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synthesized polyethylene glycol (PEG)-conjugated doxorubicin (PD) by linking DOX with double amino-terminated PEG via succinimide coupling and then surface-modified PD NPs with HN- 1 using an improved nanoprecipitation method to form HNPD NPs for penetration and drug delivery in oral cancer cells (Wang et al
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[6] This pathway should not be called completely independent of VEGFR2
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