Recent advancements in polymer/liposome assembly for drug delivery: From surface modifications to hybrid vesicles

Liposomes are consolidated and attractive biomimetic nanocarriers widely used in the field of drug delivery. The structural versatility of liposomes has been exploited for the development of various carriers for the topical or systemic delivery of drugs and bioactive molecules, with the possibility of increasing their bioavailability and stability, and modulating and directing their release, while limiting the side effects at the same time. Nevertheless, first-generation vesicles suffer from some limitations including physical instability, short in vivo circulation lifetime, reduced payload, uncontrolled release properties, and low targeting abilities. Therefore, liposome preparation technology soon took advantage of the possibility of improving vesicle performance using both natural and synthetic polymers. Polymers can easily be synthesized in a controlled manner over a wide range of molecular weights and in a low dispersity range. Their properties are widely tunable and therefore allow the low chemical versatility typical of lipids to be overcome. Moreover, depending on their structure, polymers can be used to create a simple covering on the liposome surface or to intercalate in the phospholipid bilayer to give rise to real hybrid structures. This review illustrates the main strategies implemented in the field of polymer/liposome assembly for drug delivery, with a look at the most recent publications without neglecting basic concepts for a simple and complete understanding by the reader

Electronic nose and isotope ratio mass spectrometry in combination with chemometrics for the characterization of the geographical origin of Italian sweet cherries

Sweet cherries from two Italian regions, Apulia and Emilia Romagna, were analysed using electronic nose (EN) and isotope ratio mass spectrometry (IRMS), with the aim of distinguishing them according to their geographic origin. The data were elaborated by statistical techniques, examining the EN and IRMS datasets both separately and in combination. Preliminary exploratory overviews were performed and then linear discriminant analyses (LDA) were used for classification. Regarding EN, different approaches for variable selection were tested, and the most suitable strategies were highlighted. The LDA classification results were expressed in terms of recognition and prediction abilities and it was found that both EN and IRMS performed well, with IRMS showing better cross-validated prediction ability (91.0%); the EN–IRMS combination gave slightly better results (92.3%). In order to validate the final results, the models were tested using an external set of samples with excellent results

Photocatalytic degradation of methyl-red by immobilised nanoparticles of TiO2 and ZnO

none6noIn this work, we report on the degradation of methyl-red (2-(4-Dimethylamino-phenylazo)-benzoic acid - C.I. 13020) under UV irradiation in the presence of nanosized ZnO and TiO2. Oxide nanocrystals with controlled size were synthesised by using non-hydrolytic approaches and tested for the photocatalysed degradation. The performances of the immobilised nanoparticles were compared with their commercial counterparts after immobilization onto a solid support. The influence of some experimental conditions, namely pH and dye concentration, were investigated by monitoring the dye decoloration spectrophotometrically. Several intermediate by-products were identified by HPLC-MS, showing that two different mechanisms were operative during the photocatalytic oxidationsee at: http://www.iwaponline.com/wst/04904/wst049040183.htmopenR. COMPARELLI; P. D. COZZOLI; M. L. CURRI; A. AGOSTIANO; G. MASCOLO; G. LOVECCHIOR., Comparelli; Cozzoli, Pantaleo Davide; M. L., Curri; A., Agostiano; G., Mascolo; G., Lovecchi

Nanocrystalline TiO2 based films onto fibers for photocatalytic degradation of organic dye in aqueous solution

Nanocrystalline titania (TiO2) synthesized via sol–gel, by using an alkoxide precursor were deposited onto commercially available silica and alumina fibers, namely E-Glass and Nextel 650, respectively. Different processing conditions and material preparation parameters, such as amount of TiO2, film composition and annealing temperature were tested in order to obtain nanocrystalline TiO2 with different morphological and structural characteristics. The materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and the Brunauer, Emmett, and Teller (BET) surface area measurements. The photocatalytic activity of the obtained coated fibers was investigated by monitoring the degradation of a model molecule, an azo dye (Methyl Red), under UV irradiation in aqueous solution. The detected photocatalytic performance of the sol–gel derived nanocrystalline TiO2 was explained on the basis of mechanism associated to the photocatalytic decomposition of organic molecules using semiconductor oxides and accounted for the structural and morphological characteristics of the TiO2 based coating. The materials with the most suited characteristics for photocatalysis were used to scale up the deposition onto a larger sample of fiber and then tested in a photocatalytic reactor. A commercially available TiO2 standard material (TiO2 P25 Degussa) was used as reference, in order to ultimately assess the viability of the coating process for real application

