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Volumn 7, Issue 3, 2011, Pages 313-323

Mechanistic enhancement of the intestinal absorption of drugs containing the polar guanidino functionality

Author keywords

guanidino containing drugs; intestinal permeability; ion pair approach; nanocarriers; oral drug absorption; prodrug approach

Indexed keywords

1 HYDROXY 2 NAPHTHOIC ACID; 2 NAPHTHOIC ACID DERIVATIVE; [3 (HYDROXYMETHYL)PHENYL]GUANIDINE; ARGATROBAN; ARGININE; CARBAMIC ACID DERIVATIVE; CHITOSAN; CIMETIDINE; DABIGATRAN; FAMOTIDINE; GUANFACINE; GUANIDINE DERIVATIVE; METFORMIN; METOPROLOL; NANOCARRIER; NANOPARTICLE; OSELTAMIVIR; POLYGLACTIN; PRODRUG; STREPTOMYCIN; UNCLASSIFIED DRUG; ZANAMIVIR;

EID: 79951928274     PISSN: 17425255     EISSN: None     Source Type: Journal    
DOI: 10.1517/17425255.2011.550875     Document Type: Review
Times cited : (15)

References (81)
  • 1
    • 0023376437 scopus 로고
    • Biochemistry and neurotoxicology of guanidino compounds. History and recent advances
    • Mori A. Biochemistry and neurotoxicology of guanidino compounds. History and recent advances. Pavlov J Biol Sci 1987;22(3):85-94
    • (1987) Pavlov J Biol Sci , vol.22 , Issue.3 , pp. 85-94
    • Mori, A.1
  • 2
    • 0037304972 scopus 로고    scopus 로고
    • A role for guanidino compounds in the brain
    • DOI 10.1023/A:1022491419813
    • Hiramatsu M. A role for guanidino compounds in the brain. Mol Cell Biochem 2003;244(1-2):57-62 (Pubitemid 36411053)
    • (2003) Molecular and Cellular Biochemistry , vol.244 , Issue.1-2 , pp. 57-62
    • Hiramatsu, M.1
  • 4
    • 69249155619 scopus 로고    scopus 로고
    • Guanidino compounds as uremic (neuro)toxins
    • De Deyn PP, Vanholder R, Eloot S, et al. Guanidino compounds as uremic (neuro)toxins. Semin Dial 2009;22(4):340-5
    • (2009) Semin Dial , vol.22 , Issue.4 , pp. 340-345
    • De Deyn, P.P.1    Vanholder, R.2    Eloot, S.3
  • 5
    • 0027728591 scopus 로고
    • Amidines and guanidines in medicinal chemistry
    • Greenhill JV, Lue P. Amidines and guanidines in medicinal chemistry. Prog Med Chem 1993;30:203-326
    • (1993) Prog Med Chem , vol.30 , pp. 203-326
    • Greenhill, J.V.1    Lue, P.2
  • 6
    • 52749088723 scopus 로고    scopus 로고
    • The chemistry and biology of organic guanidine derivatives
    • Berlinck RG, Burtoloso AC, Kossuga MH. The chemistry and biology of organic guanidine derivatives. Nat Prod Rep 2008;25(5):919-54
    • (2008) Nat Prod Rep , vol.25 , Issue.5 , pp. 919-954
    • Berlinck, R.G.1    Burtoloso, A.C.2    Kossuga, M.H.3
  • 7
    • 4744355192 scopus 로고    scopus 로고
    • Enzymes of arginine metabolism
    • Morris Jr SM. Enzymes of arginine metabolism. J Nutr 2004;134(Suppl 10):2743S-2747S; discussion 65S-67S (Pubitemid 39315214)
    • (2004) Journal of Nutrition , vol.134 , Issue.10 SUPPL.
    • Morris Jr., S.M.1
  • 8
    • 33845360094 scopus 로고    scopus 로고
    • Arginine mimetic structures in biologically active antagonists and inhibitors
    • DOI 10.2174/092986706779026101
    • Masic LP. Arginine mimetic structures in biologically active antagonists and inhibitors. Curr Med Chem 2006;13(30):3627-48 (Pubitemid 44882612)
    • (2006) Current Medicinal Chemistry , vol.13 , Issue.30 , pp. 3627-3648
    • Masic, L.P.1
  • 9
    • 4744356881 scopus 로고    scopus 로고
    • Plasma membrane transporters for arginine
    • Closs EI, Simon A, Vekony N, et al. Plasma membrane transporters for arginine. J Nutr 2004;134(Suppl 10):2752S-2759S, disscussion 2765S-2767S (Pubitemid 39315216)
    • (2004) Journal of Nutrition , vol.134 , Issue.10 SUPPL.
