Oxidized Bacterial Cellulose Research Articles

An antifouling electrochemical biosensor based on oxidized bacterial cellulose and quaternized chitosan for reliable detection of involucrin in wound exudate

The monitoring of biomarkers in wound exudate is of great importance for wound care and treatment, and electrochemical biosensors with high sensitivity are potentially useful for this purpose. However, conventional electrochemical biosensors always suffer from severe biofouling when performed in the complex wound exudate. Herein, an antifouling electrochemical biosensor for the detection of involucrin in wound exudate was developed based on a wound dressing, oxidized bacterial cellulose (OxBC) and quaternized chitosan (QCS) composite hydrogel. The OxBC/QCS hydrogel was prepared using an in-situ chemical oxidation and physical blending method, and the proportion of OxBC and QCS was optimized to achieve electrical neutrality and enhanced hydrophilicity, therefore endowing the hydrogel with exceptional antifouling and antimicrobial properties. The involucrin antibody SY5 was covalently bound to the OxBC/QCS hydrogel to construct the biosensor, and it demonstrated a low limit of detection down to 0.45 pg mL−1 and a linear detection range from 1.0 pg mL−1 to 1.0 μg mL−1, and it was capable of detecting targets in wound exudate. Crucially, the unique antifouling and antimicrobial capability of the OxBC/QCS hydrogel not only extends its effective lifespan but also guarantees the sensing performance of the biosensor. The successful application of this wound dressing, OxBC/QCS hydrogel for involucrin detection in wound exudate demonstrates its promising potential in wound healing monitoring.

Platelet Vesicles Synergetic with Biosynthetic Cellulose Aerogels for Ultra-Fast Hemostasis and Wound Healing.

Achieving hemostasis in penetrating and irregular wounds is challenging because the hemostasis factor cannot arrive at the bleeding site, and substantial bleeding will wash away the blood clot. Since the inherently gradual nature of blood clot formation takes time, a physical barrier is needed before blood clot formation. Herein, an ultra-light and shape memory hemostatic aerogel consisting of oxidized bacterial cellulose (OBC) and platelet extracellular vesicles (pVEs) is reported. The OBC-pVEs aerogel provides a physical barrier for the bleeding site by self-expansion, absorbing the liquid from blood to concentrate platelets and clotting factors and accelerating the clot formation by activating platelets and transforming fibrinogen into fibrin. In the rat liver and tail injury models, the blood loss decreases by 73% and 59%, and the bleeding times are reduced by 55% and 62%, respectively. OBC-pVEs aerogel has also been shown to accelerate wound healing. In conclusion, this work introduces an effective tool for treating deep, non-compressible, and irregular wounds and offers valuable strategies for trauma bleeding and wound treatment.

Novel bioactive sponge mats composed of oxidized bacterial cellulose and chitosan-gum Arabic microcapsules loaded with cinnamon essential oil for enhancing meat preservation

Meat is prone to microbial contamination during storage, resulting in a shortened shelf life. To address this issue, absorbent preservation mats have been suggested and proven effective in slowing down the spoilage of meat. To this end, this study developed a novel bioactive sponge mat composed of oxidized bacterial cellulose (OBC) and microcapsules loaded with cinnamon essential oil (CGCM) obtained by complex coacervation of chitosan and gum Arabic. The surface charge of such microcapsules was regulated through the use of chitosan obtained from different deacetylation degrees. The physicochemical properties, antioxidant properties, and antibacterial properties of the OBC-CGCM sponge mats were investigated and their effect on meat preservation was assessed. The results concurred that the electrostatic interaction and hydrogen bonding between the CGCM and OBC sponge mat matrix led to improved thermal stability, water absorption, and tensile strength of the sponge mat. Furthermore, it demonstrated high antioxidant (reaching up to 90%) and antibacterial properties, particularly in the gas phase (up to 65%). The application of the prepared sponge mat to the preservation of meat was able to maintain the freshness and extend the shelf life of meat from 4 days to around 10 days under 4 °C, which is significantly better than that shown by commercially available preservation mats. In conclusion, the OBC-CGCM sponge mats are highly promising for meat preservation, thereby offering an attractive universal approach to constructing active biomass packaging materials.

