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Cited by 1,448

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

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

Open access
Blagden, N., de Matas, M., Gavan, P.T., York, P.·2007·Advanced Drug Delivery Reviews

Abstract

The increasing prevalence of poorly soluble drugs in development provides notable risk of new products demonstrating low and erratic bioavailability 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.

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Registry

Crossref · 10.1016/j.addr.2007.05.011

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Metadata

Authors
Blagden, N., de Matas, M., Gavan, P. T., & York, P.
Venue
Advanced Drug Delivery Reviews
Publisher
Elsevier BV
Published
2007-07
Volume
59
Issue
7
Pages
617-630
ISSN
0169-409X (ISSN-L)
OpenAlex
W1995008519
Cited by
1,448
References
40
FWCI
1.07
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates. https://app.cochat.ai/papers/10.1016/j.addr.2007.05.011
The paper
Blagden, N., de Matas, M., Gavan, P. T., & York, P. (2007). Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates. Advanced Drug Delivery Reviews. https://doi.org/10.1016/j.addr.2007.05.011

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.