2006
DOI: 10.1016/j.aca.2006.04.012
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Automated sequential injection fluorimetric set-up for multiple release testing of topical formulation

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Cited by 9 publications
(8 citation statements)
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“…Recalculation was needed to compensate for the dilutions of the liberation medium in the Franz cell and in the sampling loop together with the volume of the acceptor by fresh medium after each sampling point. This recalculation, described elsewhere [ 5 ], uses the following Equation (1), where C n is the concentration of the n sample [ 31 ]: C n, corrected = C n, measured + volume sample /volume acceptor × C n−1, measured …”
Section: Methodsmentioning
confidence: 99%
See 3 more Smart Citations
“…Recalculation was needed to compensate for the dilutions of the liberation medium in the Franz cell and in the sampling loop together with the volume of the acceptor by fresh medium after each sampling point. This recalculation, described elsewhere [ 5 ], uses the following Equation (1), where C n is the concentration of the n sample [ 31 ]: C n, corrected = C n, measured + volume sample /volume acceptor × C n−1, measured …”
Section: Methodsmentioning
confidence: 99%
“…Methods based on flow injection analysis (FIA) and sequential injection analysis (SIA) manifold have been applied, varying in the type of drug formulations (tablets, capsules, etc. ), parameters (dissolution or liberation), and active substance [ 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 ]. Among the different modifications, an important step was introducing more liberation units in one analyzer system, resulting in little time-lapse, evaluation of repeatability, and result confirmation [ 2 , 3 , 5 ].…”
Section: Introductionmentioning
confidence: 99%
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“…Automated flow methods meet this need with advantageous throughput in an affordable way. As a matter of fact, flow systems offer the possibility of combining an automated procedure for sample collection, which can be adapted to simultaneous testing of multiple samples [13] with an analysis apparatus providing real time monitoring of long-term processes associated to high sampling frequencies. In addition, this kind of systems foster sample consumption in the microliter range, introducing minimum disturbance to the volume of the acceptor medium, particularly when high sampling frequencies are involved [14].…”
Section: Introductionmentioning
confidence: 99%