Antimicrobial Food Packaging Based on Prodigiosin-Incorporated Double-Layered Bacterial Cellulose and Chitosan Composites.

Nowadays, food packaging systems have shifted from a passive to an active role in which the incorporation of antimicrobial compounds into biopolymers can promote a sustainable way to reduce food spoilage and its environmental impact. Accordingly, composite materials based on oxidized-bacterial cellulose (BC) and poly(vinyl alcohol)-chitosan (PVA-CH) nanofibers were produced by needleless electrospinning and functionalized with the bacterial pigment prodigiosin (PG). Two strategies were explored, in the first approach PG was incorporated in the electrospun PVA-CH layer, and TEMPO-oxidized BC was the substrate for nanofibers deposition (BC/PVA-CH_PG composite). In the second approach, TEMPO-oxidized BC was functionalized with PG, and afterward, the PVA-CH layer was electrospun (BC_PG/PVA-CH composite). The double-layer composites obtained were characterized and the nanofibrous layers displayed smooth fibers with average diameters of 139.63 ± 65.52 nm and 140.17 ± 57.04 nm, with and without pigment incorporation, respectively. FTIR-ATR analysis confirmed BC oxidation and revealed increased intensity at specific wavelengths, after pigment incorporation. Moreover, the moderate hydrophilic behavior, as well as the high porosity exhibited by each layer, remained mostly unaffected after PG incorporation. The composites’ mechanical performance and the water vapor transmission rate (WVTR) evaluation indicated the suitability of the materials for certain food packaging solutions, especially for fresh products. Additionally, the red color provided by the bacterial pigment PG on the external surface of a food packaging material is also a desirable effect, to attract the consumers’ attention, creating a multifunctional material. Furthermore, the antimicrobial activity was evaluated and, PVA-CH_PG, and BC_PG layers exhibited the highest antimicrobial activity against Staphylococcus aureus and Pseudomonas aeruginosa. Thus, the fabricated composites can be considered for application in active food packaging, owing to PG antimicrobial potential, to prevent foodborne pathogens (with PG incorporated into the inner layer of the food packaging material, BC/PVA-CH_PG composite), but also to prevent external contamination, by tackling the exterior of food packaging materials (with PG added to the outer layer, BC_PG/PVA-CH composite).

Oxidized bacterial cellulose reinforced nanocomposite scaffolds for bone repair

Bone tissue engineering has been widely used in promoting the repair and regeneration of bone defects. Tissue-engineered bone scaffolds can simulate the extracellular matrix environment and induce the proliferation and differentiation of osteoblasts. The first issues to be considered when constructing bone repair scaffolds include biocompatibility, stress resistance, degradability and stability. Here, a low-cost manufacturing introduces a new bone repair composite scaffold (CS/OBC/nHAP). The scaffolds were composed of only natural derived components, including nano hydroxyapatite (nHAP) formed by in-situ crystallization of Ca2+/PO42- solution and evenly dispersed in oxidized bacterial cellulose (OBC) and chitosan (CS) scaffolds. The experimental results showed that compared with CS/nHAP scaffold, CS/OBC/nHAP scaffold has significantly improve mechanical properties and water retention performance, and has a more stable degradation rate. Cell experiments showed that the CS/OBC/nHAP scaffold has good biocompatibility and significantly promote the proliferation of MC3T3-E1 cells. The rat skull defect model further proves that the CS/OBC/nHAP scaffold could induce the formation of bone tissue. Meanwhile, H&E staining experiment show that the CS/OBC/nHAP scaffold has good stability in vivo and could better promote the formation of bone tissue.

In Situ Fabrication of Nerve Growth Factor Encapsulated Chitosan Nanoparticles in Oxidized Bacterial Nanocellulose for Rat Sciatic Nerve Regeneration.

