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Merck
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文件

765139

Sigma-Aldrich

聚(乙二醇)甲醚-嵌段-聚（丙交酯-共-乙交酯）

PEG average Mn 5,000, PLGA Mn 7,000

别名:

PEG-PLGA, mPEG-b-PLGA

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About This Item

线性分子式:
H[(C3H4O2)x(C2H2O2)y]mO[C2H4O]nCH3
分類程式碼代碼:
12162002
NACRES:
NA.23

形狀

solid

饋電比

lactide:glycolide 50:50

分子量

PEG average Mn 5,000
PLGA Mn 7,000
average Mn 12,000 (total)

降解時間

1-4 weeks

轉變溫度

Tg 24 °C
Tm 38-43 °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

两亲性嵌段共聚物（AmBC）由两种化学上不同的均聚物嵌段组成。嵌段之一是亲水的，另一个是疏水的。这些大分子溶于水介质时具有自组装的特性。PEG-PLGA是最常用于药物递送应用的可生物降解的两亲嵌段共聚物之一。PEG是亲水部分，PLGA是疏水部分。

應用

可用于合成靶向纳米粒子，从而用于差异递送和控释药物。
形成“隐形”聚乙二醇化微粒

特點和優勢

  • 良好的生物相容性、低免疫原性和良好的降解性。
  • 通过改变嵌段共聚物链段的尺寸可以轻松调节其性能，以适合特定应用。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

No data available

閃點（°C）

No data available

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Thermosensitive self-assembling block copolymers as drug delivery systems.
Bonacucina, G., Cespi, M., Mencarelli, G., Giorgioni, G., &amp; Palmieri, G. F.
Polymer, 3(2), 779-811 (2011)
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
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)

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