Catalog |
name |
Description |
price |
R-C-5722 |
DSPE-PEG350-Maltotriose hydrate |
DSPE-PEG-Maltotriose hydrate,DSPE is a phospholipid that is commonly used in lipid-based drug delivery systems.It provides stability and structure to liposomes and lipid nanoparticles.The PEGylation of a drug carrier can enhance its biocompatibility,prolong circulation time in the bloodstream, and reduce immune response.Small molecules are more difficult to produce. |
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R-C-5723 |
DSPE-PEG2K-Carboxyl-HA |
DSPE-PEG-COOH-HA,DSPE-PEG-Carboxyl-hyaluronic acid,DSPE-PEG2K-COOH-HA can self-assemble into liposomes or lipid-based nanoparticles,which can encapsulate drugs or other active compounds for targeted delivery.Hyaluronic Acid(HA)is a naturally occurring polysaccharide found in the extracellular matrix of various tissues.It has high biocompatibility,biodegradability, and can interact with specific cell surface receptors.By modifying the carboxyl group,additional functional molecules,such as targeting ligands or imaging agents,can be conjugated to the lipid carrier to further enhance its specificity and therapeutic effect. |
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R-C-5724 |
DSPE-PEG-RGR(CRGRRST) |
DSPE-PEG2000-RGR,DSPE is a phospholipid used as a lipid component to form liposomes or lipid-based nanoparticles.PEGylation increases the biocompatibility of the drug carrier, improves circulation time, and reduces immunogenicity.DSPE-PEC-RGR(CRGREST) can self-assemble into liposomes or lipid-based nanoparticles,which can encapsulate drugs or other active agents. The incorporation of the RGR and CRGREST sequences facilitates targeted delivery to tumor cells, potentially improving therapeutic efficacy while minimizing off-target effects. |
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R-C-5725 |
DSPE-PEG350-RGR(CRGRRST) |
DSPE-PEG2000-RGR,DSPE is a phospholipid used as a lipid component to form liposomes or lipid-based nanoparticles.PEGylation increases the biocompatibility of the drug carrier, improves circulation time, and reduces immunogenicity.DSPE-PEC-RGR(CRGREST) can self-assemble into liposomes or lipid-based nanoparticles,which can encapsulate drugs or other active agents. The incorporation of the RGR and CRGREST sequences facilitates targeted delivery to tumor cells, potentially improving therapeutic efficacy while minimizing off-target effects. |
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R-C-5735 |
DSPE-PEG2K-N-acetyl-L-cysteine |
DSPE-PEG-N-acetyl-L-cysteine,N-acetyl-L-cysteine(NAC) is a mucolytic agent with antibacterial and antibiofilm properties against several bacterial strains. it shows potential in inhibiting biofilm formation and even disrupting mature biofilms,that NAC acts on reducing the production of exopolysaccharides and leads to disruption and degradation of EPS matrix components. |
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R-C-5741 |
DSPE-PEG2000-MMP(FITC) |
The inclusion of Matrix metalloproteinases in DSPE-PEG-MMPs allows for specific enzymatic degradation of the liposomal nanocarrier at the tumor site. This enzyme-sensitive feature enables the triggered release of the encapsulated cargo,such as drugs or imaging agents, in response to the MMP activity present.The incorporation of the Fluorescein dye in DSPE-PEG-MMPs allows for real-time tracking and visualization of the nanocarrier within the biological system.This fluorescent labeling facilitates the assessment of distribution,uptake, and release of the liposomes in preclinical studies. |
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R-C-5742 |
DSPE-PEG2000-iRG(RB) |
DSPE-PEG-iRG (RB) is a lipid-polyethylene glycol (PEG) conjugate molecule that is widely used in targeted drug delivery systems, such as liposomes or nanoparticles.rhodamine B, which is conjugated to the DSPE-PEG2000-iRG molecule. This dye allows for visualization and tracking of the delivery system in vivo. |
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R-C-5747 |
DSPE-PEG2000-oncoFAP |
DSPE-PEG-oncoFAP is a lipid-polyethylene glycol (PEG) conjugate molecule used in targeted drug delivery and imaging applications. OncoFAP is a peptide specifically designed to target and bind to fibroblast activation protein (FAP), which is overexpressed in the tumor microenvironment. The DSPE-PEG-oncoFAP conjugate combines the properties of DSPE for liposome formation, PEG for increased circulation time in the bloodstream, and oncoFAP for tumor targeting. |
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R-C-5750 |
DSPE-PEG-NHS-Tyr |
DSPE-PEG2000-NHS-Tyr is a lipid-polyethylene glycol(PEG)conjugate molecule that is functionalized with a tyrosine residue and a N-hydroxysuccinimide(NHS)group.DSPE stands for 1,2-distearoyl-sn-glycero-3-phosphoethanolamine,which is a lipid component that can self-assemble into bilayer structures.The PEG chain provides hydrophilicity and stealth properties, resulting in prolonged circulation time in the bloodstream and reduced immunogenicity.The addition of tyrosine to DSPE-PEG-NHS introduces a specific functional group that can be utilized for various applications.For example,tyrosine can serve as a site for further conjugation with a ligand,drug,or imaging agent. |
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R-C-5751 |
DSPE-PEG2000-MbCD |
DSPE-PEG-MbCD,MβCD is a cyclic oligosaccharide molecule that can form inclusion complexes with hydrophobic guest molecules. By conjugating MβCD to DSPE-PEG, the resulting DSPE-PEG-MβCD conjugate can enhance the solubility and stability of hydrophobic drugs or imaging agents.The incorporation of MβCD in DSPE-PEG-MβCD allows for the formation of liposomal systems that can encapsulate and deliver hydrophobic drugs, solubilize hydrophobic imaging agents, or promote the cellular uptake of hydrophobic compounds. |
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