Autograft is currently the gold standard in the clinical treatment of peripheral nerve injury (PNI), which, however, is limited by the availability of a donor nerve and secondary injuries. Nerve guidance conduits (NGC) provide a suitable microenvironment to promote the regeneration of injured nerves, which could be the substitutes for autografts. In this study, nerve growth factor (NGF) encapsulated chitosan nanoparticles (CSNPs) were first constructed in situ in an oxidized bacterial cellulose (OBC) conduit using the ion gel method after the introduction of a CS/NGF solution under pressure to enable a sustainable release of NGF. A novel NGF@CSNPs/OBC nanocomposite with antibacterial activity, biodegradability, and porous microstructure was successfully developed. In vitro experiments showed that the nanocomposite promoted the adhesion and proliferation of Schwann cells. When the nanocomposite was applied as NGC to repair the sciatic nerve defect of rats, a successful repair of the 10 mm nerve defect was observed after 4 weeks. At week 9, the diameter, morphology, histology, and functional recovery of the regenerated nerve was comparable to the autografts, indicating that the NGC effectively promoted the regeneration and function recovery of the nerve. In summary, the NGF@CSNPs/OBC as a novel NGC provides great potential in the treatment of PNI.

Multifunctional dopamine modification of green antibacterial hemostatic sponge

A novel hemostatic nanocomposite (OBC-PDA/PDA-MMT/Ag NPs) was prepared. As Functional hemostatic particles, hydrochloric acid modified montmorillonite coated with dopamine (PDA-MMT) doped into oxidized bacterial cellulose (OBC). In the presence of carboxyl and dopamine, silver ions (Ag+) were reduced into Ag nanoparticles (Ag NPs) distributed homogeneously on the matrix of PDA-MMT and OBC. Then, dopamine was grafted onto the oxidized bacterial cellulose under the crosslinking effect of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC). After dopamine was grafted onto the oxidized bacterial cellulose, the interaction between PDA-MMT and the whole material was enhanced, and the flexibility was also improved. OBC-PDA/PDA-MMT/Ag NPs hemostatic sponge have appropriate mechanical strength, broad-spectrum antibacterial properties and excellent biodegradability. The hemostatic sponge with addition of PDA-MMT and Ag NPs is expected to provide functional properties such as rapid hemostasis, bacteriostasis and wound healing. In addition, the hemostatic effect of the compound was confirmed in vivo. The hemostatic sponge showed greater coagulation capacity, higher adherent red blood cells and platelets, and lower blood loss. The results show that hemostatic sponge is a rapid and effective coagulant with good antibacterial properties.

Antibacterial Multi-Layered Nanocellulose-Based Patches Loaded with Dexpanthenol for Wound Healing Applications.

Antibacterial multi-layered patches composed of an oxidized bacterial cellulose (OBC) membrane loaded with dexpanthenol (DEX) and coated with several chitosan (CH) and alginate (ALG) layers were fabricated by spin-assisted layer-by-layer (LbL) assembly. Four patches with a distinct number of layers (5, 11, 17, and 21) were prepared. These nanostructured multi-layered patches reveal a thermal stability up to 200 °C, high mechanical performance (Young’s modulus ≥ 4 GPa), and good moisture-uptake capacity (240–250%). Moreover, they inhibited the growth of the skin pathogen Staphylococcus aureus (3.2–log CFU mL−1 reduction) and were non-cytotoxic to human keratinocytes (HaCaT cells). The in vitro release profile of DEX was prolonged with the increasing number of layers, and the time-dependent data imply a diffusion/swelling-controlled drug release mechanism. In addition, the in vitro wound healing assay demonstrated a good cell migration capacity, headed to a complete gap closure after 24 h. These results certify the potential of these multi-layered polysaccharides-based patches toward their application in wound healing.

Production of Bacterial Cellulose Aerogels With Improved Physico-Mechanical Properties and Antibacterial Effect.

