E. Leo

发表

Induction of Endocytosis and Pore Formation Ultrasound and Microbubble-Targeted Delivery of Macromolecules Is Regulated

W. Paulus, O. Kamp, N. Jong, 2009 .

Nuclear localization of cationic solid lipid nanoparticles containing Protamine as transfection promoter.

B. Ruozi, M. Montanari, G. Tosi, 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

pDNA condensation capacity and in vitro gene delivery properties of cationic solid lipid nanoparticles.

B. Ruozi, R. Battini, M. Montanari, 2010, International journal of pharmaceutics.

Oral tolerance elicited in mice by beta-lactoglobulin entrapped in biodegradable microspheres.

A. Pfeifer, P. Couvreur, E. Fattal, 2000, Vaccine.

Inhaled Solid Lipid Microparticles to target alveolar macrophages for tuberculosis.

M. A. Croce, E. Leo, M. Bondi, 2014, International journal of pharmaceutics.

Protein immobilization in crosslinked alginate microparticles

E. Leo, M. Bernabei, V. Iannuccelli, 2002, Journal of microencapsulation.

Application of atomic force microscopy to characterize liposomes as drug and gene carriers.

B. Ruozi, G. Tosi, M. Vandelli, 2007, Talanta.

Self-Assembled Lipid Nanoparticles for Oral Delivery of Heparin-Coated Iron Oxide Nanoparticles for Theranostic Purposes

M. Montanari, E. Leo, E. Vismara, 2017, Molecules.

Newly synthesized surfactants for surface mannosylation of respirable SLN assemblies to target macrophages in tuberculosis therapy

E. Leo, L. Costantino, C. Rustichelli, 2018, Drug Delivery and Translational Research.

Chitosan-Alginate Microparticles as a Protein Carrier

E. Leo, M. Bernabei, V. Iannuccelli, 2001, Drug development and industrial pharmacy.

Intact collagen and atelocollagen sponges: Characterization and ESEM observation

B. Ruozi, G. Tosi, F. Forni, 2007 .

Characterization of Natural Clays from Italian Deposits with Focus on Elemental Composition and Exchange Estimated by EDX Analysis: Potential Pharmaceutical and Cosmetic Uses

E. Leo, M. Romagnoli, Eleonora Maretti, 2016, Clays and Clay Minerals.

In vitro evaluation of PLA nanoparticles containing a lipophilic drug in water-soluble or insoluble form.

Maria Angela Vandelli, Flavio Forni, F. Forni, 2004, International journal of pharmaceutics.

Changing the pH of the external aqueous phase may modulate protein entrapment and delivery from poly(lactide-co-glycolide) microspheres prepared by a w/o/w solvent evaporation method.

P. Couvreur, E. Fattal, E. Leo, 1998, Journal of microencapsulation.

In vitro evaluation of a potential colonic delivery system that releases drug after a controllable lag-time

F. Forni, M. Vandelli, E. Leo, 1996 .

Design and physicochemical characterization of novel hybrid SLN-liposome nanocarriers for the smart co-delivery of two antitubercular drugs

M. Mori, F. Meneghetti, C. Castellano, 2022, Journal of Drug Delivery Science and Technology.

Gastroretentive montmorillonite-tetracycline nanoclay for the treatment of Helicobacter pylori infection.

E. Leo, M. Montorsi, C. Rustichelli, 2015, International journal of pharmaceutics.

In vivo β-carotene skin permeation modulated by Nanostructured Lipid Carriers.

C. Siligardi, E. Leo, C. Rustichelli, 2021, International journal of pharmaceutics.

Particulate adducts based on sodium risedronate and titanium dioxide for the bioavailability enhancement of oral administered bisphosphonates.

L. Ferraro, C. Bignozzi, S. Beggiato, 2010, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Flow cytometry and live confocal analysis for the evaluation of the uptake and intracellular distribution of FITC-ODN into HaCaT cells

B. Ruozi, R. Battini, M. Montanari, 2009, Journal of liposome research.

Design, Characterization, and In Vitro Assays on Muscle Cells of Endocannabinoid-like Molecule Loaded Lipid Nanoparticles for a Therapeutic Anti-Inflammatory Approach to Sarcopenia

R. Battini, E. Leo, C. Rustichelli, 2022, Pharmaceutics.

A Peptidic Thymidylate-Synthase Inhibitor Loaded on Pegylated Liposomes Enhances the Antitumour Effect of Chemotherapy Drugs in Human Ovarian Cancer Cells

Maria Paola Costi, G. Ponterini, E. Leo, 2020, International journal of molecular sciences.

Solid Lipid Nanoparticle assemblies (SLNas) for an anti-TB inhalation treatment-A Design of Experiments approach to investigate the influence of pre-freezing conditions on the powder respirability.

E. Leo, M. Romagnoli, C. Rustichelli, 2016, International journal of pharmaceutics.

Design flexibility influencing the in vitro behavior of cationic SLN as a nonviral gene vector.

