Bioactivity‐guided separation of antifungal compounds by preparative high‐performance liquid chromatography

Author(s):  
Zhidong Li ◽  
Zhuoshun Dai ◽  
Dasen Jiang ◽  
Yingping Dai ◽  
Yu Jin ◽  
...  
2017 ◽  
Vol 8 (1) ◽  
pp. 155
Author(s):  
Ivanildo Viana Borges ◽  
LEONARDO SOUSA CAVALCANTI ◽  
ACÁCIO FIGUEIRÊDO NETO ◽  
JACKSON ROBERTO GUEDES DA SILVA ALMEIDA ◽  
LARISSA ARAÚJO ROLIM ◽  
...  

In the search of molecules and antifungal compounds with low hazard, it is important the compound inespecific action, since there is a possibility of inactivity due to the resistance development. In order to increase the alternatives for the Curvularia inaequalis and Colletotrichum gloeosporioides control, husks of M. tenuiflora were collected and processed for obtaining the aqueous extract, which was then fractionated by column chromatography, thin layer chromatography and analysed by high-performance liquid chromatography (HPLC), aiming the identification of active compounds. After obtaining the phases, germination tests were carried out with C. inaequalis. The phase “one” showed the presence of flavonoids catechin and apigenin. This phase presented degradation or inhibition of chitin layer formation in C. inaequalis and the other phases presented no activity for the evaluated concentrations. Catechin also presented inhibition of C. inaequalis germination. For the evaluation of the effect of crude extract on C. gloeosporioides germination, all concentrations were effective in inhibiting germination, and when 4 mg.mL-1 or higher concentrations were used, the inhibition was 100%. The phase “one” and the catechin inhibit the C. inaequalis germination and the crude extract inhibited, similarly to phase “one”, the germination of C. gloeosporioides.


2007 ◽  
Vol 177 (4S) ◽  
pp. 295-295
Author(s):  
Michael Mullerad ◽  
Haleem J. Issaq ◽  
Alexander Kravtsov ◽  
Timothy Waybright ◽  
Brian Luke ◽  
...  

2013 ◽  
Vol 83 (2) ◽  
pp. 122-128 ◽  
Author(s):  
Cécile Renaud ◽  
Jacques Berger ◽  
Arnaud Laillou ◽  
Sylvie Avallone

Vitamin A deficiency is still one of the major public health problems in least developed countries. Fortification of vegetable oils is a strategy implemented worldwide to prevent this deficiency. For a fortification program to be effective, regular monitoring is necessary to control food quality in the producing units. The reference methods for vitamin A quantification are expensive and time-consuming. A rapid method should be useful for regular assessment of vitamin A in the oil industry. A portable device was compared to high-performance liquid chromatography (HPLC) for three plant oils (rapeseed, groundnut, and soya). The device presented a good linearity from 3 to 30 mg retinol equivalents per kg (mg RE.kg- 1). Its limits of detection and quantification were 3 mg RE.kg- 1 for groundnut and rapeseed oils and 4 mg RE.kg- 1 for soya oil. The intra-assay precision ranged from 1.48 % to 3.98 %, considered satisfactory. Accuracy estimated by the root mean squares error ranged from 3.99 to 5.49 and revealed a lower precision than HPLC (0.4 to 2.25). Although it offers less precision than HPLC, the device estimates quickly the vitamin A content of the tested oils from 3 or 4 to 15 mg RE.kg- 1.


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