ABSTRACT
This study investigated effects of UV-B radiation and CaCl2 on the enhancement of carotenoid content in germinated corn kernels. UV-B radiation and CaCl2 treatments were effective for promoting both carotenoid content and antioxidant activity. Furthermore, the carotenoid content was greater when under the combined treatments of UV-B radiation and CaCl2. Activities of superoxide dismutase and peroxidase were enhanced but malondialdehyde content was weakened by UV-B radiation plus CaCl2 compared to the UV-B radiation only. The mRNA expression of PSY, PDS, ZDS, LCYB, LCYE, BCH1, CYP97C genes involved in the carotenoid biosynthesis pathway showed different patterns in UV-B radiation and CaCl2 treatments. This reveals that the UV-B radiation can increase carotenoid content and antioxidant enzyme activity. Moreover, CaCl2 can further improve carotenoid content and reduce photooxidative damage caused by UV-B radiation.
Subject(s)
Calcium Chloride/pharmacology , Carotenoids , Ultraviolet Rays , Zea mays , Carotenoids/analysis , Carotenoids/metabolism , Germination , Zea mays/drug effects , Zea mays/metabolism , Zea mays/radiation effectsABSTRACT
[6]-Shogaol, an alkylphenol compound purified from the root and stem of ginger (Zingiber officinale), has attracted considerable interest due to its potential anticancer, antioxidative and antirheumatic properties. However, the oral bioavailability of [6]-shogaol has been severely limited because of its poor solubility. In this study, a significant quantity of high-purity [6]-shogaol (yield: 3.6%; purity: 98.65%) was extracted and encapsulated in solid lipid nanoparticles (SLNs) via high-pressure homogenization (encapsulation efficiency: 87.67%) to improve its solubility and oral bioavailability. The resulting [6]-shogaol-loaded solid lipid nanoparticles (SSLNs) were stable, homogeneous and well-dispersed. Its mean particle size and zeta potential were 73.56⯱â¯5.62â¯nm and -15.2⯱â¯1.3â¯mV, respectively. Importantly, the in vitro release profile and in vivo oral bioavailability of SSLNs were significantly improved compared with the free drug. Furthermore, the SSLNs could remarkably lower the uric acid level via inhibiting the activity of xanthine oxidase and reduce the production of interleukin-1ß (IL-1ß) and tumor necrosis factor (TNF-α) in the hyperuricemia/gouty arthritis rat model, when compared to the free [6]-shogaol. Collectively, SLNs could serve as a promising drug delivery system to improve the oral bioavailability of [6]-shogaol for effective treatment of gouty arthritis.
Subject(s)
Catechols/pharmacokinetics , Drug Carriers , Gout Suppressants/pharmacokinetics , Nanoparticles , Plant Extracts/pharmacokinetics , Administration, Oral , Animals , Biological Availability , Catechols/administration & dosage , Drug Delivery Systems , Gout/drug therapy , Gout Suppressants/administration & dosage , Humans , Lipids , Male , Plant Extracts/administration & dosage , Rats, Sprague-DawleyABSTRACT
The food matrix is a limiting factor in determining the bioaccessibility of carotenoids. The impact of food matrix change on the bioaccessibility of carotenoids during drying processes is still unknown. The effect of intermittent microwave vacuum-assisted drying (IMVD) and hot air drying (HAD) on the in vitro liberation and micellization of carotenoids in pumpkin slices was studied. This variable depended on the changes of the matrix driven by the drying process. Different changes in the cell morphology and carotenoid distribution of pumpkin slices during the two processing methods were observed. For IMVD, cell wall degradation and complete chromoplast organelle disruption contributed to the improvement in the liberation and micellization of carotenoids. In the HAD-dried sample, large pigment aggregates hindered the liberation of carotenoids. The carotenoid level in the micellar fraction appeared to be lower than that in the aqueous supernatant during the two processes, suggesting that the new obstacles formed during processing and/or digestion hindered the incorporation of carotenoids in mixed micelles.