多孔n-HA/PVA/CS复合水凝胶的制备与抑菌性能研究

以纳米羟基磷灰石、聚乙烯醇、壳聚糖为原料,采用物理交联法制备复合水凝胶(n-HA/PVA/CS),并测定其含水率、力学强度及微观结构。采用比浊法和平板计数法测定n-HA/PVA/CS复合水凝胶在酸性条件下的最低抑菌浓度和抑菌率,同时对比研究其对革兰氏阴性菌大肠杆菌(E.coli)和革兰氏阳性菌金黄色葡萄球菌(S.aureus)的抑菌性。结果表明,n-HA/PVA/CS复合水凝胶具有均匀分散的三维多孔结构,含水率75%,拉伸强度0.26 MPa。经过2%(质量分数)的醋酸溶液处理的n-HA/PVA/CS复合水凝胶材料对S.aureus和E.coli的最低抑菌质量浓度均为0.5 g/L;在该复合水凝胶质量浓度为2.0 g/L时,对S.aureus的抑菌率为84%,对E.coli的抑菌率达到99%,当其样品质量浓度为2.5 g/L时,对E.coli抑菌率接近100%。n-HA/PVA/CS复合水凝胶可望成为性能优良的人工角膜支架材料。     

Preparation,characterization, antibacterial properties,and hemostatic evaluation of ibuprofen‐loaded chitosan/gelatin composite films

Ibuprofen‐loaded chitosan/gelatin (CS/GE) composite films were fabricated in this work. The morphology of the composite film was investigated using scanning electron microscopy. The functional groups of the composite film before and after crosslinking were characterized using Fourier transform infrared spectroscopy. Meanwhile, the mechanical properties, antibacterial performance, cytocompatibility, and hemostatic activity of the composite films were investigated. The results show that the amount of CS affected the mechanical properties and liquid uptake capacities of the composite films. The composite film showed better bactericidal activity against Staphylococcus aureus than Escherichia coli. In vitro drug‐release evaluations showed that crosslinking could control the drug‐release rate and period in wound healing. Both types of CS/GE and drug‐loaded CS/GE composite films also showed excellent cytocompatibility in cytotoxicity assays. The hemostatic evaluation indicated that the composite film crosslinked by glutaraldehyde in rabbit livers had a dramatic hemostatic efficacy. Therefore, ibuprofen‐loaded CS/GE composite films are potentially applicable as a wound dressing material. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45441.     

Influences of degradability,bioactivity, and biocompatibility of the calcium sulfate content on a calcium sulfate/poly(amino acid) biocomposite for orthopedic reconstruction

The inorganic content in a bioceramic/polymer composite is considered to play an important role in promoting bone healing after implantation in vivo. In this study, two calcium sulfate/poly(amino acid) (CS/PAA) composites with CS content proportions of 50% (mass fraction, 50CS/PAA) and 65% (65CS/PAA) were synthesized via the in situ melting polymerization method, and the degradability, bioactivity, and biocompatibility of the composites were evaluated. The results indicated that 41.5% of weight loss of the 50CS/PAA was observed after soaking in simulated body fluid (SBF) for 16 weeks, whereas 56.2% of weight loss of the 65CS/PAA was observed. These results suggested that the CS content in the composite affected the degradability of the composite. After being soaked in SBF for 1 week, formation of an apatite layer was observed on the surfaces of both composites without obvious differences. The co‐culture results of the composites and the MG‐63 cells confirmed that 65CS/PAA exhibited higher proliferation and a higher alkaline phosphatase (ALP) activity than did 50CS/PAA. The implantations in bone defects of rabbits for 3 months revealed that both composites had good biocompatibility and were capable of guiding new bone formation without causing any inflammation. However, faster degradability of the 65CS/PAA composite was observed in vivo, indicating that the higher CS content in the composite results in higher degradability. In conclusion, the CS content in the composite for orthopedic reconstruction has distinct effects on the degradability, OD value, and ALP activity of the composites, whereas it has little effect on the bioactivity and bone formation. POLYM. COMPOS., 37:1886–1894, 2016. © 2015 Society of Plastics Engineers     

Fabrication and properties of degradable poly(amino acid)/nano hydroxyapatite bioactive composite

