Evidence map›Paper›PMID 37836456›Full record

ArticleNutrients2023

NXP081, DNA Aptamer-Vitamin C Complex Ameliorates DNFB-Induced Atopic Dermatitis in Balb/c Mice.

Sanggon Lee, Hyun-Jong Ahn, Yong Seek Park, Ji-Hyun Kim, Yoon-Seong Kim, Jeong-Je Cho, Cheung-Seog Park

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Causal relationships between dietary antioxidant vitamin intake and atopic dermatitis: A two-sample Mendelian randomization study.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Article
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

7 authors at 1 institution in 1 country.

Sanggon LeeDepartment of Microbiology, College of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Hyun-Jong AhnDepartment of Microbiology, College of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Yong Seek ParkDepartment of Microbiology, College of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID 0000-0002-9260-3102
Ji-Hyun KimNexmos Co., Ltd., U-Tower, 767, Sinsu-ro, Yongin-si 16827, Republic of Korea.
Yoon-Seong KimNexmos Co., Ltd., U-Tower, 767, Sinsu-ro, Yongin-si 16827, Republic of Korea.
Jeong-Je ChoDepartment of Microbiology, College of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Cheung-Seog ParkDepartment of Microbiology, College of Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.
Kyung Hee University · KR

Funding

This work was fully supported by the Nexmos Co., Ltd., Republic of Korea. KHU-20191784
6 · The paper itself

Abstract

Atopic dermatitis (AD) is a chronic inflammatory disease characterized by dry and itchy skin. Recently, it has been reported that oxidative stress is involved in skin diseases, possibly including AD. Vitamin C, also referred to as ascorbic acid, is a vital water-soluble compound that functions as an essential nutrient. It plays a significant role as both an antioxidant and an additive in various pharmaceutical and food products. Despite the fact that vitamin C is easily oxidized, we have developed NXP081, a single-stranded DNA aptamer that selectively binds to vitamin C, thereby inhibiting its oxidation. The objective of the current research was to examine the impact of NXP081, an animal model of AD induced by 2,4-dinitrofluorobenzene (DNFB). The experimental drug NXP081, when taken orally, showed promising results in reducing inflammation and improving the skin conditions caused by DNFB. The administration of NXP081 resulted in a significant reduction in ear swelling and a noticeable improvement in the appearance of skin lesions. In addition, the administration of NXP081 resulted in a significant decrease in the migration of mast cells in the skin lesions induced by DNFB. Moreover, NXP081 inhibited the production of interferon-gamma (IFN-γ) in CD4

Indexed as

Aptamers, NucleotideDermatitis, AtopicSkin DiseasesAnimalsAscorbic AcidCD4-Positive T-LymphocytesCytokinesDinitrofluorobenzeneMiceMice, Inbred BALB CSkinVitaminsAptamers, NucleotideAscorbic AcidCytokinesDinitrofluorobenzeneVitaminsatopic dermatitisDNA aptamervitamin C

Identifiers

PMID37836456
PMCPMC10574402
OpenAlexW4387106332

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.