Aerogels have gained significant interest in recent decades because of their unique properties such as high porosity, low density, high surface area, and excellent heat and noise insulation. However, their high cost and low mechanical strength limit their practical application. We developed appropriate conditions to produce aerogels with controlled density, high mechanical strength, and thermal characteristics from bacterial cellulose (BC) synthesized by the strain Komagataeibacter sucrofermentans H-110. Aerogels produced using TEMPO oxidized BC (OBC) exhibited high mechanical strength and lower shrinkage than those from native bacterial cellulose (NBC). Compared to the NBC, the use of TEMPO-oxidized BC with oxidation degrees (OD) of 1.44 and 3.04% led to the reduction of shrinkage of the aerogels from 41.02 to 17.08%. The strength of the aerogel produced from the TEMPO-oxidized BC with an oxidation degree of 1.44% was twice that of the aerogel produced from NBC. The addition of Mg2+ at concentrations of 20 and 40 mM during the preparation of the aerogels increased the strength of the aerogels by 4.9 times. The combined use of TEMPO-oxidized BC and Mg2+ allowed pore size reduction from 1,375 to 197.4 μm on the outer part of the aerogels, thereby decreasing the thermal conductivity coefficient from 0.036 to 0.0176 W/(m•K). Furthermore, novel biocomposites prepared from the aerogels based on NBC and OBC and sodium fusidate, which have high antibiotic activity against Staphylococcus aureus, were obtained. Owing to their antibacterial properties, these aerogels can be used as functional biomaterials in a wide range of applications such as in tissue engineering and fabrication of wound dressing materials.

3D printed hydrogels with oxidized cellulose nanofibers and silk fibroin for the proliferation of lung epithelial stem cells.

A novel biomaterial ink consisting of regenerated silk fibroin (SF) and 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized bacterial cellulose (OBC) nanofibrils was developed for 3D printing lung tissue scaffold. Silk fibroin backbones were cross-linked using horseradish peroxide/H2O2 to form printed hydrogel scaffolds. OBC with a concentration of 7wt% increased the viscosity of inks during the printing process and further improved the shape fidelity of the scaffolds. Rheological measurements and image analyses were performed to evaluate inks printability and print shape fidelity. Three-dimensional construct with ten layers could be printed with ink of 1SF-2OBC (SF/OBC = 1/2, w/w). The composite hydrogel of 1SF-1OBC (SF/OBC = 1/1, w/w) printed at 25 °C exhibited a significantly improved compressive strength of 267 ± 13 kPa and a compressive stiffness of 325 ± 14 kPa at 30% strain, respectively. The optimized printing parameters for 1SF-1OBC were 0.3 bar of printing pressure, 45 mm/s of printing speed and 410 μm of nozzle diameter. Furthermore, OBC nanofibrils could be induced to align along the print lines over 60% degree of orientation, which were analyzed by SEM and X-ray diffraction. The orientation of OBC nanofibrils along print lines provided physical cues for guiding the orientation of lung epithelial stem cells, which maintained the ability to proliferate and kept epithelial phenotype after 7 days’ culture. The 3D printed SF-OBC scaffolds are promising for applications in lung tissue engineering.Electronic supplementary materialThe online version of this article (10.1007/s10570-020-03526-7) contains supplementary material, which is available to authorized users.

Resorbable bacterial cellulose membranes with strontium release for guided bone regeneration.

Hybrid materials, based on bacterial cellulose (BC) and hydroxyapatite (HA), have been investigated for guided bone regeneration (GBR). However, for some GBR, degradability in the physiological environment is an essential requirement. The present study aimed to explore the use of oxidized bacterial cellulose (OxBC) membranes, associated with strontium apatite, for GBR applications. BC membranes were produced by fermentation and purified, before oxidizing and mineralizing by immersing in strontium chloride solution and sodium bibasic phosphate for 5cycles. The hybrid materials (BC/HA/Sr, BC/SrAp, OxBC/HA/Sr and OxBC/SrAp) were characterized for biodegradability and bioactivity and for their physicochemical and morphological properties. In vitro cytotoxicity and hemolytic properties of the materials were also investigated. In vivo biocompatibility was analyzed by performing histopathological evaluation at 1, 3 and 9weeks in mices. Results showed that the samples presented different strontium release profiles and that oxidation enhances degradation under physiological conditions. All the hybrid materials were bioactive. Cell viability assay indicated that the materials are non-cytotoxic and in vivo studies showed low inflammatory response and increased connective tissue repair, as well as degradation in most of the materials, especially the oxidized membranes. This study confirms the potential use of bacterial cellulose-derived hybrid membranes for GBR.

