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In this connection, umbelliprenin was co-encapsulated with doxorubicin in liposomes, and this combination, prepared with microfluidics, induced higher toxicity than liposomes prepared with the thin-film method, with an IC 50 (half-maximal inhibitory concentration) at least 2-fold lower

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The amount of GSH converted to GSS ranged from 0.420%, dependent on the conditions used

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