Investigation of Carbamazepine- Nicotinamide Cocrystal Solubility and Dissolution by a UV Imaging System

Total Page:16

File Type:pdf, Size:1020Kb

Investigation of Carbamazepine- Nicotinamide Cocrystal Solubility and Dissolution by a UV Imaging System Investigation of Carbamazepine- Nicotinamide cocrystal solubility and dissolution by a UV imaging system PhD Thesis Ning Qiao This thesis is submitted in partial fulfilment of the requirements of De Montfort University for the award of Doctor of Philosophy April 2014 Faculty of Health and Life Sciences De Montfort University Leicester CONTENTS CONTENTS CONTENTS ................................................................................................................................... I DECLARATION ........................................................................................................................... v ABSTRACT .................................................................................................................................. vi ACKNOWLEDGEMENTS ......................................................................................................... vii PUBLICATIONS ........................................................................................................................ viii LIST OF FIGURES ....................................................................................................................... x LIST OF TABLES ...................................................................................................................... xiii ABBREVIATIONS ..................................................................................................................... xv Chapter 1 Introduction .................................................................................................................. 1 1.1 Research background .......................................................................................................... 1 1.2 Research aim and objectives ............................................................................................... 2 1.3 Thesis structure ................................................................................................................... 3 Chapter 2 Literature Review ......................................................................................................... 5 2.1 Chapter overview ................................................................................................................ 5 2.2 Cocrystal background review.............................................................................................. 5 2.2.1 Cocrystal definition ...................................................................................................... 5 2.2.2 Crystal engineering ...................................................................................................... 7 2.2.3 Pharmaceutical cocrystals design strategies ................................................................. 8 2.2.4 Cocrystal formation methods ....................................................................................... 9 2.2.5 Cocrystal characterisation techniques ........................................................................ 11 2.2.6 Physicochemical properties of cocrystals .................................................................. 13 2.3 Theoretical development on solubility prediction of pharmaceutical cocrystals .............. 17 2.3.1 Prediction of cocrystal solubility ................................................................................ 17 2.3.2 Cocrystal dissolution in surfactant solutions.............................................................. 22 2.3.3 Solution mediated phase transformation .................................................................... 25 2.4 Carbamazepine (CBZ) cocrystals studies ......................................................................... 29 2.4.1 CBZ introduction ....................................................................................................... 29 I CONTENTS 2.4.2 CBZ cocrystal studies ................................................................................................ 31 2.5 Introduction of pharmaceutical cocrystal coformers: nicotinamide and succinic acid ..... 35 2.6 Definitions of basics of pharmaceutical physical chemistry [143] ................................... 36 2.7 Chapter conclusions .......................................................................................................... 45 Chapter 3 Materials and Methods ............................................................................................... 46 3.1 Chapter overview .............................................................................................................. 46 3.2 Materials ........................................................................................................................... 47 3.3 Methods............................................................................................................................. 48 3.3.1 ActiPix SDI 300 UV imaging dissolution system ...................................................... 48 3.3.2 Enspectr R532 Raman spectrometry .......................................................................... 58 3.3.3 Infrared (IR) Spectroscopy ......................................................................................... 63 3.3.4 Ultraviolet–visible spectrometry (UV-Vis) ................................................................ 65 3.3.5 Differential scanner calorimetry (DSC) ..................................................................... 66 3.3.6 Thermal gravimetric analysis (TGA) ......................................................................... 67 3.3.7 High performance liquid chromatography (HPLC) ................................................... 