Wieland-Berghausen Susanne, Schote Uwe, Frey Michaela, Schmidt Friederike
Novartis Animal Health Inc, PO Box CH-4002, Basel, Switzerland.
J Control Release. 2002 Dec 13;85(1-3):35-43. doi: 10.1016/s0168-3659(02)00269-9.
In this investigation, the water-soluble drugs nitenpyram and clomipramine HCl were encapsulated using coacervation, solvent evaporation and film-coating. The effect of different process factors on the encapsulation efficiency and the release profile of the microparticles was evaluated. For coacervation it was shown that the core to wall ratio was the most important factor. For solvent evaporation using an w/o emulsion the type and concentration of the surfactant were the most important parameters for a successful encapsulation. Additionally the coated material was tested for its stability under different conditions as a powder or compressed into tablets. It could clearly be demonstrated that the coated drug substance exhibited a better stability then the uncoated material. The particles prepared by film-coating showed the best stability.
在本研究中,使用凝聚法、溶剂蒸发法和薄膜包衣法对水溶性药物烯啶虫胺和盐酸氯米帕明进行了包封。评估了不同工艺因素对微粒包封效率和释放曲线的影响。对于凝聚法,结果表明核壁比是最重要的因素。对于使用水包油乳液的溶剂蒸发法,表面活性剂的类型和浓度是成功包封的最重要参数。此外,还测试了包衣材料作为粉末或压制成片剂在不同条件下的稳定性。可以清楚地证明,包衣药物比未包衣材料表现出更好的稳定性。通过薄膜包衣制备的颗粒表现出最佳的稳定性。