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2.1 Steps involved in solvent casting and particulate leaching.

      2.4.2 Emulsion Freeze Drying

      This method is particularly suitable for collagen‐based scaffolds. This is because the collagen has a higher sensitivity to heat denaturation and chemicals. It has been found that aortic heart valve cells can be grown by creating these porous collagen scaffolds [26]. For entrapping the ice crystals, these collagen type 1 fibers were frozen at −30 °C. The required porous materials can be obtained by removing the crystals using a process known as lyophilization. The prominent parameters that affect the pore size include temperature, pH, and solution concentration. Emulsion freeze drying method is used for producing scaffolds having heat‐sensitive bioactive molecules with pore sizes in the range 20–200 μm and with porosity greater than 90% [27, 28].

      2.4.3 Electrospinning

Schematic illustration of the fabrication of electrospun nanofibers under high voltage.

      2.4.4 Blow Film Extrusion

      Blow film extrusion is used for the manufacture of polymeric films. This method involves the extrusion of molten polymeric material, which takes the shape of a die into which it is blown, while air blown into it forms a thin film. Due to their significant advantages such as biodegradability, low cost for processing, and nontoxicity, these blown films are finding their applications in the pharmaceutical industry. Chitosan [36], polysaccharides [37], cellulose [38], and their derivatives are the most commonly used biobased polymers in film industries. Increased attention has been gained for the preparation of blown films made from starch‐based materials [39]. Chitosan‐ and starch‐based thermoplastic films have been found to be suitable for applications in pharmaceutical and food processing industries. By increasing the percentage of chitosan in the film, properties such as water vapor and oxygen barrier tend to increase, while the surface hydrophilicity is reduced. Hence, by controlling the amount of chitosan in the film, the rate of degradation of the film, and consequently, its shelf life can be tuned [39].

      2.4.5 3D Printing

      In 3D printing technique, a preprogrammed printer head moves over the target surface and ejects a fixed quantity of molten polymer on the target in order to create the final desired shape. For attaining the final 3D structure, the movable printer head deposits the polymer material in a layer‐by‐layer fashion. This process is also known as Rapid Prototyping and has prominent applications in biomedical fields such as dental implants [40], orthopedic prosthetics [41, 42], 3D surgical and medical models, and also hearing aids. 3D bioprinting, a new technique, is nothing but a variation of traditional 3D printing in which 3D biofunctional structures are engineered. It involves the deposition of living cells onto a gel medium [43]. Some studies have used nanomaterials in conjunction with biohybrid scaffolds to create additional functions [44]. Some examples show that, new bone growth could be induced by adding magnesia nanoparticles to PCL–chitosan nanofibers through modulation of signal transduction and cell proliferation [44]. In another example, it has been found that this cell proliferation could also be induced by means of magnetic heating when magnetic nanoparticles are added to PCL–chitosan nanofibers [45].

      In the field of tissue engineering, electrospinning and 3D printing are the most common techniques by which the scaffolds are fabricated. In addition to these techniques, common biomedical supplies are prepared by conventional techniques such as compression molding or injection molding. In recent years, in order to combine the advantages of both, a combination of advanced methods and conventional techniques is used to reduce the overall processing time and cost. Examples include particulate leaching and solvent casting [46].

      Generally, there are three different methods by which biobased composites are obtained. They are as follows:

      1 The reinforcement of non‐biobased polymers with biobased fillers/fibers

      2 The reinforcement of biobased polymers with non‐biobased fillers/fibers

      3 The reinforcement of biobased polymers with biobased fillers/fibers.

      2.5.1 Biobased Fillers/Reinforcements with Non‐biobased Polymers

      Fillers/additives used to produce environmental friendly materials include waste paper sludge (WPS) and ink‐eliminated sludge (IES). These materials are used in high‐density polyethylene (HDPE)/wood flour composites [47]. Research shows that, the flexural properties of the HDPE/wood flour composites increased when WPS was added as an additive. This increase in flexural strength could be further increased by using a compatibilizer such as malleated anhydride grafted polyethylene (MAPE) in between the reinforcement and the matrix. Also, there occurs a decrease in the swelling and water absorption properties when this WPS and IES are added as fillers/additives. It has been found out that the overall mechanical properties of IES‐added composites show better results than that of the WPS‐added composites. The optimum loading condition of IES‐added composites is 60 wt%. These results show a promising outcome that these composites could be used for the preparation of biobased composites.

      As these HDPE/wood flour composites find its applications in the exteriors of construction industries, their amount of durability could be calculated by investigating the damage caused due to sunlight and other weathering conditions [48]. Artificial weathering experiments could be carried out on the surface of these composites and by carefully investigating the chemical changes happening on the surface, help in finding out the durability. Further, it has been proved that, when carrying out tests such as X‐ray photoelectron spectroscopy (XPS) and Fourier Transform Infrared Spectroscopy (FTIR), the amount of weathering damage to the wood flour‐reinforced HDPE is increased to 16 times faster than unreinforced plastic. The outcomes confirm that the degradation mechanism is triggered in the polymer chain due to the presence of carbonyl groups and leads to polymer

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