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The authors report a case of erythema multiforme in a 32-year-old woman who was also taking oral terbinafine for an onychomycosis. The patient data analysis showed serological positivity for cytomegalovirus (IgM and IgG) and hepatitis C virus and serological titre of antinuclear antibody was elevated. After a brief review of the literature the authors propose the possibility of virus–drug interaction as a model of adverse drug reactions. [ABSTRACT FROM AUTHOR]

Hypothesis: Cellulose nanocrystals (CNCs) are sustainable rod-like nanoparticles that can be used to stabilize oil-in-water emulsions and can create hydrophilic coatings. Modifying the surface of CNCs can improve emulsion properties and allow for adjustable wettability., Experiments: This study explores the improvement of Pickering emulsion properties for various oils and the adjustability of coated surfaces through the physical modification of CNCs, without chemical functionalization. Bio-based additives, including antioxidant tannic acid (TA), methyl cellulose (MC), and ethyl cellulose (EC) were used as surface modifiers. The identification of optimal formulations involved varying the weight fraction of the alkyl cellulose derivatives., Findings: The findings suggest that, akin to pure CNCs, Pickering emulsions stabilized by TA and/or MC-modified CNCs demonstrate comparably high stability. The introduction of MC at a low weight fraction enhances hydrophilicity, and AFM analysis reveals smooth surfaces, mitigating the potential influence of roughness. In contrast, EC-modified CNCs result in less stable emulsions but exhibit more hydrophobic surfaces. This translates to a broad spectrum of characteristics, ranging from quasi-superhydrophilic to nearly hydrophobic (with contact angles spanning from below 11° up to 68°), all controllable through a straightforward physical coating process. This facile preparation of coated CNCs provides a versatile approach to customizing the wetting and emulsification properties of nanomaterials., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Isabelle CAPRON reports financial support was provided by INRAE. Isabelle CAPRON reports financial support was provided by French National Research Agency. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

Cellulose nanocrystals (CNCs) are hydrophilic nanoparticles that cannot be dispersed in non-polar solvents or hydrophobic polymer matrices. Here, we demonstrate the tunable modification of CNC surfaces by physical adsorption of tannic acid (TA) and two alkyl cellulose derivatives (ACDs), methyl cellulose (MC) and ethyl cellulose (EC), while maintaining their sustainable nature. We compare the impact of ACD adsorption when mixed with CNCs to CNCs precoated with tannic acid (CNC@TA), varying ACD weight fractions in CNC suspensions. Our results show that CNC@ACD and CNC@TA@ACD aqueous suspensions display good colloidal stability in water, while their surface properties are altered. We use a wide range of analytical techniques to characterize these suspensions, with a focus on their interaction with water. The two selected ACDs adsorb on both CNCs and CNC@TA at low fractions (ACD ≤ 10 % w/w), followed by an intermediate region of saturation between 10 % and 30 % w/w. At fractions above 30 % w/w, we observe the formation of CNC- or CNC@TA-reinforced ACD composites. Most samples can be redispersed in water upon freeze-drying, except for EC-rich samples redispersible in toluene. Our facile method for preparing ACD-coated CNCs allows for the creation of a range of nanomaterials with modulable wetting and emulsification properties., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)

Thermal stability is a crucial property of materials, especially when they have a wide range of thermally sensitive applications. Cellulose nanomaterials (CNMs) extracted from cellulosic biomass have garnered significant attention due to their abundance, biodegradability, sustainability, production scalability, and industrial versatility. To explore the correlation between the structure, chemistry, and morphology of CNMs and their thermal stability, we present a comprehensive literature review. We identify five major factors affecting CNMs' thermal stability, namely type, source, reaction conditions, post-treatment, and drying method, and analyze their impact on CNMs' thermal stability using several case studies from the literature. Using multiple linear least-squares regression (MLR), we establish a quantitative relationship between thermal stability and seven variables: crystallinity index of the source, dissociation constant of the reactant used, reactant concentration, reaction temperature, reaction time, evaporation rate, and post-treatment presence. By understanding these interdependencies, our statistical analysis enables the design of CNMs with predictable thermal properties and identification of optimal conditions for achieving high thermal stability. The results of our study provide crucial insights that can guide the development of CNMs with enhanced thermal stability for use in a variety of industrial applications.

