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Prinjaporn Teengam

Researcher at Chulalongkorn University

Publications -  16
Citations -  1007

Prinjaporn Teengam is an academic researcher from Chulalongkorn University. The author has contributed to research in topics: Detection limit & Oligonucleotide. The author has an hindex of 9, co-authored 13 publications receiving 643 citations.

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Multiplex Paper-Based Colorimetric DNA Sensor Using Pyrrolidinyl Peptide Nucleic Acid-Induced AgNPs Aggregation for Detecting MERS-CoV, MTB, and HPV Oligonucleotides

TL;DR: A paper-based colorimetric assay for DNA detection based on pyrrolidinyl peptide nucleic acid (acpcPNA)-induced nanoparticle aggregation is reported as an alternative to traditional colorimetry approaches.
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Electrochemistry on Paper‐based Analytical Devices: A Review

TL;DR: Recent advances in ePAD development and application are reviewed, focusing on electrode fabrication techniques and examples of applications specially focused on environmental monitoring, biological applications and clinical assays.
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Electrochemical paper-based peptide nucleic acid biosensor for detecting human papillomavirus.

TL;DR: A novel paper-based electrochemical biosensor using an anthraquinone-labeled pyrrolidinyl peptide nucleic acid probe (AQ-PNA) probe and graphene-polyaniline modified electrode to detect human papillomavirus (HPV) type 16 is promising for the screening and monitoring of the amount of HPV-DNA type 16 to identify the primary stages of cervical cancer.
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Pop-up paper electrochemical device for label-free hepatitis B virus DNA detection

TL;DR: In this article, a pop-up DNA device was proposed for point-of-care point-to-care HBV DNA detection using 3D microfluidic paper-based analytical device (μPAD) platform.
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Electrochemical impedance-based DNA sensor using pyrrolidinyl peptide nucleic acids for tuberculosis detection

TL;DR: A label-free electrochemical DNA sensor based on pyrrolidinyl peptide nucleic acid covalently immobilized on a paper-based analytical device (PAD) that exhibited very high selectivity for complementary oligonucleotides over single-base-mismatch, two- base- mismatch and non-complementary DNA targets.