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来自河豚毒素增强型局部麻醉微球的长效局部麻醉

Prolonged duration local anesthesia from tetrodotoxin-enhanced local anesthetic microspheres.

作者信息

Kohane Daniel S, Smith Sarah E, Louis David N, Colombo Gaia, Ghoroghchian Peter, Hunfeld Nicole G M, Berde Charles B, Langer Robert

机构信息

Massachusetts General Hospital and Harvard Medical School, Boston MA, USA.

出版信息

Pain. 2003 Jul;104(1-2):415-21. doi: 10.1016/s0304-3959(03)00049-6.

DOI:10.1016/s0304-3959(03)00049-6
PMID:12855352
Abstract

There is interest in developing prolonged duration local anesthesics. Here we examine whether tetrodotoxin (TTX) can be used to prolong the block from bupivacaine microspheres with and without dexamethasone. Rats received sciatic nerve blocks with 75 mg of microspheres containing 0.05% (w/w) TTX, 50% (w/w) bupivacaine and/or 0.05% (w/w) dexamethasone. 0.1% (w/w) TTX microspheres were also tested. The carrier fluid contained 1:100,000 epinephrine. Nociceptive and motor blockade of the hindpaw were quantified. Nerves and adjacent muscles were harvested 2 weeks after injection for histological assessment by light microscopy. The median nociceptive block duration in hours from the microsphere groups were: bupivacaine=6.2, 0.05% TTX=0, bupivacaine+TTX=35.3, bupivacaine+dexamethasone=31.3, TTX+dexamethasone=8.1, TTX+bupivacaine+dexamethasone=221.7. Some animals receiving particles containing 0.05% TTX had deficits in the uninjected extremity; all animals receiving 0.1% (w/w) TTX particles died. Pockets of particles were associated with localized inflammation, and all samples showed some evidence of myotoxicity in the vicinity of the injection. The nerves themselves appeared intact. In summary, coencapsulation of TTX in controlled release devices containing bupivacaine and dexamethasone resulted in very prolonged nerve blocks. As formulated here, this preparation had a narrow margin of safety. While the myotoxicity appears consistent with the well-known reversible myotoxicity associated with local anesthetics, its long-term significance remains to be established.

摘要

人们对开发长效局部麻醉剂很感兴趣。在此,我们研究河豚毒素(TTX)是否可用于延长布比卡因微球(含或不含地塞米松)的阻滞时间。大鼠接受坐骨神经阻滞,使用含0.05%(w/w)TTX、50%(w/w)布比卡因和/或0.05%(w/w)地塞米松的75毫克微球。还测试了0.1%(w/w)TTX微球。载液含有1:100,000肾上腺素。对后爪的伤害性和运动阻滞进行量化。注射后2周采集神经和相邻肌肉,通过光学显微镜进行组织学评估。微球组以小时计的中位伤害性阻滞持续时间为:布比卡因=6.2,0.05% TTX=0,布比卡因+TTX=35.3,布比卡因+地塞米松=31.3,TTX+地塞米松=8.1,TTX+布比卡因+地塞米松=221.7。一些接受含0.05% TTX颗粒的动物未注射的肢体出现功能缺陷;所有接受0.1%(w/w)TTX颗粒的动物死亡。颗粒囊袋与局部炎症相关,所有样本在注射部位附近均显示出一定程度的肌毒性证据。神经本身看起来完好无损。总之,在含有布比卡因和地塞米松的控释装置中共包封TTX可导致非常长的神经阻滞时间。按此处配方,该制剂的安全范围较窄。虽然肌毒性似乎与局部麻醉剂相关的众所周知的可逆性肌毒性一致,但其长期意义仍有待确定。

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