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81.
We study special regularity and decay properties of solutions to the IVP associated to the k-generalized KdV equations. In particular, for datum u 0 ∈ H 3/4+ (?) whose restriction belongs to H l ((b, ∞)) for some l ∈ ?+ and b ∈ ? we prove that the restriction of the corresponding solution u(·, t) belongs to H l ((β, ∞)) for any β ∈ ? and any t ∈ (0, T). Thus, this type of regularity propagates with infinite speed to its left as time evolves. 相似文献
82.
A new concept of using acrylated epoxidized soybean oil (AESO) in the production of 3D cellulose biocomposites was evaluated. Cellulose-AESO composites were prepared by dissolving pulp in N,N-dimethylacetamide/lithium chloride and adding AESO and an initiator to the solutions followed by thermal curing and compression moulding at room temperature. The resulting biocomposites were characterized by FE-SEM, FT-IR, XRD, GC, TGA and nano- and microindentation. SEM images indicated the presence of spherical morphology and FT-IR together with TGA results showed no hydrogen or covalent bonding between the two components. The existence of hydrophobic interactions between AESO molecules and cellulose hydrophobic domains was proposed. AESO aggregates captured and covered by cellulose chains increase the flexibility of the composites acting as specific plasticizer and after polymerization introduce strength to the material. It was found that the optimal amount of AESO for achieving both desired hardness and good mouldability should be below 20 %. 相似文献
83.
Double‐Wall Carbon Nanotube–Porphyrin Supramolecular Hybrid: Synthesis and Photophysical Studies 下载免费PDF全文
Dr. María Vizuete Dr. María J. Gómez‐Escalonilla Prof. José Luis G. Fierro Dr. Pedro Atienzar Prof. Hermenegildo García Prof. Fernando Langa 《Chemphyschem》2014,15(1):100-108
Double‐wall carbon nanotubes (DWCNTs) with pyridyl units covalently attached to the external wall through isoxazolino linkers and carboxylic groups that have been esterified by pentyl chains are synthesized. The properties of these modified DWCNTs are then compared with an analogous sample based on single‐wall carbon nanotubes (SWCNTs). Raman spectroscopy shows the presence of characteristic radial breathing mode vibrations, confirming that the samples partly retain the integrity of the nanotubes in the case of DWCNTs, including the internal and external nanotubes. Quantification of the pyridyl content for both samples (DWCNT and SWCNT derivatives) is based on X‐ray photoelectron spectroscopy and thermogravimetric profiles, showing very similar substituent load. Both pyridyl‐containing nanotubes (DWCNTs and SWCNTs) form a complex with zinc porphyrin (ZnP), as evidenced by the presence of two isosbestic points in the absorption spectra of the porphyrin upon addition of the pyridyl‐functionalized nanotubes. Supramolecular complexes based on pyridyl‐substituted DWCNTs and SWCNTs quench the emission and the triplet excited state identically, through an energy‐transfer mechanism based on pre‐assembly of the ground state. Thus, the presence of the intact inner wall in DWCNTs does not influence the quenching behavior, with respect to SWCNTs, for energy‐transfer quenching with excited ZnP. These results sharply contrast with previous ones referring to electron‐transfer quenching, in which the double‐wall morphology of the nanotubes has been shown to considerably reduce the lifetime of charge separation, owing to faster electron mobility in DWCNTs compared to SWCNTs. 相似文献
84.
Inside Cover: Quinone‐Rich Poly(dopamine) Magnetic Nanoparticles for Biosensor Applications (ChemPhysChem 17/2014) 下载免费PDF全文
85.
Prof. Pedro Laborda Yong-Mei Lyu Dr. Fabio Parmeggiani Dr. Ai-Min Lu Wen-Jiao Wang Ying-Ying Huang Dr. Kun Huang Juan Guo Prof. Li Liu Prof. Sabine L. Flitsch Prof. Josef Voglmeir 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(13):5346-5349
Chitin is one of the most abundant and cheaply available biopolymers in Nature. Chitin has become a valuable starting material for many biotechnological products through manipulation of its N-acetyl functionality, which can be cleaved under mild conditions using the enzyme family of de-N-acetylases. However, the chemoselective enzymatic re-acylation of glucosamine derivatives, which can introduce new stable functionalities into chitin derivatives, is much less explored. Herein we describe an acylase (CmCDA from Cyclobacterium marinum) that catalyzes the N-acylation of glycosamine with a range of carboxylic acids under physiological reaction conditions. This biocatalyst closes an important gap in allowing the conversion of chitin into complex glycosides, such as C5-modified sialosides, through the use of highly selective enzyme cascades. 相似文献
86.
87.
