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1.
Crit Rev Food Sci Nutr ; 58(9): 1495-1511, 2018 Jun 13.
Artigo em Inglês | MEDLINE | ID: mdl-28033035

RESUMO

Gelatin is a highly purified animal protein of pig, cow, and fish origins and is extensively used in food, pharmaceuticals, and personal care products. However, the acceptability of gelatin products greatly depends on the animal sources of the gelatin. Porcine and bovine gelatins have attractive features but limited acceptance because of religious prohibitions and potential zoonotic threats, whereas fish gelatin is welcomed in all religions and cultures. Thus, source authentication is a must for gelatin products but it is greatly challenging due to the breakdown of both protein and DNA biomarkers in processed gelatins. Therefore, several methods have been proposed for gelatin identification, but a comprehensive and systematic document that includes all of the techniques does not exist. This up-to-date review addresses this research gap and presents, in an accessible format, the major gelatin source authentication techniques, which are primarily nucleic acid and protein based. Instead of presenting these methods in paragraph form which needs much attention in reading, the major methods are schematically depicted, and their comparative features are tabulated. Future technologies are forecasted, and challenges are outlined. Overall, this review paper has the merit to serve as a reference guide for the production and application of gelatin in academia and industry and will act as a platform for the development of improved methods for gelatin authentication.


Assuntos
Cosméticos/análise , Aditivos Alimentares/análise , Análise de Alimentos/métodos , Gelatina/química , Preparações Farmacêuticas/análise , Animais , Bovinos , Eletroforese , Ensaio de Imunoadsorção Enzimática , Peixes , Tecnologia de Alimentos , Marcadores Genéticos , Reação em Cadeia da Polimerase , Reação em Cadeia da Polimerase em Tempo Real , Especificidade da Espécie , Suínos
2.
J Food Drug Anal ; 25(3): 654-666, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28911651

RESUMO

In order to improve the encapsulation process, a newly supercritical antisolvent process was developed to encapsulate fish oil using hydroxypropyl methyl cellulose as a polymer. Three factors, namely, temperature, pressure, and feed emulsion rate were optimized using response surface methodology. The suitability of the model for predicting the optimum response value was evaluated at the conditions of temperature at 60°C, pressure at 150 bar, and feed rate at 1.36 mL/min. At the optimum conditions, particle size of 58.35 µm was obtained. The surface morphology of the micronized fish oil was also evaluated using field emission scanning electron microscopy where it showed that particles formed spherical structures with no internal voids. Moreover, in vitro release of oil showed that there are significant differences of release percentage of oil between the formulations and the results proved that there was a significant decrease in the in vitro release of oil from the powder when the polymer concentration was high.


Assuntos
Óleos de Peixe/química , Dióxido de Carbono , Cromatografia com Fluido Supercrítico , Composição de Medicamentos , Microscopia Eletrônica de Varredura , Tamanho da Partícula , Polímeros , Solubilidade , Temperatura
3.
Artigo em Inglês | MEDLINE | ID: mdl-27643977

RESUMO

The Malayan box turtle (Cuora amboinensis) (MBT) is a vulnerable and protected species widely used in exotic foods and traditional medicines. Currently available polymerase chain reaction (PCR) assays to identify MBT lack automation and involve long targets which break down in processed or denatured tissue. This SYBR Green duplex real-time PCR assay has addressed this research gap for the first time through the combination of 120- and 141-bp targets from MBT and eukaryotes for the quantitative detection of MBT DNA in food chain and herbal medicinal preparations. This authentication ensures better security through automation, internal control and short targets that were stable under the processing treatments of foods and medicines. A melting curve clearly demonstrated two peaks at 74.63 ± 0.22 and 78.40 ± 0.31°C for the MBT and eukaryotic products, respectively, under pure, admixed and commercial food matrices. Analysis of 125 reference samples reflected a target recovery of 93.25-153.00%, PCR efficiency of 99-100% and limit of detection of 0.001% under various matrices. The quantification limits were 0.00001, 0.00170 ± 0.00012, 0.00228 ± 0.00029, 0.00198 ± 0.00036 and 0.00191 ± 0.00043 ng DNA for the pure meat, binary mixtures, meatball, burger and frankfurter products, respectively. The assay was used to screen 100 commercial samples of traditional Chinese herbal jelly powder from eight different brands; 22% of them were found to be MBT-positive (5.37 ± 0.50-7.00 ± 0.34% w/w), which was reflected through the Ct values (26.37 ± 0.32-28.90 ± 0.42) and melting curves (74.63-78.65 ± 0.22°C) of the amplified MBT target (120 bp), confirming the speculation that MBT materials are widely used in Chinese herbal desserts, exotic dishes consumed with the hope of prolonging life and youth.


Assuntos
Medicamentos de Ervas Chinesas/química , Análise de Alimentos/métodos , Contaminação de Alimentos/análise , Produtos da Carne/análise , Compostos Orgânicos/análise , Reação em Cadeia da Polimerase em Tempo Real , Tartarugas , Animais , Benzotiazóis , China , DNA/análise , DNA/genética , Diaminas , Pós/análise , Quinolinas , Tartarugas/genética
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