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https://hdl.handle.net/11147/14255
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DC Field | Value | Language |
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dc.contributor.author | Yücel, Müge | - |
dc.contributor.author | Onbaş, Rabia | - |
dc.contributor.author | Arslan Yıldız, Ahu | - |
dc.contributor.author | Yıldız, Ümit Hakan | - |
dc.date.accessioned | 2024-01-30T09:24:43Z | - |
dc.date.available | 2024-01-30T09:24:43Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 1616-5187 | - |
dc.identifier.issn | 1616-5195 | - |
dc.identifier.uri | https://doi.org/10.1002/mabi.202300402 | - |
dc.identifier.uri | https://hdl.handle.net/11147/14255 | - |
dc.description.abstract | This study describes the formation, size control, and penetration behavior of polymer nanodots (Pdots) consisting of single or few chain polythiophene-based conjugated polyelectrolytes (CPEs) via nanophase separation between good solvent and poor solvent of CPE. Though the chain singularity may be associated with dilution nanophase separation suggests that molecules of a good solvent create a thermodynamically driven solvation layer surrounding the CPEs and thereby separating the single chains even in their poor solvents. This statement is therefore corroborated with emission intensity/lifetime, particle size, and scattering intensity of polyelectrolyte in good and poor solvents. Regarding the augmented features, Pdots are implemented into cell imaging studies to understand the nuclear penetration and to differentiate the invasive characteristics of breast cancer cells. The python based red, green, blue (RGB) color analysis depicts that Pdots have more nuclear penetration ability in triple negative breast cancer cells due to the different nuclear morphology in shape and composition and Pdots have penetrated cell membrane as well as extracellular matrix in spheroid models. The current Pdot protocol and its utilization in cancer cell imaging are holding great promise for gene/drug delivery to target cancer cells by explicitly achieving the very first priority of nuclear intake. The penetration capability of cationic soft nanodots in to tumor models of breast cancer is demonstrated. The image analysis based on fluorescence intensity variation reveals the characteristics of translocation of nanodots in dense mediums such as tumor models.image | en_US |
dc.description.sponsorship | This work was supported by the Scientific and Technological Research Council of Turkey TUBITAK Project Nos: 116Z547 and 120Z588 and & Idot;YTE BAP Project No: 2021IYTE-1-0065. M.Y. acknowledged TUBITAK 2214-A International Doctoral Research Fellowship Programme for Ph.D. and R.O. acknowledged TUBITAK 2211-A National Graduate Scholarship Program. The authors acknowledged Prof. Franziska Groehn/Prof. Dirk Guldi for SLS-TCSPC utilization and Prof. Yasemin Basp & imath;nar/Dr. Tolga Sever for their help in confocal microscopy analysis. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation | Konformasyon Değişikliğine Hassas Politiyofen Türevi Polielektrolit Sentezi ve Mikroakışkan DNA Metilasyon Tarama Platformu Geliştirilmesi | tr |
dc.relation.ispartof | Macromolecular Bioscience | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Conjugated polyelectrolyte | en_US |
dc.subject | Image analysis | en_US |
dc.subject | Nanophase separation | en_US |
dc.subject | Polymer dots | en_US |
dc.subject | Breast cancer | en_US |
dc.title | The soft nanodots as fluorescent probes for cell imaging: Analysis of cell and spheroid penetration behavior of single chain polymer dots | en_US |
dc.type | Article | en_US |
dc.type | Article; Early Access | en_US |
dc.authorid | 0000-0001-7032-392X | - |
dc.authorid | 0000-0003-0348-0575 | - |
dc.authorid | 0000-0002-6922-4454 | - |
dc.department | İzmir Institute of Technology. Chemistry | en_US |
dc.department | İzmir Institute of Technology. Bioengineering | en_US |
dc.identifier.wos | WOS:001139640200001 | en_US |
dc.identifier.scopus | 2-s2.0-85181916757 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.doi | 10.1002/mabi.202300402 | - |
dc.identifier.pmid | 38102867 | en_US |
dc.relation.grantno | 116Z547 | - |
dc.authorscopusid | 57201675340 | - |
dc.authorscopusid | 57190064834 | - |
dc.authorscopusid | 57217604248 | - |
dc.authorscopusid | 8516383700 | - |
dc.identifier.wosquality | Q1 | - |
dc.identifier.scopusquality | Q2 | - |
item.fulltext | With Fulltext | - |
item.grantfulltext | embargo_20260101 | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.openairetype | Article; Early Access | - |
crisitem.author.dept | 03.01. Department of Bioengineering | - |
crisitem.author.dept | 04.01. Department of Chemistry | - |
Appears in Collections: | Bioengineering / Biyomühendislik Chemistry / Kimya PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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Macromolecular Bioscience.pdf Until 2026-01-01 | 18.69 MB | Adobe PDF | View/Open Request a copy |
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