Zafar Ameeduzzafar
Department of Pharmaceutics, College of Pharmacy, Jouf University.
J Oleo Sci. 2020;69(11):1389-1401. doi: 10.5650/jos.ess20162.
The oral route is the most prevalent route of drug administration among various routes. Dapagliflozin is an oral hypoglycemic drug used for lowering the blood glucose level. The objective of this work is to developed and optimized dapagliflozin loaded nanostructured lipid carriers (DG-NLCs) for the improvement of oral delivery. DG-NLCs were prepared by a high-pressure homogenization method (hot) and optimized by Box-Behnken design software using lipid, surfactant, and homogenization cycle as an independent variable. DG-NLCs were evaluated for particle size (Y), entrapment efficiency (Y), drug release (Y). The DG-NLCs were further evaluated for morphology, thermal and X-ray diffraction analysis, ex-vivo intestinal permeation, and stability study. Particle size (nm), entrapment efficiency (%) and drug release (%) of all seventeen formulations were found in the range of 113.71-356.22 nm, 60.43-96.54% and 63.44-83.62% respectively. Morphology of optimized formulation exhibited spherical in shape confirmed by transmission electron microscopy. Thermal and X-ray diffraction analysis of NLCs showed the drug was solubilized and lost the crystallinity. DG-NLCs-opt exhibited dual release pattern initial fast and later sustained-release (90.01±2.01% in 24 h) whereas DG-dispersion showed 31.54±1.87% release in 24 h. Korsmeyer-Peppas model was found to be the best fit model (R=0.999). The DG-NLCs-opt exhibited significant-high (p < 0.05, 1.293 µg/cm/h) flux than DG-dispersion (0.2683 µg/cm/h). Apparent permeation coefficient of DG-NLCs-opt was found to be significantly higher (p < 0.05, 4.14×10 cm/min) than DG-dispersion (8.61×10 cm/min). The formulation showed no significant changes (p < 0.05) on six months of storage study at 25±2°C/60±5%RH. The finding concluded that quality by design (QbD) based lipid nanocarrier for oral delivery could be a promising approach of dapagliflozin for the management of diabetes.
口服途径是各种给药途径中最常见的给药方式。达格列净是一种用于降低血糖水平的口服降糖药。本研究的目的是开发并优化载有达格列净的纳米结构脂质载体(DG-NLCs),以改善口服给药效果。通过高压均质法(热法)制备DG-NLCs,并使用脂质、表面活性剂和均质循环作为自变量,通过Box-Behnken设计软件进行优化。对DG-NLCs进行粒径(Y1)、包封率(Y2)、药物释放(Y3)的评估。对DG-NLCs进一步进行形态学、热分析和X射线衍射分析、离体肠道渗透和稳定性研究。所有17种制剂的粒径(nm)、包封率(%)和药物释放(%)范围分别为113.71-356.22 nm、60.43-96.54%和63.44-83.62%。通过透射电子显微镜确认,优化制剂的形态呈球形。NLCs的热分析和X射线衍射分析表明药物被溶解且失去了结晶性。优化后的DG-NLCs呈现出初始快速释放和随后持续释放的双重释放模式(24小时内释放90.01±2.01%),而DG分散体在24小时内释放31.54±1.87%。发现Korsmeyer-Peppas模型是最佳拟合模型(R=0.999)。优化后的DG-NLCs的通量显著高于DG分散体(p<0.05,1.293μg/cm/h对0.2683μg/cm/h)。优化后的DG-NLCs的表观渗透系数显著高于DG分散体(p<0.05,4.14×10 cm/min对8.61×10 cm/min)。在2:±2°C/60±5%RH条件下进行6个月的稳定性研究,该制剂无显著变化(p<0.05)。研究结果表明,基于质量源于设计(QbD)的脂质纳米载体用于口服给药可能是达格列净治疗糖尿病的一种有前景的方法。