68 3.3.8 Leica microscope ....................................................................................................... 71 3.3.9 Scanning electron microscope (SEM)[161] ............................................................... 71 3.3.10 CAM 200 surface tension meter .............................................................................. 72 3.3.11 Solubility test methods ............................................................................................. 74 3.4 Preparations....................................................................................................................... 75 3.4.1 Dissolution media preparation ................................................................................... 75 3.4.2 Test samples preparation ............................................................................................ 76 3.5 Chapter conclusions .......................................................................................................... 77 Chapter 4 Sample Characterisations ........................................................................................... 79 4.1 Chapter overview .............................................................................................................. 79 4.2 Materials and methods ...................................................................................................... 79 4.2.1 Materials .................................................................................................................... 79 4.2.2 Methods ...................................................................................................................... 79 4.3 Results ............................................................................................................................... 80 II CONTENTS 4.3.1 TGA analysis of CBZ DH .......................................................................................... 80 4.3.2 DSC analysis of test samples ..................................................................................... 80 4.3.3 IR spectroscopy analysis of CBZ-NIC cocrystal and CBZ-SUC cocrystal ............... 83 4.3.4 Raman spectroscopy analysis of CBZ-NIC cocrystal and CBZ-SUC cocrystal ........ 86 4.3.5 Molecular structures of CBZ-NIC cocrystal and CBZ-SUC cocrystal ...................... 91 4.4 Chapter conclusions .......................................................................................................... 92 Chapter 5 In Situ Monitoring of Carbamazepine-Nicotinamide Cocrystal Intrinsic Dissolution Behaviour .................................................................................................................................... 93 5.1 Chapter overview .............................................................................................................. 93 5.2 Materials and methods ...................................................................................................... 93 5.2.1 Materials .................................................................................................................... 93 5.2.2 Methods ...................................................................................................................... 94 5.3 Results ............................................................................................................................... 95 5.3.1 UV imaging dissolution tests ..................................................................................... 95 5.3.2 In situ monitoring of solid state transformation during dissolution using Raman spectroscopy ...................................................................................................................... 101 5.3.3 SEM ......................................................................................................................... 105 5.4 Discussion ......................................................................................................................
Recommended publications
  • Mechanochemical Synthesis of a Cocrystal of Two Supramolecular
    crystals Article Mechanochemical Synthesis of a Cocrystal of Two Supramolecular Hydrogen-Bonded Aggregates of 1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane (TATU) with 4-tert-Butylphenol Bearing Different Hydrogen Bonding Interactions Augusto Rivera 1,*, Jicli José Rojas 1, Jaime Ríos-Motta 1 and Michael Bolte 2 ID 1 Departamento de Química, Facultad de Ciencias, Universidad Nacional de Colombia, Sede Bogotá, Carrera 30 No. 45-03, Bogotá,Código Postal 111321, Colombia; [email protected] (J.J.R.); [email protected] (J.R.-M.) 2 Institut für Anorganische Chemie, J. W. Goethe-Universität Frankfurt, Max-von Laue-Str., 7, 60438 Frankfurt/Main, Germany; [email protected] * Correspondence: [email protected]; Tel.: +57-1-316-5000 Received: 2 July 2018; Accepted: 20 July 2018; Published: 30 July 2018 Abstract: The synthesis and single crystal structure of a new cocrystal, which is composed of OHphenolic···OHphenolic···Naminalic supramolecular heterosynthons assembled from 4-tert-butylphenol and the macrocyclic aminal TATU, is presented. This cocrystal was prepared by solvent-free assisted grinding, which is a commonly used mechanochemical method. Crystal structure, supramolecular assembly through hydrogen bonding interactions as well as the physical and spectroscopic properties of the title cocrystal are presented in this paper. Keywords: supramolecular chemistry; crystal engineering; cocrystals; hydrogen bonds; noncovalent interactions; aminal structure 1. Introduction Noncovalent interactions, such as electrostatic forces, H-bonds, halogen bonds, CH–π, π–π stacking, cation–π, anion–π, lone pair–π associations and other weak forces, play significant roles in a variety of fields, including molecular recognition, host–guest chemistry, crystal engineering, supramolecular chemistry, biochemistry, pharmaceutical chemistry, and materials science [1,2].
