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LipNanoCar Technology – A Versatile and Scalable Technology for the Production of Lipid Nanoparticles

dc.contributor.authorEsgueira, Vera L.R.
dc.contributor.authorLopes, Clara P.A.
dc.contributor.authordos Santos, Ana Catarina A.
dc.contributor.authorPinto, Fátima
dc.contributor.authorSousa, Silvia A.
dc.contributor.authorde Barros, Dragana P.C.
dc.contributor.authorLeitão, Jorge H.
dc.contributor.authorFonseca, Luis P.
dc.date.accessioned2022-12-05T12:55:45Z
dc.date.available2022-12-05T12:55:45Z
dc.date.issued2022-05-19
dc.description.abstractThe extensive knowledge in the miniemulsion technique used in biocatalysis applications by the authors allowed the development of drug delivery systems that constitutes the LipNanoCar technology core for the production of lipid nanoemulsions and solid lipid nanoparticles. The LipNanoCar technology, together with adequate formulations of different oils, fatty acids, surfactants, and temperature, allows the entrapment of several bioactive and therapeutic compounds in lipid nanoparticles for cosmetic, nutrition, and pharmaceutical applications. The LIpNanoCar technology allowed lipid nanoparticles production with average sizes ranging from 100 to 300 nm and Zeta potentials between −55 and −20 mV. Concomitantly, high entrapment or encapsulation efficiencies (%EE) were achieved, as illustrated in this work for β-carotene and vitamins derivatives (>85%) for cosmetic application, and for antibiotics currently used in chemotherapy, like rifampicin (69–85%) and pyrazinamide (14–29%) against Mycobacterium tuberculosis (TB), and ciprofloxacin (>65%) and tobramycin (~100%) in Cystic Fibrosis (CF) respiratory infections therapy. Ciprofloxacin presented, for example, a quick-release from the lipid nanoparticles using a dialysis tubing (96% in the first 7 h), but slower than the free antibiotic (95% in the first 3 h). This result suggests that ciprofloxacin is loaded near the external surface of the lipid nanoparticles. The toxicity and validation of entrapment of antibiotics in lipid nanoparticles for Cystic Fibrosis therapy were assessed using Caenorhabditis elegans as an animal model of bacterial infection. Fluorescence microscopy of an entrapped fluorescent dye (DiOC) confirmed the uptake of the lipid nanoparticles by ingestion, and their efficacy was successfully tested in C. elegans. Burkholderia contaminans IST408 and Burkholderia enocepacia K56–2 infections were tested as model bacterial pathogens difficult to eradicate in Cystic Fibrosis respiratory diseases.pt_PT
dc.description.sponsorshipThe authors thank Fundação para a Ciência e a Tecnologia (FCT) and IBB – Institute for Bioengineering and Biosciences for funding through project UIDB/04565/2020.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationIn: Louro H, Silva MJ (eds). Nanotoxicology in Safety Assessment of Nanomaterials. Springer, Cham, 2022, pp. 43-82. https://doi.org/10.1007/978-3-030-88071-2_3pt_PT
dc.identifier.doi10.1007/978-3-030-88071-2_3pt_PT
dc.identifier.eissn2214-8019
dc.identifier.issn0065-2598
dc.identifier.urihttp://hdl.handle.net/10400.18/8381
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSpringerpt_PT
dc.relationInstitute for Bioengineering and Biosciences
dc.relation.publisherversionhttps://link.springer.com/chapter/10.1007/978-3-030-88071-2_3pt_PT
dc.subjectEnvironmental Genotoxicitypt_PT
dc.subjectLipid Nanoparticlespt_PT
dc.subjectMiniemulsionpt_PT
dc.subjectEntrapmentpt_PT
dc.subjectEncapsulationpt_PT
dc.subjectAntibioticspt_PT
dc.subjectChemotherapypt_PT
dc.subjectTuberculosispt_PT
dc.subjectCystic Fibrosispt_PT
dc.subjectCaenorhabditis Eleganspt_PT
dc.subjectHealth benefitspt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.titleLipNanoCar Technology – A Versatile and Scalable Technology for the Production of Lipid Nanoparticlespt_PT
dc.typebook part
dspace.entity.typePublication
oaire.awardTitleInstitute for Bioengineering and Biosciences
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04565%2F2020/PT
oaire.citation.endPage82pt_PT
oaire.citation.startPage43pt_PT
oaire.citation.titleAdvances in Experimental Medicine and Biologypt_PT
oaire.citation.volume(Advances in Experimental Medicine and Biology;1357)pt_PT
oaire.fundingStream6817 - DCRRNI ID
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.embargofctAcesso de acordo com política editorial da revista.pt_PT
rcaap.rightsrestrictedAccesspt_PT
rcaap.typebookPartpt_PT
relation.isProjectOfPublicationcf090881-a371-430c-9bfc-2f43275b41f8
relation.isProjectOfPublication.latestForDiscoverycf090881-a371-430c-9bfc-2f43275b41f8

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