Abstract
Purpose
Less local availability and higher skin permeation restrict wide application of silver sulfadiazine (SSD) formulations against infectious burn wound.
Aim
We aimed to develop β-cyclodextrin inclusion complex-based in situ pluronic gel of SSD (β-CD-ssd P-Gel).
Methods
Formation of inclusion complex was confirmed by FT-IR, DSC, SEM, and XRD and checked for improved solubility.
Results and Discussion
Poloxamer (407/118)-based in situ gel of inclusion complex was prepared and characterized for its gelation temperature (33.50 °C), viscosity (1159.25 ± 5.60 cps), pH (6.4 ± 0.56), and drug content (91.56 ± 1.62%). The developed gel showed slow drug release and slow permeation of the drug through the skin. It showed broader zone of Staphylococcus aureus growth inhibition (31 ± 0.20 mm) and high wound contraction (98.89%) when compared with the marketed formulation (26 ± 0.20 mm and 58.00%, respectively).
Conclusions
A consistent, biocompatible, β-CD-ssd P-Gel was prepared successfully. It was found able to ensure increased local availability by forming viscous gel below body temperature, high SSD availability at the desired site, and high efficacy against infectious wound.
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Acknowledgments
Authors are thankful to the management of ISF College of Pharmacy for providing institutional scholar’s fund, necessary infrastructure, and facilities to complete this work. We acknowledge Mr. Anand Rai for helping us out with technical and editorial improvements.
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Joshi, N., Mishra, N. & Rai, V.K. Development and Evaluation of In Situ Gel of Silver Sulfadiazine for Improved Therapeutic Efficacy Against Infectious Burn Wound. J Pharm Innov 16, 537–550 (2021). https://doi.org/10.1007/s12247-020-09464-y
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DOI: https://doi.org/10.1007/s12247-020-09464-y