Preparation and characterization of bee venom-loaded PLGA particles for sustained release

被引:20
作者
Park, Min-Ho [1 ,2 ]
Jun, Hye-Suk [1 ,2 ]
Jeon, Jong-Woon [3 ]
Park, Jin-Kyu [3 ]
Lee, Bong-Joo [4 ]
Suh, Guk-Hyun [4 ]
Park, Jeong-Sook [1 ,2 ]
Cho, Cheong-Weon [1 ,2 ]
机构
[1] Chungnam Natl Univ, Coll Pharm, 99 Daehak Ro, Daejeon 34134, South Korea
[2] Chungnam Natl Univ, Inst Drug Res & Dev, 99 Daehak Ro, Daejeon 34134, South Korea
[3] Wissen Co Ltd, Daejeon, South Korea
[4] Chonnam Natl Univ, Coll Vet Med, Gwangju, South Korea
关键词
Bee venom; PLGA; sustained release; microparticle; IN-VITRO RELEASE; POLY(LACTIDE-CO-GLYCOLIDE) NANOPARTICLES; CONTROLLED DELIVERY; MICROSPHERES; DRUG; STABILITY; FORMULATION; ADSORPTION; SYSTEM;
D O I
10.1080/10837450.2016.1264415
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bee venom-loaded poly(lactic-co-glycolic acid) (PLGA) particles were prepared by double emulsion-solvent evaporation, and characterized for a sustained-release system. Factors such as the type of organic solvent, the amount of bee venom and PLGA, the type of PLGA, the type of polyvinyl alcohol, and the emulsification method were considered. Physicochemical properties, including the encapsulation efficiency, drug loading, particle size, zeta-potential and surface morphology were examined by Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and X-ray diffraction (XRD). The size of the bee venom-loaded PLGA particles was 500 nm (measured using sonication). Zeta-potentials of the bee venom-loaded PLGA particles were negative owing to the PLGA. FT-IR results demonstrated that the bee venom was completely encapsulated in the PLGA particles, indicated by the disappearance of the amine and amide peaks. In addition, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis indicated that the bee venom in the bee venom-loaded PLGA particles was intact. In vitro release of the bee venom from the bee venom-loaded PLGA particles showed a sustained-release profile over 1 month. Bee venom-loaded PLGA particles can help improve patients' quality of life by reducing the number of injections required.
引用
收藏
页码:857 / 864
页数:8
相关论文
共 40 条
[1]   PREPARATION OF BIODEGRADABLE MICROSPHERES AND MICROCAPSULES .2. POLYACTIDES AND RELATED POLYESTERS [J].
ARSHADY, R .
JOURNAL OF CONTROLLED RELEASE, 1991, 17 (01) :1-21
[2]   Fabrication of protein-loaded PLGA nanoparticles: effect of selected formulation variables on particle size and release profile [J].
Azizi, Monireh ;
Farahmandghavi, Farhid ;
Joghataei, Mohammadtaghi ;
Zandi, Mojgan ;
Imani, Mohammad ;
Bakhtiary, Mehrdad ;
Dorkoosh, Farid Abedin ;
Ghazizadeh, Fariba .
JOURNAL OF POLYMER RESEARCH, 2013, 20 (04)
[3]   Haloperidol-loaded PLGA nanoparticles: Systematic study of particle size and drug content [J].
Budhian, Avinash ;
Siegel, Steven J. ;
Winey, Karen I. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 336 (02) :367-375
[4]   Cystatin incorporated in poly(lactide-co-glycolide) nanoparticles: development and fundamental studies on preservation of its activity [J].
Cegnar, M ;
Kos, J ;
Kristl, J .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 22 (05) :357-364
[5]   Effects of solvent selection and fabrication method on the characteristics of biodegradable poly(lactide-co-glycolide) microspheres containing ovalbumin [J].
Cho, SW ;
Song, SH ;
Choi, YW .
ARCHIVES OF PHARMACAL RESEARCH, 2000, 23 (04) :385-390
[6]   Preparation and characterization of fentanyl-loaded PLGA microspheres: in vitro release profiles [J].
Choi, HS ;
Seo, SA ;
Khang, G ;
Rhee, JM ;
Lee, HB .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 234 (1-2) :195-203
[7]   CONTROLLED DELIVERY SYSTEMS FOR PROTEINS BASED ON POLY(LACTIC GLYCOLIC ACID) MICROSPHERES [J].
COHEN, S ;
YOSHIOKA, T ;
LUCARELLI, M ;
HWANG, LH ;
LANGER, R .
PHARMACEUTICAL RESEARCH, 1991, 8 (06) :713-720
[8]   Preparation and characterization of melittin-loaded poly (DL-lactic acid) or poly (DL-lactic-co-glycolic acid) microspheres made by the double emulsion method [J].
Cui, F ;
Cun, DM ;
Tao, AJ ;
Yang, MS ;
Shi, K ;
Zhao, M ;
Guan, Y .
JOURNAL OF CONTROLLED RELEASE, 2005, 107 (02) :310-319
[9]   Evaluation of ciprofloxacin-loaded Eudragit® RS100 or RL100/PLGA nanoparticles [J].
Dillen, Kathleen ;
Vandervoort, Jo ;
Van den Mooter, Guy ;
Ludwig, Annick .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 314 (01) :72-82
[10]   Methoxy poly(ethylene glycol)-poly(lactide) (MPEG-PLA) nanoparticles for controlled delivery of anticancer drugs [J].
Dong, YC ;
Feng, SS .
BIOMATERIALS, 2004, 25 (14) :2843-2849