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At least 217 records · Page 12Linked to original sources
PubMed2004

Three-MHz Ultrasound Heats Deeper Into the Tissues Than Originally Theorized.

OBJECTIVE: To measure muscle temperature of ultrasound at 1-MHz and 3-MHz frequencies at a depth of 2.5 cm and to compare treatment durations for vigorous heating (increase of 4 degrees C) and for heating to 40 degrees C. DESIGN AND SETTING: A counterbalanced, repeated-measures design with 1 fixed, independent variable, 1.5-W/cm(2) ultrasound treatment (1 MHz, 3 MHz, or control [sham]) using a Theratouch 7.7 ultrasound device. Dependent variables were end-treatment temperature at 2.5 cm, time to vigorous heating, and time to reach 40 degrees C. SUBJECTS: Eighteen healthy volunteers (age = 24.6 +/- 2.3 years, height = 173.0 +/- 9.7 cm, mass = 72.0 +/- 16.3 kg) without a history of lower leg injury. MEASUREMENTS: The medial triceps surae intramuscular temperature at 2.5 cm was measured every 10 seconds using an implantable thermocouple. Each of the 3 ultrasound frequencies was applied in counterbalanced order at 24-hour intervals. RESULTS: Ultrasound of 3 MHz produced both vigorous heating (at 3.4 minutes) and an absolute temperature of 40 degrees C (at 4 minutes). CONCLUSIONS: Our results suggest that 3-MHz ultrasound heats 0.5 cm deeper than suggested by others. With our machine, 3-MHz ultrasound was more effective in heating muscle at this depth than 1-MHz ultrasound.

Journal Article↗
PubMed1991

Immunocytochemical investigation of the tissue of origin of two lung cancer cell lines.

The constitutive cell types of the two lung cancer cell lines CaLu1 and CaLu3 have been investigated by immunocytochemical staining with markers for cytokeratins, vimentin, carcinoembryonic antigen and the epithelial cell epitope recognized by the monoclonal antibody Ber-EP4. The cells of both lines reacted with vimentin, with CAM 5.2, which is a marker for cytokeratins 8, 18 and 19, and with a specific marker for cytokeratin 19. CaLu3 cultures showed patchy staining, and CaLu1 none, when treated with a monoclonal antibody reactive with cytokeratins 13, 14 and 17. CaLu3 cells all reacted strongly with Ber-EP4 and the antibody to carcinoembryonic antigen, whereas CaLu1 gave a negative reaction with both these reagents. These results indicate that the CaLu3 line has retained antigens characteristic of some bronchial adenocarcinomata, and that the CaLu1 line was derived from a mesothelioma rather than a pleural metastasis of a squamous carcinoma.

Antibodies, Monoclonal↗
PubMed1978

Cell-mediated immunity and postexposure protection from rabies by inactivated vaccines of tissue culture origin.

A strong cell-mediated cytotoxic response (CMC), which was maximal 6-7 days after treatment, was generated in mice exposed to inactivated rabies virus vaccine. CMC response was linear and was a function of antigenic mass. Live attenuated viruses also generated a strong CMC response after intracerebral infection. Mice lethally infected with virulent strains of virus failed to develop CMC. There was, however, no difference in the rate and amount of virus-neutralizing or lytic antibodies and interferon induction in mice infected with virulent as compared to those infected with attenuated strains of virus. The level of T-cell effector function was found to be directly correlated with survival. Secondary CMC response to inactivated virus vaccine is strong, appears faster (3 days)and requires a smaller amount of antigen than does the primary CMC response. A consistent high level of CMC can be maintained for extended periods of time by repeated vaccine inoculations. When mice were treated with vaccine after being infected with street virus, high levels of CMC were found in effectively protected animals, but no CMC was found in unprotected animals. High levels of virus-neutralizing antibody were present in both surviving and dying mice. CMC responses to different antigenic components of rabies virus were also investigated.

Animals↗