    [Show full text]
  • Cocrystal Prediction Using Machine Learning Models and Descriptors
    applied sciences Article Cocrystal Prediction Using Machine Learning Models and Descriptors Medard Edmund Mswahili 1,† , Min-Jeong Lee 2,†, Gati Lother Martin 1, Junghyun Kim 3, Paul Kim 4, Guang J. Choi 2 and Young-Seob Jeong 1,* 1 Department of ICT Convergence, Soonchunhyang University, Asan-si 31538, Korea; [email protected] (M.E.M.); [email protected] (G.L.M.) 2 Department of Pharmaceutical Engineering, Soonchunhyang University, Asan-si 31538, Korea; [email protected] (M.-J.L.); [email protected] (G.J.C.) 3 Department of Future Convergence Technology, Soonchunhyang University, Asan-si 31538, Korea; [email protected] 4 Department of Medical Science, Soonchunhyang University, Asan-si 31538, Korea; [email protected] * Correspondence: [email protected] † These authors contributed equally to this work. Abstract: Cocrystals are of much interest in industrial application as well as academic research, and screening of suitable coformers for active pharmaceutical ingredients is the most crucial and challeng- ing step in cocrystal development. Recently, machine learning techniques are attracting researchers in many fields including pharmaceutical research such as quantitative structure-activity/property relationship. In this paper, we develop machine learning models to predict cocrystal formation. We extract descriptor values from simplified molecular-input line-entry system (SMILES) of compounds and compare the machine learning models by experiments with our collected data of 1476 instances. As a result, we found that artificial neural network shows great potential as it has the best accuracy, sensitivity, and F1 score. We also found that the model achieved comparable performance with about Citation: Mswahili, M.E.; Lee, M.-J.; half of the descriptors chosen by feature selection algorithms.
    [Show full text]
  • Selection of Effective Cocrystals Former for Dissolution Rate Improvement Of
    Selection of effective cocrystals former for dissolution rate improvement of active pharmaceutical ingredients based on lipoaffinity index Piotr Cysewski, Maciej Przybylek To cite this version: Piotr Cysewski, Maciej Przybylek. Selection of effective cocrystals former for dissolution rate im- provement of active pharmaceutical ingredients based on lipoaffinity index. European Journal of Pharmaceutical Sciences, Elsevier, 2017, 107, pp.87-96. 10.1016/j.ejps.2017.07.004. hal-01773096 HAL Id: hal-01773096 https://hal.archives-ouvertes.fr/hal-01773096 Submitted on 29 Apr 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Accepted Manuscript Selection of effective cocrystals former for dissolution rate improvement of active pharmaceutical ingredients based on lipoaffinity index Piotr Cysewski, Maciej Przybyłek PII: S0928-0987(17)30403-7 DOI: doi: 10.1016/j.ejps.2017.07.004 Reference: PHASCI 4127 To appear in: European Journal of Pharmaceutical Sciences Received date: 11 April 2017 Revised date: 6 June 2017 Accepted date: 3 July 2017 Please cite this article as: Piotr Cysewski, Maciej Przybyłek , Selection of effective cocrystals former for dissolution rate improvement of active pharmaceutical ingredients based on lipoaffinity index, European Journal of Pharmaceutical Sciences (2017), doi: 10.1016/j.ejps.2017.07.004 This is a PDF file of an unedited manuscript that has been accepted for publication.
