2. dx.doi.org/10.1021/ja413036q | J. Am. Chem. Soc. XXXX, XXX, XXX−XXX
dx.doi.org/10.1021/ja413036q | J. Am. Chem. Soc. XXXX, XXX, XXX−XXX
3. Introduction
Stimuli-responsive micelles have gained increasing attention due to their
potential utilization as nanocarriers for drug delivery.
Responsive materials are inspired
changes in pH,
temperature,
irradiated light,
or their combination
Enzymes as stimuli
4. Encapsulation and release of hydrophobic guests
Figure . Schematic representation of the encapsulation of hydrophobic guests in the hydrophobic core of a smart micellar
nanocarrier. Upon enzymatic cleavage of the hydrophobic end groups, the nanocarrier disassembles and the guest
molecules are released.
8. Selectivity of the Enzymatic Activation
Figure : Fluorescence emission intensity of compound 1b is unaffected
in the absence of the activating enzyme penicilin G amidase (PGA )
after 12 hours in buffer
Figure : Fluorescence emission intensity of compound 1b is
unaffected in the presence of 0.66μM of Esterase from porcine
liver (PLE enzyme) , which is not capable of breaking amide
bond .
9. Micelle Disassembly with Nile Red Fluorescence
Figure . Fluorescence spectra of Nile red (1.25 μM) in the presence
of PEG-dendron hybrid 1b (160 μM) as a function of time after the
addition of the activating enzyme, PGA (0.14 μM). Fluorescence
intensity decreased as Nile red was released into solution.
13. Summary
• New family of amphiphilic PEG-dendron hybrids.
• Enzyme-responsive hybrids and their self assembled micelles have great
potential in the field of drug delivery.
• Disassembly and release rates depended on the CMC.