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Volumn 21, Issue 3, 2003, Pages 291-298

Effect of valspodar on the pharmacokinetics of unbound paclitaxel

Author keywords

Disposition; P glycoprotein; Paclitaxel; Resistance; Valspodar

Indexed keywords

GLYCOPROTEIN P; GLYCOPROTEIN P INHIBITOR; PACLITAXEL; PROTEIN INHIBITOR; UNCLASSIFIED DRUG; VALSPODAR;

EID: 0345714781     PISSN: 01676997     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1025412509730     Document Type: Article
Times cited : (11)

References (43)
  • 1
    • 0036364467 scopus 로고    scopus 로고
    • Multidrug resistance in cancer: Role of AT-dependent transporters
    • Gottesman MM, Fojo T, Bates S: Multidrug resistance in cancer: role of AT-dependent transporters. Nature Rev Cancer 2: 48-58, 2002
    • (2002) Nature Rev Cancer , vol.2 , pp. 48-58
    • Gottesman, M.M.1    Fojo, T.2    Bates, S.3
  • 2
    • 0033873755 scopus 로고    scopus 로고
    • Development of multidrug-resistance convertors: Sense or nonsense?
    • Van Zuylen L, Nooter K, Sparreboom A, Verweij J: Development of multidrug-resistance convertors: sense or nonsense? Invest New Drugs 18: 205-220, 2000
    • (2000) Invest New Drugs , vol.18 , pp. 205-220
    • Van Zuylen, L.1    Nooter, K.2    Sparreboom, A.3    Verweij, J.4
  • 3
    • 0034496578 scopus 로고    scopus 로고
    • Does P-glycoprotein play a role in anticancer drug pharmacokinetics?
    • Sparreboom A, Nooter K: Does P-glycoprotein play a role in anticancer drug pharmacokinetics? Drug Resis Updates 3: 357-363, 2000
    • (2000) Drug Resis Updates , vol.3 , pp. 357-363
    • Sparreboom, A.1    Nooter, K.2
  • 5
    • 0023921505 scopus 로고
    • Cyclosporine metabolism in human liver: Identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugs
    • Kronbach T, Fischer V, Meyer UA: Cyclosporine metabolism in human liver: identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugs. Clin Pharmacol Ther 43: 630-635, 1988
    • (1988) Clin Pharmacol Ther , vol.43 , pp. 630-635
    • Kronbach, T.1    Fischer, V.2    Meyer, U.A.3
  • 6
    • 0345084436 scopus 로고    scopus 로고
    • The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A: Implications for drug-drug interactions and pharmacological activity of the main metabolite
    • Fischer V, Rodriguez-Gaston A, Heitz F, Tynes R, Hauck C, Cohen D, Vickers AE: The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A: implications for drug-drug interactions and pharmacological activity of the main metabolite. Drug Metab Dispos 26: 802-811, 1998
    • (1998) Drug Metab Dispos , vol.26 , pp. 802-811
    • Fischer, V.1    Rodriguez-Gaston, A.2    Heitz, F.3    Tynes, R.4    Hauck, C.5    Cohen, D.6    Vickers, A.E.7
  • 7
    • 0026014503 scopus 로고
    • In vivo circumvention of P-glycoprotein mediated multidrug resistance of tumor cells with SDZ PSC 833
    • Boesch D, Gaveriaux C, Jachezs B, Poutier-Manzanedo A, Bollinger P, Loor F: In vivo circumvention of P-glycoprotein mediated multidrug resistance of tumor cells with SDZ PSC 833. Cancer Res 51: 4226-4233, 1991
    • (1991) Cancer Res , vol.51 , pp. 4226-4233
    • Boesch, D.1    Gaveriaux, C.2    Jachezs, B.3    Poutier-Manzanedo, A.4    Bollinger, P.5    Loor, F.6
  • 10
    • 0027957132 scopus 로고
    • Metabolism of taxol by human hepatic microsomes and liver slices: Participation of cytochrome P 450 3A4 and an unknown P450 enzyme
    • Harris JW, Rahman A, Kim BR, Guengerich FP, Collins JM: Metabolism of taxol by human hepatic microsomes and liver slices: participation of cytochrome P450 3A4 and an unknown P450 enzyme. Cancer Res 54: 4026-4035, 1994
    • (1994) Cancer Res , vol.54 , pp. 4026-4035
