Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters











Database
Language
Publication year range
1.
Chemistry ; 23(24): 5652-5657, 2017 Apr 27.
Article in English | MEDLINE | ID: mdl-28272756

ABSTRACT

We report a facile chemical method for fabricating holey graphene by catalytic oxidation of highly ordered pyrolytic graphite (HOPG) using an FeIII porphyrin complex-based covalent organic framework (COF) as a bifunctional surface catalyst-template. We demonstrate regular hole formation after oxidation with H2 O2 and NaOCl, COF removal, and HOPG exfoliation.

2.
Nanoscale ; 7(19): 8689-94, 2015 May 21.
Article in English | MEDLINE | ID: mdl-25902750

ABSTRACT

With the advancement of nanocarriers for drug delivery into biomedical practice, assessments of drug susceptibility to oxidative degradation by enzymatic mechanisms of inflammatory cells become important. Here, we investigate oxidative degradation of a carbon nanotube-based drug carrier loaded with Doxorubicin. We employed myeloperoxidase-catalysed and peroxynitrite-mediated oxidative conditions to mimic the respiratory burst of neutrophils and macrophages, respectively. In addition, we revealed that the cytostatic and cytotoxic effects of free Doxorubicin, but not nanotube-carried drug, on melanoma and lung carcinoma cell lines were abolished in the presence of tumor-activated myeloid regulatory cells that create unique myeloperoxidase- and peroxynitrite-induced oxidative conditions. Both ex vivo and in vitro studies demonstrate that the nanocarrier protects the drug against oxidative biodegradation.


Subject(s)
Antibiotics, Antineoplastic/chemistry , Doxorubicin/chemistry , Drug Carriers/chemistry , Nanotubes, Carbon/chemistry , Peroxidase/metabolism , Peroxynitrous Acid/chemistry , Animals , Antibiotics, Antineoplastic/pharmacology , Biocatalysis , Cell Line, Tumor , Cell Survival/drug effects , Doxorubicin/pharmacology , Humans , Hydrogen-Ion Concentration , Mice , Oxidation-Reduction
3.
J Phys Chem C Nanomater Interfaces ; 118(31): 17193-17199, 2014 Aug 07.
Article in English | MEDLINE | ID: mdl-25126155

ABSTRACT

We report on the reversible detection of CaptAvidin, a tyrosine modified avidin, with single-walled carbon nanotube (SWNT) field-effect transistors (FETs) noncovalently functionalized with biotin moieties using 1-pyrenebutyric acid as a linker. Binding affinities at different pH values were quantified, and the sensor's response at various ionic strengths was analyzed. Furthermore, protein "fingerprints" of NeutrAvidin and streptavidin were obtained by monitoring their adsorption at several pH values. Moreover, gold nanoparticle decorated SWNT FETs were functionalized with biotin using 1-pyrenebutyric acid as a linker for the CNT surface and (±)-α-lipoic acid linkers for the gold surface, and reversible CaptAvidin binding is shown, paving the way for potential dual mode measurements with the addition of surface enhanced Raman spectroscopy (SERS).

4.
ACS Nano ; 8(6): 5610-21, 2014 Jun 24.
Article in English | MEDLINE | ID: mdl-24871084

ABSTRACT

In contrast to short-lived neutrophils, macrophages display persistent presence in the lung of animals after pulmonary exposure to carbon nanotubes. While effective in the clearance of bacterial pathogens and injured host cells, the ability of macrophages to "digest" carbonaceous nanoparticles has not been documented. Here, we used chemical, biochemical, and cell and animal models and demonstrated oxidative biodegradation of oxidatively functionalized single-walled carbon nanotubes via superoxide/NO* → peroxynitrite-driven oxidative pathways of activated macrophages facilitating clearance of nanoparticles from the lung.


Subject(s)
Lung/drug effects , Macrophages/drug effects , Nanotechnology/methods , Nanotubes, Carbon/chemistry , Peroxynitrous Acid/chemistry , Superoxides/chemistry , Acoustics , Animals , Biocompatible Materials/chemistry , Bronchoalveolar Lavage , Carbon/chemistry , Humans , Inflammation/metabolism , Lung/pathology , Macrophages/metabolism , Macrophages, Alveolar/metabolism , Mice , Mice, Inbred C57BL , Neutrophils/metabolism , Nitric Oxide/chemistry , Oxygen/chemistry , Rats
5.
J Org Chem ; 76(18): 7352-8, 2011 Sep 16.
Article in English | MEDLINE | ID: mdl-21846123

ABSTRACT

This Article describes the development of conditions for cleaving silicon-oxygen bonds using catalytic quantities of fluoride at neutral pH in mixed organic-aqueous solutions that contain buffer. A variety of silicon protecting groups can be removed under these conditions, which show tolerance for acid- and base-sensitive groups. A modified procedure also is presented using catalytic fluoride in anhydrous dimethyl sulfoxide-methanol, which generates primarily volatile silicon byproducts.

6.
J Am Chem Soc ; 132(27): 9234-5, 2010 Jul 14.
Article in English | MEDLINE | ID: mdl-20565108

ABSTRACT

This Communication describes a strategy for designing stimuli-responsive plastics that are capable of responding to chemical signals in the environment by changing shape. The plastics consist of patterned mixtures of poly(phthalaldehyde) polymers in which each polymer contains a different end-capping group, or "trigger". Each polymer within the plastic is capable of responding to a different signal and depolymerizing once the signal reacts with the trigger. This process of depolymerization enables the plastic to alter its physical features quickly and with a magnitude that depends on the length of the responsive polymer.

7.
Org Lett ; 9(12): 2301-4, 2007 Jun 07.
Article in English | MEDLINE | ID: mdl-17488122

ABSTRACT

We have investigated Ag(I) mediated folding of a tridentate compound, containing three pyridine flaps tethered to a semirigid scaffold, into a molecular basket, using both experimental and theoretical methods. The basket formation has been shown to be highly favorable in organic media (Delta G degrees = -7.2 kcal/mol), with the assembly process allowing for another ligand to bind preferentially on the outer side.


Subject(s)
Organometallic Compounds/chemistry , Pyridines/chemistry , Silver/chemistry , Ligands , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Structure
SELECTION OF CITATIONS
SEARCH DETAIL