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Tuning pore features of mineralized collagen/PCL scaffolds for cranial bone regeneration in a rat model.
Wang, Shuo; Yang, Yongdong; Koons, Gerry L; Mikos, Antonios G; Qiu, Zhiye; Song, Tianxi; Cui, Fuzhai; Wang, Xiumei.
Afiliación
  • Wang S; State Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials of Ministry of Education, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China.
  • Yang Y; State Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials of Ministry of Education, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China; Dongzhimen Hospital Affiliated Beijing University of Chinese Medicine, Beijing 100700, Chi
  • Koons GL; Department of Bioengineering, Rice University, Houston, TX 77030, USA.
  • Mikos AG; Department of Bioengineering, Rice University, Houston, TX 77030, USA.
  • Qiu Z; Beijing Allgens Medical Science and Technology Co., Ltd., Beijing 100176, China.
  • Song T; Beijing Allgens Medical Science and Technology Co., Ltd., Beijing 100176, China.
  • Cui F; State Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials of Ministry of Education, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China.
  • Wang X; State Key Laboratory of New Ceramics and Fine Processing, Key Laboratory of Advanced Materials of Ministry of Education, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China. Electronic address: wxm@mail.tsinghua.edu.cn.
Mater Sci Eng C Mater Biol Appl ; 106: 110186, 2020 Jan.
Article en En | MEDLINE | ID: mdl-31753406
ABSTRACT
Porosity is indispensable for a bone tissue-engineered scaffold for facilitating endogenous cell migration and nascent bone ingrowth. In large-sized cranial bone defect repair, porous scaffolds meet great challenges to match cranial bone regeneration and provide sufficient protection with structural integrity. Therefore, the pore features of the scaffolds for cranial bone regeneration should differ from those typical porous scaffolds used in tubular bone repair and be finely tuned. In this study, a series of porous mineralized collagen/PCL scaffolds with different pore features were fabricated via freeze-drying and applied in a Sprague Dawley rat cranial bone calvarial defect model. The pore size for four groups increased from 10-45 µm to 40-130 µm. As scaffold porosity increased, the compressive strength decreased from 2.09 ±â€¯0.12 MPa to 0.51 ±â€¯0.04 MPa. The micro-computed tomography three-dimensional reconstruction images showed that as pore size and porosity increased, the amount of new bone formation had a maximum in group 3 (pore size 20-100 µm, compressive strength 1.06 ±â€¯0.03 MPa). In addition, the histological and histomorphometric analyses showed a consistent tendency which confirmed the Micro-CT results. Meanwhile, histological findings including bony bridging, tissue response at the bone-implant interface and fibrous capsule thickness indicated that the dura mater pathway played the most important role in the regenerative process of this calvarial defect model.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cráneo / Colágeno / Andamios del Tejido Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Mater Sci Eng C Mater Biol Appl Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cráneo / Colágeno / Andamios del Tejido Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Mater Sci Eng C Mater Biol Appl Año: 2020 Tipo del documento: Article País de afiliación: China