    [Show full text]
  • Cocrystal Prediction by Artificial Neural Networks
    Cocrystal prediction by artificial neural networks Jan-Joris Devogelaer, Hugo Meekes, Paul Tinnemans, Elias Vlieg, and René de Gelder* Radboud University, Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands E-mail: [email protected] Abstract A significant amount of attention has been given to the design and synthesis of cocrys- tals by both industry and academia because of its potential to change a molecule’s physico- chemical properties. Yet, difficulties arise when searching for adequate combinations of molecules (or coformers) to form cocrystals, hampering the efficient exploration of the tar- get’s solid-state landscape. This paper reports on the application of a data-driven cocrystal prediction method, based on two types of artificial neural network models and cocrystal data present in the Cambridge Structural Database. The models accept pairs of coformers and predict whether a cocrystal is likely to form. By combining the output of multiple models of both types, our approach shows to have excellent performance on the proposed cocrystal training and validation sets, and has an estimated accuracy of 80% for molecules for which previous cocrystallization data is unavailable. 1 1 Introduction Molecular solids appear in many different ways, and the solid-state landscape of a molecule may cover various crystalline forms, ranging from polymorphs and hydrates to more complex multicomponent crystals [1, 2]. The latter have been promoted as excellent tools to modify the physico-chemical characteristics of a target compound, such as the (aqueous) solubility, bio- availability, density, and melting point [3–8]. Multicomponent crystals therefore play a pivotal role in the effective formulation of pharmaceuticals and will continue to be part of the solid form screening process in drug development.
    [Show full text]
  • Synthesis, Crystal Structure, and Solubility Analysis of a Famotidine Cocrystal
    crystals Article Synthesis, Crystal Structure, and Solubility Analysis of a Famotidine Cocrystal Yan Zhang 1,2,* , Zhao Yang 2, Shuaihua Zhang 3 and Xingtong Zhou 2 1 School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China 2 Qingdao Institute for Food and Drug Control, Qingdao 266071, China 3 School of Pharmacy, Qingdao University, Qingdao 266071, China * Correspondence: [email protected]; Tel.: +86-532-5875-9178 Received: 15 May 2019; Accepted: 10 July 2019; Published: 15 July 2019 Abstract: A novel cocrystal of the potent H2 receptor antagonist famotidine (FMT) was synthesized with malonic acid (MAL) to enhance its solubility. The cocrystal structure was characterized by X-ray single crystal diffraction, and the asymmetry unit contains one FMT and one MAL connected via intermolecular hydrogen bonds. The crystal structure is monoclinic with a P21/n space group and unit cell parameters a = 7.0748 (3) Å, b = 26.6502 (9) Å, c = 9.9823 (4) Å, α = 90, β = 104.2228 (12), γ = 90,V = 1824.42 (12) Å3, and Z = 4. The cocrystal had unique thermal, spectroscopic, and powder X-ray diffraction (PXRD) properties that differed from FMT. The solubility of the famotidine-malonic acid cocrystal (FMT-MAL) was 4.2-fold higher than FMT; the FAM-MAL had no change in FMT stability at high temperature, high humidity, or with illumination. Keywords: cocrystal; famotidine; malonic acid; crystal structure; solubility 1. Introduction Drugs with low water solubility usually show dissolution-limited absorption and low bioavailability [1]. Recent estimates suggest that approximately 40% of currently marketed drugs and up to 75% of compounds currently under development are poorly water soluble; thus, enhancing the aqueous solubility of poorly water-soluble active pharmaceutical ingredients (APIs) is a key challenge for pharmaceutical scientists [2].
