![]() For preparation of the nosode, duckweed was grown in 2000 ml of moStM (see below) comprising 158 mg/l arsenic(V) for 48 h. on the day of the experiment from the same batch of distilled and autoclaved water. All test solutions for one experiment (potencies and controls) were freshly prepared according to the multiple glass method between 6 a.m. A detailed description of the sample preparation has been given in a precursor publication. All experiments were carried out between January and September 2009. Thus, a total of 20 experiments (four experimental series with five independent experiments each) entered the final data evaluation. For the final statistical evaluation, the data from the screening experiment were pooled with those of the four repetition experiments. Furthermore, we conducted four additional full-size experiments with pure water as the only treatment parameter (systematic negative control experiments) to investigate the stability of the experimental setup over the entire study period. We subsequently performed four additional independent experiments for each of the three substances and each test organism, designed as identical repetitions of the initial screening experiment (Fig. cerevisiae in the 11 screening experiments, for the additional independent replication experiment, we selected only substances that had yielded significant effects in the screening experiments of the Lemna test system (Arsenicum album, a duckweed nosode, and gibberellic acid). Because we did not observe any significant effects on the growth curve parameters for S. In a primary screening, a total of 12 experiments were performed, 11 with different potentized substances (Table 1) and one systematic negative control experiment. The experimental investigations were performed in two parts. Reporting of the study was adapted to the latest guidelines for experimental basic research in homeopathy. we present the data obtained with the yeast bioassay and compare the results of both bioassays. ![]()
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