Aqueous Dispersion of Aramid Nanofibers Achieved by Using Tannic Acid for Ultrahigh Strength Films.

Polymer nanofibers have established a robust foundation and possess immense potential in various emerging fields such as sensors and biotechnology. In this study, aqueous dispersions of aramid nanofibers (ANFs) were successfully prepared by using tannic acid (TA). Morphological analysis revealed that TA effectively prevented self-aggregation of ANFs, and preserved the nanofiber structure during TA-assisted solvent exchange. Subsequently, the ANF and TA/ANF films were fabricated using casting and vacuum-assisted filtration techniques. Notably, the tensile strength of the casting TA/ANF film reached 393.8 MPa, exhibiting a remarkable improvement of 41.3% compared to that of the pure ANF film. These exceptional mechanical properties can be attributed to the well-dispersed nanostructures, hydrogen-bonding interactions, zigzag structures, and fiber-bridging effects. Furthermore, the TA/ANF film demonstrated superior ultraviolet (UV) shielding capabilities, visible transparency properties, and excellent resistance to chemical reagents. The above-mentioned interesting findings demonstrate its potential as a nanofiber-reinforced material for poly(vinyl alcohol) (PVA) composites.

Self-healing, environmentally stable and adhesive hydrogel sensor with conductive cellulose nanocrystals for motion monitoring and character recognition.

Conductive hydrogel-based sensors offer diverse applications in artificial intelligence, wearable electronic devices and character recognition management. However, it remains a significant challenge to maintain their satisfactory performances under extreme climatic conditions. Herein, a stretchable, self-adhesive, self-healing and environmentally stable conductive hydrogel was developed through free radical polymerization of hydroxyethyl acrylate (HEA) and poly(ethylene glycol) methacrylate (PEG) as the skeleton, followed by the incorporation of polyaniline-coated cellulose nanocrystal (CNC@PANI) as the conductive and reinforced nanofiller. Encouragingly, the as-prepared hydrogel (CHP) exhibited decent mechanical strength, satisfactory self-adhesion, prominent self-healing property (95.04 % after 60 s), excellent anti-freezing performance (below -60 °C) and outstanding moisture retention. The assembled sensor derived from CHP hydrogel possessed a low detection limit (0.5 % strain), high strain sensitivity (GF = 1.68) and fast response time (96 ms). Remarkably, even in harsh environmental temperatures from -60 °C to 80 °C, it reliably detected subtle and large-scale human motion for a long-term process (>10,000 cycles), manifesting its exceptional environmental tolerance. More interestingly, this hydrogel-based sensor could be assembled into a "writing board" for accurate handwritten numeral recognition. Therefore, the as-obtained multifunctional hydrogel could be a promising material applied in human motion detection and character recognition platforms even in harsh surroundings.

Ionic Conductive Cellulose-Based Hydrogels with Superior Long-Lasting Moisture and Antifreezing Features for Flexible Strain Sensor Applications.

Nowadays, wearable devices derived from flexible conductive hydrogels have attracted enormous attention. Nevertheless, the utilization of conductive hydrogels in practical applications under extreme conditions remains a significant challenge. Herein, a series of inorganic salt-ion-enhanced conductive hydrogels (HPE-LiCl) consisting of hydroxyethyl cellulose, hydroxyethyl acrylate, lithium chloride, and ethylene glycol/water binary solvent were fabricated via a facile one-pot method. Apart from outstanding self-adhesion, high stretchability, and remarkable fatigue resistance, the HPE-LiCl hydrogels possessed especially excellent antifreezing and long-lasting moisture performances, which could maintain satisfactory flexibility and electric conductivity over extended periods of time, even in challenging conditions such as extremely low temperatures (as low as -40 °C) and high temperatures (as high as 80 °C). Consequently, the HPE-LiCl-based sensor could timely and accurately monitor various human motion signals even in adverse environments and after long-term storage. Hence, this work presents a facile strategy for the design of long-term reliable hydrogels as smart strain sensors, especially used in extreme environments.

One-Step Method for Fabricating Janus Aramid Nanofiber/MXene Nanocomposite Films with Improved Joule Heating and Thermal Camouflage Properties.

