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Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns
Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns
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Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns
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Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns
Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns

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Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns
Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns
Journal Article

Design and Evaluation of Microemulsion-Based Drug Delivery Systems for Biofilm-Based Infection in Burns

2024
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Overview
Normal skin is the first line of defense in the human body. A burn injury makes the skin susceptible to bacterial infection, thereby delaying wound healing and ultimately leading to sepsis. The chances of biofilm formation are high in burn wounds due to the presence of avascular necrotic tissue. The most common pathogen to cause burn infection and biofilm is Pseudomonas aeruginosa. The purpose of this study was to create a microemulsion (ME) formulation for topical application to treat bacterial burn infection. In the present study, tea tree oil was used as the oil phase, Tween 80 and transcutol were used as surfactants, and water served as the aqueous phase. Pseudo ternary phase diagrams were used to determine the design space. The ranges of components as suggested by the design were chosen, optimization of the microemulsion was performed, and in vitro drug release was assessed. Based on the characterization studies performed, it was found that the microemulsion were formulated properly, and the particle size obtained was within the desired microemulsion range of 10 to 300 nm. The I release study showed that the microemulsion followed an immediate release profile. The formulation was further tested based on its ability to inhibit biofilm formation and bacterial growth. The prepared microemulsion was capable of inhibiting biofilm formation. Graphical Abstract