Evidence map›Paper›PMID 31121831›Full record

ArticleMolecules (Basel, Switzerland)2019

Functional Fragments of AIMP1-Derived Peptide (AdP) and Optimized Hydrosol for Their Topical Deposition by Box-Behnken Design.

Jeong-Jun Lee, Young-Min Han, Tae-Wan Kwon, Dong Hyun Kim, Han Sol Lee, Woo Jin Jung, Jina Kim, Sujin Kang, Sang Kyum Kim, Cheong-Weon Cho and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

14 authors at 3 institutions in 1 country.

Jeong-Jun LeeCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. daegeon0705@cnu.ac.kr.
Young-Min HanCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. gksdudals93@naver.com.
Tae-Wan KwonCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. mds_wantae@naver.com.
Dong Hyun KimCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. gcy70426@gmail.com.
Han Sol LeeCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. sol4273@naver.com.
Woo Jin JungCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. woojin@cnu.ac.kr.
Jina KimCureBio Research Center, Suwon 16229, Korea. jnkim@curebio.co.kr.ORCID 0000-0003-0764-0097
Sujin KangCureBio Research Center, Suwon 16229, Korea. sjkang@curebio.co.kr.
Sang Kyum KimCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. sangkim@cnu.ac.kr.
Cheong-Weon ChoCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. chocw@cnu.ac.kr.ORCID 0000-0001-8390-0132
Keong-Ryoon LeeLaboratory Animal Resource Center, Korea Research Institute of Bioscience and Biotechnology, Ochang 28116, Korea. kyeongrlee@kribb.re.kr.
Dae-Duk KimCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea. ddkim@snu.ac.kr.
Min Chul ParkCureBio Research Center, Suwon 16229, Korea. mcpark@curebio.co.kr.
Jae-Young LeeCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea. jaeyoung@cnu.ac.kr.
Chungnam National University · KRSeoul National University · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aminoacyl-tRNA synthetase complex-interacting multifunctional protein 1 (AIMP1)-derived peptide (AdP) has been developed as a cosmeceutical ingredient for skin anti-aging given its fibroblast-activating (FA) and melanocyte-inhibiting (MI) functions. However, a suitable strategy for the topical delivery of AdP was required due to its low-permeable properties. In this study, FA and MI domains of AdP (FA-AdP and MI-AdP, respectively) were determined by functional domain mapping, where the activities of several fragments of AdP on fibroblast and melanocyte were tested, and a hydrosol-based topical delivery system for these AdP fragments was prepared. The excipient composition of the hydrosol was optimized to maximize the viscosity and drying rate by using Box-Behnken design. The artificial skin deposition of FA-AdP-loaded hydrosol was evaluated using Keshary-Chien diffusion cells equipped with Strat-M membrane (STM). The quantification of the fluorescent dye-tagged FA-AdP in STM was carried out by near-infrared fluorescence imaging. The optimized hydrosol showed 127-fold higher peptide deposition in STM than free FA-AdP (

Indexed as

AnimalsCell LineCell ProliferationCell SurvivalCosmeceuticalsCytokinesDoxorubicinHumansMelanocytesMiceModels, BiologicalNeoplasm ProteinsOptical ImagingPeptidesRNA-Binding ProteinsSkin AgingCosmeceuticalsCytokinesDoxorubicinNeoplasm ProteinsPeptidesRNA-Binding Proteinssmall inducible cytokine subfamily E, member 1AIMP1-derived peptide (AdP)Box-Behnken designcosmeceutical peptidehydrosoltopical delivery of peptides

Identifiers

PMID31121831
PMCPMC6572189
OpenAlexW2945529119

What OpenQuestion holds

Textmetadata
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.