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Volumn 65, Issue 8, 2013, Pages 1107-1117

Pluronic F127-modified liposome-containing tacrolimus-cyclodextrin inclusion complexes: Improved solubility, cellular uptake and intestinal penetration

Author keywords

cellular uptake; cyclodextrin inclusion complex; molecular modelling; Pluronic F127 modified liposomes; solubility; tacrolimus

Indexed keywords

CYCLODEXTRIN; LIPOSOME; NANOCARRIER; PHOSPHATE; POLOXAMER; TACROLIMUS; TAUROCHOLIC ACID;

EID: 84880133034     PISSN: 00223573     EISSN: 20427158     Source Type: Journal    
DOI: 10.1111/jphp.12074     Document Type: Article
Times cited : (51)

References (44)
  • 1
    • 10444279209 scopus 로고    scopus 로고
    • Cyclodextrin-based pharmaceutics: Past, present and future
    • Davis ME, Brewster ME,. Cyclodextrin-based pharmaceutics: past, present and future. Nat Rev Drug Discov 2004; 12: 1023-1035.
    • (2004) Nat Rev Drug Discov , vol.12 , pp. 1023-1035
    • Davis, M.E.1    Brewster, M.E.2
  • 2
    • 78649654159 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrins: Basic science and product development
    • Loftsson T, Brewster ME,. Pharmaceutical applications of cyclodextrins: basic science and product development. J Pharm Pharmacol 2010; 11: 1607-1621.
    • (2010) J Pharm Pharmacol , vol.11 , pp. 1607-1621
    • Loftsson, T.1    Brewster, M.E.2
  • 3
    • 44649133855 scopus 로고    scopus 로고
    • Rationalizing the selection of oral lipid based drug delivery systems by an in vitro dynamic lipolysis model for improved oral bioavailability of poorly water soluble drugs
    • Dahan A, Hoffman A,. Rationalizing the selection of oral lipid based drug delivery systems by an in vitro dynamic lipolysis model for improved oral bioavailability of poorly water soluble drugs. J Control Release 2008; 1: 1-10.
    • (2008) J Control Release , vol.1 , pp. 1-10
    • Dahan, A.1    Hoffman, A.2
  • 4
    • 35248822616 scopus 로고    scopus 로고
    • The utility of cyclodextrins for enhancing oral bioavailability
    • Carrier RL, et al. The utility of cyclodextrins for enhancing oral bioavailability. J Control Release 2007; 2: 78-99.
    • (2007) J Control Release , vol.2 , pp. 78-99
    • Carrier, R.L.1
  • 5
    • 0034988419 scopus 로고    scopus 로고
    • Comparative studies of the enhancing effects of cyclodextrins on the solubility and oral bioavailability of tacrolimus in rats
    • Hidetoshi A, et al. Comparative studies of the enhancing effects of cyclodextrins on the solubility and oral bioavailability of tacrolimus in rats. J Pharm Sci 2001; 6: 690-701.
    • (2001) J Pharm Sci , vol.6 , pp. 690-701
    • Hidetoshi, A.1
  • 6
    • 50249163680 scopus 로고    scopus 로고
    • Development and evaluation of novel itraconazole-loaded intravenous nanoparticles
    • Chen W, et al. Development and evaluation of novel itraconazole-loaded intravenous nanoparticles. Int J Pharm 2008; 1-2: 133-140.
    • (2008) Int J Pharm , vol.12 , pp. 133-140
    • Chen, W.1
  • 7
    • 0033106029 scopus 로고    scopus 로고
    • Mechanisms of drug release from cyclodextrin complexes
    • Valentino JS, et al. Mechanisms of drug release from cyclodextrin complexes. Adv Drug Del Rev 1999; 36: 3-16.
    • (1999) Adv Drug Del Rev , vol.36 , pp. 3-16
    • Valentino, J.S.1
  • 8
    • 33846498531 scopus 로고    scopus 로고
    • A mixed polymeric micellar formulation of itraconazole: Characteristics, toxicity and pharmacokinetics
    • Yi Y, et al. A mixed polymeric micellar formulation of itraconazole: characteristics, toxicity and pharmacokinetics. J Control Release 2007; 1: 59-67.
    • (2007) J Control Release , vol.1 , pp. 59-67
    • Yi, Y.1
  • 9
    • 0034691643 scopus 로고    scopus 로고
    • Oral bioavailability and hypoglycaemic activity of tolbutamide/ cyclodextrin inclusion complexes
    • Veiga F, et al. Oral bioavailability and hypoglycaemic activity of tolbutamide/cyclodextrin inclusion complexes. Int J Pharm 2000; 1-2: 165-171.
    • (2000) Int J Pharm , vol.12 , pp. 165-171
    • Veiga, F.1
  • 10
    • 27744575591 scopus 로고    scopus 로고
    • Cyclodextrins in drug delivery: An updated review
    • Rajeswari C, et al. Cyclodextrins in drug delivery: an updated review. AAPS PharmSciTech 2005; 2: E329-E357.
    • (2005) AAPS PharmSciTech , vol.2
    • Rajeswari, C.1
  • 11
    • 70349840419 scopus 로고    scopus 로고
    • Combined hydroxypropyl-beta-cyclodextrin and poly(anhydride) nanoparticles improve the oral permeability of paclitaxel
