Fabrication and characterization of porous poly(lactic-co-glycolic acid) (PLGA) microspheres for use as a drug delivery system

被引:27
作者
Bao, Trinh-Quang [1 ]
Hiep, Nguyen-Thi [1 ]
Kim, Yang-Hee [1 ]
Yang, Hun-Mo [2 ]
Lee, Byong-Taek [1 ]
机构
[1] Soonchunhyang Univ, Coll Med, Dept Biomed Engn & Mat, Cheonan 330090, Chungnam, South Korea
[2] Soonchunhyang Univ, Dept Physiol, Coll Med, Cheonan 330090, Chungnam, South Korea
关键词
CONTROLLED-RELEASE; MICROENCAPSULATION; NANOSPHERES; PEPTIDE; PROTEIN;
D O I
10.1007/s10853-010-5101-4
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
In this work, Simvastatin (SIM) loaded porous poly(lactic-co-glycolic acid) (PLGA) microspheres were fabricated using the W/O/W1/W2 double emulsion and solvent evaporation method. The optimal conditions for fabricating porous PLGA microspheres were determined to be 20% distilled water (v/v), 10% PLGA (m/v), and a 4:1 ratio of internal polyvinyl alcohol (PVA) to dichloromethane (DCM). The pores size distribution of porous PLGA microspheres was varied from 0.01 to 40 mu m, while their particle displayed a bimodal size distribution that had two diameter peaks at around 100 mu m and 500 mu m. The SIM encapsulation efficacy was found to be very high with a yield near 80% and the porous PLGA microspheres showed the excellent biocompatibility. In addition, the drug release profile was found to be significantly different from a temporal basis. Base on the combined results of this study, SIM loaded PLGA microspheres holds great promise for use in biomedical applications, especially in drug delivery system or tissue regeneration.
引用
收藏
页码:2510 / 2517
页数:8
相关论文
共 35 条
[1]
Amit R, 2008, J CONTROL RELEASE, V128, P224
[2]
Fabrication of covered porous PLGA microspheres using hydrogen peroxide for controlled drug delivery and regenerative medicine [J].
Bae, Soon Eon ;
Son, Jun Sik ;
Park, Kwideok ;
Han, Dong Keun .
JOURNAL OF CONTROLLED RELEASE, 2009, 133 (01) :37-43
[3]
A novel enzymatically-mediated drug delivery carrier for bone tissue engineering applications: combining biodegradable starch-based microparticles and differentiation agents [J].
Balmayor, Elizabeth Rosado ;
Tuzlakoglu, Kadriye ;
Marques, Alexandra P. ;
Azevedo, Helena S. ;
Reis, Rui L. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2008, 19 (04) :1617-1623
[4]
Beom SK, 2008, ARCH PHARM RES, V31, P1050
[5]
Fabrication of PLG microspheres with precisely controlled and monodisperse size distributions [J].
Berkland, C ;
Kim, KK ;
Pack, DW .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (01) :59-74
[6]
Novel fabrication techniques to produce microspheres by thermally induced phase separation for tissue engineering and drug delivery [J].
Blaker, Jonny J. ;
Knowles, Jonathan C. ;
Day, Richard M. .
ACTA BIOMATERIALIA, 2008, 4 (02) :264-272
[7]
Adipose tissue engineering using mesenchymal stem cells attached to injectable PLGA spheres [J].
Choi, YS ;
Park, SN ;
Suh, H .
BIOMATERIALS, 2005, 26 (29) :5855-5863
[8]
CHUNG YW, 2010, J TAIWAN INST CHEM E, V41, P203
[9]
PREPARATION OF POROUS AND NONPOROUS BIODEGRADABLE POLYMERIC HOLLOW MICROSPHERES [J].
CROTTS, G ;
PARK, TG .
JOURNAL OF CONTROLLED RELEASE, 1995, 35 (2-3) :91-105
[10]
Large porous particles for pulmonary drug delivery [J].
Edwards, DA ;
Hanes, J ;
Caponetti, G ;
Hrkach, J ;
BenJebria, A ;
Eskew, ML ;
Mintzes, J ;
Deaver, D ;
Lotan, N ;
Langer, R .
SCIENCE, 1997, 276 (5320) :1868-1871