Quality by design-oriented formulation optimization and characterization of guar gum-pectin based oral colon targeted liquisolid formulation of xanthohumol

瓜尔胶 果胶 差示扫描量热法 溶解度 休止角 溶解 生物利用度 瓜尔 黄腐酚 溶解试验 化学 造粒 材料科学 色谱法 食品科学 有机化学 药理学 复合材料 医学 钥匙(锁) 生态学 物理 生物制药分类系统 生物 热力学
作者
Sourabh Chatterjee,Leander Corrie,Mahesh Hanmantrao,Sukriti Vishwas,Rajan Kumar,Faisal Al-Otaibi,Mohammad Javed Ansari,Zia ur Rehman,Omji Porwal,Rubiya Khursheed,Vancha Harish,Gaurav Gupta,Bimlesh Kumar,Pankaj Kumar Singh,Gowthamarajan Kuppusamy,Anindita De,S. Swathi,Umashankar Marakanam Srinivasan,Monica Gulati,Kamal Dua,Sachin Kumar Singh
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier]
卷期号:82: 104350-104350 被引量:9
标识
DOI:10.1016/j.jddst.2023.104350
摘要

In the present study a colon targeted liquisolid powder of xanthohumol was developed using Central Composite Design (CCD). Xanthohumol is a drug obtained from hops plants that can be effective in the treatment of UC. It possesses poor aqueous solubility, permeability and dissolution rate limited oral bioavailability. Hence, it was thought to enhance its dissolution rate by formulating liquisolid powder. Liquisolid technology is simple, single step and cost effective techniques to enhance dissolution rate of lipophilic drugs. Further, the formulation was targeted to colon using optimized combination of guar gum and pectin. Liquisolid powder of xanthohumol was formulated using Transcutol P as non-volatile solvent, polysaccharide mixture of guar gum and pectin as carrier, Syloid XDP as coating agent. The ratio of guar gum, pectin and Syloid XDP affecting angle of repose, drug loading and dissolution of drug in 5 h were optimized using CCD. The optimized formulation showed angle of repose of 26.78°, drug loading of 89.34% and dissolution of drug in 5 h of 5.23%, respectively. The formulation showed site-specific release of liquisolid with less than 10% drug release in initial 5 h due to the release restricting property of guar gum and pectin followed by a burst release of xanthohumol between 5th and 12th hour indicating colon specific release of xanthohumol. The powder X-ray diffraction studies, differential scanning calorimetry and scanning electron microscopy revealed about complete solubility of xanthohumol in the Transcutol P and complete adsorption of the liquid on surface of Syloid XDP, guar gum and pectin. The accelerated stability studies indicated that the formulation was stable. The overall results of study indicated about successful development of colon targeted liquisolid formulation of xanthohumol that can be further explored for pre-clinical studies.
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