Bajwa Maryam, Tabassam Naila, Hameed Huma, Irfan Ali, Zaman Muhammad, Khan Mahtab Ahmad, Shazly Gamal A, Mehboob Tooba, Riaz Tehseen, Jardan Yousef A Bin
Faculty of Pharmaceutical Sciences, University of Central Punjab, Lahore 54000, Pakistan.
Department of Chemistry, Government College University Faisalabad, Faisalabad 38000, Pakistan.
Gels. 2023 Oct 20;9(10):830. doi: 10.3390/gels9100830.
The current research aims to create a sol-gel-based nanocarrier containing terbinafine formulated for transdermal delivery of the drug into the skin. Sol-gel-based nanocarriers were prepared via the cold method using poloxamer-188, poloxamer-407, and distilled water. The prepared formulation was examined for pH, gelation temperature, Fourier transform infrared spectrophotometer (FTIR) analysis, thermal stability analysis, X-ray diffraction (XRD), scanning electron microscopy (SEM), particle size analysis, zeta potential, and anti-microbial activity. The in-vitro drug release study of F1 was found to be 94%, which showed greater drug release as compared to F2 and F3. The pH of the formulation was found to be within the range applicable to the skin. The gelation temperature was detected at 28 °C. The SEM images of formulations have spotted various particles well-segregated from each other. Analysis of formulations showed a mean globule size diameter of 428 nm, zeta potential values of 0.04 mV, refractive index (1.329), and viscosity (5.94 cP). FTIR analysis confirmed various functional groups' presence in the prepared formulation. Thermal analysis has confirmed the stability of the drug within the prepared formulation. The growth of inhibition was found to be 79.2% in 60 min, which revealed that the prepared formulation has shown good permeation from the membrane. Hence, the sol-gel-based nanocarrier formulation of terbinafine was successfully developed and evaluated.
当前的研究旨在制备一种基于溶胶-凝胶的纳米载体,其中含有特比萘芬,用于将药物经皮递送至皮肤。基于溶胶-凝胶的纳米载体通过冷法使用泊洛沙姆-188、泊洛沙姆-407和蒸馏水制备。对制备的制剂进行了pH值、凝胶化温度、傅里叶变换红外光谱仪(FTIR)分析、热稳定性分析、X射线衍射(XRD)、扫描电子显微镜(SEM)、粒径分析、zeta电位和抗菌活性检测。发现F1的体外药物释放研究为94%,与F2和F3相比显示出更高的药物释放。发现制剂的pH值在适用于皮肤的范围内。检测到凝胶化温度为28℃。制剂的SEM图像显示各种颗粒彼此分离良好。制剂分析显示平均球粒直径为428nm,zeta电位值为0.04mV,折射率(1.329)和粘度(5.94cP)。FTIR分析证实了制备的制剂中存在各种官能团。热分析证实了药物在制备的制剂中的稳定性。发现60分钟内抑制生长率为79.2%,这表明制备的制剂显示出良好的从膜渗透性能。因此,成功开发并评估了基于溶胶-凝胶的特比萘芬纳米载体制剂。