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Article: Advances and Prospects of Prolamine Corn Protein Zein as Promising Multifunctional Drug Delivery System for Cancer Treatment

TitleAdvances and Prospects of Prolamine Corn Protein Zein as Promising Multifunctional Drug Delivery System for Cancer Treatment
Authors
Keywordsantitumor
drug delivery
nanomedicine
zein
Issue Date15-May-2023
PublisherTaylor and Francis Group
Citation
International Journal of Nanomedicine, 2023, v. 18, p. 2589-2621 How to Cite?
AbstractZein is a type of prolamine protein that is derived from corn, and it has been recognized by the US FDA as one of the safest biological materials available. Zein possesses valuable characteristics that have made it a popular choice for the preparation of drug carriers, which can be administered through various routes to improve the therapeutic effect of antitumor drugs. Additionally, zein contains free hydroxyl and amino groups that offer numerous modification sites, enabling it to be hybridized with other materials to create functionalized drug delivery systems. However, despite its potential, the clinical translation of drug-loaded zein-based carriers remains challenging due to insufficient basic research and relatively strong hydrophobicity. In this paper, we aim to systematically introduce the main interactions between loaded drugs and zein, administration routes, and the functionalization of zein-based antitumor drug delivery systems, in order to demonstrate its development potential and promote their further application. We also provide perspectives and future directions for this promising area of research.
Persistent Identifierhttp://hdl.handle.net/10722/362422
ISSN
2010 Impact Factor: 4.976
2023 SCImago Journal Rankings: 1.273

 

DC FieldValueLanguage
dc.contributor.authorLuo, Xi-
dc.contributor.authorWu, Sudan-
dc.contributor.authorXiao, Meng-
dc.contributor.authorGu, Huan-
dc.contributor.authorZhang, Huan-
dc.contributor.authorChen, Jianping-
dc.contributor.authorLiu, Yang-
dc.contributor.authorZhang, Chen-
dc.contributor.authorZhang, Jinming-
dc.date.accessioned2025-09-24T00:51:25Z-
dc.date.available2025-09-24T00:51:25Z-
dc.date.issued2023-05-15-
dc.identifier.citationInternational Journal of Nanomedicine, 2023, v. 18, p. 2589-2621-
dc.identifier.issn1176-9114-
dc.identifier.urihttp://hdl.handle.net/10722/362422-
dc.description.abstractZein is a type of prolamine protein that is derived from corn, and it has been recognized by the US FDA as one of the safest biological materials available. Zein possesses valuable characteristics that have made it a popular choice for the preparation of drug carriers, which can be administered through various routes to improve the therapeutic effect of antitumor drugs. Additionally, zein contains free hydroxyl and amino groups that offer numerous modification sites, enabling it to be hybridized with other materials to create functionalized drug delivery systems. However, despite its potential, the clinical translation of drug-loaded zein-based carriers remains challenging due to insufficient basic research and relatively strong hydrophobicity. In this paper, we aim to systematically introduce the main interactions between loaded drugs and zein, administration routes, and the functionalization of zein-based antitumor drug delivery systems, in order to demonstrate its development potential and promote their further application. We also provide perspectives and future directions for this promising area of research.-
dc.languageeng-
dc.publisherTaylor and Francis Group-
dc.relation.ispartofInternational Journal of Nanomedicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectantitumor-
dc.subjectdrug delivery-
dc.subjectnanomedicine-
dc.subjectzein-
dc.titleAdvances and Prospects of Prolamine Corn Protein Zein as Promising Multifunctional Drug Delivery System for Cancer Treatment-
dc.typeArticle-
dc.identifier.doi10.2147/IJN.S402891-
dc.identifier.pmid37213352-
dc.identifier.scopuseid_2-s2.0-85159824363-
dc.identifier.volume18-
dc.identifier.spage2589-
dc.identifier.epage2621-
dc.identifier.eissn1178-2013-
dc.identifier.issnl1176-9114-

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