsaicin-related effects on mortality, clinical observations, body weight, or food consumption in either species. Systemic exposure to vocacapsaicin and its metabolites, including capsaicin, was transient. In rats, vocacapsaicin was devoid of deleterious effects on bone healing parameters, and there was a trend for enhanced bone healing in rats treated with the mid-dose. In rabbits, vocacapsaicin administered alone or in combination with ropivacaine did not adversely affect bone healing parameters. In conclusion, a single perioperative administration of vocacapsaicin in unilateral osteotomy models was well tolerated, locally and systemically, supporting its continued development as a novel, nonopioid treatment for postsurgical pain management.
vocacapsaicin 是一种新型的辣椒素前药,正在开发为一种非阿片类、长效、局部特定的术后疼痛管理治疗药物。这些研究的目的是在两种动物模型中的骨切开术模型中检查 vocacapsaicin 的安全性和耐受性,并评估骨愈合参数。接受单侧股骨切开术的大鼠接受单次围手术期给药(通过滴注)vocacapsaicin(载体、0.15、0.3 和 0.6mg/kg)。接受单侧尺骨切开术的兔子接受单次围手术期给药(通过浸润和滴注)vocacapsaicin(载体、0.256 和 0.52mg)单独或与 0.5%罗哌卡因联合给药。在大鼠中,在第 4 和第 8 周以及在兔子中,在第 2 和第 10 周评估临床体征、体重、食物消耗、放射照相、组织病理学检查、离体骨矿物质密度测量(仅大鼠)和生物力学测试。还在兔子中收集血浆样本。在两种物种中,vocacapsaicin 均未对死亡率、临床观察、体重或食物消耗产生影响。系统性暴露于 vocacapsaicin 和其代谢物,包括辣椒素,是短暂的。在大鼠中,vocacapsaicin 对骨愈合参数没有有害影响,并且中剂量治疗的大鼠有增强骨愈合的趋势。在兔子中,单独给予 vocacapsaicin 或与罗哌卡因联合使用不会对骨愈合参数产生不利影响。总之,在单侧骨切开术模型中单次围手术期给予 vocacapsaicin 具有良好的耐受性,局部和全身,支持其作为一种新的非阿片类术后疼痛管理治疗药物的继续开发。