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https://hdl.handle.net/10216/128679Registo completo
| Campo DC | Valor | Idioma |
|---|---|---|
| dc.creator | Marina Barroso Pereira Pinheiro | |
| dc.date.accessioned | 2025-11-07T14:10:51Z | - |
| dc.date.available | 2025-11-07T14:10:51Z | - |
| dc.date.issued | 2020-05-11 | |
| dc.date.submitted | 2020-03-15 | |
| dc.identifier.other | sigarra:414414 | |
| dc.identifier.uri | https://hdl.handle.net/10216/128679 | - |
| dc.description | Aim: Design nanostructured lipid carriers (NLC) to facilitate drug delivery to tuberculosis-infected areas, exploiting macrophage mannose receptors and assess their uptake in a 3D human lung model. Materials & methods: NLCs and mannosylated-NLCs were synthetized and characterized. Their uptake and biocompatibility were tested in a 3D human lung model. Results: The formulations have appropriate size (170-202 nm) and morphology for lung deposition. Cell membrane integrity was maintained and no significant pro-inflammatory cytokine (IL-1β, IL-8 and TNF-α) secretion or morphological changes were observed 24 h post nanoparticles exposure. NLCs and mannosylated NLCs were distributed in the apical side of the lung tissue, both in macrophages and in epithelial cells. Conclusion: NLCs are biocompatible carriers and can be used for pulmonary drug delivery. | |
| dc.description.abstract | Aim: Design nanostructured lipid carriers (NLC) to facilitate drug delivery to tuberculosis-infected areas, exploiting macrophage mannose receptors and assess their uptake in a 3D human lung model. Materials & methods: NLCs and mannosylated-NLCs were synthetized and characterized. Their uptake and biocompatibility were tested in a 3D human lung model. Results: The formulations have appropriate size (170-202 nm) and morphology for lung deposition. Cell membrane integrity was maintained and no significant pro-inflammatory cytokine (IL-1β, IL-8 and TNF-α) secretion or morphological changes were observed 24 h post nanoparticles exposure. NLCs and mannosylated NLCs were distributed in the apical side of the lung tissue, both in macrophages and in epithelial cells. Conclusion: NLCs are biocompatible carriers and can be used for pulmonary drug delivery. | |
| dc.language.iso | por | |
| dc.rights | openAccess | |
| dc.rights.uri | https://creativecommons.org/licenses/by-sa/4.0/ | |
| dc.subject | Biotecnologia médica | |
| dc.subject | Medical biotechnology | |
| dc.title | Lipid nanoparticles biocompatibility and cellular uptake in a 3D human lung model | |
| dc.type | Dissertação | |
| dc.contributor.uporto | Faculdade de Medicina | |
| dc.identifier.doi | 10.34626/345n-rk80 | |
| dc.identifier.tid | 202616444 | |
| dc.subject.fos | Ciências médicas e da saúde::Biotecnologia médica | |
| dc.subject.fos | Medical and Health sciences::Medical biotechnology | |
| thesis.degree.discipline | Mestrado Integrado em Medicina | |
| thesis.degree.grantor | Faculdade de Medicina | |
| thesis.degree.grantor | Universidade do Porto | |
| thesis.degree.level | 1 | |
| Aparece nas coleções: | FMUP - Dissertação | |
Ficheiros deste registo:
| Ficheiro | Descrição | Tamanho | Formato | |
|---|---|---|---|---|
| 414414.pdf | Lipid nanoparticles biocompatibility and cellular uptake in a 3D human lung model | 10.82 MB | Adobe PDF | ![]() Ver/Abrir |
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