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Merck
CN

765139

聚(乙二醇)甲醚-嵌段-聚(丙交酯--乙交酯)

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

别名:

PEG-PLGA, mPEG-b-PLGA

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关于此项目

线性分子式:
H[(C3H4O2)x(C2H2O2)y]mO[C2H4O]nCH3
NACRES:
NA.23
UNSPSC Code:
12162002
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form

solid

Quality Level

feed ratio

lactide:glycolide 50:50

mol wt

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

degradation timeframe

1-4 weeks

transition temp

Tg 24 °C, Tm 38-43 °C

PDI

<2.0

storage temp.

2-8°C

General description

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。

Application

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

Features and Benefits

  • 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。


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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available



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分析证书(COA)

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商品

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.

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

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

查看所有文章

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)
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



全球贸易项目编号

货号GTIN
76575-5ML04061837583261
76575-25ML04061837583254
765139-1G04061832923307