Current Pharmaceutical Design - Volume 31, Issue 38, 2025
Volume 31, Issue 38, 2025
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Vegetable Oils in Skin Whitening - A Narrative Review
Plants are a source of a variety of compounds, such as vegetable oils, which are rich in fatty acids and possess skin-whitening properties. Considering the hyperpigmentation treatment challenges (lack of efficacy or aggressiveness), the constant search for new whitening substances is necessary. Given vegetable oils’ potential and application in dermatological and cosmetic products, we reviewed the scientific literature on vegetable oils with skin depigmenting activity. It was observed that a variety of species (Adansonia digitata, Arctium lappa, Argania spinosa, Astrocaryum vulgare, Bertholletia excelsa, Borago officinalis, Camellia oleifera, Cucurbita moschata, Euterpe oleraceae, Hevea brasiliensis, Moringa oleifera, Nicotiana tabacum, Oenocarpus bataua, Oenothera biennis, Panax ginseng, Passiflora edulis, Pentaclethra macroloba, Perilla frutescens, Sapindus mukorossi, Taiwanese species Taichung selective No. 4 (TCS4) (Adlay bran), Torreya grandis) were evaluated in vitro regarding their skin whitening properties. All the studies demonstrated that the oils have skin whitening properties and that the oils’ activity is related to their composition. The harvesting period, as well as the extraction method, impact on the oils’ properties, hence in their activity. The use of vegetable oils can have advantages over an isolated compound as their components can have synergistic or adding effects. When conducting skin whitening experiments, it is recommended to employ multiple assays because vegetable oils can influence skin whitening through various mechanisms. Furthermore, more clinical trials should be encouraged, considering the potential of vegetable oils as skin-lightening ingredients. More innovative and effective formulations can be obtained using vegetable oils for skin whitening purposes.
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Exploration of 4D Printing and its Applications in the Biomedical Sciences
The potential for 3D printing to completely transform future advanced manufacturing systems has been widely acknowledged. Recent developments in 3D printing technology, particularly in the areas of materials, printers, and procedures, have the potential to revolutionize numerous industries and improve our quality of life on a worldwide scale. 4D printed structures evolve and display intelligent behavior based on specific stimulus-smart material interaction mechanisms and the right design of multi-material structures from mathematical modelling. Time, printer, and shape/property/functionality evolution are the goals of 4D printing, which differs from 3D printing in that it is predictable and not dependent on any one factor. These features enable the product to be self-assembled, multi-functional, and self-repairing. The idea behind four-dimensional printing is the creation of sophisticated three-dimensional structures that can change form in response to various external stimuli. The article provides a comprehensive overview of the smart materials, activation mechanisms, and shape-changing processes used in 4D printing. 4D printing items can be engineered for diverse biomedical purposes, including cell scaffolds, vascular stents, bone scaffolds, tracheal stents, and cardiac stents, through various 3D printing methodologies, influenced by diverse challenges. Additionally, the article explores the potential of shape-changing structures and their present uses in several scientific and biomedical areas.
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Artificial Intelligence in Medicine and Imaging Applications
More LessArtificial intelligence (AI) can completely transform drug development methods by delivering faster, more accurate, efficient results. However, the effective use of AI requires the accessibility of data of excellent quality, the resolution of ethical dilemmas, and an awareness of the drawbacks of AI-based techniques. Moreover, the application of AI in drug discovery is gaining popularity as an alternative to both the complex and time-consuming process of discovering as well as developing novel medications. Importantly, machine learning (ML) as well as natural language processing, for example, may boost both productivity as well as accuracy by analyzing vast volumes of data. This review article discusses in detail the promise of AI in drug discovery as well as offers insights into various topics such as societal issues related to the application of AI in medicine (e.g., legislation, interpretability and explainability, privacy and anonymity, and ethics and fairness), the importance of AI in the development of drug delivery systems, causability and explainability of AI in medicine, and opportunities and challenges for AI in clinical adoption, threat or opportunity of AI in medical imaging, the missing pieces of AI in medicine, approval of AI and ML-based medical devices.
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Shashen Maidong Decoction’s Effects on Chronic Bronchitis: A Multi-Method Approach
Authors: Wenchao Zhou, Yaqin Hu, Yun Qiu, Hao Zheng, Juan Jiang, Jiangyi Luo, Juanjiang Wu, Hanwen Yuan, Xudong Zhou, Liming Gong, Yixing Qiu and Wei WangBackgroundShashen Maidong Decoction (SSMDD) is a traditional Chinese medicine (TCM) formula used for treating chronic bronchitis (CB).
