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Merck
CN

908649

Sigma-Aldrich

Poly(lactide-co-glycolide)-fluorescein

lactide:glycolide 50:50, Mn 10,000-20,000

Synonym(s):

PLGA, PLGA-fluorescein

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50 MG
¥800.96

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50 MG
¥800.96

About This Item

Linear Formula:
[C3H4O2]x[C2H2O2]y
UNSPSC Code:
12162002
NACRES:
NA.23

¥800.96


Please contact Customer Service for Availability

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form

powder or chunks

feed ratio

lactide:glycolide 50:50

mol wt

Mn 10,000-20,000
average Mn 10,000-20,000

composition

Dye Content, 0.15 μg/mg (polymer)

color

yellow to orange

storage temp.

−20°C

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908630908622908517
storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

feed ratio

lactide:glycolide 50:50

feed ratio

lactide:glycolide (50:50)

feed ratio

lactide:glycolide 50:50

feed ratio

lactide:glycolide 50:50

mol wt

Mn 10,000-20,000

mol wt

Mn 20,000-30,000, average Mn 20,000-30,000

mol wt

Mn 10,000-30,000, average Mn 10,000-30,000

mol wt

average Mn 5,000

composition

Dye Content, 0.15 μg/mg (polymer)

composition

Dye Content, 7.54 μg/mg (polymer)

composition

Dye Content, 3.12 μg/mg (polymer)

composition

-

color

yellow to orange

color

blue to teal

color

red to maroon

color

white to tan

Application

This fluorescein labeled PLGA is a biocompatible and biodegradable polymer. It can be used in the formation of fluorescent nanoparticles for drug delivery and bioimaging applications.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Yihan Xu et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 105(6), 1692-1716 (2016-04-22)
Poly (lactic-co-glycolic acid) (PLGA) copolymers have been broadly used in controlled drug release applications. Because these polymers are biodegradable, they provide an attractive option for drug delivery vehicles. There are a variety of material, processing, and physiological factors that impact
R Gref et al.
Science (New York, N.Y.), 263(5153), 1600-1603 (1994-03-18)
Injectable nanoparticulate carriers have important potential applications such as site-specific drug delivery or medical imaging. Conventional carriers, however, cannot generally be used because they are eliminated by the reticulo-endothelial system within seconds or minutes after intravenous injection. To address these

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