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The particles may comprise magnesium aluminometasilicate powder. The dosage form may include a pH regulating agent selected from one or more of the group comprising organic acids, inorganic acids and bases, andor include a chelating agent. In particular, it has been found that the use of organic acid(s) andor chelating agent (s) facilitate the dissolution of FujiCalin particles upon contact with gastric acid. Preferably, the weight percent of a liquid, active agent formulation is at least 5 of the total weight of the dosage form. These absorbent materials have been found to be useful for various types of dosage forms. In one embodiment of the present invention, the dosage form is adapted for rapid, possibly immediate, release of the active agent.

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