    • Closs, E.I.1    Simon, A.2    Vekony, N.3    Rotmann, A.4
  • 10
    • 38349170961 scopus 로고    scopus 로고
    • Amino acid transport across mammalian intestinal and renal epithelia
    • Broer S. Amino acid transport across mammalian intestinal and renal epithelia. Physiol Rev 2008;88(1):249-86
    • (2008) Physiol Rev , vol.88 , Issue.1 , pp. 249-86
    • Broer, S.1
  • 11
    • 0018863326 scopus 로고
    • Pharmacokinetics and metabolism of guanfacine in man: A review
    • Kiechel JR. Pharmacokinetics and metabolism of guanfacine in man: a review. Br J Clin Pharmacol 1980;10(Suppl 1):25S-32S (Pubitemid 10065106)
    • (1980) British Journal of Clinical Pharmacology , vol.10 , Issue.SUPPL. 1
    • Kiechel, J.R.1
  • 12
    • 0032696606 scopus 로고    scopus 로고
    • Effect of molecular charge on intestinal epithelial drug transport: PH-dependent transport of cationic drugs
    • Palm K, Luthman K, Ros J, et al. Effect of molecular charge on intestinal epithelial drug transport: pH-dependent transport of cationic drugs. J Pharmacol Exp Ther 1999;291(2):435-43
    • (1999) J Pharmacol Exp Ther , vol.291 , Issue.2 , pp. 435443
    • Palm, K.1    Luthman, K.2    Ros, J.3
  • 13
    • 0027260934 scopus 로고
    • Solubility, stability and ionization behaviour of famotidine
    • Islam MS, Narurkar MM. Solubility, stability and ionization behaviour of famotidine. J Pharm Pharmacol 1993;45(8):682-6 (Pubitemid 23258682)
    • (1993) Journal of Pharmacy and Pharmacology , vol.45 , Issue.8 , pp. 682-686
    • Islam, M.S.1    Narurkar, M.M.2
  • 14
    • 77957729688 scopus 로고    scopus 로고
    • High-permeability criterion for BCS classification: Segmental/pH dependent permeability considerations
    • Dahan A, Miller JM, Hilfinger JM, et al. High-permeability criterion for BCS classification: segmental/pH dependent permeability considerations. Mol Pharm 2010;7(5):1827-34
    • (2010) Mol Pharm , vol.7 , Issue.5 , pp. 1827-1834
    • Dahan, A.1    Miller, J.M.2    Hilfinger, J.M.3
  • 17
    • 22244488749 scopus 로고    scopus 로고
    • Oral delivery of peptide drugs: Barriers and developments
    • DOI 10.2165/00063030-200519030-00003
    • Hamman JH, Enslin GM, Kotze AF. Oral delivery of peptide drugs: barriers and developments. BioDrugs 2005;19(3):165-77 (Pubitemid 40994232)
    • (2005) BioDrugs , vol.19 , Issue.3 , pp. 165-177
    • Hamman, J.H.1    Enslin, G.M.2    Kotze, A.F.3
  • 18
    • 0023263447 scopus 로고
    • Clinical pharmacology of famotidine: A summary
    • Chremos AN. Clinical pharmacology of famotidine: a summary. J Clin Gastroenterol 1987;9(Suppl 2):7-12 (Pubitemid 17118612)
    • (1987) Journal of Clinical Gastroenterology , vol.9 , Issue.SUPPL. 2 , pp. 7-12
    • Chremos, A.N.1
  • 19
    • 0032588513 scopus 로고    scopus 로고
    • 2-antagonists ranitidine and famotidine across Caco-2 cell monolayers
    • DOI 10.1021/js980474k
    • Lee K, Thakker DR. Saturable transport of H2-antagonists ranitidine and famotidine across Caco-2 cell monolayers. J Pharm Sci 1999;88(7):680-7 (Pubitemid 29325994)
    • (1999) Journal of Pharmaceutical Sciences , vol.88 , Issue.7 , pp. 680-687
    • Kiho, L.1    Thakker, D.R.2
  • 20
    • 27744570434 scopus 로고    scopus 로고
    • Differential Substrate and Inhibitory Activities of Ranitidine and Famotidine Toward Human Organic Cation Transporter (hOCT1; SLC22A1), hOCT2 (SLC22A2), and hOCT3 (SLC22A3)
    • Bourdet DL, Pritchard JB, Thakker DR. Differential substrate and inhibitory activities of ranitidine and famotidine toward human organic cation transporter (hOCT1; SLC22A1), hOCT2 (SLC22A2), and hOCT3 (SLC22A3). J Pharmacol Exp Ther 2005;315(3):1288-97
    • (2005) J Pharmacol Exp Ther , vol.315 , Issue.3 , pp. 12881-12897
