Evidence map›Paper›PMID 26072363›Full record

ArticleActa biomaterialia2015

Pendant allyl crosslinking as a tunable shape memory actuator for vascular applications.

Timothy C Boire, Mukesh K Gupta, Angela L Zachman, Sue Hyun Lee, Daniel A Balikov, Kwangho Kim, Leon M Bellan, Hak-Joon Sung

Abstract read
In one paragraph

Article in Acta biomaterialia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Heparin-functionalized polymer graft surface eluting MK2 inhibitory peptide to improve hemocompatibility and anti-neointimal activity.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Timothy C Boire *† Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, United States.
Mukesh K Gupta *† Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, United States.
Angela L Zachman† Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, United States.
Sue Hyun Lee† Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, United States.
Daniel A Balikov† Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, United States.
Kwangho KimInstitute of Chemical Biology, Nashville, TN, 37235, United States.
Leon M Bellan† Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, United States.
Hak-Joon Sung† Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, United States.

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI MCGUINNESS, OWEN P · 1986 to 2011
$28.1M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Kevin L Schey · 1989 to 2026
$19.6M
THREE-TIERED PREVENTION MODEL TO BETTER SERVE ALL STUDENP30HD015052 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1985 to 2014
$18.6M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
3D Microvascular Networks in Hydrogels Fabricated with Sacrificial StructuresR00EB013630 · NIBIB · VANDERBILT UNIVERSITY · PI BELLAN, LEON MARCEL · 2013 to 2015
$709k
3D Microvascular Networks in Hydrogels Fabricated with Sacrificial StructuresK99EB013630 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BELLAN, LEON MARCEL · 2011 to 2012
$175k
3D Microvascular Networks in Biomaterials Fabricated with Sacrificial StructuresF32EB011866 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BELLAN, LEON MARCEL · 2010 to 2010
$50k
NCI NIH HHS CA68485NCI NIH HHS P30 CA068485NEI NIH HHS EY08126NEI NIH HHS P30 EY008126NIBIB NIH HHS F32 EB011866NIBIB NIH HHS K99 EB013630NIBIB NIH HHS R00 EB013630NICHD NIH HHS HD15052NICHD NIH HHS P30 HD015052NIDDK NIH HHS DK20593NIDDK NIH HHS DK58404NIDDK NIH HHS DK59637NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS U24 DK059637NIGMS NIH HHS T32 GM007347
6 · The paper itself

Abstract

Thermo-responsive shape memory polymers (SMPs) can be programmed to fit into small-bore incisions and recover their functional shape upon deployment in the body. This property is of significant interest for developing the next generation of minimally-invasive medical devices. To be used in such applications, SMPs should exhibit adequate mechanical strengths that minimize adverse compliance mismatch-induced host responses (e.g. thrombosis, hyperplasia), be biodegradable, and demonstrate switch-like shape recovery near body temperature with favorable biocompatibility. Combinatorial approaches are essential in optimizing SMP material properties for a particular application. In this study, a new class of thermo-responsive SMPs with pendant, photocrosslinkable allyl groups, x%poly(ε-caprolactone)-co-y%(α-allyl carboxylate ε-caprolactone) (x%PCL-y%ACPCL), are created in a robust, facile manner with readily tunable material properties. Thermomechanical and shape memory properties can be drastically altered through subtle changes in allyl composition. Molecular weight and gel content can also be altered in this combinatorial format to fine-tune material properties. Materials exhibit highly elastic, switch-like shape recovery near 37°C. Endothelial compatibility is comparable to tissue culture polystyrene (TCPS) and 100%PCL in vitro and vascular compatibility is demonstrated in vivo in a murine model of hindlimb ischemia, indicating promising suitability for vascular applications. STATEMENT OF SIGNIFICANCE: With the ongoing thrust to make surgeries minimally-invasive, it is prudent to develop new biomaterials that are highly compatible and effective in this workflow. Thermo-responsive shape memory polymers (SMPs) have great potential for minimally-invasive applications because SMP medical devices (e.g. stents, grafts) can fit into small-bore minimally-invasive surgical devices and recover their functional shape when deployed in the body. To realize their potential, it is imperative to devise combinatorial approaches that enable optimization of mechanical, SM, and cellular responses for a particular application. In this study, a new class of thermo-responsive SMPs is created in a robust, facile manner with readily tunable material properties. Materials exhibit excellent, switch-like shape recovery near body temperature and promising biocompatibility for minimally-invasive vascular applications.

Indexed as

Blood Vessel ProsthesisMaterials TestingAnimalsBlood Vessel Prosthesis ImplantationCross-Linking ReagentsDisease Models, AnimalHindlimbHumansHuman Umbilical Vein Endothelial CellsIschemiaMicePolystyrenesCross-Linking ReagentsPolystyrenesAllylic compoundsBiocompatibilityShape memory polymersStructure–function relationshipsThermally responsive materials

Identifiers

PMID26072363
PMCPMC4560603

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.