Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates

Blagden, N. and de Matas, M. and Gavan, P.T. and York, P. (2007) Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates. Advanced Drug Delivery Reviews, 59 (7). pp. 617-630. ISSN 0169-409X

Full content URL: http://dx.doi.org/10.1016/j.addr.2007.05.011

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Item Type:Article
Item Status:Live Archive

Abstract

The increasing prevalence of poorly soluble drugs in development provides notable risk of new products demonstrating low and erratic bioavailabilty with consequences for safety and efficacy, particularly for drugs delivered by the oral route of administration. Although numerous strategies exist for enhancing the bioavailability of drugs with low aqueous solubility, the success of these approaches is not yet able to be guaranteed and is greatly dependent on the physical and chemical nature of the molecules being developed. Crystal engineering offers a number of routes to improved solubility and dissolution rate, which can be adopted through an in-depth knowledge of crystallisation processes and the molecular properties of active pharmaceutical ingredients. This article covers the concept and theory of crystal engineering and discusses the potential benefits, disadvantages and methods of preparation of co-crystals, metastable polymorphs, high-energy amorphous forms and ultrafine particles. Also considered within this review is the influence of crystallisation conditions on crystal habit and particle morphology with potential implications for dissolution and oral absorption. © 2007 Elsevier B.V. All rights reserved.

Keywords:Dissolution rates, Metastable polymorphs, Particle morphology, Crystal engineering, Crystallization, Dissolution, Drug delivery, Polymorphism, Solubility, Supramolecular chemistry, Drug products, er 34122, glibenclamide, griseofulvin, lipoxygenase inhibitor, prostaglandin synthase inhibitor, unclassified drug, area under the curve, bioengineering, crystal, crystal structure, drug absorption, drug bioavailability, drug delivery system, drug solubility, nonhuman, physical chemistry, priority journal, review, Biological Availability, Chemistry, Pharmaceutical, Drug Design, Pharmaceutical Preparations, Solvents
Subjects:B Subjects allied to Medicine > B200 Pharmacology, Toxicology and Pharmacy
Divisions:College of Science > School of Pharmacy
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ID Code:8763
Deposited On:11 Jul 2013 15:36

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