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Merck

900946

Sigma-Aldrich

Stearic acid-modified branched polyethylenimine

Synonym(e):

Stearic acid-PEI, Stearic acid-functionalized PEI, Stearic-PEI25K

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About This Item

Lineare Formel:
H(NHCH2CH2)nNHCOCH2(CH2)15CH3
UNSPSC-Code:
12352200
NACRES:
NA.23

Form

liquid

Lagertemp.

2-8°C

Anwendung

Stearic acid-modified branched polyethylenimine was derived from Sigma-Aldrich Product 408727. Based upon an approximate Mw of 25,000 for the branched PEI, Product 900946 is approximately 60% functionalized with stearic acid units (by NMR).

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Aws Alshamsan et al.
Molecular pharmaceutics, 6(1), 121-133 (2008-12-05)
This study was conducted to formulate a nonviral delivery system for the delivery of small interfering RNA (siRNA) to B16 melanoma cells in vitro. For this purpose, oleic and stearic acid modified derivatives of branched polyethylenimine (PEI) were prepared and
Hao Liu et al.
Journal of materials chemistry. B, 2(32), 5238-5248 (2014-08-28)
This study aimed to enhance the water solubility and antitumor efficacy of (-)-gossypol. Polyethyleneimine conjugated with stearic acid (PgS) was used for loading and protecting (-)-gossypol through hydrogen bonding. Double-layered hyaluronic acid (HA)-modified PgS nanoparticles encapsulating (-)-gossypol [(-)-G-PgSHAs] were prepared
Qiaofeng Jin et al.
PloS one, 8(9), e76544-e76544 (2013-10-03)
A novel cationic microbubble (MB) for improvement of the DNA loading capacity and the ultrasound-mediated gene delivery efficiency has been developed; it has been prepared with commercial lipids and a stearic acid modified polyethylenimine 600 (Stearic-PEI600) polymer synthesized via acylation

Artikel

Professor Yoshiki Katayama (Kyushu University, Japan) discusses recent advances in drug delivery systems and strategies that exploit the EPR effect, with a special focus on stimuli-responsive systems based on novel materials.

CRISPR/Cas9 delivery via nonviral nanoparticles shows promising advancements for gene editing in disease treatment.

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