934569
NanoFabTx™ Photoactivatable Lipid
redAzoPC
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About This Item
Empirische Formel (Hill-System):
C46H72Cl4N3O8P
CAS-Nummer:
Molekulargewicht:
967.86
UNSPSC-Code:
12161503
NACRES:
NA.21
Empfohlene Produkte
Qualitätsniveau
Assay
≥90%
Form
solid
Farbe
orange to dark red
Lagertemp.
−20°C
SMILES String
[O-]P(OCC[N+](C)(C)C)(OC[C@H](OC(CCCC1=CC(Cl)=C(C(Cl)=C1)/N=N/C2=C(C=C(C=C2Cl)CCCC)Cl)=O)COC(CCCCCCCCCCCCCCCCC)=O)=O
Allgemeine Beschreibung
The NanoFabTx Photoactivatable Lipid, redAzoPC is a red-light photoswitchable lipid for controlled and targeted drug delivery. The tetra-ortho-chloro-azobenzene of redAzoPC can be isomerized from the cis to the trans conformation at 660 nm light. LNPs prepared using the NanoFabTx™ Photoactivatable Lipid, redAzoPC result in controlled drug release following deep red light irradiation.
Anwendung
Lipid nanoparticle and liposome drug delivery systems
Leistungsmerkmale und Vorteile
- Similar drug loading, encapsulation efficiency, size, and polydispersity to non-photoswitchable lipids
- Light-induced drug delivery
- Targeted and controlled release
- Overcomes limitations associated to UV-switchable lipids
Rechtliche Hinweise
NANOFABTX is a trademark of Sigma-Aldrich Co. LLC
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Analysenzertifikate (COA)
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Tufan K Mukhopadhyay et al.
Current opinion in pharmacology, 63, 102202-102202 (2022-03-13)
Many aspects of cell signaling are controlled by lipids. Several signaling lipids have been functionalized with an azobenzene photoswitch to control underlying signaling dynamics with light. Herein, we provide an overview of signaling photolipids developed to date focusing on their
Johannes Morstein et al.
Chembiochem : a European journal of chemical biology, 22(1), 73-83 (2020-08-14)
Photoswitchable lipids are emerging tools for the precise manipulation and study of lipid function. They can modulate many aspects of membrane biophysics, including permeability, fluidity, lipid mobility and domain formation. They are also very useful in lipid physiology and enable
Nisha Chander et al.
Small (Weinheim an der Bergstrasse, Germany), 17(21), e2008198-e2008198 (2021-04-22)
Encapsulation of small molecule drugs in long-circulating lipid nanoparticles (LNPs) can reduce toxic side effects and enhance accumulation at tumor sites. A fundamental problem, however, is the slow release of encapsulated drugs from these liposomal systems at the disease site
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