Raj Pooja Mongia, Raj Rakesh, Kaul Ankur, Mishra Anil K, Ram Alpana
Institute of Pharmaceutical Sciences, Guru Ghasidas Vishwavidyalaya Bilaspur C.G. 495009 India
Division of Cyclotron and Radiopharmaceutical Sciences, Institute of Nuclear Medicine and Allied Sciences (INMAS) New Delhi 110054 India.
RSC Adv. 2018 Jun 6;8(37):20809-20821. doi: 10.1039/c8ra01898g. eCollection 2018 Jun 5.
In the present investigation we have prepared and characterized curcumin (CN)-containing chitosan nanoparticles (CS-NPs) coated with Eudragit FS 30D for colon-specific drug delivery for treatment of ulcerative colitis.
CS-NPs were prepared by ionic gelation using tripolyphosphate. To specify pH sensitive delivery, CS-CN-NPs were coated with Eudragit FS 30D by using a solvent evaporation method. Different process parameters were evaluated, and the optimized formulation was characterized by particle size, size distribution, zeta potential and encapsulation efficiency before lyophilization. The lyophilized product was further subjected to Fourier-transform infrared spectroscopy, and particle morphology and drug release in different media were studied.
the kinetics of drug release from the CS-CN-NPs revealed sustained release behaviour of the developed carriers. biodistribution study by gamma-scintigraphy showed good accumulation of the developed nanocarriers in the colonic region.
sustained and pH stimulated delivery of CN to the colon was successfully attained coating of CS-NPs with Eudragit FS 30D to circumvent poor absorption and availability of CN.
在本研究中,我们制备并表征了用Eudragit FS 30D包衣的含姜黄素(CN)的壳聚糖纳米粒(CS-NPs),用于结肠特异性药物递送以治疗溃疡性结肠炎。
采用三聚磷酸钠通过离子凝胶法制备CS-NPs。为了实现pH敏感递送,通过溶剂蒸发法用Eudragit FS 30D包衣CS-CN-NPs。评估了不同的工艺参数,并在冻干前通过粒径、粒径分布、zeta电位和包封率对优化后的制剂进行了表征。对冻干产品进一步进行傅里叶变换红外光谱分析,并研究了其颗粒形态和在不同介质中的药物释放情况。
CS-CN-NPs的药物释放动力学显示所开发载体具有缓释行为。通过γ闪烁显像进行的生物分布研究表明,所开发的纳米载体在结肠区域有良好的蓄积。
通过用Eudragit FS 30D包衣CS-NPs成功实现了CN向结肠的持续且pH刺激的递送,以规避CN吸收不良和利用率低的问题。