Optical Interferometric Device for Rapid and Specific Detection of Biological Cells
Here, we report a rapid and accurate optical method for detecting cells from liquid samples in a label-free manner. The working principle of the method is based on the interference of parts of a conical laser beam, coming from a single-mode optical fiber directly, and reflected from a flat glass sur...
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Published in | Biosensors (Basel) Vol. 14; no. 9; p. 421 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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29.08.2024
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Abstract | Here, we report a rapid and accurate optical method for detecting cells from liquid samples in a label-free manner. The working principle of the method is based on the interference of parts of a conical laser beam, coming from a single-mode optical fiber directly, and reflected from a flat glass surface. The glass is functionalized by antibodies against the cells to be detected from the liquid sample. Cells bound to that surface modify the reflected beam, and hence, change the resulting interference pattern, too. By registering and interpreting the variation in the image, the presence of cells from the sample can be detected. As for a demonstration, cell suspensions from a U937 cell line were used in glass chambers functionalized by antibodies (TMG6-5 (mIgG1)) to which the cells specifically bind. The limit of detection (LOD) of the method was also estimated. This proof-of-concept setup offers a cost-effective and easy-to-use way of rapid and specific detection of any type of cells (including pathogens) from suspensions (e.g., body fluids). The possible portability of the device predicts its applicability as a rapid test in clinical diagnostics. |
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AbstractList | Here, we report a rapid and accurate optical method for detecting cells from liquid samples in a label-free manner. The working principle of the method is based on the interference of parts of a conical laser beam, coming from a single-mode optical fiber directly, and reflected from a flat glass surface. The glass is functionalized by antibodies against the cells to be detected from the liquid sample. Cells bound to that surface modify the reflected beam, and hence, change the resulting interference pattern, too. By registering and interpreting the variation in the image, the presence of cells from the sample can be detected. As for a demonstration, cell suspensions from a U937 cell line were used in glass chambers functionalized by antibodies (TMG6-5 (mIgG1)) to which the cells specifically bind. The limit of detection (LOD) of the method was also estimated. This proof-of-concept setup offers a cost-effective and easy-to-use way of rapid and specific detection of any type of cells (including pathogens) from suspensions (e.g., body fluids). The possible portability of the device predicts its applicability as a rapid test in clinical diagnostics.Here, we report a rapid and accurate optical method for detecting cells from liquid samples in a label-free manner. The working principle of the method is based on the interference of parts of a conical laser beam, coming from a single-mode optical fiber directly, and reflected from a flat glass surface. The glass is functionalized by antibodies against the cells to be detected from the liquid sample. Cells bound to that surface modify the reflected beam, and hence, change the resulting interference pattern, too. By registering and interpreting the variation in the image, the presence of cells from the sample can be detected. As for a demonstration, cell suspensions from a U937 cell line were used in glass chambers functionalized by antibodies (TMG6-5 (mIgG1)) to which the cells specifically bind. The limit of detection (LOD) of the method was also estimated. This proof-of-concept setup offers a cost-effective and easy-to-use way of rapid and specific detection of any type of cells (including pathogens) from suspensions (e.g., body fluids). The possible portability of the device predicts its applicability as a rapid test in clinical diagnostics. Here, we report a rapid and accurate optical method for detecting cells from liquid samples in a label-free manner. The working principle of the method is based on the interference of parts of a conical laser beam, coming from a single-mode optical fiber directly, and reflected from a flat glass surface. The glass is functionalized by antibodies against the cells to be detected from the liquid sample. Cells bound to that surface modify the reflected beam, and hence, change the resulting interference pattern, too. By registering and interpreting the variation in the image, the presence of cells from the sample can be detected. As for a demonstration, cell suspensions from a U937 cell line were used in glass chambers functionalized by antibodies (TMG6-5 (mIgG1)) to which the cells specifically bind. The limit of detection (LOD) of the method was also estimated. This proof-of-concept setup offers a cost-effective and easy-to-use way of rapid and specific detection of any type of cells (including pathogens) from suspensions (e.g., body fluids). The possible portability of the device predicts its applicability as a rapid test in clinical diagnostics. |
