Rump Adrian, Tetyczka Carolin, Littringer Eva, Kromrey Marie-Luise, Bülow Robin, Roblegg Eva, Weitschies Werner, Grimm Michael
Institute of Pharmacy, Biopharmaceutics and Pharmaceutical Technology, University of Greifswald, 17489 Greifswald, Germany.
Institute of Pharmaceutical Sciences, Pharmaceutical Technology and Biopharmacy, University of Graz, 8010 Graz, Austria.
Mol Pharm. 2023 Mar 6;20(3):1624-1630. doi: 10.1021/acs.molpharmaceut.2c00835. Epub 2023 Jan 27.
Gastroretentive dosage forms are intended to stay inside the stomach for a long period of time while releasing an active pharmaceutical ingredient. Such systems may offer significant benefits for numerous drugs compared to other sustained release systems, such as improved pharmacokinetics/bioavailability and reduced intake frequency and thereby improved adherence to the medical therapy. However, there is no gastroretentive product on the market with proven reliable gastroretentive properties in humans. A major obstacle is the motility pattern of the stomach in the fasting state in humans, which reliably ensures gastric emptying of even large indigestible objects into the small intestine. One promising approach to avoid gastric emptying is adhesion of the drug delivery system to the gastric mucosa. In order to achieve mucoadhesive properties, minitablets containing Carbopol 71G NF were developed and compared to minitablets without adhesive properties. In a specialized mucoadhesive test system, the adhesion time was prolonged for adhesive minitablets (240 min) compared to non-adhesive minitablets (30 min). The in vivo transit behavior was investigated using magnetic resonance imaging in 11 healthy volunteers in fasted state in a crossover setup. It was found that the gastric residence time (GRT) of the adhesive minitablets (median of 37.5 min with IQR = 22.5-52.5) was statistically significantly prolonged compared to the non-adhesive minitablets (median of 7.5 with IQR = 7.5-22.5), indicating a delay in gastric emptying by adhesion to the gastric mucosa. However, the system needs further improvement to create a clinical benefit. Furthermore, it was observed that for 9 of 22 administrations (three minitablets were given simultaneously with every administration), the minitablets were not emptied together but showed different GRTs.
胃滞留剂型旨在长时间停留在胃内,同时释放活性药物成分。与其他缓释系统相比,此类系统可能为多种药物带来显著益处,如改善药代动力学/生物利用度、降低服药频率,从而提高对药物治疗的依从性。然而,市场上尚无经证实对人体具有可靠胃滞留特性的胃滞留产品。一个主要障碍是人类空腹状态下胃的蠕动模式,它能可靠地确保即使是大的难消化物体也能排空到小肠。一种有前景的避免胃排空的方法是使药物递送系统粘附于胃黏膜。为了实现粘膜粘附特性,研发了含有卡波姆71G NF的微型片,并与无粘附特性的微型片进行比较。在一个专门的粘膜粘附测试系统中,与非粘附微型片(30分钟)相比,粘附微型片的粘附时间延长(240分钟)。在11名处于空腹状态的健康志愿者中,采用交叉试验设计,利用磁共振成像研究了体内转运行为。结果发现,与非粘附微型片(中位数为7.5分钟,四分位距为7.5 - 22.5分钟)相比,粘附微型片的胃滞留时间(GRT)(中位数为37.5分钟,四分位距为22.5 - 52.5分钟)在统计学上显著延长,表明通过粘附于胃黏膜可延迟胃排空。然而,该系统需要进一步改进以产生临床效益。此外,还观察到在22次给药中有9次(每次给药同时给予三片微型片),微型片并非一起排空,而是显示出不同的胃滞留时间。