The integration of ultraflexible and mechanically robust films with electric heaters and camouflage technology provides a promising platform for the development of wearable devices, especially for aerospace and military applications. Herein, we present a facile and efficient one-step vacuum-assisted filtration method for fabricating Janus films based on aramid nanofibers (ANF) and Ti3C2Tx (MXene). The ANF/MXene nanocomposite film exhibits remarkable properties, including high conductivity (23809.5 S/m), excellent mechanical strength (102.54 MPa), and outstanding thermal stability (575 °C). Most notably, the Janus ANF/MXene composite film demonstrates superior Joule heating performance with a low driving voltage (1-5 V), high heating temperature (30-276 °C), and rapid response time (within 5 s). Additionally, the film exhibits effective thermal camouflage (72 °C for objects with temperatures above 163 °C) and excellent electromagnetic interference shielding properties (SSE/t = 32475.6 dB cm2/g). These results demonstrate that Janus ANF/MXene films possess a unique combination of thermal camouflage, Joule heating, and electromagnetic interference shielding properties, making them highly promising for wearable devices, high-performance electrical heating, infrared stealth, and security protection applications.

Bamboo charcoal fiber bundles loaded MOF-derived magnetic Co/CoO porous polyhedron for efficiently catalytic degradation of tetracyclines hydrochloride.

The health of living things and the ecosystem of the planet have both been negatively impacted by antibiotic residue in the water environment. There has been a lot of interest in the catalyst made of metal-carbon compounds from MOFs as a potential solution for activating peroxymonosulfate (PMS) to produce reactive oxygen species to catalyze the degradation of residual antibiotics. In this study, zeolitic imidazolate frameworks (ZIF-67) on bamboo fiber bundles (BFB) were pyrolyzed to produce magnetic Co/CoO nanoparticles with porous polyhedrons mounted on bamboo charcoal fiber bundles (BCFB)(BCFB@PCo/CoO). Specific surface area of obtained BCFB@PCo/CoO with abundant active sites arrives at 302.41 m2/g. The catalytic degradation efficiency of Tetracycline hydrochloride (TCH), a target contaminant, could reach up to 99.94% within 15 minutes (PMS = 0.4g/L, Cat. = 0.2g/L). The effects of potential factors, including PMS dosage, interference ions, and temperature, on catalytic degradation efficiencies were investigated. Magnetic recovery and antimicrobial properties of the BCFB@PCo/CoO were also evaluated and the possible degradation pathways were explored. Catalytic mechanism explorations of BCFB@PCo/CoO/PMS system reveal MOF-derived magnetic Co/CoO nanoparticles embedded in BCFB promote the synergistic interaction of both radicals and non-radical pathways for catalytic degradation of TCH. The novel BCFB@PCo/CoO provides an alternative to deal with wastewater containing antibiotics.

Fe-pillared montmorillonite functionalized chitosan/gelatin foams for efficient removal of organic pollutants by integration of adsorption and Fenton degradation.

A Fe-pillared montmorillonite (Fe-MMT) functionalized bio-based foam (Fe-MMT@CS/G) was developed by using chitosan (CS) and gelatin (G) as the matrix for high-efficiency elimination of organic pollutants through the integration of adsorption and Fenton degradation. The results showed that the mechanical properties of as-obtained foam were strengthened by the addition of certain amounts of Fe-MMT. Interestingly, Fe-MMT@CS/G displayed efficient adsorption ability for charged pollutants under a wide range of pH. The adsorption processes of methyl blue (MB), methylene blue (MEB) and tetracycline hydrochloride (TCH) on Fe-MMT@CS/G were well described by the Freundlich isotherm model and pseudo-second-order kinetic model. The maximum adsorption capacities were 2208.24 mg/g for MB, 1167.52 mg/g for MEB, and 806.31 mg/g for TCH. Electrostatic interactions, hydrogen bonding and van der Waals forces probably involved the adsorption process. As expected, this foam could exhibit better removal properties toward both charged and uncharged organic pollutants through the addition of H2O2 to trigger the Fenton degradation reaction. For non-adsorbable and uncharged bisphenol A (BPA), the removal efficiency was dramatically increased from 1.20 % to 92.77 % after Fenton degradation. Additionally, it presented outstanding recyclability. These results suggest that Fe-MMT@CS/G foam is a sustainable and efficient green material for the alleviation of water pollution.

Versatile CO2-responsive Sponges Decorated with ZIF-8 for Bidirectional Separation of Oil/Water and Controllable Removal of Dyes.