Audience | Academic |
Author | Biczók, Brigitta Petrovszki, Dániel Dósa, Kevin Nagy, Krisztina Andó, István Valkai, Sándor Baumgärtner, Margaréta Kocsis, Anna E Dér, András Fáskerti, Zsombor Dakos, Kira Kirner, Berill B |
AuthorAffiliation | 3 Hungarian Research Network, Biological Research Centre, Institute of Genetics, 6726 Szeged, Hungary; ando.istvan@brc.hu 1 Hungarian Research Network, Biological Research Centre, Institute of Biophysics, 6726 Szeged, Hungary; danielpetrovszki37@gmail.com (D.P.); kocsis.anna@brc.hu (A.E.K.); nagy.krisztina@brc.hu (K.N.); der.andras@brc.hu (A.D.) 2 Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary; zsomborkongorf@gmail.com (Z.F.); baumgartnermargareta@gmail.com (M.B.); biczok.brigi@gmail.com (B.B.); d.kira00@icloud.com (K.D.); kevind737@outlook.com (K.D.); berillkirner@gmail.com (B.B.K.) |
AuthorAffiliation_xml | – name: 3 Hungarian Research Network, Biological Research Centre, Institute of Genetics, 6726 Szeged, Hungary; ando.istvan@brc.hu – name: 1 Hungarian Research Network, Biological Research Centre, Institute of Biophysics, 6726 Szeged, Hungary; danielpetrovszki37@gmail.com (D.P.); kocsis.anna@brc.hu (A.E.K.); nagy.krisztina@brc.hu (K.N.); der.andras@brc.hu (A.D.) – name: 2 Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary; zsomborkongorf@gmail.com (Z.F.); baumgartnermargareta@gmail.com (M.B.); biczok.brigi@gmail.com (B.B.); d.kira00@icloud.com (K.D.); kevind737@outlook.com (K.D.); berillkirner@gmail.com (B.B.K.) |
Author_xml | – sequence: 1 givenname: Sándor orcidid: 0000-0001-8479-8141 surname: Valkai fullname: Valkai, Sándor organization: Hungarian Research Network, Biological Research Centre, Institute of Biophysics, 6726 Szeged, Hungary – sequence: 2 givenname: Dániel orcidid: 0000-0002-7736-2144 surname: Petrovszki fullname: Petrovszki, Dániel organization: Hungarian Research Network, Biological Research Centre, Institute of Biophysics, 6726 Szeged, Hungary – sequence: 3 givenname: Zsombor surname: Fáskerti fullname: Fáskerti, Zsombor organization: Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary – sequence: 4 givenname: Margaréta orcidid: 0009-0005-0043-0662 surname: Baumgärtner fullname: Baumgärtner, Margaréta organization: Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary – sequence: 5 givenname: Brigitta surname: Biczók fullname: Biczók, Brigitta organization: Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary – sequence: 6 givenname: Kira surname: Dakos fullname: Dakos, Kira organization: Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary – sequence: 7 givenname: Kevin orcidid: 0009-0005-2283-5556 surname: Dósa fullname: Dósa, Kevin organization: Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary – sequence: 8 givenname: Berill B surname: Kirner fullname: Kirner, Berill B organization: Faculty of Science and Informatics, University of Szeged, 6720 Szeged, Hungary – sequence: 9 givenname: Anna E surname: Kocsis fullname: Kocsis, Anna E organization: Hungarian Research Network, Biological Research Centre, Institute of Biophysics, 6726 Szeged, Hungary – sequence: 10 givenname: Krisztina surname: Nagy fullname: Nagy, Krisztina organization: Hungarian Research Network, Biological Research Centre, Institute of Biophysics, 6726 Szeged, Hungary – sequence: 11 givenname: István orcidid: 0000-0002-4648-9396 surname: Andó fullname: Andó, István organization: Hungarian Research Network, Biological Research Centre, Institute of Genetics, 6726 Szeged, Hungary – sequence: 12 givenname: András orcidid: 0000-0001-6112-884X surname: Dér fullname: Dér, András organization: Hungarian Research Network, Biological Research Centre, Institute of Biophysics, 6726 Szeged, Hungary |
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Cites_doi | 10.1002/lpor.201100025 10.3390/diagnostics10100841 10.1016/j.snb.2010.09.064 10.1016/j.nantod.2009.04.001 10.1016/j.bioelechem.2015.07.010 10.3390/mi14091668 10.1016/j.mee.2021.111523 10.1085/jgp.7.2.235 10.1016/j.biomaterials.2004.04.002 10.3390/biomedicines10010188 10.1002/ijc.2910170504 10.4049/jimmunol.109.1.129 10.1016/j.bios.2013.05.007 10.1016/j.bios.2019.05.012 10.1364/AO.48.002880 10.1039/C9AN01485C 10.1016/j.imbio.2012.07.031 10.1186/1479-5876-11-197 10.1088/0957-4484/14/8/312 10.1016/j.biosx.2023.100352 |
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Snippet | Here, we report a rapid and accurate optical method for detecting cells from liquid samples in a label-free manner. The working principle of the method is... |
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SubjectTerms | Antibodies biological cells Biosensing Techniques Body fluids Cell surface Cell suspensions Cells Communication easy-to-use tool Fiber lasers Fiber optics Glass substrates Humans Interferometry label-free biosensor Laser beams Lasers Light Limit of Detection Optical Fibers Optics point of care proof of concept Sedimentation & deposition U937 Cells Viral antibodies |
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Title | Optical Interferometric Device for Rapid and Specific Detection of Biological Cells |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39329796 https://www.proquest.com/docview/3110381939 https://www.proquest.com/docview/3110408080 https://pubmed.ncbi.nlm.nih.gov/PMC11430435 https://doaj.org/article/e737b1fd31a244f389e1afceceacb425 |
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