    • Bourdet, D.L.1    Pritchard, J.B.2    Thakker, D.R.3
  • 22
    • 62649126219 scopus 로고    scopus 로고
    • Segmental dependent transport of low permeability compounds along the small intestine due to P-glycoprotein: The role of efflux transport in the oral absorption of BCS class III drugs
    • Dahan A, Amidon GL. Segmental dependent transport of low permeability compounds along the small intestine due to P-glycoprotein: the role of efflux transport in the oral absorption of BCS class III drugs. Mol Pharm 2009;6(1):19-28
    • (2009) Mol Pharm , vol.6 , Issue.1 , pp. 19-28
    • Dahan, A.1    Amidon, G.L.2
  • 23
    • 70349414560 scopus 로고    scopus 로고
    • Multiple efflux pumps are involved in the transepithelial transport of colchicine: Combined effect of P-gp and MRP2 leads to decreased intestinal absorption throughout the entire small intestine
    • Dahan A, Sabit H, Amidon GL. Multiple efflux pumps are involved in the transepithelial transport of colchicine: combined effect of P-gp and MRP2 leads to decreased intestinal absorption throughout the entire small intestine. Drug Metab Dispos 2009;37(10):2028-36
    • (2009) Drug Metab Dispos , vol.37 , Issue.10 , pp. 2028-2036
    • Dahan, A.1    Sabit, H.2    Amidon, G.L.3
  • 24
    • 61549086853 scopus 로고    scopus 로고
    • Grapefruit juice and its constituents augment colchicine intestinal absorption: Potential hazardous interaction and the role of P-glycoprotein
    • Dahan A, Amidon G. Grapefruit juice and its constituents augment colchicine intestinal absorption: potential hazardous interaction and the role of P-glycoprotein. Pharm Res 2009;26(4):883-92
    • (2009) Pharm Res , vol.26 , Issue.4 , pp. 883-92
    • Dahan, A.1    Amidon, G.2
  • 25
    • 68049113657 scopus 로고    scopus 로고
    • Small intestinal efflux mediated by MRP2 and BCRP shifts sulfasalazine intestinal permeability from high to low, enabling its colonic targeting
    • Dahan A, Amidon GL. Small intestinal efflux mediated by MRP2 and BCRP shifts sulfasalazine intestinal permeability from high to low, enabling its colonic targeting. Am J Physiol Gastrointest Liver Physiol 2009;297(2):G371-7
    • (2009) Am J Physiol Gastrointest Liver Physiol , vol.297 , Issue.2
    • Dahan, A.1    Amidon, G.L.2
  • 26
    • 74149085130 scopus 로고    scopus 로고
    • MRP2 mediated drug-drug interaction: Indomethacin increases sulfasalazine absorption in the small intestine, potentially decreasing its colonic targeting
    • Dahan A, Amidon GL. MRP2 mediated drug-drug interaction: indomethacin increases sulfasalazine absorption in the small intestine, potentially decreasing its colonic targeting. Int J Pharm 2010;386(1-2):216-20
    • Int J Pharm 2010 , vol.386 , Issue.1-2 , pp. 216-20
    • Dahan, A.1    Amidon, G.L.2
  • 27
    • 68049095727 scopus 로고    scopus 로고
    • The H2 receptor antagonist nizatidine is a P-glycoprotein substrate: Characterization of its intestinal epithelial cell efflux transport
    • Dahan A, Sabit H, Amidon G. The H2 receptor antagonist nizatidine is a P-glycoprotein substrate: characterization of its intestinal epithelial cell efflux transport. AAPS J 2009;11(2):205-13
    • (2009) AAPS J , vol.11 , Issue.2 , pp. 205-13
    • Dahan, A.1    Sabit, H.2    Amidon, G.3
  • 28
    • 58149168723 scopus 로고    scopus 로고
    • Segmental-dependent membrane permeability along the intestine following oral drug administration: Evaluation of a triple single-pass intestinal perfusion (TSPIP) approach in the rat
    • Dahan A, West BT, Amidon GL. Segmental-dependent membrane permeability along the intestine following oral drug administration: evaluation of a triple single-pass intestinal perfusion (TSPIP) approach in the rat. Eur J Pharm Sci 2009;36(2-3):320-9
