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Polymorphs, Salts, and Cocrystals: What’s in a Name?

Crystal Growth & Design · 2012 · Vol. 12(5) · pp. 2147–2152
Srinivasulu AitipamulaRahul BanerjeeArvind K. BansalKumar BiradhaM.L. CheneyAngshuman Roy ChoudhuryGautam R. DesirajuAmol G. DikundwarRitesh DubeyNagakiran DuggiralaPreetam P. GhogaleSoumyajit GhoshPramod Kumar GoswamiN. Rajesh GoudRam R. K. R. JettiPiotr KarpińskiP. KaushikDinesh KumarVineet KumarBrian MoultonArijit MukherjeeGargi MukherjeeAllan S. MyersonVibha PuriArunachalam RamananRajamannar ThennatiC. Malla ReddyNaír Rodríguez‐HornedoRobin D. RogersTayur N. Guru RowPalash SanphuiNing ShanGanesh SheteAmit K. SinghChangquan Calvin SunJennifer A. SwiftRam ThaimattamTejender S. ThakurRajesh Kumar ThaperSajesh P. ThomasSrinu TothadiV.R. VangalaNarayan VariankavalP. VishweshwarD.R. WeynaMichael J. Zaworotko

Abstract

The December 2011 release of a draft United States Food and Drug Administration (FDA) guidance concerning regulatory classification of pharmaceutical cocrystals of active pharmaceutical ingredients (APIs) addressed two matters of topical interest to the crystal engineering and pharmaceutical science communities: (1) a proposed definition of cocrystals; (2) a proposed classification of pharmaceutical cocrystals as dissociable "API-excipient" molecular complexes. The Indo–U.S. Bilateral Meeting sponsored by the Indo–U.S. Science and Technology Forum titled The Evolving Role of Solid State Chemistry in Pharmaceutical Science was held in Manesar near Delhi, India, from February 2–4, 2012. A session of the meeting was devoted to discussion of the FDA guidance draft. The debate generated strong consensus on the need to define cocrystals more broadly and to classify them like salts. It was also concluded that the diversity of API crystal forms makes it difficult to classify solid forms into three categories that are mutually exclusive. This perspective summarizes the discussion in the Indo–U.S. Bilateral Meeting and includes contributions from researchers who were not participants in the meeting.

Crystallography and molecular interactionsCrystallization and Solubility StudiesChemical Thermodynamics and Molecular StructureFood and drug administrationSession (web analytics)Crystal engineeringChemistryPolitical scienceTraditional medicineMedicineComputer sciencePharmacologyOrganic chemistry
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Amorphous pharmaceutical solids: preparation, characterization and stabilization
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Supramolecular Synthons in Crystal Engineering—A New Organic Synthesis
Angewandte Chemie International Edition in English · 1995 · 4,793 citations
Pharmaceutical Co-Crystals
Journal of Pharmaceutical Sciences · 2006 · 955 citations
Pharmaceutical Cocrystals and Their Physicochemical Properties
Crystal Growth & Design · 2009 · 1,459 citations
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