Search Results (400)

Background/Objectives: Hot-melt extrusion (HME) has gained prominence for the manufacture of sustained-release oral dosage forms, yet the application of wax-based matrices and their resilience to alcohol-induced dose dumping (AIDD) remains underexplored. This study aimed to develop and characterise wax-based sustained-release felodipine formulations, with a particular focus on excipient functionality and robustness against AIDD. Methods: Felodipine sustained-release formulations were prepared via HME using Syncrowax HGLC as a thermally processable wax matrix. Microcrystalline cellulose (MCC) and lactose monohydrate were incorporated as functional fillers and processing aids. The influence of wax content and filler type on mechanical properties, wettability, and drug release behaviour was systematically evaluated. Ethanol susceptibility testing was conducted under simulated co-ingestion conditions (4%, 20%, and 40% v/v ethanol) to assess AIDD risk. Results: MCC-containing tablets demonstrated superior sustained-release characteristics over 24 h, showing better wettability and disintegration. In contrast, tablets formulated with lactose monohydrate remained structurally intact during dissolution, overly restricting drug release. This limitation was effectively addressed through granulation, where reduced particle size significantly improved surface accessibility, with 0.5–1 mm granules achieving a satisfactory release profile. Ethanol susceptibility testing revealed divergent behaviours between the two filler systems. Unexpectedly, MCC-containing tablets showed suppressed drug release in ethanolic media, likely resulting from inhibitory effect of ethanol on filler swelling and disintegration. Conversely, formulations containing lactose monohydrate retained their release performance in up to 20% v/v ethanol, with only high concentrations (40% v/v) compromising matrix drug-retaining functionality and leading to remarkably increased drug release. Conclusions: This study highlights the pivotal role of excipient type and constitutional ratios in engineering wax-based sustained-release formulations. It further contributes to the understanding of AIDD risk through in vitro assessment and offers a rational design strategy for robust, alcohol-resistant oral delivery systems for felodipine. Full article

Here, we demonstrated a direct method to produce cellulose nanocrystals (CNCs) with a rod-like shape from microcrystalline cellulose by a ZnCl₂-based deep eutectic solvent (DES) with a high yield (~80.1%). We obtained CNCs, crystalline index (68.9%), with a width of ~30–50 nm and a length of 200–400 nm. Importantly, we were able to functionalize the CNCs with an acetyl, -(CO)CH₃, group, which could potentially modulate the hydrophobic property of the CNCs. We attributed the formation of the CNCs to the Lewis acid effect of ZnCl₂, which can hydrolyze the amorphous cellulose regime. Our study opens a new path to directly isolate cellulose nanocrystals with several functional groups on the surface of CNCs. Full article

Ionic liquids (ILs) have attained considerable attention as cellulose solvents. Nevertheless, the detailed mechanism of cellulose dissolution in ILs is not clearly defined. It is crucial to recognize the role of the individual components of the ILs to fully understand this mechanism. During this study, the effect of alkyl chain length in imidazolium cation was examined using synthesized ILs which are composed of common acetate anion and imidazolium cations with different alkyl substituents. This study also aimed to investigate the odd–even effect of alkyl chain carbons. Furthermore, whereas most published investigations on cellulose dissolution in ILs used microcrystalline cellulose (MCC), which has a far lower degree of polymerization, in this study, cotton cellulose was used. During the dissolution experiments, cotton cellulose (5% w/w) was added to each IL, and the progress of the dissolution was monitored using polarized light microscopy (PLM). The regeneration of cellulose was performed by using water as the anti-solvent, and the regenerated cellulose was characterized by Fourier-transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). During these experiments, it was noted that ILs with odd C3 and C5 carbon chains were less effective at dissolving cellulose than those with even C2 and C4 alkyl chains. Additionally, after regeneration, biomaterials for a variety of applications could be produced. Full article

The development of printable, biocompatible, biodegradable, and cost-effective bioinks, or biomaterial inks, remains a focal point in extrusion-based bioprinting research. In this study, fish gelatin (FG) was reinforced with microcrystalline cellulose (MCC) to formulate biomaterial inks. These FG/MCC composite inks were fabricated into 3D scaffolds using an extrusion bioprinter. The influence of MCC concentration on printability was systematically evaluated. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analyses confirmed the formation of hydrogen bonds between MCC and FG, indicating molecular-level interactions. Notably, MCC incorporation enhanced the rheological properties of the ink and significantly improved the compressive strength of printed scaffolds. Furthermore, MCC content modulated key scaffold characteristics, including porosity, degradation rate, swelling behavior, and microarchitecture. These findings demonstrate that FG/MCC composite hydrogels exhibit optimal properties for extrusion-based 3D bioprinting, offering a promising platform for tissue engineering applications. Full article

