Biopharmaceutics & Drug Disposition

雜志介紹

Biopharmaceutics & Drug Disposition雜志介紹

《Biopharmaceutics & Drug Disposition》是一本以English為主的混合獲取國際優秀期刊，中文名稱生物制藥與藥物處置，本刊主要出版、報道醫學-PHARMACOLOGY & PHARMACY領域的研究動態以及在該領域取得的各方面的經驗和科研成果，介紹該領域有關本專業的最新進展，探討行業發展的思路和方法，以促進學術信息交流，提高行業發展。該刊已被國際權威數據庫SCIE收錄，為該領域相關學科的發展起到了良好的推動作用，也得到了本專業人員的廣泛認可。該刊最新影響因子為1.7，最新CiteScore 指數為3.6。

本刊近期中國學者發表的論文主要有：

• Effect of high uric acid on the disposition of metformin: in vivo and in vitro studies.

  Author: Zhang G¹, Ma Y¹, Xi D², Rao Z¹, Sun X^1,3, Wu X¹.

• TGF-β1 elevates P-gp and BCRP in hepatocellular carcinoma through HOTAIR/miR-145 axis.

  Author: Kong J¹, Qiu Y¹, Li Y¹, Zhang H¹, Wang W¹.

• Investigating the bioavailabilities of olerciamide A via the rat's hepatic, gastric and intestinal first-pass effect models.

  Author: Zhao C¹, Ying Z², Hao D¹, Zhang W¹, Ying X¹, Yang G².

• Mechanistic study of absorption and first-pass metabolism of GL-V9, a derivative of wogonin.

  Author: Xing H¹, Ren C¹, Kong Y¹, Ning C¹, Kong D¹, Zhang Y¹, Zhao D¹, Li N¹, Wang Z¹, Chen X¹, Lu Y¹.

英文介紹

Biopharmaceutics & Drug Disposition雜志英文介紹

Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes:

- animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites,

- in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man

- studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition,

- simulation and modeling in drug discovery and development

- theoretical treatises

- includes themed issues and reviews

and exclude manuscripts on

- bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation

- analytical methods