在体外溶出实验中对阿霉素磁性毫微粒体外释放性能的影响主要考察了三个因素：毫微粒平均粒径大小、毫微粒的载药量以及交联剂含量。
In the drug release kinetics investigation, influences of the content of drug, the microsphere size and the content of crossing-linker on the drug-release were studied.
在体外溶出实验中对阿霉素磁性毫微粒体外释放性能的影响主要考察了三个因素：毫微粒平均粒径大小、毫微粒的载药量以及交联剂含量。
In the drug release kinetics investigation, influences of the content of drug, the microsphere size and the content of crossing-linker on the drug-release were studied.
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