2010
DOI: 10.1016/j.biomaterials.2010.07.048
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Mesenchymal stem cells as cellular vehicles for delivery of nanoparticles to brain tumors

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Cited by 212 publications
(143 citation statements)
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“…Though, this technology offers significant release by the use of nanoparticles in vivo that has been demanding to the competent approval, ineffective distribution in solid tumors and unable to attack the micro metastatic lesions [184]. To defeat these barriers, the use of SCs as nanoparticles release agents that can travel to develop malignancies and to set down the overloaded nanoparticles that are related to the cancer [185,186].…”
Section: Nanoparticles Carrier Function Of Stem Cellsmentioning
confidence: 99%
“…Though, this technology offers significant release by the use of nanoparticles in vivo that has been demanding to the competent approval, ineffective distribution in solid tumors and unable to attack the micro metastatic lesions [184]. To defeat these barriers, the use of SCs as nanoparticles release agents that can travel to develop malignancies and to set down the overloaded nanoparticles that are related to the cancer [185,186].…”
Section: Nanoparticles Carrier Function Of Stem Cellsmentioning
confidence: 99%
“…4 The DNA probe was complementary to the highly repetitive human satellite III sequences located close to the centromeric region of the human Y-chromosome DYZ1 locus (CEPY) and was labeled with the SpectrumOrange fluorochrome (Vysis; Abbott Laboratories, Abbott Park, IL, USA). Cryosections were then analyzed under an Axioscope ® 2 fluorescence microscope.…”
Section: Fluorescence In Situ Hybridizationmentioning
confidence: 99%
“…4 In this work, we defined the optimal dose of Fc-diOHLNCs that MIAMI cells could carry without deleterious effects on viability for at least 7 days after their uptake. For this purpose, we had to take drug and LNC matrix component concentrations into account.…”
Section: Optimization and Quantification Of Fc-dioh Internalization Bmentioning
confidence: 99%
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“…They showed efficient internalization of the NPs into MSCs that were able to migrate toward an experimental human glioma model. They suggested MSCs as potential cellular carriers for delivery of NPs into brain tumors (Roger et al, 2010). In 2011, A dual-targeting drug carrier (PAMAM-PEG-WGA-Tf) was developed based on the PEGylated fourth generation PAMAM dendrimer with Tf and wheat germ agglutinin (WGA) on the periphery and DOX loaded in the interior (He et al, 2011).…”
Section: Recent Advancements For Crossing Bbbmentioning
confidence: 99%