Literature DB >> 24215347

Cucurbit[n]uril type hosts for the reversal of steroidal neuromuscular blocking agents.

Donal H Macartney1.   

Abstract

The ideal neuromuscular blocking agent (NMBA) is regarded as being a non-depolarizing equivalent of succinylcholine, having a rapid onset and short duration of action, with minimal side effects. In the absence of a single drug, the administration of an aminosteroid NMBA, such as rocuronium, followed by reversal using an acetylcholinesterase inhibitor, such as neostigmine, is commonly employed. A different and safer approach to rapidly reversing the action of the NMBA, by encapsulating it with a macrocyclic or acyclic host molecule, such as the cyclodextrin sugammadex or more recently, cucurbituril-type hosts such as cyclic cucurbit[7]uril and the acyclic glycoluril tetramer calabadion 1, is described.

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Year:  2013        PMID: 24215347     DOI: 10.4155/fmc.13.164

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  2 in total

1.  Acyclic Cucurbit[n]uril-type Receptors: Preparation, Molecular Recognition Properties and Biological Applications.

Authors:  Shweta Ganapati; Lyle Isaacs
Journal:  Isr J Chem       Date:  2017-11-14       Impact factor: 3.333

2.  In Vitro selectivity of an acyclic cucurbit[n]uril molecular container towards neuromuscular blocking agents relative to commonly used drugs.

Authors:  Shweta Ganapati; Peter Y Zavalij; Matthias Eikermann; Lyle Isaacs
Journal:  Org Biomol Chem       Date:  2015-12-09       Impact factor: 3.876

  2 in total

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