Description
Book SynopsisThis book is the first to combine computational material science and modeling of molecular solid states for pharmaceutical industry applications.
Table of ContentsList of Contributors xiii
Preface xvii
Editor’s biography xix
1 Computational Pharmaceutical Solid‐State Chemistry: An Introduction 1
Yuriy A. Abramov
1.1 Introduction 1
1.2 Pharmaceutical Solid‐State Landscape 2
1.2.1 Some Definitions 2
1.2.2 Impact of Solid‐State Form on API and Product Properties 4
1.2.3 Challenges of Pharmaceutical Industry Related to Solid Form Selection 6
1.3 Pharmaceutical Computational Solid‐State Chemistry 8
1.4 Conclusions 9
Acknowledgment 10
References 10
2 Navigating the Solid Form Landscape with Structural Informatics 15
Peter T. A. Galek, Elna Pidcock, Peter A. Wood, Neil Feeder, and Frank H. Allen
2.1 Introduction 15
2.2 The CSD System 17
2.3 Hydrogen‐Bond Propensity: Theory and Applications to Polymorphism 18
2.3.1 Methodology 18
2.3.2 Case Study 1: Ritonavir 19
2.4 Hydrogen‐Bond Landscapes: Developing the Propensity Approach 21
2.4.1 Methodology 21
2.4.2 Case Study 2: Metastable versus Stable Form of Piroxicam 22
2.4.3 Case Study 3: Exploring the Likely Hydrogen‐Bond Landscape of Axitinib (Inlyta®) 25
2.5 Informatics‐Based Cocrystal Screening 25
2.5.1 Methodology 25
2.5.2 Case Study 4: Paracetamol 26
2.5.3 Case Study 5: AMG 517 – Sorbic Acid Cocrystal 29
2.6 Conclusions and Outlook 32
References 33
3 Theoretical Hydrogen‐Bonding Analysis for Assessment of Physical Stability of Pharmaceutical Solid Forms 37
Yuriy A. Abramov
3.1 Introduction 37
3.2 Experimental Scales of H‐Bonding Basicity and Acidity 39
3.2.1 In Solution Phase 39
3.2.2 In Solid‐State Phase 40
3.3 Theoretical Study of H‐Bonding Strength in Solution and in Solid State 40
3.3.1 Supermolecular Approach 41
3.3.2 Descriptor‐Based Approaches 41
3.3.3 Solid‐State H‐bonding Strength 42
3.4 Application to Solid Form Selection 47
3.4.1 Examples of Theoretical H‐Bonding Analysis to Support Solid Form Selection 48
3.4.2 Consideration of Limitations of Hydrogen‐Bonding Propensity Approach 50
3.5 Conclusion 52
Acknowledgment 53
References 53
4 Improving Force Field Parameters for Small‐Molecule Conformation Generation 57
Dmitry Lupyan, Yuriy A. Abramov, and Woody Sherman
4.1 Introduction 57
4.2 Methods 62
4.3 Results and Discussion 66
4.3.1 Close S⋯O Interactions 66
4.3.2 Halogen X⋯O Interactions 75
4.3.3 Generalization of the Approach to Other Interactions 77
4.3.4 An Improved OPLS Force Field (OPLS2) 80
4.4 Conclusion 81
References 82
5 Advances in Crystal Structure Prediction and Applications to Pharmaceutical Materials 87
Graeme M. Day
5.1 Introduction 87
5.1.1 Motivation 88
5.2 Crystal Structure Prediction Methodologies 89
5.2.1 Molecular Geometry 89
5.2.2 Crystal Structure Searching 99
5.2.3 Structure Ranking 102
5.3 Applications of Crystal Structure Prediction 105
5.3.1 Crystal Structure Determination 106
5.3.2 Solid Form Screening 108
5.4 Summary 110
References 110
6 Integrating Computational Materials Science Tools in Form and Formulation Design 117
Joseph F. Krzyzaniak, Paul A. Meenan, Cheryl L. Doherty, Klimentina Pencheva, Suman Luthra, and Aurora Cruz‐Cabeza
6.1 Introduction 117
6.2 From Molecule to Crystal Structure 119
