Biomaterials have been intensively investigated due to the increase in the elderly population and high prevalence of several disorders, such as cardiovascular and orthopedic diseases. Polymeric and composite polymeric materials in combination with different processing techniques, such as electrospinning, solution blow spinning, ultrathin film preparation, and 3D printing are promising for obtaining biomaterials with patient-specific applications. Here, we provide a review on recent advances and perspectives for synthetic and natural polymers as well as composites in the design of biomaterials. After introducing basic information about biomaterials, we describe the fundamentals of manufacturing techniques and highlight possible biomedical applications.

Abstract The immobilization of the enzyme tyrosinase (Tyr) in lipid matrices can be explored to produce biosensors for detecting polyphenols, which is relevant for the food industry. Herein, we shall demonstrate the importance of the lipid composition to immobilize the enzyme tyrosinase in Langmuir-Blodgett (LB) films. Tyr could be incorporated into Langmuir monolayers of arachidic acid (AA), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and 1,2-dipalmitoyl-sn-glycero-3-phospho-(1’-rac-glycerol) (sodium salt) (DPPG), having as the main effect an expansion in the monolayers. Results from polarization-modulated infrared reflection-absorption spectroscopy (PM-IRRAS) pointed to electrostatic interactions between the charged residues of Try and the lipid headgroups, in addition to changes in the order of lipid chains. The interaction between Tyr and DPPC in Langmuir monolayers can be correlated with the superior performance of DPPC/Tyr LB films used as biosensors to detect catechol by cyclic voltammetry. The molecular-level interactions assessed via PM-IRRAS are therefore believed to drive an immobilization process for Tyr in the lipid LB matrix and may serve as a general criterion to identify matrices that preserve enzyme activity.

The molecular control in Langmuir-Blodgett (LB) films may be exploited in charge storage electrodes provided a suitable choice of molecular architecture and components is made. In this paper, we employed a naphtyl-1,3,4-oxadiazole amphiphile (NFT1) and its complex [Ru(bpy)2NFT1]PF6 (RuNFT1) (bpy = 2,2’-bipyridine) in heterostructured LB films in a proof-of-principle production of charge storage. The optimized architecture contained a one-layer RuNFT1 deposited on a 9-layer NFT1 LB film, where the efficient packing of NFT1 inferred from spectroscopic measurements and Brewster angle microscopy (BAM) images was considered as relevant for ion diffusion. This packing was achieved owing to the π-stacking warranted by the planarity of the NFT1 naphtyl 1,3,4-oxadiazole ring, as confirmed with density functional theory (DFT) calculations. The top layer of the redox-active RuNFT1 provided an additional contribution with its Faradaic charge storage to the double layer capacitance of NFT1. Taken together, these results demonstrate that synergy may be achieved in combining distinct compounds in LB films toward efficient charge storage.

Immunosensors based on impedance spectroscopy for diagnosing hepatitis C are reported where the sensing units were made with the antigenic peptide PPLLESWKDPDYVPPWHG (NS5A-1) derived from the NS5A protein of the hepatitis C virus (HCV) immobilized in layer-by-layer (LbL) films with silk fibroin (SF) and deposited on gold interdigitated electrodes. The electrical response of the sensing units varied upon immersion into solutions containing the antibody anti-HCV owing to the biomolecular recognition of NS5A-1. This was associated with morphological changes on the LbL films caused by adsorption of NS5A-1 and inferred from atomic force microscopy images. Buffer solutions with different anti-HCV concentrations down to 2 ng mL-1 could be clearly distinguished by analyzing the impedance spectroscopy data with a multidimensional projection technique. The specificity toward anti-HCV antibodies was confirmed in control experiments where no significant changes in the electrical response were measured by exposing the sensing units to solutions containing an anti-human immunodeficiency virus (HIV) antibody. The high sensitivity and selectivity of the units made with LbL films demonstrate the feasibility of measuring electrical impedance as an immunosensing strategy to detect hepatitis C.