    • (2009) Eur J Pharm Sci , vol.36 , Issue.2-3 , pp. 320-9
    • Dahan, A.1    West, B.T.2    Amidon, G.L.3
  • 29
  • 30
    • 0029936885 scopus 로고    scopus 로고
    • Transfer of metformin across monolayers of human intestinal Caco-2 cells and across rat intestine
    • DOI 10.1016/0378-5173(95)04259-8
    • Nicklin P, Keates AC, Page T, et al. Transfer of metformin across monolayers of human intestinal Caco-2 cells and across rat intestine. Int J Pharm 1996;128(1-2):155-62 (Pubitemid 26091018)
    • (1996) International Journal of Pharmaceutics , vol.128 , Issue.1-2 , pp. 155-162
    • Nicklin, P.1    Keates, A.C.2    Page, T.3    Bailey, C.J.4
  • 31
    • 33644664085 scopus 로고    scopus 로고
    • Metformin is a superior substrate for renal organic cation transporter OCT2 rather than hepatic OCT1
    • Kimura N, Masuda S, Tanihara Y, et al. Metformin is a superior substrate for renal organic cation transporter OCT2 rather than hepatic OCT1. Drug Metab Pharmacokinet 2005;20(5):379-86
    • (2005) Drug Metab Pharmacokinet , vol.20 , Issue.5 , pp. 379-86
    • Kimura, N.1    Masuda, S.2    Tanihara, Y.3
  • 32
    • 0036689433 scopus 로고    scopus 로고
    • Interactions of n-tetraalkylammonium compounds and biguanides with a human renal organic cation transporter (hOCT2)
    • DOI 10.1023/A:1019870831174
    • Dresser MJ, Xiao G, Leabman MK, et al. Interactions of n-tetraalkylammonium compounds and biguanides with a human renal organic cation transporter (hOCT2). Pharm Res 2002;19(8):1244-7 (Pubitemid 34985011)
    • (2002) Pharmaceutical Research , vol.19 , Issue.8 , pp. 1244-1247
    • Dresser, M.J.1    Xiao, G.2    Leabman, M.K.3    Gray, A.T.4    Giacomini, K.M.5
  • 33
    • 34748922537 scopus 로고    scopus 로고
    • Metformin transport by a newly cloned proton-stimulated organic cation transporter (plasma membrane monoamine transporter) expressed in human intestine
    • DOI 10.1124/dmd.107.015495
    • Zhou M, Xia L, Wang J. Metformin transport by a newly cloned proton-stimulated organic cation transporter (plasma membrane monoamine transporter) expressed in human intestine. Drug Metab Dispos 2007;35(10):1956-62 (Pubitemid 47481592)
    • (2007) Drug Metabolism and Disposition , vol.35 , Issue.10 , pp. 1956-1962
    • Zhou, M.1    Xia, L.2    Wang, J.3
  • 34
    • 67650717860 scopus 로고    scopus 로고
    • The first bioreversible prodrug of metformin with improved lipophilicity and enhanced intestinal absorption
    • Huttunen KM, Mannila A, Laine K, et al. The first bioreversible prodrug of metformin with improved lipophilicity and enhanced intestinal absorption. J Med Chem 2009;52(14):4142-8
    • (2009) J Med Chem , vol.52 , Issue.14 , pp. 4142-8
    • Huttunen, K.M.1    Mannila, A.2    Laine, K.3
  • 35
    • 27744470403 scopus 로고    scopus 로고
    • Pharmacology and clinical potential of direct thrombin inhibitors
    • DOI 10.2174/138161205774580598
    • Linkins LA, Weitz JI. Pharmacology and clinical potential of direct thrombin inhibitors. Curr Pharm Des 2005;11(30):3877-84 (Pubitemid 41632243)
    • (2005) Current Pharmaceutical Design , vol.11 , Issue.30 , pp. 3877-3884
    • Linkins, L.-A.1    Weitz, J.I.2
  • 36
    • 0032996541 scopus 로고    scopus 로고
    • Pharmacokinetics of zanamivir after intravenous, oral, inhaled or intranasal administration to healthy volunteers
    • Cass LM, Efthymiopoulos C, Bye A. Pharmacokinetics of zanamivir after intravenous, oral, inhaled or intranasal administration to healthy volunteers. Clin Pharmacokinet 1999;36(Suppl 1):1-11 (Pubitemid 29322452)
    • (1999) Clinical Pharmacokinetics , vol.36 , Issue.SUPPL. 1 , pp. 1-11
    • Cass, L.M.R.1    Efthymiopoulos, C.2    Bye, A.3
  • 37
    • 0033385681 scopus 로고    scopus 로고
