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Antibodies Modified by Gold Nanoparticles or Quantum Dots For Specific Detection of Sarcosine on The Membrane: Use in Rapid Diagnostics

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F18%3A43915222" target="_blank" >RIV/60461373:22330/18:43915222 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/18:10392581

  • Result on the web

    <a href="https://www.nanocon.eu/files/uploads/01/NANOCON2017_Proceedings_content.pdf" target="_blank" >https://www.nanocon.eu/files/uploads/01/NANOCON2017_Proceedings_content.pdf</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Antibodies Modified by Gold Nanoparticles or Quantum Dots For Specific Detection of Sarcosine on The Membrane: Use in Rapid Diagnostics

  • Original language description

    Paper tests are very cheap and fast diagnostic tools for self-testing in a wide range of health problems. Thus, the diagnostics of tumor development is of a great medical and socio-economic significance. Malignant prostate cancers are the most common malignancy in men. Procedures have been developed to diagnose this disease based on the monitoring of tumor marker molecules. Most commonly, PSA and fPSA are used. Although these tumor markers are significantly increased, the cancer at the biopsy is not always confirmed. Thus, the finding of other marker molecules is urgently needed. Recent studies have shown that changes in content of the amino acid sarcosine are associated with prostate tumors. Polyclonal chicken antibodies against sarcosine (AntiSar) were prepared. AntiSar antibodies were labeled with gold nanoparticles Au20 (size 20-30 nm, zeta potential - 38 mV) and CdTe QDs (emission 530 green QDs and 650 nm yellow QDs). Dot blot and flow lateral chromatography were used to develop a newly designed sarcosin detection procedure. The aggregation or fluorescence intensities were evaluated by newly designed software. Sarcosine was analyzed in a concentration range (0-150 μM) in PBS, arteficial urine and urine sample buffer. The calibration curves obtained in the concentration range (0-12 μM) were strictly linear (R2 = 0.99) with a relative error of 10%. Using the proposed methods sarcosine concentrations as low as 250-500 nM were analyzed. Moreover, the results obtained show a higher sensitivity (by 20-40%) of sarcosine detection using QDs in comparison with using gold nanoparticles.

  • Czech name

  • Czech description

Classification

  • Type

    D - Article in proceedings

  • CEP classification

  • OECD FORD branch

    21002 - Nano-processes (applications on nano-scale); (biomaterials to be 2.9)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Article name in the collection

    Nanocon 2017

  • ISBN

    978-80-87294-81-9

  • ISSN

  • e-ISSN

    neuvedeno

  • Number of pages

    6

  • Pages from-to

    517-523

  • Publisher name

    Tanger s.r.o.

  • Place of publication

    Ostrava

  • Event location

    Brno

  • Event date

    Oct 18, 2017

  • Type of event by nationality

    WRD - Celosvětová akce

  • UT code for WoS article

    000452823300085