胃内浮力制剂的制备与评价。

Drug design and delivery Pub Date : 1989-03-01
Y Machida, K Inouye, T Tokumura, M Iwata, T Nagai
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引用次数: 0

摘要

介绍了两种浮在胃液中的药物制剂的设计和制备。一种是浮力片剂,由粉末状大豆蛋白、药物和碳酸氢钠组成。另一种是由药物膜、含碳酸氢钠的气泡膜和外药物释放调节膜组成的层压膜型制剂。以酸溶性药物肉桂碱为模型药物,采用羧乙烯基聚合物、乙基纤维素和羟丙基纤维素制备膜。两种制剂在体外酸性溶出试验介质中均表现出良好的浮力和缓释性能。在一项用比格犬进行的吸收研究中,口服浮力片剂或薄膜型制剂24小时后仍可在血液中发现肉桂碱。将含有硫酸钡的类似浮力片剂口服给一名健康志愿者,经x线摄影证实,片剂漂浮了近三个小时。
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Preparation and evaluation of intragastric buoyant preparations.

The design and preparation of two drug formulations which float in gastric juice are described. One, a buoyant tablet, consisted of powdered soybean protein, drug and sodium bicarbonate. The other, a laminated film-type preparation, consisted of a drug film, an effervescing film containing sodium bicarbonate and outer drug release regulating films. Cinnarizine, an acid-soluble drug, was chosen as model drug, and carboxyvinyl polymer, ethyl cellulose and hydroxypropyl cellulose were used in the preparation of the films. Both formulations showed favorable buoyancy in an in vitro acidic dissolution test medium and also sustained release properties. In an absorption study using beagle dogs, cinnarizine was found in the blood even 24 hr after oral administration of the buoyant tablet or film-type preparation. Similar buoyant tablets containing barium sulfate were administered orally to a healthy volunteer, and it was confirmed by roentgenography that the tablets floated for almost three hours.

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