    [Show full text]
  • Non-Covalent Derivatives: Cocrystals and Eutectics
    Molecules 2015, 20, 14833-14848; doi:10.3390/molecules200814833 OPEN ACCESS molecules ISSN 1420-3049 www.mdpi.com/journal/molecules Review Non-Covalent Derivatives: Cocrystals and Eutectics Emily Stoler † and John C. Warner †,* The Warner Babcock Institute for Green Chemistry, 100 Research Drive, Wilmington, MA 01887, USA; E-Mail: [email protected] † These authors contributed equally to this work. * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +1-978-229-5420; Fax: +1-978-229-5401. Academic Editor: Kei Saito Received: 9 June 2015 / Accepted: 5 August 2015 / Published: 14 August 2015 Abstract: Non-covalent derivatives (NCDs) are formed by incorporating one (or more) coformer molecule(s) into the matrix of a parent molecule via non-covalent forces. These forces can include ionic forces, Van der Waals forces, hydrogen bonding, lipophilic-lipophilic interactions and pi-pi interactions. NCDs, in both cocrystal and eutectic forms, possess properties that are unique to their supramolecular matrix. These properties include critical product performance factors such as solubility, stability and bioavailability. NCDs have been used to tailor materials for a variety of applications and have the potential to be used in an even broader range of materials and processes. NCDs can be prepared using little or no solvent and none of the reagents typical to synthetic modifications. Thus, NCDs represent a powerfully versatile, environmentally-friendly and cost-effective opportunity. Keywords: non-covalent derivative; cocrystals; eutectics; green chemistry 1. Introduction A non-covalent derivative (NCD) [1] is formed when one (or more) coformer molecule(s) is incorporated into the matrix of the target molecule by way of non-covalent forces [2–4].
    [Show full text]
  • Cocrystal Construction Between Rosuvastatin Calcium and L- Asparagine with Enhanced Solubility and Dissolution Rate
    Original Article DOI: 10.4274/tjps.galenos.2021.62333 Cocrystal Construction Between Rosuvastatin Calcium and L- asparagine with Enhanced Solubility and Dissolution Rate Venkata Deepthi Vemuri1*, Srinivas Lankalapalli 2 1Maharajah’s College of Pharmacy, Phool Baugh, Vizianagaram-535002, India 2GITAM Institute of Pharmacy, GITAM (Deemed to be University), Visakhapatnam, Andhra Pradesh, INDIA Corresponding author: Corresponding author: Venkata Deepthi Vemuri* Mailing address: Maharajah’s College of Pharmacy, Phool Baugh, Vizianagaram-535002, Andhra Pradesh, India Mobile phone: +91-9032292387 E-mail: [email protected] https://orcid.org/0000-0003-3243-4340 20.12.2020 03.04.2021 Abstract Background: Rosuvastatin calcium, a synthetic BCS class-II drug with low solubility and high permeability utilized in hyperlipidaemia management. In the present investigation, an attempt was made towards the modification of the physicochemical properties of rosuvastatin calcium by applying crystalproof engineering to prepare a cocrystal form. Cocrystals of rosuvastatin calcium with GRAS status co-former L-Asparagine were prepared by utilizing solvent evaporation method. Result: The Obtained cocrystals was evaluated by Fourier transform infrared spectroscopy, powder X-ray diffraction, FT-Nuclear magnetic resonance spectroscopy, Scanning electron microscopy, and differential scanning calorimetry. Powder X-ray diffraction studies revealed the presence of unique crystalline peaks, which provides the interaction details of API and the co-former. The changes in the thermal behaviour of cocrystals were confirmed by differential scanning calorimetry studies. Alteration in the chemical shift values of FT-NMR at OH group confirms the hydrogen bond interaction between drug and co-former. Comparative studies on the solubility and dissolution rate were conducted and exhibited an almost 2-fold higher than the parent drug.
