Microcrystalline Cellulose Research Articles

Improved Fog Collection on a Hybrid Surface with Acylated Cellulose Coating.

Fog collection serves as an efficient method to alleviate water scarcity in foggy, water-stressed regions. Recent research has focused on constructing a hybrid surface to enhance fog collection efficiency, with one approach being the prevention of liquid film formation at hydrophilic sites. Inspired by the desert beetle, a coating (10-MCC) made by partially acylating microcrystalline cellulose (MCC) exhibits hydrophilic sites alongside a hydrophobic skeleton enabling rapid droplet capture despite its overall hydrophobicity. The captured droplets quickly coalesce into a large droplet driven by the wetting gradient created by the hydrophobic backbone and hydrophilic sites. To achieve greater fog collection efficiency, a hydrophobic-superhydrophobic hybrid surface is formed by combining a coating of 10-MCC with a superhydrophobic surface. The construction of superhydrophobic surfaces typically involves creating a rough surface with a distinctive structure produced by the anodization technique and modifying it with stearic acid. The superhydrophobic surface exhibits excellent corrosion resistance and mechanical stability. Moreover, the hybrid surface shows high efficiency in fog collection, with a tested maximum efficiency of approximately 1.5092 g/cm2/h, 1.77 times that of the original Al sheets. The results demonstrate a remarkable enhancement in fog collection capacity. Furthermore, this work serves as an inspiration for the low-cost and innovative design of engineered surfaces for efficient fog collection.

Development of Bilayer Polysaccharide-Based Films Combining Extrusion and Electrospinning for Active Food Packaging

The development of active food packaging is desirable for food safety and to avoid food loss and waste. In this work, we developed antioxidant bilayer films combining extrusion and electrospinning techniques. These films consisted of a first layer of thermoplastic cornstarch (TPS), incorporated with microcrystalline cellulose (MCC). The second layer consisted of gallic acid (GA) encapsulated at different concentrations in 1:1 chitosan/poly(ethylene-co-vinyl alcohol) (CS/EVOH) nanofibers. This layer was directly electrospun onto the TPS/MCC film. The morphological, structural, wettability, permeability to oxygen, and antioxidant properties were investigated for the first layer and the bilayer films. Water contact angle measurements revealed the hydrophobic nature of the first layer (θ0 = 100.6°). The oxygen permeability (OP) was accessed through the peroxide value (PV) of canola oil, kept in containers covered by the films. PV varied from 66.6 meq/kg for the TPS/MCC layer to 60.5 meq/kg for a bilayer film. Intermolecular hydrogen bonds, mediated by GA, contributed slightly to improving the mechanical strength of the bilayer films. The bilayer film incorporated with GA at 15.0% reached a radical scavenging activity against the DPPH radical of (903.8 ± 62.2) μmol.L−1.Eq. Trolox.g−1. This result proved the effectiveness of the GA nanoencapsulation strategy.

Advanced Fabrication and Characterization of Hydrothermal Responsive Fabric from Microcrystalline Cellulose-Reinforced Shape Memory Polyurethane Filament

Demands for smart textiles have recently increased quickly in terms of functionality and responsiveness to wearers and environmental changes. This paper explores the development of hydrothermal responsive shape memory woven fabric from Microcrystalline Cellulose Reinforced Shape Memory Polyurethane Microcomposite Filament. The concentration of microcrystalline cellulose and drawing ratio of the filaments were first optimized according to the tensile strength and shape recovery ratio and taken as 15 wt% and 2.0 respectively. Hydrothermal responsive shape memory micro-composite filaments were then produced from shape memory polyurethane (SMPU) and microcrystalline cellulose (MCC) with optimized concentration and draw ratio by wet spinning process. The physical, mechanical, thermal and shape memory performances of the filaments were studied. The optimized filament was found to have a tensile strength of 0.91 cN/dtex and elongation of 385.2% in which the strength is much more improved when compared to a pure SMPU filament of strength 0.72 cN/dtex. The shape fixity and shape recovery results of the micro-composite filament were found to be 71.2% and 93.6% respectively. A woven fabric was manufactured from pure polyester, cotton as warp and SMPU-MCC filaments as weft and its breathability and shape memory properties were investigated. The air permeability of SMPU-PE fabrics was found to be 172.9 mm/s and 155.1 mm/s in its fixed temporary shape and recovered shape respectively. The water vapour permeability of SMPU-CT fabric was found to be 612.01 g/m2.h and 540.28 g/m2.h in its fixed temporary and recovered shape respectively which shows smart breathable fabrics can be made and adopted with enhanced properties.

