메뉴 건너뛰기




Volumn 150, Issue 3, 2011, Pages 318-325

G3.5 PAMAM dendrimers enhance transepithelial transport of SN38 while minimizing gastrointestinal toxicity

Author keywords

7 ethyl 10 hydroxy camptothecin; Caco 2; Oral drug delivery; PAMAM dendrimers; Transepithelial transport

Indexed keywords

10-HYDROXY-CAMPTOTHECIN; CACO-2; ORAL DRUG DELIVERY; PAMAM DENDRIMERS; TRANSEPITHELIAL TRANSPORT;

EID: 79955051898     PISSN: 01683659     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jconrel.2010.11.022     Document Type: Article
Times cited : (92)

References (37)
  • 1
    • 0038387390 scopus 로고    scopus 로고
    • The dawning era of polymer therapeutics
    • DOI 10.1038/nrd1088
    • R. Duncan The dawning era of polymer therapeutics Nat. Rev. Drug Discov. 2 5 2003 347 360 (Pubitemid 37361705)
    • (2003) Nature Reviews Drug Discovery , vol.2 , Issue.5 , pp. 347-360
    • Duncan, R.1
  • 2
    • 29544448116 scopus 로고    scopus 로고
    • Polymer conjugates: Nanosized medicines for treating cancer
    • DOI 10.1016/j.tibtech.2005.11.006, PII S0167779905003021
    • M.J. Vicent, and R. Duncan Polymer conjugates: nanosized medicines for treating cancer Trends Biotechnol. 24 1 2006 39 47 (Pubitemid 43017749)
    • (2006) Trends in Biotechnology , vol.24 , Issue.1 , pp. 39-47
    • Vicent, M.J.1    Duncan, R.2
  • 3
    • 75749149269 scopus 로고    scopus 로고
    • HPMA copolymers: Origins, early developments, present, and future
    • J. Kopecek, and P. Kopeckova HPMA copolymers: origins, early developments, present, and future Adv. Drug Deliv. Rev. 62 2 2010 122 149
    • (2010) Adv. Drug Deliv. Rev. , vol.62 , Issue.2 , pp. 122-149
    • Kopecek, J.1    Kopeckova, P.2
  • 4
    • 70349988803 scopus 로고    scopus 로고
    • PEG conjugates in clinical development or use as anticancer agents: An overview
    • G. Pasut, and F.M. Veronese PEG conjugates in clinical development or use as anticancer agents: an overview Adv. Drug Deliv. Rev. 61 13 2009 1177 1188
    • (2009) Adv. Drug Deliv. Rev. , vol.61 , Issue.13 , pp. 1177-1188
    • Pasut, G.1    Veronese, F.M.2
  • 5
    • 0034461768 scopus 로고    scopus 로고
    • Drug-like properties and the causes of poor solubility and poor permeability
    • DOI 10.1016/S1056-8719(00)00107-6, PII S1056871900001076
    • C.A. Lipinski Drug-like properties and the causes of poor solubility and poor permeability J. Pharmacol. Toxicol. Meth. 44 1 2000 235 249 (Pubitemid 32239479)
    • (2000) Journal of Pharmacological and Toxicological Methods , vol.44 , Issue.1 , pp. 235-249
    • Lipinski, C.A.1
  • 6
    • 38849106122 scopus 로고    scopus 로고
    • Effective oral chemotherapy for breast cancer: Pill ars of strength
    • DOI 10.1093/annonc/mdm285
    • M. Findlay, G. von Minckwitz, and A. Wardley Effective oral chemotherapy for breast cancer: pillars of strength Ann. Oncol. 19 2 2008 212 222 (Pubitemid 351201700)
    • (2008) Annals of Oncology , vol.19 , Issue.2 , pp. 212-222
    • Findlay, M.1    Von Minckwitz, G.2    Wardley, A.3
  • 7
    • 34248393937 scopus 로고    scopus 로고
    • Comparative cost-minimisation of oral and intravenous chemotherapy for first-line treatment of non-small cell lung cancer in the UK NHS system
