TY - JOUR
T1 - Polymers for biodegrable medical devices XI. Microencapsulation studies
T2 - Characterization of hydrocortisone-loaded poly-hydroxybutyrate-hydroxyvalerate microspheres
AU - Embleton, J. K.
AU - Tighe, B. J.
PY - 2002/11/1
Y1 - 2002/11/1
N2 - Hydrocortisone-loaded monolithic microspheres were prepared, using a single emulsion solvent evaporation process, from a range of poly-β-hydroxybutyrate-hydroxyvalerate copolymers in which both molecular weight and hydroxyvalerate content were varied. Many similarities were observed in the effects of process parameters and co-polymer composition on the morphologies of the microspheres, and the morphologies of microcapsules prepared (and previously reported) by a double emulsion process. The yields of the single emulsion process were generally superior to those of the double emulsion process, although these were adversely affected by hydrocortisone incorporation as the molecular weight of the copolymer was reduced. The predominant effect of hvdrocortisone incorporation was on polymer morphology, characterized by the appearance of small surface pores; an effect which increased with increasing drug loading. Changes in polymer molecular weight, copolymer composition and process temperature, together with the incorporation of polycaprolactone in the form of a solvent blend, enabled microspheres with a range of morphologies to be produced providing the potential for control of drug release.
AB - Hydrocortisone-loaded monolithic microspheres were prepared, using a single emulsion solvent evaporation process, from a range of poly-β-hydroxybutyrate-hydroxyvalerate copolymers in which both molecular weight and hydroxyvalerate content were varied. Many similarities were observed in the effects of process parameters and co-polymer composition on the morphologies of the microspheres, and the morphologies of microcapsules prepared (and previously reported) by a double emulsion process. The yields of the single emulsion process were generally superior to those of the double emulsion process, although these were adversely affected by hydrocortisone incorporation as the molecular weight of the copolymer was reduced. The predominant effect of hvdrocortisone incorporation was on polymer morphology, characterized by the appearance of small surface pores; an effect which increased with increasing drug loading. Changes in polymer molecular weight, copolymer composition and process temperature, together with the incorporation of polycaprolactone in the form of a solvent blend, enabled microspheres with a range of morphologies to be produced providing the potential for control of drug release.
KW - Biodegradable polymers
KW - Hydrocortisone
KW - Hydroxyvalerate
KW - Poly-hydroxybutyrate
KW - Porous microspheres
UR - http://www.scopus.com/inward/record.url?scp=0036827499&partnerID=8YFLogxK
UR - https://www.tandfonline.com/doi/abs/10.1080/0265204021000022725
U2 - 10.1080/0265204021000022725
DO - 10.1080/0265204021000022725
M3 - Article
C2 - 12569022
AN - SCOPUS:0036827499
SN - 0265-2048
VL - 19
SP - 737
EP - 752
JO - Journal of Microencapsulation
JF - Journal of Microencapsulation
IS - 6
ER -