摘要
研究药物在胃肠道的吸收程度和转运机制对于口服药物的剂型设计具有指导性作用。药物吸收和转运的研究模型分为物化模型（物化参数）和生物学模型（亚细胞片段、细胞、游离组织和器官）。
That is indicators to investigate the absorption and transit of drug in gastrointestinal tract for designing oral dosage . The models of absorption and transit are included physical chemical model and biological model (subcellular fraction, cell, isolated tissue, organ). The benefits and errors of the models were reviewed.
出处
《药学进展》
CAS
1998年第2期93-96,共4页
Progress in Pharmaceutical Sciences
