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R-C-4710 DSPE-polyethylene glycol550-VSNKYFSNIHWGC uPA peptide (VSNKYFSNIHWGC)-conjugated,antisense-miR-21 and antisense-miR-10b coloaded PLGA-b-PEG-NPs (called uPA-Anti-miR-21-Anti-miR-10b-NPs) that simultaneously antagonized miR-21-induced inhibition of apoptosis and miR-10b-induced metastasis to achieve TNBC therapy.Our products are only used for scientific research, not for human body. price>
R-C-4723 DSPE-PEG-RINNIPWSEAMMC 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a long circulating liposome membrane, formation of micelles in water dispersion, the critical micelle concentration (CMC) ratio of surfactant is 102 times lower, so the drug stability is better, even by hemodilution, can maintain the integrity of the micelle particle, has certain targeting, easy accumulation in solid tumors. Peptide is a compound formed by α-amino acids linked together by peptide bond,which is the intermediate product of protein hydrolysis. price>
R-C-4724 DSPE-HYD-PEG-iRGD DSPE-Hyd-PEG-iRGD is a PH-responsive liposome, which uses hydrazone bond to design PH-responsive nano drug micelles, and its core is composed of DOX connected by hydrazone bond. Under acidic conditions, the hydrazone bond breaks and the drug is released. When the drug carrier reaches the endosomes or lysosomes of tumor cells, acid hydrolysis will occur to release the drug, achieving the effect of targeted drug delivery. price>
R-C-4725 DSPE-HYD-polyethylene glycol350-iRGD DSPE-Hyd-PEG-iRGD is a PH-responsive liposome, which uses hydrazone bond to design PH-responsive nano drug micelles, and its core is composed of DOX connected by hydrazone bond. Under acidic conditions, the hydrazone bond breaks and the drug is released. When the drug carrier reaches the endosomes or lysosomes of tumor cells, acid hydrolysis will occur to release the drug, achieving the effect of targeted drug delivery. price>
R-C-4726 DSPE-Hydrazide-PEG550-iRGD DSPE-Hyd-PEG-iRGD is a PH-responsive liposome, which uses hydrazone bond to design PH-responsive nano drug micelles, and its core is composed of DOX connected by hydrazone bond. Under acidic conditions, the hydrazone bond breaks and the drug is released. When the drug carrier reaches the endosomes or lysosomes of tumor cells, acid hydrolysis will occur to release the drug, achieving the effect of targeted drug delivery. price>
R-C-4727 iRGD-PEG750-HYD-DSPE DSPE-Hyd-PEG-iRGD is a PH-responsive liposome, which uses hydrazone bond to design PH-responsive nano drug micelles, and its core is composed of DOX connected by hydrazone bond. Under acidic conditions, the hydrazone bond breaks and the drug is released. When the drug carrier reaches the endosomes or lysosomes of tumor cells, acid hydrolysis will occur to release the drug, achieving the effect of targeted drug delivery. price>
R-C-4731 DSPE-PEG350-RINNIPWSEAMMC 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a long circulating liposome membrane, formation of micelles in water dispersion, the critical micelle concentration (CMC) ratio of surfactant is 102 times lower, so the drug stability is better, even by hemodilution, can maintain the integrity of the micelle particle, has certain targeting, easy accumulation in solid tumors. Peptide is a compound formed by α-amino acids linked together by peptide bond,which is the intermediate product of protein hydrolysis. price>
R-C-4733 DSPE-polyethylene glycol550-RINNIPWSEAMMC 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a long circulating liposome membrane, formation of micelles in water dispersion, the critical micelle concentration (CMC) ratio of surfactant is 102 times lower, so the drug stability is better, even by hemodilution, can maintain the integrity of the micelle particle, has certain targeting, easy accumulation in solid tumors. Peptide is a compound formed by α-amino acids linked together by peptide bond,which is the intermediate product of protein hydrolysis. price>
R-C-4735 DSPE-N3 CAS:2839508-98-2 1,2-Distearoyl-sn-Glycero-3-Phosphoethanolamine-N-azide(DSPE-azide,DSPE-N3)is a phophalipid capped with azide group.The azide capped head can be used to react with alkynes cyclocytidine in an aqueous solution with or without copper catalyst;18:0PE N3; Phospholipid-azide;The primary amino group of DSPE directly modifies the N3 active group. price>
R-C-4740 DSPE-PEG-TK-MAL DSPE-PEG2k-TK-MAL,DSPE phospholipids have the function of emulsifying and solubilizing drugs as pharmaceutical excipients. Modification of phospholipid molecules can make these preparations have the ability to release and target under specific conditions. Common modification methods include:; Introduce polymer to improve the blood circulation time and disintegration time of the preparation; Introducing rabbit epidemic factor to enhance targeting; Introduce markers for diagnosis and tracking. price>
