Evidence map›Paper›PMID 30235826›Full record

ArticleSensors (Basel, Switzerland)2018

A Disposable and Multi-Chamber Film-Based PCR Chip for Detection of Foodborne Pathogen.

Nam Ho Bae, Sun Young Lim, Younseong Song, Soon Woo Jeong, Seol Yi Shin, Yong Tae Kim, Tae Jae Lee, Kyoung G Lee, Seok Jae Lee, Yong-Jun Oh and 1 more

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2018. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Application of Microfluidics for Bacterial Identification.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  3. Review
  4. Article
  5. 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

11 authors.

Nam Ho BaeDepartment of Materials Science and Engineering, Hanbat National University, Daejeon 34158, Korea. nhbae@nnfc.re.kr.
Sun Young LimNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. sylim@nnfc.re.kr.
Younseong SongNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. yssong@nnfc.re.kr.
Soon Woo JeongNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. swjeong@nnfc.re.kr.
Seol Yi ShinNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. syshin@nnfc.re.kr.
Yong Tae KimDepartment of Chemical Engineering & Biotechnology, Korea Polytechnic University, 237 Sangidaehak-ro, Siheung-si 15073, Gyeonggi-do, Korea. ytkim@kpu.ac.kr.
Tae Jae LeeNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. tjlee@nnfc.re.kr.
Kyoung G LeeNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. kglee@nnfc.re.kr.
Seok Jae LeeNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. sjlee@nnfc.re.kr.
Yong-Jun OhDepartment of Materials Science and Engineering, Hanbat National University, Daejeon 34158, Korea. yjoh@hanbat.ac.kr.
Yoo Min ParkNano-Bio Application Team, National NanoFab Center (NNFC), 291 Deahak-ro, Yuseong-gu, Daejeon 34141, Korea. ympark@nnfc.re.kr.

Funding

Ministry of Science ICT and Future Planning 2018R1C1B3001553National Research Foundation of Korea 2017M3A7B4039936Rural Development Administration PJ01252602
6 · The paper itself

Abstract

Since the increment of the threat to public health caused by foodborne pathogens, researches have been widely studied on developing the miniaturized detection system for the on-site pathogen detection. In the study, we focused on the development of portable, robust, and disposable film-based polymerase chain reaction (PCR) chip containing a multiplex chamber for simultaneous gene amplification. In order to simply fabricate and operate a film-based PCR chip, different kinds of PCR chambers were designed and fabricated using polyethylene terephthalate (PET) and polyvinyl chloride (PVC) adhesive film, in comparison with commercial PCR, which employs a stereotyped system at a bench-top scale. No reagent leakage was confirmed during the PCR thermal cycling using the film PCR chip, which indicates that the film PCR chip is structurally stable for rapid heat cycling for DNA amplification. Owing to use of the thin film to fabricate the PCR chip, we are able to realize fast thermal transfer from the heat block that leads to short PCR amplification time. Moreover, using the film PCR chip, we could even amplify the target pathogen with 10 CFU mL

Indexed as

AnimalsBacillus cereusFood ContaminationHot TemperatureMilkPolymerase Chain Reactionfilm PCR chippathogen DNA amplificationPCRpoint-of-care testing

Identifiers

PMID30235826
PMCPMC6165562

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.