Diana Trujillo-Benítez Myrna Luna-Gutirrez Guillermina Ferro-Flores Blanca Ocampo-García Clara Santos-Cuevas Gerardo Bravo-Villegas Enrique Morales-vila Pedro Cruz-Nova Lorenza Díaz-Nieto Janice García-Quiroz Erika Azorín-Vega Antonio Rosato Laura Melndez-Alafort 《Molecules (Basel, Switzerland)》2022,27(1)
Fibroblast activation protein (FAP) is expressed in the microenvironment of most human epithelial tumors. 68Ga-labeled FAP inhibitors based on the cyanopyrrolidine structure (FAPI) are currently used for the detection of the tumor microenvironment by PET imaging. This research aimed to design, synthesize and preclinically evaluate a new FAP inhibitor radiopharmaceutical based on the 99mTc-((R)-1-((6-hydrazinylnicotinoyl)-D-alanyl) pyrrolidin-2-yl) boronic acid (99mTc-iFAP) structure for SPECT imaging. Molecular docking for affinity calculations was performed using the AutoDock software. The chemical synthesis was based on a series of coupling reactions of 6-hidrazinylnicotinic acid (HYNIC) and D-alanine to a boronic acid derivative. The iFAP was prepared as a lyophilized formulation based on EDDA/SnCl2 for labeling with 99mTc. The radiochemical purity (R.P.) was verified via ITLC-SG and reversed-phase radio-HPLC. The stability in human serum was evaluated by size-exclusion HPLC. In vitro cell uptake was assessed using N30 stromal endometrial cells (FAP positive) and human fibroblasts (FAP negative). Biodistribution and tumor uptake were determined in Hep-G2 tumor-bearing nude mice, from which images were acquired using a micro-SPECT/CT. The iFAP ligand (Ki = 0.536 nm, AutoDock affinity), characterized by UV-Vis, FT-IR, 1H–NMR and UPLC-mass spectroscopies, was synthesized with a chemical purity of 92%. The 99mTc-iFAP was obtained with a R.P. >98%. In vitro and in vivo studies indicated high radiotracer stability in human serum (>95% at 24 h), specific recognition for FAP, high tumor uptake (7.05 ± 1.13% ID/g at 30 min) and fast kidney elimination. The results found in this research justify additional dosimetric and clinical studies to establish the sensitivity and specificity of the 99mTc-iFAP. 相似文献
88.
Pedro L. R. Guedes Carolina P. F. Carvalho Adriana A. F. Carbonel Manuel J. Simes Marcelo Y. Icimoto Jair A. K. Aguiar Maria Kouyoumdjian Marcos L. Gazarini Marcia R. Nagaoka 《Molecules (Basel, Switzerland)》2022,27(3)
During liver fibrogenesis, there is an imbalance between regeneration and wound healing. The current treatment is the withdrawal of the causing agent; thus, investigation of new and effective treatments is important. Studies have highlighted the action of chondroitin sulfate (CS) in different cells; thus, our aim was to analyze its effect on an experimental model of bile duct ligation (BDL). Adult Wistar rats were subjected to BDL and treated with CS for 7, 14, 21, or 28 days intraperitoneally. We performed histomorphometric analyses on Picrosirius-stained liver sections. Cell death was analyzed according to caspase-3 and cathepsin B activity and using a TUNEL assay. Regeneration was evaluated using PCNA immunohistochemistry. BDL led to increased collagen content with corresponding decreased liver parenchyma. CS treatment reduced total collagen and increased parenchyma content after 21 and 28 days. The treatment also promoted changes in the hepatic collagen type III/I ratio. Furthermore, it was observed that CS treatment reduced caspase-3 activity and the percentage of TUNEL-positive cells after 14 days and cathepsin B activity only after 28 days. The regeneration increased after 14, 21, and 28 days of CS treatment. In conclusion, our study showed a promising hepatoprotective action of CS in fibrogenesis induced by BDL. 相似文献
89.
Luis D. Vargas Gustavo A. Chapela Orlando Guzmán Pedro Díaz Leyva Rodrigo Sánchez 《Molecular physics》2020,118(9-10)
We analyse by discrete molecular dynamics the self-assembly of SW trimer particles that contain a different number of attractive and repulsive spheres. They also have different geometries: linear, obtuse, rectangular and equilateral. We identify that some of these molecules exhibit liquid–vapour equilibria while others do not. For all of them, we show the morphological phase diagram built up from the different supra-molecular structures formed by each type of trimer. We simulated 14 different systems with a total of 321 states. The main features of the supra-molecular structures depend only on the composition and geometry of the trimer: triple SW trimers do not form supra-structures, double SW trimers and single SW trimers form monolayers, bilayers and worm-like micelles. The liquid–vapour coexistence properties are also exhibited. These trimers can be used to model complex amphiphiles beyond the standard ones, such as the Gemini and the Bola surfactants as well as colloidal particles. 相似文献
90.
Carlota Leonardo-Sousa Andreia Neves Carvalho Romina A. Guedes Pedro M. P. Fernandes Natlia Aniceto Jorge A. R. Salvador Maria Joo Gama Rita C. Guedes 《Molecules (Basel, Switzerland)》2022,27(7)
Proteasome inhibitors have shown relevant clinical activity in several hematological malignancies, namely in multiple myeloma and mantle cell lymphoma, improving patient outcomes such as survival and quality of life, when compared with other therapies. However, initial response to the therapy is a challenge as most patients show an innate resistance to proteasome inhibitors, and those that respond to the therapy usually develop late relapses suggesting the development of acquired resistance. The mechanisms of resistance to proteasome inhibition are still controversial and scarce in the literature. In this review, we discuss the development of proteasome inhibitors and the mechanisms of innate and acquired resistance to their activity—a major challenge in preclinical and clinical therapeutics. An improved understanding of these mechanisms is crucial to guiding the design of new and more effective drugs to tackle these devastating diseases. In addition, we provide a comprehensive overview of proteasome inhibitors used in combination with other chemotherapeutic agents, as this is a key strategy to combat resistance. 相似文献