0000000000089536

AUTHOR

Piersandro Pallavicini

0000-0002-5223-0233

showing 13 related works from this author

Gold nanostars coated with neutral and charged polyethylene glycols: A comparative study of in-vitro biocompatibility and of their interaction with S…

2015

Gold nanostars (GNS) have been coated with four different polyethylene glycols (PEGs) equipped with a -SH function for grafting on the gold surface. These PEGs have different chain lengths with average MW = 2000, 3000, 5000 and average number of -O-CH2-CH2 - units 44, 66, and 111, respectively. Two are neutral and two are terminated with -COOH and -NH2 functions, thus bearing negative and positive charges at physiological pH, thanks to the formation of carboxylate and ammonium groups. The negative charge of the GNS coated with PEG carboxylate has also been exploited to further coat the GNS with the PAH (polyallylamine hydrochloride) cationic polymer. Vitality tests have been carried out on …

Polyethylene glycolBiocompatibilityCell SurvivalMetal NanoparticlesPolyethylene glycolCell morphologyBiochemistryPolyethylene GlycolsInorganic Chemistrychemistry.chemical_compoundNeuroblastomaMicroscopy Electron TransmissionCell Line TumorPEG ratioOrganic chemistryHumansCarboxylatechemistry.chemical_classificationGold nanostarsMolecular StructureEndocytosiCationic polymerizationGold nanostarPolymerEndocytosisTwo-photon luminescenceNanomedicinechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiocompatibilityGoldPolyallylamine hydrochlorideNuclear chemistry
researchProduct

Gold nanostar–polymer hybrids for siRNA delivery: Polymer design towards colloidal stability and in vitro studies on breast cancer cells

2017

To overcome the low bioavailability of siRNA (small interfering RNA) and to improve their transfection efficiency, the use of non-viral delivery carriers is today a feasible approach to transform the discovery of these incredibly potent and versatile drugs into clinical practice. Polymer-modified gold nanoconstructs (AuNCs) are currently viewed as efficient and safe intracellular delivery carriers for siRNA, as they have the possibility to conjugate the ability to stably entrap and deliver siRNAs inside cells with the advantages of gold nanoparticles, which can act as theranostic agents and radiotherapy enhancers through laser-induced hyperthermia. In this study, AuNCs were prepared by coat…

3003siRNA deliverySmall interfering RNAPolymersMetal NanoparticlesPharmaceutical ScienceGold Colloid02 engineering and technologyPolyethylene Glycol01 natural sciencesPolyethylene GlycolsGold Colloidchemistry.chemical_compoundDrug Delivery SystemsMCF-7 CellDrug StabilityCoatingRNA Small InterferingPolymerDrug Carrierchemistry.chemical_classificationDrug CarriersTumorLipoic acidGold nanostarPolymer021001 nanoscience & nanotechnologyColloidal goldMCF-7 Cells0210 nano-technologyDrug carrierHydrophobic and Hydrophilic InteractionsBreast NeoplasmHumanBiological AvailabilityReproducibility of ResultBreast NeoplasmsNanotechnologyPolyethylene glycolengineering.materialSmall InterferingTransfection010402 general chemistryCell LineHydrophobic and Hydrophilic InteractionMetal NanoparticleCell Line TumorAmphiphileHumansGene SilencingParticle SizeGold nanostarsReproducibility of ResultsGold nanostars; Lipoic acid; MCF-7; PEG; PHEA; siRNA delivery; Biological Availability; Breast Neoplasms; Cell Line; Tumor; Drug Carriers; Drug Delivery Systems; Drug Stability; Gene Silencing; Gold; Gold Colloid; Humans; Hydrophobic and Hydrophilic Interactions; MCF-7 Cells; Metal Nanoparticles; Particle Size; Polyethylene Glycols; Polymers; RNA; Small Interfering; Reproducibility of Results; Transfection; 3003PHEAPEG0104 chemical scienceschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoengineeringRNAGoldMCF-7Drug Delivery SystemInternational Journal of Pharmaceutics
researchProduct

Optical method for predicting the composition of self-assembled monolayers of mixed thiols on surfaces coated with silver nanoparticles.

