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1.
Biomaterials ; 313: 122794, 2025 Feb.
Article in English | MEDLINE | ID: mdl-39241552

ABSTRACT

Complex tissue damage accompanying with bacterial infection challenges healthcare systems globally. Conventional tissue engineering scaffolds normally generate secondary implantation trauma, mismatched regeneration and infection risks. Herein, we developed an easily implanted scaffold with multistep shape memory and photothermal-chemodynamic properties to exactly match repair requirements of each part from the tissue defect by adjusting its morphology as needed meanwhile inhibiting bacterial infection on demand. Specifically, a thermal-induced shape memory scaffold was prepared using hydroxyethyl methacrylate and polyethylene glycol diacrylate, which was further combined with the photothermal agent iron tannate (FeTA) to produce NIR light-induced shape memory property. By varying ingredients ratios in each segment, this scaffold could perform a stepwise recovery under different NIR periods. This process facilitated implantation after shape fixing to avoid trauma caused by conventional methods and gradually filled irregular defects under NIR to perform suitable tissue regeneration. Moreover, FeTA also catalyzed Fenton reaction at bacterial infections with abundant H2O2, which produced excess ROS for chemodynamic antibacterial therapy. As expected, bacteriostatic rate was further enhanced by additional photothermal therapy under NIR. The in vitro and vivo results showed that our scaffold was able to perform high efficacy in both antibiosis, inflammation reduction and wound healing acceleration, indicating a promising candidate for the regeneration of complex tissue damage with bacterial infection.


Subject(s)
Anti-Bacterial Agents , Tissue Scaffolds , Wound Healing , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/therapeutic use , Animals , Tissue Scaffolds/chemistry , Mice , Wound Healing/drug effects , Infrared Rays , Photothermal Therapy , Tissue Engineering/methods , Tannins/chemistry , Tannins/pharmacology , Smart Materials/chemistry , Staphylococcus aureus/drug effects , Male , Polyethylene Glycols/chemistry
2.
Mikrochim Acta ; 191(10): 573, 2024 09 04.
Article in English | MEDLINE | ID: mdl-39227417

ABSTRACT

Tannic acid (TA)-derived carbon dots (TACDs) were synthesized for the first time via a solvothermal method using TA as one of the raw materials, which may effectively inhibit amyloid fibril aggregation and disaggregate mature fibril. The fluorescent property of TACDs were modulated by adjusting the ratio of TA to o-phenylenediamine (oPD), and TACDs fabricated with the precursor ratio as 1:1 showed the best fluorescent property. Circular dichroism spectra (CD) showed that the structure of ß-sheet decreased as the concentration of TACDs increased. The inhibition efficiency, as confirmed by thioflavin T (ThT) and transmission electron microscopy (TEM), is extraordinary at 98.16%, whereas disaggregation efficiency is noteworthy at 97.97%, and the disaggregated lysozyme fibrils did not reaggregate after 7 days. More critically, TACDs can also alleviate the cellular toxicity caused by Aß fibrils and improve cell viability. This work offers a new perspective on the design of scavengers for amyloid plaques.


Subject(s)
Carbon , Protein Aggregates , Tannins , Tannins/chemistry , Tannins/pharmacology , Carbon/chemistry , Humans , Protein Aggregates/drug effects , Muramidase/chemistry , Muramidase/metabolism , Cell Survival/drug effects , Quantum Dots/chemistry , Amyloid beta-Peptides/chemistry , Amyloid beta-Peptides/metabolism , Amyloid/chemistry , Amyloid/metabolism , Phenylenediamines/chemistry , Phenylenediamines/pharmacology , Animals , Polyphenols
3.
Int J Nanomedicine ; 19: 9145-9160, 2024.
Article in English | MEDLINE | ID: mdl-39258005

ABSTRACT

Background: Triple negative breast cancer (TNBC) is one of the worst prognosis types of breast cancer that urgently needs effective therapy methods. However, cancer is a complicated disease that usually requires multiple treatment modalities. Methods: A tumor microenvironment (TME)-responsive PFC/TRIM37@Fe-TA@HA (abbreviated as PTFTH) nanoplatform was constructed by coating Fe3+ and tannic acid (TA) on the surface of TRIM37-siRNA loaded phase-transition perfluorocarbon (PFC) nanodroplets and further modifying them with hyaluronic acid (HA) to achieve tumor-specific mild photothermal/gene/ferroptosis synergistic therapy (MPTT/GT/ Ferroptosis) in vitro. Once internalized into tumor cells through CD44 receptor-mediated active targeting, the HA shell of PTFTH would be preliminarily disassembled by hyaluronidase (HAase) to expose the Fe-TA metal-phenolic networks (MPNs), which would further degrade in response to an acidic lysosomal environment, leading to HAase/pH dual-responsive release of Fe3+ and PFC/TRIM37. Results: PTFTH showed good biocompatibility in vitro. On the one hand, the released Fe3+ could deplete the overexpressed glutathione (GSH) through redox reactions and produce Fe2+, which in turn converts endogenous H2O2 into highly cytotoxic hydroxyl radicals (•OH) for chemodynamic therapy (CDT). On the other hand, the local hyperthermia generated by PTFTH under 808 nm laser irradiation could not only improve CDT efficacy through accelerating the Fe2+-mediated Fenton reaction, but also enhance TRIM37-siRNA delivery for gene therapy (GT). The consumption of GSH and accumulation of •OH synergistically augmented intracellular oxidative stress, resulting in substantial tumor cell ferroptosis. Moreover, PTFTH possessed outstanding contrast enhanced ultrasound (CEUS), photoacoustic imaging (PAI) and magnetic resonance imaging (MRI) ability. Conclusion: This PTFTH based multiple-mode therapeutic strategy has successfully achieved a synergistic anticancer effect in vitro and has the potential to be translated into clinical application for tumor therapy in future.


