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Biomedical subjects

Richard A Farrer

Publications and source records attributed to Richard A Farrer.

7 recordsLinked to original sources

Selective functionalization of 3-D polymer microstructures.

We demonstrate the selective functionalization of 3-D polymer microstructures that were created using multiphoton absorption polymerization. By fabricating different portions of the structures with acrylic and methacrylic polymers, we are able to take advantage of the differential reactivities of these materials to perform functionalization chemistry on a single polymeric component. We demonstrate the selective deposition of metal to create structures, such as a functional microinductor. Our strategy is quite general and can be extended readily to the deposition of materials, such as metal oxides and biomolecules.

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Ultrafast orientational dynamics of nanoconfined benzene.

Ultrafast optical Kerr effect spectroscopy has been used to study the orientational dynamics of benzene and benzene-d(6) confined in nanoporous sol-gel glass monoliths with a range of average pore sizes. All of the observed orientational diffusion of confined benzene is found to occur on a slower time scale than in the bulk, even in pores with diameters that are significantly larger than a benzene molecule. The orientational dynamics of benzene-d(6) are found to be inhibited to a lesser extent than those of benzene, which is attributed to the differences in wetting properties of the two liquids on silica. The decays are fit well by a sum of two exponentials, the faster of which depends on pore size. Similar results are found in pores that have been modified with trimethylsilyl groups, although the relaxation is faster than in unmodified pores. Comparison to Raman line width data for confined benzene-d(6) suggests that the liquid exhibits significant structuring at the pore walls, with the benzene molecules lying flat on the surfaces of unmodified pores.

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Optical Kerr effect spectroscopy using time-delayed pairs of pump pulses with orthogonal polarizations.

We characterize in detail a recently introduced technique in which perpendicularly polarized pulses with controllable intensities and timing are used for the excitation step in optical Kerr effect spectroscopy. We examine the ratio of pump pulse intensities required to cancel the contribution of reorientational diffusion or of a Raman-active intramolecular vibration to the signal as a function of the delay time between excitation pulses. These results indicate that the signal can be described well as arising from the sum of independent third-order responses initiated by each pump pulse. This conclusion is further supported by using data obtained with a single pump pulse to model decays obtained with two pump pulses.

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Highly efficient multiphoton-absorption-induced luminescence from gold nanoparticles.

We demonstrate that highly efficient photoluminescence is generated from gold nanoparticles as small as a few nanometers in diameter upon irradiation with sub-100-fs pulses of 790-nm light. Strong emission is observed at excitation intensities comparable to or less than those typically used for multiphoton imaging of fluorescently labeled biological samples. The particles have polarized emission, can radiate more efficiently than single molecules, do not exhibit significant blinking, and are photostable under hours of continuous excitation. These observations suggest that metal nanoparticles are a viable alternative to fluorophores or semiconductor nanoparticles for biological labeling and imaging.

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Orientational dynamics of liquids confined in nanoporous sol-gel glasses studied by optical kerr effect spectroscopy.

When a liquid is restricted to volumes on a molecular distance scale, its orientational and translational dynamics are perturbed strongly by the confinement. Nanoporous sol-gel glasses are an excellent model system for studying the effects of confinement on the behavior of liquids, and in this Account we review experiments in which ultrafast optical Kerr effect spectroscopy has been used to study the orientational dynamics of liquids confined in these media. We contrast the effects of confinement on the orientational dynamics of weakly wetting, strongly wetting, and networked liquids, and we discuss the influence of factors such as pore size, molecular shape, and surface chemistry.

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Production, analysis, and application of spatially resolved shells in solid-phase polymer spheres.

Two-photon fluorescence microscopy has been used to interrogate the interior functionality of polymer resin beads. By employing this technique, the spatial distribution of the initial functionality contained within the polymer matrix has been determined. Spatially resolved, concentric shells were then produced synthetically in these polymer spheres via a series of protection/deprotection reactions in which two-photon fluorescence microscopy was employed to monitor each successive step. To demonstrate the potential utility of these techniques in combinatorial screening, a set of beads was prepared containing a unique tripeptide sequence in each of the three concentric shells within each individual bead. The set was then screened for the binding affinity of each tripeptide toward a fluorescent ligand.

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In situ observation of molecular diffusion in solid supports using two-photon fluorescence microscopy.

We demonstrate that two-photon fluorescence microscopy is a useful tool for monitoring the diffusion of molecules through polymeric solid supports. As a proof of principle, TentaGel beads were bound to a cover slip, and diffusion of Rhodamine 6G through single beads was observed in real time. Diffusion experiments performed in 40 different beads indicate that there is a considerable degree of heterogeneity in diffusion rates from bead to bead.

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