Applications of tumor chip technology.
Applications of tumor chip technology.
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DOI:
10.1039/c8lc00330k
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发表时间:
2018-09-26
期刊:
影响因子:
6.1
通讯作者:
Hughes CCW
中科院分区:
文献类型:
--
作者:
Hachey SJ;Hughes CCW
Over the past six decades the inflation-adjusted cost to bring a new drug to market has been increasing constantly and doubles every 9 years - now reaching in excess of $2.5 billion. Overall, the likelihood of FDA approval for a drug (any disease indication) that has entered phase I clinical trials is a mere 9.6%, with the approval rate for oncology far below average at only 5.1%. Lack of efficacy or toxicity is often not revealed until the later stages of clinical trials, despite promising preclinical data. This indicates that the current in vitro systems for drug screening need to be improved for better predictability of in vivo outcomes. Microphysiological systems (MPS), or bioengineered 3D microfluidic tissue and organ constructs that mimic physiological and pathological processes in vitro, can be leveraged across preclinical research and clinical trial stages to transform drug development and clinical management for a range of diseases. Here we review the current state-of-the-art in 3D tissue-engineering models developed for cancer research, with a focus on tumor-on-a-chip, or tumor chip, models. From our viewpoint, tumor chip systems can advance innovative medicine to ameliorate the high failure rates in anti-cancer drug development and clinical treatment.
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影响因子:
3.7
作者:
Chan JM;Zervantonakis IK;Rimchala T;Polacheck WJ;Whisler J;Kamm RD
通讯作者:
Kamm RD
影响因子:
3.2
作者:
Acosta, Miguel A.;Jiang, Xiao;Gamcsik, Michael P.
通讯作者:
Gamcsik, Michael P.
DOI:
10.1016/j.jconrel.2014.05.004
发表时间:
2014-09-28
期刊:
Journal of controlled release : official journal of the Controlled Release Society
影响因子:
--
作者:
Bhise NS;Ribas J;Manoharan V;Zhang YS;Polini A;Massa S;Dokmeci MR;Khademhosseini A
通讯作者:
Khademhosseini A
影响因子:
3.7
作者:
Beckwitt CH;Clark AM;Wheeler S;Taylor DL;Stolz DB;Griffith L;Wells A
通讯作者:
Wells A
影响因子:
46.9
作者:
Bhatia, Sangeeta N.;Ingber, Donald E.
通讯作者:
Ingber, Donald E.