Evidence map›Paper›PMID 34641110›Full record

ArticlePolymers2021

Nanoplasmonic Structure of a Polycarbonate Substrate Integrated with Parallel Microchannels for Label-Free Multiplex Detection.

Yi-Jung Lu, Han-Yun Hsieh, Wen-Chang Kuo, Pei-Kuen Wei, Horn-Jiunn Sheen, Hidetoshi Tahara, Te-Wei Chiu, Yu-Jui Fan

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2021. 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
0.5field-weighted citation impact, top 39% 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, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Highly Sensitive TiOBiosensors · 2022
    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 at 6 institutions in 2 countries.

Yi-Jung LuDivision of Family and Operative Dentistry, Department of Dentistry, Taipei Medical University Hospital, Taipei 11031, Taiwan.
Han-Yun HsiehInstitute of Applied Mechanics, National Taiwan University, Taipei 10617, Taiwan.ORCID 0000-0002-7756-0167
Wen-Chang KuoInstitute of Applied Mechanics, National Taiwan University, Taipei 10617, Taiwan.
Pei-Kuen WeiResearch Center for Applied Sciences, Academia Sinica, Nankang, Taipei 11529, Taiwan.
Horn-Jiunn SheenInstitute of Applied Mechanics, National Taiwan University, Taipei 10617, Taiwan.
Hidetoshi TaharaDepartment of Cellular and Molecular Biology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima 734-8553, Japan.ORCID 0000-0003-3054-4175
Te-Wei ChiuDepartment of Materials and Mineral Resources Engineering, National Taipei University of Technology, Taipei 10608, Taiwan.ORCID 0000-0002-2625-2906
Yu-Jui FanSchool of Biomedical Engineering, Taipei Medical University, Taipei 11031, Taiwan.
Hiroshima University · JPNational Taiwan University · TWNational Taipei University of Technology · TWResearch Center for Applied Science, Academia Sinica · TWTaipei Medical University · TWTaipei Medical University Hospital · TW

Funding

Ministry of Science and Technology, Taiwan 110-2636-E-038-004Taipei Medical University Hospital 110TMU-TMUH-05
6 · The paper itself

Abstract

In this study, a multiplex detection system was proposed by integrating a localized surface plasmon resonance (LSPR) sensing array and parallel microfluidic channels. The LSPR sensing array was fabricated by nanoimprinting and gold sputter on a polycarbonate (PC) substrate. The polydimethylsiloxane (PDMS) microfluidic channels and PC LSPR sensing array were bound together through (3-aminopropyl)triethoxysilane (APTES) surface treatment and oxygen plasma treatment. The resonant spectrum of the LSPR sensing device was obtained by broadband white-light illumination and polarized wavelength measurements with a spectrometer. The sensitivity of the LSPR sensing device was measured using various ratios of glycerol to water solutions with different refractive indices. Multiplex detection was demonstrated using human immunoglobulin G (IgG), IgA, and IgM. The anti-IgG, anti-IgA, and anti-IgM were separately modified in each sensing region. Various concentrations of human IgG, IgA, and IgM were prepared to prove the concept that the parallel sensing device can be used to detect different targets.

Indexed as

biosensormultiplex detectionnanoimprintingsurface plasmon resonance (SPR)

Identifiers

PMID34641110
PMCPMC8512492
OpenAlexW3201986945

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.