Evidence map›Paper›PMID 30497010›Full record

ArticleColloids and surfaces. B, Biointerfaces2019

Immunofunctional photodegradable poly(ethylene glycol) hydrogel surfaces for the capture and release of rare cells.

Paige J LeValley, Mark W Tibbitt, Ben Noren, Prathamesh Kharkar, April M Kloxin, Kristi S Anseth, Mehmet Toner, John Oakey

Abstract read
In one paragraph

Article in Colloids and surfaces. B, Biointerfaces, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Urinary biomarkers for lung cancer detection.The journal of liquid biopsy · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Microfluidics for the Isolation and Detection of Circulating Tumor Cells.Advances in experimental medicine and biology · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Cell Separations and Sorting.Analytical chemistry · 2020
    Review
  15. 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

8 authors.

Paige J LeValleyDepartment of Chemical Engineering, University of Wyoming, Laramie, WY 82071, United States; Department of Biomolecular and Chemical Engineering, University of Delaware, Newark, DE 19716, United States.
Mark W TibbittDepartment of Chemical and Biological Engineering, University of Colorado Boulder,Boulder, CO 80309, United States; Department of Mechanical and Process Engineering, ETH Zürich, Zürich, 8092, Switzerland.
Ben NorenDepartment of Chemical Engineering, University of Wyoming, Laramie, WY 82071, United States.
Prathamesh KharkarDepartment of Biomolecular and Chemical Engineering, University of Delaware, Newark, DE 19716, United States.
April M KloxinDepartment of Biomolecular and Chemical Engineering, University of Delaware, Newark, DE 19716, United States.
Kristi S AnsethDepartment of Chemical and Biological Engineering, University of Colorado Boulder,Boulder, CO 80309, United States; BioFrontiers Institute, University of Colorado Boulder, Boulder, CO 80309, United States; Howard Hughes Medical Institute, University of Colorado Boulder, Boulder, CO 80309, United States.
Mehmet TonerBioMEMS Resource Center, Center for Engineering in Medicine and Surgical Services, Massachusetts General Hospital, Shriners Hospital for Children and Harvard Medical School, Boston, MA 02114, United States.
John OakeyDepartment of Chemical Engineering, University of Wyoming, Laramie, WY 82071, United States. Electronic address: joakey@uwyo.edu.

Funding

Wyoming INBRE Phase 4- Equipment Supplement for x-ray diffractometer for Center for Advanced Scientific InstrumentationP20GM103432 · NIGMS · UNIVERSITY OF WYOMING · PI Robert Scott Seville · 2012 to 2026
$56.8M
This renovation project will create over 1455 sq. ft. of state- of-the-art reseaP20GM104316 · NIGMS · UNIVERSITY OF DELAWARE · PI FOX, JOSEPH M · 2014 to 2024
$26.8M
Pilot Research Subproject ProgramP30GM110758 · NIGMS · UNIVERSITY OF DELAWARE · PI BEEBE, THOMAS PAUL · 2014 to 2018
$5.8M
Mechanics of Bipolar Mitotic Spindle AssemblyR01GM102428 · NIGMS · UNIVERSITY OF WYOMING · PI GATLIN, JESSE C · 2012 to 2016
$1.3M
Spindle Assembly and Scaling via Microfluidic Encapsulation of Xenopus NucleiR15GM101636 · NIGMS · UNIVERSITY OF WYOMING · PI OAKEY, JOHN S · 2012 to 2012
$313k
NIGMS NIH HHS P20 GM103432NIGMS NIH HHS P20 GM104316NIGMS NIH HHS P30 GM110758NIGMS NIH HHS R01 GM102428NIGMS NIH HHS R15 GM101636
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) play a central role in cancer metastasis and represent a rich source of data for cancer prognostics and therapeutic guidance. Reliable CTC recovery from whole blood therefore promises a less invasive and more sensitive approach to cancer diagnosis and progression tracking. CTCs, however, are exceedingly rare in whole blood, making their quantitative recovery challenging. Several techniques capable of isolating these rare cells have been introduced and validated, yet most suffer from low CTC purity or viability, both of which are essential to develop a clinically viable CTC isolation platform. To address these limitations, we introduce a patterned, immunofunctional, photodegradable poly(ethylene glycol) (PEG) hydrogel capture surface for the isolation and selective release of rare cell populations. Flat and herringbone capture surfaces were successfully patterned via PDMS micromolding and photopolymerization of photolabile PEG hydrogels. Patterned herringbone surfaces, designed to convectively transport cells to the capture surface, exhibited improved capture density relative to flat surfaces for target cell capture from buffer, buffy coat, and whole blood. Uniquely, captured cells were released for collection by degrading the hydrogel capture surface with either bulk or targeted irradiation with cytocompatible doses of long wavelength UV light. Recovered cells remained viable following capture and release and exhibited similar growth rates as untreated control cells. The implementation of molded photodegradable PEG hydrogels as a CTC capture surface provides a micropatternable, cytocompatible platform that imparts the unique ability to recover pure, viable CTC samples by selectively releasing target cells.

Indexed as

Antibodies, ImmobilizedAntigens, NeoplasmBiocompatible MaterialsCell SeparationHumansHydrogelsLung NeoplasmsMicrofluidic Analytical TechniquesNeoplastic Cells, CirculatingPhotolysisPolyethylene GlycolsTumor Cells, CulturedAntibodies, ImmobilizedAntigens, NeoplasmBiocompatible MaterialsHydrogelsPolyethylene GlycolsBiomaterialsCirculating tumor cellImmunocaptureMicrofluidics

Identifiers

PMID30497010
PMCPMC6545105

What OpenQuestion holds

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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.