6.2.1 Single Crystal Structure 120
6.2.2 Structural Analysis 120
6.2.3 Molecular Packing and HB Geometry Analyses 122
6.2.4 Full Interaction Maps 123
6.2.5 Crystal Structure Prediction 124
6.3 From Crystals to Particles 131
6.4 From Particles to Dosage Forms 134
6.4.1 Structural Investigation of Crystal Surfaces and Structure Dehydration 137
6.4.2 Structural Investigations of Crystal Surfaces and Chemical Stability 139
6.5 Conclusion 141
Acknowledgments 142
References 142
7 Current Computational Approaches at Astrazeneca for Solid‐State and Property Predictions 145
Sten O. Nilsson Lill, Staffan Schantz, Viktor Broo, and Anders Broo
7.1 Introduction 145
7.2 Polymorphism 146
7.3 Conformer Search 157
7.4 Molecular Perturbations to Achieve Solubility for GPR119 Ligands 158
7.5 Solid‐State Nuclear Magnetic Resonance and Azd8329 Case Study 163
7.6 CCDC Tools 168
7.7 Tautomerism 169
7.8 Conclusions 170
Acknowledgments 170
References 170
8 Synthonic Engineering: From Molecular and Crystallographic Structure to the Rational Design of Pharmaceutical Solid Dosage Forms 175
Kevin J. Roberts, Robert B. Hammond, Vasuki Ramachandran, and Robert Docherty
8.1 Introduction 175
8.2 The Crystal 177
8.2.1 Crystallography 177
8.2.2 Crystal Chemistry and Crystal Packing of Drug Molecules 179
8.2.3 Deconstructing the Supra‐Molecular Interactions in Bulk – Intrinsic Synthons 181
8.3 Morphology and Surface Structure 185
8.3.1 Nucleation and the Crystal Growth Process 185
8.3.2 Particle Morphology and Surface Structure 186
8.3.3 Crystal Morphology Prediction 188
8.3.4 Deconstructing the Supra‐Molecular Interactions at Surfaces – Extrinsic Synthons 190
8.3.5 Grid Searching – Probing Inter‐molecular Interactions at Surfaces and Environments 190
8.4 The Crystallisation Perspective 191
8.4.1 Nucleation, Surface Energies and Directed Polymorphism 191
8.4.2 The Impact of Solvent on Morphology 194
8.4.3 The Impact of Impurities on Morphology 196
8.5 The Drug Product Perspective 197
8.5.1 Excipient Compatibility 197
8.5.2 Inhaled Drug Delivery Design 199
8.5.3 Mechanical Properties 201
8.5.4 Dissolution 203
8.6 Summary and Future Outlook: Synthonic Engineering Particle Passport and the Future of the Drug Product Design 205
Acknowledgements 207
References 207
9 New Developments in Prediction of Solid‐State Solubility and Cocrystallization Using COSMO‐RS Theory 211
Christoph Loschen and Andreas Klamt
9.1 Introduction 211
9.2 COSMO‐RS 212
9.3 Prediction of Drug Solubility Using COSMO‐RS 215
9.4 Solubility Prediction with Multiple Reference Solvents 218
9.5 Melting Point and Fusion Enthalpy QSPR Models 221
9.6 Cocrystal Screening 225
9.7 Solvate Formation 229
9.8 Summary 231
References 231
10 Modeling and Prediction of Solid Solubility by Ge Models 235
Larissa P. Cunico, Anjan K. Tula, Roberta Ceriani, and Rafiqul Gani
10.1 Introduction 235
10.2 Framework 236
10.2.1 Thermodynamic Basis 238
10.2.2 The Necessary Property‐Related Information for Solid Solubility Prediction and the Developed Databases 238
10.2.3 SLE Thermodynamic Consistency Tests 241
10.2.4 SolventPro 252
10.3 Conclusion 259
References 260
11 Molecular Simulation Methods to Compute Intrinsic Aqueous Solubility of Crystalline Drug‐Like Molecules 263
David S. Palmer and Maxim V. Fedorov
