In the present study, we focused our attention on Crataegus laciniata Ucria (Rosaceae), which is wild growing in western Sicily (Italy). The chemical profile of the C. laciniata flower’s (CLF) ethanolic (70%) extract showed the presence of both C-flavonoid and O-flavonoid derivatives. Beyond the main metabolites, like hyperoside and vitexin, there are several luteolin derivates, in addition to catechin and epicatechin dimers or trimers. Regarding the antioxidant activities, CLF showed a strong ability to scavenge DPPH and ABTS radicals and a good Fe³⁺-reducing antioxidant power. The investigation into the key enzymes in diabetes showed strong inhibition on α-amylase and α-glucosidase, whereas the skin-whitening properties are linked to inhibitory effects on tyrosinase. Moreover, we employed Danio rerio (zebrafish) for toxicity assessment, as it represents an ideal in vivo model due to its high correlation with humans in response to pharmaceutical and cosmetic testing. Zebrafish embryos exposed to CLF (25–100 µg/mL) showed marked depigmentation compared to phenylthiourea (PTU), in addition to a high survival percentage and the absence of malformations. In conclusion, this experimental study outlines that C. laciniata flowers could be a potential source of bioactive compounds for application in the pharmaceutical and cosmeceutical industries.

Background/Objectives: Ultraviolet B (UVB) radiation contributes significantly to skin aging and skin disorders by promoting oxidative stress, inflammation, and collagen degradation. Natural antioxidants such as theaflavins and thearubigins from Camellia sinensis L. (black tea) have shown photoprotective effects. This study aimed to optimize the extraction of theaflavins and thearubigins from black tea leaves and evaluate the efficacy of the extract against UVB-induced damage using a transfersome-based topical formulation. Methods: Extraction of theaflavins and thearubigins was optimized via response surface methodology (Box-Behnken Design), yielding an extract rich in active polyphenols. This extract was incorporated into transfersomes that were characterized for size, polydispersity, zeta potential, storage stability, and entrapment efficiency. Human dermal fibroblasts (NHDF) were used to assess cytotoxicity, protection against UVB-induced viability loss, collagen degradation, and expression of inflammatory (IL6, COX2, iNOS) and matrix-degrading (MMP1) markers. Cellular uptake of the extract’s bioactive marker compounds was measured via LC-MS/MS. Results: The transfersomes (~60 nm) showed a good stability and a high entrapment efficiency (>85%). The transfersomes significantly protected NHDF cells from UVB-induced cytotoxicity, restored collagen production, and reduced gene expression of MMP1, IL6, COX2, and iNOS. Cellular uptake of key extract’s polyphenols was markedly enhanced by the nanoformulation compared to the free extract. Conclusions: Black tea extract transfersomes effectively prevented UVB-induced oxidative and inflammatory damage in skin fibroblasts. This delivery system enhanced bioavailability of the extract and cellular protection, supporting the use of the optimized extract in cosmeceutical formulations targeting photoaging and UV-induced skin disorders.

The tomato leaf miner (Tuta absoluta) is recognized as a highly destructive pest affecting members of the Solanaceae family, particularly tomato crops, where infestations may cause total crop loss. Its rapid spread and increasing resistance to chemical insecticides underscore the urgent need for innovative, environmentally compatible control strategies. In this context, the present study investigates the bioactivity of surface extracts derived from four Salvia species (S. buchananii, S. corrugata, S. discolor, and S. namaensis) against T. absoluta larvae, focusing on their insecticidal and feeding-deterrent effects. Chemical characterization through LC–MS analysis demonstrated that these Salvia species contain diverse secondary metabolites, including diterpenoids, triterpenoids, and flavonoids. Initial screening using a leaf-dip bioassay at a concentration of 2.50 mg/mL showed that S. discolor was particularly effective among the Salvia extracts tested. Subsequent dose–response assays with S. discolor extracts (0.16–5.00 mg/mL) confirmed strong larvicidal and feeding inhibitory effects, with LC₅₀ and FI₅₀ values of 0.12 and 0.13 mg/mL, respectively. Additionally, weak inhibition of acetylcholinesterase (AChE) was observed, suggesting a minor contribution of neurotoxic effects to the overall activity of the extract. The findings suggest that S. discolor extracts may be useful for managing T. absoluta infestations, pending evaluation of their effects on non-target organisms.

