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In vitro drug release from the dual nanodrug CPVA-FLOX/17-AAG and CPVA-FLOX/PCL. (A) 17-AAG, and (B) PCL (C) FLOX release in simulated gastric fluid (pH 1.2). (D) FLOX release from CPVA-FLOX nanogel-drug conjugate at physiological condition (pH 7.4). Shown data are means ± SD (n = 3).
