Evidence map›Paper›PMID 28254113›Full record

ArticleThe Kaohsiung journal of medical sciences2017

Development and in vivo evaluation of self-microemulsion as delivery system for α-mangostin.

Wen-Ke Xu, Hui Jiang, Kui Yang, Ya-Qin Wang, Qian Zhang, Jian Zuo

Open access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.6field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Journal of inflammation research · 2021
    Article
  10. Review
  11. Nanoparticle Drug Delivery Systems for α-Mangostin.Nanotechnology, science and applications · 2020
    Review
  12. Review
  13. Article
  14. Review
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

6 authors at 1 institution in 1 country.

Wen-Ke XuDepartment of Pharmacy, Yijishan Hospital, Wannan Medical College, Wuhu, China.
Hui JiangDepartment of Pharmacy, Yijishan Hospital, Wannan Medical College, Wuhu, China.
Kui YangDepartment of Pharmacy, Yijishan Hospital, Wannan Medical College, Wuhu, China.
Ya-Qin WangDepartment of Pharmacy, Yijishan Hospital, Wannan Medical College, Wuhu, China.
Qian ZhangDepartment of Pharmacy, Yijishan Hospital, Wannan Medical College, Wuhu, China.
Jian ZuoDepartment of Pharmacy, Yijishan Hospital, Wannan Medical College, Wuhu, China; Anhui Provincial Engineering Technology Research Center of Polysaccharides Drug, Wuhu, China. Electronic address: zuojian8178@163.com.
Wannan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

α-Mangostin (MG) is a versatile bioactive compound isolated from mangosteen and possesses significant pharmacokinetic shortages. To augment the potential clinical efficacy, MG-loaded self-microemulsion (MG-SME) was designed and prepared in this study, and its potential as a drug loading system was evaluated based on the pharmacokinetic performance and tissue distribution feature. The formula of MG-SME was optimized by an orthogonal test under the guidance of ternary phase diagram, and the prepared MG-SME was characterized by encapsulation efficiency, size distribution, and morphology. Optimized high performance liquid chromatography method was employed to determine concentrations of MG and characterize the pharmacokinetic and tissue distribution features of MG in rodents. It was found that diluted MG-SME was characterized as spherical particles with a mean diameter of 24.6 nm and an encapsulation efficiency of 87.26%. The delivery system enhanced the area under the curve of MG by 4.75 times and increased the distribution in lymphatic organs. These findings suggested that SME as a nano-sized delivery system efficiently promoted the digestive tract absorption of MG and modified its distribution in tissues. The targeting feature and high oral bioavailability of MG-SME promised a good clinical efficacy, especially for immune diseases.

Indexed as

Administration, OralAnimalsArea Under CurveBiological AvailabilityChromatography, High Pressure LiquidDrug CompoundingDrug Delivery SystemsEmulsionsFactor Analysis, StatisticalFemaleGarcinia mangostanaGastrointestinal AbsorptionMaleMiceMice, Inbred C57BLOrgan SpecificityEmulsionsmangostinPlant ExtractsXanthonesPharmacokineticsSelf-microemulsionTissue distributionα-Mangostin

Identifiers

PMID28254113
PMCPMC11916032
OpenAlexW2573230689

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.