Evidence map›Paper›PMID 38840668›Full record

ArticleFrontiers in bioengineering and biotechnology2024

Investigation of a new implant surface modification using phosphorylated pullulan.

Kanako Nagamoto, Ko Nakanishi, Tsukasa Akasaka, Shigeaki Abe, Kumiko Yoshihara, Mariko Nakamura, Hiroshi Hayashi, Shinji Takemoto, Masato Tamura, Yoshimasa Kitagawa and 2 more

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Kanako NagamotoOral Diagnosis and Medicine, Faculty of Dental Medicine, Hokkaido University, Sapporo, Japan.
Ko NakanishiDepartment of Biomaterials and Bioengineering, Faculty of Dental Medicine, Hokkaido University, Sapporo, Japan.
Tsukasa AkasakaDepartment of Biomaterials and Bioengineering, Faculty of Dental Medicine, Hokkaido University, Sapporo, Japan.
Shigeaki AbeDepartment of Dental and Biomedical Materials Science, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Kumiko YoshiharaHealth and Medical Research Institute, National Institute of Advanced Industrial Science and Technology, Takamatsu, Japan.
Mariko NakamuraSchool of Clinical Psychology, Kyushu University of Medical Science, Miyazaki, Japan.
Hiroshi HayashiSection for Dental Innovation, Faculty of Dental Medicine, Hokkaido University, Sapporo, Japan.
Shinji TakemotoDepartment of Biomedical Engineering, Iwate Medical University, Shiwa, Japan.
Masato TamuraDepartment of Oral Biochemistry and Molecular Biology, Graduate School of Dental Medicine, Hokkaido University, Sapporo, Japan.
Yoshimasa KitagawaOral Diagnosis and Medicine, Faculty of Dental Medicine, Hokkaido University, Sapporo, Japan.
Bart Van MeerbeekBIOMAT, Department of Oral Sciences, KU Leuven, Leuven, Belgium.
Yasuhiro YoshidaDepartment of Biomaterials and Bioengineering, Faculty of Dental Medicine, Hokkaido University, Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various implant surface treatment methods have been developed to achieve good osseointegration in implant treatment. However, some cases remain impossible to treat with implants because osseointegration is not obtained after implantation, and the implants fail. Thus, this study focused on phosphorylated pullulan because of its adhesiveness to titanium (Ti) and bone, high biocompatibility, and early replacement with bone. In this study, the response of bone-related cells to phosphorylated pullulan was evaluated to develop a new surface treatment method. Saos-2 (human osteosarcoma-derived osteoblast-like cells), MC3T3-E1 (mouse calvaria-derived osteoblast-like cells), and RAW264.7 (mouse macrophage-like cells) were used. In evaluating cellular responses, phosphorylated pullulan was added to the culture medium, and cell proliferation and calcification induction tests were performed. The proliferation and calcification of cells on the surface of Ti disks coated with phosphorylated pullulan were also evaluated. In addition, bone morphogenetic protein-2 (BMP-2), an osteogenic factor, was used to evaluate the role of phosphorylated pullulan as a drug carrier in inducing calcification on Ti disks. Phosphorylated pullulan tended to promote the proliferation of osteoblast-like cells and the formation of calcification on Ti disks coated with phosphorylated pullulan. Ti disks coated with phosphorylated pullulan loaded with BMP-2 enhanced calcification. Phosphorylated pullulan inhibited osteoclast-like cell formation. These results are due to the properties of phosphorylated pullulan, such as adhesiveness to titanium and drug-loading function. Therefore, phosphorylated pullulan effectively promotes bone regeneration when coated on titanium implants and is useful for developing a new surface treatment method.

Indexed as

cellular responsedental implantsphosphorylated pullulansurface modificationtitanium

Identifiers

PMID38840668
PMCPMC11150837

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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.