Supramolecular Synthons in Crystal Engineering of Pharmaceutical Properties
CRC Press (Verlag)
978-1-032-19611-4 (ISBN)
This comprehensive resource skillfully consolidates crystal engineering, the design of organic solids, and supramolecular synthons (i.e., structural hydrogen bond units) to achieve desired pharmaceutical properties, including solubility, dissolution, bioavailability, permeability, particle size, tableting, hydration, and mechanical strength. Covering 30 years of crystal engineering developments and pharmaceutical applications, this book will be a single and complete resource for supramolecular and structural chemists, the crystal engineering community, pharmaceutical scientists, and industrial researchers.
Key Features
Covers the fundamentals of crystal engineering and supramolecular synthons.
Details the challenges of low solubility and low permeability facing oral drug formulations.
Explains how heterosynthons provide a rational approach to address and implement solutions.
Provides case studies from academic and industrial labs to walk the reader through the actual steps.
Explores developments in the scale up and manufacture of crystal forms in pharmaceutical industry.
Ashwini Nangia (born 1960) is a senior professor of chemistry at the University of Hyderabad, India. He completed his MSc from Indian Institute of Technology Kanpur (1983) and PhD from Yale University (1988). He joined the University of Hyderabad in 1989 and was promoted to professor in 2002 and to senior professor in 2019. His research interests in crystal engineering include polymorphs, cocrystals, salts, eutectics, and amorphous forms of drugs and pharmaceuticals. He has authored more than 350 research publications, with over 18,000 citations and an h-index of 70. He is a fellow of the three premier National Science Academies of India and Royal Society of Chemistry, London. He is a recipient of the prestigious JC Bose National Fellowship. He was director of Council of Scientific and Industrial Research–National Chemical Laboratory, Pune from March 2016 to November 2020, during which time he diversified his interests to flow chemistry and process intensification in crystallization.
Chapter 1 Introduction to Supramolecular Chemistry and Crystal Engineering
1.1 Introduction
1.2 Organic synthesis
1.3 Supramolecular chemistry
1.4 Crystal engineering
1.5 Hydrogen bonding
1.6 Space groups
1.7 Summary conclusions
1.8 References
1.9 Questions and thoughts
1.10 Additional reading
Chapter 2 Crystal Engineering, Supramolecular Synthons, and Cocrystal Design
2.1 Introduction
2.2 Supramolecular synthons
2.3 Crystal engineering of pharmaceutical cocrystals
2.3.1 Cocrystals
2.3.2 Pharmaceutical cocrystals
2.4 Cocrystal design approaches
2.4.1 Hydrogen bond synthons
2.4.2 ΔpKa rule
2.4.3 Computational methods
2.4.4 Molecular electrostatic potential surface energy
2.4.5 Hansen solubility parameter
2.5 Summary conclusions
2.6 References
2.7 Questions and thoughts
Chapter 3 Pharmaceutical Solid-State Forms
3.1 Introduction
3.2 Pharmaceutical multi-component crystals
3.2.1 Drug salts and pharmaceutical cocrystals
3.2.2 Pharmaceutical cocrystals via crystal engineering
3.2.3 Coamorphous solids
3.2.4 Solid solutions and eutectics
3.2.5 Ionic liquids
3.2.6 Ionic cocrystals
3.2.7 Nanocrystalline drugs
3.2.8 Supramolecular gels of drugs
3.2.9 Salt−cocrystal continuum or hybrid quasi-state of proton
3.2.10 Cocrystal polymorphs
3.2.11 Ternary and higher organic cocrystals
3.3 Summary conclusions
3.4 References
3.5 Questions and thoughts
Chapter 4 Design and Methodology of Pharmaceutical Cocrystals
4.1 Introduction
4.2 Complementarity between API and coformer
4.3 Preparation methods of cocrystals
4.3.1 Spray drying
4.3.2 Freeze drying
