Evidence map›Paper›PMID 26666701›Full record

ArticleScientific reports2015

Thermodynamic Insights and Conceptual Design of Skin-Sensitive Chitosan Coated Ceramide/PLGA Nanodrug for Regeneration of Stratum Corneum on Atopic Dermatitis.

Sang-Myung Jung, Gwang Heum Yoon, Hoo Chul Lee, Moon Hee Jung, Sun Il Yu, Seung Ju Yeon, Seul Ki Min, Yeo Seon Kwon, Jin Ha Hwang, Hwa Sung Shin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 51 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.

Sang-Myung JungDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Gwang Heum YoonDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Hoo Chul LeeDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Moon Hee JungDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Sun Il YuDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Seung Ju YeonDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Seul Ki MinDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Yeo Seon KwonDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Jin Ha HwangDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Hwa Sung ShinDepartment of Biological Engineering, Inha University, Incheon, 402-751, Korea.
Inha University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atopic dermatitis (AD) is a complex skin disease primarily characterized by psoriasis of the stratum corneum. AD drugs have usually been used in acidic and hydrophilic solvents to supply moisture and prevent lipid defects. Ceramide is a typical treatment agent to regenerate the stratum corneum and relieve symptoms of AD. However, ceramide has limitation on direct use for skin because of its low dispersion properties in hydrophilic phase and side effects at excessive treatment. In this study, ceramide imbedded PLGA nanoparticles were developed with chitosan coating (Chi-PLGA/Cer) to overcome this problem. The chitosan coating enhanced initial adherence to the skin and prevented the initial burst of ceramide, but was degraded by the weakly acidic nature of skin, resulting in controlled release of ceramide with additional driving force of the squeezed PLGA nanoparticles. Additionally, the coating kinetics of chitosan were controlled by manipulating the reaction conditions and then mathematically modeled. The Chi-PLGA/Cer was not found to be cytotoxic and ceramide release was controlled by pH, temperature, and chitosan coating. Finally, Chi-PLGA/Cer was demonstrated to be effective at stratum corneum regeneration in a rat AD model. Overall, the results presented herein indicated that Chi-PLGA/Cer is a novel nanodrug for treatment of AD.

Indexed as

AnimalsAnimals, NewbornCells, CulturedCell SurvivalCeramidesChemokine CCL2ChitosanDermatitis, AtopicDermatologic AgentsDrug DesignFibroblastsGene ExpressionImmunohistochemistryLactic AcidMicroscopy, ElectronNanoparticlesCcl2 protein, ratCeramidesChemokine CCL2ChitosanDermatologic AgentsLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerTumor Necrosis Factor-alpha

Identifiers

PMID26666701
PMCPMC4678456
OpenAlexW2261382670

What OpenQuestion holds

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LicenceCC BY
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.