Poly(amino acid)/nano hydroxyapatite (PAA/n-HA) bioactive composite was prepared by in situ melting polymerization. The composition, structure and morphology as well as glass transition temperature (T_g), dynamic mechanical properties of the PAA/n-HA composite were characterized by infrared spectrometer, X-ray diffractometer, X-ray photoelectron spectroscopy, scanning electron microscope, differential scanning calorimeter, and dynamic mechanical analyzer. The results indicated that the n-HA particles were uniformly distributed into PAA matrix and some interactions were found at the interface between PAA and n-HA, and the crystallinity of PAA in the composite decreased with the increase of n-HA content. The T_g and storage modulus of the composite increased with increasing n-HA content, demonstrating that the n-HA content had obvious effects on the crystallization kinetic parameters and thermo properties of the PAA/n-HA composite. In addition, the n-HA amount had evident effects on the degradation of the PAA/n-HA composite in phosphate buffered saline (PBS), and the weight loss ratio of the composite decreased with the increase with n-HA content. The pH value of the medium was stable around 7.40 after the composite immersion into PBS for 8 weeks. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Poly(ε‐caprolactone) composites containing gentamicin‐loaded β‐tricalcium phosphate/gelatin microspheres as bone tissue supports

In this work, novel antibacterial composites were prepared by using poly(ε‐caprolactone) (PCL) as the main matrix material, and gentamicin‐loaded microspheres composed of β‐tricalcium phosphate (β‐TCP) and gelatin. The purpose is to use this biodegradable material as a support for bone tissue. This composite system is expected to enhance bone regeneration by the presence of β‐TCP and prevent a possible infection that might occur around the defected bone region by the release of gentamicin. The effects of the ratio of the β‐TCP/gelatin microspheres on the morphological, mechanical, and degradation properties of composite films as well as in vitro antibiotic release and antibacterial activities against Escherichia coli and Staphylococcus aureus were investigated. The results showed that the composites of PCL and β‐TCP/gelatin microspheres had antibacterial activities for both bacteria. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

High strength antibacterial membranes consisted of nanofibrous chitosan immobilized silver nanoparticles

Chitosan (CS) has biocompatibility and biodegradability, but the bulk CS hydrogel/membranes with its poor strength and limited antibacterial property could not satisfy the practical application. Here green dissolving/regeneration and in situ reduction strategy was combined to construct high strength antibacterial CS membranes. First nanofibrous CS hydrogels were constructed through dissolving CS in LiOH/KOH/urea aqueous system via freezing–thawing process followed regeneration. Then, Ag NPs were immobilized along CS nanofibers through in situ reductions of Ag + by the NH₂ group of CS. The obtained NCM-Ag composite dry membranes are easy for storing and can quick switch to nanofibrous hydrogels as absorbing water. Size of Ag NPs can be controlled to very small until 2 nm by concentration and limited space network. Fourier transform infrared spectroscopy and X-ray photoelectron spectrometer indicated the forceful grasp ability of CS nanofibers to Ag NPs for a stable binding, mechanical property was enhanced over 100Mpa as the nanofibrous structure and chain linked by Ag coordination. The NCM-Ag membranes had excellent antibacterial activities against both Staphylococcus aureus and Escherichia coli. Moreover, such nanofibrous CS membrane exhibited good adhesive ability to tissues. Combining all these properties, NCM-Ag membranes would be potential as antibacterial adhesion barrier to accelerate wound healing.     

Physico-chemical,thermal, and mechanical properties of PLA-nHA nanocomposites: Effect of glass fiber reinforcement

In this study, tri-layered composites were prepared by reinforcing poly-lactic acid (PLA) nano-hydroxyapatite (n-HA) (1 and 5 wt%) and 20 mol% continuous phosphate glass fibers (PGF). Initially, the effect of addition of 1 and 5% n-HA on the structural, thermal, mechanical, and thermo-mechanical properties of 100% PLA was investigated. With 5 wt% n-HA addition the tensile modulus (TM), flexural modulus (FM), tensile strength (TS), and flexural strength (FS) of 100% PLA was improve by 14.9, 47.4, 6, and 32.9%, respectively. Whereas, the un-notched impact strength of the nanocomposites suffer 2% deterioration. However, T _g decreased by 0.3°C and T _c increased by 10°C as 5 wt% n-HA was added to 100% PLA. Afterwards, the 5% n-HA/PLA composite were reinforced with 20 mol% continuous PGF and the TM, FM, TS, and FS of the tri-layered composites were 162.6, 412.5, 28.4, and 157.4% higher as compared to 100%PLA. Furthermore, the storage modulus of the 1% n-HA-filled composites was 500 MPa lower than 100%PLA, while 5 wt% n-HA-filled composites showed similar storage modulus as 100% PLA. 5 wt% n-HA-filled composite showed the highest peak of loss modulus which may be attribute to the chain segment of PLA matrix after the incorporation of HA. Thus, n-HA and PGF reinforcement resulted in improved mechanical properties of the composites and have great potential as biodegradable bone fixation device with enhanced load-bearing ability.     