Simultaneously enhancing microelastic response and degradability for poly(butylene succinate) composite monofilaments by silanized microcrystalline cellulose

Simultaneously enhancing microelastic response and degradability for poly(butylene succinate) composite monofilaments by silanized microcrystalline cellulose

DEVELOPMENT OF MYCROCRYSTALLINE CELLULOSE ORIGINATE FROM SAGO (METROXYLON SAGU) STEM BARK BY HYDROLISIS METHODE USING NITRIC ACID

Objective: Microcrystalline cellulose (MCC) is an essential excipient in tablet formulation. Mostly MCC was obtained from wooden conifer stem fiber, therefore environment issues had been came up. Alternative sources for MCC which offer friendly conifer wood need to be explored. This study aimed to isolate and determine the characteristics of MCC originated from Sago (Metroxylon sago Rottb.) stem fibers as an promising alternative of MCC. Methods: MCC was prepared through pre-hydrolysis using an acetic acid solution, alkali heating using NaOH solution, and acid hydrolysis using nitric acid 0.3 N using three variations of heating temperature, namely 90, 95 and 100 °C. The characterization carried out were pharmaceutical grade, powder properties, FTIR analysis and powder morphology by SEM. Results: The yields obtained were 66.02; 65.53 and 65.08%, respectively. The characteristics of the MCC sample based on pharmaceutical grade quality were white to yellowish white powder, odorless, tasteless, insoluble in: ether, 96% alcohol, HCl 2N and NaOH 1N. The pH of the MCC suspension were 5.07-5.12, while moisture content were 3.67-4.17%, with loss on drying value as much as 0.37-0.4%, and ash content 1-2.17%. The value of permanganate number were 0.09-0.11, Hausner factor was between 1.05-1.25, and angle of repose were between 11.4-24.8°. Conclusion: Based on the results, it can be concluded that Sago is potent natural resource for MCC. The resulting MCC revealed physicochemical and characteristic of MCC, which almost similar to Avicel PH 102 as standard.

Construction of high-performance and sustainable polylactic acid composites for 3D printing applications with plasticizer

Polylactic acid (PLA) attains much attention because of its biodegradability, biocompatibility, and high strength, but its further application was remarkably hindered by its brittleness. In order to improve the toughness of PLA, a biodegradable composite was prepared by blending ductile polycaprolactone (PCL), stiff microcrystalline cellulose (MCC), and green plasticizer tributyl citrate (TBC) with PLA by melting extrusion. The physicochemical properties and microstructure of PLA composites were thoroughly investigated using FTIR, TGA, DSC, XRD, melting rheology, optical transmittance, 3d printing, tensile tests, and SEM. The tensile tests results show that introduction of TBC exhibited a remarkable improvement effect in the elongation at break of PLA/PCL/MCC (PPM) composite, increasing from 2.9 % of PPM to up to 30 % of PPM/6TBC and PPM/8TBC. Noticeably, the strength of PPM/TBC composites (at least 33.1 MPa) was enhanced compared with that of PPM (28.2 MPa). The plasticization of TBC, enhancing the compatibility of composites, and reinforcing effect of MCC were identified as pivotal factors in toughening and reinforcing PLA. Furthermore, it is observed that the incorporation of TBC contributed to enhanced thermal stability, crystallinity, and rheology property of composites. This research supplies a novel approach to bolstering the toughness of PLA and broaden its potential applications.

