Articles

Inclusion Behavior of Naringenin/β-Cyclodextrin Supramolecular Complex

  • YANG Yun-han ,
  • DU Yao ,
  • YING Fei-xiang ,
  • YANG Jun-li ,
  • XIA Da-zhen ,
  • XIA Fu-ting ,
  • YANG Li-juan
Expand
  • 1. Key Laboratory of Intelligent Supramolecular Chemistry at the University of Yunnan Province, National and Local Joint Engineering Research Center for Green Preparation Technology of Biobased Materials, School of Chemistry & Environment, Yunnan Minzu University, Kunming 650500, China;
    2. School of Electrical and Information Technology, Yunnan Minzu University, Kunming 650500, China

Received date: 2018-11-19

  Online published: 2019-01-29

Abstract

An inclusion complex of naringenin (NAR) and β-cyclodextrin (βCD) was prepared with ultrasonication. Powder X-ray diffraction (XRD) and infrared absorption spectroscopy (IR) indicated that the inclusion complex formed had some new physical/chemical properties. 1H NMR and ROESY spectroscopy revealed that the stable supramolecular inclusion complex was formed by having the benzene ring of NAR introduced into the big end of the βCD. The formation processes of NAR/βCD inclusion complex were also studied by quantum chemical calculations. It was revealed that enthalpy and hydrogen bonding weak interaction force were the driving forces behind the formation. The optimal inclusion mode obtained from energy gap and binding energy analyses were consistent with the most inclusive mode obtained from molecular docking analysis and the NMR results. These results were further confirmed by ONIOM calculation.

Cite this article

YANG Yun-han , DU Yao , YING Fei-xiang , YANG Jun-li , XIA Da-zhen , XIA Fu-ting , YANG Li-juan . Inclusion Behavior of Naringenin/β-Cyclodextrin Supramolecular Complex[J]. Chinese Journal of Magnetic Resonance, 2019 , 36(3) : 319 -330 . DOI: 10.11938/cjmr20182691

