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The distinct ability of cell-penetrating peptides(CPPs)has lead to development of novel drug delivery methods in human cells for therapeutic purposes.The lack of specific selectivity is a main obstacle of CPPs.A novel delivery method based on acid-sensitive micelles using for the introduction and protection of TAT was developed in this study.Doxorubicin-TAT conjugate(Dox-TAT)was loaded in the luteinizing hormone-releasing hormone modified poly(ethylene glycol)-poly(L-histidine)-doxorubicin(LHRH-PEG-PHIS-Dox)micelle.