Evidence map›Paper›PMID 26690745›Full record

ArticleACS nano2016

Nanoporous Glass Integrated in Volumetric Bar-Chart Chip for Point-of-Care Diagnostics of Non-Small Cell Lung Cancer.

Ying Li, Jie Xuan, Yujun Song, Wenjin Qi, Bangshun He, Ping Wang, Lidong Qin

Abstract read
In one paragraph

Article in ACS nano, 2016. 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
3.2field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Technologies for Frugal and Sensitive Point-of-Care Immunoassays.Annual review of analytical chemistry (Palo Alto, Calif.) · 2022
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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

7 authors at 5 institutions in 2 countries.

Ying LiDepartment of Nanomedicine, Houston Methodist Research Institute , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Jie XuanDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Yujun SongDepartment of Nanomedicine, Houston Methodist Research Institute , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Wenjin QiDepartment of Nanomedicine, Houston Methodist Research Institute , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Bangshun HeDepartment of Nanomedicine, Houston Methodist Research Institute , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Ping WangDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Lidong QinDepartment of Nanomedicine, Houston Methodist Research Institute , 6670 Bertner Avenue, Houston, Texas 77030, United States.
Houston Methodist · USMethodist Hospital · USCornell University · USFirst Affiliated Hospital of Kunming Medical University · CNNanjing Medical University · CN

Funding

Development of a Point-of-Care Volumetric Bar-Chart Chip for Drug QuantitationR01DA035868 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI QIN, LIDONG, WANG, PING · 2013 to 2020
$4.3M
NIDA NIH HHS R01 DA035868
6 · The paper itself

Abstract

Point-of-care (POC) testing has the potential to enable rapid, low-cost, and large-scale screening. POC detection of a multiplexed biomarker panel can facilitate the early diagnosis of non-small cell lung cancer (NSCLC) and, thus, may allow for more timely surgical intervention for life-saving treatment. Herein, we report the nanoporous glass (NPG) integrated volumetric bar-chart chip (V-Chip) for POC detection of the three NSCLC biomarkers CEA, CYFRA 21-1, and SCCA, by the naked eye. The 3D nanostructures in the NPG membrane efficiently increase the number of binding sites for antibodies and decrease the diffusion distance between antibody and antigen, enabling the low detection limit and rapid analysis time of the NPG-V-Chip. We utilized the NPG-V-Chip to test the NSCLC biomarker panel and found that the limit of detection can reach 50 pg/mL (10-fold improvement over the original V-Chip), and the total assay time can be decreased from 4 to 0.5 h. We then detected CEA in 21 serum samples from patients with common cancers, and the on-chip results showed good correlation with the clinical results. We further assayed 10 lung cancer samples using the device and confirmed the results obtained using conventional ELISA methods. In summary, the NPG-V-Chip platform has the ability of multiplex, low detection limit, low cost, lack of need for accessory equipment, and rapid analysis time, which may render the V-Chip a useful platform for quantitative POC detection in resource-limited settings and personalized diagnostics.

Indexed as

Antibodies, NeoplasmAntigen-Antibody ComplexAntigens, NeoplasmBiomarkers, TumorCarcinoembryonic AntigenCarcinoma, Non-Small-Cell LungEarly DiagnosisGene ExpressionGlassHumansKeratin-19Lab-On-A-Chip DevicesLimit of DetectionLung NeoplasmsNanostructuresPoint-of-Care SystemsAntibodies, NeoplasmAntigen-Antibody Complexantigen CYFRA21.1Antigens, NeoplasmBiomarkers, TumorCarcinoembryonic AntigenKeratin-19Serpinssquamous cell carcinoma-related antigenbiomarker detectionmicrofluidicsnanoporous glassNSCLCpoint-of-care testingV-Chip

Identifiers

PMID26690745
PMCPMC4934604
OpenAlexW2220784393

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.