M. Montanari, E. Leo, E. Vighi, 2013, International journal of pharmaceutics.

Bile salt-coating modulates the macrophage uptake of nanocores constituted by a zidovudine prodrug and enhances its nose-to-brain delivery.

L. Ferraro, S. Beggiato, E. Leo, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Application of the “in-oil nanoprecipitation” method in the encapsulation of hydrophilic drugs in PLGA nanoparticles

E. Leo, A. Dalpiaz, B. Pavan, 2016 .

Fabrication via a nonaqueous nanoprecipitation method, characterization and in vitro biological behavior of N(6)-cyclopentyladenosine-loaded nanoparticles.

E. Leo, E. Vighi, A. Dalpiaz, 2009, Journal of pharmaceutical sciences.

A Polysorbate-Based Non-Ionic Surfactant Can Modulate Loading and Release of β-Lactoglobulin Entrapped in Multiphase Poly(DL-Lactide-co-glycolide) Microspheres

P. Couvreur, E. Fattal, E. Leo, 1999, Pharmaceutical Research.

Re-dispersible cationic solid lipid nanoparticles (SLNs) freeze-dried without cryoprotectors: characterization and ability to bind the pEGFP-plasmid.

B. Ruozi, R. Battini, M. Montanari, 2007, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

In Vivo Biodistribution of Respirable Solid Lipid Nanoparticles Surface-Decorated with a Mannose-Based Surfactant: A Promising Tool for Pulmonary Tuberculosis Treatment?

C. Siligardi, E. Leo, L. Costantino, 2020, Nanomaterials.

Surface engineering of Solid Lipid Nanoparticle assemblies by methyl α-d-mannopyranoside for the active targeting to macrophages in anti-tuberculosis inhalation therapy.

M. A. Croce, E. Leo, L. Costantino, 2017, International journal of pharmaceutics.

Doxorubicin-loaded gelatin nanoparticles stabilized by glutaraldehyde: Involvement of the drug in the cross-linking process

F. Forni, M. Vandelli, E. Leo, 1997 .

General and cardiac toxicity of doxorubicin-loaded gelatin nanoparticles.

R. Arletti, F. Forni, E. Leo, 1997, Farmaco.

PLA-microparticles formulated by means a thermoreversible gel able to modify protein encapsulation and release without being co-encapsulated.

B. Ruozi, G. Tosi, M. Vandelli, 2006, International journal of pharmaceutics.

Bead Coating Process Via an Excess of Crosslinking Agent

M. Vandelli, E. Leo, M. Bernabei, 1995 .

Development and characterization of biodegradable nanospheres as delivery systems of anti-ischemic adenosine derivatives.

F. Forni, M. Vandelli, E. Leo, 2005, Biomaterials.

Enhanced anti-hyperproliferative activity of human thymidylate synthase inhibitor peptide by solid lipid nanoparticle delivery.

Maria Paola Costi, E. Leo, M. Hanuskovà, 2015, Colloids and surfaces. B, Biointerfaces.

Conveying a newly designed hydrophilic anti-human thymidylate synthase peptide to cisplatin resistant cancer cells: are pH-sensitive liposomes more effective than conventional ones?

Maria Paola Costi, E. Leo, F. Genovese, 2017, Drug development and industrial pharmacy.

The Influence of 2‐Hydroxypropyl‐β‐cyclodextrin on the Haemolysis Induced by Bile Acids

G. Salvioli, M. Vandelli, E. Leo, 1996, The Journal of pharmacy and pharmacology.

Studying the in vitro behavior of cationic solid lipid nanoparticles as a nonviral vector.

E. Leo, E. Vighi, 2012, Nanomedicine.

Surface drug removal from ibuprofen-loaded PLA microspheres.

F. Forni, E. Leo, M. Bernabei, 2000, International journal of pharmaceutics.

In vivo fate and immune pulmonary response after nasal administration of microspheres loaded with phosphorylcholine-thyroglobulin.

P. Couvreur, E. Caudron, E. Fattal, 1999, International journal of pharmaceutics.

PVP Solid Dispersions for the Controlled Release of Furosemide from a Floating Multiple-Unit System

E. Leo, M. Bernabei, V. Iannuccelli, 2000, Drug development and industrial pharmacy.

Drugs/lamellae interface influences the inner structure of double-loaded liposomes for inhaled anti-TB therapy: An in-depth small-angle neutron scattering investigation.

M. Mori, F. Meneghetti, C. Castellano, 2019, Journal of colloid and interface science.

Influence of secondary preparative parameters and aging effects on PLGA particle size distribution: a sedimentation field flow fractionation investigation

E. Leo, E. Vighi, C. Contado, 2012, Analytical and Bioanalytical Chemistry.

Nasal biocompatible powder of geraniol oil complexed with cyclodextrins for neurodegenerative diseases: Physicochemical characterization and in vivo evidences of nose to brain delivery.

