Objective:To evaluate the effects of cryopreservation of APBSCs in -80"C un-controlled freezer and liquid nitrogen, and to search for the efficient combined cryoprotectant and the highest cell concentration for cryopreservating peripheral blood stem cell (PBSC). Methods: To compare the effect of three combined cryoprotectants, evaluation of in vitro proliferative capacity by colony-forming unitGranulocyte-macrophage (CFU-GM) and burst-forming Unit-erythroid (BFU-E) assay, immunophenotyping for CD34+/CD38 cells by FCM, and viability assessment by trypan blue exclusion were performed. Results: The cryoprotectant 10%DMSO+HES+auto-Plasma resulted in the highest recovery rates. CFU-GM and BFU-E were (78.7+9.8)%, (69.8+14.1)%, respectively. The recovery rates of CFU-GM and BFU-E in A/C groups were (68.3+6.2)%/ (65.8:t=7.2)% and (63.4+9.7)%/ (60.4+ 10.5)%, respectively. The recovery rates of CD34+/CD38 cells and cell viability with the three combined reagents were 90% and 80%, respectively. Conclusion: 5%DMSO+ HES+auto-PLASMA is an ideal combined cryoprotectant for cryopreserving PBSC. The cell concentrations may be cryopreserved at 4xl08 ml l.