Subject(s)
Ferroptosis , Glutathione , Hyaluronic Acid , Nanoparticles , Photothermal Therapy , RNA, Small Interfering , Tannins , Triple Negative Breast Neoplasms , Tumor Microenvironment , Humans , Ferroptosis/drug effects , Glutathione/metabolism , Glutathione/chemistry , Tumor Microenvironment/drug effects , Cell Line, Tumor , Tannins/chemistry , Tannins/pharmacology , Nanoparticles/chemistry , Hyaluronic Acid/chemistry , Female , Triple Negative Breast Neoplasms/therapy , Triple Negative Breast Neoplasms/genetics , RNA, Small Interfering/chemistry , RNA, Small Interfering/pharmacology , RNA, Small Interfering/genetics , Photothermal Therapy/methods , Fluorocarbons/chemistry , Fluorocarbons/pharmacology , Tripartite Motif Proteins/genetics , Tripartite Motif Proteins/metabolism , Genetic Therapy/methods , Combined Modality Therapy/methods , Animals , Iron/chemistry , Hyaluronoglucosaminidase/genetics , Hyaluronoglucosaminidase/metabolism
4.
Chem Senses ; 492024 Jan 01.
Article in English | MEDLINE | ID: mdl-39223911

ABSTRACT

Astringency, commonly described as a drying, roughening, and/or puckering sensation associated with polyphenol-rich foods affects their palatability. While the compounds eliciting astringency are known, its mechanism of action is debated. This study investigated the role of transient receptor potential (TRP) channels A1 and V1 in astringency perception. If TRP A1 or V1 have a functional role in astringency perception, then desensitizing these receptors should decrease perceived astringency. Thirty-seven panelists underwent unilateral lingual desensitization of TRP A1 and V1 channels using mustard oil and capsaicin, respectively. Panelists then evaluated four astringent stimuli: epicatechin (EC), epigallocatechin gallate (EGCG), tannic acid (TA), and potassium alum (Alum), via 2-AFC and intensity ratings. When TRPA1 receptors were desensitized on one half of the tongue via mustard oil, no significant differences were observed between the treated and untreated sides for both 2-AFC and intensity ratings. Similarly, when TRPV1 receptors were desensitized on one half of the tongue via capsaicin, no significant differences were observed between the treated and untreated sides for both 2-AFC and intensity ratings. These findings challenge the notion that TRP channels play a pivotal role in astringency perception.


Subject(s)
Capsaicin , Mustard Plant , Plant Oils , TRPA1 Cation Channel , TRPV Cation Channels , Tannins , Humans , TRPV Cation Channels/metabolism , TRPA1 Cation Channel/metabolism , Male , Adult , Female , Capsaicin/pharmacology , Mustard Plant/chemistry , Plant Oils/pharmacology , Plant Oils/chemistry , Tannins/pharmacology , Tannins/chemistry , Transient Receptor Potential Channels/metabolism , Young Adult , Taste Perception/drug effects , Taste Perception/physiology , Catechin/analogs & derivatives , Catechin/pharmacology , Catechin/chemistry , Middle Aged , Alum Compounds/pharmacology , Taste/drug effects , Taste/physiology , Astringents/pharmacology , Tongue/drug effects , Tongue/metabolism
5.
ACS Appl Mater Interfaces ; 16(38): 51411-51420, 2024 Sep 25.
Article in English | MEDLINE | ID: mdl-39269915

ABSTRACT

Maintaining the differentiated phenotype and function of primary hepatocytes in vitro and in vivo represents a distinct challenge. Our paper describes microcapsules comprised of a bioactive polymer and overcoated with an ultrathin film as a means of maintaining the function of entrapped hepatocytes for at least two weeks. We previously demonstrated that heparin (Hep)-based microcapsules improved the function of entrapped primary hepatocytes by capturing and releasing cell-secreted inductive signals, including hepatocyte growth factor (HGF). Further enhancement of hepatic function could be gained by loading exogenous HGF into microcapsules. In this study, we demonstrate that an ultrathin coating of tannic acid (TA) further enhances endogenous HGF signaling for entrapped hepatocytes and increases by 2-fold the rate of uptake of exogenous HGF by Hep microcapsules. Hepatocytes in overcoated microcapsules exhibited better function and hepatic gene expression than in capsules without a TA coating. Our study showcases the potential application of ultrathin coatings to modulate the bioactivity of microcapsules and may enable the use of encapsulated hepatocytes for modeling drug toxicity or treating liver diseases.


