The Cocoa Pod Husk (CPH) accounts for 67–76% of the total cocoa fruit weight, making it its main agro-industrial waste of cocoa production. A valorization of this waste is possible through the extraction of pectin. In this study, pectin was extracted from CPH powder by acid hydrolysis using citric acid and sulfuric acid. Fourier transform infrared spectroscopy (FT-IR) was employed as a qualitative and quantitative characterization technique. The FT-IR of the pectin samples showed the bands visible at 1732 and 1626 cm⁻¹ corresponding to the esterified and free carboxylic groups, respectively. These bands can be differentiated according to their degree of methyl esterification (DE) by analyzing the area under the curve. The extracted pectin showed no significant difference in yields (p ≤ 0.05) between the two acids; however, significant differences (p ≤ 0.05) were observed in DE and methoxylation percentage (MeO). According to the FT-IR results, pectin extracted with citric acid presented a lower DE (7.43%) and MeO (1.12%) compared to pectin extracted with sulfuric acid, which showed a DE of 18.15% and a 2.96% MeO. Pectin with a DE below 50% is classified as low-methylated, making it unsuitable for the food industry. However, these create a raw material that has a potential use in the pharmaceutical and bioenergy industries.

Cocoa drying is the post-harvest thermal process used to condition the beans to a moisture content between 6.5 and 7% for storage and further processing. Convective drying is an energy-intensive process where time and temperature are considered critical factors for the degradation of bioactive compounds in edible products. In the present study, the energy parameters, vibrational spectroscopy, and changes in bioactive compounds of cocoa beans were studied during thin-layer hot air drying at 50 °C, 60 °C, and 70 °C. Moisture loss, specific energy consumption (SEC), energy efficiency, total phenolics (TPs), total flavonoids (TFs), and antioxidant activity (DPPH) were determined. Fourier transform infrared (FT-IR) spectroscopy with attenuated total reflectance (ATR) was used to characterize the samples, and a multivariate analysis was applied to find interactions among the components. The obtained SEC was 18,947.30–24,469.51 kJ/kg, and the energy efficiency was 9.73–12.31%. When the temperature was 70 °C, the best values for SEC and energy efficiency were obtained. The results also showed that the convective drying generated changes in the TP levels for the three temperatures, mainly after 300 min, with maximum levels between 360 and 600 min, at 70 °C; however, it does not have a clear relationship with the TFs and the antioxidant activity. The FT-IR and the multivariate analysis revealed changes in several signals in the 1800 to 400 cm⁻¹ range, confirming the variation in the associated signal with phenolic compounds.

Background: In Mexico, the fruit of the Manilkara zapota (L.) P. Royen (Chicozapote) tree is widely consumed; however, numerous studies have identified bioactive compounds within its leaves. Purpose: To evaluate the bioactive properties of M. zapota leaf extracts, focusing on their anti-oxidant, anti-diabetic, and anti-hypertensive potentials, and assessing their efficacy in mitigating inflammation. Materials and Methods: This study evaluated the anti-oxidant properties of aqueous (AE), ethanolic (EE), and hydroalcoholic (HE) extracts, utilizing 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays. Anti-diabetic activity was assessed by inhibiting the enzymes α-amylase and α-glucosidase, while anti-hypertensive efficacy was measured via angiotensin-converting enzyme (ACE) inhibition. The anti-inflammatory potential was also examined in vivo using a murine model of 12- O-tetradecanoylphorbol-13-acetate-induced ear edema. Results: The DPPH assay revealed that all extracts exhibited equivalent anti-oxidant capacities at the same concentration, with no significant statistical difference ( p < 0.05). Conversely, the ABTS assay demonstrated that AE possessed superior activity (4.6−28.5%) across varying concentrations. EE exhibited the most potent inhibition of α-amylase, α-glucosidase, and ACE, with 81.8%, 58.9%, and 87.8%, respectively. In anti-inflammatory assays, EE at a 5 mg dosage significantly outperformed other extracts. Conclusion: These findings suggest that M. zapota leaf extracts, mainly through EE, could offer a viable natural alternative for reducing inflammation and potentially managing diabetes and hypertension.

Cocoa pod husk (CPH), a major agro-industrial residue, contains valuable bioactive compounds whose recovery can support sustainable waste valorization. This study evaluated the influence of increasing ethanol concentrations on the ultrasound-assisted extraction (UAE) of bioactive compounds from CPH and their antioxidant, antihypertensive, and antihyperglycemic activity. Dried and milled CPH was extracted using ethanol–water mixtures (0–100% ethanol) under fixed ultrasonic conditions. Cocoa pod husk powder characterization and the resulting extracts were analyzed in terms of chemical composition (lignocellulosic compounds, proximate and elemental composition, and bromatological composition), antioxidant capacity, and in vivo antihypertensive and antihyperglycemic effects in Wistar rats. The results showed that solvent polarity strongly modulated extraction efficiency: absolute ethanol yielded the highest phenolic (171.43 mg GAE/g) and flavonoid (132.05 mg QE/g) content, whereas hydroalcoholic mixtures, particularly 50:50, enhanced overall antioxidant performance, especially in FRAP. The chemical analysis results showed the selective recovery of compounds such as quercetin, hesperidin, and theobromine, and FTIR-PCA results revealed distinct solvent-dependent chemical profiles. In vivo assays indicated modest blood pressure stabilization and a more pronounced antihyperglycemic effect after chronic administration. Overall, UAE proved an effective, rapid, and solvent-efficient method for CPH valorization, highlighting its potential for producing natural antioxidants applicable to food, nutraceutical, and cosmetic formulations.