ObjectivesThis study aims to explore the mechanism of SSMDD against CB, focusing on its active components and their impact on Interleukin 6 (IL-6), a key inflammatory factor.
Materials and MethodsNetwork pharmacology, a method that helps identify potential active components and their interactions in a biological network, was used to predict SSMDD’s effects. Molecular docking, a computational approach for predicting the binding affinity between small molecules and target proteins, was utilized to elucidate the mechanisms of action. Transcriptomic analysis, ELISA, and Western blot assays were subsequently implemented for mechanism validation.
ResultsNetwork pharmacology analysis identified quercetin and kaempferol as key active components of SSMDD, with a high affinity for IL-6. Transcriptomic data confirmed the regulation of inflammation-related pathways by SSMDD, aligning with the predicted targets. In the ELISA determination, compared with the model group, the IL-6 levels in the samples treated with quercetin and kaempferol were reduced by 55% and 36%, respectively. The Western blot results showed that the expression of IL-6 protein in these samples decreased by 33% and 25%, respectively.
ConclusionSSMDD exhibits anti-inflammatory activity against CB by targeting IL-6. This study provides a deeper understanding of the mechanisms through which SSMDD exerts its therapeutic effects on CB. Moreover, these findings also suggest that SSMDD may offer insights for future treatments of other inflammatory diseases, potentially improving patient outcomes and developing novel therapeutic strategies. Future studies should explore the effects of additional targets and active compounds within SSMDD and evaluate its broader applications in inflammatory conditions.
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Investigation into the Mechanisms of Paeoniae Radix Rubra in the Treatment of Venous Thrombosis Using Network Pharmacology, Bioinformatics, and Molecular Docking Techniques
Authors: Shuo Xu, Ajiao Hou, Jiaxu Zhang, Jinhao Xue, Shiwen Gao, Hai Jiang and Liu YangObjectiveThis study investigates the potential targets and mechanisms of Paeoniae Radix Rubra (PRR) in treating Venous Thrombosis (VTE) by employing network pharmacology, bioinformatics analysis, and molecular docking validation.
MethodsActive components of PRR were identified via TCMSP. VTE-related genes were screened from GEO datasets, and WGCNA analyzed key modules. A Protein-Protein Interaction (PPI) network was constructed using Cytoscape, followed by immune infiltration analysis. Core targets were functionally annotated via GO and KEGG pathways. Molecular docking and molecular dynamics simulations validated interactions between PRR components and core targets.
ResultsA total of 30 active components of PRR and 21 potential targets for the treatment of VTE were identified. From the PPI network, 10 hub genes were screened. KEGG pathway enrichment analysis demonstrated that the target genes were significantly enriched in pathways, such as the cGMP-PKG signaling pathway, B cell receptor signaling pathway, Th1 and Th2 cell differentiation, and IL-17 signaling pathway. Molecular docking results revealed that MAPK1, NFATC1, and SELP all had good affinity with the screened active components. Among them, MAPK1 and beta-sitosterol exhibited the highest binding energy of -8.73 kcal/mol. Molecular dynamics simulation results from RMSD, RMSF, HBond, and SASA analyses indicated that the beta-sitosterol-MAPK1 complex maintained good stability.
ConclusionThrough this study, it was found that PRR may act on targets, such as MAPK1 and NFATC1, through components like beta-sitosterol and Stigmasterol. Among them, the complex (beta-sitosterol - MAPK1) may be the key active component that plays a role in treating VTE.
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Volumes & issues
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Volume 31 (2025)
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Volume (2025)
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Volume 30 (2024)
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Volume 29 (2023)
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Volume 28 (2022)
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Volume 27 (2021)
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Volume 26 (2020)
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Volume 25 (2019)
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Volume 24 (2018)
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Volume 23 (2017)
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Volume 22 (2016)
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Volume 21 (2015)
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Volume 20 (2014)
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Volume 19 (2013)
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Volume 18 (2012)
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Volume 17 (2011)
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Volume 16 (2010)
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Volume 15 (2009)
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Volume 14 (2008)
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Volume 13 (2007)
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Volume 12 (2006)
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Volume 11 (2005)
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Volume 10 (2004)
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Volume 9 (2003)
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Volume 8 (2002)
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Volume 7 (2001)
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Volume 6 (2000)
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