Subject(s)
Capsules , Heparin , Hepatocytes , Hepatocytes/metabolism , Hepatocytes/cytology , Hepatocytes/drug effects , Capsules/chemistry , Animals , Heparin/chemistry , Heparin/pharmacology , Tannins/chemistry , Tannins/pharmacology , Hepatocyte Growth Factor/metabolism , Hepatocyte Growth Factor/chemistry , Hepatocyte Growth Factor/pharmacology , Spheroids, Cellular/drug effects , Spheroids, Cellular/metabolism , Humans , Coated Materials, Biocompatible/chemistry , Coated Materials, Biocompatible/pharmacology , Mice
6.
Biomolecules ; 14(9)2024 Sep 06.
Article in English | MEDLINE | ID: mdl-39334895

ABSTRACT

Conventional pulp capping materials have limited anti-inflammatory capacity. It is necessary to develop more effective pulp capping material for the treatment of inflamed pulps. Tannic acid (TA) is a natural, water-soluble polyphenol with antimicrobial and anti-inflammatory properties. This study aimed to investigate the effects of a tannin-containing hydroxypropyl chitin hydrogel (HPCH/TA hydrogel) as an innovative pulp capping material. The physicochemical properties of the composite hydrogels were characterized. The effects of HPCH/TA hydrogel as a pulp capping material were evaluated in vitro and in vivo. The underlying mechanism of the anti-inflammatory effects of HPCH/TA hydrogel was explored. The HPCH/TA hydrogel demonstrated favorable temperature sensitivity, injectability, and antibacterial properties. In vitro, the HPCH/TA hydrogel effectively promoted the proliferation of human dental pulp cells and inhibited interleukin-1ß, interleukin-6, and tumor necrosis factor-α expression, possibly by suppressing the nuclear factor kappa-B pathway. In vivo, on the fourth day after capping, the HPCH/TA hydrogel group showed lower inflammatory scores compared to the control and iRoot BP Plus (commercial pulp capping material) group. By the sixth week, complete reparative dentin formation was observed in the HPCH/TA hydrogel group, with no difference in thickness compared to the iRoot BP Plus group. Collectively, the HPCH/TA hydrogel holds promise as a bioactive pulp capping material for promoting the repair of inflamed pulp in vital pulp therapy.


Subject(s)
Chitin , Dental Pulp , Hydrogels , Tannins , Tannins/chemistry , Tannins/pharmacology , Hydrogels/chemistry , Dental Pulp/drug effects , Dental Pulp/metabolism , Chitin/chemistry , Chitin/pharmacology , Chitin/analogs & derivatives , Humans , Animals , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/administration & dosage , Dental Pulp Capping , Cell Proliferation/drug effects , Pulp Capping and Pulpectomy Agents/chemistry , Pulp Capping and Pulpectomy Agents/pharmacology , Rats , Male
7.
ACS Appl Mater Interfaces ; 16(38): 51618-51629, 2024 Sep 25.
Article in English | MEDLINE | ID: mdl-39259880

ABSTRACT

Conductive hydrogels exhibit tremendous potential for wearable bioelectronics, biosensing, and health monitoring applications, yet concurrently enhancing their biocompatibility and antimicrobial properties remains a long-standing challenge. Herein, we report an all-natural conductive supramolecular hydrogel (GT5-DACD2-B) prepared via the Schiff base reaction between the biofriendly dialdehyde cyclodextrin and gelatin. The potent antibacterial agent fusidic acid (FA) is incorporated through host-guest inclusion, enabling 100% inhibition of Staphylococcus aureus proliferation. The biocompatibility of our hydrogel is bolstered with tannic acid (TA) facilitating antibacterial effects through interactions with gelatin, while borax augments conductivity. This supramolecular hydrogel not only exhibits stable conductivity and rapid response characteristics but also functions as a flexible sensor for monitoring human movement, facial expressions, and speech recognition. Innovatively integrating biocompatibility, antimicrobial activity, and conductivity into a single system, our work pioneers a paradigm for developing multifunctional biosensors with integrated antibacterial functionalities, paving the way for advanced wearable bioelectronics with enhanced safety and multifunctionality.


Subject(s)
Anti-Bacterial Agents , Biosensing Techniques , Electric Conductivity , Hydrogels , Staphylococcus aureus , Wearable Electronic Devices , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Staphylococcus aureus/drug effects , Hydrogels/chemistry , Hydrogels/pharmacology , Humans , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Tannins/chemistry , Tannins/pharmacology , Microbial Sensitivity Tests , Gelatin/chemistry
8.
ACS Appl Mater Interfaces ; 16(38): 50335-50343, 2024 Sep 25.
Article in English | MEDLINE | ID: mdl-39264146

ABSTRACT

Near-infrared (NIR) organic materials have been widely developed for tumor phototherapy due to their deep tumor penetration, good biodegradability, and high photothermal conversion (PCE). However, most of the NIR organic dyes are easily destroyed by photooxidation due to their big and long conjugated structures, such as cyanine dyes. Under light irradiation, the reactive oxygen species (ROS) produced by these NIR dyes can easily break their conjugated skeleton, resulting in a dramatic decrease in phototherapeutic efficiency. Herein, an NIR organic dye cyanine dye (CyS) and a photosensitizer methylene blue (MB) were chosen to prepare nanocarrier CMTNPs by facile self-assembling with a natural antioxidant, tannic acid (TA). TA can greatly enhance the stability of NIR cyanine dyes by scavenging ROS. Furthermore, CMTNPs have a character of pH/thermal dual response, allowing for controlled release of MB in the slightly acidic tumor environment during photothermal therapy. The released MB can turn on both fluorescence and photodynamic therapy effects. In vitro and in vivo experiments demonstrated the remarkable tumor ablation ability of CMTNPs. Thus, our study provided an antiphotobleaching and controlled release photosensitizer strategy through the introduction of antioxidant TA into the nanocarrier for efficient collaborative photothermal/photodynamic therapy.


