Ciprofloxacin in Layered Double Hydroxides: Looking for the Best Synthesis Method.

It is important to develop new methods of release to improve pharmacokinetic parameters of drugs, especially antibiotics, whose plasmatic concentration is determinant to ensure an effective treatment. Layered double hydroxides (LDH) are inorganic and biocompatible materials with high drug intercalation capacity and release properties that can be tuned by controlling the pH value. These materials can be an excellent choice to achieve a sustained release and an optimal drug concentration in plasm. In this work, LDH were synthesized with intercalated ciprofloxacin (CIP) by three different methods: coprecipitation, reconstruction and ion exchange. LDH-CIP complexes were characterized by XRD, TG-DSC, TEM, SEM, FTIR, electrophoretic mobilities, and drug release and dissolution kinetics in NaCl solutions and under physiological conditions. The coprecipitation and reconstruction methods lead to the formation of ill-defined products, whereas the ion exchange method rendered the best intercalation results. CIP release was controlled by dissolution at pH<3 and by desorption and ion exchange at intermediate and high pH. In comparison with a commercial formulation, the LDH-CIP complex prepared by ion exchange presented a slower release profile. The fast dissolution at gastric pH raises the need of developing some type of coating for protecting LDH materials.

Synthesis of Layered Double Hydroxides Intercalated With Drugs for Controlled Release: Successful Intercalation of Ibuprofen and Failed Intercalation of Paracetamol.

This work examines the effect of drug structure and ionization degree on the formation and properties of biocompatible layered double hydroxides (LDH) intercalated with ibuprofen and paracetamol. Ibuprofen (pKa = 5.3) is in its anionic form, whereas paracetamol (pKa 9.4) is only partially ionized at the synthesis pH (9.0), and thus intercalation is expected to be different in the two cases. Chemical analyses, X-ray diffraction, electron microscopy, infrared spectroscopy and thermal analyses were applied to characterize the materials. Dissolution kinetics and drug release kinetics were also investigated, in an ample range of pH (3.0-9.0) in NaCl solutions, and in physiological buffers (1.2, 4.5 and 6.8). All characterization techniques showed that an efficient intercalation of ibuprofen took place, resulting in a material with 30% of its weight corresponding to the drug. On the contrary, all techniques revealed a very poor intercalation of paracetamol (1.2%). The dissolution kinetics of LDHs was highly pH-dependent, being higher as pH decreased. The drug release kinetics, conversely, increased as pH increased. In physiological buffers the release rate depended not only on the pH but also on the type of buffer. This last behavior is useful to control the release in different parts of the digestive system.

Quantum chemical study on surface complex structures of phosphate on gibbsite.

Quantum mechanics calculations based on the density functional theory (DFT) were used to identify phosphate surface complexes on gibbsite at low and high pH. The different phosphate species were represented using the Al6(OH)18(H2O)6 cluster model considering four different geometries: monodentate mononuclear (Pmm), monodentate binuclear (Pmb), bidentate mononuclear (Pbm) and bidentate binuclear (Pbb). The corresponding adsorption reactions were modelled via ligand exchange between phosphate species and surface functional groups (hydroxyls and protonated hydroxyls at high and low pH, respectively). The theoretical results indicate that phosphate surface complexes are thermodynamically more favored at acid pH, in agreement with experimental evidences. The first step in these reactions, i.e., the generation of required aluminum vacant sites, was predicted to be particularly favorable when singly coordinated aquo groups are released. Stretching and bending vibrational frequencies associated with the different surface structures were calculated at both pH conditions. The corresponding values at low pH were found to be shifted to higher frequencies with respect to those ones at high pH. ATR-FTIR studies were also carried out. The resulting spectra are dominated by a strong band within the 800-840 cm(-1) interval due to P-OH stretching modes. The corresponding peak appearing around 820 cm(-1) at high pH is shifted to lower frequencies with respect to the position at low pH, a tendency well predicted by DFT calculations.

An ATR-FTIR study of different phosphonic acids adsorbed onto boehmite.

An ATR-FTIR study of the vibrational spectra of N,N-bis(2-hydroxyethyl) aminomethylphosphonic acid (BHAMP), 1-hydroxyethane-1,1'-diphosphonic acid (HEDP) and nitrilotris(methylenephosphonic acid) (NTMP) adsorbed onto boehmite is presented. The study was performed in the pH range from 5 to 9, and bands assignments are given in the 1200-900 cm(-1) wavenumber range, where the bands associated with various P-O(H) vibrations can be found. The three phosphonic acids adsorb onto boehmite by forming inner-sphere surface complexes. ATR-FTIR data indicates the presence of both protonated and deprotonated mononuclear surface species. In all cases, the surface-bound ions undergo protonation reactions as pH is decreased. The results are in good agreement with previously proposed surface complexation models.

An ATR-FTIR study of different phosphonic acids in aqueous solution.

An ATR-FIR study of the vibrational spectra of 1-hydroxyethane-1,1'-diphosphonic acid (HEDP), nitrilotris(methylenephosphonic acid) (NTMP) and N,N-bis(2-hydroxyethyl)aminomethylphosphonic acid (BHAMP) in aqueous solution is presented. The study was performed in the range of pH from 5 to 9, and bands assignments are given in the 2000-890 cm(-1) range. However, as phosphonates display bands due to the PO stretching vibration mainly in the 900-1200 cm(-1) range, the study is focused in this midinfrared region, which shows important changes as the pH changes, specially the nu(POH) at approximately 925 cm(-1) and nu(PO(3)(2-)) at approximately 970 cm(-1) vibrations. IR analyses give also evidences for the zwitterionic nature of BHAMP and NTMP in solution with a strong indication that the zwitterion in both compounds remains intact throughout the pH range investigated. The successive protonation steps with the decrease of pH were evidenced in the IR spectra of the three studied phosphonates.