药物的

The transporters play important roles in drug absorption, distribution and excretion, and lead to consequences for interindividual differences in disposition kinetics, interaction profiles of clinical drugs, susceptibility to side effects and treatment efficacy.

参与药物跨膜转运的转运体功能受影响，将可能导致诸多临床药物的疗效、毒副作用甚至药物相互作用的发生。

Howerer, solid dispersion is one of the technologies of increasing the bioavailability of indissolvable drug, which force drug being at high disperdion state, Generally, drug particle diameter in solid dispersions was 0.001～0.1um, mainly dispersed condition was molecularity, metastable amorphism and colloidal state.

而固体分散体是增加难溶性药物的生物利用度的常用方法之一，其主要是使难溶性药物在水溶性载体中处于高度分散状态，一般而言，药物在固体分散体中的粒径为0.001～0.1μm，分散状态以分子状态、亚稳定态及无定形态或胶体状态多见。

Will amino acid introduces in fighting tumor medicaments element, can raise its to be opposite of tumor cell alternative, thing of antidote of the fat dissolve sex that enhances medicaments, delay is right cellular noxiousness.

将氨基酸引入抗肿瘤药物分子中，可以提高其对肿瘤细胞的选择性，增强药物的脂溶性、缓解药物对细胞的毒性等。

In this paper, the micronization of phytosterol particles is researched by the RESS (rapid expansion of supercritical solutions) process.

通过药物颗粒的微细化，降低其粒度，增大比表面积，进而提高药物颗粒的溶解度，可以有效地改善难溶药物的生物利用度。

It is a leading publication in psychopharmacology offering a wide range of articles reporting on clinical trials and studies,side effects,drug interactions,overdose management, pharmacogenetics,pharmacokinetics,and psychiatric effects of non-psychiatric drugs.

这是一份在精神药理学领域的领头刊物，它刊登文章的范围很广，包括临床试验和研究、副作用、药物相互作用、过量管理、遗传药理学、药物动力学以及非治疗精神病药物的精神病治疗效果等。

Tp the time required for one-half of the atoms in a group of radioactive atoms to decay.

放射性药物radiopharmaceuticals是指药物的本身含有放射性核素，用于人体疾病的诊断与治疗的特殊药物。

"Many patients who had lost their response to the drug benefited from re-treatment at intervals shorter than every eight weeks," Hanauer says.

Hanauer说：「很多使用这种药物的患者，在使用这种药物不产生治疗效果后，通过一段少于8周的停药期，可以再次恢复对这种药物治疗的反应。

CYP and P-gp mediated PP-CD interactions and the research methods have been discussed in this review.

本文综述了药物代谢酶CYP及药物转运蛋白P-gp介导的植物制剂—化学药物的相互作用及常用的研究方法。

There were a certain relationship between haemoconcentration and tess score（p.05）,tess score influence male sexual function.conclusion:within a certain chloropromazine ＆clozapine haemoconcentration,higher haemoconcentration,higher impairment to sexual function,there were significant relationship between haemoconcentration and sexual function;also severely side effect with the haemoconcentration higher,there were a certain relationship between haemoconcentration and side effect,side effect also influence male sexual function.

药物血浓度与tess评分呈现一定相关性（p.05），对性功能产生影响(p.05)。结论：氯丙嗪、氯氮平的药物在一定范围内血浓度越高，对男性性功能影响越大，呈现显著正相关；而药物的副反应随血药浓度递增而增大，显现出一定的正相关性，对性功能产生一定影响。

In 2004, for example, the US Food and Drug Administration issued new guidelines on botanical drugs that made it much easier to get extracts into clinical trials if there was some history of prior use, and that obviated the need to characterize all compounds in an extract.

例如，2004年美国国家食品和药物监督局修改了对草本药物的标准，使得有应用历史记录的草本药物提取物更容易进入临床实验。而且这消除了对草药提取物中所有成分都要进行检测的规定。

Plunder melds and run with this jewel!

掠夺melds和运行与此宝石！

My dream is to be a crazy growing tree and extend at the edge between the city and the forest.

此刻，也许正是在通往天国的路上，我体验着这白色的晕旋。