RESUMEN
Among different microbial-induced calcium carbonate precipitation (MICCP) mechanisms utilized for biomineralization, ureolysis leads to the greatest yields of calcium carbonate. Unfortunately, it is reported that urea-induced growth inhibition can delay urea hydrolysis but it is not clear how this affects MICCP kinetics. This study investigated the impact of urea addition on the MICCP performance of Lysinibacillus sphaericus MB284 not previously grown on urea (thereafter named bio-agents), compared with those previously cultured in urea-rich media (20 g/L) (hereafter named bio-agents+ or bio-agents-plus). While it was discovered that initial urea concentrations exceeding 3 g/L temporarily hindered cell growth and MICCP reactions for bio-agents, employing bio-agents+ accelerated the initiation of bacterial growth by 33% and led to a 1.46-fold increase in the initial yield of calcium carbonate in media containing 20 g/L of urea. The improved tolerance of bio-agents+ to urea is attributed to the presence of pre-produced endogenous urease, which serves to reduce the initial urea concentration, alleviate growth inhibition, and expedite biomineralization. Notably, elevating the initial concentration of bio-agents+ from OD600 of 0.01 to 1, housing a higher content of endogenous urease, accelerated the initiation of MICCP reactions and boosted the ultimate yield of biomineralization by 2.6 times while the media was supplemented with 20 g/L of urea. These results elucidate the advantages of employing bio-agents+ with higher initial cell concentrations to successfully mitigate the temporary inhibitory effects of urea on biomineralization kinetics, offering a promising strategy for accelerating the production of calcium carbonate for applications like bio self-healing of concrete.
Asunto(s)
Bacillaceae , Carbonato de Calcio , Precipitación Química , Urea , Ureasa , Carbonato de Calcio/metabolismo , Carbonato de Calcio/farmacología , Carbonato de Calcio/química , Urea/metabolismo , Urea/farmacología , Bacillaceae/metabolismo , Cinética , Ureasa/metabolismo , Biomineralización , Medios de Cultivo/químicaRESUMEN
Hierarchical fibrous scaffolds (HFS) consist of nanoscale fibers arranged in larger macroscale structures, much in the same pattern as in native tissue such as tendon and bone. Creation of continuous macroscale nanofiber yarns has been made possible using modified electrospinning set-ups that combine electrospinning with techniques such as twisting, drawing, and winding. In this paper, a modified electrospinning setup was used to create continuous yarns of twisted type I collagen nanofibers, also known as collagen nanoyarns (CNY), from collagen solution prepared in acetic acid. Fabricated CNYs were cross-linked and characterized using SEM imaging and mechanical testing, while denaturation of collagen and dissolution of the scaffolds were assessed using circular dichroism (CD) and UV-vis spectroscopy, respectively. HeLa cells were then cultured on the nanoyarns for 24 h to assess cell adhesion on the scaffolds. Scanning electron micrographs revealed a twisted nanofiber morphology with an average nanofiber diameter of 213 ± 60 nm and a yarn diameter of 372 ± 23 µm that shrank by 35% after covalent cross-linking. Structural denaturation assessment of native collagen using circular dichroism (CD) spectroscopy showed that 60% of the triple-helical collagen content in CNYs was retained. Cross-linking of CNYs significantly improved their mechanical properties as well as stability in buffered saline with no sign of degradation for 14 days. In addition, CNY strength and stiffness increased significantly with cross-linking although in the wet state, significant loss in these properties, with a corresponding increase in elasticity, was observed. HeLa cells cultured on cross-linked CNYs for 24 h adhered to the yarn surface and oriented along the nanofiber alignment axis, displaying the characteristic spindle-like morphology of cells grown on surfaces with aligned topography. Collectively, the results demonstrate the promising potential of collagen nanoyarns as a new class of shapable biomaterial scaffold and building block for generating macroscale fiber-based tissues.
