Immunoliposomes: A review on functionalization strategies and targets for drug delivery

Bibliographic Details
Main Author: Eloy, Josimar O. [UNESP]
Publication Date: 2017
Other Authors: Petrilli, Raquel [UNESP], Trevizan, Lucas Noboru Fatori [UNESP], Chorilli, Marlus [UNESP]
Format: Other
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.colsurfb.2017.07.085
http://hdl.handle.net/11449/175063
Summary: Nanoparticles, especially liposomes, have gained prominence in the field of drug delivery for the treatment of human diseases, particularly cancer; they provide several advantages, including controlled drug release, protection of the drug against degradation, improved pharmacokinetics, long circulation, and passive targeting to tumors and inflammatory sites due to the enhanced permeability and retention effect. The functionalization of liposomes with monoclonal antibodies or antibody fragments to generate immunoliposomes has emerged as a promising strategy for targeted delivery to and uptake by cells overexpressing the antigens to these antibodies, with a consequent reduction in side effects. In this review, we address functionalization strategies for the non-covalent and covalent attachment of monoclonal antibodies and their fragments to liposomal surfaces. The main reaction occurs between the sulfhydryl groups of thiolated antibodies and maleimide-containing liposomes. Furthermore, we explore the main targeting possibilities with these ligands for the treatment of a variety of pathologies, including HER2- and EGFR-positive cancers, inflammatory and cardiovascular diseases, infectious diseases, and autoimmune and neurodegenerative diseases, which have not previously been reviewed together. Overall, many studies have shown selective delivery of immunoliposomes to target cells, with promising in vivo results, particularly for cancer treatment. Although clinical trials have been conducted, immunoliposomes have not yet received clinical approval. However, immunoliposomes are promising formulations that are expected to become available for therapeutic use after clinical trials prove their safety and efficacy, and after scaling issues are resolved.
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spelling Immunoliposomes: A review on functionalization strategies and targets for drug deliveryFunctionalizationImmunoliposomesLiposomesMonoclonal antibodiesTargeted deliveryNanoparticles, especially liposomes, have gained prominence in the field of drug delivery for the treatment of human diseases, particularly cancer; they provide several advantages, including controlled drug release, protection of the drug against degradation, improved pharmacokinetics, long circulation, and passive targeting to tumors and inflammatory sites due to the enhanced permeability and retention effect. The functionalization of liposomes with monoclonal antibodies or antibody fragments to generate immunoliposomes has emerged as a promising strategy for targeted delivery to and uptake by cells overexpressing the antigens to these antibodies, with a consequent reduction in side effects. In this review, we address functionalization strategies for the non-covalent and covalent attachment of monoclonal antibodies and their fragments to liposomal surfaces. The main reaction occurs between the sulfhydryl groups of thiolated antibodies and maleimide-containing liposomes. Furthermore, we explore the main targeting possibilities with these ligands for the treatment of a variety of pathologies, including HER2- and EGFR-positive cancers, inflammatory and cardiovascular diseases, infectious diseases, and autoimmune and neurodegenerative diseases, which have not previously been reviewed together. Overall, many studies have shown selective delivery of immunoliposomes to target cells, with promising in vivo results, particularly for cancer treatment. Although clinical trials have been conducted, immunoliposomes have not yet received clinical approval. However, immunoliposomes are promising formulations that are expected to become available for therapeutic use after clinical trials prove their safety and efficacy, and after scaling issues are resolved.School of Pharmaceutical Sciences of Araraquara São Paulo State University UNESP Department of Drugs and MedicinesSchool of Pharmaceutical Sciences of Ribeirão Preto São Paulo State University USP Department of Pharmaceutical SciencesSchool of Pharmaceutical Sciences of Araraquara São Paulo State University UNESP Department of Drugs and MedicinesSchool of Pharmaceutical Sciences of Ribeirão Preto São Paulo State University USP Department of Pharmaceutical SciencesUniversidade Estadual Paulista (Unesp)Eloy, Josimar O. [UNESP]Petrilli, Raquel [UNESP]Trevizan, Lucas Noboru Fatori [UNESP]Chorilli, Marlus [UNESP]2018-12-11T17:14:04Z2018-12-11T17:14:04Z2017-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/other454-467application/pdfhttp://dx.doi.org/10.1016/j.colsurfb.2017.07.085Colloids and Surfaces B: Biointerfaces, v. 159, p. 454-467.1873-43670927-7765http://hdl.handle.net/11449/17506310.1016/j.colsurfb.2017.07.0852-s2.0-850278566892-s2.0-85027856689.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengColloids and Surfaces B: Biointerfaces1,071info:eu-repo/semantics/openAccess2025-03-29T05:20:18Zoai:repositorio.unesp.br:11449/175063Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-03-29T05:20:18Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Immunoliposomes: A review on functionalization strategies and targets for drug delivery
