Evidence map›Paper›PMID 27928655›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2017

In Vivo Pharmacokinetics of Puerarin via Different Drug Administration Routes Based on Middle Cerebral Artery Occlusion Model.

Pengyue Li, Jie Bai, Boyu Dong, Yang Lu, Shengwei Zhang, Shuang Guo, Ning Tan, Mengdi Zhao, Shouying Du, Puning Cao

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Article in European journal of drug metabolism and pharmacokinetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Pengyue LiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Jie BaiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Boyu DongSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Yang LuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China. landocean28@163.com.
Shengwei ZhangSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Shuang GuoSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Ning TanSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Mengdi ZhaoSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Shouying DuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China. dsydulaoshi@126.com.
Puning CaoSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100102, China.
Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesPueraria labata has traditionally been applied in the treatment of stroke in Chinese clinics. Puerarin is the key ingredient in it for brain protection effect. To find a superior administration route for puerarin in the treatment of ischemic cerebrovascular disease, the pharmacokinetics of puerarin based on the middle cerebral artery occlusion (MCAO) rat via different administration routes were studied and compared.

methodsTen rats (MCAO model) divided into two groups were treated with puerarin via intravenous and intranasal routes. Samples of brain and plasma were collected by microdialysis and tested by high-performance liquid chromatography with tandem mass spectrometric detection (HPLC-MS/MS).

resultsIn olfactory bulb, the intranasal group got a higher C

conclusionsThe 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.

Indexed as

Administration, IntranasalAnimalsBiological AvailabilityBrainDisease Models, AnimalInfarction, Middle Cerebral ArteryInfusions, IntravenousIsoflavonesMicrodialysisRats, Sprague-DawleyVasodilator AgentsIsoflavonespuerarinVasodilator Agents

Identifiers

PMID27928655
OpenAlexW2559899277

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.