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Since the number of antibiotic-resistant bacterial infections is growing and cases are getting worse every year, the search for new alternative bactericidal wound dressing treatments is becoming crucial. Within this context, the use of polysaccharides from plants and seeds in innovative biopolymer technologies is of key importance. In this work, bio-nano-composite guar gum/polyvinyl alcohol (PVOH) membranes loaded with aluminum-doped zinc oxide nanoparticles were produced via electrospinning. Citric acid was added to the mixture to increase spinnability. However, depending on the pH, zinc oxide nanoparticles are partially dissociated, decreasing their bactericidal efficiency. Thus, a second successful alkaline thermo-chemical regrowth step was added to the process to treat the obtained fibers. This alkaline thermo-chemical treatment reconstituted both the nanoparticles and their bactericidal properties. The Staphylococcus aureus antibacterial assay results show that the membranes obtained after the alkaline thermo-chemical treatment presented a 57% increase in growth inhibition.
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PURPOSE: In deep burns, wound contraction and hypertrophic scar formation can generate functional derangement and debilitation of the affected part. In order to improve the quality of healing in deep second-degree burns, we developed a new treatment in a preclinical model using nanostructured membranes seeded with mesenchymal stem cells (MSCs). METHODS: Membranes were obtained by reconstitution of bacterial cellulose (reconstituted membrane [RM]) and produced by a dry-cast process, then RM was incorporated with 10% tamarind xyloglucan plus gellan gum 1:1 and 10% lysozyme (RMGT-LZ) and with 10% gellan gum and 10% lysozyme (RMG-LZ). Membrane hydrophobic/hydrophilic characteristics were investigated by static/dynamic contact-angle measurements. They were cultivated with MSCs, and cell adhesion, proliferation, and migration capacity was analyzed with MTT assays. Morphological and topographic characteristics were analyzed by scanning electron microscopy. MSC patterns in flow cytometry and differentiation into adipocytes and osteocytes were checked. In vivo assays used RMG-LZ and RMGT-LZ (with and without MSCs) in Rattus norvegicus rats submitted to burn protocol, and histological sections and collagen deposits were analyzed and immunocytochemistry assay performed. RESULTS: In vitro results demonstrated carboxyl and amine groups made the membranes moderately hydrophobic and xyloglucan inclusion decreased wettability, favoring MSC adhesion, proliferation, and differentiation. In vivo, we obtained 40% and 60% reduction in acute/chronic inflammatory infiltrates, 96% decrease in injury area, increased vascular proliferation and collagen deposition, and complete epithelialization after 30 days. MSCs were detected in burned tissue, confirming they had homed and proliferated in vivo. CONCLUSION: Nanostructured cellulose-gellan-xyloglucan-lysozyme dressings, especially when seeded with MSCs, improved deep second-degree burn regeneration.
Assuntos
Bandagens , Queimaduras/terapia , Celulose/química , Glucanos/química , Células-Tronco Mesenquimais/citologia , Muramidase/química , Nanoestruturas/química , Polissacarídeos Bacterianos/química , Xilanos/química , Animais , Vasos Sanguíneos/patologia , Queimaduras/patologia , Adesão Celular , Diferenciação Celular , Proliferação de Células , Celulose/ultraestrutura , Colágeno/metabolismo , Inflamação/patologia , Masculino , Transplante de Células-Tronco Mesenquimais/métodos , Células-Tronco Mesenquimais/ultraestrutura , Nanoestruturas/ultraestrutura , Ratos Wistar , CicatrizaçãoRESUMO
Biological scaffolds have become an attractive approach for repairing the infarcted myocardium and have been shown to facilitate constructive remodeling in injured tissues. This study aimed to investigate the possible utilization of bacterial cellulose (BC) membrane patches containing cocultured cells to limit myocardial postinfarction pathology. Myocardial infarction (MI) was induced by ligating the left anterior descending coronary artery in 45 Wistar rats, and patches with or without cells were attached to the hearts. After one week, the animals underwent echocardiography to assess for ejection fraction and left ventricular end-diastolic and end-systolic volumes. Following patch formation, the cocultured cells retained viability of >90% over 14 days in culture. The patch was applied to the myocardial surface of the infarcted area after staying 14 days in culture. Interestingly, the BC membrane without cellular treatment showed higher preservation of cardiac dimensions; however, we did not observe improvement in the left ventricular ejection fraction of this group compared to coculture-treated membranes. Our results demonstrated an important role for BC in supporting cells known to produce cardioprotective soluble factors and may thus provide effective future therapeutic outcomes for patients suffering from ischemic heart disease.