    [Show full text]
  • Preparation and Characterization of Carbamazepine Cocrystal in Polymer Solution
    pharmaceutics Article Preparation and Characterization of Carbamazepine Cocrystal in Polymer Solution Hao Zhang 1, Ying Zhu 1, Ning Qiao 1,2,* ID , Yang Chen 1,2 and Linghuan Gao 3 1 College of Materials Science and Engineering, North China University of Science and Technology, Tangshan 063210, China; [email protected] (H.Z.); [email protected] (Y.Z.); [email protected] (Y.C.) 2 Hebei Provincial Key Lab of Inorganic Nonmetallic Materials, College of Materials Science and Engineering, North China University of Science and Technology, Tangshan 063210, China 3 College of Basic Medical Sciences, North China University of Science and Technology, Tangshan 063210, China; [email protected] * Correspondence: [email protected]; Tel.: +86-315-880-5620 Received: 1 October 2017; Accepted: 29 November 2017; Published: 1 December 2017 Abstract: In this study, we attempted to prepare carbamazepine (CBZ) cocrystal through the solution method in ethanol-water solvent mixture (volume ratio 1:1) and polyvinyl pyrrolidone (PVP) solution. Nicotinamide (NIC) and saccharin (SAC) were selected as cocrystal coformers. Cocrystal screening products were characterized by Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), and Powder X-ray Diffraction (PXRD) techniques. Characterization results show that in ethanol-water solvent mixture, pure CBZ-NIC cocrystal can be prepared, while CBZ-SAC cocrystal cannot be obtained. The addition of PVP can inhibit CBZ-NIC cocrystal formation and facilitate CBZ-SAC cocrystal formation. Keywords: cocrystal preparation; polyvinyl pyrrolidone; carbamazepine; nicotinamide; saccharin 1. Introduction Pharmaceutical cocrystal is a crystalline material with two components present in definite stoichimetric amounts [1]. One of the pharmaceutical cocrystal components is an active pharmaceutical ingredient (API), and the other component is a cocrystal coformer (CCF).
    [Show full text]
  • Improved Solubility and Dissolution Rates in Novel Multicomponent Crystals of Piperine with Succinic Acid
    Scientia Pharmaceutica Article Improved Solubility and Dissolution Rates in Novel Multicomponent Crystals of Piperine with Succinic Acid Erizal Zaini 1,* , Afriyani 1, Lili Fitriani 1 , Friardi Ismed 2, Ayano Horikawa 3 and Hidehiro Uekusa 3 1 Department of Pharmaceutics, Faculty of Pharmacy, Andalas University, Padang 25163, Indonesia; [email protected] (A.); lilifi[email protected] (L.F.) 2 Laboratory of Biota Sumatera and Faculty of Pharmacy, Andalas University, Padang 25163, Indonesia; [email protected] 3 Department of Chemistry, School of Science, Tokyo Institute of Technology, Tokyo 1528551, Japan; [email protected] (A.H.); [email protected] (H.U.) * Correspondence: [email protected] Received: 18 March 2020; Accepted: 9 April 2020; Published: 13 April 2020 Abstract: The objectives of this study were to prepare and characterize a novel piperine–succinic acid multicomponent crystal phase and to evaluate the improvement in the solubility and dissolution rate of piperine when prepared in the multicomponent crystal formation. The solid-state characterization of the novel multicomponent crystal was performed by powder X-ray diffraction (XRD), differential scanning calorimetry (DSC), and Fourier transform-infrared (FT-IR) spectroscopy. Solubility and dissolution rate profiles were evaluated in distilled water. The physical stability was evaluated under high relative humidity (75% and 100% RH). The determination of the single crystal X-ray diffraction structure revealed that this novel multicomponent crystal was a cocrystalline phase of piperine–succinic acid (2:1 molar ratio). The differential scanning calorimetry thermogram of the cocrystal showed a single and sharp endothermic peak at 110.49 ◦C.
    [Show full text]
  • Cocrystals of Spironolactone and Griseofulvin Based on an in Silico Screening Method
    This is a repository copy of Cocrystals of spironolactone and griseofulvin based on an in silico screening method. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/119702/ Version: Accepted Version Article: Grecu, T., Prohens, R., McCabe, J.F. et al. (4 more authors) (2017) Cocrystals of spironolactone and griseofulvin based on an in silico screening method. CrystEngComm, 19 (26). pp. 3592-3599. ISSN 1466-8033 https://doi.org/10.1039/c7ce00891k Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ Please do not adjust margins Journal Name ARTICLE Cocrystals of Spironolactone and Griseofulvin Based on an in Silico Screening Method Received 00th January 20xx, Accepted 00th January 20xx DOI: 10.1039/x0xx00000x a b c a d d www.rsc.org/ Tudor Grecu, Rafel Prohens, James F. McCabe, Elliot J. Carrington, James S. Wright, Lee Brammer,d and Christopher A. Hunter*e Cocrystal formation is considered as one of the most effective solid-state methods to alter the physicochemical properties of active pharmaceutical ingredients (APIs).
