Evidence map›Paper›PMID 34565474›Full record

ArticleBiomaterials research2021

Evaluation of cellular response and drug delivery efficacy of nanoporous stainless steel material.

Inho Bae, Kyung-Seob Lim, Jun-Kyu Park, Ju Han Song, Sin-Hye Oh, Jung-Woo Kim, Zijiao Zhang, Chan Park, Jeong-Tae Koh

Abstract read
In one paragraph

Article in Biomaterials research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
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  5. Review
  6. 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

9 authors.

Inho BaeHard-tissue Biointerface Research Center; Department of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, Republic of Korea.
Kyung-Seob LimNational Primate Research Center & Futuristic Animal Resource and Research Center, Korea Research Institute of Bioscience and Biotechnology, Ochang, 28116, Republic of Korea.
Jun-Kyu ParkDepartment of Polymer Science and Engineering, Sunchon National University, Suncheon, 57922, Republic of Korea.
Ju Han SongHard-tissue Biointerface Research Center; Department of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, Republic of Korea.
Sin-Hye OhHard-tissue Biointerface Research Center; Department of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, Republic of Korea.
Jung-Woo KimHard-tissue Biointerface Research Center; Department of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, Republic of Korea.
Zijiao ZhangHard-tissue Biointerface Research Center; Department of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, Republic of Korea.
Chan ParkDepartment of Prosthodontics, School of Dentistry, Chonnam National University, Gwangju, 61186, Republic of Korea.
Jeong-Tae KohHard-tissue Biointerface Research Center; Department of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, Republic of Korea. jtkoh@chonnam.ac.kr.ORCID http://orcid.org/0000-0001-6279-6487

Funding

national research foundation of korea NRF-2019R1A5A2027521
6 · The paper itself

Abstract

objectiveVarious surface modification techniques that can further improve the function and usability of stainless steel as a medical device have been reported. In the present study, the physical and biological properties of nanoporous stainless steel as well as its usefulness for drug delivery were assessed.

methodsThe specimen was prepared with a circular disk shape (15 mm in diameter and 1 mm in thickness). The disk was subjected to electropolishing at a constant voltage of 20 V and 10 A for 10 min in an acidic environment (50% H

resultsThe surface roughness of the postpolishing group was greater than that of the nonpolishing group. Platelet adhesion and SMC adhesion and migration were inhibited in the postpolishing group compared to those in the prepolishing group. In the postpolishing group, the total amount of EVL on the surface (i.e., drug storage rate) was higher and the drug release rate was lower, with half the amount of the EVL released within 4 days compared with only 1 day for that of the prepolishing group.

conclusionTaken together, this stainless steel with a nanoporous surface could be used as a medical device for controlling cellular responses and carrying drugs.

Indexed as

Cellular responseDrug deliveryNanoporous structureStainless steelSurface modification

Identifiers

PMID34565474
PMCPMC8474832

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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.