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Highly Water-Soluble Cucurbit[8]uril Derivative as a Broad-Spectrum Neuromuscular Block Reversal Agent.

Hong-Kun LiuFurong LinShang-Bo YuYan WuShuai LuYue-Yang LiuQiao-Yan QiJin CaoWei ZhouXiaopeng LiHui WangDan-Wei ZhangZhan-Ting LiDa Ma
Published in: Journal of medicinal chemistry (2022)
Broad-spectrum agents for the reversal of residual curarization induced by neuromuscular blocking agents are of great significance. Here, we report a highly water-soluble cucurbit[8]uril (CB[8]) derivative as a broad-spectrum neuromuscular block reversal agent induced by both benzylisquinolinium and aminosteroid neuromuscular block agents by the supramolecular sequestration strategy. The UV/Vis competition titration assays suggest the high binding affinity of the CB[8] derivative toward both benzylisquinolinium-type cisatracurium besylate and aminosteroid-type rocuronium, vecuronium, and pancuronium, at the level of 10 7 M -1 . In vivo studies demonstrate that the administration of the CB[8] derivative could significantly accelerate the recovery time compared to the placebo or neostigmine groups. The reversal activity of the CB[8] derivative is comparable to or higher than that of clinically approved sugammadex. Acute toxicity evaluations reveal that the CB[8]-derivative displays outstanding biocompatibility, with the maximum tolerance dose as high as 960 mg kg -1 .
Keyphrases
  • water soluble
  • liver failure
  • oxidative stress
  • high throughput
  • mass spectrometry
  • hepatitis b virus
  • study protocol
  • acute respiratory distress syndrome
  • case control