Preservation of Tomatoes (Lycopersicum esculentum) with Composite Biofilms Based on Starch and Microcrystalline Cellulose (MCC)

Preservation of Tomatoes (Lycopersicum esculentum) with Composite Biofilms Based on Starch and Microcrystalline Cellulose (MCC)

Preparation of amino cellulose aerogel and its formaldehyde adsorption properties

The aerogel prepared from cellulose has the advantages of low density, high porosity, large specific surface area, good gas diffusion and adsorption space, which is a good gas adsorption material. In this study, microcrystalline cellulose was used as raw material, and LiBr ionic liquid was used as a solvent system. In addition, cellulose aerogel was modified by polyethyleneimine, which retained three-dimensional network structure and had excellent formaldehyde adsorption capacity. The adsorption capacity of polyethyleneimine-modified cellulose aerogel (PCA) to formaldehyde can reach 12.3 mg/g at 25 ℃. It was found that the adsorption capacity of PCA aerogel for formaldehyde changed with the increase in nitrogen content. The adsorption of formaldehyde was mainly through the chemical adsorption of the Schiff base reaction between NH2 and formaldehyde molecules in polyethylenimine (PEI).

Effect of microcrystalline cellulose on mechanical properties of flax-jute-epoxy hybrid composite materials using vacuum bagging

Nowadays, synthetic fibres are replaced with hybrid composite fibres which consist of low energy production, biodegradability, resource renewability, less hazardous and easy handling of manufactured composites. The present work focuses on the effect of microcrystalline cellulose (MCC) particles by varying the percentage concentration (0 wt %, 2 wt % and 4 wt %) in the flax-jute-epoxy composite materials. The MCC particle is mixed with epoxy resin as matrix material and flax-jute fibres as reinforcements in the composite panels fabricated using the vacuum bagging method. The tensile, flexural, impact, hardness and thermogravimetric tests were performed on the fabricated composite panels per the ASTM standard. The experimental results show that with the addition of 2 wt % MCC particle, sample 2 has higher tensile strength, flexural strength and impact strength than sample 1 (0 wt % MCC) and sample 3 (4 wt % MCC). It can be noted that due to the addition of MCC particles, overall mechanical properties improved as a result of good interfacial bonding between matrix and fibres which are evident through SEM analysis. Similarly, thermal stability of the composites also improved in the flax-jute hybrid fibre composites particularly in 2 wt % MCC.

Fabrication and characterization of biocomposite pellets from cassava starch and oil palm empty fruit bunch fibers

Oil palm empty fruit bunches (OPEFB) are lignocellulosic biomass that can be used to produce a biocomposite as an alternative to substitute non-renewable materials, such as plastic. Generally, the production of biocomposites uses OPEFB, which has been processed into cellulose, microcrystalline cellulose, or nanocellulose and is mixed with starch. However, the OPEFB pretreatment into various types of cellulose requires a long process and many chemicals. The OPEFB pretreatment with less process, such as cutting to shorter fibers and without chemicals, was expected to shorten the process. This study aims to produce and evaluate the characteristics of biocomposite pellets from a combination of cassava starch and OPEFB fibers. Short OPEFB fibers (3-5 mm) with varying concentrations of 0, 5, 10, 15, and 20% were added to the cassava starch before mixing with other materials. The twin screw extruder used to produce biocomposite pellets was set at six temperature zones ranging from 85-140 °C and the screw speed in the range of 160-190 rpm. The results show that higher concentrations of OPEFB fibers produced darker pellets, which tended to be greyish. The biocomposite pellets had densities of 1.322-1.417 g cm-3. SEM results show some agglomerations on the surface of starch-OPEFB fibers biocomposite pellets. The water solubility of biocomposite pellets ranged from 32.97 – 36.44%. In conclusion, biocomposite pellets could be produced from a mixture of cassava starch and OPEFB fibers up to 20%. In its application for rigid packaging production, the biocomposite pellets’ performance could be improved by mixing them with recycled polypropylene.

