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Curcumin-loaded soluplus® based ternary solid dispersions with enhanced solubility, dissolution and antibacterial, antioxidant, anti-inflammatory activities

姜黄素 溶解度 抗氧化剂 溶解 三元运算 化学 核化学 色谱法 化学工程 有机化学 生物化学 工程类 计算机科学 程序设计语言
作者
Memoona Ishtiaq,Hina Manzoor,Ikram Ullah Khan,Sajid Asghar,Muhammad Irfan,Norah A. Albekairi,Abdulrahman Alshammari,Abdulrahman F. Alqahtani,Saad H. Alotaibi,Rabia Munir,Pervaiz Akhtar Shah,Liaqat Hussain,Muhammad Abubakar Saleem,Fizza Abdul Razzaq,Syed Haroon Khalid
出处
期刊:Heliyon [Elsevier BV]
卷期号:10 (14): e34636-e34636 被引量:2
标识
DOI:10.1016/j.heliyon.2024.e34636
摘要

Amorphous solid dispersion (ASD) has emerged to be an outstanding strategy among multiple options available for improving solubility and consequently biological activity. Interestingly several binary SD systems continue to exhibit insufficient solubility over time. Therefore, the goal of current research was to design ternary amorphous solid dispersions (ASDs) of hydrophobic model drug curcumin (CUR) to enhance the solubility and dissolution rate in turn, presenting enhanced anti-bacterial, antioxidant and anti-inflammatory activity. For this purpose several ternary solid dispersions (TSDs) consisting of Soluplus®, Syloid® XDP 3150, Syloid® 244 and Poloxamer® 188 in combination with HPMC E5 (binary carrier) were prepared using solvent evaporation method. Both solubility and dissolution testing of prepared solid dispersion were performed to determine the increase in solubility and dissolution. Solid state investigation was carried out utilizing infrared spectroscopy, also known as Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM),Differential scanning calorimetry (DSC) and X-ray diffraction (XRD).Optimized formulations were also tested for their biological effectiveness including anti-bacterial, anti-oxidant and anti-inflammatory activity. Amid all Ternary formulations F3 entailing 20 % soluplus® remarkably improved the solubility (186 μg/ml ± 3.95) and consequently dissolution (91 % ± 3.89 %) of curcumin by 3100 and 9 fold respectively. These finding were also supported by FTIR, SEM, XRD and DSC. In-vitro antibacterial investigation of F3 also demonstrated significant improvement in antibacterial activity against both gram positive (

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