polyDL-lactide-b-poly(ethylene glycol)-b-polyDL-lactide(PELA) were used as the microsphere matrix to encapsulate plasmid DNA. The PDLLA
PELA
pBR322-loaded PDLLA and pBR322-loaded PELA microspheres were prepared by solvent extraction method based on the formation of multiple w1/o/w2 emulsion. The microspheres were characterized by surface morphology
mean particle size
particle size distribution and loading efficiency. The integrity of DNA molecules after being extracted from microspheres was determined by agarose gel electrophoresis. The result suggested that plasmid DNA molecules could retain their integrity after being encapsulated by PELA. The PELA microspheres could prevent plasmid DNA from being digested by DNase. The in vitro degradation and release profiles of plasmid DNA-loaded microspheres were measured in pH = 7.4 buffer solution at 37 ℃. The in vitrodegradation profiles of the microspheres were evaluated by the deterioration in microspheres surface morphology
the molecular weight reduction of polymer
the mass loss of microspheres
the changes of pH values of degradation medium
and the changes of particle size. The in vitro release profiles of the microspheres were assessed by measurement of the amount of DNA presented in the release medium at determined intervals. The release profiles were correlation with the degradation profiles. The release of plasmid DNA from PELA microspheres showed a similar biphasic trend
that is
an initial burst release was followed by a slow
but sustained release.
Abstract
PolyDL-lactide (PDLLA) and the block copolymer
polyDL-lactide-b-poly(ethylene glycol)-b-polyDL-lactide(PELA) were used as the microsphere matrix to encapsulate plasmid DNA. The PDLLA
PELA
pBR322-loaded PDLLA and pBR322-loaded PELA microspheres were prepared by solvent extraction method based on the formation of multiple w1/o/w2 emulsion. The microspheres were characterized by surface morphology
mean particle size
particle size distribution and loading efficiency. The integrity of DNA molecules after being extracted from microspheres was determined by agarose gel electrophoresis. The result suggested that plasmid DNA molecules could retain their integrity after being encapsulated by PELA. The PELA microspheres could prevent plasmid DNA from being digested by DNase. The in vitro degradation and release profiles of plasmid DNA-loaded microspheres were measured in pH = 7.4 buffer solution at 37 ℃. The in vitrodegradation profiles of the microspheres were evaluated by the deterioration in microspheres surface morphology
the molecular weight reduction of polymer
the mass loss of microspheres
the changes of pH values of degradation medium
and the changes of particle size. The in vitro release profiles of the microspheres were assessed by measurement of the amount of DNA presented in the release medium at determined intervals. The release profiles were correlation with the degradation profiles. The release of plasmid DNA from PELA microspheres showed a similar biphasic trend
that is
an initial burst release was followed by a slow
but sustained release.
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Keywords
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