Evidence map›Paper›PMID 31984222›Full record

ArticleACS biomaterials science & engineering2018

Fabrication of Functional Biomaterial Microstructures by in Situ Photopolymerization and Photodegradation.

Paige J LeValley, Ben Noren, Prathamesh M Kharkar, April M Kloxin, Jesse C Gatlin, John S Oakey

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Microfluidic encapsulation ofSTAR protocols · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. Article
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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

6 authors.

Paige J LeValleyDepartment of Chemical Engineering, University of Wyoming, Laramie, Wyoming 82071, United States.
Ben NorenDepartment of Chemical Engineering, University of Wyoming, Laramie, Wyoming 82071, United States.
Prathamesh M KharkarDepartment of Biomolecular and Chemical Engineering, University of Delaware, Newark, Delaware 19716, United States.
April M KloxinDepartment of Biomolecular and Chemical Engineering, University of Delaware, Newark, Delaware 19716, United States.ORCID 0000-0002-4594-2953
Jesse C GatlinDepartment of Molecular Biology, University of Wyoming, Laramie, Wyoming 82071, United States.
John S OakeyDepartment of Chemical Engineering, University of Wyoming, Laramie, Wyoming 82071, United States.ORCID 0000-0003-1023-1964

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

The in situ fabrication of poly(ethylene glycol) diacrylate (PEGDA) hydrogel microstructures within poly(dimethylsiloxane) (PDMS)-based microfluidic networks is a versatile technique that has enabled unique applications in biosensing, medical diagnostics, and the fundamental life sciences. Hydrogel structures have previously been patterned by the lithographic photopolymerization of PEGDA hydrogel forming solutions, a process that is confounded by oxygen-permeable PDMS. Here, we introduce an alternate PEG patterning technique that relies upon the optical sculpting of features by patterned light-induced erosion of photodegradable PEGDA deemed negative projection lithography. We quantitatively compared the hydrogel micropatterning fidelity of negative projection lithography to positive projection lithography, using traditional PEGDA photopolymerization, within PDMS devices. We found that the channel depth, the local oxygen atmosphere, and the UV exposure time dictated the size and resolution of hydrogel features formed using positive projection lithography. In contrast, negative projection lithography was observed to deliver high-resolution functional features with dimensions on the order of single micrometers enabled by its facilely controlled mechanism of feature formation that is insensitive to oxygen. Next, the utility of photodegradable PEGDA was further assessed by encapsulating or conjugating bioactive molecules within photodegradable PEG matrixes to provide a route to the formation of complex and dynamically reconfigurable chemical microenvironments. Finally, we demonstrated that negative projection lithography enabled photopatterning of multilayered microscale objects without the need for precise mask alignment. The described approach for photopatterning high-resolution photolabile hydrogel microstructures directly within PDMS microchannels could enable novel microsystems of increasing complexity and sophistication for a variety of clinical and biological applications.

Indexed as

biomaterialshydrogel patterningmicrofluidicsprojection lithography

Identifiers

PMID31984222
PMCPMC6980224

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Registered trials

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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.