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Publicação:
Functionalized lipid-based drug delivery nanosystems for the treatment of human infectious diseases

dc.contributor.authorAlmeida Furquim de Camargo, Bruna [UNESP]
dc.contributor.authorFonseca-Santos, Bruno
dc.contributor.authorGonçalves Carvalho, Suzana [UNESP]
dc.contributor.authorCorrêa Carvalho, Gabriela [UNESP]
dc.contributor.authorDelello Di Filippo, Leonardo [UNESP]
dc.contributor.authorSousa Araújo, Victor Hugo [UNESP]
dc.contributor.authorLobato Duarte, Jonatas [UNESP]
dc.contributor.authorPolli Silvestre, Amanda Letícia [UNESP]
dc.contributor.authorBauab, Taís Maria [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2023-03-02T02:50:42Z
dc.date.available2023-03-02T02:50:42Z
dc.date.issued2022-01-01
dc.description.abstractInfectious diseases are still public health problems. Microorganisms such as fungi, bacteria, viruses, and parasites are the main causing agents related to these diseases. In this context, the search for new effective strategies in prevention and/or treatment is considered essential, since current drugs often have side effects or end up, causing microbial resistance, making it a serious health problem. As an alternative to these limitations, nanotechnology has been widely used. The use of lipid-based drug delivery nanosystems (DDNs) has some advantages, such as biocompatibility, low toxicity, controlled release, the ability to carry both hydrophilic and lipophilic drugs, in addition to be easel scalable. Besides, as an improvement, studies involving the conjugation of signalling molecules on the surfaces of these nanocarriers can allow the target of certain tissues or cells. Thus, this review summarizes the performance of functionalized lipid-based DDNs for the treatment of infectious diseases caused by viruses, including SARS-CoV-2, bacteria, fungi, and parasites.en
dc.description.affiliationSchool of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationFaculty of Pharmaceutical Sciences Campinas State University (UNICAMP)
dc.description.affiliationUnespSchool of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.identifierhttp://dx.doi.org/10.1080/1040841X.2022.2047007
dc.identifier.citationCritical Reviews in Microbiology.
dc.identifier.doi10.1080/1040841X.2022.2047007
dc.identifier.issn1549-7828
dc.identifier.issn1040-841X
dc.identifier.scopus2-s2.0-85131160016
dc.identifier.urihttp://hdl.handle.net/11449/241902
dc.language.isoeng
dc.relation.ispartofCritical Reviews in Microbiology
dc.sourceScopus
dc.subjectdrug delivery nanosystem
dc.subjectfunctionalization
dc.subjectinfectious diseases
dc.subjectnanotechnology
dc.subjectTargeting
dc.titleFunctionalized lipid-based drug delivery nanosystems for the treatment of human infectious diseasesen
dc.typeResenhapt
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
unesp.author.orcid0000-0002-8442-0840[1]
unesp.author.orcid0000-0002-4259-0008[2]
unesp.author.orcid0000-0002-0139-457X[3]
unesp.author.orcid0000-0002-4071-5364[4]
unesp.author.orcid0000-0001-6365-8756[5]
unesp.author.orcid0000-0003-1731-9918[6]
unesp.author.orcid0000-0002-7276-3686[7]
unesp.author.orcid0000-0003-1957-6993[8]
unesp.author.orcid0000-0002-1929-6003[9]
unesp.author.orcid0000-0002-6698-0545[10]
unesp.departmentCiências Biológicas - FCFpt
unesp.departmentFármacos e Medicamentos - FCFpt

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