Design and Development of Gastro-retentive Gel Forming System Comprising Curcumin Loaded Nanostructured Lipid Carrier for Stomach Specific Delivery

IF 2.7 4区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Journal of Cluster Science Pub Date : 2024-10-03 DOI:10.1007/s10876-024-02702-0
Mohankumar Dhasaiyan, Arjunan Karuppaiah, Habibur Rahman
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Abstract

This study delved on development of curcumin loaded Nanostructured Lipid carrier (NLC) incorporated into gastro-retentive oral in-situ gel for specifically designed to the stomach delivery. Curcumin is less soluble in stomach pH, so a high amount of drug would be required to produce the desired effects. The solubility of curcumin was enhanced by incorporating curcumin into NLC through size reduction. Subsequently, it was formulated into GRDDS for targeted stomach-specific delivery. The curcumin loaded NLC was fabricated using a high shear homogenization technique. Through lipid screening, Precirol ATO 5 and Labrafac PG were chosen as a lipids, and tween 80 was selected as a surfactant in this formulation. A formulation (NLC-F4) comprising 2% lipids and 800 mg of surfactant was chosen as the best formulation, average mean particle size was found to be 119.3 ± 0.13 nm, PDI was found to be 0.127 ± 0.02, Zeta potential was found to be -30 ± 0.17 mV and % of encapsulation efficiency were found to be 83.4 ± 1.5%. FT-IR investigation showed no interactions. Scanning Electron Microscopy (SEM) revealed smooth and spherical shaped particles, while Differential Scanning Calorimetry (DSC) assessment suggested that curcumin is complexed in the NLC formulation. The in vitro drug release of curcumin from NLC-F4 showed 8 times enhanced drug release compared with the pure curcumin in pH 1.2 buffer. In vitro antioxidant and anti-inflammatory studies revealed significant effects compared to reference standards. Drug release kinetics followed first order release and Weibull kinetics models. The curcumin loaded NLC was fabricated into oral in-situ gel to enhances the gastric retention time and prolong release of drug in the stomach. The system exhibited quick gelation time, optimal viscosity, gastric buoyant density, 24 h floating time, good gel strength, and sustained drug release. These investigations revealed that an oral in-situ gelling system containing curcumin loaded NLC has potential as a carrier for stomach specific delivery and could serve as an alternative dosage form compared to conventional ones for treating gastric ulcers in patients.

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设计和开发含有姜黄素的纳米结构脂质载体的胃部特异性给药胃黏膜凝胶成型系统
这项研究深入探讨了将姜黄素载入纳米结构脂质载体(NLC)并入胃保留口服原位凝胶的开发问题,该凝胶专为胃部给药而设计。姜黄素在胃的 pH 值中溶解度较低,因此需要大量药物才能产生预期效果。将姜黄素加入 NLC 后,通过减小体积提高了姜黄素的溶解度。随后,将其配制成胃特异性靶向给药 GRDDS。姜黄素负载 NLC 是利用高剪切匀浆技术制成的。通过脂质筛选,该配方选择了 Precirol ATO 5 和 Labrafac PG 作为脂质,并选择吐温 80 作为表面活性剂。结果发现,平均粒径为 119.3 ± 0.13 nm,PDI 为 0.127 ± 0.02,Zeta 电位为 -30 ± 0.17 mV,封装效率为 83.4 ± 1.5%。傅立叶变换红外光谱(FT-IR)调查显示没有相互作用。扫描电子显微镜(SEM)显示颗粒光滑且呈球形,而差示扫描量热法(DSC)评估则表明姜黄素在 NLC 配方中发生了络合。在 pH 值为 1.2 的缓冲液中,NLC-F4 的姜黄素体外药物释放量是纯姜黄素的 8 倍。体外抗氧化和抗炎研究显示,与参考标准相比,其抗氧化和抗炎效果显著。药物释放动力学遵循一阶释放和 Weibull 动力学模型。将负载姜黄素的 NLC 制成口服原位凝胶,可以延长药物在胃中的滞留时间和释放时间。该体系具有凝胶化时间快、粘度最佳、胃浮力密度大、24 小时漂浮时间长、凝胶强度高和药物释放持久等特点。这些研究表明,含有姜黄素负载 NLC 的口服原位凝胶系统具有作为胃特异性给药载体的潜力,与传统剂型相比,可作为治疗胃溃疡患者的替代剂型。
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来源期刊
Journal of Cluster Science
Journal of Cluster Science 化学-无机化学与核化学
CiteScore
6.70
自引率
0.00%
发文量
166
审稿时长
3 months
期刊介绍: The journal publishes the following types of papers: (a) original and important research; (b) authoritative comprehensive reviews or short overviews of topics of current interest; (c) brief but urgent communications on new significant research; and (d) commentaries intended to foster the exchange of innovative or provocative ideas, and to encourage dialogue, amongst researchers working in different cluster disciplines.
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