ABSTRACT
A thermally remendable polymer was synthesized by the Diels-Alder reaction between dithienylfuran and maleimide monomers to generate a photoresponsive diarylethene. UV light (312 nm) and visible light (>435 nm) "gate" the reversibility of the Diels-Alder reaction and turn the self-healing properties of the polymer "off" and "on", respectively. After exposure to UV light, the strength of the polymer as an adhesive is enhanced. Visible light weakens the adhesive.
ABSTRACT
Anthracene endoperoxide ligands anchored to the surfaces of gold nanoparticles undergo bond breaking and release singlet oxygen when the nanoparticles convert 532 nm laser light to heat localized near their surfaces.
Subject(s)
Anthracenes/chemistry , Gold/chemistry , Metal Nanoparticles/chemistry , Singlet Oxygen/chemistry , Hot Temperature , Lasers , Light , Photochemotherapy , Spectrophotometry, UltravioletABSTRACT
Light is used to 'gate' the Diels-Alder reaction using a photoresponsive dithienylfuran backbone and turn the reversibility of the Diels-Alder reaction 'off' and 'on' at 100 °C. These features make the reported system an excellent candidate for developing the next generation of self-healing polymers and photothermal drug delivery vehicles.
ABSTRACT
The ability of gold (Au) nanoparticles (NPs) to generate heat efficiently by absorbing visible and near-infrared (NIR) light holds great promise as a means to trigger chemical and biochemical events near the NPs. Previous demonstrations show that pulsed laser irradiation can selectively elicit the release of a fluorescent dye covalently anchored to the NP surface through a heat-labile linker without measurably changing the temperature of the surroundings. This article reports that the authors demonstrate the biological efficacy of this approach to photodelivery by showing that the decorated Au NPs are rapidly internalized by cells, are stable under physiological conditions, are nontoxic, and exhibit nonlethal photorelease following exposure to pulsed laser radiation. These observations, further supported by the versatility of our delivery motif, reaffirm the potential for further development of nonlethal photothermal therapeutics and their future relevance to such fields as gene therapy and stem-cell differentiation.
Subject(s)
Gold/chemistry , Gold/radiation effects , Nanocapsules/chemistry , Nanocapsules/radiation effects , Oocytes/chemistry , Oocytes/radiation effects , Animals , Cells, Cultured , Cricetinae , Cricetulus , Hot Temperature , Light , Radiation Dosage , Xenopus laevisABSTRACT
Photothermal release of DNA from gold nanoparticles either by thermolysis of the Au-S bonds used to anchor the oligonucleotides to the nanoparticle or by thermal denaturation has great therapeutic potential, however, both processes have limitations (a decreased particle stability for the former process and a prohibitively slow rate of release for the latter). Here we show that these two mechanisms are not mutually exclusive and can be controlled by adjusting laser power and ionic strength. We show this using two different double-stranded (ds)DNA-nanoparticle conjugates, in which either the anchored sense strand or the complementary antisense strand was labeled with a fluorescent marker. The amounts of release due to the two mechanisms were evaluated using fluorescence spectroscopy and capillary electrophoresis, which showed that irradiation of the decorated particles in 200 mM NaOAc containing 10 mM Mg(OAc)(2) with a pulsed 532 nm laser operating at 100 mW favors denaturation over Au-S cleavage to an extent of more than six-to-one. Due to the use of a pulsed laser, the process occurs on the order of minutes rather than hours, which is typical for continuous wave lasers. These findings encourage continued research toward developing photothermal gene therapeutics.
Subject(s)
DNA, Single-Stranded/chemistry , Gold/chemistry , Metal Nanoparticles/chemistry , Sulfur/chemistry , Temperature , Base Sequence , DNA, Single-Stranded/genetics , DNA, Single-Stranded/isolation & purification , Electrophoresis, Capillary , Models, Molecular , Nucleic Acid Conformation , Nucleic Acid Denaturation , Oligodeoxyribonucleotides, Antisense/chemistry , Oligodeoxyribonucleotides, Antisense/genetics , Oligodeoxyribonucleotides, Antisense/isolation & purification , Particle Size , Spectrometry, Fluorescence , Surface PropertiesABSTRACT
Photoisomerization of a coordinating, photochromic dithienylethene bearing a pyridine and a methylpyridinium group was investigated as a means to reversibly modulate the luminescence from CdSe-ZnS core-shell quantum dots. Resonance energy transfer and electron transfer are both plausible quenching mechanisms based on an increase in the spectral donor-acceptor overlap and an anodic shift in the reduction potential accompanying the isomerization reaction of the dithienylethene photoswitch. Photochemical degradation of both the quantum dot and photochromic quencher was observed after repeated cycling between the two isomers, suggesting irreversible electron transfer from the quantum dot to the dithienylethene as the dominant luminescence quenching mechanism.
Subject(s)
Pyridinium Compounds/chemistry , Quantum Dots , Thiophenes/chemistry , Cadmium Compounds/chemistry , Isomerism , Luminescence , Selenium Compounds/chemistry , Spectrophotometry, Ultraviolet , Sulfides/chemistry , Zinc Compounds/chemistryABSTRACT
A close-packed monolayer of zinc 5,10,15,20-tetrakis(3-carboxyphenyl)porphyrin has been prepared and deposited on the thin native oxide covering the surface of an SOI-MOSFET (silicon-on-insulator metal-oxide-semiconductor field effect transistor) using Langmuir-Blodgett techniques. When the device is exposed to amine vapors in a nitrogen atmosphere, the amine coordinates to the zinc atom. The resulting change in electron distribution within the porphyrin leads to a large change in the drain current of the transistor, biased via a back gate. This change is sensitive to both the amount of amine present and the base strength of the amine. Only very small changes in drain current were observed with a monolayer of free base porphyrin or palmitic acid. After exposure to high pyridine concentrations, the device response saturates, but partially recovers after overnight exposure to flowing nitrogen gas. Interestingly, the device response is instantaneously reset by exposure to visible light, suggesting that photode-ligation occurs. An electrical model for the hybrid device that describes its response to ligand binding in terms of a change in the work function of the porphyrin monolayer has been developed. A transistor response to a few hundred attomoles of bound pyridine can be readily detected. This extreme sensitivity, coupled with the ability to reset the device using light, suggests that such systems might be useful as sensors.
