Preparation and characterization of ibuprofen-loaded microspheres consisting of poly(3-hydroxybutyrate) and methoxy poly (ethylene glycol)-b-poly (D,L-lactide) blends or poly(3-hydroxybutyrate) and gelatin composites for controlled drug release

被引:37
作者
Bidone, Juliana [1 ]
Melo, Ana Paula P. [1 ]
Bazzo, Giovana C. [2 ]
Carmignan, Francoise [1 ]
Soldi, Marli S. [2 ]
Pires, Alfredo T. N. [2 ]
Lemos-Senna, Elenara [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Ciencias Farmaceut, Lab Farmacotecn, Florianopolis, SC, Brazil
[2] Univ Fed Santa Catarina, Dept Quim, Grp Estudos Mat Polimer POLIMAT, Florianopolis, SC, Brazil
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2009年 / 29卷 / 02期
关键词
Microspheres; Poly(3-hydroxybutyrate); Methoxy poly (ethylene glycol)-b-poly (D; L-lactide); Gelatin; Ibuprofen; Controlled release; IN-VITRO; POLYHYDROXYALKANOATES; COPOLYMER; DELIVERY;
D O I
10.1016/j.msec.2008.10.016
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
Poly-(3-hydroxybutyrate) (P(3HB)) is a biodegradable and biocompatible polymer that has been used to obtain polymer-based drug carriers. However, due to the high crystallinity degree of this polymer, drug release from P(3HB) microspheres frequently occurs at excessive rates. In this study. two strategies for prolonging ibuprofen release from P(3HB)-based microspheres were tested: blending with poly(D,L-lactide)-b-polyethylene glycol (mPEC-PLA); and obtaining composite particles with gelatin (GEL). SEM micrographs showed particles that were spherical and had a tough surface. A slight decrease of the crystallinity degree of P(3HB) was observed only in the DSC thermogram obtained from unloaded-microspheres prepared from 1:1 P(3HB):mPEG-PLA blend. For IBF-loaded microspheres, a reduction of around 10 degrees C in the melting temperature of P(3HB) was observed, indicating that the crystalline structure of the polymer was affected in the presence of the drug. DSC studies also yielded evidence of the presence of a molecular dispersion coexisting with a crystalline dispersion in the drug in the matrix. Similar results were obtained from X-ray diffractograms. In spite of 1:1 mPEG-PLA:P(3HB) blends having contributed to the reduction of the burst effect, a more controlled drug release was provided by the use of the 3:1 P(3HB):mPEGPLA blend. This result indicated that particle hydration played an important role in the drug release. On the other hand, the preparation of P(3HB):GEL composite microspheres did not allow control of the IBF release. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:588 / 593
页数:6
相关论文
共 11 条
[1]
CARMINGNAN J, 2008, LATIN AM J PHARM, V27, P131
[2]
The application of polyhydroxyalkanoates as tissue engineering materials [J].
Chen, GQ ;
Wu, Q .
BIOMATERIALS, 2005, 26 (33) :6565-6578
[3]
Biodegradable ibuprofen-loaded PLGA microspheres for intraarticular administration -: Effect of Labrafil addition on release in vitro [J].
Fernández-Carballido, A ;
Herrero-Vanrell, R ;
Molina-Martínez, IT ;
Pastoriza, P .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 279 (1-2) :33-41
[4]
In vitro and in vivo degradation studies for development of a biodegradable patch based on poly(3-hydroxybutyrate) [J].
Freier, T ;
Kunze, C ;
Nischan, C ;
Kramer, S ;
Sternberg, K ;
Sass, M ;
Hopt, UT ;
Schmitz, KP .
BIOMATERIALS, 2002, 23 (13) :2649-2657
[5]
Characterization and application of poly(β-hydroxyalkanoates) family as composite biomaterials [J].
Galego, N ;
Rozsa, C ;
Sánchez, R ;
Fung, J ;
Vázquez, A ;
Tomás, JS .
POLYMER TESTING, 2000, 19 (05) :485-492
[6]
Nifedipine solid dispersion in microparticles of ammonio methacrylate copolymer and ethylcellulose binary blend for controlled drug delivery - Effect of drug loading on release kinetics [J].
Huang, Jingjun ;
Wigent, Rodney J. ;
Bentzley, Catherine M. ;
Schwartz, Joseph B. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 319 (1-2) :44-54
[7]
Huang YY, 2001, J MICROENCAPSUL, V18, P457
[8]
Physical solid-state properties and dissolution of sustained-release matrices of polyvinylacetate [J].
Novoa, GAG ;
Heinämäki, J ;
Mirza, S ;
Antikainen, O ;
Colarte, AI ;
Paz, AS ;
Yliruusi, J .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 59 (02) :343-350
[9]
Biosynthetic polyhydroxyalkanoates and their potential in drug delivery [J].
Pouton, CW ;
Akhtar, S .
ADVANCED DRUG DELIVERY REVIEWS, 1996, 18 (02) :133-162
[10]
Polymer blends and composites from renewable resources [J].
Yu, Long ;
Dean, Katherine ;
Li, Lin .
PROGRESS IN POLYMER SCIENCE, 2006, 31 (06) :576-602