Injectable hydrogels embedded with alginate microspheres for controlled delivery of bone morphogenetic protein-2

被引:19
|
作者
Zhu, Youjia [1 ]
Wang, Jiulong [1 ]
Wu, Jingjing [2 ]
Zhang, Jun [3 ]
Wan, Ying [2 ]
Wu, Hua [4 ,5 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Dept Stomatol, Wuhan 430071, Peoples R China
[2] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Wuhan 430074, Peoples R China
[3] Royal Mil Coll Canada, Dept Chem & Chem Engn, Kingston, ON K7K 7B4, Canada
[4] Xiamen Univ, Affiliated Hosp 1, Dept Nucl Med, Xiamen 316003, Peoples R China
[5] Xiamen Univ, Affiliated Hosp 1, Minnan PET Ctr, Xiamen 316003, Peoples R China
基金
中国国家自然科学基金;
关键词
chitosan; dextran-polylactide copolymer; microsphere-embedded hydrogel; bone morphogenetic protein-2; controlled release; PERIODONTAL TISSUE REGENERATION; RHEOLOGICAL CHARACTERIZATION; CHITOSAN; RELEASE; ENHANCEMENT; CHONDROCYTE; COMPOSITE; SCAFFOLDS; COPOLYMER; RHBMP-2;
D O I
10.1088/1748-6041/11/2/025010
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Some delivery carriers with injectable characteristics were built using the thermosensitive chitosan/dextran-polylactide/glycerophosphate hydrogel and selected alginate microspheres for the controllable release of bone morphogenetic protein-2 (BMP-2). BMP-2 was first loaded into the microspheres with an average size of around 20 mu m and the resulting microspheres were then embedded into the gel in order to achieve well-controlled BMP-2 release. The microsphere-embedded gels show their incipient gelation temperature at around 32 degrees C and pH at about 7.1. Some gels had their elastic modulus close to 1400 Pa and the ratio of elastic modulus to viscous modulus at around 34, revealing that they behaved like mechanically strong gels. Optimized microsphere-embedded gels were found to be able to administer the BMP-2 release without significant initial burst release in an approximately linear manner over a period of time longer than four weeks. The release rate and the released amount of BMP-2 from these gels could be regulated individually or cooperatively by the initial BMP-2 load and the dextran-polylactide content in the gels. Measurements of the BMP-2 induced alkaline phosphatase activity in C2C12 cells confirmed that C2C12 cells responded to BMP-2 in a dose-dependent way and the released BMP-2 from the microsphere-embedded gels well retained their bioactivity. In vivo assessment of some gels revealed that the released BMP-2 maintained its osteogenesis functions.
引用
收藏
页数:16
相关论文
共 50 条
  • [1] Chitosan-Based Hydrogels Embedded with Hyaluronic Acid Complex Nanoparticles for Controlled Delivery of Bone Morphogenetic Protein-2
    Min, Qing
    Yu, Xiaofeng
    Liu, Jiaoyan
    Wu, Jiliang
    Wan, Ying
    PHARMACEUTICS, 2019, 11 (05):
  • [2] Oxidized alginate hydrogels for bone morphogenetic protein-2 delivery in long bone defects
    Priddy, Lauren B.
    Chaudhuri, Ovijit
    Stevens, Hazel Y.
    Krishnan, Laxminarayanan
    Uhrig, Brent A.
    Willett, Nick J.
    Guldberg, Robert E.
    ACTA BIOMATERIALIA, 2014, 10 (10) : 4390 - 4399
  • [3] Bone morphogenetic protein-2 sustained delivery by hydrogels with microspheres repairs rabbit mandibular defects
    Song, Wei-Yi
    Liu, Guo-Min
    Li, Juan
    Luo, Yun-Gang
    TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2016, 13 (06) : 750 - 761
  • [4] Heparin-Conjugated Fibrin as an Injectable System for Sustained Delivery of Bone Morphogenetic Protein-2
    Yang, Hee Seok
    La, Wan-Geun
    Bhang, Suk Ho
    Jeon, Jeong-Yi
    Lee, Jong Ho
    Kim, Byung-Soo
    TISSUE ENGINEERING PART A, 2010, 16 (04) : 1225 - 1233
  • [5] Response Surface Methodology for Statistical Optimization of Chitosan/Alginate Nanoparticles as a Vehicle for Recombinant Human Bone Morphogenetic Protein-2 Delivery
    Zohri, Maryam
    Javar, Hamid Akbari
    Gazori, Taraneh
    Khoshayand, Mohammad Reza
    Aghaee-Bakhtiari, Seyed Hamid
    Ghahremani, Mohammad Hossein
    INTERNATIONAL JOURNAL OF NANOMEDICINE, 2020, 15 : 8345 - 8356
  • [6] Collagen I derived recombinant protein microspheres as novel delivery vehicles for bone morphogenetic protein-2
    Mumcuoglu, Didem
    de Miguel, Laura
    Jekhmane, Shehrazade
    Siverino, Claudia
    Nickel, Joachim
    Mueller, Thomas D.
    van Leeuwen, Johannes P.
    van Osch, Gerjo J.
    Kluijtmans, Sebastiaan G.
    MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2018, 84 : 271 - 280
  • [7] Improvement in the delivery system of bone morphogenetic protein-2: a new approach to promote bone formation
    Zhang, Quan
    He, Qi-Fen
    Zhang, Tong-Han
    Yu, Xiao-Lin
    Liu, Qin
    Deng, Fei-long
    BIOMEDICAL MATERIALS, 2012, 7 (04)
  • [8] Three dimensional cell printing with sulfated alginate for improved bone morphogenetic protein-2 delivery and osteogenesis in bone tissue engineering
    Park, Jisun
    Lee, Su Jeong
    Lee, Hwangjae
    Park, Su A.
    Lee, Jae Young
    CARBOHYDRATE POLYMERS, 2018, 196 : 217 - 224
  • [9] Application of alginate microbeads as a carrier of bone morphogenetic protein-2 for bone regeneration
    Lee, Yun Hwan
    Lee, Byung-Woo
    Jung, Yun Chan
    Yoon, Byung-Il
    Woo, Heung-Myong
    Kang, Byung-Jae
    JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2019, 107 (02) : 286 - 294
  • [10] Biodegradable gelatin microparticles as delivery systems for the controlled release of bone morphogenetic protein-2
    Patel, Zarana S.
    Yamamoto, Masaya
    Ueda, Hiroki
    Tabata, Yasuhiko
    Mikos, Antonios G.
    ACTA BIOMATERIALIA, 2008, 4 (05) : 1126 - 1138