We report on the synthesis of single-crystalline tellurium nanowires with different aspect-ratios prepared via facile surfactant-assisted synthesis under mild conditions. Short and long Te nanowires were synthesized by the reduction of tellurium dioxide by hypophosphorous acid with the assistance of polyoxyethylene (23) laurylether and cetyltrimethylammonium bromide, respectively. We obtained uniform single-crystal Te nanowires with diameter below 30 nm and tunable length from 600 nm to 5 µm. Short and long Te nanowires showed remarkable nonlinear absorption and their third-order nonlinear optical properties were investigated by the Z-scan technique with single 80 ps laser pulses at 532 nm. For the first time, it was observed a distinguished switching behavior from saturated absorption to reverse saturated absorption as a function of the laser intensity in one-dimensional Te nanostructures. Although both short and long Te nanowires display such interesting behavior, the short ones exhibited superior optical limiting performance.

Interface effects between metal electrodes and organic films are crucial for the overall performance of organic electronics devices. We investigate effects from gold electrodes deposited on spin-coated films of poly(p-phenylene vinylene) (PPV). While a thin Au layer (16 nm) did not affect the absorption and emission spectra of PPV, a 64 nm thick Au layer induced blue shifts in both spectra owing to the reduction in the effective conjugation degree of PPV segments. Upon combining photoluminescence and Raman scattering spectroscopies, we noted that the Au clusters interact preferentially with the phenyl rings of the polymer chain, leading to shifts in the vibrational modes at 1100 and 555 cm-1 and a significant change in the electron-phonon coupling inferred from the Huang-Rhys parameters. These results are consistent with theoretical predictions in ab initiocalculations, which imply that the final properties of polymeric devices may be tuned with adequate conditions for electrode deposition.

This review deals with surface-enhancved Raman scattering (SERS) employing Langmuir-Blodgett (LB) films, which serve as model systems for developing theoretical and experimental studies to elucidate the SERS effect. In addition, LB films have be used as integral parts of molecular architectures for SERS-active substrates. On the other hand, SERS and surface-enhaced resonant Raman scattering (SERRS) have allowed various properties of LB films to be investigated, especially those associated with molecular-level interactions. In the paper, emphasis is placed on single molecule detection (SMD), where the target molecule is diluted on an LB matrix of spectral silent material (low Raman cross section). The perspectives and challenges for combining SERS and LB films are also discussed.

In this work we take advantage of the polyelectrolyte character of some Brazilian native gums to fabricate electrically conductive, nanostructured films. The gums Sterculia urens, (caraia), Sterculia striata (chicha) or Anadenanthera macrocarpa Benth were assembled in conjunction with poly(o-methoxyaniline) (POMA) in the form of layered nanostructured films using the layer-by-layer (LbL) technique. All the LbL films displayed a well-defined electroactivity, as confirmed via cyclic voltammetry. In comparison to POMA LbL films fabricated with conventional polyelectrolytes (viz. poly(vinyl sulfonic acid)-PVS), the presence of the gums in the LbL films increased remarkably the electrochemical stability of the films.

O complexo [{RuCl3(dppb)}2(µ-4,4'-bipy)] (dppb = PPh2(CH2)4PPh2; 4,4'-bipy= 4,4'-bipiridil) foi obtido por meio da reação entre 4,4'-bipiridina e mer-[RuCl3(dppb)].H2O, em bom rendimento. As características do complexo binuclear obtido, estudadas por medidas de FT-IR, UV-Vis, EPR e análise elementar foram similares às do complexo [RuCl3(dppb)L] (L= N-heterociclo). [{RuCl3(dppb)}2(µ-4,4'-bipy)] é solúvel em solventes fracamente polares, facilitando a sua utilização para produzir filmes de Langmuir e Langmuir-Blodgett (LB). Enquanto que filmes cast e o complexo em solução são vermelhos, filmes LB são azul-esverdeados, provavelmente devido à oxidação da bisfosfina. A natureza nanoestruturada dos filmes LB, se manifestou nas medidas eletroquímicas, já que estes filmes exibem maior corrente de pico do que os filmes cast e dip-coated. As respostas eletroquímicas destes filmes são caracterizadas pelo processo RuIII RuIII/RuII RuII, o qual difere do complexo em solução. Neste último caso, um processo irreversível é observado devido à formação de novas espécies. A eletroatividade dos filmes LB/[{RuCl3(dppb)}2(µ-4,4' -bipy)] indica a possibilidade de utilização em dispositivos eletroquímicos.

