Littérature scientifique sur le sujet « Cyclodextrin Molecules »
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Articles de revues sur le sujet "Cyclodextrin Molecules"
Cardoso, T., C. I. C. Galhano, M. F. Ferreira Marques et A. Moreira da Silva. « Thymoquinoneβ-Cyclodextrin Nanoparticles System : A Preliminary Study ». Spectroscopy : An International Journal 27 (2012) : 329–36. http://dx.doi.org/10.1155/2012/902486.
Texte intégralPereva, Stiliyana, Valya Nikolova, Silvia Angelova, Tony Spassov et Todor Dudev. « Water inside β-cyclodextrin cavity : amount, stability and mechanism of binding ». Beilstein Journal of Organic Chemistry 15 (17 juillet 2019) : 1592–600. http://dx.doi.org/10.3762/bjoc.15.163.
Texte intégralBrown, SE, JH Coates, CJ Easton, SF Lincoln, Y. Luo et AKW Stephens. « Cyclodextrin Inclusion Complexes of Two Non-Steroidal Antiinflammatory Drugs and of an Analgesic Drug ». Australian Journal of Chemistry 44, no 6 (1991) : 855. http://dx.doi.org/10.1071/ch9910855.
Texte intégralBelyakova, L. A., A. M. Varvarin, D. Yu Lyashenko et O. V. Khora. « Designing Adsorption Centres for Biological Active Molecules on a Silica Surface ». Adsorption Science & ; Technology 23, no 9 (novembre 2005) : 703–19. http://dx.doi.org/10.1260/026361705776316596.
Texte intégralWang, Runmiao, Hui Zhou, Shirley W. I. Siu, Yong Gan, Yitao Wang et Defang Ouyang. « Comparison of Three Molecular Simulation Approaches for Cyclodextrin-Ibuprofen Complexation ». Journal of Nanomaterials 2015 (2015) : 1–8. http://dx.doi.org/10.1155/2015/193049.
Texte intégralSzékely-Szentmiklósi, Blanka, et B. Tőkés. « Study of Cyclodextrin/Fluoroquinolone Inclusion Complexes by Capillary Electrophoresis ». Acta Medica Marisiensis 59, no 2 (1 avril 2013) : 107–10. http://dx.doi.org/10.2478/amma-2013-0026.
Texte intégralSivakumar, Ponnurengam M., Shohreh Peimanfard, Ali Zarrabi, Arezoo Khosravi et Matin Islami. « Cyclodextrin-Based Nanosystems as Drug Carriers for Cancer Therapy ». Anti-Cancer Agents in Medicinal Chemistry 20, no 11 (8 juillet 2020) : 1327–39. http://dx.doi.org/10.2174/1871520619666190906160359.
Texte intégralBelyakova, L. A. « Encapsulation of benzene carboxylic acids using cyclodextrins ». Himia, Fizika ta Tehnologia Poverhni 12, no 1 (30 mars 2021) : 40–51. http://dx.doi.org/10.15407/hftp12.01.040.
Texte intégralWelliver, Mark, et John P. McDonough. « Anesthetic Related Advances with Cyclodextrins ». Scientific World JOURNAL 7 (2007) : 364–71. http://dx.doi.org/10.1100/tsw.2007.83.
Texte intégralBraga, Susana Santos. « Cyclodextrins as Multi-Functional Ingredients in Dentistry ». Pharmaceutics 15, no 9 (31 août 2023) : 2251. http://dx.doi.org/10.3390/pharmaceutics15092251.
Texte intégralThèses sur le sujet "Cyclodextrin Molecules"
Huang, Tian He. « Investigation of cyclodextrin formulations by combined experimental and molecular modeling techniques ». Thesis, University of Macau, 2018. http://umaclib3.umac.mo/record=b3952153.
Texte intégralBinti, Mohtar Noratiqah. « Cyclodextrin-based formulations for pulmonary delivery of chemotherapeutic molecules ». Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10054726/.
Texte intégralSala, Andrea. « Supramolecular derivatisation of bioactive molecules via co-crystallization and cyclodextrin inclusion complexation ». Master's thesis, University of Cape Town, 2018. http://hdl.handle.net/11427/29711.
Texte intégralMvula, Eino Natangwe. « Preparation and solid state properties of cyclodextrin complexes of selected drug molecules ». Master's thesis, University of Cape Town, 1999. http://hdl.handle.net/11427/17902.