11.1 Introduction 263
11.2 Definitions of Solubility 264
11.3 Solubility and Thermodynamics 264
11.3.1 Solubility and Free Energy of Solution 264
11.3.2 Computation of Solubility from the Thermodynamic Cycle of Solid to Supercooled Liquid to Aqueous Solution 265
11.3.3 Computation of Solubility from the Thermodynamic Cycle of Solid to Gas Phase to Aqueous Solution 267
11.4 Calculation of ΔGhyd 269
11.4.1 Implicit Continuum Solvent Models 270
11.4.2 Explicit Solvent Models: Atomistic Simulations 270
11.4.3 Explicit Solvent Models: Molecular Theories of Liquids 271
11.5 Calculation of ΔGsub 275
11.5.1 Crystal Polymorphism 275
11.5.2 Crystal Structure Prediction 275
11.5.3 Calculation of ΔGsub 276
11.5.4 Calculation of ΔHsub 276
11.5.5 Calculation of ΔSsub 277
11.5.6 Other Methods to Compute ΔGsub 278
11.6 Experimental Data 279
11.7 Conclusion and Future Outlook 280
Acknowledgments 280
References 280
12 Calculation of NMR Tensors: Application to Small‐Molecule Pharmaceutical Solids 287
Luis Mafra, Sergio Santos, Mariana Sardo, and Heather Frericks Schmidt
12.1 SSNMR Spectroscopy: A Short Introduction 287
12.2 The Chemical Shielding Tensors: Fundamentals 288
12.3 Computational Approaches to the Calculation of Chemical Shift Tensors in Solids 290
12.3.1 Cluster Approach 290
12.3.2 Periodic Approach 291
12.3.3 Pitfalls and Practical Considerations 292
12.4 NICS 294
12.5 Case Studies Combining Experimental and Computational NMR Methods 294
12.5.1 NMR Assignment of Polymorphs Aided by Computing NMR Parameters 295
12.5.2 Calculated vs Experimental Chemical Shift Tensors Using Different NMR Methods 302
12.5.3 Studying Crystal Packing Interactions 312
12.5.4 Employing Chemical Shifts for Crystal Structure Elucidation/Determination 315
12.6 Summary 325
References 326
13 Molecular Dynamics Simulations of Amorphous Systems 331
Bradley D. Anderson and Tian‐Xiang Xiang
13.1 Introduction 331
13.2 MD Simulation Methodology 332
13.3 Polymer Properties—MD Simulation Versus Experiment 334
13.3.1 Glass Transition Temperature (Tg) 334
13.3.2 Amorphous Structure and Dynamics 337
13.4 Hydrogen Bonding Patterns, Water Uptake, and Distribution in Amorphous Solids 342
13.4.1 Poly(D,L)lactide 343
13.4.2 Polyvinylpyrrolidone 345
13.4.3 Hydroxypropylmethylcellulose Acetate Succinate (HPMCAS) 347
13.4.4 Amorphous Indomethacin 350
13.5 Amorphous Drug–Polymer Blends 354
13.5.1 Molecular Interactions Probed by MD Simulation 354
13.5.2 Solubility and Miscibility Prediction 357
13.5.3 Molecular Mobility and Small‐Molecule Diffusion in Amorphous Dispersions 361
13.5.4 Plasticization by Water Clusters 365
13.6 Summary 367
References 368
14 Numerical Simulations of Unit Operations in Pharmaceutical Solid Dose Manufacturing 375
Ekneet Kaur Sahni, Shivangi Naik, and Bodhisattwa Chaudhuri
14.1 Introduction 375
14.2 Numerical Method 376
14.2.1 Contact Drying in an Agitated Filter Dryer 376
14.2.2 Coating in a Conventional Pan Coater 378
14.2.3 Modeling of milling in a Wiley Mill 379
14.3 Experimental Method for Milling 380
14.4 Results and Discussion 380
14.4.1 Simulation of Contact Drying 380
14.4.2 Simulation of Tablet Coating 384
14.4.3 Simulation of Size Fragmentation (Milling) 387
14.5 Summary and Conclusions 391
References 392
Index 395
