Sustained release of calcium hydroxide from poly(dl-lactide-co-glycolide) acid microspheres for apexification Article uri icon

abstract

  • Calcium hydroxide (CH) loaded poly(dl-lactide-co-glycolide) acid (PLGA) microspheres (MS) might be used for apexification requiring a sustained release of Ca2 . The aim of this study was to formulate and characterize CH-PLGA-MS. The CH-loaded MS were prepared by either oil-in-water (O/W) or water-in-oil/in-water (W/O/W) emulsion solvent evaporation technique. MS produced by the O/W technique exhibited a larger diameter (18.63 ± 7.23 μm) than the MS produced by the W/O/W technique (15.25 ± 7.37 μm) (Mann–Whitney U test P < 0.001). The CH encapsulation efficiency (Ee) and Ca2 release were calculated from data obtained by absorption techniques. Ca2 release profile was evaluated for 30 days. To know the Ee, the CH-loaded MS were dissolved in 1 M NaOH to release all its content and a Ca2 colorimetric marker was added to this solution. The reagent marked the Ca2 in blue color, which was then measured by a UV–Vis system (650 nm). The percentage of Ee was calculated on the basis of the theoretical loading. The Ee of the O/W-produced MS was higher (24 %25) than the corresponding percentage of the W/O/W-produced MS (11 %25). O/W- and W/O/W-produced MS released slower and lower Ca2 than a control CH paste with polyethylene glycol 400 (Kruskal–Wallis test). O/W-produced MS released higher Ca2 than W/O/W-produced MS (statistically significant differences; P < 0.05). In conclusion, the CH-PLGA-MS were successfully formulated; the technique of formulation influenced the size, encapsulation efficiency and release profile. The MS were better sustained release system than the CH paste. © 2015, The Society of The Nippon Dental University.
  • Calcium hydroxide (CH) loaded poly(dl-lactide-co-glycolide) acid (PLGA) microspheres (MS) might be used for apexification requiring a sustained release of Ca2%2b. The aim of this study was to formulate and characterize CH-PLGA-MS. The CH-loaded MS were prepared by either oil-in-water (O/W) or water-in-oil/in-water (W/O/W) emulsion solvent evaporation technique. MS produced by the O/W technique exhibited a larger diameter (18.63 ± 7.23 μm) than the MS produced by the W/O/W technique (15.25 ± 7.37 μm) (Mann–Whitney U test P < 0.001). The CH encapsulation efficiency (Ee) and Ca2%2b release were calculated from data obtained by absorption techniques. Ca2%2b release profile was evaluated for 30 days. To know the Ee, the CH-loaded MS were dissolved in 1 M NaOH to release all its content and a Ca2%2b colorimetric marker was added to this solution. The reagent marked the Ca2%2b in blue color, which was then measured by a UV–Vis system (650 nm). The percentage of Ee was calculated on the basis of the theoretical loading. The Ee of the O/W-produced MS was higher (24 %25) than the corresponding percentage of the W/O/W-produced MS (11 %25). O/W- and W/O/W-produced MS released slower and lower Ca2%2b than a control CH paste with polyethylene glycol 400 (Kruskal–Wallis test). O/W-produced MS released higher Ca2%2b than W/O/W-produced MS (statistically significant differences; P < 0.05). In conclusion, the CH-PLGA-MS were successfully formulated; the technique of formulation influenced the size, encapsulation efficiency and release profile. The MS were better sustained release system than the CH paste. © 2015, The Society of The Nippon Dental University.

publication date

  • 2016-01-01