Subject(s)
Infrared Rays , Methylene Blue , Nanoparticles , Photochemotherapy , Photosensitizing Agents , Tannins , Tannins/chemistry , Tannins/pharmacology , Animals , Mice , Photosensitizing Agents/chemistry , Photosensitizing Agents/pharmacology , Humans , Nanoparticles/chemistry , Methylene Blue/chemistry , Methylene Blue/pharmacology , Photothermal Therapy , Drug Carriers/chemistry , Reactive Oxygen Species/metabolism , Mice, Inbred BALB C , Neoplasms/drug therapy , Neoplasms/therapy , Neoplasms/pathology , Cell Line, Tumor , Polyphenols
9.
ACS Appl Mater Interfaces ; 16(36): 48352-48362, 2024 Sep 11.
Article in English | MEDLINE | ID: mdl-39221854

ABSTRACT

Chitosan-based biomass packaging materials are a promising material for food preservation, but their limited solubility, antioxidant capacity, UV resistance, and mechanical properties severely restrict their application. In this study, we developed a novel chitosan-based coating/packaging composite (QCTO) using quaternary ammonium salt and tannic acid (TA)-modified chitosan (QCS-TA) and oxidized chitosan (OCS). The introduction of quaternary ammonium salt and TA effectively improves the water solubility and antibacterial, antioxidant, and UV-resistant properties of chitosan. The Schiff-base bond formed between OCS and QCS-TA, along with the TA-mediated multiple interactions, conferred the prepared composite film with good mechanical properties (69.9 MPa tensile strength) and gas barrier performance to water (14.3 g·h-1·m-2) and oxygen (3.5 g·mm·m-2·h-1). Meanwhile, the prepared QCTO composites demonstrate excellent biocompatibility and safety and are applied as coatings for strawberries and bananas as well as packaging films for mushrooms. These preservation experiments demonstrated that the prepared composites are able to effectively reduce weight loss, prevent microbial growth, maintain color, and significantly prolong the shelf life of fresh products (bananas, strawberries, and mushrooms extended shelf life by 6, 5, and 6 days, respectively). Therefore, the developed QCTO coating/packaging film shows great potential for applications in the field of food preservation and packaging.


Subject(s)
Anti-Bacterial Agents , Antioxidants , Chitosan , Food Packaging , Food Preservation , Ultraviolet Rays , Chitosan/chemistry , Chitosan/pharmacology , Food Preservation/methods , Antioxidants/chemistry , Antioxidants/pharmacology , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Tannins/chemistry , Tannins/pharmacology
10.
Acta Pharm ; 74(3): 539-550, 2024 Sep 01.
Article in English | MEDLINE | ID: mdl-39279521

ABSTRACT

Prostate cancer is a significant global health concern that requires innovative therapeutic investigations. Here, the potential anticancer properties of tannic acid were evaluated by examining its effects on apoptosis in prostate cancer cell lines. PC-3 and LnCaP prostate adeno carcinoma cells, along with PNT1A prostate control cells, were cultured and divided into untreated and tannic acid-treated groups. Cell proliferation, cytotoxicity, and effects of tannic acid on the cell death mechanism were evaluated. mRNA expression levels of 84 genes were explored in cells following tannic acid treatment. Notably, tannic acid-induced down-regulation of several pro-survival genes, including ATM, BCL2, BCL2A1, BIK, BIRC2, BIRC3, BRE, CASP3, CASP6, CASP8, CHEK2, CRADD, PPIA, RPA3, TNFSF18, TRAF1, TRAF2, TRAF4, and TRAF5 in both cell lines. Moreover, tannic acid treatment led to the up-regulation of various pro-apoptotic genes, such as BCL10, BIRC3, BNIP3, CASP1, CASP5, CD40, CIDEB, DAPK2, FASLG, GADD45A, MYD88, RPA 3, TNFRSF10D, TNFRSF17, TNFRSF8, TNFSF13B, TNFSF4, TNFSF7, TNFSF8, TNFSF9, TP53, TRAF1, and TRAF2 in both PC-3 and LnCap cells. These findings highlight tannic acid's ability to induce apoptosis in prostate cancer cells through pro-apoptotic pathways. This study concludes that tannic acid selectively inhibits prostate cancer cell growth.


Subject(s)
Apoptosis , Cell Proliferation , Gene Expression Regulation, Neoplastic , Prostatic Neoplasms , Tannins , Humans , Male , Apoptosis/drug effects , Prostatic Neoplasms/genetics , Prostatic Neoplasms/drug therapy , Prostatic Neoplasms/pathology , Tannins/pharmacology , Cell Line, Tumor , Gene Expression Regulation, Neoplastic/drug effects , Cell Proliferation/drug effects , PC-3 Cells , Cell Survival/drug effects , Down-Regulation/drug effects , Polyphenols
11.
Biomed Mater ; 19(6)2024 Sep 19.
Article in English | MEDLINE | ID: mdl-39255828

