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Key Documents

909858

Sigma-Aldrich

Carboxylic acid-poly(ethylene glycol)-b-poly(lactide-co-glycolide)

PEG average Mn 5,000, PLGA average Mn 20,000, lactide:glycolide 50:50

Sinonimo/i:

COOH-PEG-PLGA, Carboxylic acid PEG-PLGA

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About This Item

Formula condensata:
H[(C3H4O2)x(C2H2O2)y]mO[C2H4O]nC2H3O2
Codice UNSPSC:
12352106
NACRES:
NA.23

Forma fisica

powder or chunks

Rapporto d’alimentazione

lactide:glycolide 50:50

PM

PEG average Mn 5,000 (by NMR)
PLGA average Mn 20,000 (by NMR)

Colore

white to tan

Temperatura di conservazione

−20°C

Applicazioni

Carboxylic acid-poly(ethylene glycol)-b-poly(lactide-co-glycolide) is a functionalized, amphiphilic, diblock copolymer composed of a hydrophilic PEG block and a hydrophobic PLGA block. These biodegradable, biocompatible polymers can self-assemble to form nanoparticles, such as micelles and polymersomes, in both aqueous and non-aqueous media. Due to these properties, these polymers are widely used in polymeric nanoparticle formulation to achieve controlled and targeted delivery of therapeutic agents (e.g. APIs, genetic material, peptides, vaccines, and antibiotics). The carboxylic acid functional group on the PEG chain enables rapid and facile surface functionalization, allowing for these materials to be used in applications such as targeted drug delivery.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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The goal of this study was to develop and characterize a novel intravaginal film platform for targeted delivery of small interfering RNA (siRNA)-loaded nanoparticles (NP) to dendritic cells as a potential gene therapy for the prevention of sexually transmitted human
Soroush Ardekani et al.
Scientific reports, 5, 16258-16258 (2015-11-21)
Nitroglycerin (NTG) markedly enhances nitric oxide (NO) bioavailability. However, its ability to mimic the anti-inflammatory properties of NO remains unknown. Here, we examined whether NTG can suppress endothelial cell (EC) activation during inflammation and developed NTG nanoformulation to simultaneously amplify

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