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The objective of the present study was the development and evaluation of Norfloxacin lipid microspheres as topical gels for adjunct therapy to overcome complex clinical challenges presented by moist, thermally coagulated burn wounds.
Norfloxacin-loaded lipid microspheres were prepared using the melt diffusion technique with Compritol ATO HD5, stearic acid, Tween 20, Span 80, and Transcutol P and incorporated into topical gels formulated with Carbopol 971P NF.
The lipid microspheres exhibited an average size of 65.22+23.39 μm and drug entrapment efficiency of 81.58 ± 0.81%. The scanning electron microscopy confirmed spherical particle morphology, while differential scanning calorimetry indicated the amorphous nature of norfloxacin within the microspheres. In vitro studies demonstrated an extended release of norfloxacin, with 72.33 ± 1.46% released from microspheres and 63.18 ± 1.24% from topical gels after 8 hours. Ex vivo studies revealed 28.16 ± 0.63% of norfloxacin permeating through second-degree burnt porcine skin and 21.12 ± 1.38% through intact porcine skin after 8 hours from topical gels. In vitro antibacterial studies indicated a lower MIC90 for the lipid microspheres compared to the pure drug.
The melt diffusion technique yielded micron-sized spherical particles with a drug entrapment efficiency exceeding 80%. In vitro and ex vivo studies confirmed the extended release and enhanced permeation of norfloxacin. Furthermore, in vitro antibacterial evaluations demonstrated increased effectiveness of the microspheres, attributed to improved solubility and sustained drug release.
The approach shows promise in enhancing Norfloxacin availability for managing burn wound complexities. However, preclinical, clinical, and regulatory evaluations are required to establish the utility of the proposed approach. Further investigations into its application for other types of chronic or infected wounds could broaden its therapeutic potential.
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