Dissolution kinetics and mechanism of Mg-Al layered hydroxides: A simple approach to describe drug release in acid media

MARA PARELLO; RICARDO ROJAS; CARLA E. GIACOMELLI

JOURNAL OF COLLOID AND INTERFACE SCIENCE

ACADEMIC PRESS INC ELSEVIER SCIENCE

Lugar: Amsterdam; Año: 2010 vol. 351 p. 134 - 139

0021-9797

Layered double hydroxides (LDHs) weathering in acidic media is one of the main features that affects their applications in drug delivery systems. In this work, the dissolution kinetics of biocompatible Mg–Al LDHs was studied at different initial pH values and solid concentrations using a simple and fast experimental method that coupled flow injection analysis and amperometric detection. A carbonate intercalated sample was used to determine the controlling step of the process and the dissolution mechanism. Finally, the study was extended to an ibuprofen intercalated LDH. The obtained results showed that the weathering process was mainly controlled by the exposed area and surface reactivity of LDHs particles. The dissolution mechanism at the particle surface was described in two steps: fast formation of surface reactive sites by hydroxyl group protonation and slow detachment of metal ions from surface. At strongly acidic conditions, the reaction rate was pH dependent due to the equilibrium between protonated (active) and deprotonated (inactive) hydroxyl groups. On the other hand, at mildly acidic conditions, the dissolution behavior was also ruled by the equilibrium attained between the particle surface reactive sites and the dissolved species. LDHs solubility and dissolution rate presented strong dependence with the interlayer anion. The ibuprofen intercalated sample was more soluble and more rapidly dissolved than the carbonate intercalated one in acetic/acetate buffer. On the other hand, the dissolution mechanism was invariant with the interlayer anion.applications in drug delivery systems. In this work, the dissolution kinetics of biocompatible Mg–Al LDHs was studied at different initial pH values and solid concentrations using a simple and fast experimental method that coupled flow injection analysis and amperometric detection. A carbonate intercalated sample was used to determine the controlling step of the process and the dissolution mechanism. Finally, the study was extended to an ibuprofen intercalated LDH. The obtained results showed that the weathering process was mainly controlled by the exposed area and surface reactivity of LDHs particles. The dissolution mechanism at the particle surface was described in two steps: fast formation of surface reactive sites by hydroxyl group protonation and slow detachment of metal ions from surface. At strongly acidic conditions, the reaction rate was pH dependent due to the equilibrium between protonated (active) and deprotonated (inactive) hydroxyl groups. On the other hand, at mildly acidic conditions, the dissolution behavior was also ruled by the equilibrium attained between the particle surface reactive sites and the dissolved species. LDHs solubility and dissolution rate presented strong dependence with the interlayer anion. The ibuprofen intercalated sample was more soluble and more rapidly dissolved than the carbonate intercalated one in acetic/acetate buffer. On the other hand, the dissolution mechanism was invariant with the interlayer anion.