Assuntos
Terapia Baseada em Transplante de Células e Tecidos , Celulose/metabolismo , Infarto do Miocárdio/terapia , Função Ventricular Esquerda/fisiologia , Animais , Terapia Baseada em Transplante de Células e Tecidos/métodos , Coração/fisiopatologia , Miocárdio/metabolismo , Neovascularização Fisiológica , Ratos Wistar , Volume Sistólico/fisiologia , Remodelação Ventricular/fisiologiaRESUMO
In this work, bacterial cellulose was subjected to a high-power ultrasonic treatment for different time intervals. The morphological analysis, scanning electron microscopy, and atomic force microscopy revealed that this treatment changed the width and height of the microfibrillar ribbons and roughness of their surface, originating films with new nanostructures. Differential thermal analysis showed a higher thermal stability for ultrasonicated samples with a pyrolysis onset temperature of 208 degrees C for native bacterial cellulose and 250 and 268 degrees C for the modified samples. The small-angle X-ray scattering experiments demonstrated that the treatment with ultrasound increased the thickness of the ribbons, while wide-angle X-ray scattering experiments demonstrated that the average crystallite dimension and the degree of crystallinity also increased. A model is proposed where the thicker ribbons and crystallites result from the fusion of neighboring ribbons due to cavitation effects.
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Bactérias/química , Celulose/química , Nanoestruturas , Ultrassom , Microscopia de Força Atômica , Microscopia Eletrônica de Varredura , Espalhamento de RadiaçãoRESUMO
Hyaluronic acid (HA) and galactomannans (such as guar gum - GG and locust bean gum - LBG) are biomacromolecules with various applications due to their physicochemical characteristics in solution, especially their ability to form films or hydrogels in some conditions. Some of these applications are possible because they are nontoxic and biocompatible. Mixtures of HA and GG or LBG, at pH 7.4, were prepared at 25 g·L-1 of HA:LBG or HA:GG with percentages of 50:50, 60:40, 70:30 and 80:20 (w/w) and evaluated by rheology and NMR experiments regarding the interactions. The best synergism observed was between HA:LBG, most pronounced at 50% (w/w), where the dynamic modulus values G' and Gâ³ indicated the formation of physical gels with viscoelastic behavior close to that of HA. 2D NOESY spectra revealed hydrogen interconnectivity of H-1 glucuronic acid units of HA with H-5 mannose units of the main galactomannan chains. This synergism, besides producing a hydrogel with interesting properties, also can decrease the cost by partially replacing HA in many applications, such as in nutraceutical foods, support for tissue engineering and cosmetics.
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Ácido Hialurônico/química , Mananas/química , Galactanos/química , Galactose/análogos & derivados , Gomas Vegetais/químicaRESUMO
The influence of Na2SO4 as a kosmotropic salt on the thermogelation of xyloglucan (XG) solutions was measured by rheology. The gelation occurred at lower temperatures and shorter times when the salt concentration was increased above 0.5â¯mol.L-1. For Na2SO4 concentrations equal to 1â¯mol.L-1, a not thermoreversible elastic hydrogel was obtained. Salts containing various types of anions were used, and it was observed that SO42-, HPO42- and H2PO4- promoted the formation of a gelled network. The gel structure was observed using confocal laser scanning microscopy and scanning electron microscopy. In XG containing SO42 at 1â¯mol.L-1aggregates and gels were formed by interconnected sub-micrometer XG particles. Increasing the concentration of SO42- led to conformation changes in the XG, from a twisted/helical to an extended/flat conformation, as observed using circular dichroism. The naturally occurring hydrophobic sequences promoted an economically feasible XG gelling that may produce thermo and kosmo-sensitive hydrogels.
