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MAL-PEG-PCL, PEG MW 400-10k

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

Category MAL-PEG-PCL
Catalog NO. BPG-1379
Product Name MAL-PEG-PCL, PEG MW 400-10k
Molecular Weight Customizable
MAL-PEG-PCL, PEG MW 400-10k
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Fast track to get specific molecular weight products:

CatalogMolecular WeightAvailability
BPG-1379-1 MAL-PEG-PCL, PEG MW 400 In stock Inquiry
BPG-1379-2 MAL-PEG-PCL, PEG MW 600 In stock Inquiry
BPG-1379-3 MAL-PEG-PCL, PEG MW 1k In stock Inquiry
BPG-1379-4 MAL-PEG-PCL, PEG MW 2k In stock Inquiry
BPG-1379-5 MAL-PEG-PCL, PEG MW 3.4k In stock Inquiry
BPG-1379-6 MAL-PEG-PCL, PEG MW 5k In stock Inquiry
BPG-1379-7 MAL-PEG-PCL, PEG MW 10k In stock Inquiry
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Product Information

Description Polyethylene glycol and polycaprolactone coupled compounds are widely used in the field of biomedicine. Drugs modified by the PEG-PCL series of derivatives have better water solubility, encapsulation efficiency and drug loading. PEGylation can improve the stability of the drug. PCL has good biocompatibility, degradability and other properties. It does not cause toxic side effects to the human body and can therefore be used as a carrier material for different types of drugs. In addition, PCL has good flexibility, slow degradation rate and good film formation, so it can be used for postoperative tissue engineering.
Synonyms PCL-PEG-MAL
Solubility Soluble in water, DMSO and DMF. Freshly prepared before use.
Storage -20°C for long-term preservation, keep in dry and avoid sunlight. Avoid repeated freezing and thawing.
References 1. Gao H, Qian J, Cao S, et al. Precise glioma targeting of and penetration by aptamer and peptide dual-functioned nanoparticles. Biomaterials, 2012, 33(20): 5115-5123.
2. Zhang P, Hu L, Yin Q, et al. Transferrin-conjugated polyphosphoester hybrid micelle loading paclitaxel for brain-targeting delivery: synthesis, preparation and in vivo evaluation. Journal of Controlled Release, 2012, 159(3): 429-434.

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PEGylation of Peptides and Proteins

PEGylation of Peptides
and Proteins

Reduce the Immunogenicity of Peptide/Protein Drugs

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