The complex wastewater containing water-soluble dyes and water-insoluble oils has given rise to significant environmental concerns that demand urgent remediation. Herein, a novel "smart" multifunctional sponge (ZIF-8@PMS) stepwise decorated with ZIF-8 nanoparticles and CO2-responsive copolymer (poly(2-(diethylamino) ethyl methacrylate-co-3-(trimethoxysilyl)propyl acrylate-co-stearyl methacrylate) was successfully prepared for CO2 controllable oil/water separation and dyes removal. The results revealed that the sponge coated with CO2-responsive copolymer for three cycles (ZIF-8@PMS-3) exhibited optimal comprehensive properties. The ZIF-8@PMS-3 had excellent compressive-resilient characteristics and chemical stability. As expected, it displayed tunable wettability and charged state under the regulation of CO2. Based on these features, ZIF-8@PMS-3 presented highly efficient removal of oil and dyes, even for the dye-containing oil/water emulsions, via a synergistic combination of adsorption and separation methods. The adsorption capacity for oil and various organic solvents ranged from 21.3 to 50 g g-1. The maximum adsorption capacities toward anionic dyes: methyl orange with 1205.89 mg g-1 and methyl blue with 880.00 mg g-1 in the presence of CO2 through electrostatic interaction. In the absence of CO2, it achieved maximum adsorption capacities for cationic dyes, including malachite green with 1246.15 mg g-1 and rhodamine B with 203 mg g-1, primarily driven by π-π interactions. According to distinct adsorption mechanisms, ZIF-8@PMS-3 could selectively adsorb either anionic or cationic dyes by exploiting CO2 as a trigger. Furthermore, the separation efficiencies for both types of oil/water emulsions surpassed 99.9%, with respective fluxes of 1566.99 L m-2 h-1 (water-in-oil emulsion) and 310.37 L m-2 h-1 (oil-in-water emulsion). Additionally, the as-prepared sponges exhibited remarkable antibacterial properties and exceptional recyclability. Therefore, the ZIF-8@PMS-3 holds substantial promise for potential applications in practical industrial wastewater treatment.

Highly water dispersible collagen/polyaniline nanocomposites with strong adhesion for electrochromic films with enhanced cycling stability.

Electrochromic materials have attracted extensive attention recently due to their versatile applications in smart windows, displays, antiglare rearview mirrors, and so on. Herein we report a new electrochromic composite prepared from collagen and polyaniline (PANI) through a self-assembly assisted co-precipitation method. The introduction of hydrophilic collagen macromolecules into PANI nanoparticles makes the collagen/PANI (C/PANI) nanocomposite obtain excellent dispersibility in water, which provides good environmental-friendly solution processability. Furthermore, the C/PANI nanocomposite exhibits excellent film-forming properties and adhesion to the ITO glass matrix. The resulting electrochromic film of the C/PANI nanocomposite displays significantly improved cycling stability compared with the pure PANI film after 500 coloring-bleaching cycles. On the other hand, the composite films also exhibit yellow, green and blue polychromatic properties at different applied voltages and high average transmittance at the bleaching state. The C/PANI electrochromic material illustrates scaling potential for the application of electrochromic devices.

Characterization of two infection-induced transcription factors of Magnaporthe oryzae reveals their roles in regulating early infection and effector expression.

The initial stage of rice blast fungus, Magnaporthe oryzae, infection, before 36 h postinoculation, is a critical timespan for deploying pathogen effectors to overcome the host's defences and ultimately cause the disease. However, how this process is regulated at the transcription level remains largely unknown. This study functionally characterized two M. oryzae Early Infection-induced Transcription Factor genes (MOEITF1 and MOEITF2) and analysed their roles in this process. Target gene deletion and mutant phenotype analysis showed that the mutants Δmoeitf1 and Δmoeitf2 were only defective for infection growth but not for vegetative growth, asexual/sexual sporulation, conidial germination, and appressoria formation. Gene expression analysis of 30 putative effectors revealed that most effector genes were down-regulated in mutants, implying a potential regulation by the transcription factors. Artificial overexpression of two severely down-regulated effectors, T1REP and T2REP, in the mutants partially restored the pathogenicity of Δmoeitf1 and Δmoeitf2, respectively, indicating that these are directly regulated. Yeast one-hybrid assay and electrophoretic mobility shift assay indicated that Moeitf1 specifically bound the T1REP promoter and Moeitf2 specifically bound the T2REP promoter. Both T1REP and T2REP were predicted to be secreted during infection, and the mutants of T2REP were severely reduced in pathogenicity. Our results indicate crucial roles for the fungal-specific Moeitf1 and Moeitf2 transcription factors in regulating an essential step in M. oryzae early establishment after penetrating rice epidermal cells, highlighting these as possible targets for disease control.

