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http://dx.doi.org/10.5012/bkcs.2011.32.5.1465

The Evaluation of Fabrication Parameters Process Effect on the Formation of Poly(lactic-co-glycolic acid) (PLGA) Microspheres  

Bao, Trinh-Quang (Department of Biomedical Engineering and Materials, College of Medicine, Soonchunhyang University)
Lee, Byong-Taek (Department of Biomedical Engineering and Materials, College of Medicine, Soonchunhyang University)
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Abstract
In this study, a poly(lactic-co-glycolic acid) (PLGA) microspheres was fabricated using emulsion solvent evaporation technique. During the procedure fabrication, some parameters process have effected on the formation of micro-carriers. The structure and morphology of micro-carriers were evaluated by SEM observation. Beside, heparin incorporated into microspheres was determined using toluidine blue method. Specifically, the effects of some parameters process such as ultrasonic levels, PLGA concentrations and freeze-dry times on the size, structure, porous formation and heparin entrapment of micro-carriers were studied carefully. We found that, the morphology and structure of carriers were influenced by the all above parameters. The diameter of the carriers varied from 20 to 400 ${\mu}M$ depending on experimental conditions. At suitable freeze-dry time, the pores were automatically formation on surface of microspheres with a significantly in the numbers of pore. After heparin incorporated porous PLGA microspheres, it was suggested that the highly heparin incorporated into porous PLGA microspheres could enhance of angiogenesis for tissue regeneration easily.
Keywords
Porous PLGA microspheres; Drug delivery system; Heparin;
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1 Chengji, C.; Steven, P. S. Pharmaceutical Research 2007, 24, 2381-2393.   DOI
2 Chung, H. J.; Kim, H. K.; Joon, J. J.; Park, T. G. Pharmaceutical Research 2006, 23, 1835-1841.   DOI
3 Kuo, Y. C.; Shih, K. H. Colloids and Surfaces B: Biointerfaces 2009, 71, 282-287.   DOI   ScienceOn
4 Yi, Y. Y.; Tai, S. C.; Ngee, P. N. Biomaterials 2001, 22, 231-241.   DOI   ScienceOn
5 Zonghua, L.; Yanpeng, J.; Fanna, L.; Ziyong, Z. Journal of Biomedical Materials Research Part A 2007, 83A, 206-812.
6 Hoffart, V.; Ubrich, N.; Simonin, C.; Babak, V.; Vigneron, C.; Hoffman, M.; Lecompte, T.; Maincent, P. Drug Development and Industrial Pharmacy 2002, 28, 1091-1099.   DOI   ScienceOn
7 Yu, H. L.; Chiung, H. C.; Yu, S. W.; Yuan, M. H.; Shu, F. C.; Yi, J. C. Biomaterials 2009, 30, 3332-3342.   DOI   ScienceOn
8 Yi, Y. Y.; Tai, S. C.; Ngee, P. N. Biomaterials 2001, 22, 231-241.   DOI   ScienceOn
9 Sergio, F.; Hans, P. M.; Bruno, G. Journal of Controlled Release 2005, 102, 313-332.   DOI   ScienceOn
10 Manca, M. L.; Mourtas, S.; Dracopoulos, V.; Fadda, A. M.; Antimisiaris, S. G. Colloids and Surfaces B: Biointerfaces 2008, 68, 220-231.
11 Langer, R. Nature 1998, 392, 1-5.   DOI
12 Leong, K. W.; Amore, P. D.; Marletta, M.; Langer, R. Journal of Biomedical Materials Research 1986, 20, 51-64.   DOI   ScienceOn
13 Chung, H. J.; Park, T. G. Tissue Engineering: Part A 2008, 15, 1392-1400.