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1.
Food Res Int ; 132: 109061, 2020 06.
Article in English | MEDLINE | ID: mdl-32331671

ABSTRACT

Genotypes of bananas and plantains have been studied for biofortification purposes, mainly due to content of resistant starch (RS) and polyphenols. This study aims to identify banana and plantain genotypes with a high content of resistant starch, phenolic compounds and minerals, and to evaluate the impact of the ripening stage and domestic thermal processing to select superior genotypes with high levels of functional compounds. In this study, it was used bunches of bananas and plantain genotypes. The phenolic compounds profiles were determined by HPLC-DAD in pulps and peels. The resistant starch and the minerals (K, Na, Zn, Cu and Fe) were evaluated in pulps and peels of unripe fruit. The results of phenolic compounds were studied in three ripening stages, and after thermal processing (ripe stage) of two genotypes, which were most promising for biofortification studies. Resistant starch and minerals were analysed in the unripe fruits. The peel biomass showed the highest values of phenolic compounds and minerals. The total starch content in the pulp varied from 42.3% ('FC06-02') to 80.6% ('Pelipita'). Plantains and cooking bananas presented the highest contents of starch and resistant starch (stage 2 - green with yellow traces). The pulps of the dessert genotypes 'Khai' and 'Ouro da Mata', and cooking genotype 'Pacha Nadam' stood out due to their minerals high contents (P, K and Fe; Zn and Fe; Ca, Mg and Zn, respectively). The dessert bananas (e.g., 'Ney Poovan') and cooking bananas (e.g., 'Tiparot') had the highest concentrations of phenolic compounds, mainly in ripe fruit (stage 5 - yellow with green). In addition, the thermal processing of Musa spp. fruit led to increasing these secondary metabolites, mainly the cooking of fruit with peel by boiling, which should be preferred in domestic preparations.


Subject(s)
Antioxidants/analysis , Cooking , Fruit/chemistry , Musa/chemistry , Nutritive Value , Plantago/chemistry , Catechin/analysis , Minerals/analysis , Musa/genetics , Phenols/analysis , Plant Breeding , Polyphenols/analysis , Starch
2.
Biol Trace Elem Res ; 173(2): 362-71, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26926909

ABSTRACT

The protective role of Arctium lappa (AL) on the testes of rats acutely exposed to cadmium (Cd) was tested. The rats were randomly divided into a control group (C-group) and three major experimental groups, which were further subdivided into minor groups (n = 6) according to the experimental period (7 or 56 days). The C-group was subdivided into C-7 and C-56 [receiving a single saline solution, intraperitoneal (i.p.), on the first day]; the AL-group, AL-7, and AL-56, received AL extract (300 mg/kg/daily); the Cd group, Cd-7 and Cd-56, received a single i.p. dose of CdCl2 (1.2 mg/kg body weight (BW)) on the first day; the CdAL group, CdAL-7 and CdAL-56, received the same Cd dose, followed by AL extract. Water or AL extract was administered daily by gavage. After either 7 or 56 days, the testis and accessory glands were removed after whole-body perfusion. Exposure to Cd and CdAL decreased the weight of the testis and epididymis, the gonadosomatic index, seminiferous tubular (ST) diameter, and ST volumetric proportion, and increased the volumetric proportion of interstitium after 56 days. In the epididymis caput, the tubular volumetric proportion decreased along with an increase of interstitial volumetric proportion and epithelium height after 56 days. The alterations observed were less severe only after 7 days. A progressive testicular damage resulted mainly in tubules lined only by Sertoli cells. The sperm number and cell debris decreased in the epididymis. We demonstrated that the testicular damage induced by single acute i.p. exposure to Cd occurred despite the daily oral intake of AL extract.


Subject(s)
Arctium/chemistry , Cadmium/toxicity , Plant Extracts/pharmacology , Testis/metabolism , Animals , Epididymis/metabolism , Epididymis/pathology , Male , Plant Extracts/chemistry , Rats , Rats, Wistar , Testis/pathology
3.
Parasite ; 8(2 Suppl): S144-6, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11484340

ABSTRACT

Serum samples belonging to three outbreaks in Argentina (47 patients) taken at different times post-ingestion were analysed employing IIF and ELISA simultaneously. Results show that: a) the number of patients diagnosed by a unique technique, especially by ELISA (31 patients), was lower than the one obtained by the simultaneous use of both assays (38 patients); b) four patients out of the seven diagnosed by a unique technique were negative by the other assay over the period of time evaluated. Therefore, it can be concluded that the use of a sole immunoserological technique can not only lead to the delay in the detection but also to the misdiagnosis of this parasitic infection.


Subject(s)
Antibodies, Helminth/blood , Trichinella spiralis , Trichinellosis/diagnosis , Animals , Argentina/epidemiology , Disease Outbreaks , Enzyme-Linked Immunosorbent Assay/methods , Fluorescent Antibody Technique, Indirect , Humans , Reproducibility of Results , Sensitivity and Specificity , Serologic Tests/methods , Trichinellosis/epidemiology , Trichinellosis/immunology
4.
Biomed Chromatogr ; 10(1): 43-5, 1996.
Article in English | MEDLINE | ID: mdl-8821872

ABSTRACT

By reversed phase HPLC the highly pure lycopene produces only one peak, that corresponds to the all-trans polyunsaturated system. Commercial standards, however, show generally two peaks that correspond to the molecule in all-trans configuration (about 90%) and probably to its 13-cis geometrical isomer (about 10%), respectively, independent of the solvent used to inject the sample. An anomalous HPLC behaviour was observed by analysing a commercial sample of lycopene by normal-phase HPLC. In this case the chromatogram showed different profiles depending on the solvent used to prepare the solution to be injected. A relationship between such unusual behaviour and the polarity of the solvent used to dissolve the sample was tentatively found. It is worth emphasizing that in the same HPLC conditions the behaviour of beta-carotene does not show the above described phenomenon.


Subject(s)
Anticarcinogenic Agents/analysis , Carotenoids/analysis , Chromatography, High Pressure Liquid/methods , Acetonitriles , Anticarcinogenic Agents/chemistry , Carotenoids/chemistry , Lycopene , Methanol , Methylene Chloride , Molecular Conformation , Solvents
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