CO2-responsive functional cotton fibers decorated with Ag nanoparticles for "smart" selective and enhanced dye adsorption.

Novel Ag nanoparticles (NPs) decorated CO2-responsive cotton fiber (PCCF@Ag) as eco-friendly adsorbent was prepared via in-situ growth of Ag NPs on the poly(2-(dimethylamino) ethyl methacrylate-co-4-acryloyloxybenzophenone) coated cotton fiber. The as-prepared PCCF@Ag displayed excellent adsorption performance toward both anionic and cationic dyes with or without CO2 stimulation, even under a wide range of pH from 3 to 11. The maximum adsorption capacities of the as-prepared PCCF@Ag toward anionic dye (1538.5 mg g-1 for MO) and cationic dyes (944.0 mg g-1 for MEB and 415.6 mg g-1 for NR) were satisfactory. The adsorption processes were described better by the Langmuir isotherm and pseudo-second-order kinetic models, respectively. Notably, upon CO2 stimulation, the PCCF@Ag exhibited significantly enhanced adsorption capacity toward anionic dyes, following ultrafast adsorption rate, which made the PCCF@Ag could selectively adsorb anionic dyes from mixture because of greatly different adsorption rates between anionic dyes (adsorption equilibrium within 2 min) and cationic dyes (adsorption equilibrium over 12 h). Additionally, the PCCF@Ag could maintain over 91.0% of adsorption capacity even after ten cycles, indicating its outstanding reusability. Meanwhile, the as-obtained PCCF@Ag exhibited excellent antibacterial activity. Overall, the as-obtained PCCF@Ag could be considered as a promising dye scavenger for wastewater remediation.

Fabrication of super-high transparent cellulose films with multifunctional performances via postmodification strategy.

A transparent versatile cellulose platform film was prepared from Eucalyptus pulp in this work. Based on such cellulose platform, multifunctional cellulose films with ultraviolet-shielding, photochromism, and strong mechanical strength were fabricated via nucleophilic postmodification strategy by introducing a versatile spiropyran moiety into cellulose molecules. The fabricated cellulose films exhibited super-high transmittance up to 96% and performed notable ultraviolet-shielding capacity at 200-400 nm. Moreover, the photochromic performance of cellulose films with color changes could be clearly observed by the naked eyes, and the fluorescent blue could be excited. Besides, the tensile stress of multi-functional cellulose film was about 80 MPa, which was almost 8 times stronger than that of the commercial polyethylene film at the same thickness. It is noteworthy that these superior performances promote such a cellulose platform to be a versatile precursor for fabricating various multi-functional cellulose used in the fields of out-door coating, transparent packaging, optical screen,etc.

Facile and Scalable Fabrication of Antibacterial CO2-Responsive Cotton for Ultrafast and Controllable Removal of Anionic Dyes.

A novel CO2-responsive cotton as an eco-friendly adsorbent derived from poly(4-acryloyloxybenzophenone-co-2-(dimethylamino) ethyl methacrylate) and cotton was fabricated via a facile and fast dip-coating method. As expected, upon CO2 stimulation, the protonated cotton presented CO2-induced "on-off" selective adsorption behaviors toward anionic dyes owing to electrostatic interactions. The adsorption isotherms and kinetics of the CO2-responsive cotton toward anionic dyes obeyed the Langmuir isotherm and pseudo-second-order kinetics models, respectively. It is noteworthy that the CO2-responsive cotton exhibited high adsorption capacity and ultrafast adsorption rate toward anionic dyes with the maximum adsorption capacities of 1785.71 mg g-1 for methyl orange (MO), 1108.65 mg g-1 for methyl blue (MB), and 1315.79 mg g-1 for naphthol green B (NGB), following the adsorption equilibrium times of 5 min for MO, 3 min for MB, and 4 min for NGB. Moreover, the CO2-responsive cotton also exhibited high removal efficiency toward anionic dyes in synthetic dye effluent. Additionally, the CO2-responsive cotton could be facilely regenerated via heat treatment under mild conditions and presented stable adsorption properties even after 15 cycles. Finally, the as-prepared CO2-responsive cotton exhibited outstanding antibacterial activity against E. coli and S. aureus. In summary, this novel CO2-responsive cotton can be viewed as a promising eco-friendly adsorbent material for potential scalable application in dye-contaminated wastewater remediation.

