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. 2010 Jul 13;12(4):569–575. doi: 10.1208/s12248-010-9215-z

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© The Author(s) 2010

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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Fig. 4 — Dissolution profiles of tablets composed of a physical mixture () and controlled crystallized dispersions of 35% w/w fenofibrate in mannitol. Controlled crystallized dispersions were prepared by slow freezing (closed symbols) or fast freezing (open symbols) and a low (−25°C) crystallization temperature (circles) or a high (−15°C) crystallization temperature (triangles). Process 1 corresponds to (●), process 2 corresponds to (▲), process 3 corresponds to (○), and process 4 corresponds to (△) (n = 3–6; mean ± standard deviation)

Inline graphic — Dissolution profiles of tablets composed of a physical mixture () and controlled crystallized dispersions of 35% w/w fenofibrate in mannitol. Controlled crystallized dispersions were prepared by slow freezing (closed symbols) or fast freezing (open symbols) and a low (−25°C) crystallization temperature (circles) or a high (−15°C) crystallization temperature (triangles). Process 1 corresponds to (●), process 2 corresponds to (▲), process 3 corresponds to (○), and process 4 corresponds to (△) (n = 3–6; mean ± standard deviation)