In this study, doxorubicin (DOX) loaded polymeric micelles (PMs) were synthesized based on biodegradable poly(εcaprolactone)-poly(ethylene glycol)-poly(ε-caprolactone) (PCEC) triblock copolymers. So four parameters (shaking speed (rpm) X 1 , time of contact (hour) X 2 , amount of triethylamine (TEA) (μL) X 3 , DOX% X 4 ) were optimized. Then by adding valspodar (PSC 833) or D-α-Tocopherol polyethylene glycol 1000 succinate (TPGS 1000) to the formulations DOX/PSC 833-PMs or DOX/ TPGS 1000-PMs were prepared by a nanoprecipitation method. The synthesized micelles exhibited high drug-loading encapsu-lation efficiency (> 78.98 %), high stability, and pH-dependent drug release. The results showed that the encapsulation efficiencies were not compromised by co-encapsulation of two agents. Finally, it was observed that the association of both DOX and PSC 833 or both DOX and TPGS 1000 within a single micelle formulation elicited the most soluble DOX as compared to DOX loaded formulations (DOX-PMs) while using a lower amount of polymer compared to separated micelle formulations.