Objectives: In this paper we propose embedding natural fillers, such as pristine and functionalized chitin nanocrystals, into resin adhesives to produce photopolymerizable dental filled adhesives with enhanced biocompatibility, hydrophobicity, mechanical resistance, and anti-bacterial properties., Methods: Chitin nanocrystals (ChNC) were functionalized with decanoyl chloride and methacrylic anhydride to produce ChNC-C10 and ChNC-MA, respectively. These hydrophobically functionalized chitin nanocrystals were incorporated into a resin adhesive at concentrations of 0.5-3.0 wt% to assess the materials' physical and mechanical properties through Fourier-transform infrared (FTIR) spectroscopy, solid-state NMR spectroscopy, X-ray diffraction (XRD), elemental analysis, scanning electron microscopy (SEM), thermogravimetric analysis (TGA), flexural strength, microhardness, and water sorption tests., Results: The analytical techniques confirmed the successful preparation of chitin nanocrystals from commercial chitin powder derived from shrimp shells and the efficient hydrophobization of their surface. Electron microscope images indicated that the increased hydrophobicity of ChNC-C10 promotes the formation of layered structures throughout the resin adhesive, while ChNC-MA tends to form aggregates in the matrix. Adhesives filled with ChNC-C10 enhanced their flexural strength, microhardness, and thermal stability and decreased their water sorption and degree of conversion. Adhesives filled with ChNC-MA resulted in improvements in microhardness, in water sorption and degree of conversion, although they did not exhibit augmentation of their flexural strength and thermal stability., Significance: In light of the improved physical and mechanical properties with respect to the control, resin adhesives filled with anti-bacterial chitin nanocrystals are promising new materials for dental applications, especially those filled with low/moderate amounts of ChNC-C10., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Dynamic covalent bonds bear great potential for the development of adaptive and self-healing materials. Herein, we introduce a versatile concept not only for the design of low-molecular-weight liquid crystals but also for their in situ postsynthetic modification by using the dynamic covalent nature of imine bonds. The methodology allows systematic investigations of structure-property relationships as well as the manipulation of the materials' behavior (liquid crystallinity) and the introduction of additional properties (here, fluorescence) by a solvent-free method. For the first time, the transamination reaction is followed by variable-temperature 19 F solid-state NMR in the mesophase, providing insights into the reaction dynamics in a liquid crystalline material. Finally, the application potential for the design of liquid crystalline materials with adaptive properties is demonstrated by a sequential combination of these reactions.

Multicomponent low molecular weight gelators (LMWGs) may self-assemble by co-assembly (CA), social self-sorting (SSS), or narcissistic self-sorting (NSS). Understanding the nuances of the self-assembly processes is important to predict the behavior of multicomponent organogels. Here, we investigate the effect of molecular structure on self-assembly in a series of amino-acid based bicomponent LMWGs that differ in headgroup and alkyl chain length. Packing preference of the organogels was determined using differential scanning calorimetry, nuclear magnetic resonance spectroscopy and small angle X-ray scattering. From 66 bicomponent samples we found 50 CA, 14 SSS and 2 NSS. Furthermore, we performed statistical analysis to investigate the role of hydrophobicity and chain length on the overall pathway of self-assembly for these systems. We found the hydrophobicity of the headgroup strongly affected the assembly preference of the organogel, but alkyl chain length only played a small role., (© 2022 Wiley-VCH GmbH.)

The properties of chiral nematic and iridescent cellulose nanocrystal films with different monovalent cations (CNC-X) obtained through evaporation-induced self-assembly (EISA) can be modified by a variety of external stimuli. Here, we study the transformations of their optical and structural properties when the films are thermally annealed at 200 °C and 240 °C for up to 2 days. The chiral nematic structure of the most thermally stable films is not destroyed even after extensive heating due to the thermochemical stability of the cellulose backbone and the presence of surface alkali counterions, which suppress catalysis of early stage degradation. Despite the resilience of the cholesteric structure and the overall integrity of heated CNC-X films, thermal annealing is often accompanied by reduction of iridescence, birefringence, and transparency, as well as formation of degradation products. The versatility, sustainability, and stability of CNC-X films highlight their potential as temperature indicators and photonic devices., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Bioderived cellulose nanocrystals (CNCs) are used to create light, flexible, biocompatible, and biodegradable electronic devices. Herein, surface modification of cellulose nanocrystals was employed to fabricate cationic and anionic CNCs. Subsequently, we demonstrated rectification behavior from a fixed junction between two agarose hydrogels doped with cationic and anionic cellulose nanocrystals. The current rectification ratio reaches 70 reproducibly, which is significantly higher than that for analogous diodes generated with microfibrillated cellulose (∼15) and the first polyelectrolyte gel diode (∼40). The current-voltage characteristics of the CNC-hydrogel diode are influenced by concentration, gel thickness, scanning frequency, and applied voltage. The high surface area of CNC resulted in high charge density after surface modification, which in turn resulted in good rectification behavior from only small amounts of dopant material.

