Evidence map›Paper›PMID 30038494›Full record

ArticleInternational journal of nanomedicine2018

Galactosylated PLGA nanoparticles for the oral delivery of resveratrol: enhanced bioavailability and in vitro anti-inflammatory activity.

Frederick Yk Siu, Shaotang Ye, Hui Lin, Shoujun Li

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 96 citations in OpenAlex.

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  15. Nanoparticles Enhance Solubility and Neuroprotective Effects of Resveratrol in Demyelinating Disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
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  19. Nano-Nutraceuticals for Health: Principles and Applications.Revista brasileira de farmacognosia : orgao oficial da Sociedade Brasileira de Farmacognosia · 2023
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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

4 authors at 2 institutions in 1 country.

Frederick Yk SiuCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, People's Republic of China, shoujunli@scau.edu.cn.
Shaotang YeCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, People's Republic of China, shoujunli@scau.edu.cn.
Hui LinCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, People's Republic of China, shoujunli@scau.edu.cn.
Shoujun LiCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, People's Republic of China, shoujunli@scau.edu.cn.
South China Agricultural University · CNKey Laboratory of Guangdong Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResveratrol (RES) is a natural anti-inflammatory and antioxidant compound with poor water solubility and oral bioavailability. The present study takes the advantages of nanocarriers combined with a ligand (galactose) anchoring to orally deliver RES in an attempt to improve its bioavailability and pharmacological activity.

methodsRES-loaded galactosylated nanoparticles (RES-GNPs) were prepared by solvent diffusion technique using poly(lactic-co-glycolic acid), synthesized

resultsThe resulting RES-GNPs were 108.4 nm around in particle size with a polydispersity index of 0.217. Furthermore, RES-GNPs possessed a high EE and a slow drug release in water. After oral administration, RES-GNPs significantly enhanced the oral bioavailability of RES, up to 335.7% relative to RES suspensions. In situ single-pass intestinal perfusion and cellular uptake experiments showed that GNPs could improve the intestinal permeability and transcellular transport of RES. Moreover, the anti-inflammatory efficacy of RES-GNPs in RAW 264.7 cells model was superior to free RES and RES-GNPs.

conclusionThe results indicate that RES-GNPs can effectively promote the intestinal absorption of RES and strengthen its bioactivity, which may be a promising system for the treatment of inflammatory diseases.

Indexed as

Administration, OralAnimalsAnti-Inflammatory AgentsBiological AvailabilityCaco-2 CellsDrug LiberationEndocytosisGalactosamineHumansInflammationIntestinal AbsorptionIntestinal MucosaLactic AcidMaleNanoparticlesParticle SizeAnti-Inflammatory AgentsGalactosamineLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerResveratrolStilbenesanti-inflammationgalactosylationoral bioavailabilitypolymeric nanoparticlesresveratrol

Identifiers

PMID30038494
PMCPMC6049601
OpenAlexW2884628200

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.