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The drug effect was monitored with electrochemical (cyclic voltammetry and electrochemical impedance spectroscopy), as well as spectroscopic techniques (surface enhanced Raman scattering), during its passive partitioning/penetration through the mixed Langmuir and Langmuir Blodgett monolayers after their transfer on gold electrodes.
Therapeutic effect was monitored by follow-up of body weight and 111In-DTPA-octreotide SPECT/CT when ongoing decrease in body weight was registered.
The silencing effect was monitored by Western blotting.
No growth-inhibiting or -stimulating effect was monitored when cells were followed up for 5 days.
Cytopathic effect was monitored by staining viable cells with crystal violet [58].
The cytopathic effect was monitored daily.
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The capacitance shift due to the hybridization effect is monitored by means of a charge-sensitive amplifier and digitalized by means of a comparator and a counter.
The capacitive shift due to the hybridization effect is monitored by means of a charge sensitive amplifier and a differential stage.
In this study, we designed and fabricated a new kind of multifunctional core/shell nanospheres as biodegradable targeted drug carriers, the controlled drug release progress and therapeutic effect were monitored in-situ by the fluorescent state of the cells.
This effect is monitored by sodium/alkali hazard, which is expressed as the SAR.
In these techniques, a disturbance signal is provided to specific parameters at the PCC and their effect is monitored for ID.
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