[{RuCl3(dppb)}2(µ-4,4'-bipy)] was prepared from the reaction of the 4,4'-bipyridine and mer-[RuCl3(dppb)].H2O, in good yield. The characteristics of the binuclear complex studied with FT-IR, UV-Vis, EPR and elemental analysis were similar to those of the [RuCl3(dppb)L] (L= N-heterocycle). [{RuCl3(dppb)}2(µ-4,4'-bipy)] is soluble in weakly polar organic solvents, facilitating its use in the production of Langmuir and Langmuir-Blodgett (LB) films production. While the cast films and the complex in solution were red, the LB films were green-bluish, probably due to oxidation of the bisphosphine. The nanostructured nature of the LB films was manifested in electrochemical measurements, as these films exhibited higher peak currents than cast or dip-coated films. For all films, the electrochemical response was dominated by the RuIII RuIII/RuII RuII process, which differed from that of the binuclear compound. For the latter, an irreversible process appeared due to formation of new species. The electroactivity of LB films from [{RuCl3(dppb)}2(µ-4,4'-bipy)] also pointed to their possible use in electrochemical devices.

Chitosan incorporated in the aqueous subphase is found to affect the Langmuir monolayers of cholesterol, causing the surface pressure and the surface potential isotherms to become more expanded. The mean molecular area per cholesterol molecule in the condensed monolayer increases from 53 Ų in the absence of chitosan to 61 Ų for a concentration of 0.100 mg/mL of chitosan in the subphase. If additional chitosan is incorporated in the subphase, no change is noted, which points to saturation in the effects from chitosan. The interaction between chitosan and cholesterol probably occurs via hydrogen bonding. The monolayer expansion is also manifested in the monolayer morphology, as indicated by Brewster angle microscopy measurements, where larger cholesterol domains are visualized when chitosan is present in the subphase.

This paper discusses fundamental concepts for the characterization of Langmuir monolayers and Langmuir-Blodgett (LB) films, with emphasis on investigations of material properties at the molecular level. By way of illustration, results for phospholipid monolayers interacting with the drug dipyridamole are highlighted. These results were obtained with several techniques, including in situ grazing incidence X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy, fluorescence microscopy, in addition to surface pressure and surface potential isotherms. Also mentioned are the difficulties in producing Langmuir and LB films from macromolecules, and how molecular-level interactions in mixed polymer LB films can be exploited in sensors.

This paper discusses water at interfaces with emphasis on the electrical properties of adsorbed films. Two issues are addressed, namely adsorption of organic molecules at the air/water interface in Langmuir monolayers and the influence of adsorbed water on the electrical properties of nanostructured organic films deposited onto solid substrates. In Langmuir monolayers the focus will be on the interaction of the adsorbed molecules with the underlying water, particularly with regard to the surface potential and lateral conductance of the monolayers. It will be shown that these electrical measurements are extremely sensitive to small changes in the subphase, including trace amounts of impurities. Phase transitions due to structuring of the monolayer will be discussed at the light of theoretical models that deal with proton transfer along the monolayers. Attempts will be made to connect the interpretation at the molecular level with experimental findings from techniques such as Brewster angle microscopy and fluorescence microscopy, which provide information at the mesoscopic or microscopic scale. The gradient of the dielectric constant for water at the monolayer interface is inferred from modeling the monolayer surface potential in terms of the dipole moments of the molecules. For deposited films, the discussion will be centered on the electrical properties of nanostructured films produced with either the Langmuir-Blodgett (LB) or the layer-by-layer (LBL) methods. The strong effects from adsorbed water will be presented, with mention to sensor applications where the extreme sensitivity of the electrical properties to water is exploited and to doping of a conducting polymer induced by X-ray irradiation.

A study is presented of the formation and optical properties of polymeric heterostructures from poly(p-phenylene vinylene) (PPV) and poly(o-methoxyaniline) (POMA) produced via the self-assembly technique. POMA layers were obtained in a non self-limiting process from its emeraldine salt, semiconducting form in HCl solution. Thermal conversion of PPV was performed at low temperatures with the substitution of the counter-ion Cl in the PPV precursor by a long sulfonic chain, the dodecylbenzenesulfonate (DBS) ion. The optical properties of PPV films converted in this way are not affected by POMA, which can be used as transparent electrode of PPV luminescent devices.