Evidence map›Paper›PMID 31549085›Full record

ArticleResearch (Washington, D.C.)2019

Geometric Flow Control Lateral Flow Immunoassay Devices (GFC-LFIDs): A New Dimension to Enhance Analytical Performance.

E Eriksson, J Lysell, H Larsson, K Y Cheung, D Filippini, W C Mak

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
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.

E ErikssonBiosensors and Bioelectronics Centre, IFM-Linköping University, 58183 Linköping, Sweden.
J LysellBiosensors and Bioelectronics Centre, IFM-Linköping University, 58183 Linköping, Sweden.
H LarssonBiosensors and Bioelectronics Centre, IFM-Linköping University, 58183 Linköping, Sweden.
K Y CheungIKE-Linköping University, 58185 Linköping, Sweden.
D FilippiniOptical Devices Laboratory, IFM-Linköping University, 58183 Linköping, Sweden.ORCID https://orcid.org/0000-0002-4938-1524
W C MakBiosensors and Bioelectronics Centre, IFM-Linköping University, 58183 Linköping, Sweden.ORCID https://orcid.org/0000-0003-3274-6029

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nitrocellulose (NC) membrane based lateral flow immunoassay device (LFID) is one of the most important and widely used biosensor platforms for point-of-care (PoC) diagnostics. However, the analytical performance of LFID has limitations and its optimization is restricted to the bioassay chemistry, the membrane porosity, and the choice of biolabel system. These bottom neck technical issues resulted from the fact that the conventional LFID design principle has not evolved for many years, which limited the LFID for advanced biosensor applications. Here we introduce a new dimension for LFID design and optimization based on geometric flow control (GFC) of NC membranes, leading to highly sensitive GFC-LFID. This novel approach enables comprehensive flow control via different membrane geometric features such as the width (

Identifiers

PMID31549085
PMCPMC6750055

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.