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764817

Sigma-Aldrich

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

average Mn (1100-1000-1100), lactide:glycolide 75:25

别名:

PLGA-PEG-PLGA

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About This Item

分類程式碼代碼:
12162002
NACRES:
NA.23
价格与库存信息目前不能提供

描述

typical PEG PDI<1.1; overall PDI≤2.0 (THF, PS)

品質等級

100

形狀

semisolid

饋電比

lactide:glycolide 75:25

分子量

PEG average Mn 1,000
PLGA average Mn 2,200
average Mn (1100-1000-1100)

降解時間

2-3 weeks

轉變溫度

Tm 230-235 °C

蛋白質二硫鍵異構酶

<2.0

儲存溫度

2-8°C

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相关类别

一般說明

PLGA-PEG-PLGA is an amphiphilic triblock copolymer which can self-assemble into micelles in aqueous medium due to the hydrophobic interactions present in the hydrophobic segments. The PEG segment imparts hydrophilicity and improves the biocompatibility of the copolymer. The PLGA segment forms a hydrophobic core and can solubilize hydrophobic drugs. These copolymers are widely used as nanocarriers for the sustained release of drugs.[1]

應用

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

特點和優勢

Biocompatible, degradable, thermosensitive, high stability, small size (<200 nm) and properties can be easily modified.[1]

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCP0962
MKCP5201
MKCM8663
MKCM5667
MKCG3703

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Zhimei Song et al.
Journal of colloid and interface science, 354(1), 116-123 (2010-11-04)
The aim of this study was to assess the potential of new copolymeric micelles to modify the pharmacokenetics and tissue distribution of Curcumin (CUR), a hydrophobic drug. In the present study, a poly (d,l-lactide-co-glycolide)-b-poly(ethylene glycol)-b-poly(d,l-lactide-co-glycolide) (PLGA-PEG-PLGA) copolymer was synthesized and
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., &amp; 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

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