Habibullah Sk, Mohanty Biswaranjan, Babu Anashwara, Sivakumar Gomathi, Maji Samarendra, Pal Kunal, Sagiri Sai Sateesh
Department of Pharmaceutics, University Department of Pharmaceutical Sciences, Utkal University, Vani Vihar, Bhubaneswar, Odisha 751004, India.
Department of Pharmaceutics, School of Pharmacy, DRIEMS University, Tangi, Cuttack, Odisha 754022, India.
Int J Biol Macromol. 2025 Jul;318(Pt 4):145312. doi: 10.1016/j.ijbiomac.2025.145312. Epub 2025 Jun 16.
This study evaluated the role of plant-based biphasic gel (bigel) formulations prepared using various ratios of xanthan gum (XG) hydrogel and Candelilla wax-based oleogel for the delayed release of curcumin (CUR). Microscopic studies revealed that the bigel exhibited a bicontinuous phase distribution. FTIR analysis suggested increased hydrogen bonding with a higher proportion of hydrogel in the bigel formulations. The percentage of stress-relaxation in the mechanical study decreased as the hydrogel proportion was increased within the formulations, indicating a rise in elastic components (89.84-27.10 %; CX1-CX5). An examination of the electrical characteristics of the bigels showed an increase in impedance values with higher oleogel concentration (1.2 × 10-1.0 × 10; CX1-CX5). An in vitro release study showed a delayed release in the bigel (31.96 to 24.90 %), whereas the control formulation showed a release of 43.43 % at the end of the experiment. The control formulation showed an anomalous diffusion pattern, whereas bigel formulations exhibited Fickian diffusion-mediated release kinetics. As per the ex vivo intestinal permeation study, the drug was released from the gel formulations through Fickian diffusion (CX1, CX2, and CX4) and anomalous diffusion (CX3 and CX5). The stability study, evaluated by the heat-cool method, confirmed that the dosage form was stable after 6 cycles.
本研究评估了使用不同比例的黄原胶(XG)水凝胶和小烛树蜡基油凝胶制备的植物基双相凝胶(双凝胶)制剂对姜黄素(CUR)缓释的作用。显微镜研究表明,双凝胶呈现双连续相分布。傅里叶变换红外光谱(FTIR)分析表明,双凝胶制剂中较高比例的水凝胶会增加氢键作用。在力学研究中,随着制剂中水凝胶比例的增加,应力松弛百分比降低,表明弹性成分增加(89.84 - 27.10%;CX1 - CX5)。对双凝胶电学特性的研究表明,随着油凝胶浓度升高,阻抗值增加(1.2×10 - 1.0×10;CX1 - CX5)。体外释放研究表明,双凝胶中呈现缓释(31.96%至24.90%),而对照制剂在实验结束时释放率为43.43%。对照制剂呈现非正规扩散模式,而双凝胶制剂呈现菲克扩散介导的释放动力学。根据体外肠道渗透研究,药物通过菲克扩散(CX1、CX2和CX4)和非正规扩散(CX3和CX5)从凝胶制剂中释放。通过热 - 冷方法评估的稳定性研究证实,该剂型在6个循环后是稳定的。