Evidence map›Paper›PMID 35071210›Full record

ArticleFrontiers in bioengineering and biotechnology2021

Surface Modification of Polycaprolactone Scaffold With Improved Biocompatibility and Controlled Growth Factor Release for Enhanced Stem Cell Differentiation.

Xiaoyan Qin, Yixin Wu, Shuang Liu, Lei Yang, Hongxia Yuan, Susu Cai, Julia Flesch, Zehao Li, Yujing Tang, Xiaomin Li and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 48 citations in OpenAlex.

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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 5 institutions in 2 countries.

Xiaoyan QinCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Yixin WuCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Shuang LiuCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Lei YangDepartment of Spine Surgery, The First Affiliated Hospital, Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China.
Hongxia YuanCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Susu CaiCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Julia FleschDepartment of Biology/Chemistry, University of Osnabrück, Osnabrück, Germany.
Zehao LiCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Yujing TangSINOPEC, Beijing Research Institute of Chemical Industry, Beijing, China.
Xiaomin LiSINOPEC, Beijing Research Institute of Chemical Industry, Beijing, China.
Yi ZhuangScience and Technology Department China Petrochemical Corporation, Beijing, China.
Changjiang YouDepartment of Biology/Chemistry, University of Osnabrück, Osnabrück, Germany.
Chaoyong LiuCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Changyuan YuCollege of Life Sciences and Technology, Beijing University of Chemical Technology, Beijing, China.
Beijing University of Chemical Technology · CNBeijing Chemical Industry Research Institute (China) · CNOsnabrück University · DEBeijing Institute of Petrochemical Technology · CNShenzhen Second People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polycaprolactone (PCL) has been widely used as a scaffold material for tissue engineering. Reliable applications of the PCL scaffolds require overcoming their native hydrophobicity and obtaining the sustained release of signaling factors to modulate cell growth and differentiation. Here, we report a surface modification strategy for electrospun PCL nanofibers using an azide-terminated amphiphilic graft polymer. With multiple alkylation and pegylation on the side chains of poly-L-lysine, stable coating of the graft polymer on the PCL nanofibers was achieved in one step. Using the azide-alkyne "click chemistry", we functionalized the azide-pegylated PCL nanofibers with dibenzocyclooctyne-modified nanocapsules containing growth factor, which rendered the nanofiber scaffold with satisfied cell adhesion and growth property. Moreover, by specific immobilization of pH-responsive nanocapsules containing bone morphogenetic protein 2 (BMP-2), controlled release of active BMP-2 from the PCL nanofibers was achieved within 21 days. When bone mesenchyme stem cells were cultured on this nanofiber scaffold, enhanced ossification was observed in correlation with the time-dependent release of BMP-2. The established surface modification can be extended as a generic approach to hydrophobic nanomaterials for longtime sustainable release of multiplex signaling proteins for tissue engineering.

Indexed as

cell differentiationcontrolled releasegrowth factorpolycaprolactone scaffoldsurface modification

Identifiers

PMID35071210
PMCPMC8782149
OpenAlexW4206698867

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.