123 research outputs found
Shortcut Model for Describing Isothermal Batch Preferential Crystallization of Conglomerates and Estimating the Productivity
Resolution of Racemic Guaifenesin Applying a Coupled Preferential Crystallization-Selective Dissolution Process: Rational Process Development
Preferential
crystallization is a cost efficient method to provide
pure enantiomers from a racemic mixture of a conglomerate forming
system. Exploiting small amounts of pure crystals of both enantiomers,
several batch or continuous processes were developed, capable of providing
both species. However, an intermediate production step has to be used
when pure enantiomers are not available. In such cases, partially
selective synthesis, chromatography, or crystallization processes
utilizing chiral auxiliaries have to be used to provide the initial
seed material. Recently, it was shown that a coupled Preferential
Crystallization-selective Dissolution process (CPCD) in two coupled
crystallizers can be applied if at least one pure enantiomer is available
to produce both antipodes within one batch. The corresponding process
is carried out in one reactor (crystallization tank) by seeding a
racemic supersaturated solution with the available enantiomer at a
certain temperature. The second reactor (dissolution tank) contains
a saturated racemic suspension at a higher temperature. Both reactors
are coupled via the fluid phase, allowing for a selective dissolution
of the preferentially crystallizing enantiomer from the solid racemic
feed provided in the dissolution vessel. The dissolution and crystallization
processes continue until the solid racemic material is completely
resolved and becomes enantiopure. At this point, both enantiomers
can be harvested in their pure crystalline form. For a specific pharmaceutically
relevant case study, a rational process design and the applied empirical
optimization procedure will be described. The achieved productivities
after optimization show the great potential of this approach also
for industrial applications. Also, a strategy to control this process
based on inline turbidity measurement will be presented
Gabapentin for tinnitus: a systematic review.
PURPOSE: The main aim of this study was to assess the effect of gabapentin on tinnitus via a systematic review. METHOD: An electronic search of literature as well as a hand search were conducted. Only double-blind randomized controlled trials (RCTs) that met all of the inclusion criteria were included in this review. The Cochrane Collaboration tool for risk of bias assessment was used to investigate the validity of the included studies. Meta-analysis was not appropriate due to inadequate details in reporting the data in the included studies. Hence, qualitative synthesis and interpretation of the data were carried out. RESULTS: Two studies that met the inclusion criteria were included in the review. Fourteen studies were excluded. There were substantive within-study clinical heterogeneities with regard to the baseline tinnitus handicap scores, duration of tinnitus, and severity of hearing loss in the included double-blind RCTs. CONCLUSION: The authors of both studies reported that gabapentin was not superior to placebo in their primary outcomes. However, following the assessment of risk of bias and within-study clinical heterogeneities, this review concludes that there is insufficient evidence regarding the effect of gabapentin on tinnitus
Estimation of leisure time physical activity and sedentary behaviour among school adolescents in Nepal
Industrial Crystallization: Classical Technology with Steadily Increasing Applications and Importance
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