2012

With a simple optical method, based on UV-vis absorption spectra on glass slides, it is possible to predict the composition of self-assembled monolayers of mixed thiols, grafted on monolayers of silver nanoparticles. Glass slides are modified with the layer-by-layer technique, first forming a monolayer of mercaptopropyltrimethoxysilane, then grafting a monolayer of silver nanoparticles on it. These surfaces are further coated by single or mixed thiol monolayers, by dipping the slides in toluene solutions of the chosen thiols. Exchange constants are calculated for the competitive deposition between the colorless 1-dodecanethiol or PEG5000 thiol and BDP-SH, with the latter being a thiol-beari…

Absorption spectroscopyInorganic chemistrySelf-assembled monolayerSurfaces and InterfacesCondensed Matter PhysicsMole fractionSilver nanoparticlechemistry.chemical_compoundchemistryMonolayerElectrochemistryMoleculeMoietyGeneral Materials ScienceBODIPYSpectroscopyLangmuir : the ACS journal of surfaces and colloids
researchProduct

A fluorescent molecular sensor for pH windows in traditional and polymeric biocompatible micelles: comicellization of anionic species to shift and re…

2011

A new approach is presented to obtain fluorescent sensors for pH windows that work in water and under biomimetic conditions. A single molecule that features all-covalently linked components is used, thus making it capable of working as a fluorescent sensor with an OFF/ON/OFF response to pH value. The components are a tertiary amine, a pyridine, and a fluorophore (pyrene). The forms with both protonated bases or both neutral bases quench the pyrene fluorescence, whereas the form with the neutral pyridine and protonated amine groups is fluorescent. The molecular sensor is also equipped with a long alkyl chain to make it highly hydrophobic in all its protonated and unprotonated forms, that is,…

FluorophoreTertiary aminePolymersPyridinesInorganic chemistryPhotochemistryMicelleCatalysisPolystyrene sulfonatechemistry.chemical_compoundAmphiphileAminesAlkylMicellesFluorescent Dyeschemistry.chemical_classificationPyrenesfluorescence micelles polymerization potentiometry sensorsOrganic ChemistryMolecular sensorGeneral ChemistryHydrogen-Ion ConcentrationPolyelectrolyteKineticschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoHydrophobic and Hydrophilic InteractionsChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

An Off-On-Off Fluorescent Sensor for pH Windows Based on the 13aneN4-Zn 2+ System

2016

International audience; The new ligand L was prepared and features a 13-membered tetraaza macrocyclic ring with a 1,8-naphthalimide fluorophore appended to a C atom of its backbone. The protonation constants of L as well as its complexation constants with Zn2+ ions were determined in 1:1 water/methanol solutions by potentiometric titrations. Fluorimetric pH titrations were performed with L alone and L in the presence of Zn2+ ions (1:1), and the species distributions (%) versus pH were compared. A window-shaped fluorescence trend was observed with pH for the L/Zn2+ system, which behaves as an off-on-off pH sensor. The on window is centred in the 6.5-7.5 pH range, in correspondence with the f…

inorganic chemicalsFluorophorePotentiometric titrationInorganic chemistryProtonationYeast cellsSensors; Fluorescence; Zinc; Yeast cells; Macrocyclic ligands010402 general chemistry01 natural sciencesMicelleFluorescenceInorganic Chemistrychemistry.chemical_compoundMacrocyclic ligandsCyclamLipophilicity[SDV.IDA]Life Sciences [q-bio]/Food engineeringEquilibriaMicellesIonsChemosensors010405 organic chemistryLigandSensorsChelation-enhanced fluorescencezinc[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringMetal-complexesFluorescence0104 chemical scienceschemistryCyclamTitrationMacrocycles
researchProduct

Micelles as containers for self-assembled nanodevices: a fluorescent sensor for lipophilicity

2008

Potentiometric titrations, fluorescence versus pH titrations, dynamic light scattering and fluorescence polarization anisotropy studies demonstrate that inside the nanodimensioned Triton X-100 micelles, 1-pyrenecarboxylic acid, PCOO-, forms an apical complex with the Zn2+ cation encircled by a lipophilic cyclen ligand and hugely increasing its fluorescence. The ability of the Zn2+-cyclen-PCOO- complex plus its micellar container to act as a fluorescent sensor to evaluate the lipophilicity of molecular species is demonstrated on the fatty acid series CH 3(CH2)xCOOH (x=0-16). At pH 7.4 a decrease in fluorescence is observed on the addition of fatty acids that is directly related to their chai…

chemistry.chemical_classification010405 organic chemistryChemistryStereochemistryInorganic chemistryFatty acidmicelles light scattering pH fluorescence010402 general chemistry01 natural sciencesFluorescenceMicelleAtomic and Molecular Physics and Optics3. Good health0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundCyclenLipophilicity[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryTitrationPhysical and Theoretical ChemistryApical complexFluorescence anisotropyComputingMilieux_MISCELLANEOUS
researchProduct

A micellar multitasking device: sensing pH windows and gauging the lipophilicity of drugs with fluorescent signals.

