One-step detection of human papilloma viral infection using quantum dot-nucleotide interaction specificity
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
31450441
DOI
10.1016/j.talanta.2019.07.006
PII: S0039-9140(19)30736-2
Knihovny.cz E-zdroje
- Klíčová slova
- Cancer, Human papillomavirus, Magnetic isolation, Nanotechnology, Quantum dots,
- MeSH
- biosenzitivní techniky metody MeSH
- dlaždicobuněčné karcinomy hlavy a krku virologie MeSH
- DNA sondy chemie genetika MeSH
- DNA virů krev chemie genetika MeSH
- dospělí MeSH
- fluorescenční mikroskopie metody MeSH
- fluorescenční spektrometrie metody MeSH
- hybridizace nukleových kyselin MeSH
- infekce papilomavirem diagnóza MeSH
- kvantové tečky chemie MeSH
- lidé MeSH
- limita detekce MeSH
- magnetické jevy MeSH
- nádorové buněčné linie MeSH
- Papillomaviridae chemie MeSH
- senioři MeSH
- sklo chemie MeSH
- sloučeniny kadmia chemie MeSH
- telur chemie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- cadmium telluride MeSH Prohlížeč
- DNA sondy MeSH
- DNA virů MeSH
- sloučeniny kadmia MeSH
- telur MeSH
Due to the close relationship between carcinogenesis and human papillomavirus (HPV), and since they are transmitted via huge number of asymptomatic carriers, the detection of HPV is really needed to reduce the risk of developing cancer. According to the best of our knowledge, our study provides the very first method for one-step detection of viral infection and if it has initiated the subsequent cancer proliferation. The proposed novel nanosystem consists of magnetic glass particles (MGPs), which were attached with DNA probe on their surface to hybridize with target DNAs. The MGP-probe-DNA hybrid was finally conjugated with CdTe/ZnSe core/shell quantum dots (QDs). The proposed detection system is based on a novel mechanism in which the MGPs separate out the target DNAs from different biological samples using external magnetic field for better and clear detection and the QDs give different fluorescent maxima for different target DNAs due to their ability to interact differently with different nucleotides. Firstly, the method was optimized using HPV genes cloned into synthetic plasmids. Then it was applied directly on the samples from normal and cancerous cells. After that, the real hospital samples of head and neck squamous cell carcinoma (HNSCC) with or without the infection of HPV were also analyzed. Our novel nano-system is proved successful in detecting and distinguishing between the patients suffering by HPV infection with or without subsequent cancer having detection limit estimated as 1.0 x 109 (GEq/mL). The proposed methodology is faster and cost-effective, which can be applied at the clinical level to help the doctors to decide the strategy of medication that may save the life of the patients with an early treatment.
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