Influence of Distillation Temperature in the Determination of Added Sulfites in Dehydrated Garlic Powders Using the Modified Optimized Monier-Williams Method

2016 ◽  
Vol 99 (3) ◽  
pp. 721-724
Author(s):  
Ramya Addala ◽  
Leonard Fong ◽  
Mihir Vasavada ◽  
Siva Subramanian

Abstract Influence of distillation temperature on the determination of added sulfites in dehydrated garlic originating from China and California using the modified optimized Monier-Williams method was evaluated. In the study, the temperature of the distillation was monitored and maintained from 90° to 95°C instead of boiling temperature (>95°C). Samples from 38 unsulfited dehydrated garlic powders were analyzed at the 90° to 95°C temperature and at boiling temperature (>95°C) at 94 m above sea level. At the boiling distillation temperature, 25 of the 38 unsulfited garlic samples had a positive result for sulfite content ranging from 10.2 to 14.1 ppm using the modified optimized Monier-Williams procedure. Maintaining distillation temperature between 90° and 95°C eliminated false-positive results for added sulfite and had an average spiked sulfite recovery of 95.6% with a coefficient of variation of 3.79%. Lowering of the distillation temperature decreases the possible acid hydrolysis of organosulfur compounds that can lead to positive added sulfite results in unsulfited dehydrated garlic samples.

1988 ◽  
Vol 71 (4) ◽  
pp. 857-859
Author(s):  
Walter Holak ◽  
John J Specchio

Abstract When lead and cadmium were determined in samples of canned food by the AOAC anodic stripping voltammetric method, an interference was observed which was believed to be tin(IV). This interference could cause false positive results for lead and cadmium. The electroactivity of tin(IV) was suppressed by increasing the concentration of tartaric acid in the supporting electrolyte from 0.005M to 0.1M after mixing with an equal volume of sample solution.


2017 ◽  
Vol 277 ◽  
pp. 16-20 ◽  
Author(s):  
Michele Boracchi ◽  
Salvatore Andreola ◽  
Federica Collini ◽  
Guendalina Gentile ◽  
Francesca Maciocco ◽  
...  

2017 ◽  
Author(s):  
Aidan Coville ◽  
Eva Vivalt

Under-powered studies combined with low prior beliefs about intervention effects increase the chances that a positive result is overstated. We collect prior beliefs about intervention impacts from 125 experts to estimate the false positive and false negative report probabilities (FPRP and FNRP) as well as Type S (sign) and Type M (magnitude) errors for studies in development economics. We find that the large majority of studies in our sample are generally credible. We discuss how more systematic collection and use of prior expectations could help improve the literature.


2021 ◽  
Vol 2 (Supplement_1) ◽  
pp. A32-A32
Author(s):  
N Eriksson ◽  
P Teuwen ◽  
E Mateus ◽  
C Shim ◽  
A Scott

Abstract Introduction A retrospective study on the effect of inter-scorer concordance and impact of analysing polysomnography (PSG) data prior to the Multiple Sleep Latency Test (MSLT) on clinical interpretation of Narcolepsy (N) and Idiopathic Hypersomnolence (IH). Methods Data of four individuals was randomly selected from a cohort of patients that participated in MSLT studies. De-identified MSLT fragments from four nap periods (n=16) were scored in two groups: analysis of PSG conducted prior to the respective MSLT fragments, and analysis without access to prior PSG. Individual scorers were compared to a master score set, by consensus from two experienced sleep scientists. Spearman correlation and percentage agreement statistics were applied to calculate the inter-scorer concordance in sleep latency and REM latency. Mann-Whitney test was utilised to assess differences between the two groups. A positive result was assigned as: mean (n=4) sleep latency of <10min (IH), and mean (n=4) sleep latency of <8min including (n=2) SOREMs (N). Results From 16 sets of data, four false positive results were identified when PSG was not analysed prior to scoring the MSLT fragments. Additionally, statistically significant differences were present when PSG analysis was conducted prior to scoring MSLT sleep latency and REM latency data. Discussion These results support a recommendation that PSG analysis (sleep and REM latency) should be encouraged prior to MSLT studies and performed by the same sleep scientist. Furthermore, including MSLT data in intra-lab concordance activities is important, particularly in relation to medical interpretation and practice.


1994 ◽  
Vol 40 (10) ◽  
pp. 1944-1949 ◽  
Author(s):  
S H Mishalani ◽  
J Seliktar ◽  
G D Braunstein

Abstract We evaluated the performance of four visually read pregnancy tests (TestPack Plus hCG Combo, ICON II hCG, SureCell hCG-Serum/Urine and PregnaGen 1-Step) designed to detect increased concentrations of choriogonadotropin (hCG) in either serum or urine samples. The biochemical sensitivities and specificity in both serum and urine samples were similar for each kit. All kits correctly identified pregnancy serum samples: The TestPack Plus hCG Combo and SureCell hCG-Serum/Urine were 100% specific; the other two kits exhibited a few false-positive results. For urine samples the ICON II hCG test was 100% sensitive, and the other three were 99.5% sensitive, with false-positive urine results occasionally reported by the PregnaGen 1-Step and ICON II hCG tests. Quantitative hCG concentrations could be estimated in pregnancy serum samples, but not urine samples, through determination of the time elapsed from the sample application or addition of the final reagent to the first appearance of a positive result.