Surface‐modified pliable PDLLA/PCL/β‐TCP scaffolds as a promising delivery system for bone regeneration

Surface‐modified poly(d , l ‐lactide)/polycaprolactone/β‐tricalcium phosphate complex scaffold was fabricated in this study and we hypothesized that pliable and mechanical strong scaffold would be achieved by regulation of ternary compositions; while superficial modification strategy conduced to preserve and controlled‐release of bioactive growth factors. Properties of the composite scaffolds were systematically investigated, including mechanical properties, surface morphology, porosity, wettability, and releasing behavior. Moreover, the representative cytokine, recombinant human bone morphogenetic protein‐2 (rhBMP‐2), was loaded and implanted into muscular pouch of mouse to assess bone formation in vivo. Improved osteogenesis was achieved ascribed to both amplified β‐tricalcium phosphate (β‐TCP) content and retarded initial burst release. Particularly, scaffold doped with hydroxypropyl methylcellulose (HPMC) displayed optimal osteogenic capability. The results indicated that the PDLLA/PCL/β‐TCP complex scaffold along with HPMC‐coating and rhBMP‐2 loading was a promising candidate for bone regeneration. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40951.     

Sustained release of CIP from TiO2-PVDF/starch nanocomposite mats with potential application in wound dressing

Electrospinning is an economical and alluring method to fabricate wound dressing mats from a variety of natural and synthetic materials. In this study, polyvinylidene fluoride (PVDF) and starch composite mats containing ciprofloxacin (CIP) loaded on titanium dioxide nanoparticles (TiO₂) were prepared. Fourier Transform Infrared spectra of CIP, synthesized TiO₂ NPs, TiO₂/CIP, and PVDF/starch composite mats are analyzed. Scanning electron microscopy images revealed that the fiber diameter of PVDF nanofibers thickens by increasing starch, which varies between 180 nm and 550 nm. Strain at break of PVDF, starch, PVDF/starch (2:1 w:w; P2S1), PVDF/starch (1:1 w:w; P1S1), PVDF/starch (1:2 w:w; P1S2), and nanofibers were 103 ± 11, 3 ± 0.6, 27 ± 4, 52 ± 5.2, 7.7 ± 1%, respectively. Based on strain at break and young modulus, P2S1 was selected as a suitable candidate for wound dressing to which load TiO₂/CIP as a bioactive agent. The release rate of CIP showed that about 40% of the drug is released in the first 2 days. Furthermore, the antibacterial activity of dressings was investigated using Escherichia coli and Staphylococcus aureus microorganisms and zones of clearance were obvious around the specimen on the agar plate. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48916.     

Swelling,thermal stability,antibacterial properties enhancement on composite hydrogel synthesized by chitosan-acrylic acid and ZnO nanowires

ABSTRACT

A series of antibacterial superabsorbents containing zinc oxide nanowires (ZnO NWs) based on chitosan (CS) and acrylic acid (AA) were prepared by one-step synthesis. Antibacterial influence of the content with ZnO NWs complex in superabsorbents on Escherichia coli and Staphylococcus aureus was studied, as well as water absorbency, swelling behavior, and thermal stability. Results showed that water absorbency for CS-co-AA composite hydrogel in water was 1000 g/g, because of the presence of ZnO NWs within CS-co-AA hydrogel facilitated the water absorbency ability. Furthermore, results also showed that the antibacterial effect of CS-co-AA composite hydrogels increased with an increase of ZnO NWs content.     