    • DOI 10.1007/s10198-006-0034-1, Special Issue: "Economic Evaluation in Health Care"
    • K. Le Lay, E. Myon, S. Hill, L. Riou-Franca, D. Scott, M. Sidhu, D. Dunlop, and R. Launois Comparative cost-minimisation of oral and intravenous chemotherapy for first-line treatment of non-small cell lung cancer in the UK NHS system Eur. J. Health Econ. 8 2 2007 145 151 (Pubitemid 46742894)
    • (2007) European Journal of Health Economics , vol.8 , Issue.2 , pp. 145-151
    • Le Lay, K.1    Myon, E.2    Hill, S.3    Riou-Franca, L.4    Scott, D.5    Sidhu, M.6    Dunlop, D.7    Launois, R.8
  • 8
    • 0026849216 scopus 로고
    • Potential cost savings of oral versus intravenous etoposide in the treatment of small cell lung cancer
    • S. Pashko, and D.H. Johnson Potential cost savings of oral versus intravenous etoposide in the treatment of small cell lung cancer Pharmacoeconomics 1 4 1992 293 297
    • (1992) Pharmacoeconomics , vol.1 , Issue.4 , pp. 293-297
    • Pashko, S.1    Johnson, D.H.2
  • 9
    • 4444266177 scopus 로고    scopus 로고
    • Estimating the cost of cancer: Results on the basis of claims data analyses for cancer patients diagnosed with seven types of cancer during 1999 to 2000
    • DOI 10.1200/JCO.2004.10.170
    • S. Chang, S.R. Long, L. Kutikova, L. Bowman, D. Finley, W.H. Crown, and C.L. Bennett Estimating the cost of cancer: results on the basis of claims data analyses for cancer patients diagnosed with seven types of cancer during 1999 to 2000 J. Clin. Oncol. 22 17 2004 3524 3530 (Pubitemid 41109929)
    • (2004) Journal of Clinical Oncology , vol.22 , Issue.17 , pp. 3524-3530
    • Chang, S.1    Long, S.R.2    Kutikova, L.3    Bowman, L.4    Finley, D.5    Crown, W.H.6    Bennett, C.L.7
  • 11
    • 33847017288 scopus 로고    scopus 로고
    • Dendrimers as multi-purpose nanodevices for oncology drug delivery and diagnostic imaging
    • D.A. Tomalia, L.A. Reyna, and S. Svenson Dendrimers as multi-purpose nanodevices for oncology drug delivery and diagnostic imaging Biochem. Soc. Trans. 35 Pt 1 2007 61 67
    • (2007) Biochem. Soc. Trans. , vol.35 , Issue.PART 1 , pp. 61-67
    • Tomalia, D.A.1    Reyna, L.A.2    Svenson, S.3
  • 12
    • 28744445460 scopus 로고    scopus 로고
    • Dendrimer biocompatibility and toxicity
    • DOI 10.1016/j.addr.2005.09.019, PII S0169409X0500195X, Dendrimers: a Versatile Targeting Platform
    • R. Duncan, and L. Izzo Dendrimer biocompatibility and toxicity Adv. Drug Deliv. Rev. 57 15 2005 2215 2237 (Pubitemid 41759394)
    • (2005) Advanced Drug Delivery Reviews , vol.57 , Issue.15 , pp. 2215-2237
    • Duncan, R.1    Izzo, L.2
  • 13
    • 28644434579 scopus 로고    scopus 로고
    • Designing dendrimers for biological applications
    • DOI 10.1038/nbt1171
    • C.C. Lee, J.A. MacKay, J.M. Fréchet, and F.C. Szoka Designing dendrimers for biological applications Nat. Biotechnol. 23 12 2005 1517 1526 (Pubitemid 41752929)
    • (2005) Nature Biotechnology , vol.23 , Issue.12 , pp. 1517-1526
    • Lee, C.C.1    MacKay, J.A.2    Frechet, J.M.J.3    Szoka, F.C.4
  • 14
    • 0033800262 scopus 로고    scopus 로고
    • Anionic PAMAM dendrimers rapidly cross adult rat intestine in vitro: A potential oral delivery system?