Background/Objectives: Microcrystalline cellulose (MCC) is a commonly used pharmaceutical excipient. At present, the catalytic potential of MCCs for the degradation of active pharmaceutical ingredients (APIs) has not been paid adequate attention. This study aims to investigate the representativeness of the pH value of an MCC determined in accordance with the pharmacopeia method to the acidity on its surface. Methods: We tested the differences between the catalytic activities of different MCCs and their supernatant prepared in accordance with the pharmacopeia method for the hydrolysis of ginsenoside Re, which is relatively stable in neutral or weak alkaline aqueous solutions but sensitive to acid. The sulfur content of the sulfuric acid-prepared MCC was measured using an ICP-OES. Results: All of the five tested commercially available and two self-prepared MCCs have been found to significantly promote the hydrolysis of ginsenoside Re. But their supernatants were neutral and chemically inert to Re. The sulfur content of the MCC prepared in this experiment using sulfuric acid hydrolysis was determined to be 109.60 µg/g, which is equivalent to 186 to 465 µM of sulfuric acid on the surface. Conclusions: The pH value of an MCC determined in accordance with the pharmacopeia method is not representative of the acidity on its surface. The primary reason should be that there is immobilized acid that is not so easily dissociated into the media. Ginsenoside Re is sensitive and applicable as a probe for the evaluation of the catalytic potential of pharmaceutically used MCCs. Full article

The drying process of microcrystalline cellulose and adipic acid particles in a cylindrical fluidized bed was investigated using the Gaussian spectral technique to monitor fluid–dynamic regime transitions associated with surface moisture loss. Pressure fluctuation signals were recorded and analyzed to assess hydrodynamic behavior. Excess moisture significantly alters the bubbling characteristics of the bed, leading to instability in the fluidization regime. The results demonstrated that the Gaussian spectral technique effectively captured these hydrodynamic changes, particularly at the critical moisture content threshold, when compared with the drying rate curves of the materials. For microcrystalline cellulose and adipic acid particles, it is reasonable to conclude that a mean central frequency above 5.75–6.0 Hz and a standard deviation exceeding 3.7–3.8 Hz correspond to a bubbling regime, indicating that the critical drying point has been reached. This approach provides a non-intrusive and sensitive method for identifying transitions in the drying process, offering a valuable tool for real-time monitoring and control. The ability to track fluidization regime changes with high precision reinforces the potential of this technique for optimizing drying operations in the pharmaceutical, food, and chemical industries. Full article

As health concerns and regulatory pressures over saturated and trans fats grow, there is a growing need for healthier alternatives to traditional solid fats, such as butter and hydrogenated oils, that are still widely used in the food system. In this study, cellulose particle-based Pickering emulsions (CP-PEs) were prepared from microcrystalline cellulose and ethylcellulose and then foamed to obtain edible oleofoams (CP-EOs) as a solid-fat replacer. The average size of CP-PE droplets without surfactant was 598 ± 69 nm, as confirmed by confocal and transmission electron microscopy. Foaming with citric acid/NaHCO₃ and structuring with ≥6% glyceryl monostearate resulted in CP-EOs with an overrun of 147 ± 4% and volumetric stability for 72 h. Micro-computed tomography showed a uniform microcellular network, while the rheological analysis showed solid-like behavior with a storage modulus higher than butter. Differential scanning calorimetry showed a melting enthalpy similar to unsalted butter (10.1 ± 0.9 J/g). These physicochemical properties demonstrate that CP-EOs can closely mimic the firmness, thermal profile, and mouth-feel of conventional solid fats and may provide a promising solid-fat replacer. Full article

Improving the manufacturability of drug formulations via direct compression has been of great interest for the pharmaceutical industry. Selecting excipients plays a vital role in obtaining a high-quality product without the wet granulation processing step. In particular, for diluents which are usually present in a larger amount in a formulation, choosing the correct one is of utmost importance in the production of tablets via any method. In this work, we assessed the possibility of manufacturing a small-molecule drug product, omeprazole, which has been historically manufactured via a multi-step processes such as wet granulation and multiple-unit pellet system (MUPS). For this purpose, four prototypes were developed using several diluents: a co-processed excipient (Microcelac^®), two granulated forms of alpha-lactose monohydrate (Tablettose^® 70 and Tabletose^® 100), and a preparation of microcrystalline cellulose (Avicel^® PH102) and lactose (DuraLac^® H), both of which are common excipients without any enhancement. The tablets were produced using a single punch tablet press and thoroughly characterized physically and chemically in order to assess their functionality and adherence to drug product specifications. The direct compression process was used for the manufacturing of all proposed formulations, and the prototype formulated using Microcelac^® showed the best results and performance during the compression process. In addition, it remained stable over twelve months under 25 °C/60% RH conditions. Full article