Amino grafted MCM-41 as highly efficient and reversible ecofriendly adsorbent material for the Direct Blue removal from wastewater

The very high adsorption efficiency of Direct Blue (DB), an anionic toxic azo dye, onto amino grafted mesoporous silica nanoparticles (MCM-41), was studied in this paper, for possible industrial applications. Interesting challenges and advances are proposed in this field, presenting an adsorbent able to efficiently and rapidly remove the anionic dye from water. The important added value of this work regards the system recycle, which allows both the DB and adsorbent material recover, with a global reduction of the environmental impact, in the viewpoint of the green economy. Indeed, this paper is the first example of very fast removal and recycle of great amounts of DB with adsorbent materials characterized by impressive adsorption/desorption capacities, at least of around 300mg/g for each adsorption cycle, potentially increasable by performing consecutive cycles of DB adsorption/desorption. In detail, the MCM-41 amino functionalization (MCM-41-NH2) was obtained after (MCM- 41-POST) and during (MCM-41-PRE) the synthesis of MCM-41, obtaining materials with different behavior towards the DB adsorption. The MCM-41-NH2 surface features and porous structure, before and after the dye adsorption, were carefully characterized. Considering the adsorption process, for investigating the nature of the DB/MCM-41-NH2 interaction, several parameters were studied: the contact time, the DB solutions pH values, adsorbent material and dye amount, with the additional analysis of how the adsorption process was influenced by the presence of electrolytes. The isotherms of adsorption were also considered. Although MCM-41-PRE exhibited a higher affinity towards DB molecules, the MCM-41-POST were able to rapidly desorb it, thus recycling both DB and the adsorbent material

Electrochemical Characterization and Electroanalytical Aplications of RGO_AuNPs Hybrids

A novel synthetic route for the synthesis of gold nanoparticles (AuNPs) modified graphene electrodes has been developed: Reduced Graphene Oxide (RGO) sheets are functionalized with pyrene linkers acting as growing sites for gold nanoparticles (AuNPs) of different dimensions (approximatively 5, 10 and 20 nm). The Au surface is functionalized with oleylamine or 3,4-dimethylbenzenethiol as capping agents. The hybrid material is deposited onto Carbon Screen Printed Electrodes (C-SPEs) for a deep physico-chemical and electrochemical characterization, using Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS) measurements. The role played by every single hybrid counterpart has been investigated, showing a synergistic effect, which is responsible of the enhancement of the system properties. The charge transfer from gold nanoparticles to graphene, assisted and stimulated by the pyrene linker, seems to be the key point to understand the peculiarities of this innovative material. The as prepared RGO-AuNPs hybrids have been used in the electroanalytical detection of both inorganic and organic species (arsenic, H2O2, dopamine), showing promising results in terms of sensitivities and detection limits. In particular, regarding the detection of the neurotransmitter dopamine by means of Differential Pulse Voltammetry in Phosphate Buffer Solution, a LOD of (3.3 \ub1 0.2) ppb has been reached, comparable with other electroanalytical results in the literature and in accordance with the benchmark for this molecule [1]. For arsenic detection, the hybrid devices show increased performances in comparison with bare gold or gold NPs, also allowing speciation between arsenic (III) and (V), appropriately adjusting the experimental conditions. In the case of H2O2, the hybrid devices display high electrocatalytic activity and fast electron-transfer kinetics, representing an ideal platform for developing oxidoreductase-based electrochemical biosensors as well as for detecting H2O2 in real samples. [1] J.A. Ribeiro, P.M.V. Fernandes, C.M. Pereira, F. Silva, Talanta 160 (2016) 653-679

Enhanced performances of RGO-AuNPs hybrids towards electroanalytical applications

In recent years, lot of attention has been devoted to understanding the properties of hybrid nanocomposites, \u201cbrave new materials\u201d made of two or more organic and inorganic components. These systems show enhanced or novel physico-chemical properties with respect to the single components, resulting not only from the sum of the precursors\u2019 ones, but also from interactions occurring at their interface, the so-called \u201cheterojunction\u201d. However, a remaining challenge is to understand in depth the phenomena here originating. In the present work, to start fulfilling this gap, a deep electrochemical study of hybrids made of Reduced Graphene Oxide (RGO) and Au nanoparticles (NPs) is performed, analysing carefully the role played by each single component of the material on the electrochemical properties. In more details, RGO platforms are surface functionalized with 1-aminopyrene or 1-pyrene carboxylic acid that act as heteronucleation and growing sites of the amine- or thiol-coated Au NPs of different dimensions (from 3 to 20 nm). At first, Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS) measurements are carried out in order to characterize the different hybrids. Then, the materials are applied as electroanalytical sensors for both organic and inorganic molecules (dopamine and As, respectively) with very promising results, comparable or even better than analogous systems reported in literature. Moreover, preliminary tests on H2O2 detection open the venue to the application of these materials in biosensor applications. The properties of the hybrid nanocomposite, enhanced with respect to those of the single components, are ascribed to charge transfer occurring at the heterojunction from the Au NPs to the RGO, assisted and channelled by the pyrene linker