Oxidized bacterial cellulose membrane as support for enzyme immobilization: properties and morphological features

Bacterial cellulose (BC) membrane can be architected to covalently immobilize biomolecules, generating materials with new functionality. The processes of purification (via alkaline treatment) and chemical modification (via NaIO4) to the wet BC membrane is the innovation of this work. This wet oxidized BC (OxBC) membrane could act as a support matrix for covalent immobilization of enzymes. BC produced over 5 days of static fermentation, followed by purification with K2CO3 (BC-5d-K2CO3) was selected for our study due to high porosity and surface area, which are properties that favor its chemical modification. This wet BC membrane proven suitable for NaIO4 oxidation. Time and temperature conditions were evaluated in the oxidation reaction, with oxidation BC (OxBC) performed at 1% (w/v) NaIO4 for 6 h at 55 °C under most advantageous conditions, as it provided 50% oxidation degree and preserved its morphological structure. BC and OxBC were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, Scanning electron microscopy, mechanical test, and thermal analysis. The oxidation reaction decreased BC crystallinity, tensile strength, and thermal stability and compacted the cellulose layers. BC and OxBC showed non-cytotoxicity. Fourier transform infrared confirmed that OxBC can covalently immobilize papain and that after immobilization the enzyme showed a recovered enzymatic activity of 93.1%. In addition, the oxidized membrane presented greater amount of immobilized papain in its study than BC, proving to be a more efficient support for enzymatic immobilization.

A Biodegradable Antibacterial Nanocomposite Based on Oxidized Bacterial Nanocellulose for Rapid Hemostasis and Wound Healing.

The development of biodegradable and antibacterial hemostatic materials with high blood absorption to halt the internal hemorrhage of deep noncompressible wounds remains a challenge. In this study, a novel hemostatic nanocomposite (OBC/COL/CS) was fabricated by coupling oxidized bacterial cellulose (OBC) and chitosan (CS) with collagen (COL), that is, during the electrostatic self-assembly of OBC with CS (OBC/CS), COL was ingeniously attached as a functional component by the electrostatic attraction of cationic CS and anionic OBC. The introduction of collagen was anticipated to provide functional properties such as enhanced hemostasis and promotion of wound healing so as to achieve a new functional composite. This study is the first to evaluate the performance of OBC, OBC/CS, and the OBC/COL/CS composite for rapid internal hemostasis using a rat liver injury model. To our knowledge, this is also the first study to report that OBC has a faster biodegradability in vivo than commercial hemostatic oxidized regenerated plant cellulose (ORC). The OBC/COL/CS nanocomposite exhibited appropriate mechanical strength, broad spectrum antimicrobial properties, and excellent biodegradation in vivo. Furthermore, excellent hemostatic efficacy of the composite was confirmed in vivo. OBC/COL/CS exhibited greater procoagulant properties and blood-clotting capability, higher adhesion of erythrocytes and platelets with concomitant lower blood loss, in addition to ultrafast cessation of bleeding, superior to the commercial hemostatic ORC product Surgicel gauze. The results suggest that the OBC/COL/CS is a fast and efficient procoagulant agent with good antibacterial properties and great potential for use as an absorbable hemostat for control of internal bleeding.