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The mechanical pretreatments intensities on characteristics of cellulose nanocrystals (CNC) prior to acid hydrolysis was evaluated. The cellulose was submitted to mechanical pretreatment as: magnetic stirring (CNCst), blending (CNCbl) or grinding by 20 (CNC20x) and 40 (CNC40x) passages in a super mass colloid mill. Then, all samples were submitted to H2SO4 hydrolysis and the CNC were evaluated by total mass yield (TMY%), rheological behavior, size distribution for width/length (WD), crystallinity index (CI%), OSO3- substitution degree (SD) and zeta potential (ζ). After hydrolysis samples exhibited the same SD (190⯱â¯5â¯mMol·kg-1), ζ (-55⯱â¯3â¯mV) and CI% (65⯱â¯2), differing only in TMY% and WD. The CNCst showed TMY% of 85%, WD of 8⯱â¯5â¯nm and 100-800â¯nm, with presence of cellulose nanofibers (CNF), suggesting incomplete hydrolysis. The CNCbl and CNC20x revealed TMY% of 65⯱â¯1, but differed in WD of 8⯱â¯5â¯nm and 300⯱â¯200â¯nm and 8⯱â¯5â¯nm and 200⯱â¯170â¯nm, respectively. The results showed that the grinding mechanical pretreatment is mandatory for CNF isolation, but not for CNC. Stability profile after the hydrolytic procedure, CI%, morphology and similar character generated CNC with adequate features and good yield, by simple mechanical stirring or blending, reducing the production's cost and allowing industrial-scale production.
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Celulose/química , Celulose/isolamento & purificação , Nanopartículas/química , Ácidos Sulfúricos/química , Celulose/análise , Fracionamento Químico/métodos , Hidrólise , Microscopia de Força Atômica , Nanopartículas/análise , Análise Espectral , ViscosidadeRESUMO
Formation of stable thin films of mixed xyloglucan (XG) and alginate (ALG) onto Si/SiO(2) wafers was achieved under pH 11.6, 50mM CaCl(2), and at 70 degrees C. XG-ALG films presented mean thickness of (16+/-2)nm and globules rich surface, as evidenced by means of ellipsometry and atomic force microscopy (AFM), respectively. The adsorption of two glucose/mannose-binding seed (Canavalia ensiformis and Dioclea altissima) lectins, coded here as ConA and DAlt, onto XG-ALG surfaces took place under pH 5. Under this condition both lectins present positive net charge. ConA and DAlt adsorbed irreversibly onto XG-ALG forming homogenous monolayers approximately (4+/-1)nm thick. Lectins adsorption was mainly driven by electrostatic interaction between lectins positively charged residues and carboxylated (negatively charged) ALG groups. Adhesion of four serotypes of dengue virus, DENV (1-4), particles to XG-ALG surfaces were observed by ellipsometry and AFM. The attachment of dengue particles onto XG-ALG films might be mediated by (i) H bonding between E protein (located at virus particle surface) polar residues and hydroxyl groups present on XG-ALG surfaces and (ii) electrostatic interaction between E protein positively charged residues and ALG carboxylic groups. DENV-4 serotype presented the weakest adsorption onto XG-ALG surfaces, indicating that E protein on DENV-4 surface presents net charge (amino acid sequence) different from E proteins of other serotypes. All four DENV particles serotypes adsorbed similarly onto lectin films adsorbed. Nevertheless, the addition of 0.005mol/L of mannose prevented dengue particles from adsorbing onto lectin films. XG-ALG and lectin layers serve as potential materials for the development of diagnostic methods for dengue.