    • R. Wiwattanapatapee, B. Carreño-Gómez, N. Malik, and R. Duncan Anionic PAMAM dendrimers rapidly cross adult rat intestine in vitro: a potential oral delivery system? Pharm. Res. 17 8 2000 991 998
    • (2000) Pharm. Res. , vol.17 , Issue.8 , pp. 991-998
    • Wiwattanapatapee, R.1    Carreño-Gómez, B.2    Malik, N.3    Duncan, R.4
  • 15
    • 33845350746 scopus 로고    scopus 로고
    • Transport of poly(amidoamine) dendrimers across Caco-2 cell monolayers: Influence of size, charge and fluorescent labeling
    • DOI 10.1007/s11095-006-9122-2
    • K.M. Kitchens, R.B. Kolhatkar, P.W. Swaan, N.D. Eddington, and H. Ghandehari Transport of poly (amido amine) dendrimers across Caco-2 cell monolayers: influence of size, charge and fluorescent labeling Pharm. Res. 23 12 2006 2818 2826 (Pubitemid 44885368)
    • (2006) Pharmaceutical Research , vol.23 , Issue.12 , pp. 2818-2826
    • Kitchens, K.M.1    Kolhatkar, R.B.2    Swaan, P.W.3    Eddington, N.D.4    Ghandehari, H.5
  • 16
    • 1542509564 scopus 로고    scopus 로고
    • The use of a dendrimer-propranolol prodrug to bypass efflux transporters and enhance oral bioavailability
    • DOI 10.1016/j.jconrel.2003.12.006, PII S016836590300573X
    • A. D'Emanuele, R. Jevprasesphant, J. Penny, and D. Attwood The use of a dendrimer-propranolol prodrug to bypass efflux transporters and enhance oral bioavailability J. Control. Release 95 3 2004 447 453 (Pubitemid 38340495)
    • (2004) Journal of Controlled Release , vol.95 , Issue.3 , pp. 447-453
    • D'Emanuele, A.1    Jevprasesphant, R.2    Penny, J.3    Attwood, D.4
  • 17
    • 44749084015 scopus 로고    scopus 로고
    • Potential oral delivery of 7-ethyl-10-hydroxy-camptothecin (SN-38) using poly (amido amine) dendrimers
    • R.B. Kolhatkar, P.W. Swaan, and H. Ghandehari Potential oral delivery of 7-ethyl-10-hydroxy-camptothecin (SN-38) using poly (amido amine) dendrimers Pharm. Res. 25 7 2008 1723 1729
    • (2008) Pharm. Res. , vol.25 , Issue.7 , pp. 1723-1729
    • Kolhatkar, R.B.1    Swaan, P.W.2    Ghandehari, H.3
  • 18
    • 67650140668 scopus 로고    scopus 로고
    • Transepithelial transport of PEGylated anionic poly (amido amine) dendrimers: Implications for oral drug delivery
    • D. Sweet, R. Kolhatkar, A. Ray, P. Swaan, and H. Ghandehari Transepithelial transport of PEGylated anionic poly (amido amine) dendrimers: implications for oral drug delivery J. Control. Release 138 1 2009 78 85
    • (2009) J. Control. Release , vol.138 , Issue.1 , pp. 78-85
    • Sweet, D.1    Kolhatkar, R.2    Ray, A.3    Swaan, P.4    Ghandehari, H.5
  • 19
    • 0141867744 scopus 로고    scopus 로고
    • Transport mechanism(s) of poly (amidoamine) dendrimers across Caco-2 cell monolayers
    • DOI 10.1016/S0378-5173(03)00391-0
    • M. El-Sayed, C.A. Rhodes, M. Ginski, and H. Ghandehari Transport mechanism(s) of poly (amido amine) dendrimers across Caco-2 cell monolayers Int. J. Pharm. 265 1-2 2003 151 157 (Pubitemid 37176956)
