Practical Handbook of Advanced Interventional Cardiology 2007
DOI: 10.1002/9781444312584.ch30
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Delivery of Biologics for Angiogenesis and Myogenesis

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“…Lotreleasetesting consisted of sterility, endotoxin, mycoplasma, and testing for myoblast identity, purity, potency, viability, and cell count on a pooled sample prior to transplant meeting quality control standards [13] [14] [15]. A retain sample of myoblasts was reserved from each transplant.…”
Section: Manufacture Of Allogeneic Human Myoblastsmentioning
confidence: 99%
“…Lotreleasetesting consisted of sterility, endotoxin, mycoplasma, and testing for myoblast identity, purity, potency, viability, and cell count on a pooled sample prior to transplant meeting quality control standards [13] [14] [15]. A retain sample of myoblasts was reserved from each transplant.…”
Section: Manufacture Of Allogeneic Human Myoblastsmentioning
confidence: 99%
“…The LV can only be pierced by the needle a maximum of 20 times before the possible induction of heart arrhythmia. Therefore, in a procedure with 20 injections, each injection should emit 0.5 ml of 10 8 cells/ml myoblast solution 21,22 .…”
Section: Design Scopementioning
confidence: 99%
“…The purpose of the design is to optimize the catheter procedure for the injection of myogenic or undifferentiated stem cells into the infarct boundary zones of the left ventricle (LV). Previous studies [28][29][30] have shown that the optimal method in cell delivery would be injecting the needle into an infarct boundary zone at a diagonal angle while the needle is retracting. As difficulties occur in locating and maintaining the catheter tip at the target infarct boundary zones during such an injection, a remotely controlled catheter with finer positioning capabilities may be necessary.…”
Section: Conceptual Designmentioning
confidence: 99%