Yin Qinqin, Li Jun, Zheng Qingshan, Yang Xiaolin, Lv Rong, Ma Longxiang, Liu Jin, Zhu Tao, Zhang Wensheng
Laboratory of Anesthesia and Critical Care Medicine, Translational Neuroscience Center, West China Hospital, Sichuan University, Chengdu, Sichuan, P. R. China.
North Sichuan Medical College, Nanchong, Sichuan, P. R. China.
PLoS One. 2017 Mar 23;12(3):e0174421. doi: 10.1371/journal.pone.0174421. eCollection 2017.
The quaternary lidocaine derivative (QX-314) in combination with bupivacaine can produce long-lasting nerve blocks in vivo, indicating potential clinical application. The aim of the study was to investigate the efficacy, safety, and the optimal formulation of this combination.
QX-314 and bupivacaine at different concentration ratios were injected in the vicinity of the sciatic nerve in rats; bupivacaine and saline served as controls (n = 6~10). Rats were inspected for durations of effective sensory and motor nerve blocks, systemic adverse effects, and histological changes of local tissues. Mathematical models were established to reveal drug-interaction, concentration-effect relationships, and the optimal ratio of QX-314 to bupivacaine.
0.21.5% QX-314 with 0.030.5% bupivacaine produced 5.8~23.8 h of effective nerve block; while 0.5% bupivacaine alone was effective for 4 h. No systemic side effects were observed; local tissue reactions were similar to those caused by 0.5% bupivacaine if QX-314 were used < 1.2%. The weighted modification model was successfully established, which revealed that QX-314 was the main active ingredient while bupivacaine was the synergist. The formulation, 0.9% QX-314 plus 0.5% bupivacaine, resulted in 10.1 ± 0.8 h of effective sensory and motor nerve blocks.
The combination of QX-314 and bupivacaine facilitated prolonged sciatic nerve block in rats with a satisfactory safety profile, maximizing the duration of nerve block without clinically important systemic and local tissue toxicity. It may emerge as an alternative approach to post-operative pain treatment.
季铵利多卡因衍生物(QX - 314)与布比卡因联合使用可在体内产生持久的神经阻滞,显示出潜在的临床应用价值。本研究旨在探讨这种联合用药的疗效、安全性及最佳配方。
将不同浓度比例的QX - 314和布比卡因注射到大鼠坐骨神经附近;布比卡因和生理盐水作为对照(n = 6~10)。观察大鼠有效感觉和运动神经阻滞的持续时间、全身不良反应以及局部组织的组织学变化。建立数学模型以揭示药物相互作用、浓度 - 效应关系以及QX - 314与布比卡因的最佳比例。
0.2%1.5%的QX - 314与0.03%0.5%的布比卡因联合使用可产生5.8~23.8小时的有效神经阻滞;而单独使用0.5%布比卡因的有效时间为4小时。未观察到全身副作用;若QX - 314使用量<1.2%,局部组织反应与0.5%布比卡因引起的反应相似。成功建立了加权修正模型,该模型显示QX - 314是主要活性成分,布比卡因是增效剂。配方为0.9% QX - 314加0.5%布比卡因时,可产生10.1±0.8小时的有效感觉和运动神经阻滞。
QX - 314与布比卡因联合使用可促进大鼠坐骨神经阻滞时间延长,安全性良好,在不产生具有临床意义的全身和局部组织毒性的情况下,最大限度地延长了神经阻滞时间。它可能成为术后疼痛治疗的一种替代方法。