AgNPs loaded microemulsion using gallic acid inhibits MCF-7 breast cancer cell line and solid ehrlich carcinoma

Abstract

The objective of this present work is to optimize and prepare silver nanoparticles(AgNPs) in Dioctyl sodium sulfosuccinate (AOT) microemulsion (ME) for oral use and to investigate its antibacterial and anticancer activity in vitro and in vivo. In vitro drug release study confirmed that faster release of drug at the tumor cells compared to the blood circulation. It also showed a potential antibacterial activity against pathogenic bacteria. The optimized AgNPs loaded ME confirmed significant cytotoxicity against MCF-7 cancer cell line with IC50 16.72?±?0.014?μg/mL and significant reduction in solid Ehrlich tumor growth in compared to the control, placebo and pure drug.     

Preparation of chitosan‐graft‐(methyl methacrylate)/Ag nanocomposite with antimicrobial activity

It has been found that composites of chitosan (CS) and Ag nanoparticles can exhibit excellent antibacterial activities. However, the weak mechanical performances of these composite materials limit their wide application. Grafting of vinyl monomers onto CS is one of the most effective methods to improve the performances of CS without sacrificing its properties. A nanocomposite of chitosan‐graft‐(methyl methacrylate) (CS‐g‐MMA) containing Ag nanoparticles was prepared by in situ chemical reduction of Ag ions in an aqueous acetic acid solution of CS and graft copolymerization of MMA onto CS. Transmission electron micrographs, X‐ray diffraction patterns and UV‐visible spectra of the nanocomposite confirmed the formation of Ag nanocrystals. X‐ray photoelectron spectroscopy proved that Ag? O bonds exist in the composite. Thermogravimetric analysis/differential scanning calorimetry showed that the decomposition temperature of CS was 319.8 °C while that of the CS‐g‐MMA/Ag composite shifted to a higher temperature of 422.1 °C. Antimicrobial experiments showed that the antimicrobial rates of the CS‐g‐MMA/Ag composite to E. coli, B. subtilis, S. aureus and P. aeruginosa were 93–98%. CS molecules can act as stabilizing agents to prevent the aggregation of Ag nanoparticles in the process of synthesizing CS‐g‐MMA/Ag nanocomposites. The antimicrobial activity of the as‐prepared nanocomposites is higher than that of CS alone. Copyright © 2009 Society of Chemical Industry     

Chitosan/alginate nanoparticles stabilized by poloxamer for the controlled release of 5‐fluorouracil

In this study, stable 5‐fluorouracil (5‐FU)‐loaded chitosan (CS)/alginate (Alg) nanoparticles (NPs) were prepared with poloxamer as a surfactant. The effects of the Alg concentration, CS/Alg weight ratio, and poloxamer concentration on the properties of the 5‐FU‐loaded CS/Alg NPs were studied. The results of dynamic light scattering and transmission electron microscopy indicated that stable 5‐FU‐loaded CS/Alg NPs of around 200 nm with low‐size polydispersities were achieved. Furthermore, the in vitro release of the 5‐FU‐loaded CS/Alg NPs was investigated in phosphate buffer solution at pH 7.4. The results show that the encapsulation efficiency of 5‐FU depended on the drug feeding amount (DFA), poloxamer concentration, Alg concentration, and CS concentration. However, the in vitro release rate of the 5‐FU‐loaded CS/Alg NPs was only related to the DFA, Alg concentration, and CS concentration and was independent of the poloxamer concentration. The time of 5‐FU release from the CS/Alg NPs could becontrolled to be sustained for more than 12 h. According to this study, CS/Alg NPs stabilized by poloxamer could serve as a suitable candidate for the controlled release of 5‐FU. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Composite chitosan/poly(ethylene oxide) electrospun nanofibrous mats as novel wound dressing matrixes for the controlled release of drugs

The aim of this study was to develop novel biomedical electrospun nanofiber mats for controlled drug release, in particular to release a drug directly to an injury site to accelerate wound healing. Here, nanofibers of chitosan (CS), poly(ethylene oxide) (PEO), and a 90 : 10 composite blend, loaded with a fluoroquinolone antibiotic, such as ciprofloxacin hydrochloride (CipHCl) or moxifloxacin hydrochloride (Moxi), were successfully prepared by an electrospinning technique. The morphology of the electrospun nanofibers was investigated by scanning electron microscopy. The functional groups of the electrospun nanofibers before and after crosslinking were characterized by Fourier transform infrared spectroscopy. X‐ray diffraction results indicated an amorphous distribution of the drug inside the nanofiber blend. In vitro drug‐release evaluations showed that the crosslinking could control the rate and period of drug release in wound‐healing applications. The inhibition of bacterial growth for both Escherichia coli and Staphylococcus aureus were achieved on the CipHCl‐ and Moxi‐loaded nanofibers. In addition, both types of CS/PEO and drug‐containing CS/PEO nanofibers showed excellent cytocompatibility in the cytotoxicity assays. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42060.     

