Evidence map›Paper›PMID 30195262›Full record

ArticleJournal of biomedical materials research. Part B, Applied biomaterials2019

Cellular Response to 3-D Printed Bioactive Silicate and Borosilicate Glass Scaffolds.

Weitao Jia, Grace Y Lau, Wenhai Huang, Changqing Zhang, Antoni P Tomsia, Qiang Fu

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part B, Applied biomaterials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Bioprinting Technologies and Bioinks for Vascular Model Establishment.International journal of molecular sciences · 2023
    Review
  4. Review
  5. 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

6 authors at 4 institutions in 2 countries.

Weitao JiaDepartment of Orthopedic Surgery, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai, 200233, China.
Grace Y LauMaterials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, 94720, USA.
Wenhai HuangSchool of Materials Science and Engineering, Institute of Bioengineering and Information Technology Materials, Tongji University, Shanghai, 200092, China.
Changqing ZhangDepartment of Orthopedic Surgery, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai, 200233, China.
Antoni P TomsiaMaterials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, 94720, USA.
Qiang FuMaterials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, 94720, USA.
Lawrence Berkeley National Laboratory · USShanghai Sixth People's Hospital · CNCorning (United States) · USTongji University · CN

Funding

Complex Nanocomposites for Bone RegenerationR01DE015633 · NIDCR · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI TOMSIA, ANTONI P · 2003 to 2013
$9.2M
NIDCR NIH HHS R01 DE015633
6 · The paper itself

Abstract

The repair and regeneration of loaded segmental bone defects is a challenge for both materials and biomedical science communities. Our recent work demonstrated the capability of bioactive glass in supporting bone healing and defect bridging using a rabbit femur segmental defect model without growth factors or bone marrow stromal cells (BMSCs). Here in the current work, a comprehensive in vitro evaluation of bioactive silicate (13-93) and borosilicate (2B6Sr) glass scaffolds was conducted to provide further understanding of their biological performances and to establish a correlation between in vitro and in vivo behaviors. Our in vitro evaluation using a murine MC3T3-E1 cell line confirmed the capability of both scaffolds to support cell attachment, vascular endothelial growth factor (VEGF) formation, and to stimulate mineral deposition and osteoblast marker gene expression. In particular, borosilicate (2B6Sr) glass showed a better capability in supporting the mineralization and gene expression than silicate (13-93) glass, consistent with a faster bone healing ability in vivo. The current in vitro results, combined with our previous in vivo findings, provide a strong basis for the further translational evaluation of bioactive glass scaffolds and for potential preclinical practice. © 2018 Wiley Periodicals, Inc. J. Biomed. Mater. Res. Part B, 2018. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B: 818-824, 2019.

Indexed as

Calcification, PhysiologicMaterials TestingPrinting, Three-DimensionalAnimalsCell LineGlassMiceOsteoblastsSilicatesTissue ScaffoldsSilicatesangiogenesisBioactive glassmineralization

Identifiers

PMID30195262
PMCPMC6408292
OpenAlexW2891719315

What OpenQuestion holds

Textmetadata
LicenceTDM
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.