Texte intégralA large number of pharmaceutically important drugs are poorly soluble in water. This study focuses on the 'smart' molecule that can enhance the solubility and hence increase the bioavailability of these drugs. This molecule is a cyclodextrin and is known to form inclusion compounds with various drug molecules. The preparation of β-cyclodextrin CP-CD), y-cyclodextrin (y-CD), heptakis(2,6-di-OJ, methyl)-β-cyclodextrin (Dimeb) and heptakis(2,3,6·tri-0-methyl)- β-cyclodextrin (Trimeb) 3, complexes with clofibric acid as well as the heptakis(2,3,6j·tri-O-methyl)- β-cyclodextrin (Trimeb) complex with clofibrate is reported. The complexes were characterised by thermogravimetric analysis (TG), differential scanning calorimetry (DSC), ultraviolet spectrophotometry (UV), infrared spectroscopy (IR), X-ray powder diffraction (XRD) and single crystal X-ray analysis.
Wandstrat, Michelle Marie. « MATERIALS AND MODIFICATION OF ELECTRODES FOR THE DETECTION OF BIOLOGICAL MOLECULES ». Miami University / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=miami1164817458.
Texte intégralDutta, Ashutosh. « Exploration of diversified interactions of some significant compounds prevalent in several environments by physicochemical contrivance ». Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2787.
Texte intégralWahlström, Anna. « NMR studies on interactions between the amyloid β peptide and selected molecules ». Doctoral thesis, Stockholms universitet, Institutionen för biokemi och biofysik, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-60346.
Texte intégralAt the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 4: Manuscript. Paper 5: Manuscript.
Brown, Susan Elizabeth. « Molecular recognition by cyclodextrins / ». Title page, contents and abstract only, 1994. http://web4.library.adelaide.edu.au/theses/09PH/09phb8798.pdf.
Texte intégralCherraben, Sawsen. « Machines moléculaires à base de cyclodextrines fonctionnalisées ». Thesis, Sorbonne université, 2019. https://accesdistant.sorbonne-universite.fr/login?url=http://theses-intra.upmc.fr/modules/resources/download/theses/2019SORUS633.pdf.
Texte intégralControlling motion and directionality at the molecular level is a major challenge. This thesis project focused on the development of a family of cyclodextrin (CDs) based molecular machines. The objective was to exploit the inherent asymmetry of CDs and to functionalize them selectively in order to be able to apply a stimulus directly to them. Hence, controlling their movements in supramolecular architectures becomes possible. In the first approach, we developed a pH-sensitive switch of the pseudo-rotaxane type based on CDs selectively functionalized by amines on the primary rim. A remarkable control of threading and dethreading by a pH stimulus were obtained, along with a modulation of the dethreading kinetics by variation in the number of amines. In a second approach, we designed a system using a chemical fuel to obtain unidirectional motion of a functionalized CD through its active transport. The key step is the cleavage of protective groups located on the axis by the catalytic function carried by the CD, which should preferably take place through the primary rim, ensuring its directed transport. For this purpose, a first three-station [2]rotaxane CDMe model was synthesized by a post-functionalization approach of a one-station [2]rotaxane with amide stoppers. Its study showed the formation of 3 mechano-isomers during the protective reaction with a non-statistical distribution indicating a probable kinetic bias. This promising work opens up longer-term perspectives on the development of chemically fueled molecular motors with active CD transport
Mansour, Ali Taher. « New enantioselective transformations induced by cyclodextrins : applications in the preparation of molecular building blocks of biological interest ». Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS186/document.
Texte intégralThis work revolves around the synthesis of ennatiomerically pure cyclobutane derivatives of GABA, and their use in the preparation of hybrid γ/α-peptides that could adopt a well-defined three dimensional secondary structure. In this aim we developed two strategies. The first one employed native β-Cyclodextrin as a supramolecular chiral host to achieve enantiodifferentiating photochemical cyclizations. Attempting to perform an intramolecular [2+2] cyclization of N-allyl-N-(4-methoxyphenyl)acrylamide, we only obtained a δ-lactam resulting from a 6π electrocyclization, whereas the electrocyclization of 1,3-Dihydro‑2H‑azepin-2-one allowed access to a 45% enantiomerically enriched bicyclic γ-lactam precursor of (+)-cis-3,4CB-GABA. The second strategy was based on a racemic synthesis of N-Boc-cis-3,4CB-GABA followed by a separation of the two enantiomers using a semi-preparative HPLC fitted with a chiral column. This allowed access to optically pure (-) and (+)-cis-3,4CB-GABA, on a gram scale. Furthermore, the enantiomerically pure (-) and (+)-cis-3,4CB-GABA, were used to synthesize, and fully characterize two series [the (S,S/R) and the (R,R/R)] of short diasteriomeric hybrid γ/α-peptides composed of alternating cis-3,4CB-GABA and D-Alanine. Analysis of the conformational behavior of the dipeptides from both series by X-Ray diffraction on a single crystal, showed no intramolecular interactions but rather an array of intermolecular hydrogen bonding between the dipeptide molecules. On the other hand, a series of 1D and 2D NMR experiments showed that the tetrapeptide of the (S,S/R)-series could attain a 12/10 helical structuration, whereas its diasteriomeric analog of the (R,R/R)-series, displayed evidence of an unprecedented 7/9 folding pattern in solution
Livres sur le sujet "Cyclodextrin Molecules"
Ahern, Cormac. Dendrimeric cyclodextrins for molecular inclusion. Dublin : University College Dublin, 1997.