Development of eco-friendly CO2-responsive cellulose nanofibril aerogels as "green" adsorbents for anionic dyes removal.

A novel CO2-responsive cellulose nanofibril aerogel as a "green" adsorbent derived from poly(methacrylic acid-co-2-(dimethylamino) ethyl methacrylate) and carboxylated cellulose nanofibrils was successfully prepared via stepwise cation-induced gelation and freeze drying method. This aerogel exhibited CO2-triggered adsorption behavior towards anionic dyes with a rapid adsorption rate and a high adsorption capacity, as well as satisfactory mechanical properties. Upon CO2 stimulation, the charged aerogel can selectively adsorb anionic dyes from aqueous solutions based on an electrostatic interaction. The maximum adsorption capacities of this aerogel towards methyl blue (MB), naphthol green B (NGB), and methyl orange (MO) were 598.8, 621.1 and 892.9 mg g-1, respectively, accompanied by fast adsorption equilibriums towards MB and NGB within 7 min, and MO within 12 min. Meanwhile, the adsorption isotherms and the kinetics of the CO2-responsive adsorbents followed the Freundlich isotherm and the pseudo-second-order model, respectively. Furthermore, the resulting CO2-responsive adsorbent exhibited outstanding recyclability, as its adsorption performance can still be maintained even after twenty cycles. Accordingly, the resultant CO2-responsive cellulose nanofibril aerogel could be a promising adsorbent material for the removal of anionic dyes in wastewater remediation.

Ultra-efficient and stable heterogeneous iron-based Fenton nanocatalysts for degrading organic dyes at neutral pH via a chelating effect under nanoconfinement.

An ultra-efficient and stable heterogeneous iron-based Fenton nanocatalyst has been developed for degrading organic dyes at neutral pH via a chelating effect under nanoconfinement. The catalyst demonstrates an exceptionally high degradation capacity of 2600 mg g-1 for methylene blue and rapid degradation efficiencies at neutral and basic conditions. Moreover, MPOPs are highly stable and recyclable without any obvious performance loss and iron leaching under different pH conditions.

Study on the release behaviors of berberine hydrochloride based on sandwich nanostructure and shape memory effect.

Nanofibrous drug delivery systems (DDSs) recently have attracted remarkable interest, especially their potential to program dosage of the encased drug intelligently. Despite this, the exploration of efficient strategy to precisely program drug release from nanofibrous DDS still remains a significant challenge. In this study, we electrospun a near-body temperature (Ttrans ≈ 42 °C) sensitive shape memory polyurethane in three stages through sequential electrospinning technology, and prepared a sort of sandwich structural membrane, comprising of top, inner and bottom layers, wherein a natural antibacterial agent, berberine hydrochloride (BCH), was imbedded inside the middle layer. As demonstrated by the results obtained from tensile testing and morphology characterization, the prepared sandwich structural membrane and the nanofibrous membrane with homogenous structure exhibited not only desirable mechanical properties but also surface morphologies. In addition, the release period can be significantly prolonged in virtue of the sandwich structure. As revealed by the experiment of in vitro drug release, it took nearly 144 h to release 80 wt% BCH from sandwich structural membrane, while as little as 72 h was observed to release the same amount of BCH from that with homogenous structure. More interestingly, the encapsulated BCH is capable to be released in a controlled manner owning to the thermo-sensitive shape memory effect, and the release rate of BCH can be accelerated by stretching and fixing the nanofibrous membranes into certain ratios prior to release. Collectively, this study provides a facile strategy to design and prepare a reliable and smart DDS, i.e. sandwich structural membrane, which may enhance the availability of BCH and also intelligently avoid the bacterial infection.

Stomatocyte-like hollow polydopamine nanoparticles for rapid removal of water-soluble dyes from water.

