Phosdrin Residues in Fruits and Vegetables

1964 ◽  
Vol 47 (2) ◽  
pp. 272-280
Author(s):  
N Bluman

Abstract The enzyme inhibition-spectrophotometric procedure for Phosdrin residues submitted by the manufacturer has been slightly modified and studied collaboratively on apples, tomatoes, and cabbages. This method is based on the ability of Phosdrin to inhibit cholinesterase. Phosdrin is extracted from crops with chloroform, transferred into water, purified to remove organic impurities, and determined quantitatively by the acetylcholinesterase inhibition procedure. The uninhibited cholinesterase hydrolyzes acetylcholine to acetic acid and choline. The acetylcholine not hydrolyzed is reacted with alkaline hydroxylamine and a ferric salt to form a red complex, the absorbance of which is measured spectrophotometrically at 540 mμ. The recoveries at the 0.164 and 0.328 ppm levels of addition ranged from 73.2 to 109.8% for apples, 70.1 to 111.0% for tomatoes, and 68.9 to 117.0% for cabbages. The mean recoveries for apples, tomatoes, arid cabbages were 95.9, 94.9, and 91.6%, respectively; the over-all recovery was 94.1%. The method is recommended as official, first action for quantitative determination of Phosdrin residues in fruits and vegetables.

2018 ◽  
Vol 8 (4) ◽  
pp. 42-47
Author(s):  
Tien Nguyen Huu ◽  
Tram Le Thi Bao ◽  
Ngoc Nguyen Thi Nhu ◽  
Thang Phan Phuoc ◽  
Khan Nguyen Viet

Background: Curcumin is a major ingredient in turmeric (Curcuma longa L., Zingiberaceae), which has important activities such as anti-tumor, anti-inflammatory, antioxidant, anti-ischemia, protection of gastric mucosa etc,. Curcumin can be considered as a biological marker of turmeric and turmeric products. Objectives: Developing an HPLC method for quantification of curcumin in turmeric powder and turmeric - honey ball pills; applying this method for products on the market. Materials and methods: turmeric powder and turmeric - honey ball pills collected in Thua Thien Hue province. After optimization process, the method was validated and applied to evaluate the content of curcumin. Results: The chromatography analysis was performed with: Zorbaz Eclipse XDB-C18 (150 × 4.6 nm; 5 µm); Mobile phase: acetonitril: 2% acetic acid (45:55), Flow rate was kept constant at 1.0 ml/min; Detector PDA (420 nm). The method was validated for the HPLC system compatibility, specificity, linearity range, precision and accuracy; the recovery greater than 98%. Conclusion: The developed HPLC method can determine curcumin in turmeric powder and turmeric - honey ball pills. Key words: Curcumin, turmeric powder, turmeric-honey ball pills, quantitative determination, HPLC


1999 ◽  
Vol 82 (6) ◽  
pp. 1399-1405 ◽  
Author(s):  
Philemon Manirakiza ◽  
Adrian Covaci ◽  
Paul Schepens

Abstract A rapid and accurate method has been developed for the quantitative determination of capsaicin and its most important analogues, dihydrocapsaicin and nordihydrocapsaicin in chili peppers. These components were extracted with methylene chlo ride and separated from interfering substances with activated charcoal. Further cleanup on Florisil cartridges and elution with ethyl acetate were performed before gas chromatographic with mass spectrometric quantitation. The concentrations found were 440 ± 64 μg/g capsaicin, 81 ± 10 μg/g dihydrocapsaicin, and 11 ± 2 μg/g nordihydrocapsaicin. The mean recovery values for triplicate analysis were between 85-94%.


2017 ◽  
Vol 52 (2) ◽  
pp. 153-158 ◽  
Author(s):  
SO Aremu ◽  
CC Nweze

The vitamin A content of the fresh fruits was determined by the extraction and quantitative determination of the pro-vitamin A carotenoid-?-carotene. The Retinol Equivalent (RE) was then obtained using standard conversion formula. The result indicated that the fruit with the minimum vitamin A content and percentage among the six samples was found in mango 301.61 ± 1.03 (7%), which was followed closely by watermelon 350.12 ± 19.01 (8%), guava 504.1 ± 0.75 (11%), tomato 542.86 ± 20.20 (12%), pawpaw 683.93 ± 5.15 (16%) and the highest content was found in carrot 2054.10 ± 1.28 (46%) in (RE/100 g). Statistical calculations and analysis showed that there was significant difference in vitamin A content among the fruits (p<0.05). Thus, besides major nutrients fruits and vegetables contribute very good amount of micro nutrient-vitamin A from ?-carotene.Bangladesh J. Sci. Ind. Res. 52(2), 153-158, 2017


1977 ◽  
Vol 60 (3) ◽  
pp. 590-593 ◽  
Author(s):  
T Powell Gaines

Abstract A method is described for determining protein nitrogen (PN) in plants. Plant tissue extracted with 0.5% acetic acid to remove nonprotein nitrogen (NPN) prior to Kjeldahl analysis gave results very close to true PN, whereas AOAC crude PN method 2.049 gave results much too high. True PN was determined as the mean of 3 independently derived values and was used as the basis for comparing the proposed PN method with AOAC method 2.049. Failure of the AOAC method to differentiate between NPN and/or inorganic ammoniacal N and actual PN causes values derived from this method to be too high when it was used to determine PN in plants.


1965 ◽  
Vol 48 (4) ◽  
pp. 771-774
Author(s):  
D P Johnson ◽  
H A Stansbury

Abstract A method has been developed for detecting residues of carbaryl (1-naphthyl methylcarbamate) as well as its hydrolysis product, 1-naphthol, in dead bees. The method is based on extraction of the bees with benzene, followed by a cleanup involving liquid partitioning and chromatography on Florisil. The quantitative determination involves hydrolysis of carbaryl to 1-naphthol and coupling of the latter with p-nitrobenzenediazonium fluoborate in acetic acid to form a yellow substance. For separate analysis, free 1-naphthol is separated from methylene chloride into a basic aqueous solution. The sensitivity of the method is about 0.1 ppm; recoveries averaged 85.6 ± 6.6% for 1- naphthol and 83.8 ± 2.7% for carbaryl.


2018 ◽  
Vol 71 (4) ◽  
pp. 285
Author(s):  
Graham S. Chandler ◽  
Wolfgang H. F. Sasse

The quantitative determination of the products of bromination of acridine in concentrated sulfuric acid and glacial acetic acid is described. In both cases, the only monobromo products were the 2- and 4-substituted compounds. With sulfuric acid, the 4-isomer predominates whereas in acetic acid, the 2-isomer is predominant. This work expands substantially on the tiny amount of previous work on halogenation of dibenzo-annelated pyridines.


1972 ◽  
Vol 44 (8) ◽  
pp. 1434-1438 ◽  
Author(s):  
Leif. Bertilsson ◽  
Arthur J. Atkinson ◽  
James R. Althaus ◽  
Ase. Harfast ◽  
Jan Erik. Lindgren ◽  
...  

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