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1.
Opt Lett ; 38(23): 5032-5, 2013 Dec 01.
Article in English | MEDLINE | ID: mdl-24281502

ABSTRACT

We experimentally investigate the self-reflectivity of intense strongly focused femtosecond laser pulses used for single-shot femtosecond laser ablation of silicon-on-insulator (SOI). We model the self-reflectivity using 2D finite-difference time-domain simulations of a single femtosecond laser pulse interacting with a submicrometer-sized time- and space-dependent plasma induced by the incident pulse itself and find excellent agreement with our experimental results. The simulation shows that the laser-induced plasma scatters the incident pulse into the guided modes of the device layer of the SOI.

2.
Opt Lett ; 37(7): 1148-50, 2012 Apr 01.
Article in English | MEDLINE | ID: mdl-22466177

ABSTRACT

We have investigated the direct fabrication of subsurface waveguide amplifiers in Er-Yb zinc polyphosphate glass by utilizing the relationship between the initial glass composition and the resulting changes to the network structure after modification by fs laser pulses. Waveguides, exhibiting internal gain of 1 dB/cm at 1.53 µm when pumped with 500 mW at 976 nm, were directly fabricated using a regenerative amplified Ti:sapphire 1 kHz, 180 fs laser system. Optical properties as well as insertion losses and internal gain are reported.

3.
Opt Express ; 19(9): 7929-36, 2011 Apr 25.
Article in English | MEDLINE | ID: mdl-21643042

ABSTRACT

We report the relationship between the initial glass composition and the resulting microstructural changes after direct femtosecond laser waveguide writing with a 1 kHz repetition rate Ti:sapphire laser system. A zinc polyphosphate glass composition with an oxygen to phosphorus ratio of 3.25 has demonstrated positive refractive index changes induced inside the focal volume of a focusing microscope objective for laser pulse energies that can achieve intensities above the modification threshold. The permanent photo-induced changes can be used for direct fabrication of optical waveguides using single scan writing techniques. Changes to the localized glass network structure that produce positive changes in the refractive index of zinc phosphate glasses upon femtosecond laser irradiation have been studied using scanning confocal micro-Raman and fluorescence spectroscopy.


Subject(s)
Glass/chemistry , Glass/radiation effects , Lasers , Phosphates/chemistry , Phosphates/radiation effects , Spectrometry, Fluorescence/methods , Spectrum Analysis, Raman/methods , Zinc Compounds/chemistry , Zinc Compounds/radiation effects , Materials Testing/methods
4.
J Clin Microbiol ; 48(11): 4287-90, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20861343

ABSTRACT

Laser tweezers Raman spectroscopy was used to detect the cellular response of Escherichia coli cells to penicillin G-streptomycin and cefazolin. Time-dependent intensity changes of several Raman peaks at 729, 1,245, and 1,660 cm(-1) enabled untreated cells and cells treated with the different antibiotic drugs to be distinguished.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacteriological Techniques/methods , Escherichia coli/chemistry , Escherichia coli/drug effects , Optical Tweezers , Spectrum Analysis, Raman/methods , Cefazolin/pharmacology , Escherichia coli/metabolism , Penicillin G/pharmacology , Streptomycin/pharmacology
5.
Anal Chem ; 82(7): 2703-10, 2010 Apr 01.
Article in English | MEDLINE | ID: mdl-20196565

ABSTRACT

Laser tweezers Raman spectroscopy (LTRS) was used to characterize the Raman fingerprints of the metabolic states of Escherichia coli (E. coli) cells and to determine the spectral changes associated with cellular response to the antibiotic Cefazolin. The Raman spectra of E. coli cells sampled at different time points in the bacterial growth curve exhibited several spectral features that enabled direct identification of the growth phase of the bacteria. Four groups of Raman peaks were identified based on similarities in the time-dependent behavior of their intensities over the course of the growth curve. These groupings were also consistent with the different biochemical species represented by the Raman peaks. Raman peaks associated with DNA and RNA displayed a decrease in intensity over time, while protein-specific Raman vibrations increased at different rates. The adenine ring-breathing mode at 729 and the 1245 cm(-1) vibration peaked in intensity within the first 10 h and decreased afterward. Application of principal component analysis (PCA) to the Raman spectra enabled accurate identification of the different metabolic states of the bacterial cells. The Raman spectra of cells exposed to Cefazolin at the end of log phase exhibited a different behavior. The 729 and 1245 cm(-1) Raman peaks showed a slight decrease in intensity from 4 to 10 h after inoculation. Moreover, a shift in the spectral position of the adenine ring-breathing mode from 724 to 729 cm(-1), which was observed during normal bacterial growth, was inhibited during antibiotic drug treatment. These results suggest that potential Raman markers exist that can be used to identify E. coli cell response to antibiotic drug treatment.


Subject(s)
Anti-Bacterial Agents/chemistry , Cefazolin/chemistry , Escherichia coli/metabolism , Spectrum Analysis, Raman/methods , Anti-Bacterial Agents/pharmacology , Cefazolin/pharmacology , DNA, Bacterial/analysis , Optical Tweezers , Principal Component Analysis , RNA, Bacterial/analysis
6.
Biomed Opt Express ; 1(4): 1138-1147, 2010 Oct 10.
Article in English | MEDLINE | ID: mdl-21258536

ABSTRACT

Laser tweezers Raman spectroscopy (LTRS) was used to acquire the Raman spectra of leukemic T lymphocytes exposed to the chemotherapy drug doxorubicin at different time points over 72 hours. Changes observed in the Raman spectra were dependent on drug exposure time and concentration. The sequence of spectral changes includes an intensity increase in lipid Raman peaks, followed by an intensity increase in DNA Raman peaks, and finally changes in DNA and protein (phenylalanine) Raman vibrations. These Raman signatures are consistent with vesicle formation, cell membrane blebbing, chromatin condensation, and the cytoplasm of dead cells during the different stages of drug-induced apoptosis. These results suggest the potential of LTRS as a real-time single cell tool for monitoring apoptosis, evaluating the efficacy of chemotherapeutic treatments, or pharmaceutical testing.

7.
J Opt Soc Am A Opt Image Sci Vis ; 19(12): 2484-94, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12469745

ABSTRACT

We describe a postgrowth method to produce passband filters with different center wavelengths from a single growth run by irreversibly changing the refractive index of a layer or a series of layers within the filter. This leads to a new type of filter, the passband-shifting filter, whose center wavelength can be irreversibly shifted from lambda0 to lambda0 - deltalambda after the filter has been grown. The passband shift can be controlled exactly by proper design of the multilayer. We present the theory behind passband-shifting-filter design along with transfer-matrix simulations and preliminary experimental results for a two-cavity filter, using lateral oxidation of AlxGa1-x As-based materials to effect the passband shift.

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