1Department of Phytopharmaceutical, Sekolah Tinggi Ilmu Kesehatan Nasional, Surakarta, Indonesia
2*Department of Pharmaceuticals and Pharmaceutical Technology, Sekolah Tinggi Ilmu Kesehatan Nasional, Surakarta, Indonesia
3Department of Medical Laboratory Technology Program, Sekolah Tinggi Ilmu Kesehatan Nasional, Surakarta, Indonesia
Transfersomes are ultra-deformable lipid vesicles that have shown great potential in enhancing transdermal drug delivery. Caesalpinia sappan L. is a medicinal plant rich in brazilin and phenolic compounds with proven antibacterial activity. Despite the potential, its topical efficacy is limited by poor skin penetration. Therefore, this study aims to develop a transfersomal gel containing C. sappan extract, evaluate the effect of Tween 80 concentration on vesicle characteristics, and assess its antibacterial activity against Staphylococcus aureus. Transfersomes were prepared using the thin-film hydration method with varying Tween 80 concentrations and characterized for particle size and pH. The optimized transfersomal formulation was then incorporated into a carbopol-based gel and evaluated for physicochemical properties, stability, and antibacterial activity using the agar well diffusion method. The results showed that increasing Tween 80 concentration significantly reduced vesicle size (p < 0.05), with the smallest particles obtained at the highest surfactant concentration. Transfersomal gel demonstrated acceptable physicochemical characteristics and exhibited significant antibacterial activity against Staphylococcus aureus compared to the negative control (p < 0.05). This study indicates that transfersomal gel is a promising delivery system to enhance topical antibacterial effectiveness of C. sappan extract.
Keywords: Transfersome, Caesalpinia sappan, antibacterial gel, drug delivery system, Tween 80.
How to cite this article: Hanif AA, Setiawan I, Nirwana AP. Development and Characterization of Transfersomal Gel Containing Caesalpinia sappan L. Extract for Enhanced Topical Antibacterial Delivery. Int J Drug Deliv Technol. 2026;16(3): 165-172. DOI: 10.25258/ijddt.16.3.21
Source of support: Nil.
Conflict of interest: None