Caracterização de biocompósitos de poli(3- hidroxibutirato-co-3-hidroxivalerato) (PHBV)/coproduto da agroindústria do suco de manga.

SIAc. JICTAC. Ref.: 2232

Adsorção de fibronectina a arcabouços de polihidroxibutirato aplicáveis à engenharia óssea Adsorption of fibronectin onto polyhydroxybutyrate scaffolds applied to bone engineering

Fibronectina sérica humana foi adicionada à superfície de arcabouços de polihidroxibutirato (PHB) a fim de otimizar a adesão de osteoblastos humanos (HOB). Visando a criar sítios para a imobilização de fibronectina (FN), os arcabouços foram previamente tratados por meio de reação com etilenodiamina. O tratamento modificou a morfologia e a composição química dos arcabouços, possibilitando um aumento no teor de FN adsorvido à superfície. Imagens de AFM mostraram que as moléculas de FN assumiram conformações distintas, de acordo com a superfície na qual foi imobilizada. A FN adicionada aos arcabouços não modificados possivelmente assumiu uma conformação estendida, expondo os grupamentos RGD. Com isso, houve um aumento na adesão de HOB a estes materiais. Por outro lado, a FN na superfície dos arcabouços previamente tratados possivelmente apresentou-se na forma compacta, suprimindo a adesão de HOB.<br>Human plasma fibronectin (FN) was adsorbed onto the surface of polyhydroxybutyrate (PHB) scaffolds with aim of improving adhesion of human osteoblasts (HOB). PHB scaffolds were modified via reaction with ethylenediamine in order to create sites for FN immobilization. Morphological and chemical composition changes were observed for treated scaffolds which led to an increase in the concentration of FN adsorbed onto scaffold surfaces. AFM images showed that FN molecules assumed distinct conformation according to the surface to which they were adsorbed. It is believed that the FN molecules added to non-treated scaffolds assumed an unfolded conformational owing to the exposure of their RGD domains, thus promoting an increased HOB adhesion. On the other hand, FN molecules which were added to the surface of previously treated scaffolds are believed to have assumed a folded conformation, hiding some RGD domains and inhibiting HOB adhesion

Inhomogeneous high harmonic generation in krypton clusters.

High order harmonic generation from clusters is a controversial topic: conflicting theories exist, with different explanations for similar experimental observations. From an experimental point of view, separating the contributions from monomers and clusters is challenging. By performing a spectrally and spatially resolved study in a controlled mixture of clusters and monomers, we are able to isolate a region of the spectrum where the emission purely originates from clusters. Surprisingly, the emission from clusters is depolarized, which is the signature of statistical inhomogeneous emission from a low-density source. The harmonic response to laser ellipticity shows that this generation is produced by a new recollisional mechanism, which opens the way to future theoretical studies.Molecular control with tailored UV pulse

High-order harmonic generation from the dressed autoionizing states

In high-order harmonic generation, resonant harmonics (RH) are sources of intense, coherent extreme-ultraviolet radiation. However, intensity enhancement of RH only occurs for a single harmonic order, making it challenging to generate short attosecond pulses. Moreover, the mechanism involved behind such RH was circumstantial, because of the lack of direct experimental proofs. Here, we demonstrate the exact quantum paths that electron follows for RH generation using tin, showing that it involves not only the autoionizing state, but also a harmonic generation from dressed-AIS that appears as two coherent satellite harmonics at frequencies ±2Ω from the RH (Ω represents laser frequency). Our observations of harmonic emission from dressed states open the possibilities of generating intense and broadband attosecond pulses, thus contributing to future applications in attosecond science, as well as the perspective of studying the femtosecond and attosecond dynamics of autoionizing states