ABSTRACT

Development of a low-cost and biocompatible hydrogel dressing with antimicrobial, antioxidant, and low swelling properties is important for accelerating wound healing. Here, a multifunctional alginate hydrogel dressing was fabricated using the D-(+)-gluconic acidδ-lactone/CaCO3system. The addition of hyaluronic acid and tannic acid (TA) provides the alginate hydrogel with anti-reactive oxygen species (ROS), hemostatic, and pro-wound healing properties. Notably, soaking the alginate hydrogel in a poly-ϵ-lysine (EPL) aqueous solution enables the alginate hydrogel to be di-crosslinked with EPL through electrostatic interactions, forming a dense network resembling 'armor' on the surface. This simple one-step soaking strategy provides the alginate hydrogel with antibacterial and anti-swelling properties. Swelling tests demonstrated that the cross-sectional area of the fully swollen multifunctional alginate hydrogel was only 1.3 times its initial size, thus preventing excessive wound expansion caused by excessive swelling. After 5 h ofin vitrorelease, only 7% of TA was cumulatively released, indicating a distinctly slow-release behavior. Furthermore, as evidenced by the removal of 2,2-diphenyl-1-picrylhydrazyl free radicals, this integrated alginate hydrogel systems demonstrate a notable capacity to eliminate ROS. Full-thickness skin wound repair experiment and histological analysis of the healing site in mice demonstrate that the developed multifunctional alginate hydrogels have a prominent effect on extracellular matrix formation and promotion of wound closure. Overall, this study introduces a cost-effective and convenient multifunctional hydrogel dressing with high potential for clinical application in treating open wounds.


Subject(s)
Alginates , Anti-Bacterial Agents , Free Radical Scavengers , Hemostatics , Hydrogels , Reactive Oxygen Species , Tannins , Wound Healing , Wound Healing/drug effects , Alginates/chemistry , Animals , Hydrogels/chemistry , Hydrogels/pharmacology , Mice , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Free Radical Scavengers/chemistry , Free Radical Scavengers/pharmacology , Hemostatics/chemistry , Hemostatics/pharmacology , Reactive Oxygen Species/metabolism , Tannins/chemistry , Tannins/pharmacology , Hyaluronic Acid/chemistry , Hyaluronic Acid/pharmacology , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Antioxidants/pharmacology , Antioxidants/chemistry , Bandages , Male , Picrates/chemistry , Biphenyl Compounds/chemistry , Polylysine/chemistry
12.
Molecules ; 29(17)2024 Sep 09.
Article in English | MEDLINE | ID: mdl-39275112

ABSTRACT

Food packaging films play a vital role in preserving and protecting food. The focus has gradually shifted to safety and sustainability in the preparation of functional food packaging materials. In this study, a bisquaternary ammonium salt of tannic acid (BQTA) was synthesized, and the bioplastics based on BQTA and polyvinyl alcohol (PVA) were created for packaging applications. The impact of BQTA on antibacterial effect, antioxidant capacity, opacity, ultraviolet (UV) protective activity, mechanical strength, thermal stability, and anti-fog of the resultant bioplastics was examined. In vitro antibacterial experiments confirmed that BQTA possesses excellent antimicrobial properties, and only a trace amount addition of BQTA in PVA composite film could inhibit about 100% of Escherichia coli and Staphylococcus aureus. Compared to BQTA/PVA bioplastics with pure PVA, the experiment findings demonstrate that BQTA/PVA bioplastics show strong antioxidant and UV protection action and the performance of fruit preservation. It also revealed a small improvement in thermal stability and tensile strength. The small water contact angle, even at low BQTA concentrations, gave BQTA/PVA bioplastics good anti-fog performance. Based on the findings, bioplastics of BQTA/PVA have the potential to be used to create packaging, and they can be applied as the second (inner) layer of the primary packaging to protect food freshness and nutrition due to their antioxidant activity and biocompatibility.


Subject(s)
Anti-Bacterial Agents , Antioxidants , Escherichia coli , Food Packaging , Polyvinyl Alcohol , Quaternary Ammonium Compounds , Staphylococcus aureus , Tannins , Polyvinyl Alcohol/chemistry , Food Packaging/methods , Tannins/chemistry , Tannins/pharmacology , Staphylococcus aureus/drug effects , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/chemical synthesis , Escherichia coli/drug effects , Antioxidants/pharmacology , Antioxidants/chemistry , Antioxidants/chemical synthesis , Quaternary Ammonium Compounds/chemistry , Quaternary Ammonium Compounds/pharmacology , Sterilization/methods , Food Preservation/methods , Tensile Strength , Ultraviolet Rays , Microbial Sensitivity Tests
13.
J Control Release ; 374: 154-170, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39127448

ABSTRACT

To realize high-quality vascularized bone regeneration, we developed a multifunctional hydrogel (SHPP-ZB) by incorporating BMP-2@ZIF-8/PEG-NH2 nanoparticles (NPs) into a sodium alginate/hydroxyapatite/polyvinyl alcohol hydrogel loaded with PDGF-BB, allowing for the sequential release of angiogenic and osteogenic growth factors (GFs) during bone repair. ZIF-8 served as a protective host for BMP-2 from degradation, ensuring high encapsulation efficiency and long-term bioactivity. The SHPP-ZB hydrogel exhibited enhanced mechanical strength and injectability, making it suitable for complex bone defects. It provided a swelling interface for tissue interlocking and the early release of Zn2+ and tannin acid (TA) to exert antioxidant and antibacterial effects, followed by the sequential release of angiogenic and osteogenic GFs to promote high-quality vascularized bone regeneration. In vitro experiments demonstrated the superior angiogenic and osteogenic properties of SHPP-ZB compared to other groups. In vivo experiments indicated that the sequential delivery of GFs via SHPP-ZB hydrogel could improve vascularized bone regeneration. Further, RNA sequencing analysis of regenerative bone tissue revealed that SHPP-ZB hydrogel promoted vascularized bone regeneration by regulating JUN, MAPK, Wnt, and calcium signaling pathways in vivo. This study presented a promising approach for efficient vascularized bone regeneration in large-scale bone defects.