Trouver le texte intégralHartwell, Edward Y. Chemically-modified and immobilised cyclodextrins as molecular reaction vessels. Birmingham : University of Birmingham, 1994.
Trouver le texte intégralMareeswaran, Paulpandian Muthu, Palaniswamy Suresh et Seenivasan Rajagopal, dir. Photophysics of Supramolecular Architectures. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150491901220101.
Texte intégral(Editor), J. L. Atwood, J. E. Davies (Editor) et T. Osa (Editor), dir. Clathrate Compounds, Molecular Inclusion Phenomena and Cyclodextrins (Advances in Inclusion Science). Springer, 1985.
Trouver le texte intégralDavies, J. E., T. Osa et J. L. Atwood. Clathrate Compounds, Molecular Inclusion Phenomena, and Cyclodextrins : Proceedings of the Third International Symposium on Clathrate Compounds and Molecular Inclusion Phenomena and the Second International Symposium on Cyclodextrins, Tokyo, Japan, July 23-27 1984. Springer, 2012.
Trouver le texte intégralDavies, J. E., T. Osa et J. L. Atwood. Clathrate Compounds, Molecular Inclusion Phenomena, and Cyclodextrins : Proceedings of the Third International Symposium on Clathrate Compounds and ... 23–27, 1984. Springer, 2011.
Trouver le texte intégralChapitres de livres sur le sujet "Cyclodextrin Molecules"
Harata, K., K. Uekama, M. Otagiri et F. Hirayama. « Crystal Structures of Cyclodextrin Complexes with Chiral Molecules ». Dans Clathrate Compounds, Molecular Inclusion Phenomena, and Cyclodextrins, 583–94. Dordrecht : Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-009-5376-5_62.
Texte intégralRibeiro-Claro, Paulo J. A., et Ana M. Amado. « Structural Rigidity Vs. Structural Disorder in α-Cyclodextrin Inclusion Compounds ». Dans Spectroscopy of Biological Molecules : Modern Trends, 269–70. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_120.
Texte intégralSanz-Garcia, T., G. Gonzalez-Gaitano, N. Iza, A. Galvez-Garcia et G. Tardajos. « NMR Study of the Inclusion Complex Between β-Cyclodextrin and Propafenone ». Dans Spectroscopy of Biological Molecules : New Directions, 333–34. Dordrecht : Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4479-7_149.
Texte intégralKonsta, A. A., et L. Apekis. « Investigation of β-Cyclodextrin Inclusion Complexes by Broad Band Dielectric Spectroscopy ». Dans Spectroscopy of Biological Molecules : Modern Trends, 273–74. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_122.
Texte intégralBügler, Jürgen H., Menno de Jong, Johan F. J. Engbersen et David N. Reinhoudt. « Functionalized Cyclodextrin-Calix[4]Arene Host Molecules for Detection of Organic Analytes ». Dans Sensor Technology in the Netherlands : State of the Art, 305–9. Dordrecht : Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5010-1_49.
Texte intégralJunquera, Elena, Oscar Pastor et Emilio Aicart. « Encapsulation of the Salicylic Acid/Salicylate System by Hydroxypropyl-β-Cyclodextrin at 25 °C. A Fluorescence Enhancement Study in Aqueous Solutions ». Dans Spectroscopy of Biological Molecules : Modern Trends, 397–98. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_178.
Texte intégralBreslow, Ronald. « Cyclodextrins ». Dans Molecular Encapsulation, 43–69. Chichester, UK : John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470664872.ch2.
Texte intégralPopova, E. I., I. N. Karpov, I. N. Topchieva et O. I. Mikhalev. « Molecular Necklaces Containing Reporter Molecules ». Dans Proceedings of the Ninth International Symposium on Cyclodextrins, 563–66. Dordrecht : Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4681-4_134.