Lavandula dentata is a medicinal and aromatic plant rich in specialised secondary metabolites, but the biomedical potential of leaf-surface metabolites recovered from pruning biomass remains poorly investigated. In this study, a pruning-derived leaf-surface extract of L. dentata was obtained by brief acetone immersion followed by n-hexane partitioning. Its chemical profile was investigated by ultra-high-performance liquid chromatography coupled with high-resolution tandem mass spectrometry analysis combined with feature-based molecular networking, which revealed an enrichment in methoxylated flavonoids and pentacyclic triterpenes, including oleanane- and ursane-like derivatives. The biological activity of the extract was evaluated in HCT116 colorectal cancer cells, MDA-MB-231 triple-negative breast cancer cells, and HaCaT keratinocytes. After 24 h treatment, the extract selectively reduced HCT116 cell viability in a concentration-dependent manner, with an IC₅₀ of 27.8 ± 1.049 μg/mL, whereas MDA-MB-231 and HaCaT cells were less sensitive. Mechanistic analyses in HCT116 cells showed increased early and late apoptotic populations, mitochondrial membrane depolarisation, and enhanced cleavage of caspase-9, caspase-3, and PARP. These findings indicate that a chemically profiled L. dentata leaf-surface extract selectively impairs colorectal cancer cell survival by activating mitochondria-mediated apoptosis. The study also supports the valorisation of pruning-derived aromatic plant biomass as a source of bioactive natural products with potential biomedical relevance.

Crataegus L. (Rosaceae) comprises several species rich in nutrients and bioactive compounds with nutraceutical relevance. The present study aimed to investigate the polyphenolic profile, antioxidant activity, and in vitro antihyperglycemic-related activity of fruits from 11 Crataegus taxa collected in Western Sicily, a region characterized by a high diversity of this genus. Total polyphenol quantification indicated that, among the tested extracts, Crataegus laciniata exhibited the highest content (25.54 mg GAE/g). Using high-resolution Orbitrap Q-Exactive PLUS ESI-MS instrument (Thermo Fisher Scientific, Waltham, MA, USA), a comprehensive phytochemical characterization was performed. Hyperoside quantification revealed that Crataegus aff. insengae, Crataegus zichichii, and Crataegus drepanensis are rich in this bioactive compound (1.47, 1.22, 1.22 mg/g DW). Multivariate analysis, including principal component analysis (PCA), highlighted hyperoside and vitexin as the main contributors to sample differentiation. Additionally, Crataegus laciniata, Crataegus drepanensis, and Crataegus aff. insengae showed the highest antioxidant activity in chemical assays (DPPH, ABTS, and FRAP) and in Caco-2 and H9c2 cell models through the modulation of intracellular reactive oxygen species (ROS). Regarding antihyperglycemic-related activity, Crataegus laciniata, Crataegus azarolus var. azarolus, and Crataegus drepanensis extracts showed the best inhibitory activity against α-glucosidase and α-amylase. Overall, the study highlights the value of Crataegus fruits as sources of bioactive compounds for food and nutraceutical research and supports their further valorization.

Salvia somalensis Vatke is a source of specialized metabolites with potential biological and agrochemical applications. Previous studies on the dichloromethane plant surface extract demonstrated strong antifungal activity associated with abietane diterpenoids. Building on these findings, the present study aimed to characterize the methanolic extract of S. somalensis and evaluate its antifungal potential against major phytopathogenic fungi, with the broader goal of exploring the extract as a sustainable source of antifungal metabolites for crop protection. LC-MS analysis of the methanolic extract revealed a diverse phytochemical profile comprising phenolic acids, including caffeic acid, ferulic acid, and rosmarinic acid, as well as abietane-type diterpenoids such as carnosol, rosmanol, and carnosic acid. Quantitative analysis showed that carnosic acid was present only at low levels (0.09% w/w of fresh biomass). The extract exhibited antifungal activity against Botrytis cinerea, Colletotrichum coccodes, Fusarium oxysporum, Rhizoctonia solani, and Sclerotinia sclerotiorum. More than 80% inhibition of mycelial growth was observed against B. cinerea and C. coccodes at 1000 μg/mL. In addition, as in vitro cultivation of this species has not previously been explored, micropropagated plants and callus culture were established. Phytochemical profiling revealed distinct chemical compositions in the in vitro biomass. Extracts obtained from micropropagated plants inhibited mycelial growth of the tested phytopathogens by 60–70% at 1000 μg/mL, except for F. oxysporum, which showed 35.29% inhibition at the same concentration. Collectively, these findings highlight S. somalensis as a source of bioactive metabolites with antifungal potential.