Glycosylated nanoplatforms: From glycosylation strategies to implications and opportunities for cancer theranostics

dc.authoridRahi, Amid/0000-0002-9190-5977
dc.authoridZirak Hassan Kiadeh, Shahrzad/0000-0002-8798-8255
dc.authorscopusid57224488480
dc.authorscopusid57193347865
dc.authorscopusid57211854405
dc.authorscopusid59147427700
dc.authorscopusid55328555300
dc.authorscopusid57305831500
dc.authorscopusid57202500098
dc.authorwosidRahi, Amid/AAH-4695-2019
dc.authorwosidZare, Iman/AFM-7138-2022
dc.authorwosidZahed Nasab, Shima/ADR-0872-2022
dc.authorwosidVAROL, Mehmet/AES-2638-2022
dc.contributor.authorZare, Iman
dc.contributor.authorKhosravı, Arezoo
dc.contributor.authorVarol, Ayseguel
dc.contributor.authorVarol, Tugba Oren
dc.contributor.authorVarol, Mehmet
dc.contributor.authorSezen, Serap
dc.contributor.authorZarrabi, Ali
dc.contributor.otherGenetik ve Biyomühendislik / Genetic and Bio-Engineering
dc.date.accessioned2024-09-11T07:39:27Z
dc.date.available2024-09-11T07:39:27Z
dc.date.issued2024
dc.departmentOkan Universityen_US
dc.department-temp[Zare, Iman] Sina Med Biochem Technol Co Ltd, Res & Dev Dept, Shiraz 7178795844, Iran; [Kiadeh, Shahrzad Zirak Hassan; Nasab, Shima Zahed] Univ Tehran, Dept Life Sci Engn, Fac New Sci & Technol, POB 14395-1561, Tehran, Iran; [Varol, Ayseguel] Johannes Gutenberg Univ Mainz, Inst Pharmaceut & Biomed Sci, Dept Pharmaceut Biol, Mainz, Germany; [Varol, Tugba Oren] Mugla Sitki Kocman Univ, Fac Sci, Dept Chem, Kotekli Campus, TR-48000 Mugla, Turkiye; [Varol, Mehmet] Mugla Sitki Kocman Univ, Fac Sci, Dept Mol Biol & Genet, Kotekli Campus, TR-48000 Mugla, Turkiye; [Sezen, Serap] Sabanci Univ, Fac Engn & Nat Sci, TR-34956 Istanbul, Turkiye; [Sezen, Serap] Sabanci Univ, Nanotechnol Res & Applicat Ctr, TR-34956 Istanbul, Turkiye; [Zarepour, Atefeh] Saveetha Univ, Saveetha Inst Med & Tech Sci, Saveetha Dent Coll & Hosp, Dept Res Analyt, Chennai 600077, India; [Mostafavi, Ebrahim] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA; [Rahi, Amid] Kerman Univ Med Sci, Pathol & Stem Cell Res Ctr, Kerman, Iran; [Khosravi, Arezoo] Istanbul Okan Univ, Fac Engn & Nat Sci, Dept Genet & Bioengn, TR-34959 Istanbul, Turkiye; [Zarrabi, Ali] Istinye Univ, Fac Engn & Nat Sci, Dept Biomed Engn, TR-34396 Istanbul, Turkiye; [Zarrabi, Ali] Yuan Ze Univ, Grad Sch Biotechnol & Bioengn, Taoyuan, Taiwanen_US
dc.descriptionRahi, Amid/0000-0002-9190-5977; Zirak Hassan Kiadeh, Shahrzad/0000-0002-8798-8255en_US
dc.description.abstractGlycosylated nanoplatforms have emerged as promising tools in the field of cancer theranostics, integrating both therapeutic and diagnostic functionalities. These nanoscale platforms are composed of different materials such as lipids, polymers, carbons, and metals that can be modified with glycosyl moieties to enhance their targeting capabilities towards cancer cells. This review provides an overview of different modification strategies employed to introduce glycosylation onto nanoplatforms, including chemical conjugation, enzymatic methods, and bioorthogonal reactions. Furthermore, the potential applications of glycosylated nanoplatforms in cancer theranostics are discussed, focusing on their roles in drug delivery, imaging, and combination therapy. The ability of these nanoplatforms to selectively target cancer cells through specific interactions with overexpressed glycan receptors is highlighted, emphasizing their potential for enhancing efficacy and reducing the side effects compared to conventional therapies. In addition, the incorporation of diagnostic components onto the glycosylated nanoplatforms provided the capability of simultaneous imaging and therapy and facilitated the real-time monitoring of treatment response. Finally, challenges and future perspectives in the development and translation of glycosylated nanoplatforms for clinical applications are addressed, including scalability, biocompatibility, and regulatory considerations. Overall, this review underscores the significant progress made in the field of glycosylated nanoplatforms and their potential to revolutionize cancer theranostics.en_US
dc.description.sponsorshipNational Institute of Biomedical Imaging and Bioengineering [5T32EB009035]en_US
dc.description.sponsorshipE.M. would like to acknowledge the support from the National Institute of Biomedical Imaging and Bioengineering (5T32EB009035) .en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.citation0
dc.identifier.doi10.1016/j.jconrel.2024.05.032
dc.identifier.endpage178en_US
dc.identifier.issn0168-3659
dc.identifier.issn1873-4995
dc.identifier.pmid38782062
dc.identifier.scopus2-s2.0-85194377986
dc.identifier.scopusqualityQ1
dc.identifier.startpage158en_US
dc.identifier.urihttps://doi.org/10.1016/j.jconrel.2024.05.032
dc.identifier.urihttps://hdl.handle.net/20.500.14517/6182
dc.identifier.volume371en_US
dc.identifier.wosWOS:001250735300001
dc.identifier.wosqualityQ1
dc.institutionauthorKhosravi A.
dc.language.isoen
dc.publisherElsevieren_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGlycosylated nanoplatformsen_US
dc.subjectDrug deliveryen_US
dc.subjectNanomedicineen_US
dc.subjectCancer theranosticsen_US
dc.subjectGlycosylation strategiesen_US
dc.titleGlycosylated nanoplatforms: From glycosylation strategies to implications and opportunities for cancer theranosticsen_US
dc.typeReviewen_US
dspace.entity.typePublication
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