dc.contributor.advisor | Šnejdrová, Eva | |
dc.creator | Hafezi, Ramin | |
dc.date.accessioned | 2021-06-24T08:52:29Z | |
dc.date.available | 2021-06-24T08:52:29Z | |
dc.date.issued | 2021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11956/126182 | |
dc.description.abstract | Thesis title: Formulation and characterization of oxime loaded PLGA nanoparticles Author: Ramin Hafezi Supervisor: PharmDr. Eva Šnejdrová, Ph.D. Advisor: PharmDr. Juraj Martiška, Ph.D. Department: Department of Pharmaceutical Technology The diploma thesis was focused on PLGA nanoparticles (NPs) which could be loaded with oximes, prepared by a double emulsion technique, and characterised by size, polydispersity and zeta potential. The theoretical part deals with the most common methods of the NPs preparation, the polymers and stabilizers employed, and drug delivery to brain. In the experimental part the effect of various formulation factors on NP characteristics were studied: linear or branched PLGA derivative, the concentrations of polymer, the volumes of primary emulsion. Dichloromethane (DCM) or Dimethyl sulfoxide (DMSO) as solvent for polymers were used and Poloxamer 407 or Didodecyldimethylammonium bromide (DDAB) as an outer phase stabilizer were employed. By comparison among the collected results, it seemed 1% A2 in DMSO and stabilization with poloxamer 407 could be best candidate for the oxime loaded drug delivery systems as it was possible to produce nanoparticles with size from 152 to 168 nm with PDI of below 0.15. Electrostatic stability in case of using DDAB was resulted excellent and... | en_US |
dc.language | English | cs_CZ |
dc.language.iso | en_US | |
dc.publisher | Univerzita Karlova, Farmaceutická fakulta v Hradci Králové | cs_CZ |
dc.subject | nanoparticles | en_US |
dc.subject | rifampicin | en_US |
dc.subject | particles size | en_US |
dc.subject | zeta potential | en_US |
dc.subject | encapsulation efficiency | en_US |
dc.subject | dissolution | en_US |
dc.subject | nanočástice | cs_CZ |
dc.subject | rifampicin | cs_CZ |
dc.subject | velikost částic | cs_CZ |
dc.subject | zeta potenciál | cs_CZ |
dc.subject | enkapsulační účinnost | cs_CZ |
dc.subject | disoluce | cs_CZ |
dc.title | Formulation and characterization of oxims loaded PLGA nanoparticles | en_US |
dc.type | diplomová práce | cs_CZ |
dcterms.created | 2021 | |
dcterms.dateAccepted | 2021-06-02 | |
dc.description.department | Department of Pharmaceutical Technology | en_US |
dc.description.department | Katedra farmaceutické technologie | cs_CZ |
dc.description.faculty | Faculty of Pharmacy in Hradec Králové | en_US |
dc.description.faculty | Farmaceutická fakulta v Hradci Králové | cs_CZ |
dc.identifier.repId | 217251 | |
dc.title.translated | Formulace a charakterizace PLGA nanočástic s oximy | cs_CZ |
dc.contributor.referee | Paraskevopoulos, Georgios | |
thesis.degree.name | Mgr. | |
thesis.degree.level | magisterské | cs_CZ |
thesis.degree.discipline | Farmacie | cs_CZ |
thesis.degree.discipline | Pharmacy | en_US |
thesis.degree.program | Pharmacy | en_US |
thesis.degree.program | Farmacie | cs_CZ |
uk.thesis.type | diplomová práce | cs_CZ |
uk.taxonomy.organization-cs | Farmaceutická fakulta v Hradci Králové::Katedra farmaceutické technologie | cs_CZ |
uk.taxonomy.organization-en | Faculty of Pharmacy in Hradec Králové::Department of Pharmaceutical Technology | en_US |
uk.faculty-name.cs | Farmaceutická fakulta v Hradci Králové | cs_CZ |
uk.faculty-name.en | Faculty of Pharmacy in Hradec Králové | en_US |
uk.faculty-abbr.cs | FaF | cs_CZ |
uk.degree-discipline.cs | Farmacie | cs_CZ |
uk.degree-discipline.en | Pharmacy | en_US |
uk.degree-program.cs | Farmacie | cs_CZ |
uk.degree-program.en | Pharmacy | en_US |
thesis.grade.cs | Velmi dobře | cs_CZ |
thesis.grade.en | Very good | en_US |
uk.abstract.en | Thesis title: Formulation and characterization of oxime loaded PLGA nanoparticles Author: Ramin Hafezi Supervisor: PharmDr. Eva Šnejdrová, Ph.D. Advisor: PharmDr. Juraj Martiška, Ph.D. Department: Department of Pharmaceutical Technology The diploma thesis was focused on PLGA nanoparticles (NPs) which could be loaded with oximes, prepared by a double emulsion technique, and characterised by size, polydispersity and zeta potential. The theoretical part deals with the most common methods of the NPs preparation, the polymers and stabilizers employed, and drug delivery to brain. In the experimental part the effect of various formulation factors on NP characteristics were studied: linear or branched PLGA derivative, the concentrations of polymer, the volumes of primary emulsion. Dichloromethane (DCM) or Dimethyl sulfoxide (DMSO) as solvent for polymers were used and Poloxamer 407 or Didodecyldimethylammonium bromide (DDAB) as an outer phase stabilizer were employed. By comparison among the collected results, it seemed 1% A2 in DMSO and stabilization with poloxamer 407 could be best candidate for the oxime loaded drug delivery systems as it was possible to produce nanoparticles with size from 152 to 168 nm with PDI of below 0.15. Electrostatic stability in case of using DDAB was resulted excellent and... | en_US |
uk.file-availability | V | |
uk.grantor | Univerzita Karlova, Farmaceutická fakulta v Hradci Králové, Katedra farmaceutické technologie | cs_CZ |
thesis.grade.code | 2 | |
dc.contributor.consultant | Martiška, Juraj | |
uk.publication-place | Hradec Králové | cs_CZ |
uk.thesis.defenceStatus | O | |