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In this paper, gelatin and xanthan are applied to produce a foam‐templated oleogel. For this reason, the oleogel is prepared at different concentrations of biopolymers and the properties of solution, cryogel, and related oleogel are determined. The results show that xanthan addition increases viscosity and foam stability of solution. Also, an increment in biopolymer concentration increases cryogel network density (ND) and firmness but has no significant effect on moisture sorption. The oil binding capacity of all oleogels is >92%. In terms of high foam stability (96.87 ± 4.42), low ND (0.016 ± 0.00), and consequently suitable oil sorption (46.10 ± 4.40), the oleogel containing 3% gelatin and 0.2% xanthan is selected as the best sample. Complementary tests exhibit that the oleogel, with thixotropic behavior and 60% structural recovery, can bind the oil at temperature <100 °C. The oleogel network can protect the edible oil from oxidative reaction during 2 month storage. Nonetheless, more studies are needed to attest the application of this oleogel type in food products. Practical Application: Biopolymers of gelatin and xanthan are GRAS and available so that they are applied in many food products. This research shows that the cryogel of these biopolymers, as a hydrophilic oleogelator, can be utilized to structure oil and produce oleogel in an indirect method. This procedure that forms strong gel and keeps oil even at high temperatures can be of interest to scientists who are searching for solid fat substitutes in food products such as cakes, biscuits, and muffins.

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Some physicochemical and microstructural characteristics of hard-to-cook (HTC) and easy-to-cook (ETC) pinto beans and small-type lentils were compared. The development of HTC seeds was monitored over 6 months for changes in physicochemical properties. Results indicated that hardness, extent of water absorption and solid loss of HTC legumes were, respectively, 21-97%, 7-72% and 62-236% higher than those of ETC legumes. In addition, darkening of HTC beans and lentils was significantly higher than those of ETC ones. Scanning electron microscope observations indicated deteriorations in cytoplasmic contents of cotyledon cells of hard seeds. Phytic acid and total phenolic contents were, respectively, decreased 36-61% and 43-61% during storage, whereas hardness of seeds was increased 3-6 times. The soaking of hard seeds in sodium solutions resulted in the improvement in legume texture.

Acrylamide is a potential cause of a wide spectrum of toxic effects and is classified as probably "carcinogenic in humans". The discovery of acrylamide in human foods has given rise to extensive studies exploring its formation mechanisms and levels of exposure and has spurred search into suitable analytical procedures for its determination in foodstuffs. However, the exact chemical mechanisms governing acrylamide formation are not yet known and cheap, convenient, and rapid screening methods are still to be developed. Acrylamide in food is produced by heat-induced reactions between the amino group of asparagine and the carbonyl group of reducing sugars along with thermal treatment of early Maillard reaction products (Nglycosides). Similarly, the decarboxylated Schiff base and decarboxylated Amadori compounds of asparagine as well as the Strecker aldehyde have been proposed as direct precursors and intermediates of acrylamide. Corresponding chromatographic methods are used to determine various structural groups present in Maillard reaction model systems. Gas chromatography-mass spectrometry and liquid chromatography with tandem mass spectrometry analysis are both acknowledged as the main, useful, and authoritative methods for acrylamide determination. This review is an attempt to summarize the state-of-the-art knowledge of acrylamide chemistry, formation mechanisms, and analytical methods. Special attention is given to comparison of different chromatographic techniques, particularly the novel, simple, and low-cost methods of its determination.