Page 39 - 81_04
P. 39

enhance curcumin skin permeability from hydrophilic                                          J. González-Albadalejo et al.
     matrix gel. AAPS PharmSciTech 2013; 14: 1303-12.
     (f) Radjaram A, Hafid AF, Setyawan D. Dissolution            Carina V, Alaimo A, Rizzi M, Simoni D,
     enhancement of curcumin by hydroxypropyl-ß-                  D'Alessandro N. The antitumor activities of curcumin
     cyclodextrin complexation. Int J Pharm Pharm Sci             and of its isoxazole analogue are not affected by
     2013; 5: 401-5. (g) Mangolim CS, Moriwaki C,                 multiple gene expression changes in an MDR model
     Nogueira AC, Sato F, Baesso ML, Neto AM, Matioli             of the MCF-7 breast cancer cell line: Analysis of the
     G. Curcumin-ß-cyclodextrin inclusion complex:                possible molecular basis. Int J Mol Med 2007; 20:
     stability, solubility, characterisation by FT-IR, FT-        329-35.
     Raman, X-ray diffraction and photoacoustic              143. Kumar KA, Jayaroopa P. Isoxazoles: molecules with
     spectroscopy, and food application. Food Chem 2014;          potential medicinal properties. Int J Pharm Chem Biol
     153: 361-70. (h) Jantarat C, Sirathanarun P,                 Sci 2013; 3: 294-304.
     Ratanapongsai S, Watcharakan P, Sunyapong S,            144.Ahsan MJ, Khalilullah H, Yasmin S, Jadav SS,
     Wadu A. Curcumin-hydroxypropyl-ß-cyclodextrin                Govindasamy J. Synthesis, characterisation, and in
     inclusion complex preparation methods: effect of             vitro anticancer activity of curcumin analogues
     common solvent evaporation, freeze drying, and pH            bearing pyrazole/pyrimidine ring targeting EGFR
     shift on solubility and stability of curcumin. Trop J        tyrosine kinase. Bio Med Res Int 2013; 239354: 1-14.
     Pharm Res 2014; 13: 1215-23. (i) Kongprathet T,         145.Hamed OA, Mehdawi N, Taha AA, Hamed EM, Al-
     Wanichwecharungruang S. Sustaining guest                     Nuri MA, Hussein AS. Synthesis and antibacterial
     molecules on bio-surfaces by grafting the surfaces           activity of novel curcumin derivatives containing
     with cyclodextrins. Carbohydrate Pol 2015; 119: 110-         heterocyclic moiety. Iran J Pharm Res 2013; 12: 47-
     7.                                                           56.
                                                             146.Sundarananthavalli S, Kulandaisamy A, Christopher
135.Harada T, McTernan HL, Pham DT, Lincoln SF, Kee               CC. Synthesis, characterization, analgesic, anti-
     TW. Femtosecond transient absorption spectroscopy            inflammatory, anti-ulcer, wound healing and
     of the medicinal agent curcumin in diamide linked ?-         antimicrobial effects of curcuminoids. Int J ChemTech
     cyclodextrin dimers. J Phys Chem 2015; B 119: 2425-          Res 2011; 3: 2040-6.
     33.                                                     147.Cornago P, Claramunt RM, Bouissane L, Alkorta I,
                                                                  Elguero J. A study of the tautomerism of ß-dicarbonyl
136.Mareeswaran PM, Babu E, Sathish V, Kim B, Woo                 compounds with special emphasis on curcuminoids.
     SI, Rajagopal S. p-Sulfonatocalix[4]arene as a carrier       Tetrahedron 2008; 64: 8089-94.
     for curcumin. New J Chem 2014; 38: 1336-45.             148. Cornago P, Cabildo P, Sanz D, Claramunt RM,
                                                                  Torralba MC, Torres MR, Elguero J. Structures of
137.Magro M, Campos R, Baratella D, Lima G, Holà K,               hemicurcuminoids in the solid state and in solution.
     Divoky C, Stollberger R, Malina O, Aparicio C,               Eur J Org Chem 2013; 6043-54.
     Zoppellaro G, Zboril R, Vianello F. A magnetically      149. Nieto CI, Cabildo P, Claramunt RM, Cornago P, Sanz
     drivable nanovehicle for curcumin wih antioxidant            D, Torralba MC, Torres MR, Ferraro M, Alkorta I,
     capacity and MRI relaxation properties. Chem Eur J           Elguero J. The structure of ß-diketones related to
     2014; 20: 11913-20.                                          curcumin determined by X-ray crystallography, NMR
                                                                  (solution and solid state) and theoretical calculations.
138.(a) Arezki A, Brulé E, Jaouen G. Synthesis of the First       Struct Chem 2015; DOI: 10.1007/s11224-015-0704-7.
     Ferrocenyl Derivatives of Curcuminoids.                 150. Sánchez Alegre YR. Determinación in vitro del
     Organometallics 2009; 39: 1606-9. (b) Li PZ, Liu ZQ.         carácter antioxidante y neuroprotector de nuevas
     Ferrocenyl-substituted curcumin: can it influence            dicetonas aromáticas antioxidantes en condiciones de
     antioxidant ability to protect DNA? Eur J Med Chem           estrés oxidativo. Trabajo Fin de Máster. Proyecto de
     2011; 46: 1821-6. (c) Arezki A, Chabot G, Quentin L,         Investigación, Máster en Ciencia y Tecnología
     Scherman D, Jaouen G, Brulé E. Synthesis and                 Química, UNED, Septiembre 2015.
     biological evaluation of novel ferrocenyl curcuminoid
     derivatives. Med Chem Comm 2011; 2: 190-5.                       @Real Academia Nacional de Farmacia. Spain

139. Huang QM, Wang SW, Li Q, Pan W, Deng PX, Zhou
     H, Pan ZQ. Synthesis and characterization of
     curcumin bridged porphyrins as photosensitizers.
     Chem J Chin Univ 2012; 33: 732-7.

140.Khan MA, El-Khatib R, Rainsford KD, Whitehouse
     MW. Synthesis and antiinflammatory properties of
     some aromatic and heterocyclic aromatic
     curcuminoids. Bioorg Chem 2012; 40: 30-8.

141.Claramunt RM, Nieto CI, Sanz D, Elguero J.
     Curcumin derived pyrazoles and related compounds.
     Afinidad 2015; [enviado para su publicación].

142. Poma P, Notarbartolo M, Labbozzetta M, Maurici A,

    310
   34   35   36   37   38   39   40   41   42   43   44