Development of organic–inorganic oxidized bacterial cellulose nanobiocomposites: ternary complexes

Bacterial cellulose (BC) and oxidized BC (OBC) nanobiocomposites, incorporating alginate and zinc acetate (as Zn2+ precursor) with different concentrations, have been prepared. Periodate oxidation used to obtain OBC. According to the ATR-FTIR spectra, intermolecular interactions between the functional groups of BC and OBC, and carboxyl groups of alginate were confirmed. Characteristic diffraction peaks of ZnO nanoparticles (NPs) in nanobiocomposites containing zinc acetate confirmed the formation of ZnO nanoparticles. Water absorption was decreased with increasing alginate concentration due to the molecular chains accumulation and entanglement. Cross-linking of Zn2+ ions with alginate and BC or OBC led to decrease in water absorption and increase in tensile strength with increasing zinc acetate concentration up to 5% (w/v). The percentage of ZnO NPs in the BC-Alg3-ZnAc5 nanobiocomposites was the highest (36.2%), which was in accordance with the results obtained According to the FE-SEM micrographs, OBC revealed a more open structure with larger pores. An accumulated, chain-like, and strong structure was shown in combination of 3% alginate and 5% zinc acetate. BC-Alg0-ZnAc5 nanobiocomposites represented the highest antibacterial activity against Escherichia coli and Staphylococcus aureus. Moreover, nanobiocomposites were more sensitive against S. aureus than E. coli.

Development and biocompatibility evaluation of biodegradable bacterial cellulose as a novel peripheral nerve scaffold.

Peripheral nerve injury is a serious medical problem and severely affects normal life of patient. Bacterial cellulose (BC) is considered as a novel promising biomaterial for tissue engineering, but the poor biodegradability limits its application. In this study, biodegradable bacterial cellulose scaffolds were prepared with different oxidation degrees (O.Ds.) using sodium periodate, evaluating their potential application in peripheral nerve repair. The chemical structure and surface morphology of the oxidized bacterial cellulose (OBC) scaffolds were characterized using Fourier transform infrared spectroscopy, Wide angle X-ray diffraction, and Scanning electron microscope. The porosity, mechanical properties, and degradation behavior of the OBC series scaffolds were extensively examined. Cellular viability and blood compatibility of OBC scaffolds were studied by MTT assay and hemolytic test using Schwann cells (SCs) and red blood cells (RBCs), respectively. The results demonstrated that the biodegradability of OBC scaffolds was improved significantly. OBC scaffolds with lower O.Ds. displayed high porosity with interconnected pores, suitable mechanical property, and biodegradability for peripheral nerve repair. In vitro cytotoxicity and hemolysis test analysis indicated that OBC0.05/3 scaffold is cellular and blood compatible, demonstrating its potential application as a good candidate for peripheral nerve repair. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 1288-1298, 2018.

Biomimetic Design of Oxidized Bacterial Cellulose-gelatin-hydroxyapatite Nanocomposites

Oxidized Bacterial Cellulose (OBC)-hydroxyapatite (HAp)-gelatin (Gel) nanocomposites were prepared by a biomimetic process. HAp nanocrystals were precipitated in a mixed solution of Na2HPO4 (pH 9.2) and Gel solution at 37 °C, and OBC was used to generate a three-dimensional (3D) network stent. The tensile strength of OBC-HAp-G was higher than 0.3 MPa, and the complete degradation time was approximately 90 d in Simulated Body Fluid (SBF). Fourier transform infrared spectroscopy demonstrated that a coordinate bond had formed possibly between HAp and the cellulose hydroxyl. X-ray diffraction showed that both the oxidation of bacterial cellulose and an increase in Gel content induced the formation of tiny HAp crystallites during composite fabrication. Specific surface area and porosity measurements indicated that a low Gel concentration contributed to retention of porous structure. The Ca and P contents on the surface of materials increased initially and then decreased with an increase in Gel content, as measured by energy dispersive spectroscopy. From the thermogravimetric data, the increase in decomposition temperature suggested the formation of chemical bonds among OBC, HAp, and Gel. The above results suggest that the OBC-HAp-G0.3 composite is a potential bone scaffold material.

