Preparation of Biodegradable PLGA Nanospheres Employing a Fast Solvent Evaporation Method
The traditional W1/O/W2 emulsion method has a limit on the control of particle size to a nano-scale with high drug encapsulation efficiency (EE%). In the present study, we modified the solvent removal time and rate to develop an oral peptide drug delivery system using sCT as a model drug. We monitor...
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Published in | Journal of industrial and engineering chemistry (Seoul, Korea) pp. 1043 - 1046 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
한국공업화학회
01.11.2007
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Subjects | |
Online Access | Get full text |
ISSN | 1226-086X 1876-794X |
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Summary: | The traditional W1/O/W2 emulsion method has a limit on the control of particle size to a nano-scale with high drug encapsulation efficiency (EE%). In the present study, we modified the solvent removal time and rate to develop an oral peptide drug delivery system using sCT as a model drug. We monitored the effect of the type of poly (vinyl alcohol) (PVA) within the W2 phase on the EE%. SEM images and particle size measurements revealed that the outer surfaces of representative nanosphere samples were very fine and even; the particle size was 383.2 ± 8.7 nm with a narrow size distribution (polydispersity index = 0.25 ± 0.004). The EE% increased depending on the solvent removal time and rate from 11.4 ± 1.3 to 28.8 ± 3.0 and 52.5 ± 6.5, compared to control nanospheres, respectively. The EE% of sCT was also enhanced by controlling the molecular weight of PVA within the W2 phase. KCI Citation Count: 12 |
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Bibliography: | G704-000711.2007.13.6.001 http://www.cheric.org/article/692391 |
ISSN: | 1226-086X 1876-794X |