    • Clinical pharmacokinetics of the prodrug oseltamivir and its active metabolite Ro 64-0802
    • He G, Massarella J, Ward P. Clinical pharmacokinetics of the prodrug oseltamivir and its active metabolite Ro 64-0802. Clin Pharmacokinet 1999;37(6):471-84 (Pubitemid 30032251)
    • (1999) Clinical Pharmacokinetics , vol.37 , Issue.6 , pp. 471-484
    • He, G.1    Massarella, J.2    Ward, P.3
  • 38
    • 77953262416 scopus 로고    scopus 로고
    • Permissive secondary mutations enable the evolution of influenza oseltamivir resistance
    • Bloom JD, Gong LI, Baltimore D. Permissive secondary mutations enable the evolution of influenza oseltamivir resistance. Science 2010;328(5983):1272-5
    • Science , vol.328 , Issue.5983 , pp. 1272-5
    • Bloom, J.D.1    Gong, L.I.2    Baltimore, D.3
  • 39
    • 77957345957 scopus 로고    scopus 로고
    • Novel influenza A(H1N1) 2009 in vitro reassortant viruses with oseltamivir resistance
    • Ottmann M, Duchamp MB, Casalegno JS, et al. Novel influenza A(H1N1) 2009 in vitro reassortant viruses with oseltamivir resistance. Antivir Ther 2010;15(5):721-6
    • (2010) Antivir Ther , vol.15 , Issue.5 , pp. 721-6
    • Ottmann, M.1    Duchamp, M.B.2    Casalegno, J.S.3
  • 43
    • 69249117394 scopus 로고    scopus 로고
    • Current prodrug design for drug discovery
    • Hsieh PW, Hung CF, Fang JY. Current prodrug design for drug discovery. Curr Pharm Des 2009;15(19):2236-50
    • (2009) Curr Pharm des , vol.15 , Issue.19 , pp. 2236-50
    • Hsieh, P.W.1    Hung, C.F.2    Fang, J.Y.3
  • 44
    • 0042143281 scopus 로고    scopus 로고
    • Targeted prodrug design to optimize drug delivery
    • Han HK, Amidon GL. Targeted prodrug design to optimize drug delivery. AAPS PharmSci 2000;2(1):E6
    • (2000) AAPS PharmSci , vol.2 , Issue.1
    • Han, H.K.1    Amidon, G.L.2
  • 45
    • 2942612987 scopus 로고    scopus 로고
    • Membrane transporter/receptor-targeted prodrug design: Strategies for human and veterinary drug development
    • DOI 10.1016/j.addr.2004.02.006, PII S0169409X04000699, Veterinary Drug Delivery: Part VI
    • Majumdar S, Duvvuri S, Mitra AK. Membrane transporter/receptor-targeted prodrug design: strategies for human and veterinary drug development. Adv Drug Deliv Rev 2004;56(10):1437-52 (Pubitemid 38748825)
    • (2004) Advanced Drug Delivery Reviews , vol.56 , Issue.10 , pp. 1437-1452
    • Majumdar, S.1    Duvvuri, S.2    Mitra, A.K.3
  • 50
    • 56949097636 scopus 로고    scopus 로고
    • Novel linear triaryl guanidines, N-substituted guanidines and potential prodrugs as antiprotozoal agents
    • Arafa RK, Ismail MA, Munde M, et al. Novel linear triaryl guanidines, N-substituted guanidines and potential prodrugs as antiprotozoal agents. Eur J Med Chem 2008;43(12):2901-8
    • (2008) Eur J Med Chem , vol.43 , Issue.12 , pp. 2901-8
    • Arafa, R.K.1    Ismail, M.A.2    Munde, M.3
  • 52
    • 33644853189 scopus 로고    scopus 로고
    • Metabolism-directed optimisation of antithrombotics: The prodrug principle
    • Peterlin-Masic L, Cesar J, Zega A. Metabolism-directed optimisation of antithrombotics: the prodrug principle. Curr Pharm Des 2006;12(1):73-91
    • (2006) Curr Pharm des , vol.12 , Issue.1 , pp. 73-91
    • Peterlin-Masic, L.1    Cesar, J.2    Zega, A.3
  • 54
    • 0036038490 scopus 로고    scopus 로고
    • Reduction of N-hydroxylated compounds: Amidoximes (N-hydroxyamidines) as pro-drugs of amidines
    • DOI 10.1081/DMR-120005643
    • Clement B. Reduction of N-hydroxylated compounds: amidoximes (N-hydroxyamidines) as pro-drugs of amidines. Drug Metab Rev 2002;34(3):565-79 (Pubitemid 35006065)
    • (2002) Drug Metabolism Reviews , vol.34 , Issue.3 , pp. 565-579
    • Clement, B.1
  • 55
    • 27544492348 scopus 로고    scopus 로고
    • Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and Ro 48-3656 ([[1-[(2s)-2-[[4-[(hydroxyamino) iminomethyl]benzoyl]amino]-1- oxopropyl]-4- piperidinyl]oxy]-acetic acid)
    • Clement B, Mau S, Deters S, et al. Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and Ro 48-3656 ([[1-[(2s)-2-[[4-[(hydroxyamino) iminomethyl]benzoyl]amino]-1- oxopropyl]-4- piperidinyl]oxy]-acetic acid). Drug Metab Dispos 2005;33(11):1740-7
    • (2005) Drug Metab Dispos , vol.33 , Issue.11 , pp. 1740-7
    • Clement, B.1    Mau, S.2    Deters, S.3
  • 56
    • 42549117180 scopus 로고    scopus 로고
    • Pharmaceutical and pharmacological importance of peptide transporters
    • DOI 10.1211/jpp.60.5.0002
    • Brandsch M, Knutter I, Bosse-Doenecke E. Pharmaceutical and pharmacological importance of peptide transporters. J Pharm Pharmacol 2008;60(5):543-85 (Pubitemid 351589044)
    • (2008) Journal of Pharmacy and Pharmacology , vol.60 , Issue.5 , pp. 543-585
    • Brandsch, M.1    Knutter, I.2    Bosse-Doenecke, E.3
  • 57
    • 0028883462 scopus 로고
    • Absolute bioavailability and metabolic disposition of valaciclovir, the L-valyl ester of acyclovir, following oral administration to humans
    • Soul-Lawton J, Seaber E, On N, et al. Absolute bioavailability and metabolic disposition of valaciclovir, the L-valyl ester of acyclovir, following oral administration to humans. Antimicrob Agents Chemother 1995;39(12):2759-64
    • (1995) Antimicrob Agents Chemother , vol.39 , Issue.12 , pp. 2759-64
    • Soul-Lawton, J.1    Seaber, E.2    On, N.3
  • 59
    • 77249109864 scopus 로고    scopus 로고
    • Enhancing the intestinal absorption of molecules containing the polar guanidino functionality: A double-targeted prodrug approach
    • Sun J, Dahan A, Amidon GL. Enhancing the intestinal absorption of molecules containing the polar guanidino functionality: a double-targeted prodrug approach. J Med Chem 2010;53(2):624-32
    • (2010) J Med Chem , vol.53 , Issue.2 , pp. 624-32
    • Sun, J.1    Dahan, A.2    Amidon, G.L.3
  • 60
    • 78649913370 scopus 로고    scopus 로고
    • Specificity of a prodrug-activating enzyme hVACVase: The leaving group effect
    • Sun J, Dahan A, Walls Z, et al. Specificity of a prodrug-activating enzyme hVACVase: the leaving group effect. Mol Pharm 2010;7(6):2362-8
    • (2010) Mol Pharm , vol.7 , Issue.6 , pp. 2362-8
    • Sun, J.1    Dahan, A.2    Walls, Z.3
  • 61
    • 67349130543 scopus 로고    scopus 로고
    • Quasi-equilibrium analysis of the ion-pair mediated membrane transport of low-permeability drugs
    • Miller JM, Dahan A, Gupta D, et al. Quasi-equilibrium analysis of the ion-pair mediated membrane transport of low-permeability drugs. J Control Release 2009;137(1):31-7
    • (2009) J Control Release , vol.137 , Issue.1 , pp. 31-7
    • Miller, J.M.1    Dahan, A.2    Gupta, D.3
  • 62
    • 77955235031 scopus 로고    scopus 로고
    • Enabling the intestinal absorption of highly polar antiviral agents: Ion-pair facilitated membrane permeation of zanamivir heptyl ester and guanidino oseltamivir
    • Miller JM, Dahan A, Gupta D, et al. Enabling the intestinal absorption of highly polar antiviral agents: ion-pair facilitated membrane permeation of zanamivir heptyl ester and guanidino oseltamivir. Mol Pharm 2010;7(4):1223-34
    • (2010) Mol Pharm , vol.7 , Issue.4 , pp. 1223-34
    • Miller, J.M.1    Dahan, A.2    Gupta, D.3
  • 63
    • 33846042608 scopus 로고    scopus 로고
    • Formulation and evaluation of famotidine floating tablets
    • DOI 10.2174/156720107779314730
    • Jaimini M, Rana AC, Tanwar YS. Formulation and evaluation of famotidine floating tablets. Curr Drug Deliv 2007;4(1):51-5 (Pubitemid 46066414)
    • (2007) Current Drug Delivery , vol.4 , Issue.1 , pp. 51-55
