Dual-Ligand Functionalized pH-And Thermo-Sensitive Niosomes for Precise Targeted Therapy and Imaging of HER-2 Breast Cancer

dc.authorid Zarrabi, Ali/0000-0003-0391-1769
dc.authorscopusid 57908570400
dc.authorscopusid 57324389500
dc.authorscopusid 58941029500
dc.authorscopusid 58941394900
dc.authorscopusid 56700291100
dc.authorscopusid 58943413400
dc.authorscopusid 57202500098
dc.authorwosid Zarrabi, Ali/U-2602-2019
dc.contributor.author Saharkhiz, Shaghayegh
dc.contributor.author Nasri, Negar
dc.contributor.author Naderi, Nazanin
dc.contributor.author Saharkhiz, Shiva
dc.contributor.author Zarepour, Atefeh
dc.contributor.author Ghalehshahi, Saeid Shirzadi
dc.contributor.author Zarrabi, Ali
dc.date.accessioned 2025-07-15T19:03:53Z
dc.date.available 2025-07-15T19:03:53Z
dc.date.issued 2025
dc.department Okan University en_US
dc.department-temp [Saharkhiz, Shaghayegh; Nasri, Negar; Ghalehshahi, Saeid Shirzadi] Univ Isfahan, Fac Biol Sci & Technol, Dept Biotechnol, Esfahan, Iran; [Naderi, Nazanin] Shahid Beheshti Univ, Fac Life Sci & Biotechnol, Dept Cell & Mol Biol, Tehran 1983969411, Iran; [Saharkhiz, Shiva] Shahid Chamran Univ, Fac Biol, Dept Cellular & Mol Biol, Ahvaz, Iran; [Zarepour, Atefeh] Kocaeli Univ, Fac Arts & Sci, Dept Biol, TR-41001 Kocaeli, Turkiye; [Goodarzi, Reza] Azad Univ Shiraz, Fac Biol, Dept Biol Sci & Technol, Shiraz, Iran; [Khosravi, Arezoo] Istanbul Okan Univ, Fac Engn & Nat Sci, Dept Genet & Bioengn, TR-34959 Istanbul, Turkiye; [Khosravi, Arezoo] Yuan Ze Univ, Grad Sch Biotechnol & Bioengn, Taoyuan 320315, Taiwan; [Zarrabi, Ali] Istinye Univ, Fac Engn & Nat Sci, Dept Biomed Engn, TR-34396 Istanbul, Turkiye en_US
dc.description Zarrabi, Ali/0000-0003-0391-1769 en_US
dc.description.abstract In current study, we examined dual-targeted pH- and thermo-sensitive niosome platforms (pTSNs) for targeted delivery of Gemcitabine (GEM) and CdSe/ZnS QDs to HER-2-positive breast cancer cells for therapeutic and imaging purposes. The niosomal particles were prepared using thin-film hydration method and functionalized with Trastuzumab monoclonal antibody (Trz) and Folic acid (FA), as targeting agents. The fabricated formulation was characterized through different analyses, including DLS, Zeta potential, FTIR, SEM, and Fluorescence Microscopy. Besides, bioactivite features of the fabricated particles were evaluated using different analysis included determining loading and release profile, cell viability assessment, and relative cellular uptake. Characteristics results revealed a neutral, round-shaped, homogenous population of dual-targeted pTSNs with an average size of 200 nm that were correctly functionalized with conjugates. Moreover, it showed about 94.5 % entrapment efficiency (EE%), as well as up to 92 % drug release at pH 6.5 and 42 degrees C, while that amount was about 35 % at pH 7.4 and 37 degrees C. MTT and relative assessments demonstrated a 4.5-fold higher growth inhibition of SKBR-3 cells and 2600 times more cellular uptake by Trz and FA-conjugated pTSNs compared to non-targeted and nonsensitive particles. Overall, the developed platform proves to be a suitable carrier for the effective delivery of chemotherapeutic agents to cancer cells. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1016/j.mtchem.2025.102829
dc.identifier.issn 2468-5194
dc.identifier.scopus 2-s2.0-105008496205
dc.identifier.scopusquality Q2
dc.identifier.uri https://doi.org/10.1016/j.mtchem.2025.102829
dc.identifier.uri https://hdl.handle.net/20.500.14517/8083
dc.identifier.volume 47 en_US
dc.identifier.wos WOS:001520322200001
dc.identifier.wosquality Q1
dc.language.iso en en_US
dc.publisher Elsevier Sci Ltd en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Smart-Delivery en_US
dc.subject Dual-Targeted en_US
dc.subject pH-Sensitive en_US
dc.subject Thermo-Sensitive en_US
dc.subject Theranostic en_US
dc.title Dual-Ligand Functionalized pH-And Thermo-Sensitive Niosomes for Precise Targeted Therapy and Imaging of HER-2 Breast Cancer en_US
dc.type Article en_US

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