Assuntos
Alginatos/química , Vírus da Dengue/metabolismo , Glucanos/química , Lectinas/química , Vírion/metabolismo , Xilanos/química , Alginatos/metabolismo , Concanavalina A/química , Concanavalina A/metabolismo , Dengue/metabolismo , Vírus da Dengue/química , Vírus da Dengue/ultraestrutura , Glucanos/metabolismo , Ácido Glucurônico/química , Ácido Glucurônico/metabolismo , Ácidos Hexurônicos/química , Ácidos Hexurônicos/metabolismo , Concentração de Íons de Hidrogênio , Lectinas/metabolismo , Microscopia de Força Atômica , Dióxido de Silício/química , Dióxido de Silício/metabolismo , Espectroscopia de Infravermelho com Transformada de Fourier , Vírion/química , Xilanos/metabolismoRESUMO
Sodium alginate (Alg) reacted with antibiotic gentamicin sulfate (GS) in an aqueous-phase condition mediated by carbodiimide chemistry, in the molar ratios Alg: GS of (1:0.5), (1:1) and (1:2). The Alg-GS conjugated derivatives were characterized by elemental analysis for nitrogen content, Fourier transform infrared spectroscopy in the attenuated total reflection mode (FTIR-ATR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), thermogravimetric analyses (TGA) and water sorption measurements. XPS and FTIR-ATR analyses clearly indicated that GS molecules covalently attached to the backbone of the alginate chains by amide bond formation. The highest amount of GS bound to Alg (43.5⯱â¯0.4â¯wt%) and the highest swelling ratio (4962⯱â¯661%) were observed for the Alg-GS (1:2) sample. Bioluminescence assays with Pseudomonas aeruginosa PAO1/lecA:lux and colony forming counting of Staphylococcus aureus and Escherichia coli upon contact with all Alg-GS conjugates revealed microbicidal activity; however, Alg-GS (1:2) was the most efficient, due to the highest GS content.
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Alginatos/química , Anti-Infecciosos/química , Gentamicinas/química , Hidrogéis/química , Carbodi-Imidas/química , Quitosana/química , Ácido Glucurônico/química , Ácidos Hexurônicos/química , Pseudomonas aeruginosa/efeitos dos fármacos , Espectroscopia de Infravermelho com Transformada de Fourier , Staphylococcus aureus/efeitos dos fármacos , TermogravimetriaRESUMO
The biotechnological evolution towards the development of antigens to detect leprosy has been progressing. However, the identification of leprosy in paucibacillary patients, based solely on the antigen-antibody interaction still remains a challenge. The complexity of clinical manifestations requires innovative approaches to improve the sensitivity of assays to detect leprosy before the onset of symptoms, thus avoiding disabilities and contributing, indirectly, to reduce transmission. In this study, the strategies employed for early leprosy diagnosis were: i. using a phage-displayed mimotope (APDDPAWQNIFNLRR) which mimics an immunodominant sequence (PPNDPAWQRNDPILQ) of an antigen of Mycobacterium leprae known as Ag85B; ii. engineering the mimotope by adding a C-terminal flexible spacer (SGSG-C); iii. conjugating the mimotope to a carrier protein to provide better exposure to antibodies; iv. amplifying the signal using biotin-streptavidin detection system in an ELISA; and v. coating the optimized mimotope on a quartz crystal microbalance (QCM) sensor for label-free biosensing. The ELISA sensitivity increased up to 91.7% irrespective of the immunological profile of the 132 patients assayed. By using comparative modeling, the M. tuberculosis Ag85B was employed as a template to ascertain which features make the mimotope a good antigen in terms of its specificity. For the first time, a sensitive QCM-based immunosensor to detect anti M. leprae antibodies in human serum was used. M. leprae antibodies could also be detected in the sera of paucibacillary patients; thus, the use of a mimotope-derived synthetic peptide as bait for antibodies in a novel analytical label-free immunoassay for leprosy diagnosis exhibits great potential.
