Catalog name Description price
R-C-3430 DSPE-PEG550-PVTRPPR PVTRPPR was modified on the surface of stealth liposomes,and pvtrppr polypeptide was used as the targeting head group.The drug loaded stealth liposome could target the drug to the tumor blood vessels through the tumor penetrating peptide pvtrppr,and penetrate the whole tumor tissue directly,so as to improve the therapeutic effect of the drug. price>
R-C-3431 PVTRPPR-PEG750-DSPE PVTRPPR was modified on the surface of stealth liposomes,and pvtrppr polypeptide was used as the targeting head group.The drug loaded stealth liposome could target the drug to the tumor blood vessels through the tumor penetrating peptide pvtrppr,and penetrate the whole tumor tissue directly,so as to improve the therapeutic effect of the drug. price>
R-C-3432 DSPE-PEG350-T7(HAIYPRH) T7(HAIYPRH) is a short peptide screened by phage display technology,which can specifically bind to TfR with a binding constant as high as 10 nmol·L −1. Moreover,due to the different binding sites,endogenous TF will not inhibit, but will promote the binding of T7 modified nanoparticles to TfR.Therefore,T7 is more suitable as a target molecule,and there are many reports on the application of T7 peptide alone. price>
R-C-3433 T7(HAIYPRH)-PEG550-DSPE T7(HAIYPRH) is a short peptide screened by phage display technology,which can specifically bind to TfR with a binding constant as high as 10 nmol·L −1. Moreover,due to the different binding sites,endogenous TF will not inhibit, but will promote the binding of T7 modified nanoparticles to TfR.Therefore,T7 is more suitable as a target molecule,and there are many reports on the application of T7 peptide alone. price>
R-C-3434 DSPE-polyethylene glycol750-T7(HAIYPRH) T7(HAIYPRH)is a short peptide screened by phage display technology,which can specifically bind to TfR with a binding constant as high as 10 nmol·L −1. Moreover,due to the different binding sites,endogenous TF will not inhibit, but will promote the binding of T7 modified nanoparticles to TfR.Therefore,T7 is more suitable as a target molecule,and there are many reports on the application of T7 peptide alone. price>
R-C-3435 DSPE-PEG350-R9 Cell penetrating peptide (CPP) is a kind of short peptide with strong penetration effect on cell membrane,which can promote cell uptake.Liposome modified by CPP can improve the rate of liposome entry into the cell,which is a new direction of targeted drug delivery carrier research. price>
R-C-3436 R9-PEG550-DSPE Cell penetrating peptide (CPP) is a kind of short peptide with strong penetration effect on cell membrane,which can promote cell uptake.Liposome modified by CPP can improve the rate of liposome entry into the cell,which is a new direction of targeted drug delivery carrier research. price>
R-C-3437 DSPE-polyethylene glycol750-R9 Cell penetrating peptide (CPP) is a kind of short peptide with strong penetration effect on cell membrane,which can promote cell uptake.Liposome modified by CPP can improve the rate of liposome entry into the cell,which is a new direction of targeted drug delivery carrier research. price>
R-C-3438 DSPE-polyethylene glycol350-ADH1 Liposomes can passively enter tumor tissue through enhanced retention and retention effect(EPR).Compared with radiotherapy and chemotherapy alone, liposomes have certain clinical treatment advantages.However,the liposome can not reach the target site immediately after injection and stay at the tumor site for a long time. price>
R-C-3439 DSPE-PEG550-ADH1 Liposomes can passively enter tumor tissue through enhanced retention and retention effect(EPR).Compared with radiotherapy and chemotherapy alone, liposomes have certain clinical treatment advantages.However,the liposome can not reach the target site immediately after injection and stay at the tumor site for a long time. price>