2021
DOI: 10.1080/10408347.2021.1910927
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An Overview of Analytical Methods for the Estimation of Propofol in Pharmaceutical Formulations, Biological Matrices, and Hair Marker

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Cited by 3 publications
(2 citation statements)
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“…Previous studies have shown that propofol functions as a sedative via acting mainly on the β subunit of GABA receptors, directly opening the chloride (Cl − ) channels, and then inducing postsynaptic inhibition. 15 , 16 Remimazolam functions as a sedative via activating benzodiazepine receptors located on the α subunit of GABA receptors, increasing the frequency of Cl − channels opening, and then inducing postsynaptic inhibition. 17 , 18 These support that the two drugs can play synergistic effect of sedation.…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies have shown that propofol functions as a sedative via acting mainly on the β subunit of GABA receptors, directly opening the chloride (Cl − ) channels, and then inducing postsynaptic inhibition. 15 , 16 Remimazolam functions as a sedative via activating benzodiazepine receptors located on the α subunit of GABA receptors, increasing the frequency of Cl − channels opening, and then inducing postsynaptic inhibition. 17 , 18 These support that the two drugs can play synergistic effect of sedation.…”
Section: Discussionmentioning
confidence: 99%
“…This is because the excess release of glutamate may lead to excitotoxicity in both acute and chronic insults, such as ischemic stroke and neurodegenerative disorders [3,40]. Neuroprotective agents, e.g., riluzole, lamotrigine, and lubeluzole, have decreased glutamatergic transmission before it becomes neurotoxic [41][42][43]. In our study, DHC inhibited depolarization-evoked glutamate release in a concentration-dependent manner, with concentrations ranging from 50 to 1 µM and IC 50 values of 20.8 µM.…”
Section: Discussionmentioning
confidence: 55%