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Técnicas Biossensoriais , Imunoensaio , Hanseníase/diagnóstico , Mycobacterium leprae/isolamento & purificação , Técnicas de Microbalança de Cristal de Quartzo , Adulto , Animais , Biomarcadores/análise , Feminino , Humanos , Masculino , Camundongos , Camundongos Endogâmicos BALB CRESUMO
Polysaccharide TEMPO-oxidation was monitored using automatic continuous online monitoring of polymerization reactions (ACOMP). The products of oxidation, obtained at different pHs (9, 7 and 5) and different concentrations of catalyst TEMPO, were evaluated by Automatic Continuous Mixing (ACM) and Size Exclusion Chromatography (SEC). The degree of oxidation was higher at pH 9 and polysaccharide degradation was observed under different pH conditions, but was much higher without catalyst TEMPO. The rate constant (k) was dependent on reaction pH and TEMPO concentration. The amount of -COOH per g of polysaccharide, at pH 9, in the presence and absence of TEMPO was different, 0.215 and 0.395mmolg-1, respectively. This suggested a secondary and non-selective polysaccharide oxidation occurring at a lower rate in the absence of catalyst. TEMPO protects the polysaccharide from degradation caused by secondary oxidant species, acting as a catalyst and "sacrificial molecule" at higher concentrations.
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Óxidos N-Cíclicos , Polissacarídeos/química , Catálise , Oxirredução , PolimerizaçãoRESUMO
Low-cost piezoelectric devices, such as simple frequency monitoring quartz crystal microbalance (QCM) devices, have good clinical utility as fast diagnostic tools for the detection of several diseases. However, unspecific antigen recognition, poor molecular probe adsorption and the need for sample dilution are still common drawbacks that hinder their use in routine diagnosis. In this work, piezoelectric sensors were previously coated with thin films of bacterial cellulose nanocrystals (CN) to provide a more sensitive and adapted interface for the attachment of monoclonal immunoglobulin G (IgGNS1) and to favor specific detection of non-structural protein 1 (NS1) of dengue fever. The assembly of the immunochip surface was analyzed by atomic force microscopy (AFM) and the NS1 detection was followed by quartz crystal microbalance with (QCM-D) and without energy dissipation monitoring (QCM). The CN surface was able to immobilize 2.30±0.5mgm-2 of IgGNS1, as confirmed by AFM topography and phase images along with QCM-D. The system was able to detect the NS1 protein in serum with only 10-fold dilution in the range of 0.01-10µgmL-1 by both QCM and QCM-D. The limits of detection of the two devices were 0.1µgmL-1 for QCM-D and 0.32µgmL-1 for QCM. As a result, QCM-D and QCM apparatuses can be used to follow NS1 recognition and have good potential for more sensitive, fast and/or less expensive diagnostic assays for dengue.
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Vírus da Dengue/isolamento & purificação , Dengue/diagnóstico , Nanopartículas/química , Polissacarídeos Bacterianos/química , Técnicas de Microbalança de Cristal de Quartzo/instrumentação , Proteínas não Estruturais Virais/sangue , Anticorpos Imobilizados/química , Bactérias/química , Técnicas Biossensoriais/instrumentação , Celulose/química , Dengue/sangue , Dengue/virologia , Desenho de Equipamento , Humanos , Imunoensaio/instrumentação , Dispositivos Lab-On-A-Chip , Nanopartículas/ultraestrutura , Proteínas não Estruturais Virais/análiseRESUMO
Gelation kinetics of aqueous solutions of xyloglucan (XG) extracted from H. courbaril seeds were investigated, in-situ, during enzymatic removal of galactose units by oscillatory shear rheological measurements, at different XG and enzyme (ß-galactosidase) concentrations. Increasing the enzyme concentration (Cenz) led to an increase of the gelation rate. Master curves of the evolution of the storage shear modulus at different Cenz could be formed by time-Cenz superposition showing that Cenz influenced the kinetics, but not the gelation process and the final gel stiffness. The behaviour of gels formed by XG with different molar mass (Mw), prepared by endoglucanase hydrolysis, was evaluated as a function of the temperature. It was found that cooling led to a decrease of the crosslink density causing a decrease of the gel stiffness. The decrease of the crosslink density was sufficient to depercolate the network formed by relatively small XG with Mw=105gmol-1, but gels formed by XG with Mw≥8×105gmol-1 persisted down to 10°C. It is shown that the melting temperature and the gel stiffness at high temperatures can be controlled independently by varying the molar mass and the concentration of XG chains.
