Cell viability and noninvasive in vivo MRI tracking of 3D cell encapsulating self-assembled microcontainers

被引:15
|
作者
Gimi, Barjor
Artemov, Dmitri
Leong, Timothy
Gracias, David H.
Gilson, Wesley
Stuber, Matthias
Bhujwalla, Zaver M.
机构
[1] Univ Texas, SW Med Ctr Dallas, Childrens Med Ctr Dallas, Dept Radiol, Irving, TX 75062 USA
[2] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD USA
[3] Johns Hopkins Univ, Dept Chem Engn, Baltimore, MD 21218 USA
关键词
cell therapy; cell encapsulation; magnetic resonance microscopy; self-assembly; microcapsules; implantation;
D O I
10.3727/000000007783464803
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Several molecular therapies require the implantation of cells that secrete biotherapeutic molecules and imaging the location and microenvironment of the cellular implant to ascertain its function. We demonstrate noninvasive in vivo magnetic resonance imaging (MRI) of self-assembled microcontainers that are capable of cell encapsulation. Negative contrast was obtained to discern the microcontainer with MRI; positive contrast was obtained in the complete absence of background signal. MRI on a clinical scanner highlights the translational nature of this research. The microcontainers were loaded with cells that were dispersed in an extracellular matrix, and implanted both subcutaneously and in human tumor xenografts in SCID mice. MRI was performed on the implants, and microcontainers retrieved postimplantation showed cell viability both within and proximal to the implant. The microcontainers are characterized by their small size, three dimensionality. controlled porosity, ease of parallel fabrication, chemical and mechanical stability, and non-invasive traceability in vivo.
引用
收藏
页码:403 / 408
页数:6
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