    • Harris, J.W.1    Rahman, A.2    Kim, B.R.3    Guengerich, F.P.4    Collins, J.M.5
  • 13
    • 0032559438 scopus 로고    scopus 로고
    • Determination of paclitaxel in human plasma using single solvent extraction prior to isocratic reversed-phase high-performance liquid chromatography with ultraviolet detection
    • Sparreboom A, De Bruijn P, Nooter K, Loos WJ, Stoter G, Verweij J: Determination of paclitaxel in human plasma using single solvent extraction prior to isocratic reversed-phase high-performance liquid chromatography with ultraviolet detection. J Chromatogr B 705: 159-164, 1998
    • (1998) J Chromatogr B , vol.705 , pp. 159-164
    • Sparreboom, A.1    De Bruijn, P.2    Nooter, K.3    Loos, W.J.4    Stoter, G.5    Verweij, J.6
  • 15
    • 0032144286 scopus 로고    scopus 로고
    • Linearized colorimetric assay for Cremophor EL application to pharmacokinetics after 1-hour paclitaxel infusions
    • Brouwer E, Verweij J, Hauns B, Loos WJ, Nooter K, Mross K, Stoter G, Sparreboom A: Linearized colorimetric assay for Cremophor EL. application to pharmacokinetics after 1-hour paclitaxel infusions. Anal Biochem 261: 198-202, 1998
    • (1998) Anal Biochem , vol.261 , pp. 198-202
    • Brouwer, E.1    Verweij, J.2    Hauns, B.3    Loos, W.J.4    Nooter, K.5    Mross, K.6    Stoter, G.7    Sparreboom, A.8
  • 20
    • 0033926580 scopus 로고    scopus 로고
    • Interrelationships of paclitaxel disposition, infusion duration and Cremophor EL kinetics in cancer patients
    • Van Zuylen L, Gianni L, Verweij J, Mross K, Brouwer E, Loos WJ, Sparreboom A: Interrelationships of paclitaxel disposition, infusion duration and Cremophor EL kinetics in cancer patients. Anticancer Drugs 11: 3331-3337, 2000
    • (2000) Anticancer Drugs , vol.11 , pp. 3331-3337
    • Van Zuylen, L.1    Gianni, L.2    Verweij, J.3    Mross, K.4    Brouwer, E.5    Loos, W.J.6    Sparreboom, A.7
  • 24
    • 0034901124 scopus 로고    scopus 로고
    • A phase I trial of doxorubicin, paclitaxel, and valspodar (PSC 833), a modulator of multidrug resistance
    • Advani R, Fisher GA, Lum BL, Hausdorff J, Halsey J, Litchman M, Sikic BI: A phase I trial of doxorubicin, paclitaxel, and valspodar (PSC 833), a modulator of multidrug resistance. Clin Cancer Res 7: 1221-1229, 2001
    • (2001) Clin Cancer Res , vol.7 , pp. 1221-1229
    • Advani, R.1    Fisher, G.A.2    Lum, B.L.3    Hausdorff, J.4    Halsey, J.5    Litchman, M.6    Sikic, B.I.7
  • 26
    • 0028894301 scopus 로고
    • Nonlinear pharmacokinetics and metabolism of paclitaxel and its pharmacokinetic/pharmacodynamic relationships in humans
    • Gianni L, Kearns CM, Giani A, Capri G, Vigano L, Locatelli A, Bonadonna G, Egorin MJ: Nonlinear pharmacokinetics and metabolism of paclitaxel and its pharmacokinetic/pharmacodynamic relationships in humans. J Clin Oncol 13: 180-190, 1995
    • (1995) J Clin Oncol , vol.13 , pp. 180-190
    • Gianni, L.1    Kearns, C.M.2    Giani, A.3    Capri, G.4    Vigano, L.5    Locatelli, A.6    Bonadonna, G.7    Egorin, M.J.8
  • 28
    • 0034880214 scopus 로고    scopus 로고
    • Cremophor EL: The downsides and potential of vehicle selection for drug formulation
    • Gelderblom H, Verweij J, Nooter K, Sparreboom A: Cremophor EL: the downsides and potential of vehicle selection for drug formulation. Eur J Cancer 37: 1587-1595, 2001
    • (2001) Eur J Cancer , vol.37 , pp. 1587-1595
    • Gelderblom, H.1    Verweij, J.2    Nooter, K.3    Sparreboom, A.4
  • 29
  • 31
    • 0029921281 scopus 로고    scopus 로고
    • Nonlinear pharmacokinetics of paclitaxel in mice results from the pharmaceutical vehicle Cremophor EL
    • Sparreboom A, Van Tellingen O, Nooijen WJ, Beijnen JH: Nonlinear pharmacokinetics of paclitaxel in mice results from the pharmaceutical vehicle Cremophor EL. Cancer Res 56: 2112-2115, 1996
