Quantitative Analysis of Cellular Drug Transport, Disposition, and Delivery
Aus der Reihe
Methods in Pharmacology and Toxicology
-
- Hardcover ausgewählt
- Taschenbuch
- eBook
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Sprache:Englisch
Fr. 209.00
inkl. gesetzl. MwSt.,
Beschreibung
Produktdetails
Einband
Gebundene Ausgabe
Erscheinungsdatum
08.06.2021
Abbildungen
XVII, 453 p. 109 illus., 91 illus. in color.
Herausgeber
Gus R. Rosania + weitereVerlag
Springer UsSeitenzahl
453
Maße (L/B/H)
26/18.3/3.1 cm
Gewicht
1078 g
Auflage
21001 Auflage 1st edition 2021
Sprache
Englisch
ISBN
978-1-07-161249-1
This thorough book explores some of the most important methods and concepts affecting the quantitative analysis of the transport, targeting, and disposition of chemicals within cells, which in turn impact the macroscopic pharmacokinetics of chemical agents in the whole organism. The first half of the volume focuses on small organic molecules with drug-like characteristics, while the second half delves into the cellular pharmacokinetics of biologics and other macromolecules, including peptide therapeutics, cyclotides, antibodies, as well as nanoparticles, thus creating a comprehensive treatise that approaches cellular pharmacokinetics from the different perspectives of pharmaceutical scientists, chemical biologists, medicinal chemists, and protein engineers dealing with very different chemical agents spanning a wide range of sizes, physicochemical properties, and targeting mechanisms. Written for the
Methods in Pharmacology and Toxicology
series, chapters provide the kind of key detail and expert implementation advice that leads to excellent results in the lab. Synthetic biologists, biophysicists, and bioengineers are amongst the long list of scientists who could benefit from reading this book or from using it as a textbook.
Authoritative and practical,
Quantitative Analysis of Cellular Drug Transport, Disposition, and Delivery
builds on a long history of drug development and the adding of quantitative methods at the cellular scale in order to inspire new approaches to drug development that are better able to take advantage of phenomena such as soluble-to-insoluble phase transitions or bispecific targeting, which could ultimately be exploited for the development of more effective drug delivery systems and therapeutic agents.
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