Subject(s)
Alginates , Becaplermin , Bone Morphogenetic Protein 2 , Bone Regeneration , Hydrogels , Osteogenesis , Bone Regeneration/drug effects , Animals , Hydrogels/chemistry , Hydrogels/administration & dosage , Osteogenesis/drug effects , Bone Morphogenetic Protein 2/administration & dosage , Alginates/chemistry , Becaplermin/administration & dosage , Nanoparticles/chemistry , Durapatite/chemistry , Durapatite/administration & dosage , Angiogenesis Inducing Agents/administration & dosage , Angiogenesis Inducing Agents/pharmacology , Angiogenesis Inducing Agents/chemistry , Male , Polyvinyl Alcohol/chemistry , Polyethylene Glycols/chemistry , Tannins/chemistry , Tannins/administration & dosage , Tannins/pharmacology , Neovascularization, Physiologic/drug effects , Humans , Rats, Sprague-Dawley , Mice
14.
Colloids Surf B Biointerfaces ; 244: 114183, 2024 Dec.
Article in English | MEDLINE | ID: mdl-39208607

ABSTRACT

One way to effectively address endophyte infection and loosening is the creation of multifunctional coatings that combine anti-inflammatory, antibacterial, and vascularized osteogenesis. This study started with the preparation of strontium-doped titanium dioxide nanotubes (STN) on the titanium surface. Next, tannic acid (TA), gentamicin sulfate (GS), and pluronic F127 (PF127) were successfully loaded into the STN via layer-by-layer self-assembly, resulting in the STN@TA-GS/PF composite coatings. The findings demonstrated the excellent hydrophilicity and bioactivity of the STN@TA-GS/PF coating. STN@TA-GS/PF inhibited E. coli and S. aureus in vitro to a degree of roughly 80.95 % and 92.45 %, respectively. Cellular investigations revealed that on the STN@TA-GS/PF surface, the immune-system-related RAW264.7, the vasculogenic HUVEC, and the osteogenic MC3T3-E1 showed good adhesion and proliferation activities. STN@TA-GS/PF may influence RAW264.7 polarization toward the M2-type and encourage MC3T3-E1 differentiation toward osteogenesis at the molecular level. Meanwhile, the STN@TA-GS/PF coating achieved effective removal of ROS within HUVEC and significantly promoted angiogenesis. In both infected and non-infected bone defect models, the STN@TA-GS/PF material demonstrated strong anti-inflammatory, antibacterial, and vascularization-promoting osteogenesis properties. In addition, STN@TA-GS/PF had good hemocompatibility and biosafety. The three-step process used in this study to modify the titanium surface for several purposes gave rise to a novel concept for the clinical design of antimicrobial coatings with immunomodulatory properties.


Subject(s)
Anti-Bacterial Agents , Anti-Inflammatory Agents , Coated Materials, Biocompatible , Escherichia coli , Nanotubes , Prostheses and Implants , Staphylococcus aureus , Strontium , Titanium , Titanium/chemistry , Titanium/pharmacology , Nanotubes/chemistry , Mice , Animals , Strontium/chemistry , Strontium/pharmacology , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/chemistry , Staphylococcus aureus/drug effects , Humans , Coated Materials, Biocompatible/chemistry , Coated Materials, Biocompatible/pharmacology , Escherichia coli/drug effects , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , RAW 264.7 Cells , Human Umbilical Vein Endothelial Cells/drug effects , Microbial Sensitivity Tests , Surface Properties , Tannins/chemistry , Tannins/pharmacology , Osteogenesis/drug effects , Poloxamer/chemistry , Poloxamer/pharmacology , Cell Proliferation/drug effects , Gentamicins/pharmacology , Gentamicins/chemistry , Particle Size
15.
Sci Adv ; 10(33): eado7249, 2024 Aug 16.
Article in English | MEDLINE | ID: mdl-39151007

ABSTRACT

Ferroptosis, caused by disorders of iron metabolism, plays a critical role in various diseases, making the regulation of iron metabolism essential for tissue repair. In our analysis of degenerated intervertebral disc tissue, we observe a positive correlation between the concentration of extracellular iron ions (ex-iron) and the severity of ferroptosis in intervertebral disc degeneration (IVDD). Hence, inspired by magnets attracting metals, we combine polyether F127 diacrylate (FDA) with tannin (TA) to construct a magnetically attracting hydrogel (FDA-TA). This hydrogel demonstrates the capability to adsorb ex-iron and remodel the iron metabolism of cells. Furthermore, it exhibits good toughness and self-healing properties. Notably, it can activate the PI3K-AKT pathway to inhibit nuclear receptor coactivator 4-mediated ferritinophagy under ex-iron enrichment conditions. The curative effect and related mechanism are further confirmed in vivo. Consequently, on the basis of the pathological mechanism, a targeted hydrogel is designed to reshape iron metabolism, offering insights for tissue repair.


