Analysis of Phytochemical Composition of Camellia oleifera Oil and Evaluation of its Anti-Inflammatory Effect in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages

In China, Camellia oleifera oil (COO) is not only a common edible oil but also a traditional remedy widely applied to ameliorate a variety of illnesses associated with inflammation, such as mouth ulcers, thrush, eczema, etc. However, there has been a lack of relevant biological research on the anti-inflammatory capacity of COO, and the specific bioactive lipid phytochemicals contributing to the anti-inflammatory effect need further research. In this study, the RAW 264.7 macrophages model was used to investigate the anti-inflammatory capacity of COO. Our data showed that 33–200 μg/mL COO markedly inhibited the lipopolysaccharide lipopolysaccharide (LPS)-stimulated nitric oxide (NO.) secretion via the suppression of Nos2 and Cox-2 expression. The enzyme immunoassay confirmed that COO also exhibited a strong suppressive effect on the expression of proinflammatory cytokines such as Tnf-α and Il-6. To further explore the correlation between the anti-inflammatory effects and the lipid phytochemicals in COO, 10 samples were collected and screened for their chemical compositions. It was interestingly demonstrated that the polyphenol extracts of COO play a vital role in its anti-inflammatory properties. In addition, an oil-in-water (O/W) emulsion-based system was also developed to deliver the liposoluble COO into the cells, and the feasibility of this system was confirmed. Our research confirms the anti-inflammatory potential of COO and highlights that the main functional ingredient is polyphenol extracts. This may provide a scientific basis for the comprehensive utilization and development of COO and related functional foods.     

Characterization of the Chemical Composition of Chinese Moringa oleifera Seed Oil

This work focused on physicochemical property assaying, fatty acid composition, triacylglycerol (TAG) profiles, and unsaponifiable matter composition of the Chinese Moringa oleifera seed oil. The results indicated that there was no significant difference in approximate nutritional components between M. oleifera seeds from China and India, while variations in the mineral element contents are significant. Both the Soxhlet extraction method and the aqueous enzymatic extraction method were adopted to extract oil from Chinese M. oleifera seeds. Oil yield obtained using the Soxhlet extraction method was higher than that obtained using the aqueous enzymatic extraction method. While both the iodine value and unsaponifiable matter content of the aqueous enzymatic extracted oil were a little higher than that of the Soxhlet extracted oil. Both oils possess a very low acid value and peroxide value, suggesting their good quality as edible oil. Fatty acid composition results indicated that this oil was especially high in oleic acid. Characterization of the TAG composition was achieved by a two-dimensional high-performance liquid chromatography (HPLC) coupling of nonaqueous reverse-phase and silver ion HPLC with the atmospheric pressure chemical ionization mass spectrometry method. A total of 22 TAG including 16 regioisomers were determined. Composition results of unsaponifiable matters revealed that this oil possesses a number of phytosterols, in which β-sitosterol and stigmasterol are most predominant.     

Ultrasound-assisted extraction of oil from Moringa oleifera Lam. seed using various solvents

The present research analyzes the extraction of oil from Moringa oleifera Lam. seed using ultrasound-assisted extraction (UAE) technique under different operating conditions such as temperature, solvent type, and time. Three factors with three levels Box-Behnken response surface design was employed to optimize and investigate the effect of process variables on the response (oil yield). The independent variables showed significant effect on the extraction process. Interactive effects of the extraction process variables were analyzed by Pareto analysis of variance (ANOVA), and second-order polynomial model was used to plot the 3D response surface plot. Optimum extraction conditions for the maximizing the extraction yield of oil (59%) was found to be: temperature of 35°C, solvent type of 2, and time of 20 min. FT-IR was used to analysis the oil. From the results, it can be concluded that the UAE is the effective technique to extract the oil from Moringa oleifera Lam. seed.     

乙醇提取-丙酮沉淀法提取分离茶皂素的工艺研究

以油茶饼粕为原料，采用乙醇提取-丙酮沉淀法对茶皂素进行提取分离。以茶皂素纯度和得率为考察指标，对乙醇体积分数、液料比、提取温度、提取时间、提取次数、提取液浓缩程度和丙酮用量等工艺参数进行了单因素优化。结果表明：体积分数95%的乙醇为提取溶剂，乙醇与预处理过的油茶饼粕液料比为9：1（mL：g），提取温度为70℃，提取时间为4 h，提取次数为2次，提取液浓缩至刚好有固体析出，丙酮用量为4倍浓缩液体积量时提取分离效果较佳，得到的茶皂素纯度为85.17%，得率为9.82%。不同溶剂打浆对产品纯化效果的比较发现：丙酮、乙酸乙酯、无水乙醇、体积分数95%的乙醇作为打浆纯化溶剂用于提高茶皂素纯度效果均不明显。     

Production of yellow wine from Camellia Oleifera meal pretreated by mixed cultured solid‐state fermentation

Camellia oleifera meal was evaluated to be a potential feedstock for the production of yellow wine (YW), and process conditions were investigated. In this study, C. oleifera meal was firstly pretreated using mixed cultured Bacillus subtilis and Aspergillus niger under solid‐substrate fermentation to degrade the tea saponin (TS) for the following YW fermentation. Response surface methodology helped evaluate the effects of the selected operating parameters, and the optimal condition at a fixed time of 4 days, which gave a 67.84 ± 0.23% degradation rate of TS, was reached as inoculum concentration of 16%, initial moisture content of 55% and temperature of 30 °C. Finally, 7‐day fermentation was harvested to be the most suitable pretreatment for producing YW from C. oleifera meal, and the twice‐feeding fermentation for YW was obtained as wheat koji 12% and active yeast 1.2%. In addition, ample amino acids, phenolic components and the trace TS endowed the C. oleifera wine, the more nutritional characteristics.     

Antioxidant Stability in Vegetable Oils Monitored by the ASTM D7545 Method

The PetroOXY method was used to evaluate the kinetics of oxidation of two edible vegetable oils, extracted from moringa and passion fruit. This method, which uses pure oxygen at 700 kPa is effective and fast and our experiments were carried out at temperatures 110–140 °C with BHA antioxidant additive concentration ranging from 0 to 500 ppm. Moringa and passion fruit oils followed first-order kinetics although, in the case of passion fruit oil, mathematical approximations in the first-order kinetic expression resulted in a final equation that could also be interpreted as deriving from zero-order kinetics. The higher stability of moringa oil was characterized by an activation enthalpy ca. 50 % higher than the one related to passion fruit oil.