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Generally, we found that the silica-coated CdSe QDs show much higher cellular internalization efficiency, possibly because of cytocompatibility of silica shell.
The targeted lipid prodrugs B-R-ACV and B-12HS-ACV exhibited much higher cellular accumulation than B-ACV, R-ACV and 12HS-ACV in both cell lines.
cRGD-conjugated unimolecular micelles (i.e., H40-DOX-cRGD) exhibited a much higher cellular uptake in U87MG human glioblastoma cells due to integrin αvβ3-mediated endocytosis than non-targeted unimolecular micelles (i.e., H40-DOX), thereby leading to a significantly higher cytotoxicity.
In the cellular uptake study using KB cells positive for the folate-receptor (FR), FHP and FPHP nanoparticles showed a much higher cellular uptake than did unconjugated HP nanoparticles.
In vitro cellular uptake studies with HT-29 cells showed that the optimized curcumin-loaded PLGA nanoparticle exhibited a much higher cellular uptake of curcumin (i.e. 7.01 ± 0.33 μg/106 cells) than a native curcumin solution (3.74 ± 0.56 μg/106 cells).
Human gliomas are of much higher cellular diversity than the rat glioma cell lines used in this study.
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It has also been shown that 10 μM 9cRA actives GRQCIMFI, but this concentration is much higher than cellular levels; therefore, it is expected that 9cRA will not activate this molecular switch.
It is assumed that the difference is due mainly to the much higher penetration of cellular phones compared with the early 1990s.
The two bands are more prominent because the concentration of the SmD antibody used for immunoprecipitation was much higher than the cellular concentration of immunoprecipitated antigen in the larch anthers.
They are capable of achieving much higher throughput than current cellular systems, which can be classified as single-hop cellular networks (SCNs).
The cellular industry has seen much higher license prices and most cellular systems have been quite successful.
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