Subject(s)
Ferroptosis , Hydrogels , Iron , Iron/metabolism , Hydrogels/chemistry , Humans , Ferroptosis/drug effects , Animals , Tannins/chemistry , Tannins/pharmacology , Intervertebral Disc Degeneration/metabolism , Wound Healing/drug effects , Phosphatidylinositol 3-Kinases/metabolism , Signal Transduction , Proto-Oncogene Proteins c-akt/metabolism
16.
Food Funct ; 15(17): 8893-8903, 2024 Aug 27.
Article in English | MEDLINE | ID: mdl-39129514

ABSTRACT

As the involvement of the intestinal microbiota in the etiopathology of irritable bowel syndrome, subtype diarrhoea (IBS-D) is now increasingly recognised, a preliminary, quasi-experimental, before-after and prospective study was conducted on 28 patients to test the effect of a tannin-based supplement on the composition and activity of the microbiota, after 8 weeks of treatment. No statistically significant differences were found in α- or ß-diversity. However, sparse Partial Least Squares Discriminant Analysis (sPLS-DA) and Boruta algorithm did reveal significant changes in the relative abundance of specific groups of bacteria, highlighting the involvement of recognized of IBS-D biomarkes, namely Blautia (adj p = 3.5 × 10-11), Eubacterium hallii group (adj p = 5.1 × 10-12) and Dorea (adj p = 1.8 × 10-18), which resulted significantly depleted by the treatment. The modulation of the composition of the gut microbiota had an impact also in the production of short chain fatty acids (SCFAs), which were modulated: acetate and butyrate (n.s. and p = 0.000143) increased while propionate and formate resulted to be significantly reduced (p = 0.00476 and p = 0.00011, respectively), following the supplementation. Finally, the sPLS analysis showed that the strongest association between faecal microbiome composition and clinical symptoms of IBS-D was given by Catenibacterium, which showed a positive correlation with evacuation-related symptoms. Such preliminary findings suggest that tannin supplementation could play an outstanding role in microbiota modulation in IBS-D patients, potentially improving their symptomatology, by selectively acting on the growth and the activity of specific groups of taxa.


Subject(s)
Bacteria , Dietary Supplements , Feces , Gastrointestinal Microbiome , Irritable Bowel Syndrome , Tannins , Humans , Gastrointestinal Microbiome/drug effects , Pilot Projects , Irritable Bowel Syndrome/microbiology , Irritable Bowel Syndrome/drug therapy , Female , Male , Adult , Middle Aged , Tannins/pharmacology , Bacteria/classification , Bacteria/drug effects , Bacteria/genetics , Bacteria/isolation & purification , Feces/microbiology , Prospective Studies , Fatty Acids, Volatile/metabolism , Young Adult , Diarrhea/microbiology , Diarrhea/drug therapy
17.
Colloids Surf B Biointerfaces ; 244: 114160, 2024 Dec.
Article in English | MEDLINE | ID: mdl-39142232

ABSTRACT

The delay of diabetic wound healing puts a huge burden on the society. The key factors hindering wound healing include bacterial infection, unresolved inflammation and poorly generated blood vessels. In this paper, glycidyl trimethyl ammonium chloride (GTA) was grafted to chitosan (CS) to obtain quaternary ammonium grafted chitosan (QCS) with enhanced antibacterial performance, and then cross-linked by dialdehyde terminated poly(ethylene oxide) (PEO DA) to construct QCS/PEO DA hydrogel with tissue adhesion, biodegradation and self-healing properties. The QCS/PEO DA hydrogel is loaded with tannin acid (TA) and deferoxamine (DFO) to enhance antioxidant property and angiogenesis. At the same time, the TA and DFO loaded TA@DFO/hydrogel preserved the biocompatibility and biodegradability of chitosan. Moreover, the multifunctional hydrogel behaved excellent hemostatic properties in mice model and significantly promoted the healing efficacy of diabetic wounds. Overall, the TA@DFO/hydrogel is promising anti-infection dressing material for diabetic wound healing.


Subject(s)
Anti-Bacterial Agents , Chitosan , Deferoxamine , Diabetes Mellitus, Experimental , Hydrogels , Quaternary Ammonium Compounds , Tannins , Wound Healing , Chitosan/chemistry , Chitosan/pharmacology , Wound Healing/drug effects , Tannins/chemistry , Tannins/pharmacology , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Animals , Hydrogels/chemistry , Hydrogels/pharmacology , Mice , Deferoxamine/pharmacology , Deferoxamine/chemistry , Quaternary Ammonium Compounds/chemistry , Quaternary Ammonium Compounds/pharmacology , Diabetes Mellitus, Experimental/drug therapy , Microbial Sensitivity Tests , Male , Drug Carriers/chemistry , Staphylococcus aureus/drug effects , Humans , Escherichia coli/drug effects
18.
Int J Biol Macromol ; 278(Pt 4): 134961, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39179081