4.3.3 Hot melt extrusion
4.3.4 Rotary evaporator method
4.3.5 Vapor-assisted tumbling
4.4 Drug−drug cocrystals
4.5 Drug−nutraceutical cocrystals
4.6 Ternary and higher order cocrystals
4.7 Cocrystals of different stoichiometry
4.8 Zwitterionic cocrystals
4.9 Halogen-bonded pharmaceutical cocrystals
4.10 Characterization methods of cocrystals
4.11 Summary conclusions
4.12 References
4.13 Questions and thoughts
Chapter 5 Applications of Pharmaceutical Cocrystals
5.1 Introduction
5.2 Bioavailability improvement
5.3 Hydration stability
5.4 Chemical degradation stability
5.5 Tableting
5.6 Mechanical properties
5.7 Phase diagram and solubility measurements
5.8 Permeability and plasma concentration
5.9 Spring and Parachute model
5.10 Summary conclusions
5.11 References
5.12 Questions and thoughts
Chapter 6 Continuous Manufacturing of Cocrystals and Salts
6.1 Introduction
6.2 Batch and flow chemistry
6.3 Flow chemistry and pharmaceutical cocrystals manufacturing
6.4 Case studies of pharmaceutical cocrystals and salts
6.5 Continuous process technologies
6.6 Flow guide for the synthetic chemist
6.7 Summary conclusions
6.8 References
6.9 Questions and thoughts
Chapter 7 Commercial Outlook of Pharmaceutical Cocrystals
7.1 Introduction
7.2 Present status
7.3 Patenting and regulatory aspects
7.4 Entresto® drug-drug cocrystal salt
7.5 Seglentis® US-FDA approval
7.6 Summary conclusions
7.7 References
7.8 Questions and thoughts
Chapter 8 Controlling Polymorphism
8.1 Introduction
8.2 Definition and importance
8.3 Polymorphism and cocrystallization
8.4 Tailored additives to control crystal size and morphology
8.5 Summary conclusions
8.6 References
8.7 Questions and thoughts
Chapter 9 Supramolecular Heterosynthon in High Bioavailability Drugs
9.1 Introduction
9.2 Common heterosynthons in drugs
9.3 Heterosynthon model for high bioavailability drugs
9.4 Models for permeability enhancement
9.5 Cocrystal drugs beyond the Rule of 5
9.6 Improving cell penetration by atom replacement
9.7 Summary conclusions
9.9 Questions and thoughts
Chapter 10 Other Applications of Cocrystals
10.1 Introduction
10.2 Property engineering
10.3 Mechanochemistry
10.4 Energetic cocrystals
10.5 Summary conclusions
10.6 References
10.7 Questions and thoughts
Chapter 11 AI ML ChatGPT in Chemistry
11.1 Introduction
11.2 Retrosynthetic reaction prediction
11.3 Medicinal molecules
11.4 MOFs and inorganic materials
11.5 Cocrystals
11.6 Summary conclusions
11.7 References
11.8 Questions and thoughts
Chapter 12 3D Electron Diffraction
12.1 Introduction
12.2 Advantages of ED
12.3 Resurgence of ED
12.4 New pharmaceutical challenges solved by ED
12.5 Summary conclusions
12.6 References
12.7 Questions and thoughts
Chapter 13 Challenges, Conclusions, and Future Directions
13.1 Introduction
13.2 Carboxamide−pyridine-N-oxide heterosynthon
13.3 Browsing the literature
13.4 Challenges in pharmaceutical cocrystal technology
13.5 Conclusions
13.6 References
13.7 Suggested reading
Index
| Erscheinungsdatum | 22.08.2024 |
|---|---|
| Reihe/Serie | xx xx |
| Zusatzinfo | 13 Tables, black and white; 12 Line drawings, color; 4 Line drawings, black and white; 1 Halftones, color; 1 Halftones, black and white; 106 Illustrations, color; 67 Illustrations, black and white |
| Verlagsort | London |
| Sprache | englisch |
| Maße | 156 x 234 mm |
| Gewicht | 526 g |
| Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Pharmakologie / Pharmakotherapie |
| Naturwissenschaften ► Chemie ► Organische Chemie | |
| Technik | |
| ISBN-10 | 1-032-19611-4 / 1032196114 |
| ISBN-13 | 978-1-032-19611-4 / 9781032196114 |
| Zustand | Neuware |
| Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
| Haben Sie eine Frage zum Produkt? |
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