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亚洲龙蒿提取物DA-9601的胃内滞留漂浮型胃滞留片在比格犬体内的胃内滞留及胃保护作用

In vivo gastric residence and gastroprotective effect of floating gastroretentive tablet of DA-9601, an extract of Artemisia asiatica, in beagle dogs.

作者信息

Kim Jeong Soo, Cha Kwang Ho, Kang Seung Yeob, Won Donghan, Jang Sun Woo, Son Miwon, Son Moon Ho, Choi Ho Jung, Lee Young Won, Kang Myung Joo

机构信息

Dong-A Pharmaceutical Co. Ltd., Giheung-gu, Yongin, Gyeonggi, South Korea.

College of Veterinary Medicine and Research Institute of Veterinary Medicine, Chungnam National University, Daejeon, South Korea.

出版信息

Drug Des Devel Ther. 2016 Jun 9;10:1917-25. doi: 10.2147/DDDT.S102918. eCollection 2016.

Abstract

OBJECTIVE

DA-9601, an extract of Artemisia asiatica containing eupatilin and jaceosidin as active compounds, has been prescribed to treat gastritis in Asia. In recent times, sustained-release, floating gastroretentive (GR) tablets of DA-9601 are available on the market. In the present study, the physical properties and in vitro drug release profile, in vivo gastric residence time, and gastroprotective effect of GR tablet were compared to those of immediate release (IR) tablets of DA-9601.

METHOD

In vitro buoyancy behavior (floating lag time and duration) and release profile of eupatilin were assessed in acidic medium. The in vivo intragastric behaviors of the barium sulfate-loaded IR and GR tablets were evaluated in beagle dogs by radiographic studies. Local gastroprotective effect was compared in an experimentally induced gastric lesion in beagle dogs after oral administration of IR (three times per day) or GR (twice daily) tablets for 15 days.

RESULTS

Upon contact with gastric juice, a low-density floating tablet (apparent density of 0.93 g/cm(3)) was buoyant on the medium and was upheld for 14 hours, providing sustained drug release profile, whereas the IR tablet disintegrated within 10 minutes, showing complete drug release within 2 hours. In vivo radiographic studies showed that the GR tablet was retained for >4 hours in the stomach. Both DA-9601 formulations remarkably alleviated gastric mucosal injury compared to placebo group, when observed by gastric endoscopy.

CONCLUSION

Twice-daily GR tablets exhibited a prolonged gastric residence time and a remarkable mucosal restoration effect in animal models. Therefore, the GR system of DA-9601 could be a substitute dosage form for the treatment of gastritis, while reducing the dosing frequency and thus improving patient compliance.

摘要

目的

DA - 9601是一种亚洲龙蒿提取物,含有紫铆亭和香叶木素作为活性成分,在亚洲已被用于治疗胃炎。近年来,DA - 9601的缓释、胃内滞留(GR)片已上市。在本研究中,将GR片的物理性质、体外药物释放曲线、体内胃滞留时间和胃保护作用与DA - 9601的速释(IR)片进行了比较。

方法

在酸性介质中评估紫铆亭的体外漂浮行为(漂浮滞后时间和持续时间)和释放曲线。通过射线照相研究在比格犬中评估硫酸钡负载的IR片和GR片的体内胃内行为。在比格犬实验性诱导的胃损伤中,比较口服IR片(每日三次)或GR片(每日两次)15天后的局部胃保护作用。

结果

与胃液接触后,低密度漂浮片(表观密度为0.93 g/cm³)在介质上漂浮并维持14小时,提供持续的药物释放曲线,而IR片在10分钟内崩解,在2小时内显示完全药物释放。体内射线照相研究表明,GR片在胃中保留超过4小时。通过胃镜观察,与安慰剂组相比,两种DA - 9601制剂均显著减轻了胃黏膜损伤。

结论

每日两次的GR片在动物模型中表现出延长的胃滞留时间和显著的黏膜修复作用。因此,DA - 9601的GR系统可以作为治疗胃炎的替代剂型,同时减少给药频率,从而提高患者依从性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8b5/4907637/3367327a8837/dddt-10-1917Fig1.jpg

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