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    LNP delivery system excipient mPEG-DSPE-2K

    LNP delivery system excipient mPEG-DSPE-2K

    140.00 USD ($)/Gram

    Product Details:

    • Shelf Life 24 Months
    • Taste Other
    • Smell No Smell
    • Storage Freezer
    • HS Code 3907209090
    • Molecular Formula C45H87NNaO11P
    • Solubility Sparingly soluble in Chloroform and Methanol
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    LNP delivery system excipient mPEG-DSPE-2K Price And Quantity

    • 140.00 USD ($)/Gram
    • 1 Gram

    LNP delivery system excipient mPEG-DSPE-2K Product Specifications

    • 24 Months
    • Freezer
    • 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000]
    • No Smell
    • Other
    • 147867-65-0
    • Medicine Grade
    • 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000]
    • 53 ~ 54
    • Not less than 95.0%
    • Sparingly soluble in Chloroform and Methanol
    • White or off-white solid
    • DSPE-MPEG2000 is used as one of the LNP Delivery System Excipients for mRNA medicines or drugs.
    • Powder
    • Other
    • C45H87NNaO11P
    • 3907209090

    LNP delivery system excipient mPEG-DSPE-2K Trade Information

    • Shanghai or Beijing
    • 10000 Gram Per Month
    • 10 Days
    • Yes
    • If order is confirmed we will reimburse the sample cost
    • 1g/bottle, 5g/bottle or according to the requirements from customers.
    • Asia Australia North America Western Europe Middle East Africa Eastern Europe South America Central America
    • All India
    • ISO

    Product Description

    MPEG2000-DSPE combines the amphiphilic properties of phospholipids and the hydrophilic polymer properties of PEG. In recent years, its application in drug carriers such as long-circulating liposomes, polymer micelles, and long-circulating nanoparticles has achieved rapid development. According to the management of pharmaceutical excipients in my country, the molecular weight of polyethylene glycol in the MPEG2000-DSPE molecule is about 2000, which is suitable for the preparation of long-circulating liposomes, so that liposomes will not be captured by MPS-rich tissues immediately after intravenous injection. As a result, the circulation time in the blood is prolonged, thereby increasing the chance of entering pathological tissues.

    The amount of MPEG2000-DSPE in doxorubicin liposome DOXIL accounted for 20% of the total lipid, and compared with ordinary doxorubicin liposome Mycoet, the kinetic difference was obvious. The plasma half-life of liposomal doxorubicin, DOXIL is 2.5d, while Myocet is only 0.07h.



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