Comparative Selective Conversion of Biomass-Derived Mono- and Polysaccharides into Lactic Acid with Lanthanide Lewis Acid Catalysts

Comparative Selective Conversion of Biomass-Derived Mono- and Polysaccharides into Lactic Acid with Lanthanide Lewis Acid Catalysts

Field assessment of active ingredient quantity in pharmaceutical tablets with limited calibration of near infrared spectra: An application to ciprofloxacin tablets

Portable near-infrared (NIR) spectrophotometers have emerged as valuable tools for identifying substandard and falsified pharmaceuticals (SFPs). Integration of these devices with chemometric and machine learning models enhances their ability to provide quantitative chemical insights. However, different NIR spectrophotometer models vary in resolution, sensitivity, and responses to environmental factors such as temperature and humidity, necessitating instrument-specific libraries that hinder the wider adoption of NIR technology. This study addresses these challenges and seeks to establish a robust approach to promote the use of NIR technology in post-market pharmaceutical analysis. We developed support vector machine and partial least squares regression models based on binary mixtures of lab-made ciprofloxacin and microcrystalline cellulose, then applied the models to ciprofloxacin dosage forms that were assayed with high performance liquid chromatography (HPLC). A receiver operating characteristic (ROC) analysis was performed to set spectrophotometer independent NIR metrics to evaluate ciprofloxacin dosage forms as “meets standard,” “needs HPLC assay,” or “fails standard.” Over 200 ciprofloxacin tablets representing 50 different brands were evaluated using spectra acquired from three types of NIR spectrophotometer with 85% of the prediction agreeing with HPLC testing. This study shows that non-brand-specific predictive models can be applied across multiple spectrophotometers for rapid screening of the conformity of pharmaceutical active ingredients to regulatory standard.

Silver-doped microcrystalline cellulose as a material for simple detection of urinary cysteine using a smartphone

Silver-doped microcrystalline cellulose as a material for simple detection of urinary cysteine using a smartphone

Pioglitazone does not enhance exogenous glucose oxidation or metabolic clearance rate during aerobic exercise in men under acute high altitude exposure.

Insulin insensitivity decreases exogenous glucose oxidation and metabolic clearance rate (MCR) during aerobic exercise in unacclimatized lowlanders at high altitude (HA). Whether use of an oral insulin sensitizer prior to acute HA exposure enhances exogenous glucose oxidation is unclear. This study investigated the impact of Pioglitazone (PIO) on exogenous glucose oxidation and glucose turnover compared to placebo (PLA) during aerobic exercise at HA. Using a randomized, crossover design, native lowlanders (n=7 males, mean±SD, age: 23±6 yr, body mass: 84±11 kg) consumed 145 g (1.8 g/min) glucose while performing 80-min of steady-state (1.43±0.16 V̇O2 L/min) treadmill exercise at HA (460 mmHg) following short-term (5 days) use of PIO (15 mg oral dose per day) or PLA (microcrystalline cellulose pill). Substrate oxidation and glucose turnover were determined using indirect calorimetry and stable isotopes (13C-glucose and [6,6-2H2]-glucose). Exogenous glucose oxidation was not different between PIO (0.31±0.03 g/min) and PLA (0.32±0.09 g/min). Total carbohydrate oxidation (PIO: 1.65±0.22 g/min, PLA: 1.68±0.32 g/min) or fat oxidation (PIO: 0.10±0.0.08 g/min, PLA: 0.09±0.07 g/min) were not different between treatments. There was no treatment effect on glucose rate of appearance (PIO: 2.46±0.27, PLA: 2.43±0.27 mg/kg/min), disappearance (PIO: 2.19±0.17, PLA: 2.20 ± 0.22 mg/kg/min), or MCR (PIO: 1.63±0.37, PLA: 1.73±0.40 mL/kg/min). Results from this study indicate that PIO is not an effective intervention to enhance exogenous glucose oxidation or MCR during acute HA exposure. Lack of effect with PIO suggests the etiology of glucose metabolism dysregulation during acute HA exposure may not result from insulin resistance in peripheral tissues.

