Determination of formation constants and structural characterization of cyclodextrin inclusion complexes with two phenolic isomers: carvacrol and thymol

Scholarly Works

• Gan, C.; Langa, E.; Wang, G.; Van Bambeke, F.; Ballestero, D.; Pino-Otín, M. R. Mechanisms of action and resistance prevention of synergistic thymol and carvacrol combinations with antibiotics in Staphylococcus aureus and Acinetobacter baumannii. Natural products and bioprospecting 2025, 15, 36. doi:10.1007/s13659-025-00518-7
• Hbaieb, S.; Kallel, J.; Jaoued, N.; Riahi, E.; Bordes, C.; Chevalier, Y. Nmr Study of Hydroxypropyl-Cyclodextrin Inclusion Complexes with Active Molecules of Plant Mother Tinctures. Elsevier BV 2025. doi:10.2139/ssrn.5355069
• Mohammad, A. A.; Oladzadabbasabadi, N.; Kareem, H. R.; Al-Musawi, M. H.; PourvatanDoust, S.; Ghorbani, M. Investigating the impact of thymol/ɤ-cyclodextrin concentrations on the properties of electrospun PLA/PVP nanofibers for packaging applications. Colloids and Surfaces A: Physicochemical and Engineering Aspects 2024, 701, 134923. doi:10.1016/j.colsurfa.2024.134923
• Gao, Q.; Zheng, J.; Van der Meeren, P.; Zhang, B.; Fu, X.; Huang, Q. A comparative study on stabilizing and releasing thymol by pre-formed V-type starch and β-cyclodextrin. Food Hydrocolloids 2024, 156, 110233. doi:10.1016/j.foodhyd.2024.110233
• Panigrahi, S. D.; Klebba, K. C.; Rodriguez, E. N.; Mayhan, C. M.; Kotagiri, N.; Kumari, H. Enhancing antibacterial efficacy through macrocyclic host complexation of fluoroquinolone antibiotics for overcoming resistance. Scientific reports 2024, 14, 24637. doi:10.1038/s41598-024-73568-5
• Zhang, Y.; Li, H.; Hai, X.; Guo, X.; Di, X. Designing green and recyclable switchable supramolecular deep eutectic solvents for efficient extraction of flavonoids from Scutellariae Radix and mechanism exploration. Journal of chromatography. A 2024, 1730, 465084. doi:10.1016/j.chroma.2024.465084
• Dorofte, A. L.; Dima, C.; Bleoanca, I.; Aprodu, I.; Alexe, P.; Kharazmi, M. S.; Jafari, S. M.; Dima, Ș.; Borda, D. Mechanism of β–cyclodextrin - thyme nanocomplex formation and release: In silico behavior, structural and functional properties. Carbohydrate Polymer Technologies and Applications 2024, 7, 100422. doi:10.1016/j.carpta.2024.100422
• Etri, K.; Pluhár, Z. Exploring Chemical Variability in the Essential Oils of the Thymus Genus. Plants (Basel, Switzerland) 2024, 13, 1375. doi:10.3390/plants13101375
• Krekhova, F.; Meshcheva, D.; Shishov, A.; Bulatov, A. In situ formation of natural deep eutectic solvent on membrane after fat hydrolysis for lindane isomers determination in peanut paste. Talanta 2024, 271, 125737. doi:10.1016/j.talanta.2024.125737
• Kelanne, N.; Yang, B.; Laaksonen, O. Potential of cyclodextrins in food processing for improving sensory properties of food. Food Innovation and Advances 2024, 3, 1–10. doi:10.48130/fia-0024-0001
• Kelanne, N.; Yang, B.; Laaksonen, O. Potential of cyclodextrins in food processing for improving sensory properties of food. Food Innovation and Advances 2024, 0, 1–10. doi:10.48130/fia-2024-0001
• Georgiou, N.; Kakava, M. G.; Routsi, E. A.; Petsas, E.; Stavridis, N.; Freris, C.; Zoupanou, N.; Moschovou, K.; Kiriakidi, S.; Mavromoustakos, T. Quercetin: A Potential Polydynamic Drug. Molecules (Basel, Switzerland) 2023, 28, 8141. doi:10.3390/molecules28248141
• Nakhle, L.; Kfoury, M.; Ruellan, S.; Greige-Gerges, H.; Landy, D. Insights on cyclodextrin inclusion complexes in deep eutectic solvents:Water mixtures. Journal of Molecular Structure 2023, 1293, 136260. doi:10.1016/j.molstruc.2023.136260
• Naziruddin, M.; Jawaid, M.; Elais, R.; Sanny, M.; Fouad, H.; Yusof, N.; Abdul-Mutalib, N. Supercritical fluid extraction of torch ginger: Encapsulation, metabolite profiling, and antioxidant activity. Journal of King Saud University - Science 2023, 35, 102700. doi:10.1016/j.jksus.2023.102700
• Naeem, A.; Yu, C.; Zang, Z.; Zhu, W.; Deng, X.; Guan, Y. Synthesis and Evaluation of Rutin-Hydroxypropyl β-Cyclodextrin Inclusion Complexes Embedded in Xanthan Gum-Based (HPMC-g-AMPS) Hydrogels for Oral Controlled Drug Delivery. Antioxidants (Basel, Switzerland) 2023, 12, 552. doi:10.3390/antiox12030552
• Nakhle, L.; Kfoury, M.; Greige-Gerges, H.; Landy, D. Retention of a plethora of essential oils and aromas in deep eutectic solvent:water:cyclodextrin mixtures. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2022, 103, 35–44. doi:10.1007/s10847-022-01174-x
• Oliveira, W. P.; Miguel, L. M. Encapsulation of volatile oils with antimicrobial activity in chitosan-βCD molecular inclusion complexes by spray drying. Drying Technology 2022, 41, 754–766. doi:10.1080/07373937.2022.2115510
• Kinart, Z.; Tomaš, R. Studies of the Formation of Inclusion Complexes Derivatives of Cinnamon Acid with α-Cyclodextrin in a Wide Range of Temperatures Using Conductometric Methods. Molecules (Basel, Switzerland) 2022, 27, 4420. doi:10.3390/molecules27144420
• Peimanfard, S.; Zarrabi, A.; Trotta, F.; Matencio, A.; Cecone, C.; Caldera, F. Developing Novel Hydroxypropyl-β-Cyclodextrin-Based Nanosponges as Carriers for Anticancer Hydrophobic Agents: Overcoming Limitations of Host-Guest Complexes in a Comparative Evaluation. Pharmaceutics 2022, 14, 1059. doi:10.3390/pharmaceutics14051059
• Bai, M.-Y.; Zhou, Q.; Zhang, J.; Li, T.; Cheng, J.; Liu, Q.; Xu, W.-R.; Zhang, Y.-C. Antioxidant and antibacterial properties of essential oils-loaded β-cyclodextrin-epichlorohydrin oligomer and chitosan composite films. Colloids and surfaces. B, Biointerfaces 2022, 215, 112504. doi:10.1016/j.colsurfb.2022.112504

Explore citations to this article at