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In vitro release studies showed the release kinetics of Acyclovir from Carb-NS to be prolonged in comparison with those observed with NS, with no initial burst effect.
On average, the decoding time decreases from 7.6 to 6.7 ns with EOP and even to 5.3 ns with ROP and 5.1 ns with UOP.
The delay tuning range is 0 1.8 ns with increment of 164.2 ps.
Timing resolution was 2.2 ns with the PDC and 1.5 ns without the PDC.
The time window is 124 ns with 4096 samples acquired in the fast time totally.
First-order Gaussian derivative pulses of ns with center frequency 3 GHz are used.
There is only moderate decrease from 21.8 to 19.1 ns with increasing emission energy.
The terminal NPT simulation time was 0.5 ns with the timestep of 1 fs.
At the highest flow rates, complete mixing was achieved in 160 ns with only approximately 9% premixing of the reactants.
The input pulse has duration in the range of 1 to 50 ns, with wavelength equal to 1549.1 nm.
Maintaining isobaric and isothermal conditions, we performed the relaxation up to 1.5 ns with a time step of 0.5 fs.
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