    • (2003) International Journal of Pharmaceutics , vol.265 , Issue.1-2 , pp. 151-157
    • El-Sayed, M.1    Rhodes, C.A.2    Ginski, M.3    Ghandehari, H.4
  • 20
    • 42549146106 scopus 로고    scopus 로고
    • Endocytosis inhibitors prevent poly(amidoamine) dendrimer internalization and permeability across caco-2 cells
    • DOI 10.1021/mp700089s
    • K.M. Kitchens, R.B. Kolhatkar, P.W. Swaan, and H. Ghandehari Endocytosis inhibitors prevent poly (amido amine) dendrimer internalization and permeability across Caco-2 cells Mol. Pharm. 5 2 2008 364 369 (Pubitemid 351579139)
    • (2008) Molecular Pharmaceutics , vol.5 , Issue.2 , pp. 364-369
    • Kitchens, K.M.1    Kolhatkar, R.B.2    Swaan, P.W.3    Ghandehari, H.4
  • 21
    • 77955466733 scopus 로고    scopus 로고
    • Cellular entry of G3.5 poly (amido amine) dendrimers by clathrin- and dynamin-dependent endocytosis promotes tight junctional opening in intestinal epithelia
    • D.S. Goldberg, H. Ghandehari, and P.W. Swaan Cellular entry of G3.5 poly (amido amine) dendrimers by clathrin- and dynamin-dependent endocytosis promotes tight junctional opening in intestinal epithelia Pharm. Res. 27 8 2010 1547 1557
    • (2010) Pharm. Res. , vol.27 , Issue.8 , pp. 1547-1557
    • Goldberg, D.S.1    Ghandehari, H.2    Swaan, P.W.3
  • 22
    • 2942613703 scopus 로고    scopus 로고
    • Transport of dendrimer nanocarriers through epithelial cells via the transcellular route
    • DOI 10.1016/j.jconrel.2004.03.022, PII S0168365904001440
    • R. Jevprasesphant, J. Penny, D. Attwood, and A. D'Emanuele Transport of dendrimer nanocarriers through epithelial cells via the transcellular route J. Control. Release 97 2004 259 267 (Pubitemid 38759483)
    • (2004) Journal of Controlled Release , vol.97 , Issue.2 , pp. 259-267
    • Jevprasesphant, R.1    Penny, J.2    Attwood, D.3    D'Emanuele, A.4
  • 23
    • 0025996996 scopus 로고
    • Intracellular roles of SN-38, a metabolite of the camptothecin derivative CPT-11, in the antitumor effect of CPT-11
    • Y. Kawato, M. Aonuma, Y. Hirota, H. Kuga, and K. Sato Intracellular roles of SN-38, a metabolite of the camptothecin derivative CPT-11, in the antitumor effect of CPT-11 Cancer Res. 51 16 1991 4187 4191
    • (1991) Cancer Res. , vol.51 , Issue.16 , pp. 4187-4191
    • Kawato, Y.1    Aonuma, M.2    Hirota, Y.3    Kuga, H.4    Sato, K.5
  • 24
    • 0036023423 scopus 로고    scopus 로고
    • Human carboxylesterase 2 is commonly expressed in tumor tissue and is correlated with activation of irinotecan
    • G. Xu, W. Zhang, M.K. Ma, and H.L. McLeod Human carboxylesterase 2 is commonly expressed in tumor tissue and is correlated with activation of irinotecan Clin. Cancer Res. 8 8 2002 2605 2611 (Pubitemid 34856347)
    • (2002) Clinical Cancer Research , vol.8 , Issue.8 , pp. 2605-2611
    • Xu, G.1    Zhang, W.2    Ma, M.K.3    McLeod, H.L.4
