Engineering BSA-dextran particles encapsulated bead-on-string nanofiber scaffold for tissue engineering applications

被引:41
作者
Li, Tingxiao [1 ,2 ]
Ding, Xin [1 ,2 ]
Tian, Lingling [3 ]
Ramakrishna, Seeram [3 ]
机构
[1] Donghua Univ, Minist Educ China, Key Lab Text Sci & Technol, Shanghai 201620, Peoples R China
[2] Donghua Univ, Coll Text, Shanghai 201620, Peoples R China
[3] Natl Univ Singapore, Ctr Nanofibers & Nanotechnol, Dept Mech Engn, Singapore 117576, Singapore
关键词
STEM-CELL DIFFERENTIATION; DRUG-DELIVERY; MORPHOLOGY; RELEASE; MATRIX; REGENERATION; FIBROBLASTS; FABRICATION; FIBERS;
D O I
10.1007/s10853-017-1245-9
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Electrospun bead-on-string nanofiber, with unique beads structure could act as reservoirs for particle drugs, is a promising fibrous structure with continuous drug release for regulating cellular functions such as cell adhesion and proliferation in tissue engineering applications. In this study, we reported on the encapsulation and sustained release of model drug (BSA) from poly (lactic-co-glycolic acid) (PLGA) beaded nanofibers loaded with BSA-dextran (B-D) particles. Smooth PLGA nanofiber scaffold with B-D particles was fabricated as a positive control. Fluorescent images of inversed florescence microscopy suggested that B-D particles tended to accumulate within beads structure of beaded nanofibers but appeared randomly along smooth nanofibers. The entrapment of B-D particles within beaded nanofibers resulted in alleviative burst release compared with smooth nanofiber and sustained release of BSA over 31 days. The holes on the surface of nanofibers caused by the release of B-D particles would accelerate the degradation of nanofibers. Tensile testing result demonstrated that beaded structure would decrease the Young's Modulus, tensile strength and elongation compared with smooth nanofibers. Cultivation of human mesenchymal stem cells on particle drugs encapsulated beaded nanofibers indicated that cells could attached and proliferated well on beaded structure nanofibers, suggesting that such beaded nanofibers with a controlled and continuous release profiles was a promising candidate scaffold for tissue regeneration.
引用
收藏
页码:10661 / 10672
页数:12
相关论文
共 32 条
[1]   Progress in the Field of Electrospinning for Tissue Engineering Applications [J].
Agarwal, Seema ;
Wendorff, Joachim H. ;
Greiner, Andreas .
ADVANCED MATERIALS, 2009, 21 (32-33) :3343-3351
[2]   Use of electrospinning technique for biomedical applications [J].
Agarwal, Seema ;
Wendorff, Joachim H. ;
Greiner, Andreas .
POLYMER, 2008, 49 (26) :5603-5621
[3]   Nanofiber technology: Designing the next generation of tissue engineering scaffolds [J].
Barnes, Catherine P. ;
Sell, Scott A. ;
Boland, Eugene D. ;
Simpson, David G. ;
Bowlin, Gary L. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (14) :1413-1433
[4]   Electrospun chitosan-based nanofibers and their cellular compatibility [J].
Bhattarai, N ;
Edmondson, D ;
Veiseh, O ;
Matsen, FA ;
Zhang, MQ .
BIOMATERIALS, 2005, 26 (31) :6176-6184
[5]  
Bu N, 2012, J PHYS D, V45, P4172
[6]   The influence of fiber diameter of electrospun substrates on neural stem cell differentiation and proliferation [J].
Christopherson, Gregory T. ;
Song, Hongjun ;
Mao, Hai-Quan .
BIOMATERIALS, 2009, 30 (04) :556-564
[7]   Beaded nanofibers formed during electrospinning [J].
Fong, H ;
Chun, I ;
Reneker, DH .
POLYMER, 1999, 40 (16) :4585-4592
[8]   Amphiphilic beads as depots for sustained drug release integrated into fibrillar scaffolds [J].
Gaharwar, Akhilesh K. ;
Mihaila, Silvia M. ;
Kulkarni, Ashish A. ;
Patel, Alpesh ;
Di Luca, Andrea ;
Reis, Rui L. ;
Gomes, Manuela E. ;
van Blitterswijk, Clemens ;
Moroni, Lorenzo ;
Khademhosseini, Ali .
JOURNAL OF CONTROLLED RELEASE, 2014, 187 :66-73
[9]   Nanostructured materials for applications in drug delivery and tissue engineering [J].
Goldberg, Michael ;
Langer, Robert ;
Jia, Xinqiao .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2007, 18 (03) :241-268
[10]   Tissue engineering - Current challenges and expanding opportunities [J].
Griffith, LG ;
Naughton, G .
SCIENCE, 2002, 295 (5557) :1009-+