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Volumn 53, Issue 11, 2010, Pages 2304-2310

Preparation and characterization of inclusion complexes of antitumor camptothecin with cucurbit[n = 7, 8]urils

Author keywords

camptothecin; complexes; cucurbit n uril (n = 7, 8); dissolution properties; stability

Indexed keywords

ANTI-TUMORS; ANTICANCER DRUG; AQUEOUS SOLUBILITY; AQUEOUS SOLUTIONS; CAMPTOTHECINS; CO-EVAPORATION METHOD; COMPLEXES; CUCURBIT[N]URIL (N = 7, 8); DISSOLUTION RATES; FOURIER TRANSFORMATIONS; INCLUSION COMPLEX; PHOSPHATE BUFFER SOLUTIONS; PHYSICAL MIXTURES; POWDER X RAY DIFFRACTION; SOLID INCLUSION COMPLEXES; STABILITY CONSTANTS;

EID: 78649343690     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-010-4067-z     Document Type: Article
Times cited : (15)

References (29)
  • 1
    • 7144248725 scopus 로고
    • Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminata1
    • 1:CAS:528:DyaF28XkvVant7c%3D 10.1021/ja00968a057
    • M.E. Wall M.C. Wani C.E. Cook 1966 Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminata1 J Am Chem Soc 88 3888 3890 1:CAS:528:DyaF28XkvVant7c%3D 10.1021/ja00968a057
    • (1966) J Am Chem Soc , vol.88 , pp. 3888-3890
    • Wall, M.E.1    Wani, M.C.2    Cook, C.E.3
  • 3
    • 65349103770 scopus 로고    scopus 로고
    • Review on supermolecules as chemical drugs
    • 1:CAS:528:DC%2BD1MXksFaksL8%3D 10.1007/s11426-009-0103-2
    • C.H. Zhou F.F. Zhang L.L. Gan Y.Y. Zhang R.X. Geng 2009 Review on supermolecules as chemical drugs Sci China Series B-Chem 52 4 415 458 1:CAS:528:DC%2BD1MXksFaksL8%3D 10.1007/s11426-009-0103-2
    • (2009) Sci China Series B-Chem , vol.52 , Issue.4 , pp. 415-458
    • Zhou, C.H.1    Zhang, F.F.2    Gan, L.L.3    Zhang, Y.Y.4    Geng, R.X.5
  • 4
    • 0032119526 scopus 로고    scopus 로고
    • Cyclodextrin drug carrier systems
    • 1:CAS:528:DyaK1cXksV2itr0%3D 10.1021/cr970025p
    • K. Uekama F. Hirayama T. Irie 1998 Cyclodextrin drug carrier systems Chem Rev 98 2045 2076 1:CAS:528:DyaK1cXksV2itr0%3D 10.1021/cr970025p
    • (1998) Chem Rev , vol.98 , pp. 2045-2076
    • Uekama, K.1    Hirayama, F.2    Irie, T.3
  • 5
    • 65249158453 scopus 로고    scopus 로고
    • Design of artificial nucleases and studies of their interaction with DNA
    • 10.1007/s11426-009-0029-8
    • J.J. Zhabg Y. Shao L. Wei Y. Li X. Sheng F. Liu G.Y. Lu 2009 Design of artificial nucleases and studies of their interaction with DNA Sci China Series B-Chem 52 4 402 414 10.1007/s11426-009-0029-8
    • (2009) Sci China Series B-Chem , vol.52 , Issue.4 , pp. 402-414
    • Zhabg, J.J.1    Shao, Y.2    Wei, L.3    Li, Y.4    Sheng, X.5    Liu, F.6    Lu, G.Y.7
  • 6
    • 0034716334 scopus 로고    scopus 로고
    • New cucurbituril homologues: Syntheses, isolation, characterization, and X-ray crystal structures of cucurbit[n]uril (n = 5, 7, and 8)
    • 1:CAS:528:DC%2BD3cXhs1Gjtw%3D%3D 10.1021/ja993376p
    • J. Kim I.S. Jung S.Y. Kim E. Lee J. Kang K.S. Sakamoto K. Yamaguchi K. Kim 2000 New cucurbituril homologues: Syntheses, isolation, characterization, and X-ray crystal structures of cucurbit[n]uril (n = 5, 7, and 8) J Am Chem Soc 122 540 541 1:CAS:528:DC%2BD3cXhs1Gjtw%3D%3D 10.1021/ja993376p