Cellulose-derived materials, such as microcellulose and nanocellulose, are sustainable materials with a wide range of applications. Here, through a multi-analytical approach, we investigate the thermal degradation of microfibrillar cellulose filaments (CFs); acidic cellulose nanocrystals (CNC-H), containing sulfate half-ester groups on the surface; and neutralized cellulose nanocrystals (CNC-Na), where the protons are replaced by sodium ions. CFs have a simple degradation mechanism, associated with extensive dehydration, decarboxylation, and decarbonylation, and the highest thermal stability of the three (∼325 °C) despite the abundance of amorphous regions and inhomogeneous fibrous mass that make them structurally and morphologically less homogeneous than high-crystallinity CNCs. CNC-H decompose in a complex way below 200 °C, with large char fractions and evaporation of sulfur compounds at high temperatures, while sodium counterions in CNC-Na can improve the thermal stability up to 300 °C, where the pyrolysis leads to partial rehydration and formation of sodium hydroxide on the surface.

Diffraction gratings are important for modern optical components, such as optical multiplexers and signal processors. Although liquid crystal (LC) gratings based on thermotropic LCs have been extensively explored, they often require expensive molecules and complicated manufacturing processes. Lyotropic LCs, which can be broadly obtained from both synthetic and natural sources, have not yet been applied in optical gratings. Herein, a facile grating fabrication method using a biosourced lyotropic LC formed by cellulose nanocrystals (CNCs), a material extracted from plants, is reported. Hydrogel sheets with vertically aligned uniform periodic structures are obtained by fixing the highly oriented chiral nematic LC of CNCs in polymer networks under the cooperative effects of gravity on phase separation and a magnetic field on LC orientation. The hydrogel generates up to sixth-order diffraction spots and shows linear polarization selectivity, with tunable grating periodicity controlled through LC concentration regulation. This synthesis strategy can be broadly applied to various grating materials and opens up a new area of optical materials from lyotropic LCs., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The functionalization of cellulose nanocrystal (CNC) aerogels was achieved through a two-step synthetic procedure. CNC aerogels were prepared under hydrothermal conditions, followed by solvent exchange and critical point drying. The CNC aerogels were functionalized with a methacrylate group and then underwent thiol-ene click chemistry to impart a range of functionalities onto the surface of the CNC aerogel. The use of the functionalized aerogels as oil absorbents was then investigated, with the most hydrophobic CNC aerogel, 1 H,1 H,2 H,2 H-perfluorodecanethiol-functionalized CNC aerogel, exhibiting the highest absorption of xylenes at 2.9 mL g -1 .

Candida albicans biofilm represents a major clinical problem due to its intrinsic tolerance to anti-fungal compounds and it has been highly related to infections in catheterized patients. Few compounds are described as able to inhibit biofilm formation or to interfere with preformed biofilm of C. albicans. Here we report the in vitro evaluation of anti-biofilm activity on C. albicans ATCC 10231 of a series of new and already known amine and amide indole derivatives. Among the studied compounds, fifteen resulted active on C. albicans ATCC 10231 biofilm, with BMIC 50 ≤ 16 μg/mL. Three of them (7, 23 and 33) showed a selectivity towards mature biofilm and the most active of them was the compound 23 (BMIC 50  = 4 μg/mL). On the other hands, two different compounds (21 and 22) were selective towards biofilm formation with BMIC 50 values of 8 μg/mL. Otherwise, compounds 16 and 17 resulted active on biofilm formation, with BMIC 50 of 8 μg/mL and 2 μg/mL respectively, and on mature biofilm with BMIC 50 of 2 μg/mL. These two last compounds also showed an interesting activity towards the planktonic cells of C. albicans. A selection of the more active compounds was also evaluated on different C. albicans strains (PMC1042, PMC1083 and ATCC 10261), showing a comparable or higher anti-biofilm activity, especially on mature biofilm. In vivo toxicity studies using the Galleria mellonella larvae, were finally carried out on more active indole derivatives, showing that they are poorly toxic even at the highest concentrations tested (500-1000 μg/mL)., (Copyright © 2019 Elsevier Masson SAS. All rights reserved.)