    [Show full text]
  • X-Ray Crystallography and Its Role in Understanding The…
    J. Indian Inst. Sci. A Multidisciplinary Reviews Journal ISSN: 0970-4140 Coden-JIISAD © The Author(s) 2017. X‑Ray Crystallography and its Role in Understanding the Physicochemical Properties of Pharmaceutical Cocrystals Srinivasulu Aitipamula1* and Venu R. Vangala2* REVIEW ARTICLE Abstract | Properties of a matter are intrinsically dependent on the inter‑ nal arrangement of molecules in the solid state. Therefore, knowledge of three-dimensional structure of the matter is a prerequisite for struc‑ ture–property correlations and design of functional materials. Over the past century, X-ray crystallography has evolved as a method of choice for accurate determination of molecular structure at atomic resolution. The structural information obtained from crystallographic analysis paved the way for rapid development in electronic devices, mineralogy, geo‑ sciences, materials science, pharmaceuticals, etc. Knowledge of the structural information of active pharmaceutical ingredients (APIs) is a prerequisite for rational drug design and synthesis of new chemical entities for development as new medicines. Over the past two decades, X-ray crystallography has played a key role in the design of pharmaceu‑ tical cocrystals—crystalline solids containing an API and one or more of pharmaceutically acceptable coformers. These materials have proved X-ray crystallography: An analytical technique used for promising for fne-tuning several important properties of APIs. This short determining the atomic and molecular structure of a crys- review highlights the history of crystallography, early breakthroughs, and tal, in which the crystalline at- the role of crystallography in understanding the physicochemical proper‑ oms cause a beam of incident X-rays to diffract into many ties of pharmaceutical cocrystals. specifc directions.
    [Show full text]
  • Pharmaceutical Cocrystals: from Serendipity to Design to Application, Drug Discov Today (2018)
    Drug Discovery Today Volume 00, Number 00 December 2018 REVIEWS POST SCREEN Pharmaceutical cocrystals: from serendipity to design to application Reviews Oisin N. Kavanagh, Denise M. Croker, Gavin M. Walker and Michael J. Zaworotko Synthesis and Solid State Pharmaceutical Centre (SSPC), Bernal Institute, University of Limerick, Limerick, Ireland The field of pharmaceutical cocrystals has reached a tipping point, particularly because cocrystals can improve the physicochemical properties of drugs without compromising their therapeutic benefit. Accounts of cocrystal investigations in the literature started in earnest in 2003 and patent applications soon followed. The frequency of both has steadily accelerated, demonstrating an enhanced understanding of the design, characterisation, and manufacture of cocrystals and heightened interest from industry. Indeed, there were four new product approvals from 2014 to 2017 and more are in the pipeline. Here, we review all marketed drug products that are based upon pharmaceutical cocrystal drug 1 substances, starting with the first recorded example, Beta-Chlor in 1963, with a particular emphasis on their discovery, rationale for use, and market impact. Introduction part of an aspect of preclinical research that has been termed 3 Solid form optimisation: serendipity or design? ‘Molecules, Materials and Medicines’, or M [8]. In 2013, Merck and Pfizer announced a joint collaborative effort to It is no secret that many new chemical entities suffer from low 1 bring a promising new antidiabetic, Steglatro , to market [1]. They solubility and/or poor permeability; up to 90% of new drugs closed out 2017 by obtaining US Food and Drug Administration receive BCS II classification [9]. This presents a major challenge (FDA) approval with analysts predicting blockbuster status for for pharmaceutical science.
    [Show full text]