Stomatocyte-like hollow polydopamine nanoparticles (SHPNs) are synthesized for rapid removal of water-soluble dyes from water. They demonstrate an exceptionally high adsorption capacity of 2896 mg g-1 for methylene blue (MB) and can rapidly sequester MB from water within 20 seconds. Moreover, SHPNs can be regenerated easily using a mild washing procedure.

Rapid microwave-assisted bio-synthesized silver/Dandelion catalyst with superior catalytic performance for dyes degradation.

Silver nanoparticles were synthesized under microwave irradiation, a facile and efficient way, using dandelion extract as reducing and capping agents. The as-synthesized silver nanoparticles/Dandelion compounds (AgNPs/Dandelion) were characterized by field emission scanning electron microscope (FESEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), X-ray diffraction analysis (XRD), fourier transform infrared (FTIR) spectroscopy, dynamic light scattering (DLS), Zeta potential and ultraviolet visible (UV-vis) spectroscopy. The catalytic degradation activity of AgNPs/Dandelion for Methyl orange (MO) and Rhodamine B (RhB) in the presence of NaBH4 were recorded by UV-vis spectroscopy. AgNPs/Dandelion exhibit excellent catalytic degradation activity for RhB and MO with rate constants of 0.1038 s-1 and 0.0393 s-1, respectively.

Facile Fabrication of Sandwich Structural Membrane With a Hydrogel Nanofibrous Mat as Inner Layer for Wound Dressing Application.

A common problem existing in wound dressing is to integrate the properties of against water erosion while maintaining a high water-uptake capacity. To tackle this issue, we imbedded one layer of hydrogel nanofibrous mat into two hydrophobic nanofibrous mats, thereafter, the sandwich structural membrane (SSM) was obtained. Particularly, SSM is composed of three individual nanofibrous layers which were fabricated through sequential electrospinning technology, including two polyurethane/antibacterial agent layers, and one middle gelatin/rutin layer. The obtained SSM is characterized in terms of morphology, component, mechanical, and functional performance. In addition to the satisfactory antibacterial activity against Staphylococcus aureus and Escherichia coli, and antioxidant property upon scavenging DPPH free radicals, the obtained SSM also shows a desirable thermally regulated water vapor transmission rate. More importantly, such SSM can be mechanically stable and keep its intact morphology without appearance damage while showing a high water-absorption ratio. Therefore, the prepared sandwich structural membrane with hydrogel nanofibrous mat as inner layer can be expected as a novel wound dressing.

Extraction of lotus fibres from lotus stems under microwave irradiation.

An efficient technology for preparing lotus fibres under microwave irradiation was developed. The lotus fibres were characterized by scanning electron microscopy, Fourier transform infrared spectrometry, X-ray diffraction and thermogravimetry. Lotus fibres prepared are a kind of hollow fibres which are composed of a superfine fibre and an external shell. The effect of the treatment time with hydrogen peroxide under microwave irradiation on components, whiteness, moisture regain, removal rate of impurities, fineness, tensile strength and breaking elongation of lotus fibres was investigated. The results show that the cellulose content in lotus fibres increases with increase in treatment time. Whiteness and moisture regain of lotus fibres increase with increase in treatment time with hydrogen peroxide. The removal rate of impurities and the fineness of lotus fibres are improved after they are treated with hydrogen peroxide. Microwave irradiation is supposed to be an efficient method for producing lotus fibres.

Interaction between azo dye Acid Red 14 and pepsin by multispectral methods and docking studies.

The interaction of synthetic azo dye Acid Red 14 with pepsin was studied by fluorescence spectroscopy, UV-vis spectroscopy, circular dichroism and molecular docking. Results from the fluorescence spectroscopy show that Acid Red 14 has a strong capability to quench the intrinsic fluorescence of pepsin with static quenching. Binding constant, number of the binding sites and thermodynamic parameters were measured at different temperatures. The result indicates that Acid Red 14 interact with pepsin spontaneously by hydrogen bonding and van der Waals interactions. Three-dimensional fluorescence spectra and circular dichroism spectra reveal that Acid Red 14 could slightly change the structure of pepsin. The hydrogen bond is formed between Acid Red 14 and Tyr-189 and Thr-218 residues of pepsin. Furthermore, the binding between Acid Red 14 and pepsin inhibits pepsin activity. The study can provide a way to analyze the biological safety of Acid Red 14 on digestive proteases or other proteins.