Mathew E, Speaker T J
Temple University School of Pharmacy, Philadelphia, PA 19140, USA.
J Microencapsul. 1998 Sep-Oct;15(5):675-80. doi: 10.3109/02652049809008249.
A series of dextran molecular weight markers were encapsulated in decylamine carboxymethylcellulose microcapsules to serve as probes of capsule retentivity. The capsules were prepared by allowing microdrops of aqueous sodium carboxymethylcellulose to fall into aqueous decylamine acetate solution. Salt exchange reaction at the droplet pseudointerface resulted in self-assembling films which essentially instantaneously enclosed the droplets. Concentrations of anionic polymer were varied in the range from 1-3%. Chromophore-bearing dextrans were incorporated into these capsules by blending the dextrans with the carboxymethylcellulose prior to the encapsulation step. Four dextrans of differing (light scattering) molecular weights were used: 2 x 10(6), 6 x 10(5), 7 x 10(4), and 1.9 x 10(4) amu. The mass balance of dextran retained in the capsules, released on washing the capsules or which escaped encapsulation was determined spectrophotometrically. To measure total dextran in a population of washed capsules, the capsules were lysed in a 0.3 M solution of sodium chloride. To monitor dextran release, washed capsules were suspended in water and dextran concentration in the supernatant was measured. Encapsulation efficiency exceeded 80% for high molecular weight dextran but was lower with the smaller dextrans.
一系列葡聚糖分子量标记物被包裹在癸胺羧甲基纤维素微胶囊中,用作胶囊保留率的探针。通过使羧甲基纤维素钠水溶液的微滴落入醋酸癸胺水溶液中来制备微胶囊。液滴假界面处的盐交换反应导致自组装膜,该膜基本上瞬间包裹住液滴。阴离子聚合物的浓度在1%-3%的范围内变化。在包封步骤之前,通过将葡聚糖与羧甲基纤维素混合,将带有发色团的葡聚糖掺入这些微胶囊中。使用了四种不同(光散射)分子量的葡聚糖:2×10⁶、6×10⁵、7×10⁴和1.9×10⁴原子质量单位。通过分光光度法测定保留在微胶囊中、在洗涤微胶囊时释放或未被包封而逸出的葡聚糖的质量平衡。为了测量一批洗涤后的微胶囊中的总葡聚糖,将微胶囊在0.3M氯化钠溶液中裂解。为了监测葡聚糖的释放,将洗涤后的微胶囊悬浮在水中,并测量上清液中的葡聚糖浓度。高分子量葡聚糖的包封效率超过80%,但较小分子量的葡聚糖的包封效率较低。