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Merck

764825

Sigma-Aldrich

Poly(ethylene glycol) methyl ether-block-poly(lactide-co-glycolide)

PEG Mn 2,000, PLGA Mn 4,500

Synonym(e):

PEG-PLGA, Polyethylene glycol, mPEG-b-PLGA

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About This Item

Lineare Formel:
H[(C3H4O2)x(C2H2O2)y]mO[C2H4O]nCH3
UNSPSC-Code:
12162002
NACRES:
NA.23

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Form

pellets

Zufuhrverhältnis

lactide:glycolide 65:35

Mol-Gew.

PEG Mn 2,000
PLGA Mn 4,500
average Mn 6,500 (total)

Zeitrahmen für den Abbau

1-4 weeks

Übergangstemp.

Tm 241-246 °C

PDI

≤2.0

Lagertemp.

2-8°C

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Allgemeine Beschreibung

Amphiphilic block copolymers (AmBC) are made up of two chemically different homopolymer blocks. One of the block is hydrophilic and the other one is hydrophobic. These macromolecules have the properties to self-assemble when dissolved in an aqueous media. PEG-PLGA is one the most commonly used biodegradable amphiphilic block copolymers for drug delivery applications. PEG is the hydrophilic part and PLGA is the hydrophobic part.[1]

Anwendung

Used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs. [2][3]
forming "stealth" pegylated microparticles

Leistungsmerkmale und Vorteile

  • Good biocompatibility, low immunogenicity and good degradability.
  • Properties can be easily modulated by changing the block copolymer segment sizes to suit a particular application.[1]

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Thermosensitive self-assembling block copolymers as drug delivery systems.
Bonacucina, G., Cespi, M., Mencarelli, G., Giorgioni, G., & Palmieri, G. F.
Polymer, 3(2), 779-811 (2011)
PLGA-PEG Encapsulated sitamaquine nanoparticles drug delivery system against Leishmania donovani
Kumara, R., Sahoo, G. C., Pandeya, K., Dasa, V. N. R., Yousuf, M., Ansaria, S. R., & Dasa, P.
Journal of Scientific and Innovative Research, 3(1), 85-90 (2014)
Frank Gu et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(7), 2586-2591 (2008-02-15)
There has been progressively heightened interest in the development of targeted nanoparticles (NPs) for differential delivery and controlled release of drugs. Despite nearly three decades of research, approaches to reproducibly formulate targeted NPs with the optimal biophysicochemical properties have remained

Artikel

Micelle formation addresses low solubility in IV drug delivery, overcoming clinical limitations.

Local delivery of bioactive molecules using an implantable device can decrease the amount of drug dose required as well as non-target site toxicities compared to oral or systemic drug administration.

The development of drugs that target specific locations within the human body remains one of the greatest challenges in biomedicine today.

AliAliphatic polyesters, including polylactide and polyglycolide, are biodegradable polymers widely used in medical applications.

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