Development of a Polyethylene Breathable Packaging Film with Modified Microcrystalline Cellulose for Fresh Products

In this study, a material based on polyethylene (PE) and microcrystalline cellulose (MC) was developed as a breathable packaging film. Surface functionalization of MC with 3-aminopropyltriethoxysilane (APTES) has been shown to be an efficient option to tailor their properties and increase opportunities for the application of MC on the reinforcement of polymers such as polyethylene (PE). The functionalization of MC with the mentioned silane derivative was achieved using a green method and later used in the development of composites with PE in three percentages (1, 3, and 5%). All the materials were prepared by melt blending and characterized in terms of structural properties (ATR-FTIR and FTIR in transmittance mode, EDX, and SEM), thermal properties (DSC and TGA), thermomechanical properties (DMA), contact angle measurements and permeability to water vapor. The materials demonstrated the potential to be used as breathable film packaging for fresh products.

Optimization of toothtablets incorporating Albizia myriophylla Benth. stem extract obtained by eco-friendly microwave-assisted extraction

Albizia myriophylla Benth. stems are composed of the bioactive compound lupinifolin, which has exhibited anti-Streptococcus mutans activity. Extracting this plant for incorporation into oral healthcare products is challenging. This study aimed to optimize the eco-friendly microwave-assisted extraction of A. myriophylla stems. It also optimized toothtablets incorporating A. myriophylla stem extract. First, lupinifolin was isolated, and its structure was determined for use as a biomarker in this study. Next, three extraction parameters—the solvent-to-solid ratio, microwave power, and microwave time—were screened using a one-factor-at-a-time approach before being optimized using a Box–Behnken design. The results showed that the optimized conditions that maximized the extraction yield and lupinifolin content were a solvent-to-solid ratio of 23:1, microwave power of 800 W, and microwave time of 70 s. This extract contained 16.27 ± 0.43 % lupinifolin. The extract exhibited a minimum inhibitory concentration of 32 μg/mL and a minimum bactericidal concentration of 256 μg/mL. The half-maximal inhibitory concentration with human gingival fibroblast cells was 102.70 ± 1.02 μg/mL for the extract and 76.75 ± 1.03 μg/mL for lupinifolin. The extract was solidified using microcrystalline cellulose and colloidal silicon dioxide before being incorporated into the toothtablet formulation. Three factors in toothtablet production—compression force, microcrystalline cellulose content, and hydrated silica content—were also screened using a one-factor-at-a-time approach before being optimized using a Box–Behnken design. The results showed that the optimized conditions that approached the desired properties were a compression force of 2500 psi, microcrystalline cellulose content of 12 %, and hydrated silica content of 10 %. The developed toothtablets contained 35.64 ± 0.45 mg of lupinifolin per 650 mg toothtablet (or approximately 5.5 % lupinifolin per toothtablet) and retained their anti-S. mutans activity. They appeared safe for human gingival fibroblasts, even when treated for 2 min, with a maximum concentration of 2000 μg/mL. In conclusion, the developed toothtablets incorporating A. myriophylla stem extract can potentially serve as a high-quality, antibacterial, and safe alternative to traditional toothpaste.

Biocomposites and bionanocomposites from poly(lactide) and cellulosic materials – a review

Abstract Global environmental concerns have recently accelerated interest in the usage of biodegradable polymers to replace petroleum-based conventional plastics. Lactic acid-based polymers are some of the most promising and widely studied biobased materials, which are suitable for packaging and biomedical applications. This is mainly due to their appealing characteristics such as relatively good mechanical properties, biocompatibility, and multiple end-of-life options such as recyclability and biodegradability in industrial composting conditions. However, the use of lactic acid-based polymers in advanced applications is constrained by their inherent brittleness, poor melt strength, and relatively high cost. These disadvantages can be remedied by reinforcement with cellulose nanomaterials which can enhance their mechanical properties while maintaining their biodegradability. This review provides an overview of recent studies on the development of biodegradable lactic acid-based polymer composites and nanocomposites reinforced with cellulose nanofibrils (CNFs), cellulose nanocrystals (CNCs) and microcrystalline cellulose (MCC). The different processing methods and chemical modification techniques utilised on modification and functionalisation of cellulosic nanomaterials for improving the properties of lactic acid-based polymer nanocomposites are also discussed.

