Department of Pharmacy, University of Salerno, Via Giovanni Paolo II 132, I-84084 Fisciano, (SA), Italy.
Department of Pharmacy, University of Salerno, Via Giovanni Paolo II 132, I-84084 Fisciano, (SA), Italy; PhD Program in Drug Discovery and Development, University of Salerno, Via Giovanni Paolo II 132, I-84084 Fisciano, (SA), Italy.
Int J Biol Macromol. 2018 Dec;120(Pt B):2303-2312. doi: 10.1016/j.ijbiomac.2018.08.140. Epub 2018 Aug 29.
A gastro-retentive delivery system loaded with piroxicam with a bimodal release profile in gastrointestinal-tract was developed. Piroxicam is characterized by high oral absorption, long half-life, but its elimination is impaired in elderly patients. To overcome fluctuations in plasma levels, floating gastro-retentive gel-beads with sustained release properties were manufactured using prilling. Beads matrix was designed as a hollow/multipolymeric system based on alginate, ALM-pectin and hydroxypropilmethylcellulose. This research studied variables able to affect particles micromeritics, hollow inner structure, floating properties and drug-release profiles in gastro-intestinal tract. The gastro-retentive formulation (F4) acted as a floating-system able to provide the desired bimodal drug-release pattern controlling and delaying in vitro piroxicam release. The in vivo anti-inflammatory activity of the floating beads resulted prolonged up to 48 h, compared to standard piroxicam. This formulation may be proposed to treat chronic inflammatory-diseases in elderly patients, needing a rapid onset of drug action followed by a maintenance dose.
开发了一种载有吡罗昔康的胃滞留递送系统,其在胃肠道中具有双模式释放特征。吡罗昔康具有口服吸收高、半衰期长的特点,但在老年患者中其消除受到损害。为了克服血浆水平的波动,使用制粒法制造了具有持续释放特性的漂浮胃滞留凝胶珠。珠基质被设计为基于海藻酸钠、ALM-果胶和羟丙基甲基纤维素的中空/多聚合物系统。本研究研究了能够影响颗粒微观结构、中空内部结构、漂浮性能和在胃肠道中药物释放特征的变量。胃滞留配方(F4)作为一种漂浮系统,能够提供所需的双模式药物释放模式,控制和延迟体外吡罗昔康的释放。与标准吡罗昔康相比,漂浮珠的体内抗炎活性延长至 48 小时。这种配方可用于治疗需要快速起效药物作用后维持剂量的老年患者的慢性炎症性疾病。