Comparison of protein loaded poly(ε-caprolactone) microparticles prepared by the hot-melt technique

被引:0
|
作者
Lin, WJ [1 ]
Yu, CC [1 ]
机构
[1] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei 100, Taiwan
关键词
PCL; BSA; PEG; microparticles; hot-melt technique;
D O I
10.1080/02652040010019569
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This study was systematically designed to compare bovine serum albumin (BSA) loaded poly(epsilon -caprolactone) (PCL) microparticles based on a 2(3) factorial experiment. The microparticles were prepared by the holt-melt technique without using an organic solvent for polymer solubilization. The influence of the particle size of protein, protein/polymer ratio, and hydrophilic PEG on the surface morphology, particle size as well as the yield of PCL microparticles, encapsulation efficiency of BSA, and in vitro release properties were investigated. The structure of BSA remained its integrity using this technique. The mean particle size of BSA-loaded microparticles were in the range of 12.7 +/-0.1-16.9 +/-0.8 mum, and all of the particles were smooth on the surface. The production yield of microparticles and the encapsulation efficiencies were high, and the values were in the range of 94.8 +/-1.6%-98.1 +/-1.0% and 94.9 +/-9.6%-98.6 +/-0.3%, respectively. The burst release of BSA was in the range of 8.2 +/-0.4%-61.0 +/-0.8%, which strongly depended on the formulation. None of three variables affected the yield of microparticles prepared from eight formulations (p > 0.05). However, the particle size of BSA significantly affected the size and the burst release as well as the cumulative release of protein in these microparticles (p < 0.05). The initial loading of BSA in terms of BSA/PCL ratio and the amount of PEG blended with PCL significantly affected all of the properties, except the yield (p < 0.05). The smaller the particle size of the BSA, the smaller the size of the resulting microparticles. Since the total surface area of the small particles was larger than that of the large particles, this accounted for the high burst release of protein from the microparticles encapsulating triturated-BSA.
引用
收藏
页码:585 / 592
页数:8
相关论文
共 50 条
  • [1] Paracetamol-Loaded Poly(ε-Caprolactone) Layered Silicate Nanocomposites Prepared Using Hot-Melt Extrusion
    Campbell, Kayleen
    Qi, Sheng
    Craig, Duncan Q. M.
    McNally, Tony
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (12) : 4831 - 4843
  • [2] Comparison of chitosan and gelatin coated microparticles: prepared by hot-melt method
    Lin, WJ
    Kang, WW
    JOURNAL OF MICROENCAPSULATION, 2003, 20 (02) : 169 - 177
  • [3] Ibuprofen-loaded poly(ε-caprolactone) layered silicate nanocomposites prepared by hot melt extrusion
    Kayleen T. Campbell
    Duncan Q. M. Craig
    Tony McNally
    Journal of Materials Science: Materials in Medicine, 2010, 21 : 2307 - 2316
  • [4] Ibuprofen-loaded poly(ε-caprolactone) layered silicate nanocomposites prepared by hot melt extrusion
    Campbell, Kayleen T.
    Craig, Duncan Q. M.
    McNally, Tony
    JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2010, 21 (08) : 2307 - 2316
  • [5] Influence of pluronics on protein-loaded poly(ε-caprolactone) microparticles
    Lin, WJ
    Huang, LI
    JOURNAL OF MICROENCAPSULATION, 2001, 18 (02) : 191 - 197
  • [6] Mechanism and Kinetics of Drug Release from Poly(E-Caprolactone) Based Extrudates Prepared By Hot-Melt Extrusion
    Zhang, Cong
    Chen, Xia
    Liu, Guiting
    Chen, Rong
    Guo, Shaoyun
    JOURNAL OF MACROMOLECULAR SCIENCE PART B-PHYSICS, 2016, 55 (03): : 285 - 298
  • [7] Blends of poly(ε-caprolactone-b-lactic acid) and poly(lactic acid) for hot-melt applications
    Stolt, M
    Viljanmaa, M
    Södergård, A
    Törmälä, P
    JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 91 (01) : 196 - 204
  • [8] Production of Lysozyme-PLGA-Loaded Microparticles for Controlled Release Using Hot-Melt Extrusion
    Farinha, Susana
    Moura, Claudia
    Afonso, Maria Dina
    Henriques, Joao
    AAPS PHARMSCITECH, 2020, 21 (07)
  • [9] Development of biodegradable hot-melt adhesive based on poly-ε-caprolactone and soy protein isolate for food packaging system
    Choi, WY
    Lee, CM
    Park, HJ
    LWT-FOOD SCIENCE AND TECHNOLOGY, 2006, 39 (06) : 591 - 597
  • [10] Production of Lysozyme-PLGA-Loaded Microparticles for Controlled Release Using Hot-Melt Extrusion
    Susana Farinha
    Cláudia Moura
    Maria Diná Afonso
    João Henriques
    AAPS PharmSciTech, 21