Convergence of Cell Pharmacology and Drug Delivery

被引:18
作者
Aijaz, Ayesha [1 ]
Vaninov, Natalie [2 ]
Allen, Ashley [2 ]
Barcia, Rita N. [2 ]
Parekkadan, Biju [1 ,2 ]
机构
[1] Rutgers State Univ, Dept Biomed Engn, Piscataway Township, NJ USA
[2] Sentien Biotechnol Inc, Lexington, MA USA
基金
美国国家卫生研究院;
关键词
MESENCHYMAL STEM-CELLS; MARROW STROMAL CELLS; BONE-MARROW; PROCOAGULANT ACTIVITY; IN-VITRO; INHIBIT; DISEASE; GAMMA; LUNG;
D O I
10.1002/sctm.19-0019
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Cellular therapy is enabling new approaches to tackle significant unmet needs in areas such as regenerative medicine and immunotherapy. The pharmacology of cell therapeutics becomes of critical importance to assure that these new drugs work reproducibly and effectively. Cell pharmacology can benefit from adapting principles of classical molecular drug pharmacokinetics (PK) and pharmacodynamics (PD) to quantitatively understand rate-limiting constraints of cell fate after administration. Future innovations focused on improvements in drug delivery using a PK/PD perspective can aid in designing a cell therapeutic product to overcome any pharmacological barriers for a given disease application. Herein, we present a perspective on the development of an ex vivo mesenchymal stromal therapeutic using a PK/PD framework and also present examples of general cell engineering techniques that implicitly influence the PK/PD curve by genetically modifying cells to regulate their in vivo duration, biodistribution, and activity. Stem Cells Translational Medicine 2019;8:874&879
引用
收藏
页码:874 / 879
页数:6
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