    • (2000) J Am Chem Soc , vol.122 , pp. 540-541
    • Kim, J.1    Jung, I.S.2    Kim, S.Y.3    Lee, E.4    Kang, J.5    Sakamoto, K.S.6    Yamaguchi, K.7    Kim, K.8
  • 7
    • 0142042903 scopus 로고    scopus 로고
    • Cucurbit[n]uril analogues
    • 1:CAS:528:DC%2BD3sXnt1Ols7Y%3D 10.1021/ol035468w
    • J. Lagona J.C. Fettinger L. Isaacs 2003 Cucurbit[n]uril analogues Org Lett 5 3745 3747 1:CAS:528:DC%2BD3sXnt1Ols7Y%3D 10.1021/ol035468w
    • (2003) Org Lett , vol.5 , pp. 3745-3747
    • Lagona, J.1    Fettinger, J.C.2    Isaacs, L.3
  • 8
    • 0041472445 scopus 로고    scopus 로고
    • Cucurbituril homologues and derivatives: New opportunities in supramolecular chemistry
    • 1:CAS:528:DC%2BD3sXjvFCnt7s%3D 10.1021/ar020254k
    • J.W. Lee S. Samal N. Selvapalam H.J. Kim K. Kim 2003 Cucurbituril homologues and derivatives: New opportunities in supramolecular chemistry Acc Chem Res 36 621 630 1:CAS:528:DC%2BD3sXjvFCnt7s%3D 10.1021/ar020254k
    • (2003) Acc Chem Res , vol.36 , pp. 621-630
    • Lee, J.W.1    Samal, S.2    Selvapalam, N.3    Kim, H.J.4    Kim, K.5
  • 9
    • 33846669779 scopus 로고    scopus 로고
    • Functionalized cucurbiturils and their applications
    • 1:CAS:528:DC%2BD2sXhtVKltbw%3D 10.1039/b603088m
    • K. Kim N. Selvapaam Y.H. Ko K.M. Park D. Kim J. Kim 2007 Functionalized cucurbiturils and their applications Chem Soc Rev 36 267 279 1:CAS:528:DC%2BD2sXhtVKltbw%3D 10.1039/b603088m
    • (2007) Chem Soc Rev , vol.36 , pp. 267-279
    • Kim, K.1    Selvapaam, N.2    Ko, Y.H.3    Park, K.M.4    Kim, D.5    Kim, J.6
  • 10
    • 0034306199 scopus 로고    scopus 로고
    • Self-assembled architectures from glycoluril
    • 1:CAS:528:DC%2BD3cXlvVKisL8%3D 10.1021/ie000079g
    • J.A. Elemans A.W. Rowan A.E. Nolte 2000 Self-assembled architectures from glycoluril Ind Eng Chem Res 39 3419 3428 1:CAS:528:DC%2BD3cXlvVKisL8%3D 10.1021/ie000079g
    • (2000) Ind Eng Chem Res , vol.39 , pp. 3419-3428
    • Elemans, J.A.1    Rowan, A.W.2    Nolte, A.E.3
  • 11
    • 18444369800 scopus 로고
    • Cucurbituril: Supramolecular perspectives for an old ligand
    • 1:CAS:528:DyaK2cXlsFKkuro%3D 10.1007/BF00708781
    • P. Cintas 1994 Cucurbituril: Supramolecular perspectives for an old ligand J Incl Phenom Molec Reco Chem 17 205 220 1:CAS:528:DyaK2cXlsFKkuro%3D 10.1007/BF00708781
    • (1994) J Incl Phenom Molec Reco Chem , vol.17 , pp. 205-220
    • Cintas, P.1
  • 12
    • 0041429631 scopus 로고    scopus 로고
    • Facile synthesis of cucurbit[n]uril derivatives via direct functionalization: Expanding utilization of cucurbit[n]uril
    • 1:CAS:528:DC%2BD3sXmtVSlsro%3D 10.1021/ja036536c
    • S.Y. Jon N. Selvapalam D.H. Oh J.K. Kang S.Y. Kim Y.J. Jeon J.W. Lee K. Kim 2003 Facile synthesis of cucurbit[n]uril derivatives via direct functionalization: Expanding utilization of cucurbit[n]uril J Am Chem Soc 125 10186 10187 1:CAS:528:DC%2BD3sXmtVSlsro%3D 10.1021/ja036536c
    • (2003) J Am Chem Soc , vol.125 , pp. 10186-10187
