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1)  apparent drug loading
表观载药量
2)  drug loading
载药量
1.
Determination of Entrapment Efficiency and Drug Loading of Brucine Solid Lipid Nanoparticles Lyophilized Powder by HPLC
HPLC法测定马钱子碱固脂纳米粒冻干粉的包封率和载药量
2.
The diameter,entrapment efficiency,drug loading, zeta potential and stability of DT-13-SLN were investigated.
方法:以乳化-蒸发法制备DT-13-SLN,通过正交设计优化处方和制备工艺条件,测定其粒径、zeta电位、药物包封率和载药量,以透射电镜观察纳米粒形态,并考察DT-13-SLN的稳定性,对DT-13-SLN的冻干粉进行差示扫描量热(DSC)分析,以确定DT-13-SLN的生成。
3.
The orthogonal test design by adopting the standard of drug encapsulation efficiency and drug loading was applied to obtain the optimal formulation of the microcapsula.
以药物的包封率和载药量作为制备工艺优化指标,通过正交试验得出微囊的最优处方。
3)  loading capacity
载药量
1.
Their properties including size,Zeta potential,microcosmic morphology,loading capacity and stability were investigated by photon correlation spectroscopy(PCS),Z.
NLC作为ATRA的药物载体,载药量提高到146。
2.
Drug loading capacity was analyzed by agarose gel electrophoresis.
方法 逆相蒸发法制备 3种不同的空白脂质体 ,与反义寡核苷酸混合得到复合物 ,显微镜观察其形态 ,琼脂糖电泳分析载药量 ,流式细胞仪测定阳性细胞百分率和平均荧光强度。
4)  Loading quantity
载药量
1.
The complex efficiency and loading quantity were determined using ultraviolet spectrophotometry.
方法:采用筛分法测定微囊粒径,紫外分光光度法测定微囊的包封率及载药量,恒重法测定微囊中的含水量。
5)  drug-loading
载药量
1.
Optimization of preparation and formulation was accomplished by evaluating the drug-loading amounts and the entrapment efficiency of luteolin liposomes.
方法采用薄膜分散法和冻干工艺进行木犀草素脂质体制备,并以载药量、包封率为评价指标,优化制备处方和工艺。
6)  inscription [英][ɪn'skrɪpʃn]  [美][ɪn'skrɪpʃən]
药量记载
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