Therefore, for drugs like doxorubicin or cisplatin to achieve therapeutic efficacy, they must first be released from the liposomal carrier into the tumor microenvironment and subsequently diffuse across the cellular membrane into the intracellular space [103]
However, after 3 h of treatment, the accumulation of non-targeted NPs NanoSU6668 (ICG) at CNV was significantly lower than that of T-MNS (ICG), and the accumulation of NanoSU6668 (ICG) was significantly reduced after 12 h treatment
[DOI] [PMC free article] [PubMed] [Google Scholar] Rohr O, Schwartz C, Aunis D, Schaeffer E (1999) CREB and COUP-TF mediate transcriptional activation of the human immunodeficiency virus type 1 genome in Jurkat T cells in response to cyclic AMP and dopamine
Golan R, Weissenberg R, Lewin LM
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The selenoenzymes inhibit proinflammatory cell metabolisms and protect cell components against oxidation [2]