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作 者:Emma Steijvers Armaan Ghei Zhidao Xia
出 处:《Biomaterials Translational》2022年第1期65-80,I0001,I0002,共18页生物材料转化电子杂志(英文)
基 金:The work was partially supported by the‘Health Technology Centre,HTC’Accelerate project of Swansea University Medical School and the Institute for Innovative Materials,Processing and Numerical Technologies(IMPACT)project,Swansea University.
摘 要:Bone grafts have traditionally come from four sources:the patients’own tissue(autograft),tissue from a living or cadaveric human donor(allograft),animal donors(xenograft)and synthetic artificial biomaterials(ceramics,cement,polymers,and metal).However,all of these have advantages and drawbacks.The most commercially successful bone grafts so far are allografts,which hold 57%of the current bone graft market;however,disease transmission and scarcity are still significant drawbacks limiting their use.Tissue-engineered grafts have great potential,in which human stem cells and synthetical biomaterials are combined to produce bone-like tissue in vitro,but this is yet to be approved for widespread clinical practice.It is hypothesised that artificial bone allografts can be mass-manufactured to replace conventional bone allografts through refined bone tissue engineering prior to decellularisation.This review article aims to review current literature on(1)conventional bone allograft preparation;(2)bone tissue engineering including the use of synthetic biomaterials as bone graft substitute scaffolds,combined with osteogenic stem cells in vitro;(3)potential artificial allograft manufacturing processes,including mass production of engineered bone tissue,osteogenic enhancement,decellularisation,sterilisation and safety assurance for regulatory approval.From these assessments,a practical route map for mass production of artificial allografts for clinical use is proposed.
关 键 词:BIOMATERIALS bone graft decellularisation stem cells tissue engineering
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