    • Jaimini, M.1    Rana, A.C.2    Tanwar, Y.S.3
  • 64
    • 63649106584 scopus 로고    scopus 로고
    • Release mechanisms behind polysaccharides-based famotidine controlled release matrix tablets
    • Elmowafy EM, Awad GA, Mansour S, et al. Release mechanisms behind polysaccharides-based famotidine controlled release matrix tablets. AAPS PharmSciTech 2008;9(4):1230-9
    • (2008) AAPS PharmSciTech , vol.9 , Issue.4 , pp. 1230-9
    • Elmowafy, E.M.1    Awad, G.A.2    Mansour, S.3
  • 65
    • 54349104720 scopus 로고    scopus 로고
    • Optimization studies on floating multiparticulate gastroretentive drug delivery system of famotidine
    • Gupta R, Pathak K. Optimization studies on floating multiparticulate gastroretentive drug delivery system of famotidine. Drug Dev Ind Pharm 2008;34(11):1201-8
    • (2008) Drug Dev Ind Pharm , vol.34 , Issue.11 , pp. 1201-8
    • Gupta, R.1    Pathak, K.2
  • 66
    • 77949757639 scopus 로고    scopus 로고
    • Floating controlled drug delivery system of famotidine loaded hollow microspheres (microballoons) in the stomach
    • Ramachandran S, Shaheedha SM, Thirumurugan G, et al. Floating controlled drug delivery system of famotidine loaded hollow microspheres (microballoons) in the stomach. Curr Drug Deliv 2010;7(1):93-7
    • (2010) Curr Drug Deliv , vol.7 , Issue.1 , pp. 93-7
    • Ramachandran, S.1    Shaheedha, S.M.2    Thirumurugan, G.3
  • 67
    • 70449530507 scopus 로고    scopus 로고
    • A novel gastric-resident osmotic pump tablet: In vitro and in vivo evaluation
    • Guan J, Zhou L, Nie S, et al. A novel gastric-resident osmotic pump tablet: in vitro and in vivo evaluation. Int J Pharm 2010;383(1-2):30-6
    • (2010) Int J Pharm , vol.383 , Issue.1-2 , pp. 30-6
    • Guan, J.1    Zhou, L.2    Nie, S.3
  • 68
    • 72949088835 scopus 로고    scopus 로고
    • A novel gastro-retentive osmotic pump capsule using asymmetric membrane technology: In vitro and in vivo evaluation
    • Guan J, Zhou L, Pan Y, et al. A novel gastro-retentive osmotic pump capsule using asymmetric membrane technology: in vitro and in vivo evaluation. Pharm Res 2010;27(1):105-14
    • (2010) Pharm Res , vol.27 , Issue.1 , pp. 105-14
    • Guan, J.1    Zhou, L.2    Pan, Y.3
  • 69
    • 0022649008 scopus 로고
    • Bioavailability of metformin. Comparison of solution, rapidly dissolving tablet, and three sustained release products
    • Pentikainen PJ. Bioavailability of metformin. Comparison of solution, rapidly dissolving tablet, and three sustained release products. Int J Clin Pharmacol Ther Toxicol 1986;24(4):213-20 (Pubitemid 16113669)
    • (1986) International Journal of Clinical Pharmacology Therapy and Toxicology , vol.24 , Issue.4 , pp. 213-220
    • Pentikainen, P.J.1
  • 70
    • 0035848418 scopus 로고    scopus 로고
    • Preclinical evaluation of pharmacokinetic-pharmacodynamic rationale for oral CR metformin formulation
    • DOI 10.1016/S0168-3659(00)00374-6, PII S0168365900003746
    • Stepensky D, Friedman M, Srour W, et al. Preclinical evaluation of pharmacokinetic-pharmacodynamic rationale for oral CR metformin formulation. J Control Release 2001;71(1):107-15 (Pubitemid 32195445)
    • (2001) Journal of Controlled Release , vol.71 , Issue.1 , pp. 107-115
    • Stepensky, D.1    Friedman, M.2    Srour, W.3    Raz, I.4    Hoffman, A.5
  • 72
    • 0037161332 scopus 로고    scopus 로고
    • In vitro evaluation of a system for pH-controlled peroral delivery of metformin
    • DOI 10.1016/S0168-3659(02)00022-6, PII S0168365902000226
    • Di Colo G, Falchi S, Zambito Y. In vitro evaluation of a system for pH-controlled peroral delivery of metformin. J Control Release 2002;80(1-3):119-28 (Pubitemid 34273753)
    • (2002) Journal of Controlled Release , vol.80 , Issue.1-3 , pp. 119-128
