21,800 research outputs found
Offset frequency dynamics and phase noise properties of a self-referenced 10 GHz Ti:sapphire frequency comb
This paper shows the experimental details of the stabilization scheme that
allows full control of the repetition rate and the carrier-envelope offset
frequency of a 10 GHz frequency comb based on a femtosecond Ti:sapphire laser.
Octave-spanning spectra are produced in nonlinear microstructured optical
fiber, in spite of the reduced peak power associated with the 10 GHz repetition
rate. Improved stability of the broadened spectrum is obtained by
temperature-stabilization of the nonlinear optical fiber. The carrier-envelope
offset frequency and the repetition rate are simultaneously frequency
stabilized, and their short- and long-term stabilities are characterized. We
also measure the transfer of amplitude noise of the pump source to phase noise
on the offset frequency and verify an increased sensitivity of the offset
frequency to pump power modulation compared to systems with lower repetition
rate. Finally, we discuss merits of this 10 GHz system for the generation of
low-phase-noise microwaves
The reverse protraction factor in the induction of bone sarcomas in radium-224 patients
More than 50 bone sarcomas have occurred among a collective of about 800 patients who had been injected in Germany after World War II with large activities of radium-224 for the intended treatment of bone tuberculosis and ankylosing spondylitis.^In an earlier analysis it was concluded that, at equal mean absorbed doses in the skeleton, patients with longer exposure time had a higher incidence of bone sarcomas.^The previous analysis was based on approximations; in particular, it did not account for the varying times at risk of the individual patients.^In view of the implications of a reverse protraction factor for basic considerations in radiation protection, the need was therefore felt to reevaluate the data from the continued follow-up by more rigorous statistical methods.^A first step of the analysis demonstrates the existence of the reverse dose-rate effect in terms of a suitably constructed rank-order test.^In a second step of the analysis it is concluded that the data are consistent with a linear no-threshold dose dependence under the condition of constant exposure time, while there is a steeper than linear dependence on dose when the exposure times increase proportionally to dose.^A maximum likelihood fit of the data is then performed in terms of a proportional hazards model that includes the individual parameters, dose, treatment duration, and age at treatment.^The fit indicates proportionality of the tumor rates to mean skeletal dose with an added factor (1 + 0.18.tau), where tau is the treatment time in months.^This indicates that a protraction of the injections over 15 months instead of 5 months doubles the risk of bone sarcoma
Dibenzo[a,g]quinolizin-8-ones: synthesis, estrogen receptor affinities, and cytostatic activity
A number of acetoxy-substituted dibenzo[a,g]quinolizin-8-ones were
synthesized by the reaction of 1-oxoisoquinolines with substituted homophthalic acid
anhydride. All of the derivatives with acetoxy groups in positions 3 and 10 bind to the
estrogen receptor. Relative binding affinities (RBA) ranged from 1.8 to 5.6 (estradiol:
RBA = 100) when the substituent at C-6 was a short alkyl group. Introduction of
additional oxygen functions in the 2- and/or 11-position decreased binding affinities.
Analyses of the enantiomers of 6-methyl (6b) and 6-ethyl (6c) derivatives revealed that
the receptor binding is mainly due to one optical isomer (e.g. (-)-6b, 9.9; (+)-6b, 0.6).
In hormone-sensitive human MCF-7 breast cancer cells, compounds with one acetoxy
group in each aromatic ring strongly inhibited cellular growth. Despite marked differences
in receptor affinity, the enantiomers displayed similar activities in this cell
culture. In hormone-independent MDA-MB 231 mammary tumor cells, only a weak
cytostatic effect was recorded at 10-5 M. In the immature mouse uterine weight test,
minimal estrogenic activity was observed. At higher doses, a significant anti-estrogenic
effect became evident. It is assumed that the estrogen antagonism is responsible for
the specific cytostatic effect in MCF-7 breast cancer cells
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