1986 ◽  
Vol 32 (6) ◽  
pp. 1013-1016 ◽  
Author(s):  
T E Torresani ◽  
R Scherz

Abstract We evaluated the usefulness, in routine newborn screening for congenital hypothyroidism, of a time-resolved fluoroimmunoassay kit (DELFIA Neonatal TSH) for the determination of thyrotropin (TSH) in dried blood spots. A total of 11 531 dried blood samples from newborns were tested in parallel in each of two Swiss screening laboratories, by RIA and DELFIA. Six cases of confirmed congenital hypothyroidism were detected during the study period. The rate of false-positive results, after single TSH determination in the DELFIA assay, was 0.16%. Correlation of RIA and DELFIA results for TSH was very good in both laboratories (0.959 and 0.97, respectively). The new method fulfills the criteria for precision and sensitivity of a screening assay. Screening results are usually available the day after the sample arrives in the laboratory, thus favoring early diagnosis and allowing treatment to begin by the seventh or eighth postnatal day.


Author(s):  
B. T. Stegniy ◽  
S. S. Drahut ◽  
V. A. Kutsenko ◽  
T. P. Ramazanova ◽  
N. V. Marchenko ◽  
...  

The purpose of the work. Comparison the diagnostic ability of the ELISA test kits «DIA®-Brucella ab. combi-V» and «ID Screen® Brucellosis Serum Indirect Multi-species» for the detection of antibodies to brucellosis pathogens in various farm animals. Materials and methods. For the analysis there were used 29 positive samples to brucellosis with specific antibodies in different concentrations, 26 of which are serums (22 — from cattle, 2 — from pigs, 1 — from goat, 1 — from camel) and 3 — milk samples from cows. There were used 32 serums (23 — from cattle, 6 — from sheep, 2 — from pigs, 1 — from goat), and 2 milk samples from cows that don’t contain antibodies to brucellosis pathogens for determining the ability of test kits to detect correctly negative samples. There were also used serums from cattle containing antibodies that can lead to false positive results, 1 sample with antibodies to Francisella tularensis, 1 — to Yersinia 03 and 1 — to Yersinia 09. To compare the results in the two test kits, comparative ratios were used that allowed to determine how many times the result obtained in both test kits was higher or less than cut off, that differentiated positive samples from negative. Results of the work. When analyzing 22 cattle serums containing antibodies to B. abortus, the “DIA®-Brucella ab. combi-V” kit determined all samples positive with a results 5.3–10.6 times higher than cut off. The “ID Screen® Brucellosis Serum Indirect Multi-species” test kit identified only 18 positive serums with a maximum value of 1.3 above the cut off. The result of the analysis of 3 samples was doubtful and 1 serum was negative. When analyzing 4 sera from different animals containing antibodies to brucellosis pathogens, the “DIA®-Brucella ab. combi-V” test kit identified all positive samples with the results 8.1–9.4 times higher than cut off. The “ID Screen® Brucellosis Serum Indirect Multi-species” test kit detected specific antibodies in only 3 serums — from pigs and camel. When the goat serum was tested, a doubtful (uncertain) result of the analysis was obtained. When analyzing 3 milk samples from cows containing antibodies to B. abortus in different concentrations there was received a positive result to brucellosis in both test kits. However, ability of the “DIA®-Brucella ab. combi-V” test kit to detect specific antibodies was significantly higher than in comparison test kit. When investigating 32 serums from different animals and 2 milk samples that didn’t contain antibodies to the brucellosis pathogens, a negative result of the analysis was obtained in both test kits. When analyzing cattle serums containing antibodies that can lead to false positive results, both test kits identified 1 sample with antibodies to Francisella tularensis and 1 serum with antibodies to Yersinia 03 with negative result. When analyzing 1 serum with antibodies to Yersinia 09 the result of the analysis was false positive. Conclusions. Studies have shown that the “DIA®-Brucella ab. combi-V” test kit has a high diagnostic capacity. When analyzing 29 blood serums, including samples from different animals, and milk samples from cows containing antibodies to brucellosis pathogens, the test kit identified all samples as positive with results 5.3–10.8 times above the cut off. The “ID Screen® Brucellosis Serum Indirect Multi-species” test kit detected antibodies to brucellosis pathogens only in 24 samples with a maximum value 1.3 times higher than cut off. When investigating 4 serums, 3 samples of which are from cattle and 1 — from goat, the result of the analysis was doubtful (uncertain), 1 cattle serum was identified as negative. The ability of test kits to detect correctly negative samples was comparable. When analyzing 32 serums from different animals and 2 milk samples from cows that do not contain antibodies to brucellosis pathogens, in both test kits, a negative result of the analysis was obtained. For the 3 negative cattle serums, the analysis of which on brucellosis may be incorrect (the presence of antibodies to Yersinia О3, Yersinia О9, Francisella tularensis), in both test kits, for 1 sample with antibodies to Yersinia О9 a false positive result was obtained


Author(s):  
Funda Karbancioglu-Guler ◽  
Dilek Heperkan

The occurrence of fumonisin in dried figs was investigated by Enzyme Linked Immunoassay (ELISA) and High Performance Liquid Chromatography (HPLC). Total fumonisins (FB1, FB2, FB3) in dried figs were determined using ELISA, whereas only fumonisin B1 (FB1) was determined by HPLC. In the period 2003-2004, one hundred and fifty five dried fig samples were taken during their drying in 7 different districts in the Aegean Region. Among a total of 115 samples, the incidence of total fumonisin in the dried figs was 82% within the range of 0.16 - 108.34 mg/g when determined by ELISA. In comparison, FB1 was detected in 86 samples (74.8%) within the range between 0.046 and 3.649 mg/g by HPLC. Correlation between ELISA and HPLC methods was observed for all samples. However, no correlation between methods was recorded for the samples with less than 1 mg/g Fumonisin B1 level (obtained by HPLC). Although there was a correlation between methods for all the samples, fumonisin levels obtained by ELISA were much higher than those obtained by HPLC. False positive results were obtained by ELISA in 11 out of 115 dried fig samples. The results indicated that ELISA can be used as a screening method for determining the occurence of fumonisin in dried figs.


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