References

[1] FIELDEN S P, LEIGH D A, MCTERNAN C T, et al. Spontaneous assembly of rotaxanes from a primary amine, crown ether and electrophile[J]. J Am Chem Soc, 2018, 140(19):6049-6052.
[2] FALAISE C, MOUSSAWI M A, FLOQUET S, et al. Probing dynamic library of metal-oxo building blocks with g-cyclodextrin[J]. J Am Chem Soc, 2018, 140:11189-11201.
[3] YILDIZ Z I, CELEBIOGLU A, KILIC M E, et al. Menthol/cyclodextrin inclusion complex nanofibers:Enhanced water-solubility and high-temperature stability of menthol[J]. J Food Eng, 2018, 224:27-36.
[4] ZHAO F, YANG Y H, ZHAO X Q, et al. Study on inclusion behavior and properties of tetrahydropalmatine with β-cyclodextrin and its derivatives[J]. Chin Tradit Herbal Drugs, 2018, 49(15):3609-3618. 赵芳, 杨云汉, 赵雪秋, 等. 延胡索乙素与β-环糊精及其衍生物的包合行为研究[J]. 中草药, 2018, 49(15):3609-3618.
[5] KARPUS A, YESYPENKO O, BOIKO V, et al. Synthesis of an enantiomerically pure inherently chiral calix
[4] arene phosphonic acid and its evaluation as organocatalyst[J]. J Org Chem, 2018, 83(3):1146-1153.
[6] ZOHEB H, HAILEY F T, EMILY F B, et al. Molecular recognition of methionine-terminated peptides by cucurbit
[8] uril[J]. J Am Chem Soc, 2018, 140:12263-12269.
[7] JIE K C, ZHOU Y J, LI E R, et al. Linear positional isomer sorting in nonporous adaptive crystals of a pillar
[5] arene[J]. J Am Chem Soc, 2018, 140:3190-3193.
[8] YANG L J, WANG S H, ZHOU S Y, et al. Supramolecular system of podophyllotoxin and hydroxypropyl-β-cyclodextrin:Characterization, inclusion mode, docking calculation, solubilization, stability and cytotoxic activity[J]. Mater Sci Eng C, 2017, 76:1136-1145.
[9] YANG L J, CHANG Q, ZHOU S Y, et al. Host-guest interaction between brazilin and hydroxypropyl-β-cyclodextrin:Preparation, inclusion mode, molecular modelling and characterization[J]. Dyes Pigments, 2017, 150(2018):193-201.
[10] JI P, ZHAO W M, YU T. Recent research progress of naringenin[J]. Chin J New Drugs, 2015, 12:1382-1386. 季鹏, 赵文明, 于桐. 柚皮素的最新研究进展[J]. 中国新药杂志, 2015, 12:1382-1386.
[11] SUN L J, HU X F, CHENG X, et al. NMR characterization of flavanone naringenin 7-O-glycoside diastereomer[J]. Chinese J Magn Reson, 2017, 34(4):465-473.孙丽娟, 胡小芳, 程寻, 等. 柚皮素7-O-葡萄糖苷非对映异构体的NMR波谱分析[J]. 波谱学杂志, 2017, 34(4):465-473.
[12] HATICE G A, TUBA A. Naringenin inhibits prostate cancer metastasis by blocking voltage-gated sodium channels[J]. Biomed Pharmacother, 2018, 106:770-775.
[13] MD S, GAN S Y, YONG H H, et al. In vitro neuroprotective effects of naringenin nanoemulsion against β-amyloid toxicity through the regulation of amyloidogenesis and tau phosphorylation[J]. Int J Biol Macromol, 2018, 118:1211-1219.
[14] ZAIDUN N H, THENT Z C, LATIFF A A. Combating oxidative stress disorders with citrus flavonoid:Naringenin[J]. Life Sci, 2018, 208:111-122.
[15] KARIM N, JIA Z, ZHENG X, et al. A recent review of citrus flavanone naringenin on metabolic diseases and its potential sources for high yield-production[J]. Trends Food Sci Tech, 2018, 79:35-54.
[16] ZHAO H, RONG X Y, LIU S, et al. Preparation and pharmaceutical characteristics of naringenin nanocrystals[J]. Chin Tradit Herbal Drugs, 2018, 49(13):3026-3032. 赵涵, 戎欣玉, 刘爽, 等. 柚皮素纳米晶体的制备及药剂学性质研究[J]. 中草药, 2018, 49(13):3026-3032.
[17] YANG L J, MA S X, ZHOU S Y, et al. Preparation and characterization of inclusion complexes of naringenin with β-cyclodextrin or its derivative[J]. Carbohydrate Polymers, 2013, 98(1):861-869.
[18] ZHU Q Y, HE P Z. Structural elucidation of D-camphor and β-cyclodextrin inclusion complex[J]. Chinese J Magn Reson, 2015, 32(1):87-94. 朱庆英, 何佩芝. D-樟脑与β-环糊精包合物的结构表征[J]. 波谱学杂志, 2015, 32(1):87-94.
[19] LUNDBERG M, MOROKUMA A K. The ONIOM method and its applications to enzymatic reactions[J]. Chem Rev, 2015, 115(12):5678-5796.
[20] BANI-YASEEN A D. Computational molecular perspectives on the interaction of propranolol with β-cyclodextrin in solution:Towards the drug-receptor mechanism of interaction[J]. J Mol Liqui, 2017, 227:280-290.
[21] FRISCH M J, TRUCKS G W, SCHLEGEL H B, et al. Gaussian 03, revision D. 01[OL]. Wallingford, CT:Gaussian, Inc., 2004-01-01.
[22] ZHANG C L, LIU J C, YANG W B, et al. Experimental and molecular docking investigations on the inclusion mechanism of the complex of phloridzin and hydroxypropyl-β-cyclodextrin[J]. Food Chem, 2017, 215:124-128.
[23] MORRIS G M, HUEY R, LINDSTROM W, et al. AutoDock4 and AutoDockTools4:Automated docking with selective receptor flexibility[J]. J Comput Chem, 2009, 30(16):2785-2791.
[24] ZHOU Z G, YUAN Y Y, LIU H B, et al. An NMR study on prucalopride[J]. Chinese J Magn Reson, 2018, 35(1):119-127.周中高, 元洋洋, 刘红波, 等. 普卡必利的NMR研究[J]. 波谱学杂志, 2018, 35(1):119-127.
[25] FANG H Y. Spectral analyses of a novel ibuprofen-phillygenin ester[J]. Chinese J Magn Reson, 2018, 35(1):98-108.樊宏宇. 新型连翘脂素-布洛芬酯合物的波谱学数据解析[J]. 波谱学杂志, 2018, 35(1):98-108.
[26] RAJENDIRAN N, SIVA S. Inclusion complex of sulfadimethoxine with cyclodextrins:Preparation and characterization[J]. Carbohydr Polym, 2014, 101:828-836.
[27] SIVA S, KOTHAI NAYAKI S, RAJENDIRAN N. Spectral and molecular modeling investigations of supramolecular complexes of mefenamic acid and aceclofenac with a-and b-cyclodextrin[J]. Spectrochim Acta A Mol Biomol Spectrosc, 2017, 174:349-362.
[28] HAIAHEM S, NOUAR L, DJILANI I, et al. Host-guest inclusion complex between β-cyclodextrin and paeonol:A theoretical approach[J]. C R CHIM, 2013, 16(4):372-379.
[29] GEJJI S P, TAURIAN O E, LUNELL S. Theoretical study of the short asymmetric[O…H…O] hydrogen bond in solid potassium hydrogen diformate, including electron correlation[J]. J Phys Chem, 1990, 94(11):4449-4452.
[30] STEINER T, SAENGER W. Geometry of C-H…O hydrogen bonds in carbohydrate crystal structures. Analysis of neutron diffraction data[J]. J Am Chem Soc, 1992, 114(26):10146-10154.
Outlines

/