L. Ferraro, S. Beggiato, E. Leo, 2021, Journal of controlled release : official journal of the Controlled Release Society.

Brain uptake of a Zidovudine prodrug after nasal administration of solid lipid microparticles.

L. Ferraro, S. Beggiato, E. Leo, 2014, Molecular pharmaceutics.

Drug release from perforated matrices containing hydroxypropylcellulose

M. Vandelli, E. Leo, M. Bernabei, 1998 .

Self‐assembled organogelators as artificial stratum corneum models: Key‐role parameters for skin permeation prediction

E. Leo, C. Rustichelli, Eleonora Maretti, 2019, International journal of pharmaceutics.

OF NATURAL CLAYS FROM ITALIAN DEPOSITS WITH 1 THE FOCUS ON ELEMENTAL COMPOSITION AND EXCHANGE ESTIMATED 2 BY EDX ANALYSIS FOR POTENTIAL PHARMACEUTICAL AND COSMETIC 3 USES 4

E. Leo, M. Romagnoli, Eleonora Maretti, 2016 .

Nasal administration of nanoencapsulated geraniol/ursodeoxycholic acid conjugate: Towards a new approach for the management of Parkinson's disease.

L. Ferraro, S. Beggiato, E. Leo, 2020, Journal of controlled release : official journal of the Controlled Release Society.

Organo-modified bentonite for gentamicin topical application: Interlayer structure and in vivo skin permeation

E. Leo, G. Ori, M. Montorsi, 2018, Applied Clay Science.

Study of the Influence of Several Stabilizing Agents on the Entrapment and InVitro Release of pBC 264 from Poly(Lactide-Co-Glycolide) Microspheres Prepared by a W/O/W Solvent Evaporation Method

P. Couvreur, E. Fattal, E. Leo, 1996, Pharmaceutical Research.

The role of protamine amount in the transfection performance of cationic SLN designed as a gene nanocarrier

B. Ruozi, M. Montanari, E. Leo, 2012, Drug delivery.

pH-Promoted Release of a Novel Anti-Tumour Peptide by “Stealth” Liposomes: Effect of Nanocarriers on the Drug Activity in Cis-Platinum Resistant Cancer Cells

Maria Paola Costi, G. Ponterini, E. Leo, 2018, Pharmaceutical Research.

Complementary use of flow and sedimentation field-flow fractionation techniques for size characterizing biodegradable poly(lactic acid) nanospheres.

E. Leo, M. Zborowski, C. Contado, 2007, Journal of chromatography. A.

Development and characterization of PLGA nanoparticles as delivery systems of a prodrug of zidovudine obtained by its conjugation with ursodeoxycholic acid

E. Leo, E. Vighi, C. Contado, 2014, Drug delivery.

Targeting the central nervous system: in vivo experiments with peptide-derivatized nanoparticles loaded with Loperamide and Rhodamine-123.

M A Vandelli, F Forni, G Tosi, 2007, Journal of controlled release : official journal of the Controlled Release Society.

In vivo penetration of bare and lipid-coated silica nanoparticles across the human stratum corneum.

E. Leo, M. Romagnoli, S. Scalia, 2014, Colloids and surfaces. B, Biointerfaces.

In vivo detection of lipid-based nano- and microparticles in the outermost human stratum corneum by EDX analysis.

E. Leo, M. Romagnoli, V. Iannuccelli, 2013, International journal of pharmaceutics.

Nanoparticle formulation may affect the stabilization of an antiischemic prodrug.

G. Tosi, E. Leo, C. Contado, 2006, International journal of pharmaceutics.

Dynamic dialysis for the drug release evaluation from doxorubicin-gelatin nanoparticle conjugates.

F. Forni, E. Leo, R. Cameroni, 1999, International journal of pharmaceutics.

The Impact of Lipid Corona on Rifampicin Intramacrophagic Transport Using Inhaled Solid Lipid Nanoparticles Surface-Decorated with a Mannosylated Surfactant

C. Siligardi, E. Leo, L. Costantino, 2019, Pharmaceutics.

pH-Promoted Release of a Novel Anti-Tumour Peptide by “Stealth” Liposomes: Effect of Nanocarriers on the Drug Activity in Cis-Platinum Resistant Cancer Cells

Maria Paola Costi, G. Ponterini, E. Leo, 2018, Pharmaceutical Research.

Optimization of the encapsulation and release of beta-lactoglobulin entrapped poly(DL-lactide-co-glycolide) microspheres.

P. Couvreur, E. Fattal, E. Leo, 1999, International journal of pharmaceutics.

Chitosan/heparin polyelectrolyte complexes as ion-paring approach to encapsulate heparin in orally administrable SLN: In vitro evaluation

M. Montanari, E. Leo, A. Dalpiaz, 2021 .

Drugs acting on the beta isoform of human topoisomerase II (p180).

B. Gatto, E. Leo, 2003, Current medicinal chemistry. Anti-cancer agents.