2016
DOI: 10.1007/s13318-016-0388-4
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In Vivo Pharmacokinetics of Puerarin via Different Drug Administration Routes Based on Middle Cerebral Artery Occlusion Model

Abstract: The in vivo experiments based on the MCAO model showed that, compared with intravenous route, the bioavailability and brain-targeting of drug were highly improved via intranasal route. In pathological conditions, compared with normal rats, the AUC of puerarin in brain and DTI increased significantly.

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Cited by 11 publications
(7 citation statements)
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“…At the end of the experiment, all the animals were euthanized, using urethane (Li et al, 2017). The hippocampus of the rats (n = 5) were dissected on an ice stage and preserved at −80 °C for oxidative stress markers and TNF-α analysis.…”
Section: Methodsmentioning
confidence: 99%
“…At the end of the experiment, all the animals were euthanized, using urethane (Li et al, 2017). The hippocampus of the rats (n = 5) were dissected on an ice stage and preserved at −80 °C for oxidative stress markers and TNF-α analysis.…”
Section: Methodsmentioning
confidence: 99%
“…The main ingredients in the extract are flavonoids, and they may interact with each other in disposition and transportation through blood-brain barrier (BBB). So, pharmacokinetic parameters of the Extract group and the Puerarin group [7] were calculated by the non-compartmental method and compared with each other. For i.v.…”
Section: Pharmacokinetics Comparison Of Puerarin Between Puerarin Andmentioning
confidence: 99%
“…Puerarin could be widely distributed in areas of the brain after administration. Brain diseases such cerebral vascular ischemia could influence the brain-targeting of puerarin (Li et al., 2017; Kong et al., 2019). More puerarin was transported into brain with a shorter t 1/2 in middle cerebral artery occluasion rats model compared with control group via intranasal route (Li et al., 2017).…”
Section: Pharmacokinetics Of Puerarinmentioning
confidence: 99%
“…Brain diseases such cerebral vascular ischemia could influence the brain-targeting of puerarin (Li et al., 2017; Kong et al., 2019). More puerarin was transported into brain with a shorter t 1/2 in middle cerebral artery occluasion rats model compared with control group via intranasal route (Li et al., 2017). After intraperitoneal injection, AUC 0-120 min of puerarin in the embolic hippocampus was significantly higher than that in the normal hippocampus at 40 and 20 mg/kg.…”
Section: Pharmacokinetics Of Puerarinmentioning
confidence: 99%