Additive Manufacturing of Wet-Spun Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-Based Scaffolds Loaded with Hydroxyapatite

被引:4
作者
Pecorini, Gianni [1 ]
Braccini, Simona [1 ]
Simoni, Stefano [1 ]
Corti, Andrea [1 ]
Parrini, Gianluca [2 ]
Puppi, Dario [1 ]
机构
[1] Univ Pisa, Dept Chem & Ind Chem, BIOLab Res Grp, UdR INSTM PISA, Via Moruzzi 13, I-56124 Pisa, Italy
[2] Fabr Machinale, Via Giuntini 13, I-56021 Cascina, Pisa, Italy
关键词
3D printing; bone tissue engineering; composite materials; osteoinductive materials; polyhydroxyalkanoates; polymeric blends; IN-VITRO ASSESSMENT; MECHANICAL-PROPERTIES; COMPOSITE SCAFFOLDS; THERMAL-DEGRADATION; MC3T3-E1; CELLS; TISSUE; FABRICATION; PHBV; REGENERATION; MORPHOLOGY;
D O I
10.1002/mabi.202300538
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tissue engineering represents an advanced therapeutic approach for the treatment of bone tissue defects. Polyhydroxyalkanoates are a promising class of natural polymers in this context thanks to their biocompatibility, processing versatility, and mechanical properties. The aim of this study is the development by computer-aided wet-spinning of novel poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV)-based composite scaffolds for bone engineering. In particular, PHBV scaffolds are loaded with hydroxyapatite (HA), an osteoinductive ceramic, in order to tailor their biological activity and mechanical properties. PHBV blending with poly(lactide-co-glycolide) (PLGA) is also explored to increase the processing properties of the polymeric mixture used for composite scaffold fabrication. Different HA percentages, up to 15% wt., can be loaded into the PHBV or PHBV/PLGA scaffolds without compromising their interconnected porous architecture, as well as the polymer morphological and thermal properties, as demonstrated by scanning electron microscopy, thermogravimetric analysis, and differential scanning calorimetry. In addition, HA loading results in increased scaffold compressive stiffness to levels comparable to those of trabecular bone tissue, as well as in higher in vitro MC3T3-E1 cell viability and production of mineralized extracellular matrix, in comparison to what observed for unloaded scaffolds. The observed mechanical and biological properties suggest the suitability of the developed scaffolds for bone engineering.
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页数:16
相关论文
共 94 条
[1]   Porous scaffolds for bone regeneration [J].
Abbasi, Naghmeh ;
Hamlet, Stephen ;
Love, Robert M. ;
Nguyen, Nam-Trung .
JOURNAL OF SCIENCE-ADVANCED MATERIALS AND DEVICES, 2020, 5 (01) :1-9
[2]   Recent Advances in Synthetic and Natural Biomaterials-Based Therapy for Bone Defects [J].
Alvarez Echazu, Maria I. ;
Perna, Oriana ;
Olivetti, Christian E. ;
Antezana, Pablo E. ;
Municoy, Sofia ;
Tuttolomondo, Maria V. ;
Galdoporpora, Juan M. ;
Alvarez, Gisela S. ;
Olmedo, Daniel G. ;
Desimone, Martin F. .
MACROMOLECULAR BIOSCIENCE, 2022, 22 (04)
[3]  
Amini AR, 2012, TISSUE ENG PT A, V18, P1376, DOI [10.1089/ten.tea.2011.0076, 10.1089/ten.TEA.2011.0076]
[4]   Potential Applications of Polyhydroxyalkanoates as a Biomaterial for the Aging Population [J].
Ang, Shaik Ling ;
Sivashankari, Ramamoorthi ;
Shaharuddin, Bakiah ;
Chuah, Jo-Ann ;
Tsuge, Takeharu ;
Abe, Hideki ;
Sudesh, Kumar .
POLYMER DEGRADATION AND STABILITY, 2020, 181
[5]   Effect of wettability and surface functional groups on protein adsorption and cell adhesion using well-defined mixed self-assembled monolayers [J].
Arima, Yusuke ;
Iwata, Hiroo .
BIOMATERIALS, 2007, 28 (20) :3074-3082
[6]  
Baek J.-Y., 2012, J NANOMATER, V2012, P1165
[7]   Bone regeneration with hydroxyapatite-based biomaterials [J].
Bal, Zeynep ;
Kaito, Takashi ;
Korkusuz, Feza ;
Yoshikawa, Hideki .
EMERGENT MATERIALS, 2020, 3 (04) :521-544
[8]   Biodegradable Elastomers for Tissue Engineering and Cell-Biomaterial Interactions [J].
Bettinger, Christopher J. .
MACROMOLECULAR BIOSCIENCE, 2011, 11 (04) :467-482
[9]  
Breuls Roel G M, 2008, Open Orthop J, V2, P103, DOI 10.2174/1874325000802010103
[10]  
Brown-Woodman PDC, 1998, TERATOLOGY, V57, P321, DOI 10.1002/(SICI)1096-9926(199806)57:6<321::AID-TERA5>3.0.CO