Evidence map›Paper›PMID 23192284›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2013

HP-β-CD-PLGA nanoparticles improve the penetration and bioavailability of puerarin and enhance the therapeutic effects on brain ischemia-reperfusion injury in rats.

Hai-quan Tao, Qingfeng Meng, Ming-hui Li, Hui Yu, Mei-fang Liu, Dan Du, Shou-li Sun, Hai-cheng Yang, Yan-ming Wang, Wei Ye and 4 more

Expression of concernAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-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

15 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  5. Assessment of 28-day oral exposure toToxicology reports · 2022
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  13. Puerarin inhibits proliferation and induces apoptosis in human glioblastoma cell lines.International journal of clinical and experimental medicine · 2015
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Hai-quan TaoDepartment of Neurosurgery, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Qingfeng Meng
Ming-hui Li
Hui Yu
Mei-fang Liu
Dan Du
Shou-li Sun
Hai-cheng Yang
Yan-ming Wang
Wei Ye
Li-zhuang Yang
Da-ling Zhu
Chuan-lu Jiang
Hai-sheng Peng
Harbin Medical University · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well known that puerarin attenuates ischemia-reperfusion injury and promotes function recovery of ischemic region. However, due to its reverse physiochemical properties, puerarin does not easily cross the blood-brain barrier. The aim of the present study is to create puerarin nanoparticles which increase and prolong the puerarin concentration in the brain. Using emulsion solvent evaporation techniques, we designed puerarin-loaded poly(D,L-lactic-co-glycolic acid) nanoparticles. Hydroxypropyl beta cyclodextrin (HP-β-CD) was used to increase the solubility of puerarin and gelatin to enhance viscosity of inner water phase, which improved puerarin entrapment. The drug release kinetics and nanoparticle degradation in phosphate buffered saline (PBS) were analyzed by electronic microscopy and high-performance liquid chromatography. Computerized tomography scans were used to detect the infarction volume and electroencephalogram (EEG) was recorded to estimate the recovery of brain function. The results showed that the combined HP-β-CD and gelatin significantly improved the entrapment efficiency. The infarction volume was significantly decreased on days 3 and 7 after the administration of puerarin nanoparticles compared with that of control and pure puerarin. EEG was also significantly improved. Puerarin nanoparticles are potentially applicable for the brain injury induced by ischemic-reperfusion.

Indexed as

2-Hydroxypropyl-beta-cyclodextrinAnimalsbeta-CyclodextrinsBiological AvailabilityBlood-Brain BarrierBrain IschemiaChromatography, High Pressure LiquidDrug CarriersGelatinIsoflavonesLactic AcidMaleNanoparticlesPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerRats2-Hydroxypropyl-beta-cyclodextrinbeta-CyclodextrinsDrug CarriersGelatinIsoflavonesLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerpuerarinVasodilator Agents

Identifiers

PMID23192284
OpenAlexW1983059715

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.