TY - JOUR
T1 - Application of acid-catalyzed hydrolysis of dispersed organic solvent in developing new microencapsulation process technology
AU - Lee, Honghwa
AU - Lee, Sunhwa
AU - Bhattacharjee, Himanshu
AU - Sah, Hongkee
N1 - Funding Information:
This study was supported by a grant from the Korean Health Technology R&D Project, Ministry for Health, Welfare and Family Affairs, Republic of Korea (A092018).
PY - 2012/6
Y1 - 2012/6
N2 - The aim of this study was to evaluate a new microencapsulation technology employing an acid-catalyzed solvent extraction method in conjunction to an emulsion-based microencapsulation process. Its process consisted of emulsifying a dispersed phase of poly(D,L-lactide-co-glycolide) and isopropyl formate in an aqueous phase. This step was followed by adding hydrochloric acid to the resulting oil-in-water emulsion, in order to initiate the hydrolysis of isopropyl formate dissolved in the aqueous phase. Its hydrolysis caused the liberation of water-soluble species, that is, isopropanol and formic acid. This event triggered continual solvent leaching out of emulsion droplets, thereby initiating microsphere solidification. This new processing worked well for encapsulation of progesterone and ketoprofen that were chosen as a nonionizable model drug and a weakly acidic one, respectively. Furthermore, the structural integrity of poly(D,L-lactide-co-glycolide) was retained during microencapsulation. The new microencapsulation technology, being conceptually different from previous approaches, might be useful in preparing various polymeric particles.
AB - The aim of this study was to evaluate a new microencapsulation technology employing an acid-catalyzed solvent extraction method in conjunction to an emulsion-based microencapsulation process. Its process consisted of emulsifying a dispersed phase of poly(D,L-lactide-co-glycolide) and isopropyl formate in an aqueous phase. This step was followed by adding hydrochloric acid to the resulting oil-in-water emulsion, in order to initiate the hydrolysis of isopropyl formate dissolved in the aqueous phase. Its hydrolysis caused the liberation of water-soluble species, that is, isopropanol and formic acid. This event triggered continual solvent leaching out of emulsion droplets, thereby initiating microsphere solidification. This new processing worked well for encapsulation of progesterone and ketoprofen that were chosen as a nonionizable model drug and a weakly acidic one, respectively. Furthermore, the structural integrity of poly(D,L-lactide-co-glycolide) was retained during microencapsulation. The new microencapsulation technology, being conceptually different from previous approaches, might be useful in preparing various polymeric particles.
KW - Acid-catalysis
KW - Microencapsulation
KW - Microspheres
KW - PLGA
UR - http://www.scopus.com/inward/record.url?scp=84861058414&partnerID=8YFLogxK
U2 - 10.3109/02652048.2011.651502
DO - 10.3109/02652048.2011.651502
M3 - Article
C2 - 22299629
AN - SCOPUS:84861058414
SN - 0265-2048
VL - 29
SP - 380
EP - 387
JO - Journal of Microencapsulation
JF - Journal of Microencapsulation
IS - 4
ER -