Ramesh Sreela, Zvoníček Vít, Pěček Daniel, Pišlová Markéta, Beránek Josef, Hofmann Jiří, Dumicic Aleksandra
Zentiva, k.s., U Kabelovny 130, 10237 Prague, Czech Republic.
Pharmaceutics. 2025 Jan 25;17(2):161. doi: 10.3390/pharmaceutics17020161.
: Omeprazole undergoes degradation in acidic conditions, which makes it unstable in low pHs found in the gastric environment. The vast majority of already marketed omeprazole formulations use enteric polymer coatings to protect the drug from exposure to acidic pH in the stomach, allowing for drug release in the small intestine where the pH is higher. This study aimed to explore the technical aspects of using stomach acid neutralizers as an alternative to polymeric coatings for omeprazole. : After evaluating various neutralizers, magnesium oxide and sodium bicarbonate were chosen to be incorporated into capsules containing omeprazole, which then underwent in vitro dissolution testing to assess their ability to maintain optimal pH levels and ensure appropriate dissolution kinetics. Hygroscopicity and chemical stability of the selected formulation were tested to prove pharmaceutical quality of the product. An in vivo pharmacokinetic study was conducted to demonstrate the efficacy of the omeprazole-sodium bicarbonate formulation in providing faster absorption in humans. : Sodium bicarbonate was selected as the most suitable antacid for ensuring omeprazole stabilization. Its quantity was optimized to effectively neutralize stomach acid, facilitating the rapid release and absorption of omeprazole. In vitro studies demonstrated the ability of the formulation to neutralize gastric acid within five minutes. In vivo studies indicated that maximum concentrations of omeprazole were achieved within half an hour. The product met the requirements of pharmaceutical quality. : An easily manufacturable, fast-absorbing oral formulation was developed as an alternative to enteric-coated omeprazole.
奥美拉唑在酸性条件下会发生降解,这使其在胃环境中低pH值时不稳定。绝大多数已上市的奥美拉唑制剂使用肠溶聚合物包衣来保护药物免受胃酸pH值的影响,使药物在pH值较高的小肠中释放。本研究旨在探索使用胃酸中和剂替代奥美拉唑聚合物包衣的技术方面。
在评估了各种中和剂后,选择氧化镁和碳酸氢钠加入含有奥美拉唑的胶囊中,然后进行体外溶出度测试,以评估它们维持最佳pH值水平并确保适当溶出动力学的能力。对所选制剂的吸湿性和化学稳定性进行了测试,以证明产品的药学质量。进行了一项体内药代动力学研究,以证明奥美拉唑-碳酸氢钠制剂在人体中提供更快吸收的功效。
碳酸氢钠被选为确保奥美拉唑稳定的最合适抗酸剂。对其用量进行了优化,以有效中和胃酸,促进奥美拉唑的快速释放和吸收。体外研究表明该制剂在五分钟内具有中和胃酸的能力。体内研究表明,半小时内达到了奥美拉唑的最大浓度。该产品符合药学质量要求。
开发了一种易于制造、吸收迅速的口服制剂,作为肠溶包衣奥美拉唑的替代品。