Asunto(s)
Materiales Biocompatibles , Nanofibras , Humanos , Andamios del Tejido/química , Células HeLa , Colágeno/química , Colágeno Tipo I , Nanofibras/química , Ingeniería de TejidosRESUMEN
Investigations into the piezoelectricity of natural polymers is a continuing area of interest due to their potential role in the complex interplay of mechanical and electrical forces present in biological organisms. Their synthetic counterparts, when electrospun using the air gap electrospinning method, are known to have increased crystallinity and tensile strength as compared to randomly aligned nanofibers composed of the same constituent polymers. Using the air gap electrospinning method with the naturally-occurring, semi-crystalline polymer chitin, the nanofibers were determined to have a 300% increase in tensile strength over randomly collected ones. Additionally, a 400% increase in piezoelectric response in the aligned nanofiber chitin mats was measured. The increased tensile strength and piezoelectricity in aligned chitin nanofibers is a consequence of an increase in α-chitin crystallinity in the nanofibers induced by the air gap collection method.
RESUMEN
Electrospun natural polymeric bandages are highly desirable due to their low-cost, biodegradability, non-toxicity and antimicrobial properties. Functionalization of these nanofibrous mats with two-dimensional nanomaterials is an attractive strategy to enhance the antibacterial effects. Herein, we demonstrate an electrospinning process to produce encapsulated delaminated Ti3C2T z (MXene) flakes within chitosan nanofibers for passive antibacterial wound dressing applications. In vitro antibacterial studies were performed on crosslinked Ti3C2T z /chitosan composite fibers against Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus aureus (S. aureus) - demonstrating a 95% and 62% reduction in colony forming units, respectively, following 4 h of treatment with the 0.75 wt% Ti3C2T z - loaded nanofibers. Cytotoxicity studies to determine biocompatibility of the nanofibers indicated the antibacterial MXene/chitosan nanofibers are non-toxic. The incorporation of Ti3C2T z single flakes on fiber morphology was analyzed by scanning electron microscopy (SEM) and transmission electron microscopy equipped with an energy-dispersive detector (TEM-EDS). Our results suggest that the electrospun Ti3C2T z /chitosan nanofibers are a promising candidate material in wound healing applications.
RESUMEN
Conducting hydrogels possessing antibacterial activity were developed using a two-step free-radical aqueous polymerization method to incorporate polyaniline chains into an adsorbent Guar gum/acrylic acid hydrogel network. The material properties of the synthesized samples were characterized using FTIR spectroscopy, thermal analysis and scanning electron microscopy techniques. Conducting hydrogels were tested for antibacterial activities against gram-positive Staphylococcus aureus and gram-negative Escherichia coli bacteria and demonstrated antibacterial activity. Synthesized hydrogel samples can be potential adsorbent materials for dye removal applications.
Asunto(s)
Antibacterianos/química , Antibacterianos/farmacología , Galactanos/química , Hidrogeles/química , Mananos/química , Gomas de Plantas/química , Polisacáridos Bacterianos/química , Acrilatos/química , Antibacterianos/síntesis química , Materiales Biocompatibles , Colorantes/aislamiento & purificación , Escherichia coli/efectos de los fármacos , Hidrogeles/síntesis química , Azul de Metileno/aislamiento & purificación , Microscopía Electrónica de Rastreo , Polimerizacion , Espectroscopía Infrarroja por Transformada de Fourier , Staphylococcus aureus/efectos de los fármacosRESUMEN
Human platelet-derived growth factor-BB (hPDGF-BB) is a basic polypeptide growth factor released from platelets at the injury site. It is a multifunctional molecule that regulates DNA synthesis and cell division and induces biological effects that are implicated in tissue repair, atherosclerosis, inflammatory responses, and neoplastic diseases. This paper is an overview of the toxicology data generated from a broad testing platform to determine bone, soft tissue, and systemic responses following administration of rhPDGF-BB. Moreover, the systemic and local toxicity of recombinant human PDGF-BB (rhPDGF-BB) in combination with either beta-tricalcium phosphate (ß-TCP) or collagen combined with ß-TCP was studied to determine dermal sensitization, irritation, intramuscular tissue responses, pyrogenicity, genotoxicity, and hemolytic properties. All data strongly suggest that rhPDGF-BB either alone or in combination with ß-TCP or collagen with ß-TCP is biocompatible and has neither systemic nor local toxicity, supporting its safe use in enhancing wound healing in patients.