CAJ | 학술논문

　　背景：与传统的给药方法相比，药物微囊系统可以控制药物的释放，具有良好的靶向性和生物相容性，可将药物浓聚在病灶组织，在临床上起到巨大作用。目的：将不同囊材与明胶复凝聚制备达卡巴嗪磁性微囊(以下简称磁性微囊)，探讨最佳囊材及制备工艺。方法：采用化学共沉淀法制备Fe3O4结果与结论：溶液复凝聚法好于乳液复凝聚法，采用溶液复凝聚法制备磁性微囊较好的囊材是明胶-海藻酸钠，药物包埋率37.90%，收率72.31%，平均磁化强度8.53 emu/g，其次是明胶-壳聚糖。单凝聚法囊材明胶好于壳聚糖，药物包埋率51.58%、收率64.50%、平均磁化强度6.93 emu/g。单凝聚法制备工艺优于复凝聚法。磁性材料。采用溶液复凝聚法分别制备明胶-阿拉伯胶磁性微囊、明胶-海藻酸钠磁性微囊、明胶-羧甲基纤维素钠磁性微囊、明胶-壳聚糖磁性微囊；再分别采用乳液复凝聚法制备明胶-阿拉伯胶磁性微囊、明胶-海藻酸钠磁性微囊、明胶-羧甲基纤维素钠磁性微囊、明胶-壳聚糖磁性微囊；采用单凝聚法分别制备明胶及壳聚糖磁性微囊。以微囊的包埋率、磁化率、微囊尺寸和释放性能为评价指标，确定磁性微囊的最佳制备工艺。
　　배경：여전통적급약방법상비，약물미낭계통가이공제약물적석방，구유량호적파향성화생물상용성，가장약물농취재병조조직，재림상상기도거대작용。목적：장불동낭재여명효복응취제비체잡파진자성미낭(이하간칭자성미낭)，탐토최가낭재급제비공예。방법：채용화학공침정법제비Fe3O4결과여결론：용액복응취법호우유액복응취법，채용용액복응취법제비자성미낭교호적낭재시명효-해조산납，약물포매솔37.90%，수솔72.31%，평균자화강도8.53 emu/g，기차시명효-각취당。단응취법낭재명효호우각취당，약물포매솔51.58%、수솔64.50%、평균자화강도6.93 emu/g。단응취법제비공예우우복응취법。자성재료。채용용액복응취법분별제비명효-아랍백효자성미낭、명효-해조산납자성미낭、명효-최갑기섬유소납자성미낭、명효-각취당자성미낭；재분별채용유액복응취법제비명효-아랍백효자성미낭、명효-해조산납자성미낭、명효-최갑기섬유소납자성미낭、명효-각취당자성미낭；채용단응취법분별제비명효급각취당자성미낭。이미낭적포매솔、자화솔、미낭척촌화석방성능위평개지표，학정자성미낭적최가제비공예。
BACKGROUND:Compared with conventional medications, drug micro-capsule system can control the release of drugs and have wel target properties and biocompatibility. The drugs can be concentrated at the focus and play an important role in clinic. OBJECTIVE:To prepare dacarbazine magnetic micro-capsules with different capsule materials and gelatin complex by coacervation, and to optimize capsule materials and preparation process. METHODS:Fe 3 O 4 RESULTS AND CONCLUSION:The solution complex coacervation method was better than the emulsion coacervation method. As for the solution complex coacervation method, the optimal capsule material was gelatin-sodium alginate, with drug embedding rate 37.90%, the yield rate 72.31%, and the average magnetization intensity 8.53 emu/g. The second material was gelatin-chitosan. As a capsule material, the gelatin was better than chitosan with single coagulation method. Drug embedding rate was 51.58%, the yield rate was 64.50%, and the average magnetization was 6.93 emu/g. Single coagulation method was better than coacervation method. complex coacervation, we prepared the gelatin-Arabic gum magnetic micro-capsule, gelatin-sodium alginate magnetic micro-capsules, gelatin-sodium carboxymethyl cel ulose magnetic micro-capsules, and gelatin-chitosan magnetic micro-capsules. With the emulsion complex coacervation method, we further prepared the gelatin-Arabic gum magnetic micro-capsule, gelatin-sodium alginate magnetic micro-capsules, gelatin-sodium carboxymethyl cel ulose magnetic micro-capsules, and gelatin-chitosan magnetic micro-capsules. The magnetic gelatin micro-capsules and magnetic chitosan micro-capsules were prepared with single coagulation method. The micro-capsules were determined for the embedding rate, the magnetic susceptibility, the micro-capsule size and the release performance, to define the optimal preparation technology of dacarbazine magnetic micro-capsules.