  • 25
    • 0034746224 scopus 로고    scopus 로고
    • Irenotecan (CPT-11): Recent developments and future directions - Colorectal cancer and beyond
    • DOI 10.1634/theoncologist.6-1-66
    • M.L. Rothenberg Irinotecan (CPT-11): recent developments and future directions-colorectal cancer and beyond Oncologist 6 1 2001 66 80 (Pubitemid 32155817)
    • (2001) Oncologist , vol.6 , Issue.1 , pp. 66-80
    • Rothenberg, M.L.1
  • 26
    • 77958156329 scopus 로고    scopus 로고
    • Carboxyl terminated PAMAM-SN38 conjugates: Synthesis, characterization, and in vitro evaluation
    • N. Vijayalakshmi, A. Ray, A. Malugin, and H. Ghandehari Carboxyl terminated PAMAM-SN38 conjugates: synthesis, characterization, and in vitro evaluation Bioconjug. Chem. 21 10 2010 1804 1810
    • (2010) Bioconjug. Chem. , vol.21 , Issue.10 , pp. 1804-1810
    • Vijayalakshmi, N.1    Ray, A.2    Malugin, A.3    Ghandehari, H.4
  • 28
    • 68949218775 scopus 로고    scopus 로고
    • The gastrointestinal stability of lipid nanocapsules
    • E. Roger, F. Lagarce, and J.-P. Benoit The gastrointestinal stability of lipid nanocapsules Int. J. Pharm. 379 2 2009 260 265
    • (2009) Int. J. Pharm. , vol.379 , Issue.2 , pp. 260-265
    • Roger, E.1    Lagarce, F.2    Benoit, J.-P.3
  • 29
    • 0344731435 scopus 로고    scopus 로고
    • Bisphosphonate prodrugs: Synthesis and in vitro evaluation of novel clodronic acid dianhydrides as bioreversible prodrugs of clodronate
    • DOI 10.1021/jm9810809
    • M. Ahlmark, J. Vepsäläinen, H. Taipale, R. Niemi, and T. Järvinen Bisphosphonate prodrugs: synthesis and in vitro evaluation of novel clodronic acid dianhydrides as bioreversible prodrugs of clodronate J. Med. Chem. 42 8 1999 1473 1476 (Pubitemid 29200884)
    • (1999) Journal of Medicinal Chemistry , vol.42 , Issue.8 , pp. 1473-1476
    • Ahlmark, M.1    Vepsalainen, J.2    Taipale, H.3    Niemi, R.4    Jarvinen, T.5
  • 31
    • 0032220399 scopus 로고    scopus 로고
    • A spectrophotometric assay optimizing conditions for pepsin activity
    • R. Kimsey, and E. Harding A spectrophotometric assay optimizing conditions for pepsin activity Am. Biol. Teach. 60 3 1998 200 201
    • (1998) Am. Biol. Teach. , vol.60 , Issue.3 , pp. 200-201
    • Kimsey, R.1    Harding, E.2
  • 32
    • 0000081341 scopus 로고
    • Proteolytic and peptidolytic activities in commercial pancreatic protease preparations and their relationship to some ehey protein hydrolysate characteristics
    • M. Mullally, D. OCallaghan, R. FitzGerald, W. Donnelly, and J. Dalton Proteolytic and peptidolytic activities in commercial pancreatic protease preparations and their relationship to some ehey protein hydrolysate characteristics J. Agric. Food Chem. 42 1994 2961 2973
    • (1994) J. Agric. Food Chem. , vol.42 , pp. 2961-2973
    • Mullally, M.1    Ocallaghan, D.2    Fitzgerald, R.3    Donnelly, W.4    Dalton, J.5
  • 33
