<?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>2026-10-28T02:40:53Z</responseDate><request verb="GetRecord" identifier="oai:kostu-rdlopen.rawdatalibrary.net:kostu/10820" metadataPrefix="oai_dc">https://kostu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:kostu-rdlopen.rawdatalibrary.net:kostu/10820</identifier><datestamp>2026-10-27T23:53:26Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_kostu_10000</setSpec><setSpec>col_kostu_10001</setSpec><setSpec>com_kostu_10007</setSpec><setSpec>col_kostu_10059</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>The lenalidomide derivative loaded and quercetin modified MIL-100 based novel drug delivery system for breast cancer treatment</dc:title><dc:creator>Özsoy, Munteha</dc:creator><dc:creator>Tok, Yagmur Pirincci</dc:creator><dc:creator>Eskiler, Gamze Guney</dc:creator><dc:creator>Tok, Fatih</dc:creator><dc:creator>Karakus, Sevgi</dc:creator><dc:creator>Ozsoy, Yildiz</dc:creator><dc:creator>Özacar, Mahmut</dc:creator><dc:subject>MIL-100 (Fe)</dc:subject><dc:subject>Quercetin</dc:subject><dc:subject>Lenalidomide-like novel drug derivative</dc:subject><dc:subject>Drug delivery system</dc:subject><dc:subject>Triple negative breast cancer</dc:subject><dc:description>Lenalidomide (L0) is an immunomodulatory agent with a range of effects, including anticancer and antiinflammatory activity, and is commonly utilized in treating multiple myeloma. A derivative of lenalidomide (L1) has been synthesized to enhance its effects and to target different cancer cell types. In this study, the lenalidomide derivative L1, with the chemical structure 1-[2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-4-yl]-3(p-tolyl)urea, was loaded onto a novel drug delivery system (DDS), and its activity was assessed towards triple-negative breast cancer cell lines (TNBC). MIL-100, a subclass of metal-organic framework (MOF) structures, was synthesized via a microwave-assisted hydrothermal method. MIL-100 was modified with quercetin (QC) as a linker, and its drug loading capacity was optimized, achieving a 95.18 % encapsulation efficiency. Additionally, the antioxidant properties of QC contributed to enhancing the performance of the DDS. In vitro drug release studies of the final product, MIL-100@QC@L1, were successfully conducted. The cytotoxic influences of the formulation on MDA-MB-231 cells were assessed using the WST-1 assay. After treatment with 10 mu g/mL of MIL100@QC@L1 for 24 h, the cell viability decreased significantly to 47.8 %, showing superior results compared to treatments with L0 and L1 alone.</dc:description><dc:publisher>ELSEVIER</dc:publisher><dc:date>2025-06</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/kostu/10820</dc:identifier><dc:identifier>https://doi.org/10.1016/j.jddst.2025.106923</dc:identifier><dc:identifier>1773-2247</dc:identifier><dc:language>en</dc:language><dc:relation>JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://kostu-rdlopen.rawdatalibrary.net/tr/items/kostu/10820</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>