载药量 meaning in Chinese
drug-loading rate
Examples
- When optimized , the drug - loaded plga / pla nanoparticles contain as much as 2 . 5 % haloperidol
在最优条件下， plga / pla纳米粒载药量可高达2 . 5 %氟哌啶醇。 - The effects of different drug loadings on the drug release rate were simulated and compared with other data to validate this model
模拟不同载药量对药物释放速率的影响并与其它数据进行比较，以此来验证此模型。 - Such a result suggested that polylactide - garfted copolymer of - cyclodextrin would be a carrier of drug delivery system for peptides and proteins with high loading capacity
因此， p一环糊精及其聚乳酸接枝共聚物有望用作肤类药物释放体系的载体，并可能达到较高的载药量。 - The drug content of these nanoparticles is controlled by reducing the diffusion of the drug from the organic to the aqueous phase during the solvent evaporation stage of the preparation and by increasing the drug ? polymer interactions
通过减少制备过程中溶剂挥发时药物从有机相向水相的扩散及通过增加药物-聚合物间相互作用来控制纳米粒的载药量。 - Clsm , afm and tem testified the deposition of these drugs and the experiments carried out in ( 1 ) different initial incubation concentration , ( 2 ) different temperature , ( 3 ) different nacl concentration and ( 4 ) different ph revealed that the drugs have a relative high deposition efficiency in the high initial incubation concentration , high temperature , high nacl concentration and high ph environment , and relatively stable release properties in the low initial incubation concentration , low temperature , high nacl concentration and low ph environment
在( 1 )不同初始浓度、 ( 2 )不同温度、 ( 3 )不同盐浓度和( 4 )不同ph值下对模型药物rdb和抗癌药物dnr沉积和释放的研究发现高初始浓度、高温、高盐和高ph值环境下有利于药物的沉积；而低初始载药量、低温、高盐和低ph值环境下，沉积后的药物则具有相对平缓的释放性能。