Sreeharsha Nagaraja, Rajpoot Kuldeep, Tekade Muktika, Kalyane Dnyaneshwar, Nair Anroop B, Venugopala Katharigatta N, Tekade Rakesh K
Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
Department of Pharmaceutics, Vidya Siri College of Pharmacy, Off Sarjapura Road, Bangalore 560035, India.
Pharmaceutics. 2020 Sep 25;12(10):920. doi: 10.3390/pharmaceutics12100920.
The aim of this study was to design, optimize, and develop metronidazole (Met) loaded nanoparticles (MetNp) by employing quality-based design (QbD) as well as a risk assessment methodology. A fractional factorial design was used by selecting five independent variables viz., chitosan concentration, tripolyphosphate concentration, and acetic acid concentration as material attributes, stirring speed, and stirring time as process parameters, whereby their influence on two dependent variables such as particle size (PS) and %entrapment efficiency (%EE) was studied. MetNp were synthesized by employing an ionic-gelation technique and optimized formula obtained from the QbD design study. PS and %EE studies revealed the formation of MetNp with 558.06 ± 2.52 nm and 59.07 ± 2.15%, respectively. Furthermore, a Met release study in various simulated gastro-intestinal media suggested pH-triggered (pH > 7.0) and sustained release profile of Met from Eudragit S100 enteric-coated MetNp capsule (MetNp cap). Moreover, the stability investigation of formulations confirmed good stability with respect to their PS and residual drug content (RDC) at different temperature conditions. In conclusion, the QbD method was effectively utilized in the development of MetNp and enteric-coated MetNp cap depicting their potential to release Met through MetNp cap only in the colon region and can be utilized for the treatment of amoebiasis in the colon.
本研究的目的是采用基于质量的设计(QbD)以及风险评估方法来设计、优化和开发负载甲硝唑(Met)的纳米颗粒(MetNp)。通过选择五个自变量,即壳聚糖浓度、三聚磷酸钠浓度和乙酸浓度作为材料属性,搅拌速度和搅拌时间作为工艺参数,采用分数因子设计,研究它们对两个因变量(如粒径(PS)和包封率(%EE))的影响。采用离子凝胶技术合成MetNp,并根据QbD设计研究获得优化配方。PS和%EE研究表明,所形成的MetNp的粒径分别为558.06±2.52 nm,包封率为59.07±2.15%。此外,在各种模拟胃肠介质中的Met释放研究表明,pH触发(pH>7.0)以及Eudragit S100肠溶包衣的MetNp胶囊(MetNp cap)中Met的缓释特性。此外,制剂的稳定性研究证实,在不同温度条件下,其PS和残留药物含量(RDC)具有良好的稳定性。总之,QbD方法有效地用于MetNp和肠溶包衣的MetNp cap的开发,表明它们仅在结肠区域通过MetNp cap释放Met的潜力,可用于治疗结肠阿米巴病。