R-C-4741 DSPE-PEG350-TK-MAL DSPE phospholipids have the function of emulsifying and solubilizing drugs as pharmaceutical excipients. Modification of phospholipid molecules can make these preparations have the ability to release and target under specific conditions. Common modification methods include:; Introduce polymer to improve the blood circulation time and disintegration time of the preparation; Introducing rabbit epidemic factor to enhance targeting; Introduce markers for diagnosis and tracking. price>
R-C-4742 DSPE-polyethylene glycol550-TK-MAL DSPE phospholipids have the function of emulsifying and solubilizing drugs as pharmaceutical excipients. Modification of phospholipid molecules can make these preparations have the ability to release and target under specific conditions. Common modification methods include:; Introduce polymer to improve the blood circulation time and disintegration time of the preparation; Introducing rabbit epidemic factor to enhance targeting; Introduce markers for diagnosis and tracking. price>
R-C-4744 DSPE-PEG-GSH DSPE phospholipids have the functions of emulsification and drug solubilization as pharmaceutical excipients, and are important materials for slow-release and controlled-release drug preparations such as liposomes, fat emulsions and nanoparticles in recent years. The modification of phospholipid molecules can make these preparations have the ability to release and target under specific conditions. GSH is a blood-brain barrier shuttle peptide that can transport NPs to the blood-brain barrier through GSH transport protein. price>
R-C-4745 DSPE-PEG350-Glutathione DSPE phospholipids have the functions of emulsification and drug solubilization as pharmaceutical excipients, and are important materials for slow-release and controlled-release drug preparations such as liposomes, fat emulsions and nanoparticles in recent years. The modification of phospholipid molecules can make these preparations have the ability to release and target under specific conditions. GSH is a blood-brain barrier shuttle peptide that can transport NPs to the blood-brain barrier through GSH transport protein. price>
R-C-4746 DSPE-polyethylene glycol550-GSH DSPE phospholipids have the functions of emulsification and drug solubilization as pharmaceutical excipients, and are important materials for slow-release and controlled-release drug preparations such as liposomes, fat emulsions and nanoparticles in recent years. The modification of phospholipid molecules can make these preparations have the ability to release and target under specific conditions. GSH is a blood-brain barrier shuttle peptide that can transport NPs to the blood-brain barrier through GSH transport protein. price>
R-C-4747 DSPE-PEG750-Glutathione DSPE phospholipids have the functions of emulsification and drug solubilization as pharmaceutical excipients, and are important materials for slow-release and controlled-release drug preparations such as liposomes, fat emulsions and nanoparticles in recent years. The modification of phospholipid molecules can make these preparations have the ability to release and target under specific conditions. GSH is a blood-brain barrier shuttle peptide that can transport NPs to the blood-brain barrier through GSH transport protein. price>
R-C-4753 DSPE-PEG-cRGD-FITC Pegylated phospholipids are excellent liposome formation materials that can be used for drug delivery, gene transfection and vaccine delivery as well. Pegylation of phospholipids significantly improves the blood circulation time and stability for encapsulated drugs. Fluorescein labeled DSPE PEG products emitted green fluorescence and can be easily detected with fluorescent microscopy or spectroscopy.cRGD is an active target material,It can be used as an antitumor drug carrier and active targeted delivery. price>
R-C-4754 DSPE-PEG-peptide(PPGAYHGA) The polyethylene glycol copolymer with biodegradable and biocompatible polyester chain segments can also be used to prepare core-shell micelles, nanoparticles and microspheres.The active group at the end of the product can link some modified peptides,proteins,carbohydrates,folic acid or antibodies to make them have active targeting effect. price>
R-C-4755 DSPE-polyethylene-glycol350-peptide(PPGAYHGA) The polyethylene glycol copolymer with biodegradable and biocompatible polyester chain segments can also be used to prepare core-shell micelles,nanoparticles and microspheres.The active group at the end of the product can link some modified peptides,proteins,carbohydrates,folic acid or antibodies to make them have active targeting effect. price>
R-C-4757 DSPE-PEG750-PPGAYHGA The polyethylene glycol copolymer with biodegradable and biocompatible polyester chain segments can also be used to prepare core-shell micelles, nanoparticles and microspheres.The active group at the end of the product can link some modified peptides,proteins,carbohydrates,folic acid or antibodies to make them have active targeting effect. price>