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Johan Sebastián Díaz Tovar Dr. Giulia Kassab Dr. Natalia Mayumi Inada Prof. Dr. Vanderlei Salvador Bagnato Prof. Dr. Cristina Kurachi 《Chemphyschem》2023,24(18):e202300381
Indocyanine green is an attractive molecule for photodynamic therapy due to its near infrared absorption, resulting in a higher tissue penetration. However, its quantum yields of the triplet and singlet state have been reported to be low and then, reactive oxygen species are unlikely to be formed. Aiming to understand the ICG role in photodynamic response, its photobleaching behavior in solution has been studied under distinct conditions of CW laser irradiation at 780 and 808 nm, oxygen saturations and solvents. Sensitizer bleaching and photoproduct formation were measured by absorption spectroscopy and analyzed using the PDT bleaching macroscopic model to extract physical parameters. ICG photobleaching occurs even at lower oxygen concentrations, indicating that the molecule presents more than one way of degradation. Photoproducts were produced even in solution of less than 4 % oxygen saturation for both solvents and excitation wavelengths. Also, the amplitude of absorption related to J-dimers was increased during irradiation, but only in 50 % PBS solution. The formation of photoproducts was enhanced in the presence of J-type dimers under low oxygen concentration, and the quantum yields of triplet and singlet states were one order of magnitude and two times higher, respectively, when compared to ICG in distilled H2O. 相似文献
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Dr. Giulia Morgese Bas F. M. de Waal Dr. Silvia Varela-Aramburu Prof. Anja R. A. Palmans Prof. Lorenzo Albertazzi Prof. E. W. Meijer 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(39):17382-17386
Understanding cell/material interactions is essential to design functional cell-responsive materials. While the scientific literature abounds with formulations of biomimetic materials, only a fraction of them focused on mechanisms of the molecular interactions between cells and material. To provide new knowledge on the strategies for materials/cell recognition and binding, supramolecular benzene-1,3,5-tricarboxamide copolymers bearing benzoxaborole moieties are anchored on the surface of human erythrocytes via benzoxaborole/sialic-acid binding. This interaction based on both dynamic covalent and non-covalent chemistries is visualized in real time by means of total internal reflection fluorescence microscopy. Exploiting this imaging method, we observe that the functional copolymers specifically interact with the cell surface. An optimal fiber affinity towards the cells as a function of benzoxaborole concentration demonstrates the crucial role of multivalency in these cell/material interactions. 相似文献
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Dr. Giulia Neri Dr. Giuliana Mion Dr. Andrea Pizzi Dr. Wanda Celentano Dr. Linda Chaabane Prof. Michele R. Chierotti Prof. Roberto Gobetto Dr. Min Li Prof. Piergiorgio Messa Dr. Floryan De Campo Prof. Francesco Cellesi Prof. Pierangelo Metrangolo Prof. Francesca Baldelli Bombelli 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(44):10057-10063
In the continuous search for multimodal systems with combined diagnostic and therapeutic functions, several efforts have been made to develop multifunctional drug delivery systems. In this work, through a covalent approach, a new class of fluorinated poly(lactic-co-glycolic acid) co-polymers (F-PLGA) were designed that contain an increasing number of magnetically equivalent fluorine atoms. In particular, two novel compounds, F3-PLGA and F9-PLGA, were synthesized and their chemical structure and thermal stability were analyzed by solution NMR, DSC, and TGA. The obtained F-PLGA compounds were proven to form in aqueous solution colloidal stable nanoparticles (NPs) displaying a strong 19F NMR signal. The fluorinated NPs also showed an enhanced ability to load hydrophobic drugs containing fluorine atoms compared to analogous pristine PLGA NPs. Preliminary in vitro studies showed high cell viability and the NP ability to intracellularly deliver and release a functioning drug. 相似文献
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Dr. Claudia Mondelli Dr. Sandro Zorzi Dr. Giulia Ricci Dr. Victór Galvan Dr. Eleonora Balliana Dr. Ralf Schweins Prof. Elti Cattaruzza 《Chemphyschem》2020,21(10):966-970
Ceramics are complex objects and a rich source of information: they constitute a large part of the staple memory of past and present human activities. A deep understanding of traditional ceramics is an essential key to designing new ceramic materials. The demanding synthesis of ceramics with fine-tuned properties, such as enhanced mechanical, electrical, optical or magnetic characteristics, must be associated with cutting-edge analysis procedures in order to improve the engineering process. In this context, we describe a neutron-based non-destructive approach to investigating the nanoporosity of an historical pottery matrix as an effective investigation technique for exploring both traditional and advanced ceramic materials. 相似文献
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Yanchao Lyu Dr. Giulia Marafon Dr. Álvaro Martínez Prof. Dr. Alessandro Moretto Prof. Dr. Paolo Scrimin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(50):11758-11764
Peptide sequences functionalized with primary amines at the N- and C-terminus are able to induce the aggregation of gold nanoparticles in ethanol as a consequence of their folding into a helical conformation. Random coil peptides are unable to induce such an aggregation process. Aggregation can be monitored spectrophotometrically by following the shift of the surface plasmon resonance (SPR) band of the nanoparticles and is confirmed by transmission electron microscopy and dynamic light scattering analyses. Partial denaturation of the peptides results in diminished cross-linking ability. The helicity parameter θ222/θ208 correlates fairly well with the shift of the SPR band to longer wavelengths, supporting the relationship between the amount of helical content of a peptide sequence and its ability to induce aggregation. 相似文献