2010

A multitasking fluorescent device can be obtained by forming micelles of Triton X-100, containing a lipophilic macrocyclic Cu(2+) complex and the coordinating fluorophore Coumarin 343 (C343), which features a COOH moiety. At low pH the two micellised components do not interact, and the fluorescence of Courmarin 343 (C343) is intense. At intermediate pH, C343 is deprotonated and coordinates to the Cu(2+) centre in its apical position, with fluorescence quenching. At higher pH the deprotonated C343 is displaced from Cu(2+) by the formation of an OH(-) complex, and the fluorescence is revived. This allows the system to carry out its first task as it behaves as an "on-off-on" fluorescent sensor…

FluorophoreStereochemistryOctoxynolKineticsself-assembled devices010402 general chemistry01 natural sciencesMicelleCatalysisFluorescencechemistry.chemical_compoundfluorescent probesCoumarins[ CHIM.OTHE ] Chemical Sciences/OtherlipophilicityMoietyCarboxylateComputingMilieux_MISCELLANEOUSMicelles010405 organic chemistryChemistryOrganic ChemistryAnti-Inflammatory Agents Non-SteroidalAnticoagulantsWaterGeneral ChemistryHydrogen-Ion ConcentrationFluorescence0104 chemical sciencesPartition coefficientCrystallographyKineticsSpectrometry FluorescencepH windowsLipophilicity[CHIM.OTHE]Chemical Sciences/OtherChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

A monolayer of a Cu2+-tetraazamacrocyclic complex on glass as the adhesive layer for silver nanoparticles grafting, in the preparation of surface-act…

2011

International audience; A silane-derivatized tetraaza Cu2+ macrocyclic complex is prepared, which forms monolayers on glass surfaces, capable of allowing the further deposition of a stable monolayer of silver nanoparticles, obtaining by this, surfaces that display an enhanced antibacterial activity against Staphylococcus aureus and Escherichia coli.

Chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyGrafting01 natural sciencesCatalysisSilver nanoparticle0104 chemical sciencesChemical engineeringMonolayerMaterials ChemistryOrganic chemistry[CHIM]Chemical SciencesAdhesive0210 nano-technologyAntibacterial activityLayer (electronics)Deposition (law)
researchProduct

The Cu(II) complex of a C-lipophilized 13aneN4 macrocycle with an additional protonable amino group as micellar anion receptor.

2009

Three 13aneN4 macrocyclic ligands have been prepared bearing a -CH(2)NHR side arm (R = H, n-C(5)H(11), n-C(10)H(21)) on a carbon atom. When Cu(2+) is complexed in the macrocyclic ring, the amino group of the side arm undergoes an acid-base protonation equilibrium but it is not able to coordinate apically the metal cation even when it is deprotonated. The Cu(2+) complex with the ligand bearing the longest appended aliphatic chain is fully confined inside Triton X-100 micelles, and its ability to bind and sequestrate a series of anions inside micelles has been studied at two different pH values, i.e. both with protonated and neutral side-arm amino group. The favourable role played by the prot…

010405 organic chemistryLigandStereochemistryChemistryProtonation010402 general chemistryRing (chemistry)01 natural sciencesMicelle0104 chemical sciencesInorganic ChemistryMetalDeprotonationGroup (periodic table)visual_artvisual_art.visual_art_mediumAnion receptorDalton transactions (Cambridge, England : 2003)
researchProduct

Amphiphilic Copolymers Based on Poly[(hydroxyethyl)-d,l-aspartamide]: A Suitable Functional Coating for Biocompatible Gold Nanostars

2013

Novel amphiphilic copolymers have been synthesized based on a biocompatible poly(hydroxyethylaspartamide) (PHEA) backbone, bearing both anchoring groups for gold nanoparticles, such as thiols and disulfide, and conjugable moieties, such as amino groups, the latter as points suitable for appending further functional agents. The strategy was to functionalize α,β-poly[(N-2- hydroxyethyl)-d,l-aspartamide] (PHEA) with PEG2000-NH2 and with ethylenediamine (EDA) obtaining a partially pegylated copolymer with a large number of pendant primary amino groups. A fraction of the latter was conjugated with molecules bearing terminal thiol moieties such as 12-mercaptododecanoic acid (MDA) and disulfide gr…

