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Whenever intravenously (i.v.) inserted into mice, H-Cu9S8@CCM NPs display an increased the circulation of blood half-life (3.17 h, 6.47 times) and tumefaction buildup quantity (18.75% ID/g, 1.94 times), in comparison to H-Cu9S8 NPs (0.49 h, 9.68% ID/g) without CCM. In addition, upon 1064 nm laser and ultrasound irradiation, H-Cu9S8@CCM NPs can inhibit tumefaction development more efficiently as a result of high buildup performance and synergistic PTT-SDT functions. Consequently, the c

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