    • Di Colo, G.1    Falchi, S.2    Zambito, Y.3
  • 73
    • 22244470759 scopus 로고    scopus 로고
    • Steady-state pharmacokinetics of a novel extended-release metformin formulation
    • DOI 10.2165/00003088-200544070-00004
    • Timmins P, Donahue S, Meeker J, et al. Steady-state pharmacokinetics of a novel extended-release metformin formulation. Clin Pharmacokinet 2005;44(7):721-9 (Pubitemid 40994081)
    • (2005) Clinical Pharmacokinetics , vol.44 , Issue.7 , pp. 721-729
    • Timmins, P.1    Donahue, S.2    Meeker, J.3    Marathe, P.4
  • 75
    • 34247488674 scopus 로고    scopus 로고
    • Relative bioavailability and bioequivalence of metforphin hydrochloride extended-released and immediate-released tablets in healthy Chinese volunteers
    • Li J, Jin Y, Wang TY, et al. Relative bioavailability and bioequivalence of metforphin hydrochloride extended-released and immediate-released tablets in healthy Chinese volunteers. Eur J Drug Metab Pharmacokinet 2007;32(1):21-8 (Pubitemid 46649807)
    • (2007) European Journal of Drug Metabolism and Pharmacokinetics , vol.32 , Issue.1 , pp. 21-28
    • Li, J.1    Jin, Y.2    Wang, T.-Y.3    Lu, X.-W.4    Li, Y.-H.5
  • 76
    • 0030448509 scopus 로고    scopus 로고
    • Nanoparticles and microparticles for drug and vaccine delivery
    • Kreuter J. Nanoparticles and microparticles for drug and vaccine delivery. J Anat 1996;189(Pt 3):503-5 (Pubitemid 27011002)
    • (1996) Journal of Anatomy , vol.189 , Issue.3 , pp. 503-505
    • Kreuter, J.1
  • 77
    • 0035478442 scopus 로고    scopus 로고
    • Transcytosis of nanoparticle and dendrimer delivery systems: Evolving vistas
    • DOI 10.1016/S0169-409X(01)00184-3, PII S0169409X01001843
    • Florence AT, Hussain N. Transcytosis of nanoparticle and dendrimer delivery systems: evolving vistas. Adv Drug Deliv Rev 2001;50(Suppl 1):S69-89 (Pubitemid 32905356)
    • (2001) Advanced Drug Delivery Reviews , vol.50 , Issue.SUPPL. 1
    • Florence, A.T.1    Hussain, N.2
  • 78
    • 66449095059 scopus 로고    scopus 로고
    • Current advances in research and clinical applications of PLGA-based nanotechnology
    • Lu JM, Wang X, Marin-Muller C, et al. Current advances in research and clinical applications of PLGA-based nanotechnology. Expert Rev Mol Diagn 2009;9(4):325-41
    • (2009) Expert Rev Mol Diagn , vol.9 , Issue.4 , pp. 325-41
    • Lu, J.M.1    Wang, X.2    Marin-Muller, C.3
  • 79
    • 36049001769 scopus 로고    scopus 로고
    • Nanoparticle-based oral drug delivery system for an injectable antibiotic - Streptomycin: Evaluation in a murine tuberculosis model
    • DOI 10.1159/000110009
    • Pandey R, Khuller GK. Nanoparticle-based oral drug delivery system for an injectable antibiotic - streptomycin. Evaluation in a murine tuberculosis model. Chemotherapy 2007;53(6):437-41 (Pubitemid 350085259)
    • (2007) Chemotherapy , vol.53 , Issue.6 , pp. 437-441
    • Pandey, R.1    Khuller, G.K.2
  • 80
    • 34548630860 scopus 로고    scopus 로고
    • Chitosan nanoparticles for oral drug and gene delivery
    • Bowman K, Leong KW. Chitosan nanoparticles for oral drug and gene delivery. Int J Nanomed 2006;1(2):117-28
    • (2006) Int J Nanomed , vol.1 , Issue.2 , pp. 117-28
    • Bowman, K.1    Leong, K.W.2
  • 81
    • 70849091247 scopus 로고    scopus 로고
    • Preparation of aminoglycoside-loaded chitosan nanoparticles using dextran sulphate as a counterion
    • Lu E, Franzblau S, Onyuksel H, et al. Preparation of aminoglycoside- loaded chitosan nanoparticles using dextran sulphate as a counterion. J Microencapsul 2009;26(4):346-54
    • (2009) J Microencapsul , vol.26 , Issue.4 , pp. 346-54
    • Lu, E.1    Franzblau, S.2    Onyuksel, H.3


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