Biocompatibility and bone-repairing effects: comparison between porous poly-lactic-co-glycolic acid and nano-hydroxyapatite/poly(lactic acid) scaffolds. 2014

Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang

Copolymer composite scaffolds and bioceramic/polymer composite scaffolds are two representative forms of composite scaffolds used for bone tissue engineering. Studies to compare biocompatibility and bone-repairing effects between these two scaffolds are significant for selecting or improving the scaffold for clinical application. We prepared two porous scaffolds comprising poly-lactic-acid/poly-glycolic-acid (PLGA) and poly-lactic-acid/nano-hydroxyapatite (nHAP/PLA) respectively, and examined their biocompatibility with human bone marrow-derived mesenchymal stem cells (hMSCs) through evaluating adhesion, proliferation and osteogenic differentiation potentials of hMSCs in the scaffold. Then, the PLGA scaffold with hMSCs (PM construct) and the nHAP/PLA scaffold with hMSCs (HPM construct) were transplanted into the rat calvarial defect areas to compare their effects on the bone reconstruction. The results showed that the nHAP/PLA scaffold was in favor of adhesion, matrix deposition and osteogenic differentiation of hMSCs. For in vivo transplantation, both HPM and PM constructs led to mineralization and osteogenesis in the defect area of rat. However, the area grafted with PM construct showed a better formation of mature bone than that with HPM construct. In addition, the evaluation of in vitro and in vivo degradation indicated that the degradation rate of nHAP/PLA scaffold was much lower than that of PLGA scaffold. It is inferred that the lower degradation of nHAP/PLA scaffold should result in its inferior bone reconstruction in rat calvaria. Therefore, the preparation of an ideal composite scaffold for bone tissue engineering should be taken into account of the balance between its biocompatibility, degradation rate, osteoconductivity and mechanical property.

UI MeSH Term Description Entries
D008297 Male Males
D011091 Polyesters Polymers of organic acids and alcohols, with ester linkages--usually polyethylene terephthalate; can be cured into hard plastic, films or tapes, or fibers which can be woven into fabrics, meshes or velours. Polyester
D011100 Polyglycolic Acid A biocompatible polymer used as a surgical suture material. Polyglycolide,Biofix,Dexon (Polyester),Dexon-S,Dexon S,DexonS
D011108 Polymers Compounds formed by the joining of smaller, usually repeating, units linked by covalent bonds. These compounds often form large macromolecules (e.g., BIOPOLYMERS; PLASTICS). Polymer
D001861 Bone Regeneration Renewal or repair of lost bone tissue. It excludes BONY CALLUS formed after BONE FRACTURES but not yet replaced by hard bone. Osteoconduction,Bone Regenerations,Regeneration, Bone,Regenerations, Bone
D000077182 Polylactic Acid-Polyglycolic Acid Copolymer A co-polymer that consists of varying ratios of polylactic acid and polyglycolic acid. It is used as a matrix for drug delivery and for BONE REGENERATION. PLGA Acid,LactoSorb,PL-PG Copolymer,PLG Polymer,PLGA Compound,Poly (D,L-lactic-co-glycolic Acid),Poly (Lactic-co-glycolic Acid) -,Poly(D,L-lactide-co-glycolide),Poly(DL-lactide-co-glycolic Acid),Poly(Glycolide-co-lactide),Poly(L-lactide)-co-glycolide,Poly(Lactic-co-glycolic Acid),Poly-L-lactic-polyglycolic Acid,Polylactic-co-glycolic Acid Copolymer,RG 502,Acid, PLGA,Acids, PLGA,Copolymer, PL-PG,Copolymer, Polylactic-co-glycolic Acid,Copolymers, PL-PG,Copolymers, Polylactic-co-glycolic Acid,PL PG Copolymer,PL-PG Copolymers,PLG Polymers,PLGA Acids,PLGA Compounds,Poly L lactic polyglycolic Acid,Poly-L-lactic-polyglycolic Acids,Polylactic Acid Polyglycolic Acid Copolymer,Polylactic co glycolic Acid Copolymer,Polylactic-co-glycolic Acid Copolymers,Polymer, PLG,Polymers, PLG
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D012887 Skull Fractures Fractures of the skull which may result from penetrating or nonpenetrating head injuries or rarely BONE DISEASES (see also FRACTURES, SPONTANEOUS). Skull fractures may be classified by location (e.g., SKULL FRACTURE, BASILAR), radiographic appearance (e.g., linear), or based upon cranial integrity (e.g., SKULL FRACTURE, DEPRESSED). Linear Skull Fracture,Skull Fracture, Linear,Skull Fracture, Non-Depressed,Non-Depressed Skull Fracture,Fracture, Non-Depressed Skull,Fracture, Skull,Fractures, Linear Skull,Fractures, Non-Depressed Skull,Fractures, Skull,Linear Skull Fractures,Non Depressed Skull Fracture,Non-Depressed Skull Fractures,Skull Fracture,Skull Fracture, Non Depressed,Skull Fractures, Linear,Skull Fractures, Non-Depressed
D016062 Porosity Condition of having pores or open spaces. This often refers to bones, bone implants, or bone cements, but can refer to the porous state of any solid substance. Porosities
D016896 Treatment Outcome Evaluation undertaken to assess the results or consequences of management and procedures used in combating disease in order to determine the efficacy, effectiveness, safety, and practicability of these interventions in individual cases or series. Rehabilitation Outcome,Treatment Effectiveness,Clinical Effectiveness,Clinical Efficacy,Patient-Relevant Outcome,Treatment Efficacy,Effectiveness, Clinical,Effectiveness, Treatment,Efficacy, Clinical,Efficacy, Treatment,Outcome, Patient-Relevant,Outcome, Rehabilitation,Outcome, Treatment,Outcomes, Patient-Relevant,Patient Relevant Outcome,Patient-Relevant Outcomes

Related Publications

Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
July 2016, Artificial organs,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
December 2019, Journal of orthopaedic surgery and research,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
February 2023, International journal of biological macromolecules,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
September 2018, Journal of biomedical materials research. Part A,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
July 2013, ACS applied materials & interfaces,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
October 2008, Tissue engineering. Part A,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
May 2019, ACS biomaterials science & engineering,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
June 2005, Biomaterials,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
August 2005, Biomaterials,
Chen Zong, and Xiaodan Qian, and Zihua Tang, and Qinghong Hu, and Jiarong Chen, and Changyou Gao, and Ruikang Tang, and Xiangmin Tong, and Jinfu Wang
August 2021, Journal of biomedical materials research. Part A,
Copied contents to your clipboard!