The effect of unloading and ejection conditions on the properties of pharmaceutical tablets

This study investigates decompression and ejection conditions on tablet characteristics by comparing compact densities and tensile strengths made using regular rigid dies and custom-built die systems that enable triaxial decompression. Die-wall pressure evolution during decompression and ejection stresses did not meaningfully impact the density and tensile strength of the materials tested: microcrystalline cellulose, crystalline lactose monohydrate, and mannitol. Furthermore, the apparent differences in tensile strength between rectangular cuboids and cylindrical compacts are unrelated to decompression and ejection conditions, but rather a consequence of their shapes and of the test configurations. This suggests that elastic and plastic deformations that may occur during decompression and ejection are not significantly influenced by die-wall pressure evolution. We thus conclude that while triaxial decompression and constraint-free ejection may allow the production of defect-free compacts for materials that otherwise are defect prone using a rigid die, they seem to pose no benefits when the materials already produce defect-free compacts using a rigid die.

Development of eugenol loaded cellulose-chitosan based hydrogels; in-vitro and in-vivo evaluation for wound healing

Recent years have demonstrated that biopolymers can serve as effective woundhealing agents. We hereby report chitosan-oxidized cellulose (CS.OMCC) based hydrogels loaded with eugenol with distinctive antimicrobial, biocompatible, and angiogenic characteristics. CS.OMCC hydrogels in four different ratios were synthesized through Schiff base (-CN) between chitosan (CS) and oxidized microcrystalline cellulose (OMCC). The swelling and degradation study analyzed the maximum absorption strength and weight loss of 1165% and 56.8 %, respectively. Hydrogels were potent against E. coli and S. aureus. The zones of inhibition were dependent upon the chitosan and eugenol, where 30 % eugenol (Eu) loaded CS.OMCC 4:1 hydrogel revealed greater zones (17 mm). The hydrogels demonstrated favorable biocompatibility, adhesion, and migration potential of mouse fibroblast cells. Moreover, the in-vivo potential by Chorioallantoic membrane (CAM) assay displayed an increase in the number, length, and size of blood vessels, contributing superior angiogenic potential. Increased expression in the case of VEGF further supported the role of hydrogels in promoting angiogenesis. Our study presents eugenol loaded chitosan-oxidized cellulose hydrogels that presented a promising solution to target bacterial infection and promote angiogenesis, thereby promoting the wound healing process.

Cellulose nanocrystals as an innovative superdisintegrant for oral dispersible tablets

Oral Dispersible Tablets (ODTs), designed for rapid disintegration in the oral cavity, offer advantages such as easy administration for diverse populations and faster drug absorption. Microcrystalline cellulose (MCC) has been a traditional choice as a disintegrant, but its limitations have led to increased interest in cellulose nanocrystals (CNCs). This study focuses on obtaining and characterizing CNCs derived from MCC by sulfuric acid hydrolysis, exploring different times and drying methods (lyophilization or spray drying). At a 50 % v/v acid concentration for 60 min at 45 °C it was possible to extract CNC with a 76 % yield. When lyophilized, CNC micrographs showed large aggregates with few isolated particles, while the spray-dried samples were seen as free, elongated particles. The resulting CNCs, with enhanced properties like high hydrophilicity and surface area, are investigated for their impact on ODT formulations. All of them disintegrated faster than 10 s. A comprehensive analysis of ODTs' disintegration mechanism was also undertaken. The drying method dictates the predominant disintegration mechanism, even though this is also influenced by the nanoparticle size. Therefore, the study contributes insights into the potential of CNCs as innovative superdisintegrants, offering a promising path for improving oral drug delivery systems.