ABSTRACT

Biomedical implants are crucial for enhancing various human physiological functions. However, they are susceptible to microbial contamination after implantation, posing a risk of implant failure. To address this issue, hydrogel-based coatings are used, but achieving both effective antibacterial properties and stable adhesion remains challenging. This study introduces a hybrid hydrogel network made from Tannic Acid (TA) and Poly-l-Lysine (PLL), cross-linked through ionic and hydrogen bonds, which imparts adhesive and anti-infective properties. The physicochemical analysis revealed that the hydrogels exhibited significant porosity, favorable mechanical characteristics, and demonstrated in vitro enzymatic biodegradation. Moreover, the hydrogels demonstrated adhesion to various substrates, including Ti alloy with an adhesive strength of 42.5 kPa, and retained their integrity even after immersion in water for a minimum of 10 days. The modified Ti surfaces significantly reduced protein adsorption (∼70 %), indicating antifouling properties. The hydrogels prevented bacterial adhesion on titanium surfaces through a "contact-kill" mode of action and inhibited biofilm formation by around 94.5 % for Staphylococcus aureus and 90.8 % for Pseudomonas aeruginosa. The modified Ti retained biofilm inhibitory effects for at least six days without significant performance decline. In vitro cytotoxicity assay confirmed the biocompatibility of the hydrogels with NIH3T3 cells. Overall, these results highlight the competence of hybrid hydrogels as effective coatings for Ti implants, offering strong adhesion and biofilm prevention to mitigate implant-related infections.


Subject(s)
Anti-Bacterial Agents , Biofilms , Hydrogels , Polylysine , Staphylococcus aureus , Tannins , Polylysine/chemistry , Polylysine/pharmacology , Biofilms/drug effects , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Hydrogels/chemistry , Hydrogels/pharmacology , Mice , Animals , Tannins/chemistry , Tannins/pharmacology , NIH 3T3 Cells , Staphylococcus aureus/drug effects , Pseudomonas aeruginosa/drug effects , Titanium/chemistry , Titanium/pharmacology , Bacterial Adhesion/drug effects , Microbial Sensitivity Tests , Polyphenols
19.
Biomater Adv ; 164: 213983, 2024 Nov.
Article in English | MEDLINE | ID: mdl-39137704

ABSTRACT

The effective management of deep skin wounds remains a significant healthcare challenge that often deteriorates with bacterial infection, oxidative stress, tissue necrosis, and excessive production of wound exudate. Current medical approaches, including traditional wound dressing materials, cannot effectively address these issues. There is a great need to engineer advanced and multifunctional wound dressings to address this multifaceted problem effectively. Herein, a rationally designed composite cryogel composed of a Copper Metal-Organic Framework (Cu-MOF), tannic acid (TA), polyvinyl alcohol (PVA), and zein protein has been developed by freeze-thaw technique. Cryogels display a remarkable swelling capacity attributed to their interconnected microporous morphology. Moreover, dynamic mechanical behaviour with the characteristics of potent antimicrobial, antioxidant, and biodegradation makes it a desirable wound dressing material. It was further confirmed that the material is highly biocompatible and can release TA and copper ions in a controlled manner. In-vivo skin irritation in a rat model demonstrated that composite cryogel did not provoke any irritation/inflammation when applied to the skin of a healthy recipient. In a deep wound model, the composite cryogel significantly accelerates the wound healing rate. These findings highlight the multifunctional nature of composite cryogels and their promising potential for clinical applications as advanced wound dressings.


Subject(s)
Copper , Cryogels , Metal-Organic Frameworks , Skin, Artificial , Tannins , Wound Healing , Cryogels/chemistry , Tannins/chemistry , Tannins/pharmacology , Wound Healing/drug effects , Animals , Metal-Organic Frameworks/chemistry , Metal-Organic Frameworks/pharmacology , Copper/chemistry , Rats , Skin/drug effects , Skin/injuries , Skin/pathology , Skin/metabolism , Humans , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Bandages , Male , Polyphenols
20.
Food Chem ; 460(Pt 3): 140642, 2024 Dec 01.
Article in English | MEDLINE | ID: mdl-39111043

ABSTRACT

A double-layer film was developed with tannic acid (TA) co-pigmented purple potato anthocyanin extract (PAE)-agar as the inner layer, and K-carrageenan-oregano essential oil Pickering emulsion (OPE)/silver nanoparticles (TA-AgNPs) as the outer layer. Molecular docking and FT-IR results elucidated that intermolecular hydrogen bond was the main interaction between components in the agar-carrageenan matrix, with TA and PAE contributing to intensified anthocyanin color through π-π stacking. The incorporation of OPE/TA-AgNPs enhanced the film's hydrophobicity (WCA > 100°) and UV-vis barrier (close to 0% at 200-320 nm, effectively impeding UVA, UVB, and UVC) properties and exhibited outstanding antioxidant (DPPH scavenging rate > 88%) and antimicrobial activities. This film showed a significant color change in the pH range of 2-12 (from pink to yellow) and a considerable sensitivity to volatile amines within 2 min. The films effectively alleviated beef spoilage (extending the shelf life of beef for 1d) and reflected the freshness of beef during storage. Additionally, the digital color information of the film was obtained by a smartphone combined with RGB values analysis to quantify the freshness of beef rapidly. Therefore, this study expands the application of food packaging films with freshness preservation and monitoring in the field of animal-derived food.


Subject(s)
Anthocyanins , Food Packaging , Food Preservation , Gelatin , Metal Nanoparticles , Silver , Tannins , Tannins/chemistry , Tannins/pharmacology , Animals , Anthocyanins/chemistry , Anthocyanins/pharmacology , Silver/chemistry , Silver/pharmacology , Metal Nanoparticles/chemistry , Cattle , Food Packaging/instrumentation , Gelatin/chemistry , Food Preservation/instrumentation , Food Preservation/methods , Red Meat/analysis , Antioxidants/chemistry , Antioxidants/pharmacology , Polyphenols
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