Laccase-immobilized bacterial cellulose/TiO2 functionalized composite membranes: Evaluation for photo- and bio-catalytic dye degradation

Bacterial cellulose (BC) was prepared by the fermentation of Komagataeibacter xylinus. Subsequently, through site-directed surface oxidation chemistry, the hydroxyl groups of BC were successfully oxidized into aldehyde groups that served as anchors for covalent immobilization of laccase (Lac) to the newly developed oxidized BC (OBC) membrane. TiO2 was additionally co-immobilized to OBC to produce a novel material in which dye degradation was carried out under specific conditions. Atomic Force Microscopy (AFM) and Scanning Electron Microscope (SEM) confirmed the installation of both TiO2 and laccase on the surface of OBC nanofiber membrane. The optimum pH, temperature, thermal stability, operational stability of the OBC/Lac and OBC/TiO2-Lac membrane were also studied in detail. In addition, the effect of the temperature and pH on dye degradation was also investigated. The results showed that the oxidation process successfully introduced aldehyde groups onto the BC (FT-IR), and also improved the stability of the immobilized laccase. Compared with free laccase, the optimum pH of immobilized laccase shifted to lower pH, while the optimum temperature decreased from 55°C to 50°C. The dye degradation experiments showed that the optimum pH for dye degradation was 5.0–6.0, while the optimum temperature was ~40°C. Under UV illumination, the dye degradation efficiency was significantly improved. Therefore, functionalized composite bacterial cellulose nanofiber membranes with a combined bio- and photo- catalytic property are a potentially valid approach for industrial textile dye degradation.

Selective oxidation of bacterial cellulose by NO2–HNO3

Bacterial cellulose (BC) needs to be selectively oxidized by different oxidants such as TEMPO–NaClO–NaBr and NaIO4 in order to control its degradability in vivo. However, both of these two oxidants are difficult to remove and the oxidation process is often accompanied by undesirable degradation of the material. In this work, a highly selective and efficient method for producing oxidized bacterial cellulose (OBC) has been developed in the reaction with NO2 in HNO3 solution. Systematic characterization of the structure and property of the resulting OBCs demonstrated that the oxidation process not only avoided the secondary reaction but also significantly enhanced its mechanical properties, controllability of biodegradability and protein absorbability. Nuclear magnetic resonance (NMR) testing and Fourier transform infrared spectroscopy (FTIR) proved that the selective oxidation of BC took place only at C6 where primary alcohol groups were quickly oxidized to carboxyl groups, with a maximum oxidation degree achieved up to 32.54% after 40 h. The oxidation process not only retained the crystal structure of BC, but slightly increased its degree of crystallinity, thus contributing to the improvement of its strength and toughness. At the same time, OBC manifested more controllable degradability and higher protein adsorption than the original BC as a function of the oxidation time.

Preparation and characterization of degradable oxidized bacterial cellulose reacted with nitrogen dioxide

Bacterial cellulose (BC) is regarded as one of the most attractive and promising biomaterials in medical applications owing to its high purity and mechanical properties and excellent biocompatibility. In this study, a new kind of degradable oxidized bacterial cellulose (OBC) was prepared by oxidizing BC in the presence of nitrogen dioxide (NO2), which could be used as a scaffold for tissue engineering and tissue regeneration. The chemical structures, micromorphology, and in vitro degradability of OBC were characterized. The results demonstrated that the oxidation reaction was controllable for tailoring the degree of degradation of BC. After oxidation, the degradation of BC was accelerated, depending on the oxidation time. In the case of oxidation for 12 days, the mass loss rate of OBC increased sharply, up to 45% after being immersed in phosphate buffered saline (PBS) for 60 days, compared with only 10% for original BC in the same condition. The oxidation did not affect the crystal structure of BC, however, changed the morphology of its network. The original dense microfibril network of BC could be gradually degraded and disappeared within a desirable period of time in vitro through controlling the degree of the selective oxidation.