The development of sustainable extraction methods to obtain natural products constitutes a challenge for the food industry. The aim of this work was to compare yield, separation efficiency, chemical composition, and physicochemical properties of the mucilage extracted from fresh cladodes (FNM) and mucilage extracted from dehydrated cladodes (DNM) of O. ficus indica. Suspensions of fresh and dehydrated cladodes (4% w/w) were prepared for mucilage extraction by using a mechanical separation process. Subsequently, the separated mucilage was precipitated with ethyl alcohol (1:2 v/v) then, yield and separation efficiency were determined. The mucilage was characterized by measuring Z potential, viscosity, color, and texture attributes. Additionally, chemical proximate analysis, scanning electron microscopy, and thermogravimetric analysis (TGA) were conducted. No significant differences (p < 0.05) were detected in the yield and separation efficiencies between samples. Nevertheless, the dehydration process of cladodes prior to mucilage extraction increased protein, ashes, nitrogen free extract, and calcium content. The viscosity was higher in DNM than in FNM. The TGA revealed a different thermal behavior between samples. In addition, the DNM showed lower L (darkness/lightness), cohesiveness, adhesiveness, and springiness values than those of FNM. These results support that differences found between the chemical and physicochemical properties of DNM and those of FNM will determine the applications of the mucilage obtained from the O. ficus indica cladodes in the food, pharmaceutical, and cosmetic industries.

Arterial hypertension is one of the main risk factors in the development of cardiovascular diseases. Therefore, it is important to look for new drugs to treat hypertension. In this study, we carried out the screening of 19 compounds (triterpenes, diterpenes, sesquiterpenes, lignans, and flavonoids) isolated from 10 plants used in Mexican traditional medicine to determine whether they elicited vascular smooth muscle relaxation and, therefore, could represent novel anti-hypertension drug candidates. The vasorelaxant activity of these compounds was evaluated on the isolated rat aorta assay and the results obtained from this evaluation showed that three compounds induced a significant vasodilatory effect: meso-dihydroguaiaretic acid [half maximal effective concentration (EC₅₀), 49.9 ± 11.2 µM; maximum effect (Emax), 99.8 ± 2.7%]; corosolic acid (EC₅₀, 108.9 ± 6.7 µM; Emax, 96.4 ± 4.2%); and 5,8,4′-trihydroxy-3,7-dimethoxyflavone (EC₅₀, 122.3 ± 7.6 µM; Emax, 99.5 ± 5.4%). Subsequently, involvement of the NO/cyclic guanosine monophosphate (cGMP) and H₂S/ATP-sensitive potassium channel (K_ATP) pathways on the vasodilator activity of these compounds was assessed. The results derived from this analysis showed that the activation of both pathways contributes to the vasorelaxant effect of corosolic acid. On the other hand, the vasodilator effect of meso-dihydroguaiaretic acid and 5,8,4′-trihydroxy-3,7-dimethoxyflavone, partly involves stimulation of the NO/cGMP pathway. However, these compounds also showed an important endothelium-independent vasorelaxant effect, whose mechanism of action remains to be clarified. This study indicates that meso-dihydroguaiaretic acid, corosolic acid, and 5,8,4′-trihydroxy-3,7-dimethoxyflavone could be used as lead compounds for the synthesis of new derivatives with a higher potency to be developed as drugs for the prevention and treatment of cardiovascular diseases.

A phytochemical study of the methanol-soluble fraction of an aqueous extract of a sample of Psittacanthus calyculatus collected from the host plant Prosopsis laevigata (Smooth Mesquite) using several techniques, including co-chromatography coupled with UV detection, chromatographic purifications and IR, NMR and MS studies, resulted in the identification of gallic acid, two flavonol-3-biosides and the nonprotein amino acid N-methyl-trans-4-hydroxy-L-proline.

This study focused on the assessment of the vasorelaxant activity of the organic and aqueous extracts obtained from leaves and fruits of a Mexican hawthorn (Crataegus gracilior) on isolated rat aorta, and on the purification and identification of some of their secondary metabolites by the use of chromatographic and spectroscopic techniques. The results obtained showed that the methanol extract has a significantly more potent and effective vasorelaxant effect than the other tested extracts, with an EC₅₀ = 8.69 ± 4.34 µg/mL and an E_max = 94.6% ± 11.30%, values that are close to that of acetylcholine, the positive control. From the same extract, two major triterpenes were isolated and identified as ursolic and corosolic acids by comparison of their experimental NMR spectroscopic data with those reported in the literature. Chlorogenic acid, rutin, quercetin, kaempferol and (+)-catechin were also identified using HPLC coupled with PDAD. All these compounds have already been proven to possess on their own antihypertensive effect and other benefits on cardiovascular diseases and they can support, at least in part, the traditional use of this plant species.

Spodoptera frugiperda J. E. Smith (Lepidoptera: Noctuidae) (fall armyworm) is a pest native to the Americas that affects a variety of crops. Its control is based on chemical insecticides. However, this practice has been associated with changes in the susceptibility of pests to various insecticides. The use of plant products represents an eco-friendly alternative. The objective of this work was to evaluate the larvicidal activity of the chloroform extract of Senna crotalarioides (Kunth) H.S. Irwin & Barneby (Fabaceae) to control S. frugiperda. The chloroform extract of S. crotalarioides caused significant larval mortality, and reduced pupal weight and adult emergence. The analysis by gas chromatography coupled with mass spectrometry (GC-MS) revealed the presence of 22 compounds in the chloroform extract of S. crotalarioides leaves, with the straight-chain aliphatic fatty alcohol 1-octacosanol as the main component. This study revealed that the leaves of S. crotalarioides synthesize long chain alcohols, which increased the mortality of S. frugiperda in its larval stage, including the pupal stage. The extract also caused a decrease in the S. frugiperda pupal weight. The potential use of the chloroform extract obtained from S. crotalarioides and its principal chemical constituent is proposed as a promising alternative to control S. frugiperda.

A series of twenty segmented poly(ester-urethane)s (PEUs) were synthesized, by the reaction of four different macrodiols derived from ε-caprolactone (CL) and 1,8-octanediol (Oct), 1,6-hexamethylene diisocyanate (HDI), and three different carotenoids, (3R,3′R,6′R)-lutein (1) obtained from a renewable source such as marigold (Tagetes erecta L.), (3R,3′S)-zeaxanthin (2) and (3R,3′S)-astaxanthin (3) obtained by partial synthesis from 1, as chain-extender agents. The mechanical properties of the PEUs showed evident plastic behavior. Some PEUs samples exhibited double segregation phases attributed to PCL (soft segment) and 1, 2, and 3/HDI (hard segment) detected by DSC. This work represents the first report of the use of carotenoids as chain extenders in the synthesis of PEUs.