    • (1996) Cancer Res , vol.56 , pp. 2112-2115
    • Sparreboom, A.1    Van Tellingen, O.2    Nooijen, W.J.3    Beijnen, J.H.4
  • 34
  • 35
    • 0029044165 scopus 로고
    • Paclitaxel pharmacokinetics and pharmacodynamics
    • Kearns CM, Gianni L, Egorin MJ: Paclitaxel pharmacokinetics and pharmacodynamics. Semin Oncol 22: 16-23, 1995
    • (1995) Semin Oncol , vol.22 , pp. 16-23
    • Kearns, C.M.1    Gianni, L.2    Egorin, M.J.3
  • 36
    • 0034896260 scopus 로고    scopus 로고
    • The P-glycoprotein antagonist PSC 833 increases the plasma concentrations of 6α-hydroxypaclitaxel, a major metabolite of paclitaxel
    • Kang MH, Figg WD, Ando Y, Blagosklonny MV, Liewehr D, Fojo T, Bates SE: The P-glycoprotein antagonist PSC 833 increases the plasma concentrations of 6α-hydroxypaclitaxel, a major metabolite of paclitaxel. Clin Cancer Res 7: 1610-1617, 2001
    • (2001) Clin Cancer Res , vol.7 , pp. 1610-1617
    • Kang, M.H.1    Figg, W.D.2    Ando, Y.3    Blagosklonny, M.V.4    Liewehr, D.5    Fojo, T.6    Bates, S.E.7
  • 37
    • 0028036727 scopus 로고
    • Selective biotransformation of taxol to 6 alpha-hydroxytaxol by human cytochrome P450 2C8
    • Rahmani A, Korzekwa KR, Grohan J, Gonzalez FJ, Harris JW: Selective biotransformation of taxol to 6 alpha-hydroxytaxol by human cytochrome P450 2C8. Cancer Res 54: 5543-5546, 1994
    • (1994) Cancer Res , vol.54 , pp. 5543-5546
    • Rahmani, A.1    Korzekwa, K.R.2    Grohan, J.3    Gonzalez, F.J.4    Harris, J.W.5
  • 38
    • 0031940674 scopus 로고    scopus 로고
    • A general model for time-dissociated pharmacokinetic-pharmacodynamic relationship exemplified by paclitaxel myelosuppression
    • Karlsson MO, Molnar V, Bergh J, Freijs A, Larsson R: A general model for time-dissociated pharmacokinetic-pharmacodynamic relationship exemplified by paclitaxel myelosuppression. Clin Pharmacol Ther 63: 11-25, 1998
    • (1998) Clin Pharmacol Ther , vol.63 , pp. 11-25
    • Karlsson, M.O.1    Molnar, V.2    Bergh, J.3    Freijs, A.4    Larsson, R.5
  • 40
    • 0026489452 scopus 로고
    • Subpopulations of normal blood and bone marrow cells express a functional multidrug resistance phenotype
    • Drach D, Zhao S, Drach J, Mahadevia R, Gattringer C, Huber H, Andreeff M: Subpopulations of normal blood and bone marrow cells express a functional multidrug resistance phenotype. Blood 80: 2729-2734, 1992
    • (1992) Blood , vol.80 , pp. 2729-2734
    • Drach, D.1    Zhao, S.2    Drach, J.3    Mahadevia, R.4    Gattringer, C.5    Huber, H.6    Andreeff, M.7
  • 42
    • 0034016775 scopus 로고    scopus 로고
    • Effect of high-dose cyclosporine on etoposide pharmacodynamics in a trial to reverse P-glycoprotein (MDR1 gene) mediated drug resistance
    • Lum BL, Kaubisch S, Fisher GA, Brown BW, Sikic BI: Effect of high-dose cyclosporine on etoposide pharmacodynamics in a trial to reverse P-glycoprotein (MDR1 gene) mediated drug resistance. Cancer Chemother Pharmacol 45: 305-311, 2000
    • (2000) Cancer Chemother Pharmacol , vol.45 , pp. 305-311
    • Lum, B.L.1    Kaubisch, S.2    Fisher, G.A.3    Brown, B.W.4    Sikic, B.I.5
  • 43
    • 0027533571 scopus 로고
    • Restoration of taxol sensitivity of multidrug-resistance cell by the cyclosporine SDZ PSC 833 and the cyclopeptolide SDZ 280-446
    • Jachez B, Nordmann R, Loor F: Restoration of taxol sensitivity of multidrug-resistance cell by the cyclosporine SDZ PSC 833 and the cyclopeptolide SDZ 280-446. J Natl Cancer Inst 85: 478-483, 1993
    • (1993) J Natl Cancer Inst , vol.85 , pp. 478-483
    • Jachez, B.1    Nordmann, R.2    Loor, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.