    • Jon, S.Y.1    Selvapalam, N.2    Oh, D.H.3    Kang, J.K.4    Kim, S.Y.5    Jeon, Y.J.6    Lee, J.W.7    Kim, K.8
  • 13
    • 3142670062 scopus 로고    scopus 로고
    • Multi-nuclear platinum complexes encapsulated in cucurbit[n]uril as an approach to reduce toxicity in cancer treatment
    • Wheate NJ, Day AI, Blanch RJ, Arnold AP, Cullinance C, Collins JG. Multi-nuclear platinum complexes encapsulated in cucurbit[n]uril as an approach to reduce toxicity in cancer treatment. Chem Commun, 2004, 1424-1425
    • (2004) Chem Commun , pp. 1424-1425
    • Wheate, N.J.1    Day, A.I.2    Blanch, R.J.3    Arnold, A.P.4    Cullinance, C.5    Collins, J.G.6
  • 14
    • 20844431667 scopus 로고    scopus 로고
    • Novel molecular drug carrier: Encapsulation of oxaliplatin in cucurbit[7]uril and its effects on stability and reactivity of the drug
    • 1:CAS:528:DC%2BD2MXksFaquro%3D 10.1039/b504487a
    • Y.J. Jeon S.Y. Kim Y.H. Ko S. Sakamoto K. Yamagchi K. Kim 2005 Novel molecular drug carrier: Encapsulation of oxaliplatin in cucurbit[7]uril and its effects on stability and reactivity of the drug Org Biomol Chem 3 2122 2125 1:CAS:528:DC%2BD2MXksFaquro%3D 10.1039/b504487a
    • (2005) Org Biomol Chem , vol.3 , pp. 2122-2125
    • Jeon, Y.J.1    Kim, S.Y.2    Ko, Y.H.3    Sakamoto, S.4    Yamagchi, K.5    Kim, K.6
  • 15
    • 41249091351 scopus 로고    scopus 로고
    • Inclusion interaction between cucurbit[7]uril with Adenine and its derivatives
    • 1:CAS:528:DC%2BD1cXjsFCntLo%3D 10.1080/10610270701218570
    • Y. Huang S.F. Xue Z. Tao 2008 Inclusion interaction between cucurbit[7]uril with Adenine and its derivatives Supramol Chem 20 279 287 1:CAS:528:DC%2BD1cXjsFCntLo%3D 10.1080/10610270701218570
    • (2008) Supramol Chem , vol.20 , pp. 279-287
    • Huang, Y.1    Xue, S.F.2    Tao, Z.3
  • 16
    • 33847645406 scopus 로고    scopus 로고
    • A study on the supramolecular structure of inclusion complex of β-cyclodextrin with prazosin hydrochloride
    • 1:CAS:528:DC%2BD2sXislWhu74%3D 10.1016/j.carbpol.2006.11.007
    • L.X. Liu S.Y. Zhu 2007 A study on the supramolecular structure of inclusion complex of β-cyclodextrin with prazosin hydrochloride Carbohyd Polym 68 472 476 1:CAS:528:DC%2BD2sXislWhu74%3D 10.1016/j.carbpol.2006.11.007
    • (2007) Carbohyd Polym , vol.68 , pp. 472-476
    • Liu, L.X.1    Zhu, S.Y.2
  • 17
    • 0016422844 scopus 로고
    • The concept of dissolution efficiency
    • 1:CAS:528:DyaE2MXhsVCru7o%3D
    • K.A. Khan 1975 The concept of dissolution efficiency J Pharm Pharmacol 27 48 49 1:CAS:528:DyaE2MXhsVCru7o%3D
    • (1975) J Pharm Pharmacol , vol.27 , pp. 48-49
    • Khan, K.A.1
  • 18
    • 33750531897 scopus 로고    scopus 로고
    • Molecular recognition of aminoacid by cucurbiturils
    • 1:CAS:528:DC%2BD28XlsVOgur8%3D
    • H. Cong L.L. Tao Y.H. Yu F. Yang Y. Du S.F. Xue Z. Tao 2006 Molecular recognition of aminoacid by cucurbiturils Acta Chim Sin 64 989 996 1:CAS:528:DC%2BD28XlsVOgur8%3D
    • (2006) Acta Chim Sin , vol.64 , pp. 989-996
    • Cong, H.1    Tao, L.L.2    Yu, Y.H.3    Yang, F.4    Du, Y.5    Xue, S.F.6    Tao, Z.7
