Wound dressings have experienced continuous and significant changes since the ancient times. The development starts with the use of natural materials to simply cover the wounds to the materials of the present time that could be specially made to exhibit various extraordinary functions. The modern bandage materials made of electrospun biopolymers contain various active compounds that are beneficial to the healing of wounds. These materials are fibrous in nature, with the size of fibers segments ranging from tens of nanometers to micrometers. With the right choices of biopolymers used for these fibrous materials, they could enhance the healing of wounds significantly compared with the conventional fibrous dressing materials, such as gauze. These bandages could be made such that they contain bioactive ingredients, such as antimicrobial, antibacterial, and antiinflammatory agents, which could be released to the wounds enhancing their healing. In an active wound dressing (AWD), the main purpose is to control the biochemical states of a wound in order to aid its healing process. This review provides an overview of different types of wounds, effective parameters in wound healing and different types of wound dressing materials with a special emphasis paid to those prepared by electrospinning.
ABSTRACT:In this article, we present the drug-release rate, water uptake, water permeability, morphology, and mechanical properties of a series of active wound dressing nanofibrous mats prepared via an electrospinning process of poly(lactic acid) (PLA), poly(e-caprolactone) (PCL), and their (50/50) blends loaded with different doses of tetracycline hydrochloride antibiotic. The performance of these active wound dressings in terms of a sustained and suitable drug-release rate, adequate water uptake and water permeability, and antibacterial activities were compared with those of a commercial wound dressing (Comfeel Plus). The results show that the dressings made from PCL and PLA/PCL blends showed better performance compared with the commercial wound dressing sample as far as these properties were concerned. The improved performance could be explained on the basis of the nanofibrous structure of the mats and the hydrophilicity of PCL and PLA.
Dynamic mechanical analysis (DMA) was used to study the miscibility and various transitions (␣, , and ␥ ) in binary blends of ethylene vinyl acetate copolymer (EVA) with low-density polyethylene (LDPE) and high-density polyethylene (HDPE). Addition of a rubbery phase, such as EVA, reduced all the transition temperatures. A peak broadening of tan ␦ was observed with increasing EVA content in the blends. This can be explained by the observed reduction of the crystallinity of the systems. The presence of a single transition peak in the region of glass transition temperature (T g ) has indicated that the blends were miscible. However, morphological investigation by scanning electron microscopy (SEM) revealed the features of a two phase system in which the EVA domains would be dispersed in the polyethylene (PE) phase. The results have demonstrated that DMA is not sensitive enough to study the miscibility of polymeric blends with a similar backbone structures (such as PE and EVA) in view of the small difference in their T g . For such blends, therefore, the use of direct observations, such as microscopic examinations is necessary.
Shape memory was induced in crosslinked low‐density polyethylene by a heating‐stretching‐cooling cycle. The effect of crosslink content on thermal properties and temperature dependence recovery behavior was studied experimentally. The importance of stretching temperature and crosslink content on recovery behavior could be reasonably explained by the observed changes in the thermal properties which were attributed to the differences in crystalline structures and mechanism of crystal formation during the heating‐stretching‐cooling process. A mechanical model was developed to describe qualitatively and quantitatively the temperature dependence recovery behavior of the prepared shape memory crosslinked polyethylene at nonisothermal state under various conditions by driving constitutive equations using a set of model constants. These model constants were determined with the help of a set of optimization codes using a genetic algorithm method. By choosing a suitable set of model constants one can describe with high accuracy the temperature dependence recovery behavior of any shape memory polymer.
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