The enzyme ω-transaminase (ω-TA) has garnered significant attention due to its capacity to catalyze the synthesis of chiral amines with high efficiency. Nevertheless, the lack of stability of ω-TA and the difficulty of recycling and reuse are still challenges that limit its application. This study developed a novel magnetic nanocellulose composite carrier (NNC@Fe₃O₄@Ni), synthesized from microcrystalline cellulose via low-eutectic solvent treatment, amine modification, and metal hybridization. The NNC@Fe₃O₄@Ni was characterized by FTIR, XPS, XRD, BET, and VSM. Additionally, the performance and catalytic behavior of the immobilized enzyme were investigated. The results revealed that NNC@Fe₃O₄@Ni exhibited a high specific surface area, superparamagnetism, and dual-site functionality (amine/Ni²⁺). Response Surface Methodology (RSM) optimized the carrier-enzyme interaction parameters, yielding optimal immobilization conditions: a mass ratio of 50.8 mg g⁻¹, temperature of 12.5 °C, and duration of 58.6 min, achieving 82.91% enzyme activity recovery. Compared to free enzymes, the immobilized variant demonstrated enhanced catalytic stability, with expanded optimal pH (9.0) and temperature (30 °C). Thermal stability assessments showed 84.39% activity retention after 5 h at 30 °C and 90.30% residual activity post-120 h storage. The catalyst maintained >80% efficiency over 10 reuse cycles. These findings confirm the efficacy of magnetic nanocellulose carriers in enhancing ω-TA stability, reusability, and catalytic performance, offering a viable strategy for industrial biocatalytic processes. Full article

The effects of pomelo peel-derived dietary fibers (total dietary fiber, cellulose, and microcrystalline cellulose) on in vitro simulated gastrointestinal digestion and fermentation characteristics of silver carp fish balls were systematically investigated. Our findings revealed that pomelo peel dietary fibers significantly enhanced protein digestibility (highest increased by 18.58%), free amino acid content (most elevated by 13.27%), and slow digestion starch content (highest increased by 64.97%) in fish balls, suggesting an improved nutritional quality of fish balls. Moreover, pomelo peel-derived dietary fibers increased the content of short-chain fatty acids in the digestive fish balls at the late stage of fermentation (48 h) and caused changes in gut microbiota with reducing the ratio of Firmicutes to Bacteroidetes (F/B), the abundance of Escherichia-Shigella and Streptococcus, and increasing the levels of probiotics Bacteroides and Phascolarctobacterium. These suggested that pomelo peel-derived dietary fibers could promote the digestive characteristics of fish balls, effectively exerting prebiotic effects by regulating gut microbiota. The results could provide a scientific basis for the enhanced modification of intestinal digestion and fermentation of fish balls with dietary fibers. Full article

Achieving efficient electrocatalytic oxidation of cellulose-derived biomass is a pivotal strategy for advancing bioenergy utilization and achieving carbon neutrality. This study addresses the challenges of low conversion efficiency caused by cellulose’s high crystallinity and excessive energy consumption in conventional processes by proposing a novel integrated system combining solid heteropoly acid catalytic pretreatment and electrocatalytic oxidation. By preparing the (C₁₆TA)H₂PW solid acid catalyst, we successfully achieved hydrolysis of microcrystalline cellulose under 180 °C for 60 min, attaining a glucose yield of 40.1%. Furthermore, a non-noble metal electrocatalyst system based on foam copper (CuF) was developed, with the Co₃O₄/CuF electrode material demonstrating a Faradaic efficiency of 85.3% for formate production at 1.66 V (vs. RHE) in 1 mol L⁻¹ KOH electrolyte containing the pretreated cellulose mixture, accompanied by a partial current density of 153.2 mA cm⁻². The mechanism study indicates that hydroxyl radical-mediated C-C bond selective cleavage dominates the formate generation. This integrated system overcomes the limitations of poor catalyst stability and low product selectivity in biomass conversion, offering a sustainable strategy for green manufacturing of high-value chemicals from cellulose. Full article