Poly(vinyl alcohol)/chitosan/honey/clay responsive nanocomposite hydrogel wound dressing

Many efforts have been made to develop modern wound dressings to overcome limitations of traditional ones. Smart nanocomposite hydrogels are appropriate candidates. In this work, a novel responsive nanocomposite hydrogel based on poly(vinyl alcohol)/chitosan/honey/clay was developed and evaluated as a novel wound dressing. The morphology and properties of synthesized nanocomposite hydrogels loaded with honey as a drug model were investigated. The exfoliated morphology of nanocomposite was confirmed by X‐ray diffractometry. Swelling studies were performed at 20 and 37 °C at various pH. The results showed that swelling increased as a result of temperature rise and maximum swelling occurred at a pH of 2. In vitro release of honey was also studied at the same conditions. Corresponding results indicated faster honey release rate at higher pH values. MTT results exhibited no cytotoxicity in nanocomposite hydrogel system. Investigation of antibacterial activity revealed more than 99% antibacterial activity for proposed system. In vivo results confirmed the wound healing ability of developed system. Generally, appropriate properties of proposed system made it ideal in wound dressing applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46311.     

Synergistic Effect of Co-Delivering Ciprofloxacin and Tetracycline Hydrochloride for Promoted Wound Healing by Utilizing Coaxial PCL/Gelatin Nanofiber Membrane

Combining multiple drugs or biologically active substances for wound healing could not only resist the formation of multidrug resistant pathogens, but also achieve better therapeutic effects. Herein, the hydrophobic fluoroquinolone antibiotic ciprofloxacin (CIP) and the hydrophilic broad-spectrum antibiotic tetracycline hydrochloride (TH) were introduced into the coaxial polycaprolactone/gelatin (PCL/GEL) nanofiber mat with CIP loaded into the PCL (core layer) and TH loaded into the GEL (shell layer), developing antibacterial wound dressing with the co-delivering of the two antibiotics (PCL-CIP/GEL-TH). The nanostructure, physical properties, drug release, antibacterial property, and in vitro cytotoxicity were investigated accordingly. The results revealed that the CIP shows a long-lasting release of five days, reaching the releasing rate of 80.71%, while the cumulative drug release of TH reached 83.51% with a rapid release behavior of 12 h. The in vitro antibacterial activity demonstrated that the coaxial nanofiber mesh possesses strong antibacterial activity against E. coli and S. aureus. In addition, the coaxial mats showed superior biocompatibility toward human skin fibroblast cells (hSFCs). This study indicates that the developed PCL-CIP/GEL-TH nanofiber membranes hold enormous potential as wound dressing materials.     

Synthesis of chitosan derivative with dual‐antibacterial functional groups and its antibacterial activity

The O‐fumaryl ester (OFTMCS) of N,N,N‐trimethyl chitosan (TMCS) has been synthesized as a water‐soluble chitosan (CS) derivative bearing dual‐functional groups, with the aim of discovering novel CS derivatives with good water solubility and enhanced the antibacterial activity compared with unmodified CS. OFTMCS was characterized by FT‐IR, ¹³C NMR, XPS, XRD and Zeta potential analyses. The XPS results indicated that the degree of substitution (DS) on the C₂‐NH₂ group of the CS was 0.78, and that the DS on its C₆‐OH group was 0.31. The TGA results showed that the thermal stability of OFTMCS was lower than that of unmodified CS. The antibacterial activities of OFTMCS were investigated by assessing the mortality rates of the representative Gram‐positive and Gram‐negative bacteria Staphylococcus aureus and Escherichia coli, respectively. The results indicated that OFTMCS exhibited superior antibacterial activity to CS at a lower dosage. The synthesis of CS derivatives bearing dual‐functional groups could therefore be used as a promising strategy to enhance the antibacterial activity of CS. The antimicrobial mechanism of action of OFTMCS was discussed. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42663.     