Texte intégralJicsinszky, L., H. Hashimoto, K. Mikuni, I. Bakó et L. Szente. « Molecular Mechanics Studies on Cyclodextrin Complexes : Interaction of Crocetin with Cyclodextrins ». Dans Proceedings of the Eighth International Symposium on Cyclodextrins, 263–66. Dordrecht : Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-5448-2_57.
Texte intégralTian, He, et Qiao-Chun Wang. « Cyclodextrin-Based Switches ». Dans Molecular Switches, 301–19. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634408.ch9.
Texte intégralActes de conférences sur le sujet "Cyclodextrin Molecules"
Nozawa, Ryo, Mohammad Ferdows, Kazuhiko Murakami et Masahiro Ota. « Effects of Cyclodextrin Solutions on Methane Hydrate Formation ». Dans ASME/JSME 2007 Thermal Engineering Heat Transfer Summer Conference collocated with the ASME 2007 InterPACK Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ht2007-32987.
Texte intégralMic, Mihaela, Adrian Pı̂rnău, Mircea Bogdan et Ioan Turcu. « Inclusion complex of benzocaine and β-cyclodextrin : [sup 1]H NMR and isothermal titration calorimetry studies ». Dans PROCESSES IN ISOTOPES AND MOLECULES (PIM 2013). AIP, 2013. http://dx.doi.org/10.1063/1.4833697.
Texte intégralZavodnik, I. B., E. A. Lapshina, T. V. Ilyich, A. G. Veiko, T. A. Kovalenia et V. U. Buko. « REGULATORY, ANTIOXIDATIVE AND HEPATOPROTECTIVE EFFECTS OF PLANT POLYPHENOLS AND THEIR NANOSTRUCTURED COMPLEXES ». Dans SAKHAROV READINGS 2021 : ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. International Sakharov Environmental Institute, 2021. http://dx.doi.org/10.46646/sakh-2021-1-255-258.
Texte intégralKim, Jin-Baek, Young-Gil Kwon, Hyo-Jin Yun et Jae-Hak Choi. « Novel molecular resists based on inclusion complex of cyclodextrin ». Dans SPIE's 27th Annual International Symposium on Microlithography, sous la direction de Theodore H. Fedynyshyn. SPIE, 2002. http://dx.doi.org/10.1117/12.474286.
Texte intégralKoudoumas, E., S. Couris, P. Seta, A. Rassat et S. Leach. « Optical Limiting Action of Methano Fullerenes and Fullerenes Incorporated in Cyclodextrins ». Dans The European Conference on Lasers and Electro-Optics. Washington, D.C. : Optica Publishing Group, 1998. http://dx.doi.org/10.1364/cleo_europe.1998.cthh45.
Texte intégralWANG, YING, et DAVID F. EATON. « Control of molecular nonlinear optical properties by inclusion complexation with cyclodextrin ». Dans Conference on Lasers and Electro-Optics. Washington, D.C. : OSA, 1985. http://dx.doi.org/10.1364/cleo.1985.thm44.
Texte intégralSuharyani, Ine, Cecep Suhandi, Yayan Rizkiyan, Didi Rohadi, Muchtaridi Muchtaridi, Nasrul Wathoni et Marline Abdassah. « Molecular docking in prediction of α-mangostin/cyclodextrin inclusion complex formation ». Dans 3RD INTERNATIONAL CONFERENCE OF BIO-BASED ECONOMY FOR APPLICATION AND UTILITY. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0120782.
Texte intégralTreetharnmathurot, Benjaporn, Chitchamai Ovatlarnporn, Juraithip Wungsinthaweekul et Ruedeekorn Wiwattanapatapee. « Chemical modification and thermal stability study of β-cyclodextrin- and PAMAM-trypsin conjugates ». Dans 2009 4th IEEE International Conference on Nano/Micro Engineered and Molecular Systems. IEEE, 2009. http://dx.doi.org/10.1109/nems.2009.5068732.
Texte intégralSrihakulung, Ornin, Luckhana Lawtrakul, Pisanu Toochinda, Waree Kongprawechnon, Apichart Intarapanich et Ryo Maezono. « Theoretical investigation of molecular calculations on inclusion complexes of plumbagin with β-cyclodextrins ». Dans 2017 Fourth Asian Conference on Defence Technology - Japan (ACDT). IEEE, 2017. http://dx.doi.org/10.1109/acdtj.2017.8259589.
Texte intégralBelosludov, Rodion V., Hiroshi Mizuseki, Kyoko Ichinoseki et Yoshiyuki Kawazoe. « Theoretical Study on Inclusion Complex of Polyaniline Covered by Cyclodextrins for Molecular Device ». Dans 2001 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2001. http://dx.doi.org/10.7567/ssdm.2001.f-7-2.
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