To comparatively study the effects of cold plasma activation and chemical treatment on the adsorption capacities of biomass carbon nanofiber membranes (BCNMs), microcrystalline cellulose (MCC) and chitosan (CS) were used to fabricate porous BCNMs by electrospinning and carbonization. Two modification methods, including oxygen (O₂) plasma activation and chemical treatment using nitric acid (HNO₃), sulfuric acid (H₂SO₄), hydrogen peroxide (H₂O₂), and urea, were further employed to enhance their adsorption performance. Various carbonyl group (C=O), ether bond (C-O), carboxyl group (O-C=O) and pyridinic nitrogen (N), pyrrolic N, and quaternary N functional groups were successfully introduced onto the surface of the BCNMs by the two methods. The BCNM-O₂ showed optimal formaldehyde absorption capacity (120.67 mg g⁻¹), corresponding to its highest contents of N, O-containing functional groups, and intact network structure. However, chemical treatment in strong acid or oxidative solutions destructed the microporous structures and changed the size uniformity of fibers in the BCNMs, resulting in a decline in formaldehyde adsorption capacity. A synergistically physical–chemical adsorption took place during formaldehyde adsorption by the modified biomass nanofiber membranes, due to the coexistence of suitable functional groups and porous structures in the membranes. Full article

Fused deposition modeling (FDM) 3D printing (3DP) of PLA biocomposites reinforced with plant-derived cellulosic fibrous materials, including spun yarn, microcrystalline, microfibrillar, nanofibrillar cellulose, and cellulose nanocrystals, offers an environmentally sustainable solution to the mechanical limitations of polymer-only printed materials. Micron- and submicron-scale cellulosic fibers are valued for their renewability, non-toxicity, high surface area, and favorable elastic and specific moduli; notably, micron-scale reinforcements are particularly attractive due to their ease of large-scale industrial production and commercial viability. Similarly, PLA benefits from large-scale production, contributes to CO₂ sequestration through its raw material precursors, and requires less energy for production than non-biodegradable petroleum-derived polymers. Incorporating these raw materials, each of which offers attractive performance properties, complementary commercial strengths, and environmental benefits, as constituent phases in FDM 3D-printed biocomposites (FDMPBs) can further enhance the environmental responsiveness of an already low-waste FDM 3DP technology. Inspired by these compelling advantages, this paper critically reviews research on FDMPB with cellulosic reinforcements in a PLA matrix, uniquely categorizing studies based on the form of cellulosic reinforcement and its impact on the biocomposite’s structure and mechanical performance. Additionally, the review covers biocomposite filament production methods and the equipment involved, presenting an alternative framework for cataloging FDMPB research. A comprehensive literature analysis reveals that the wide variation in feedstocks, fiber–matrix compounding methods, equipment, and processing parameters used in filament production and 3DP complicates the comparison of FDMPB mechanical properties across studies, often resulting in conflicting outcomes. Key processing parameters have been compiled to bridge this gap and offer a more nuanced understanding of the cause-and-effect relationships governing biocomposite properties. Finally, targeted recommendations for future research on developing FDMPB with a PLA matrix and micron-scale cellulosic reinforcements are provided, addressing the knowledge gaps and challenges highlighted in the peer-reviewed literature. Full article

In this study, polymer composites based on a polypropylene (PP) matrix with the addition of cellulose and ES-40, used as a silica precursor, were investigated. These composites were designed to achieve enhanced biodegradability through the incorporation of bioavailable cellulose and to enable subsequent carbonization into carbon–silicon carbide systems. Rheological investigations revealed that the multicomponent mixtures exhibited pseudoplastic behavior over the shear rate range typical of injection molding, ensuring process stability without additional plasticization. Morphological analysis demonstrated that an optimal balance of PP, cellulose, and ES-40 promoted the formation of a three-dimensional network structure, leading to a significant increase in flexural modulus at the equal flexural strength despite some reduction in tensile strength. It was further shown that substituting fibrous cellulose with microcrystalline cellulose improved the composite homogeneity, thereby enhancing the density and mechanical properties, especially in systems with low polymer contents. Preliminary pyrolysis experiments indicated that these injection-molded composites can serve as precursors for fabricating bulk thermally stable products containing silicon carbide particles. The obtained results underscore the high potential of the developed materials for applications in conventional injection molding, the possibility of additive manufacturing, and processes requiring subsequent carbonization. Full article

Microcrystalline cellulose (MCC) possesses important attributes, including high crystallinity, a large surface area, excellent mechanical strength, chemical stability, and biodegradability. This study aims to research MCC extraction from bamboo (Phyllostachys edulis (Carrière) J. Houz.) fiber by assessing the impact of key processing variables such as acid concentration, temperature, and hydrolysis duration. Experimental results indicate that hydrolysis time and hydrochloric acid (HCl) concentration significantly influence yield. After evaluating the effects of various hydrolysis conditions, the optimal parameters were determined to be a 2.0 M HCl concentration, 90 °C, and 10 min of reaction time. The MCC produced under optimal conditions displayed improved crystallinity (77.2%) while retaining functional groups similar to those found in raw bamboo. Morphological analysis revealed an irregular rod-like shape with rough surfaces. This optimized hydrolysis process offers a viable approach for MCC production from raw bamboo and holds potential as a precursor for developing environmentally friendly biodegradable fiber materials. Full article