  • 19
    • 0035861391 scopus 로고    scopus 로고
    • Thermal analysis of cyclodextrins and their inclusion compounds
    • 1:CAS:528:DC%2BD3MXos1ChsL0%3D 10.1016/S0040-6031(01)00665-7
    • F. Giordano C. Novak J.R. Moyano 2001 Thermal analysis of cyclodextrins and their inclusion compounds Therm Acta 380 123 151 1:CAS:528: DC%2BD3MXos1ChsL0%3D 10.1016/S0040-6031(01)00665-7
    • (2001) Therm Acta , vol.380 , pp. 123-151
    • Giordano, F.1    Novak, C.2    Moyano, J.R.3
  • 20
    • 0032302537 scopus 로고    scopus 로고
    • Determination of the stability of omeprazole by means of different scanning calorimetry
    • 1:CAS:528:DyaK1cXns1ahsLY%3D 10.1007/BF02719008
    • M.A. Ruiz I. Reyes A. Parera V. Gallardo 1998 Determination of the stability of omeprazole by means of different scanning calorimetry J Therm Anal 51 29 35 1:CAS:528:DyaK1cXns1ahsLY%3D 10.1007/BF02719008
    • (1998) J Therm Anal , vol.51 , pp. 29-35
    • Ruiz, M.A.1    Reyes, I.2    Parera, A.3    Gallardo, V.4
  • 21
    • 26644448966 scopus 로고    scopus 로고
    • Physico-chemical characterization of benzocaine-β-cyclodextrin inclusion complexes
    • 1:CAS:528:DC%2BD2MXhtFWht7%2FN 10.1016/j.jpba.2005.06.010
    • L.M.A. Pinto L.F. Fraceto M.H.A. Santana T.A. Pertinhez S.O. Junior E.D. Paula 2005 Physico-chemical characterization of benzocaine-β-cyclodextrin inclusion complexes J Pharm Biom Anal 39 956 963 1:CAS:528:DC%2BD2MXhtFWht7%2FN 10.1016/j.jpba.2005.06.010
    • (2005) J Pharm Biom Anal , vol.39 , pp. 956-963
    • Pinto, L.M.A.1    Fraceto, L.F.2    Santana, M.H.A.3    Pertinhez, T.A.4    Junior, S.O.5    Paula, E.D.6
  • 22
    • 23944469637 scopus 로고    scopus 로고
    • Inclusion complex of trimethoprim with β-cyclodextrin (short communication)
    • 10.1016/j.jpba.2005.05.011
    • L. Ning Y.H. Zhang Y.N. Wu X.L. Xiong Y.H. Zhang 2005 Inclusion complex of trimethoprim with β-cyclodextrin (short communication) J Pharm Biom Anal 39 824 829 10.1016/j.jpba.2005.05.011
    • (2005) J Pharm Biom Anal , vol.39 , pp. 824-829
    • Ning, L.1    Zhang, Y.H.2    Wu, Y.N.3    Xiong, X.L.4    Zhang, Y.H.5
  • 23
    • 13544258798 scopus 로고    scopus 로고
    • Preformulation study of the inclusion complex warfarin-[beta]- cyclodextrin
    • 1:CAS:528:DC%2BD2MXhtFejtLY%3D 10.1016/j.ijpharm.2004.11.013
    • G. Zingone F. Rubessa 2005 Preformulation study of the inclusion complex warfarin-[beta]-cyclodextrin Int J Pharm 291 3 10 1:CAS:528:DC%2BD2MXhtFejtLY%3D 10.1016/j.ijpharm.2004.11.013
    • (2005) Int J Pharm , vol.291 , pp. 3-10
    • Zingone, G.1    Rubessa, F.2
  • 24
    • 18044396190 scopus 로고    scopus 로고
    • Characterization of the 13-cis-retinoic acid/cyclodextrin inclusion complexes by phase solubility, photostability, physicochemical and computational analysis
    • 1:CAS:528:DC%2BD2MXjs1Knu7c%3D 10.1016/j.ejps.2005.01.021
    • K.L. Yap X. Liu J.C. Thenmozhiyal P.C. Ho 2005 Characterization of the 13-cis-retinoic acid/cyclodextrin inclusion complexes by phase solubility, photostability, physicochemical and computational analysis Eur J Pharm Sci 25 49 56 1:CAS:528:DC%2BD2MXjs1Knu7c%3D 10.1016/j.ejps.2005.01.021