    • 0035659708 scopus 로고    scopus 로고
    • Synthesis of new carboxylesterase inhibitors and evaluation of potency and water solubility
    • DOI 10.1021/tx015508+
    • C.E. Wheelock, T.F. Severson, and B.D. Hammock Synthesis of new carboxylesterase inhibitors and evaluation of potency and water solubility Chem. Res. Toxicol. 14 12 2001 1563 1572 (Pubitemid 34016619)
    • (2001) Chemical Research in Toxicology , vol.14 , Issue.12 , pp. 1563-1572
    • Wheelock, C.E.1    Severson, T.F.2    Hammock, B.D.3
  • 34
    • 0030917983 scopus 로고    scopus 로고
    • Disposition of irinotecan and SN-38 following oral and intravenous irinotecan dosing in mice
    • DOI 10.1007/s002800050656
    • C.F. Stewart, W.C. Zamboni, W.R. Crom, and P.J. Houghton Disposition of irinotecan and SN-38 following oral and intravenous irinotecan dosing in mice Cancer Chemother. Pharmacol. 40 3 1997 259 265 (Pubitemid 27258664)
    • (1997) Cancer Chemotherapy and Pharmacology , vol.40 , Issue.3 , pp. 259-265
    • Stewart, C.F.1    Zamboni, W.C.2    Crom, W.R.3    Houghton, P.J.4
  • 35
    • 0034941111 scopus 로고    scopus 로고
    • Active transepithelial transport of irinotecan (CPT-11) and its metabolites by human intestinal Caco-2 cells
    • DOI 10.1097/00001813-200106000-00003
    • W. Yamamoto, J. Verweij, P. de Bruijn, M.J. de Jonge, H. Takano, M. Nishiyama, M. Kurihara, and A. Sparreboom Active transepithelial transport of irinotecan (CPT-11) and its metabolites by human intestinal Caco-2 cells Anticancer Drugs 12 5 2001 419 432 (Pubitemid 32643086)
    • (2001) Anti-Cancer Drugs , vol.12 , Issue.5 , pp. 419-432
    • Yamamoto, W.1    Verweij, J.2    De Bruijn, P.3    De Jonge, M.J.A.4    Takano, H.5    Nishiyama, M.6    Kurihara, M.7    Sparreboom, A.8
  • 36
    • 28744441403 scopus 로고    scopus 로고
    • Transepithelial and endothelial transport of poly (amidoamine) dendrimers
    • DOI 10.1016/j.addr.2005.09.013, PII S0169409X05001924, Dendrimers: a Versatile Targeting Platform
    • K.M. Kitchens, M.E. El-Sayed, and H. Ghandehari Transepithelial and endothelial transport of poly (amido amine) dendrimers Adv. Drug Deliv. Rev. 57 15 2005 2163 2176 (Pubitemid 41759391)
    • (2005) Advanced Drug Delivery Reviews , vol.57 , Issue.15 , pp. 2163-2176
    • Kitchens, K.M.1    El-Sayed, M.E.H.2    Ghandehari, H.3
  • 37
    • 70350055331 scopus 로고    scopus 로고
    • Synthesis and in vivo antitumor efficacy of PEGylated poly(l-lysine) dendrimer-camptothecin conjugates
    • M.E. Fox, S. Guillaudeu, J.M. Frechet, K. Jerger, N. Macaraeg, and F.C. Szoka Synthesis and in vivo antitumor efficacy of PEGylated poly(l-lysine) dendrimer-camptothecin conjugates Mol. Pharm. 6 5 2009 1562 1572
    • (2009) Mol. Pharm. , vol.6 , Issue.5 , pp. 1562-1572
    • Fox, M.E.1    Guillaudeu, S.2    Frechet, J.M.3    Jerger, K.4    MacAraeg, N.5    Szoka, F.C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.