THE USE OF GELATIN MICROPARTICLES TO DELAY THE RELEASE OF READILY WATER-SOLUBLE MATERIALS

被引:13
作者
LOU, Y [1 ]
GROVES, MJ [1 ]
机构
[1] UNIV ILLINOIS,COLL PHARM,INST TUBERCULOSIS RES,CHICAGO,IL 60607
关键词
D O I
10.1111/j.2042-7158.1995.tb05758.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
adsorption of D-arabinose onto gelatin microparticles demonstrated a Langmuirian adsorption pattern. Evaluation of the dissolution behaviour of D-arabinose-loaded gelatin microparticles suggested that the saccharide, loaded at a level below the adsorption saturation level, was released uniformly over a 14-h period after the loaded gelatin microparticles had been lyophilized for a second time. When dissolution curves were corrected for the initial burst effect seen after the gelatin microparticles had been loaded at higher levels of D-arabinose and lyophilized, steady-state release rates were also evident over prolonged periods. In addition, it was evident that the D-arabinose was adsorbed onto internal surfaces of the hydrated gelatin matrix. Calculation of this internal surface demonstrated the influence of the concentration of the glutaraldehyde used as a cross-linking agent and this parameter, in turn, influenced both the adsorption maxima and the subsequent equilibrium release rates. Application of this data base to a highly water-soluble complex polysaccharide antineoplastic agent, which has a higher molecular weight (22.4 kDa vs 150 Da), demonstrated similar behaviour in that a near zero-order release pattern over at least 16 h could be obtained by attention to the conditions under which the gelatin microparticles were made and subsequently loaded before lyophilization.
引用
收藏
页码:97 / 102
页数:6
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