TY - JOUR
T1 - Safety of real-time convection-enhanced delivery of liposomes to primate brain
T2 - A long-term retrospective
AU - Krauze, Michal T.
AU - Vandenberg, Scott R.
AU - Yamashita, Yoji
AU - Saito, Ryuta
AU - Forsayeth, John
AU - Noble, Charles
AU - Park, John
AU - Bankiewicz, Krystof S.
N1 - Funding Information:
Grant support: National Cancer Institute Specialized Program of Research Excellence grant (to K. S. Bankiewicz).
PY - 2008/4
Y1 - 2008/4
N2 - Convection-enhanced delivery (CED) is gaining popularity in direct brain infusions. Our group has pioneered the use of liposomes loaded with the MRI contrast reagent as a means to track and quantitate CED in the primate brain through real-time MRI. When co-infused with therapeutic nanoparticles, these tracking liposomes provide us with unprecedented precision in the management of infusions into discrete brain regions. In order to translate real-time CED into clinical application, several important parameters must be defined. In this study, we have analyzed all our cumulative animal data to answer a number of questions as to whether real-time CED in primates depends on concentration of infusate, is reproducible, allows prediction of distribution in a given anatomic structure, and whether it has long term pathological consequences. Our retrospective analysis indicates that real-time CED is highly predictable; repeated procedures yielded identical results, and no long-term brain pathologies were found. We conclude that introduction of our technique to clinical application would enhance accuracy and patient safety when compared to current non-monitored delivery trials.
AB - Convection-enhanced delivery (CED) is gaining popularity in direct brain infusions. Our group has pioneered the use of liposomes loaded with the MRI contrast reagent as a means to track and quantitate CED in the primate brain through real-time MRI. When co-infused with therapeutic nanoparticles, these tracking liposomes provide us with unprecedented precision in the management of infusions into discrete brain regions. In order to translate real-time CED into clinical application, several important parameters must be defined. In this study, we have analyzed all our cumulative animal data to answer a number of questions as to whether real-time CED in primates depends on concentration of infusate, is reproducible, allows prediction of distribution in a given anatomic structure, and whether it has long term pathological consequences. Our retrospective analysis indicates that real-time CED is highly predictable; repeated procedures yielded identical results, and no long-term brain pathologies were found. We conclude that introduction of our technique to clinical application would enhance accuracy and patient safety when compared to current non-monitored delivery trials.
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U2 - 10.1016/j.expneurol.2007.12.015
DO - 10.1016/j.expneurol.2007.12.015
M3 - Article
C2 - 18295759
AN - SCOPUS:41149091077
SN - 0014-4886
VL - 210
SP - 638
EP - 644
JO - Neurodegeneration
JF - Neurodegeneration
IS - 2
ER -