Lipid content in higher plants under osmotic stress

Abstract In this work, we performed investigations on the lipid content of higher plants (spinach) under hyperosmotic stress, by means of thin layer chromatography (TLC) and mass spectrometry. In particular, the experiments have been performed at different plant organization levels: whole leaves, freshly prepared protoplast suspension and mesophyll cells obtained by reformation of the cell wall from protoplast suspension. The results obtained showed that hyperosmotic stress induces changes in the phospholipid content depending on the different plant organization levels studied. All phospholipids showed an increment of their content in stressed whole leaves. In particular, phosphatidylglycerol (PG) redoubles its content by 1 h of osmotic shock. Different responses to hyperosmotic stress were reported for the other systems. In the case of protoplasts, an increment of PG, phosphatidylcholine (PC) and phosphatidylinositol (PI) together with biphosphatidylglycerol (BPG) and phosphatidylethanolamine (PE) content decreasing were observed in stressed sample. For PG, identified as PG (34:4) by elecrospray ionization mass spectrometry, the increment was of about 30%. In the case of cells, conversely, a decrease of PG content under osmotic stress was recorded. The results suggest an important role of phospholipids, in particular of PG, in the osmotic stress response

Molecular interactions, characterization and photoactivity of Chlorophyll a/chitosan/2-HP-β-cyclodextrin composite films as functional and active surfaces for ROS production

Novel photosensitizing film based on the natural hybrid polymer Chitosan/2-hydroxy-propyl-β-Cyclodextrin (CH/CD) is synthesized introducing Chlorophyll a (CH/CD/Chla) as a photoactive agent for possible application in antimicrobial photodynamic therapy (PDT). The polymer absorbs visible light, in turn able to generate reactive oxygen species (ROS) and, therefore it can be used as environmental friendly and biodegradable polymeric photosensitizer (PS). The modified film is characterized by means of different spectroscopic, calorimetric, diffraction techniques and microscopic imaging methods including time-resolved absorption spectroscopy. UV–Vis, FTIR-ATR and X-ray Photoelectron Spectroscopy (XPS) analyses suggest that Chla shows a strong affinity toward Chitosan introducing interactions with amino groups present on the polymer chains. Nanosecond laser flash photolysis technique provides evidence for the population of the excited triplet state of Chla. Photogeneration of singlet oxygen is demonstrated by both direct detection by using infrared luminescence spectroscopy and chemical methods based on the use of suitable traps. Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM) and Differential Scanning Calorimetry (DSC) analyses confirm also the occurrence of structural changes both on the film surface and within the film layer induced by the insertion of the pigment. Moreover, X-ray Diffraction data (XRD) shows the existence of an amorphous phase for the chitosan films in all the compared conditions

Three-Dimensional Self-Assembly of Networked Branched TiO2 Nanocrystal Scaffolds for Efficient Room-Temperature Processed Depleted Bulk Heterojunction Solar Cells

In this work, we report on 4% power conversion efficiency (PCE) depleted bulk heterojunction (DBH) solar cells based on a high-quality electrode with a three-dimensional nanoscale architecture purposely designed so as to maximize light absorption and charge collection. The newly conceived architecture comprises a mesoporous electron-collecting film made of networked anisotropic metal-oxide nanostructures, which accommodates visible-to-infrared light harvesting quantum dots within the recessed regions of its volume. The three-dimensional electrodes were self-assembled by spin-coating a solution of colloidal branched anatase TiO2 NCs (BNC), followed by photocatalytic removal of the native organic capping from their surface by a mild UV-light treatment and filling with small PbS NCs via infiltration. The PCE = 4% of our TiO2 BNC/PbS QD DBH solar cell features an enhancement of 84% over the performance obtained for a planar device fabricated under the same conditions. Overall, the DBH device fabrication procedure is entirely carried out under mild processing conditions at room temperature, thus holding promise for low-cost and large-scale manufacturing