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Detection of Pancreatic Cancer miRNA with Biocompatible Nitrogen-Doped Graphene Quantum Dots.
Ajgaonkar, Ryan; Lee, Bong; Valimukhametova, Alina; Nguyen, Steven; Gonzalez-Rodriguez, Roberto; Coffer, Jeffery; Akkaraju, Giridhar R; Naumov, Anton V.
  • Ajgaonkar R; School of Medicine, University of Texas Rio Grande Valley, Edinburg, TX 78539, USA.
  • Lee B; Department of Biology, Texas Christian University, Fort Worth, TX 76129, USA.
  • Valimukhametova A; Department of Physics and Astronomy, Texas Christian University, Fort Worth, TX 76129, USA.
  • Nguyen S; Department of Physics and Astronomy, Texas Christian University, Fort Worth, TX 76129, USA.
  • Gonzalez-Rodriguez R; Department of Physics and Astronomy, Texas Christian University, Fort Worth, TX 76129, USA.
  • Coffer J; Department of Physics, University of North Texas, Denton, TX 76203, USA.
  • Akkaraju GR; Department of Chemistry and Biochemistry, Texas Christian University, Fort Worth, TX 76129, USA.
  • Naumov AV; Department of Biology, Texas Christian University, Fort Worth, TX 76129, USA.
Materials (Basel) ; 15(16)2022 Aug 20.
Article in English | MEDLINE | ID: covidwho-2023877
ABSTRACT
Early-stage pancreatic cancer remains challenging to detect, leading to a poor five-year patient survival rate. This obstacle necessitates the development of early detection approaches based on novel technologies and materials. In this work, the presence of a specific pancreatic cancer-derived miRNA (pre-miR-132) is detected using the fluorescence properties of biocompatible nitrogen-doped graphene quantum dots (NGQDs) synthesized using a bottom-up approach from a single glucosamine precursor. The sensor platform is comprised of slightly positively charged (1.14 ± 0.36 mV) NGQDs bound via π-π stacking and/or electrostatic interactions to the negatively charged (-22.4 ± 6.00 mV) bait ssDNA; together, they form a complex with a 20 nm average size. The NGQDs' fluorescence distinguishes specific single-stranded DNA sequences due to bait-target complementarity, discriminating them from random control sequences with sensitivity in the micromolar range. Furthermore, this targetability can also detect the stem and loop portions of pre-miR-132, adding to the practicality of the biosensor. This non-invasive approach allows cancer-specific miRNA detection to facilitate early diagnosis of various forms of cancer.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article Affiliation country: Ma15165760

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article Affiliation country: Ma15165760