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Biopharmaceutics & Drug Disposition is a peer-reviewed journal published by Wiley, covering Drug Transport and Resistance Mechanisms, Pharmacogenetics and Drug Metabolism, Antibiotics Pharmacokinetics and Efficacy.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Biopharmaceutics & Drug Disposition 12 (3): 45–58.
Formats any DOI in Biopharmaceutics & Drug Disposition style. No sign-up. |
| Publishes research in | Drug Transport and Resistance Mechanisms Pharmacogenetics and Drug Metabolism Antibiotics Pharmacokinetics and Efficacy Analytical Methods in Pharmaceuticals Pharmacological Effects and Toxicity Studies |
| ISSN | 0142-2782 |
| Citation impact (2-yr) | 1.4 |
| h-index | 79 |
| i10-index | 1,242 |
| Total citations | 45,535 |
| Article processing charge | $3,450 |
| Top institutions publishing here | Seoul National University |
| Journal website | onlinelibrary.wiley.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
In addition to metabolic differences, the anatomical, physiological, and biochemical differences in the gastrointestinal (G.I.) tract of the human and common laboratory animals can cause significant variation in drug absorption from the oral route. Among the physiological factors, pH, bile, pancreatic juice, and mucus and fluid volume and content can modify dissolution rates, solubility, transit…
Relative plasma, brain and cerebrospinal fluid (CSF) exposures and unbound fractions in plasma and brain were examined for 18 proprietary compounds in rats. The relationship between in vivo brain-to-plasma ratio and in vitro plasma-to-brain unbound fraction (fu) was examined. In addition, plasma fu and brain fu were examined for their relationship to in vivo CSF-to-plasma…
Organic anion transporting polypeptide (OATP) family transporters accept a number of drugs and are increasingly being recognized as important factors in governing drug and metabolite pharmacokinetics. OATP1B1 and OATP1B3 play an important role in hepatic drug uptake while OATP2B1 and OATP1A2 might be key players in intestinal absorption and transport across blood-brain barrier of drugs,…
Sodium glucose cotransporter 2 (SGLT2) inhibitors have been reported to lower the serum uric acid (SUA) level. To elucidate the mechanism responsible for this reduction, SUA and the urinary excretion rate of uric acid (UE(UA)) were analysed after the oral administration of luseogliflozin, a SGLT2 inhibitor, to healthy subjects. After dosing, SUA decreased, and a…
