Shangbin Cui

Dr. Shangbin Cui

orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 March 2006 in Acta Mathematica Sinica, English Series
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Journal Article
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SCShangbin Cui
Shangbin Cui
DDDong Gao Deng
Dong Gao Deng
STShuang Ping Tao
Shuang Ping Tao

10 March 2005 in Acta Mathematica Sinica, English Series
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Journal Article
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SCShangbin Cui
Shangbin Cui

21 June 2007 in Acta Mathematica Sinica, English Series
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Journal Article
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HWHua Wang
Hua Wang
SCShangbin Cui
Shangbin Cui
DDDong Gao Deng
Dong Gao Deng

12 August 2008 in Archive for Rational Mechanics and Analysis
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Journal Article
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SCShangbin Cui
Shangbin Cui
JEJoachim Escher
Joachim Escher

26 September 2019 in Connective Tissue Research
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Journal Article
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JPJudith-Johanna Pfannkuche
Judith-Johanna Pfannkuche
WGWei Guo
Wei Guo
SCShangbin Cui
Shangbin Cui
JMJunxuan Ma
Junxuan Ma
Gernot LangGernot Lang
Gernot Lang
ZLZhen Li
Zhen Li
Low back pain is the leading cause of disability worldwide and in many patients the source of pain can be attributed to pathological changes within the intervertebral disc (IVD). As present treatment options fail to address the underlying biological problem, novel therapies are currently subject to intense research. The physiologic IVD microenvironment features a highly complex interaction of biochemical and mechanical factors influencing cell metabolism and extracellular matrix turnover and is therefore difficult to simulate for research purposes on IVD pathology. The first whole organ culture models were not able to sufficiently replicate human in vivo conditions as mechanical loading, the predominant way of IVD nutrient supply and waste exchange, remained disregarded. To mimic the unique IVD niche more realistically, whole organ culture bioreactors have been developed, allowing for dynamic loading of IVDs and nutrient exchange. Recent advancements on bioreactor systems have facilitated whole organ culture of various IVDs for extended periods. IVD organ culture bioreactors have the potential to bridge the gap between in vitro and in vivo systems and thus may give valuable insights on IVD pathology and/or potential novel treatment approaches if the respective model is adjusted according to a well-defined research question. In this review, we outline the potential of currently utilized IVD bioreactor systems and present suggestions for further developments to more reliably investigate IVD biology and novel treatment approaches.