Artursson P, Edman P, Sjöholm I
J Pharmacol Exp Ther. 1984 Dec;231(3):705-12.
Dextranase was entrapped in polyacryl starch microspheres of different compositions by emulsion polymerization. After i.v. injection in mice and rats, the particles were removed from the blood circulation by macrophages of the reticuloendothelial system. In these cells, the particles are accumulated in the lysosomes. The degradation of different 14C-labeled microparticles and their entrapped dextranase was followed in an isolated lysosomal fraction in vitro and in liver and spleen after i.v. injection in mice. The duration of entrapped dextranase in vivo was followed directly, i.e., by an enzyme assay, and indirectly by following the decrease of a stored material, [3H]dextran in the liver. The degradation of the entrapped enzyme was dependent on the composition of the particle matrix. More cross-linked spheres could better protect the entrapped enzyme in vitro and in vivo. The half-life of free dextranase in the lysosomal fraction was estimated to be about 4 hr, whereas the duration of entrapped dextranase in the liver was at least 48 hr, as measured with [3H]dextran. Finally, the effect of entrapped and free dextranase on an artificially induced storage disease was studied. The stored [3H]dextran was eliminated completely when dextranase was used in microparticles, whereas free dextranase had no effect in vivo.
通过乳液聚合将葡聚糖酶包封在不同组成的聚丙烯淀粉微球中。给小鼠和大鼠静脉注射后,网状内皮系统的巨噬细胞将这些颗粒从血液循环中清除。在这些细胞中,颗粒聚集在溶酶体中。在体外分离的溶酶体组分中以及给小鼠静脉注射后在肝脏和脾脏中,追踪不同的14C标记微颗粒及其包封的葡聚糖酶的降解情况。体内包封的葡聚糖酶的持续时间通过酶测定直接追踪,即通过酶测定,并且通过追踪肝脏中储存物质[3H]葡聚糖的减少间接追踪。包封酶的降解取决于颗粒基质的组成。更多交联的球体在体外和体内能更好地保护包封的酶。溶酶体组分中游离葡聚糖酶的半衰期估计约为4小时,而用[3H]葡聚糖测量时,肝脏中包封的葡聚糖酶的持续时间至少为48小时。最后,研究了包封的和游离的葡聚糖酶对人工诱导的储存疾病的影响。当在微粒中使用葡聚糖酶时,储存的[3H]葡聚糖被完全消除,而游离葡聚糖酶在体内没有作用。