<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-18T23:56:48Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/11314" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/11314</identifier><datestamp>2026-10-18T20:26:23Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Dual-functionality of Hibiscus sabdariffa-CuO nanoparticles in chemotherapy and textile screen-printing on cellulose-based textiles</dc:title><dc:creator>Tüzün, Elif</dc:creator><dc:creator>Erol, Ayşe</dc:creator><dc:creator>Kalındemirtaş, Ferdane Danışman</dc:creator><dc:creator>Özbaş, Fatih</dc:creator><dc:creator>Sert, Esra</dc:creator><dc:creator>Soomro, Razium Ali</dc:creator><dc:creator>Nafady, Ayman</dc:creator><dc:creator>Karakuş, Selcan</dc:creator><dc:subject>Apoptosis</dc:subject><dc:subject>Cellulose-based textiles</dc:subject><dc:subject>Copper (II) oxide nanoparticles</dc:subject><dc:subject>MCF-7</dc:subject><dc:subject>Screen printing</dc:subject><dc:subject>Cells</dc:subject><dc:subject>Cellulose</dc:subject><dc:subject>Exposure</dc:subject><dc:subject>Roselle</dc:subject><dc:subject>Scanning Electron Microscopy</dc:subject><dc:subject>Silk Screen Printing</dc:subject><dc:subject>Textiles</dc:subject><dc:subject>Cell death</dc:subject><dc:subject>Chemotherapy</dc:subject><dc:subject>Fabrics</dc:subject><dc:subject>Nanoclay</dc:subject><dc:subject>Nanoparticles</dc:subject><dc:subject>Smart textiles</dc:subject><dc:subject>Textile printing</dc:subject><dc:subject>Cancer cell lines</dc:subject><dc:subject>Cancer cells</dc:subject><dc:subject>Cellulose-based textile</dc:subject><dc:subject>Copper (II) oxide nanoparticle</dc:subject><dc:subject>CuO nanoparticles</dc:subject><dc:subject>Hibiscus sabdariffa</dc:subject><dc:subject>Oxide nanoparticles</dc:subject><dc:subject>Synthesised</dc:subject><dc:subject>Textile screen printing</dc:subject><dc:subject>Fourier transform infrared spectroscopy</dc:subject><dc:description>The dual-functional nanostructures show great promise for biomedical applications, exhibiting selective cytotoxicity against cancer cells while also serving as a crucial component in textile screen-printing for smart materials. In this study, we successfully synthesized polyethylene glycol-hibiscus extract copper (II) oxide nanoparticles (PEG/HS/CuO NPs) using a simple one-step sonosynthesis method that leverages ultrasonic irradiation. Comprehensive characterization of the synthesized PEG/HS/CuO NPs was performed using transmission electron microscopy (TEM), X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy-dispersive X-ray (EDX) analysis, and Fourier-transform infrared spectroscopy (FTIR). The incorporation of PEG/HS/CuO NPs into guar gum photochromic solution (GP) caused a significant color change after 6 ± 1 min of UV light exposure and resulted in visible coloration on cellulose-based textiles after screen printing, providing an alternative strategy for smart fabrics. Moreover, cytotoxicity experiments demonstrated the selective toxicity of green PEG/HS/CuO NPs against cancer cells. In this study, the human colon cancer cell line HCT116, breast cancer cell line MCF-7, and normal HUVEC cells were examined. PEG/HS/CuO NPs NPs induced apoptosis, cell cycle arrest, and down-regulation of CD44 antibody expression in MCF-7 cells, highlighting their potential as effective chemotherapy agents. © The Author(s) 2025.</dc:description><dc:publisher>Springer Science and Business Media B.V.</dc:publisher><dc:date>2025</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/11314</dc:identifier><dc:identifier>https://doi.org/10.1007/s10570-025-06429-7</dc:identifier><dc:identifier>0969-0239</dc:identifier><dc:language>en</dc:language><dc:relation>Cellulose</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/11314</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>