title Immunoliposomes: A review on functionalization strategies and targets for drug delivery
spellingShingle Immunoliposomes: A review on functionalization strategies and targets for drug delivery
Eloy, Josimar O. [UNESP]
Functionalization
Immunoliposomes
Liposomes
Monoclonal antibodies
Targeted delivery
title_short Immunoliposomes: A review on functionalization strategies and targets for drug delivery
title_full Immunoliposomes: A review on functionalization strategies and targets for drug delivery
title_fullStr Immunoliposomes: A review on functionalization strategies and targets for drug delivery
title_full_unstemmed Immunoliposomes: A review on functionalization strategies and targets for drug delivery
title_sort Immunoliposomes: A review on functionalization strategies and targets for drug delivery
author Eloy, Josimar O. [UNESP]
author_facet Eloy, Josimar O. [UNESP]
Petrilli, Raquel [UNESP]
Trevizan, Lucas Noboru Fatori [UNESP]
Chorilli, Marlus [UNESP]
author_role author
author2 Petrilli, Raquel [UNESP]
Trevizan, Lucas Noboru Fatori [UNESP]
Chorilli, Marlus [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Eloy, Josimar O. [UNESP]
Petrilli, Raquel [UNESP]
Trevizan, Lucas Noboru Fatori [UNESP]
Chorilli, Marlus [UNESP]
dc.subject.por.fl_str_mv Functionalization
Immunoliposomes
Liposomes
Monoclonal antibodies
Targeted delivery
topic Functionalization
Immunoliposomes
Liposomes
Monoclonal antibodies
Targeted delivery
description Nanoparticles, especially liposomes, have gained prominence in the field of drug delivery for the treatment of human diseases, particularly cancer; they provide several advantages, including controlled drug release, protection of the drug against degradation, improved pharmacokinetics, long circulation, and passive targeting to tumors and inflammatory sites due to the enhanced permeability and retention effect. The functionalization of liposomes with monoclonal antibodies or antibody fragments to generate immunoliposomes has emerged as a promising strategy for targeted delivery to and uptake by cells overexpressing the antigens to these antibodies, with a consequent reduction in side effects. In this review, we address functionalization strategies for the non-covalent and covalent attachment of monoclonal antibodies and their fragments to liposomal surfaces. The main reaction occurs between the sulfhydryl groups of thiolated antibodies and maleimide-containing liposomes. Furthermore, we explore the main targeting possibilities with these ligands for the treatment of a variety of pathologies, including HER2- and EGFR-positive cancers, inflammatory and cardiovascular diseases, infectious diseases, and autoimmune and neurodegenerative diseases, which have not previously been reviewed together. Overall, many studies have shown selective delivery of immunoliposomes to target cells, with promising in vivo results, particularly for cancer treatment. Although clinical trials have been conducted, immunoliposomes have not yet received clinical approval. However, immunoliposomes are promising formulations that are expected to become available for therapeutic use after clinical trials prove their safety and efficacy, and after scaling issues are resolved.
publishDate 2017
dc.date.none.fl_str_mv 2017-11-01
2018-12-11T17:14:04Z
2018-12-11T17:14:04Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/other
format other
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.colsurfb.2017.07.085
Colloids and Surfaces B: Biointerfaces, v. 159, p. 454-467.
1873-4367
0927-7765
http://hdl.handle.net/11449/175063
10.1016/j.colsurfb.2017.07.085
2-s2.0-85027856689
2-s2.0-85027856689.pdf
url http://dx.doi.org/10.1016/j.colsurfb.2017.07.085
http://hdl.handle.net/11449/175063
identifier_str_mv Colloids and Surfaces B: Biointerfaces, v. 159, p. 454-467.
1873-4367
0927-7765
10.1016/j.colsurfb.2017.07.085
2-s2.0-85027856689
2-s2.0-85027856689.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Colloids and Surfaces B: Biointerfaces
1,071
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 454-467
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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