    • (2005) Eur J Pharm Sci , vol.25 , pp. 49-56
    • Yap, K.L.1    Liu, X.2    Thenmozhiyal, J.C.3    Ho, P.C.4
  • 25
    • 17444420664 scopus 로고    scopus 로고
    • Cyclodextrin complexes of valdecoxib: Properties and anti-inflammatory activity in rat
    • 1:CAS:528:DC%2BD2MXjsVehsbg%3D 10.1016/j.ejpb.2004.12.005
    • K. Rajendrakumar S. Madhusudan T. Pralhad 2005 Cyclodextrin complexes of valdecoxib: Properties and anti-inflammatory activity in rat Eur J Pharm Biopharm 60 39 46 1:CAS:528:DC%2BD2MXjsVehsbg%3D 10.1016/j.ejpb.2004.12.005
    • (2005) Eur J Pharm Biopharm , vol.60 , pp. 39-46
    • Rajendrakumar, K.1    Madhusudan, S.2    Pralhad, T.3
  • 26
    • 0025258947 scopus 로고
    • Studies of cyclodextrin inclusion complexes. I. The salbutamol- cyclodextrin complex as studied by phase solubility and DSC
    • 10.1016/0378-5173(90)90132-N
    • H.C. Marques J. Hadgraft I. Kellaway 1990 Studies of cyclodextrin inclusion complexes. I. The salbutamol-cyclodextrin complex as studied by phase solubility and DSC Int J Pharm 63 259 266 10.1016/0378-5173(90)90132-N
    • (1990) Int J Pharm , vol.63 , pp. 259-266
    • Marques, H.C.1    Hadgraft, J.2    Kellaway, I.3
  • 27
    • 29144436533 scopus 로고    scopus 로고
    • Synthesis and spectral characterization of 10-hydroxycamptothecin
    • 1:CAS:528:DC%2BD2MXhtlWjtL%2FO
    • C.Y. Xu M.Z. Huang C.X. Xue 2005 Synthesis and spectral characterization of 10-hydroxycamptothecin Spectrosc Spect Anal 25 1772 1774 1:CAS:528: DC%2BD2MXhtlWjtL%2FO
    • (2005) Spectrosc Spect Anal , vol.25 , pp. 1772-1774
    • Xu, C.Y.1    Huang, M.Z.2    Xue, C.X.3
  • 28
    • 34547692974 scopus 로고    scopus 로고
    • Solid-state characterization and dissolution profiles of the inclusion complexes of omeprazole with native and chemically modified β-cyclodextrin
    • 10.1016/j.ejpb.2007.03.005
    • A. Figuerias R.A. Carvalho L. Ribeiro J.J. Torres-Labandeira F.J.B. Veiga 2007 Solid-state characterization and dissolution profiles of the inclusion complexes of omeprazole with native and chemically modified β-cyclodextrin Eur J Pharm Biopharm 67 531 539 10.1016/j.ejpb.2007.03.005
    • (2007) Eur J Pharm Biopharm , vol.67 , pp. 531-539
    • Figuerias, A.1    Carvalho, R.A.2    Ribeiro, L.3    Torres-Labandeira, J.J.4    Veiga, F.J.B.5
  • 29
    • 0035935691 scopus 로고    scopus 로고
    • Design and optimization of 20-o-linked camptothecin glycoconjugates as anticancer agents
    • 1:CAS:528:DC%2BD3MXnslOhsbY%3D 10.1021/jm010893l
    • H.G. Lerchen J. Baumgarten K.V.D. Bruch T.E. Lehmann M. Sperzel G. Kempka H.H. Fiebig 2001 Design and optimization of 20-o-linked camptothecin glycoconjugates as anticancer agents J Med Chem 44 4186 4195 1:CAS:528:DC%2BD3MXnslOhsbY%3D 10.1021/jm010893l
    • (2001) J Med Chem , vol.44 , pp. 4186-4195
    • Lerchen, H.G.1    Baumgarten, J.2    Bruch, K.V.D.3    Lehmann, T.E.4    Sperzel, M.5    Kempka, G.6    Fiebig, H.H.7


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