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ADME Processes in Pharmaceutical Sciences : Dosage, Design, and Pharmacotherapy / edited by Alan Talevi, Pablo A. Quiroga.

Springer Nature - Springer Biomedical and Life Sciences eBooks 2024 English International Available online

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Format:
Book
Author/Creator:
Talevi, Alan.
Contributor:
Quiroga, Pablo A.
Series:
Biomedical and Life Sciences Series
Language:
English
Subjects (All):
Pharmaceutical chemistry.
Pharmacology.
Toxicology.
Pharmacy.
Drugs--Design.
Drugs.
Pharmaceutics.
Structure-Based Drug Design.
Local Subjects:
Pharmaceutics.
Pharmacology.
Toxicology.
Pharmacy.
Structure-Based Drug Design.
Physical Description:
1 online resource (489 pages)
Edition:
2nd ed. 2024.
Place of Publication:
Cham : Springer Nature Switzerland : Imprint: Springer, 2024.
Summary:
The Second Edition of the ADME Processes in Pharmaceutical Sciences maintains the general structure of the first volume. The first part is dedicated to the generalities of LADME processes, including compartmental pharmacokinetics, and the second part is dedicated to burgeoning topics in the field, including pharmaceutical nanocarriers, pharmacogenomics, and pharmacokinetics of biologicals. The contents of the first edition have been kept (revised, updated and expanded) and six entirely new chapters are introduced to this second edition. American, European, and Latin American experts from both industry and academia converge in this volume intended for undergraduate and graduate Pharmacy, Medicine, and other health care careers, but also for professionals from other related fields working in relation to pharmaceuticals, such as chemists, biochemists, material scientists, bioengineers and molecular biologists. The volume is abundant in pedagogical features, including highlights, definitions, figures, tables, book recommendations, case studies and questions. ADME Processes (2nd Edition) is designed as a core textbook for pharmacology, pharmacokinetics, biopharmacy, drug design, medicinal chemistry, and pharmaceutical technology courses. .
Contents:
Part 1: The basics of ADME processes
Chapter 1-Introduction. Biopharmaceutics and Pharmacokinetics
Chapter 2-Drug release
Chapter 3-Drug Absorption
Chapter 4-Drug Distribution
Chapter 5-Drug Metabolism
Chapter 6-Drug Excretion
Chapter 7-Drug Delivery Routes
Chapter 8-Compartmental Pharmacokinetic Models
Chapter 9-Regulatory Requirements and Applications of Physiologically Based Pharmacokinetic Models
Chapter 10-Drug Drug and Food Drug Interactions of Pharmacokinetic Nature
Part 2: Specialized topics
Chapter 11-Nanocarriers: Delivery Routes
Chapter 12-Advanced Techniques for Quality Assessment of Nanocarriers
Chapter 13-Nanomedicines Obtained by Nanoprinting
Chapter 14-Absorption, Distribution, Metabolism and Excretion of Biopharmaceutical Drug Products
Chapter 15-In silico and in vitro ADME predictions
Chapter 16-Relationship Between Pharmacokinetics and Pharmacogenomics and Its Impact on Drug Choice and Dose Regimens
Chapter 17-The Relationship Between Pharmacogenomics and Pharmacokinetics and Its Impact on Drug Choice and Dosing Regimens in Pediatrics
Chapter 18-Bioavailability and Bioequivalence studies
Chapter 19-Drug transporters – Physiological role and Their Impact on Pharmacotherapy
Chapter 20-Blood Flow Distribution and Membrane Transporters As Determinant Factors Of Tissue Drug Concentration.
Notes:
Description based on publisher supplied metadata and other sources.
ISBN:
3-031-50419-4
OCLC:
1428262137

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