About: Rita Cortesi

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) дослідниця (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) hulumtuese (sq)
rdfs:label	Rita Cortesi (en) Rita Cortesi (es) Rita Cortesi (it) Rita Cortesi (nl) Rita Cortesi (ast)
skos:prefLabel	Rita Cortesi (en) Rita Cortesi (es) Rita Cortesi (it) Rita Cortesi (nl) Rita Cortesi (ast)
name	Rita Cortesi (en) Rita Cortesi (es) Rita Cortesi (it) Rita Cortesi (nl) Rita Cortesi (ast)
given name	wds:Q56957276-EB1A7957-7E54-488B-B8DB-BCC1979693CF
given name	Rita
instance of	wds:Q56957276-CA9F79ED-7BFF-483C-B456-6DC689EC3314
instance of	Homo sapiens
occupation	wds:Q56957276-93AB9097-A260-48A2-9BD5-62745990D350
employer	wds:Q56957276-5DB3E289-1CF8-4BFD-80D9-ED0A3AA25966 wds:Q56957276-7D4BF7F3-2E16-4DCD-A949-CACCBA9BEE90
sex or gender	wds:Q56957276-46FF14BC-2465-4383-A8BB-E8DDCAF6CE1B
family name	wds:Q56957276-FA145E7E-9575-462E-88E8-F2C01B9DDA0A
occupation	researcher
employer	University of Ferrara University of Nottingham
sex or gender	female organism
family name	Cortesi
ORCID iD	wds:Q56957276-EB5654BF-F6E3-4B1E-951B-8704A9D62A28
ORCID iD	https://orcid.org/0000-0002-1060-2676
ORCID iD	0000-0002-1060-2676
ResearcherID	wds:Q56957276-5E512BA5-7BD7-4C49-BE8E-E02198076D8C
ResearcherID	G-9406-2012
IRIS UNIFE author ID	wds:Q56957276-D2B76696-77FF-43F5-9DCD-0E82CDE6130C
IRIS UNIFE author ID	04384
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56957276
is author of	Colloidal dispersions for the delivery of acyclovir: a comparative study. Cationic liposomes as potential carriers for ocular administration of peptides with anti-herpetic activity Preparation and characterization of cationic microspheres for gene delivery. Preparation of liposomes by reverse-phase evaporation using alternative organic solvents Liposomes, micelles and microemulsions as new delivery systems for cytotoxic alkaloids. Nanosystems for skin hydration: a comparative study Hyaluronan-based microspheres as tools for drug delivery: a comparative study. Spray dried Eudragit microparticles as encapsulation devices for vitamin C. Production of Eudragit Microparticles by Spray-Drying Technique: Influence of Experimental Parameters on Morphological and Dimensional Characteristics Cubosome dispersions as delivery systems for percutaneous administration of indomethacin Preparation and characterisation of poly(vinyl alcohol)/cyclodextrin microspheres as matrix for inclusion and separation of drugs. Myrosinase-generated isothiocyanate from glucosinolates: Isolation, characterization and in vitro antiproliferative studies Liposomes- and ethosomes-associated distamycins: a comparative study Cationic liposomes as delivery systems for double-stranded PNA-DNA chimeras exhibiting decoy activity against NF-kappaB transcription factors Cationic lipid nanosystems as carriers for nucleic acids Nanostructured lipid dispersions for topical administration of crocin, a potent antioxidant from saffron (Crocus sativus L.). Sugar cross-linked gelatin for controlled release: microspheres and disks Gelatin microspheres: influence of preparation parameters and thermal treatment on chemico-physical and biopharmaceutical properties Production of lipospheres as carriers for bioactive compounds In Vitro Antiproliferative Activity of Isothiocyanates and Nitriles Generated by Myrosinase-Mediated Hydrolysis of Glucosinolates from Seeds of Cruciferous Vegetables Biodistribution of nanostructured lipid carriers: a tomographic study Nanoparticulate lipid dispersions for bromocriptine delivery: characterization and in vivo study Effect of nanostructured lipid vehicles on percutaneous absorption of curcumin DNA binding activity and inhibition of DNA-protein interactions. Differential effects of tetra-p-amidino-phenoxyneopentane and its 2'-bromo derivative. Kinetics of bromocriptine release from microspheres: comparative analysis between different in vitro models. Curcumin containing monoolein aqueous dispersions: a preformulative study Nanomedicines to Treat Skin Pathologies with Natural Molecules Non-phospholipid vesicles as carriers for peptides and proteins: production, characterization and stability studies Monoolein aqueous dispersions as a delivery system for quercetin. A novel multicompartimental system based on aminated poly(vinyl alcohol) microspheres/succinoylated pullulan microspheres for oral delivery of anionic drugs. Lipid Nanoparticles and Active Natural Compounds: A Perfect Combination for Pharmaceutical Applications Lipid-based nanoparticles containing cationic derivatives of PTA (1,3,5-triaza-7-phosphaadamantane) as innovative vehicle for Pt complexes: Production, characterization and in vitro studies Cross-Enzyme Inhibition by Gabexate Mesylate: Formulation and Reactivity Study Preparation and characterization of starch/cyclodextrin bioadhesive microspheres as platform for nasal administration of Gabexate Mesylate (Foy) in allergic rhinitis treatment. Production and in vitro evaluation of gelatin microspheres containing an antitumour tetra-amidine Dextran cross-linked gelatin microspheres as a drug delivery system Interchangeability of two 500 mg amoxicillin capsules with one 1000 mg amoxicillin tablet after a single oral administration. Evaluation of monooleine aqueous dispersions as tools for topical administration of curcumin: characterization, in vitro and ex-vivo studies. Ethosomes and organogels for cutaneous administration of crocin Design and characterization of fenretinide containing organogels. Cannabinoid antagonist in nanostructured lipid carriers (NLCs): design, characterization and in vivo study Clotrimazole-loaded nanostructured lipid carrier hydrogels: thermal analysis and in vitro studies Acyclovir delivery systems Clotrimazole nanoparticle gel for mucosal administration Intranasal immunization in mice with non-ionic surfactants vesicles containing HSV immunogens: a preliminary study as possible vaccine against genital herpes. Peptide-based cationic molecules for the production of positive charged liposomes and micelles Preparation and characterisation of thermoresponsive poly[(N-isopropylacrylamide-co-acrylamide-co-(hydroxyethyl acrylate)] microspheres as a matrix for the pulsed release of drugs. Cellulose acetate butyrate-pH/thermosensitive polymer microcapsules containing aminated poly(vinyl alcohol) microspheres for oral administration of DNA. Waste Material of Propolis as a Film Forming Agent Intended to Modify the Metronidazole Release: Preparation and Characterization. Evaluation of percutaneous absorption of naproxen from different liposomal formulations Investigation of the Bioequivalence of Rosuvastatin 20 mg Tablets after a Single Oral Administration in Mediterranean Arabs Using a Validated LC-MS/MS Method

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