Preparation and characterization of antimicrobial films based on nanocrystalline cellulose

Nanocrystalline cellulose (NCC) has great potential in applications in medical and food packaging due to its abundance, high specific surface area, biodegradability, biocompatibility, and reproducibility. N-Halamine is one of the most effective antibacterial agents, with broad-spectrum efficacy against microorganisms, good stability, and reproducibility. Due to the nanosize effect and high specific surface area of NCC, N-halamine-modified NCC is potentially an excellent biocidal compound. In this paper, an N-halamine precursor 1-hydroxymethyl-5,5-dimethylhydantoin (HDH) was used to modify NCC with cyanuric chloride (cych) as the bonding agent. After chlorination, the produced NCC-cych-HDH-Cl became antibacterial. The synthesized NCC-cych-HDH-Cl was added to a chitosan (CS) and polyvinyl alcohol (PVA) solution to prepare antibacterial films. The optimum mixing ratio of PVA and CS in the PVA/CS films and concentration of NCC-cych-HDH-Cl were investigated. The surface morphologies and mechanical properties of the antibacterial films were characterized with scanning electron microscopy, transmission electron microscopy, and mechanical strength tests. The results indicated that the film with 90/10 PVA/CS and 7.0% loading of NCC-cych-HDH-Cl exhibited excellent tensile strength. The antibacterial film with 5.91 × 10¹⁷ atoms/cm² of active chlorine displayed an excellent antibacterial property against Staphylococcus aureus (ATCC 6538) and Escherichia coli O157:H7 (ATCC 43895). © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47101.     

Development and characterisation of microporous biomimetic scaffolds loaded with magnetic nanoparticles as bone repairing material

Fine-tuning of the scaffolds structural features for bone tissue engineering can be an efficient approach to regulate the specific response of the osteoblasts. Here, we loaded magnetic nanoparticles aka superparamagnetic iron oxide nanoparticles (SPIONs) into 3D composite scaffolds based on biological macromolecules (chitosan, collagen, hyaluronic acid) and calcium phosphates for potential applications in bone regeneration, using a biomimetic approach. We assessed the effects of organic (chitosan/collagen/hyaluronic acid) and inorganic (calcium phosphates, SPIONs) phase over the final features of the magnetic scaffolds (MS). Mechanical properties, magnetic susceptibility and biological fluids retention are strongly dependent on the final composition of MS and within the recommended range for application in bone regeneration. The MS architecture/pore size can be made bespoken through changes of the final organic/inorganic ratio. The scaffolds undertake mild degradation as the presence of inorganic components hinders the enzyme catalytic activity. In vitro studies indicated that osteoblasts (SaOS-2) on MS9 had similar cell behaviour activity in comparison with the TCP control. In vivo data showed an evident development of integration and resorption of the MS composites with low inflammation activity. Current findings suggest that the combination of SPIONs into 3D composite scaffolds can be a promising toolkit for bone regeneration.     

Preparation and application of (Cu2O-Ag)@TA composite nanomaterials with enhanced stability and photocatalytic antibacterial activity

Food spoilage caused by bacterial growth is a serious threat to human health, so food preservation technology with long-acting antibacterial effect has been widely studied. In this work, (Cu₂O-Ag)@TA heterojunction composite antibacterial material with a core-shell structure was synthesized to improve the stability of Cu₂O. Morphological characterization shows that silver nanoparticles are uniformly distributed on the surface of Cu₂O microspheres, (Cu₂O-Ag)@TA has a core-shell structure, the particle size is about 300 nm, and the thickness of the tannic acid shell is about 6 nm. In addition, (Cu₂O-Ag)@TA exhibits excellent dispersibility and stability, it can stably release Cu²⁺ within 14 days and has enhanced reactive oxygen species release performance, thus achieving excellent antibacterial properties, with a minimum inhibitory concentrations of 96 μg ml⁻¹ against Escherichia coli and Staphylococcus aureus. In addition, adding (Cu₂O-Ag)@TA into the LbL-PVA/CS/FA composite film can improve the mechanical properties and antibacterial ability of the composite film, providing a feasible solution for new biodegradable antibacterial packaging materials.