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Bacterial cellulose (BC) derived materials represents major advances to the current regenerative and diagnostic medicine. BC is a highly pure, biocompatible and versatile material that can be utilized in several applications - individually or in the combination with different components (e.g. biopolymers and nanoparticles) - to provide structural organization and flexible matrixes to distinct finalities. The wide application and importance of BC is described by its common utilization as skin repair treatments in cases of burns, wounds and ulcers. BC membranes accelerate the process of epithelialization and avoid infections. Furthermore, BC biocomposites exhibit the potential to regulate cell adhesion, an important characteristic to scaffolds and grafts; ultra-thin films of BC might be also utilized in the development of diagnostic sensors for its capability in immobilizing several antigens. Therefore, the growing interest in BC derived materials establishes it as a great promise to enhance the quality and functionalities of the current generation of biomedical materials.
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Bactérias , Materiais Biocompatíveis , Celulose , Bactérias/metabolismo , Materiais Biocompatíveis/química , Materiais Biocompatíveis/metabolismo , Materiais Biocompatíveis/farmacologia , Celulose/biossíntese , Celulose/química , Celulose/farmacologia , Diagnóstico , Humanos , Medicina RegenerativaRESUMO
Guar (GG) and locust bean (LBG) galactomannans (GMs) oxidation at C-6 was performed with catalyst TEMPO, in which the reaction progress was monitored by consume of NaOH solution. The products were characterized by spectroscopic analysis, infrared, and (1)H-nuclear magnetic resonance, confirming the presence of aldehydes groups as intermediate of reaction to carboxylic acid. From high performance anion exchange chromatography with pulsed amperometric detection Man/Gal molar ratio was determined and demonstrated a preference to oxidize Man during the reaction on both GMs, following a first order kinetics of oxidation. The comparative macromolecular behavior of native and oxidized GMs was obtained through the analysis by high performance size exclusion chromatography, and the persistence length (Lp) was 6nm and 4nm to native LBG and GG, respectively. A more accessible OH-6 at mannose residue in LBG could be related with a two times faster reaction than GG. The selective oxidation with catalyst TEMPO proved to be efficient to increase the flexibility of the GMs during oxidation. Short reaction time and ß-elimination process were mainly observed to LBG, probably due to a more favorable oxidation access to the polysaccharide main chain.
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A three-dimensional layer-by-layer (LbL) structure composed by xanthan and galactomannan biopolymers over dioctadecyldimethylammonium bromide (DODAB) liposome template was proposed and characterized for protein drug delivery. The polymers and the surfactant interaction were sufficiently strong to create a LbL structure up to 8 layers, evaluated using quartz crystal microbalance (QCM) and zeta potential analysis. The polymer-liposome binding enthalpy was determined by isothermal titration calorimetry (ITC). The bilayer of biopolymer-coated liposomes with diameters of 165 (±15)nm, measured by dynamic light scattering (DLS), and ζ-potential of -4 (±13)mV. These bilayer-coated nanoparticles increased up to 5 times the sustained release of epidermal growth factor (EGF) at a first order rate of 0.005min(-1). This system could be useful for improving the release profile of low-stability drugs like EGF.
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Fator de Crescimento Epidérmico/administração & dosagem , Fator de Crescimento Epidérmico/química , Lipossomos/química , Mananas/química , Polissacarídeos Bacterianos/química , Preparações de Ação Retardada , Liberação Controlada de Fármacos , Galactose/análogos & derivados , Cinética , Compostos de Amônio Quaternário/químicaRESUMO
Reconstituted cellulose films were generated using residual bacterial cellulose membranes mechanically defibrillated (RBC fibrils) recycled following wound dressing production via a dry-cast process. Arabinogalactan (AG) extracted from Pereskia aculeata leaves and/or a xyloglucan (GHXG) from Guibourtia hymenifolia seeds were incorporating into the RBC at various compositions, and new films were created using the same process. Biocomposite properties were evaluated by scanning electron microscopy, contact angle (CA), and X-ray diffraction measurements. The attachment and proliferation of murine L929 fibroblasts on RBC and RBC/Hydrocolloids (HD) were also evaluated. RBC films with 20-30% GHXG replacement improved film stability and the inclusion of HD increased microfiber aggregation and reduced porous regions. Changes in the hydrophilic characteristics were also observed and owing to the adhesion effect the inclusion of HD on RBC led to a statistically significant effect of the mechanical properties of films. The RBC/AG films supported L929 adhesion similar to that observed for commercial bacterial cellulose, indicating their potential use for biomedical applications.
