Herceptin conjugated biodegradable poly(${varepsilon}$-caprolactone)-poly(ethylene glycol)-poly(${varepsilon}$-caprolactone) (PCL-PEG-PCL, PCEC) triblock copolymer has shown potential applications in drug delivery systems. In order to synthesize PCEC triblock copolymer, oligo(t-BMA) grafted PEG in the backbone were first prepared by graft radical polymerization of t-BMA in the presence of t-butylperoxybenzoate as an initiator. Then, PCL was introduced into the backbone in the presense of an initiator and a catalyst. The final product, Herceptin conjugated PCEC triblock copolymer, was confirmed with the amide bond formation between the carboxylic group of grafted PCEC polymers and the amine group of Herceptin. The targeted triblock copolymer formed nano-sized micelles with spherical shapes. The average size was in the range of 100-150 nm in diameter, showing similar fluorescent intensities for 6 days. The results of the MTT assay demonstrated that the MDA-MB231 cancer cells are more sensitive for the Herceptin conjugated PCEC micelle due to the over-expression of HER-2 receptors. The guantum dots (QDs) loaded PCEC micelles were up-taken by the MDA-MB231 cell, through the HER-2 receptor, by active binding. The overall data demonstrated that the QDs loaded PCEC micelles could be used for active targeted delivery, cancer therapy, and non-invasive imaging.