Kanke M, Koda K, Koda Y, Katayama H
Fukuyama University, Faculty of Pharmacy and Pharmaceutical Sciences, Hiroshima, Japan.
Pharm Res. 1992 Mar;9(3):414-8. doi: 10.1023/a:1015811523426.
To study the use of curdlan, a natural beta-1,3-glucan, in drug delivery, in vitro release studies were carried out with curdlan tablets containing theophylline. Tablets were readily prepared by compressing three different curdlan and theophylline mixtures, namely, a physical mixture, spray-dried curdlan particles with theophylline powder, and spray-dried particles of curdlan/theophylline solution. Drug release from the tablets prepared from spray-dried particles of curdlan/theophylline was lowest. The release rate was constant from 1 to 8 hr, and 59% cumulative release was obtained at 8 hr. Drug release from curdlan tablets was unaffected by pH or various ions; these curdlan tablets might also control drug release in vivo after oral administration. Application of Higuchi's equation indicated that drug release from curdlan tablets was diffusion-controlled. The release profiles of the curdlan tablets were compared to those of a commercial theophylline sustained-release tablet.
为研究天然β-1,3-葡聚糖凝胶多糖在药物递送中的应用,对含茶碱的凝胶多糖片剂进行了体外释放研究。通过压制三种不同的凝胶多糖与茶碱混合物(即物理混合物、茶碱粉末与喷雾干燥凝胶多糖颗粒、凝胶多糖/茶碱溶液喷雾干燥颗粒),很容易制备出片剂。由凝胶多糖/茶碱喷雾干燥颗粒制备的片剂药物释放最低。释放速率在1至8小时内恒定,8小时时累积释放率为59%。凝胶多糖片剂的药物释放不受pH值或各种离子的影响;这些凝胶多糖片剂口服给药后在体内也可能控制药物释放。应用 Higuchi 方程表明,凝胶多糖片剂的药物释放受扩散控制。将凝胶多糖片剂的释放曲线与市售茶碱缓释片剂的释放曲线进行了比较。