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Bandagens/microbiologia , Celulose/química , Celulose/farmacologia , Fenômenos Químicos , Galactanos/química , Glucanos/química , Xilanos/química , Animais , Materiais Biocompatíveis/química , Materiais Biocompatíveis/farmacologia , Adesão Celular/efeitos dos fármacos , Linhagem Celular , Proliferação de Células/efeitos dos fármacos , Membranas Artificiais , CamundongosRESUMO
The stability of perfluorinated microvesicles is mainly determined by the presence of interfacial materials and their ability to hinder the gas component diffusibility into the bloodstream. The goal of this study is to increase the persistence of the gaseous-core by introducing chitosan-coated 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) microvesicles, reducing gas diffusion from microvesicles, and increasing for a long time ultrasonic signals. Our hypothesis was based on the irreversible adhesion of chitosan towards DSPC head groups observed in thin-films models. This affinity enhanced the stabilization of gaseous-core microvesicles, in which the polysaccharide effectively reduced the phospholipid phase transition enthalpy from 383±5.5Jmg(-1) for plain to 150±9.7Jmg(-1) for chitosan-coated microvesicles, providing a more stable structure that diminished the gaseous component lost and provided the persistence of intense (19)F-NMR signals after 48h, twice as long compared to plain samples. As a result, stronger and long-lasting ultrasonic signals were produced by the more stable chitosan-containing microvesicles, thus, presenting great potential to increase the diagnostic and therapeutic applications of perfluorocarbon carries.
Assuntos
Quitosana/química , Meios de Contraste/química , Fluorocarbonos/química , Microbolhas , Fosfatidilcolinas/química , Fosfolipídeos/química , Solubilidade , UltrassonografiaRESUMO
Viscoelastic properties of aqueous solutions of xyloglucan extracted from Hymenaea courbaril seeds (Jatobá gum) were investigated by rheology over a wide range of concentrations and temperatures. The polymer was characterized in dilute solutions by light scattering measurements and size exclusion chromatography. Xyloglucan formed, in semi-dilute solutions (C 0.3 wt%), a transient network with cross-links characterized by a broad distribution of lifetimes, independent of the temperature and concentration. Progressively, at higher temperatures (>60°C), a second much weaker quasi-permanent network was formed and attributed to the exchange of intra- to inter-chain bonds. The stiffness of the second network increased with decreasing temperature, but it could be easily broken by applying a relatively weak shear stress and is readily reversible on re-heating, and partially reversible on resting at 20°C.
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Glucanos/química , Hymenaea/química , Xilanos/química , Configuração de Carboidratos , Oligossacarídeos/química , Soluções , ViscosidadeRESUMO
The interactions of the cationic surfactant DODAB with anionic xanthan (XAN) and nonionic galactomannan (GMC) polysaccharides in solution were investigated using tensiometry, differential scanning microcalorimetry (µ-DSC), zeta potential and dynamic light scattering (DLS) techniques and by the calculated thermodynamic parameters of ΔG(ves)(0), ΔG(ads)(0), Γ(max) and a(min). The surfactant formed large unilamellar vesicles (LUV) that aggregated with both the polymers in solution. Increasing DODAB concentrations resulted in greater and greater DODAB-XAN aggregates, high turbidity and even precipitation, while DODAB-GMC aggregates remained equal sized, clear solution and no precipitation observed. Further addition of DODAB to XAN solution was able to resuspend the precipitates. The interactions with both polysaccharides resulted in a more spontaneous adsorption of the DODAB-polymer aggregates at the air/solution interface with lower surfactant population.