机制(生物学)
化学
药品
动作(物理)
剂型
动力学
色谱法
活性成分
药物输送
作用机理
控制释放
材料科学
药理学
微晶纤维素
业务
毒品携带者
医学
生物化学
哲学
物理
认识论
量子力学
体外
标识
DOI:10.1002/jps.2600521210
摘要
Theoretically expected rates of release of solid drugs incorporated into solid matrices have been derived for several model systems. Mathematical relations have been obtained for cases (a) where the drug particles are dispersed in a homogeneous, uniform matrix which acts as the diffusional medium and (b) where the drug particles are incorporated in an essentially granular matrix and released by the leaching action of the penetrating solvent. Release from both planar surface and a sphere is considered. The unidimensional release rates are shown to follow our earlier equation derived for release from ointment bases. Release rates from spherical pellets by both model mechanisms are shown not to follow first‐order relationships. The analyses suggest that for the latter system the time required to release 50 per cent of the drug would normally be expected to be approximately 10 per cent of that required to dissolve the last trace of the solid drug phase in the center of the pellet.
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