Polymers and PlasticsCell SurvivalMetal NanoparticlesBioengineeringEthylenediamineengineering.materialConjugated systemPolyethylene GlycolsBiomaterialsSurface-Active Agentschemistry.chemical_compoundCoated Materials BiocompatibleCoatingCell Line TumorMaterials TestingAmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansMoleculePoly(hydroxyethyl)-DL-aspartamideParticle Sizechemistry.chemical_classificationAmphiphilic copolymersgold nanostarlipoic acidEthylenediamineschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoColloidal goldThiolengineeringGoldPeptidesgold nanoparticleBiomacromolecules
researchProduct

Thermal and Chemical Stability of Thiol Bonding on Gold Nanostars

2015

The stability of thiol bonding on the surface of star-shaped gold nanoparticles was studied as a function of temperature in water and in a set of biologically relevant conditions. The stability was evaluated by monitoring the release of a model fluorescent dye, Bodipy-thiol (BDP-SH), from gold nanostars (GNSs) cocoated with poly(ethylene glycol) thiol (PEG-SH). The increase in the BDP-SH fluorescence emission, quenched when bound to the GNSs, was exploited to this purpose. A maximum 15% dye release in aqueous solution was found when the bulk temperature of gold nanostars solutions was increased to T = 42 °C, the maximum physiological temperature. This fraction reduces 3-5% for temperatures …

Aqueous solutionSurface PropertiesAnalytical chemistryMetal NanoparticlesCondensed Matter PhysicSurfaces and InterfacesCondensed Matter PhysicsElectrochemistryPhotochemistryFluorescenceNanostructureschemistry.chemical_compoundchemistryColloidal goldElectrochemistryGeneral Materials ScienceChemical stabilityThermal stabilityGoldSulfhydryl CompoundsMaterials Science (all)Surface plasmon resonanceSurfaces and InterfaceEthylene glycolSpectroscopyLangmuir
researchProduct

Multicomponent polymeric micelles based on polyaspartamide as tunable fluorescent pH-window biosensors

2010

Abstract PHEA-PEG 5000 -C 16 is a polyaspartamide polymer with appended hydrophilic PEG 5000 functions and hydrophobic n-C 16 units forming biocompatible micelles with a CAC as low as 1.8 × 10 −7  M. The protonation and acidity constants of the polymer's amino and carboxylic groups have been determined by potentiometric titrations at five different concentrations higher than CAC, finding concentration-independent values. Viscosity and polarity of the micellar core have been investigated by means of fluorescent probes, finding local values comparable to those of pure toluene and to the core of sodium dodecyl sulphate micelles, independently on the protonation degree of the polymer. The fluor…

FluorophorePolymeric micelles Fluorescent biosensor PH window Self-assemblinGInorganic chemistryPotentiometric titrationBiomedical EngineeringBiophysicsProtonationBiosensing TechniquesMicellePolyethylene Glycolschemistry.chemical_compoundElectrochemistryOrganic chemistryMicellesPolyhydroxyethyl Methacrylatechemistry.chemical_classificationEquipment DesignGeneral MedicinePolymerHydrogen-Ion ConcentrationEquipment Failure AnalysisSpectrometry FluorescencechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPyreneSelf-assemblyPeptidesBiosensorBiotechnologyBiosensors and Bioelectronics
researchProduct

Gold nanostars co-coated with the Cu(II) complex of a tetraazamacrocyclic ligand

2015

The twelve-membered tetraazamacrocyclic ligand L1 bears an appended lipoic acid unit, whose disulphide ring is an efficient grafting moiety for the surface of gold nanostars (GNS). The GNS that were used featured a localized surface plasmon resonance (LSPR) absorption at ∼800 nm, i.e. in the near infrared (NIR). We investigated different approaches for coating them with the Cu(2+) complex of L1. While the direct reaction of [CuL1](2+) with as-prepared GNS led to aggregation, an initial coating step with polyethyleneglycol-thiol (PEG-SH) was found to be advantageous. Displacement reactions were carried out on pegylated GNS either with [CuL1](2+), directly generating [Cun(L1@GNS)](2n+), or wi…

LuminescenceLuminescent AgentsMacrocyclic CompoundsGole nanoparticelle Cooper macrocyclesStereochemistryChemistryKineticsMetal NanoparticlesPet imagingSurface Plasmon Resonanceengineering.materialPhotothermal therapyCyclamsInorganic ChemistryCrystallographyTransmetalationCoatingCoordination ComplexesHeterocyclic CompoundsengineeringMoietyGoldSurface plasmon resonanceLuminescenceCopper
researchProduct