    • Agueros M, et al. Combined hydroxypropyl-beta-cyclodextrin and poly(anhydride) nanoparticles improve the oral permeability of paclitaxel. Eur J Pharm Sci 2009; 4: 405-413.
    • (2009) Eur J Pharm Sci , vol.4 , pp. 405-413
    • Agueros, M.1
  • 12
    • 77953360626 scopus 로고    scopus 로고
    • Increased oral bioavailability of paclitaxel by its encapsulation through complex formation with cyclodextrins in poly(anhydride) nanoparticles
    • Agüeros M, et al. Increased oral bioavailability of paclitaxel by its encapsulation through complex formation with cyclodextrins in poly(anhydride) nanoparticles. J Control Release 2010; 1: 2-8.
    • (2010) J Control Release , vol.1 , pp. 2-8
    • Agüeros, M.1
  • 13
    • 58149234269 scopus 로고    scopus 로고
    • Cyclodextrin as drug carrier molecule: A review
    • Arun R, et al. Cyclodextrin as drug carrier molecule: a review. Sci Pharm 2008; 4: 567-598.
    • (2008) Sci Pharm , vol.4 , pp. 567-598
    • Arun, R.1
  • 14
    • 80051674971 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrins: Effects on drug permeation through biological membranes
    • Loftsson T, Brewster ME,. Pharmaceutical applications of cyclodextrins: effects on drug permeation through biological membranes. J Pharm Pharmacol 2011; 9: 1119-1135.
    • (2011) J Pharm Pharmacol , vol.9 , pp. 1119-1135
    • Loftsson, T.1    Brewster, M.E.2
  • 15
    • 60149100339 scopus 로고    scopus 로고
    • Micro- and macrorheology of mucus
    • Lai SK, et al. Micro- and macrorheology of mucus. Adv Drug Deliv Rev 2009; 2: 86-100.
    • (2009) Adv Drug Deliv Rev , vol.2 , pp. 86-100
    • Lai, S.K.1
  • 16
    • 60149111908 scopus 로고    scopus 로고
    • Mucus-penetrating nanoparticles for drug and gene delivery to mucosal tissues
    • Lai SK, et al. Mucus-penetrating nanoparticles for drug and gene delivery to mucosal tissues. Adv Drug Deliv Rev 2009; 2: 158-171.
    • (2009) Adv Drug Deliv Rev , vol.2 , pp. 158-171
    • Lai, S.K.1
  • 17
    • 79951896686 scopus 로고    scopus 로고
    • Cyclodextrin-based gene delivery systems
    • Ortiz Mellet C, et al. Cyclodextrin-based gene delivery systems. Chem Soc Rev 2011; 3: 1586-1608.
    • (2011) Chem Soc Rev , vol.3 , pp. 1586-1608
    • Ortiz Mellet, C.1
  • 18
    • 43449102775 scopus 로고    scopus 로고
    • Cyclodextrin-based supramolecular architectures: Syntheses, structures, and applications for drug and gene delivery
    • Li J, Loh XJ,. Cyclodextrin-based supramolecular architectures: syntheses, structures, and applications for drug and gene delivery. Adv Drug Deliv Rev 2008; 9: 1000-1017.
    • (2008) Adv Drug Deliv Rev , vol.9 , pp. 1000-1017
    • Li, J.1    Loh, X.J.2
  • 19
    • 33847105481 scopus 로고    scopus 로고
    • Integrity of liposomes in presence of cyclodextrins: Effect of liposome type and lipid composition
    • Hatzi P, et al. Integrity of liposomes in presence of cyclodextrins: effect of liposome type and lipid composition. Int J Pharm 2007; 1-2: 167-176.
    • (2007) Int J Pharm , vol.12 , pp. 167-176
    • Hatzi, P.1
  • 20
    • 69749121352 scopus 로고    scopus 로고
    • Development of a new topical system: Drug-in-cyclodextrin-in-deformable liposome
    • Gillet A, et al. Development of a new topical system: drug-in-cyclodextrin-in-deformable liposome. Int J Pharm 2009; 1-2: 174-180.
    • (2009) Int J Pharm , vol.12 , pp. 174-180
    • Gillet, A.1
  • 21
    • 79952268655 scopus 로고    scopus 로고
    • Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus
    • Yang M, et al. Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus. Angew Chem Int Ed 2011; 50: 2597-2600.
    • (2011) Angew Chem Int Ed , vol.50 , pp. 2597-2600
    • Yang, M.1
  • 22
    • 84862599039 scopus 로고    scopus 로고
    • Novel mucus-penetrating liposomes as a potential oral drug delivery system: Preparation, in vitro characterization, and enhanced cellular uptake
    • Li X, et al. Novel mucus-penetrating liposomes as a potential oral drug delivery system: preparation, in vitro characterization, and enhanced cellular uptake. Int J Nanomedicine 2011; 6: 3151-3162.
    • (2011) Int J Nanomedicine , vol.6 , pp. 3151-3162
    • Li, X.1
  • 23
    • 77954694522 scopus 로고    scopus 로고
    • Structure, dynamics, and energetics of siRNA-cationic vector complexation: A molecular dynamics study
    • Ouyang DF, et al. Structure, dynamics, and energetics of siRNA-cationic vector complexation: a molecular dynamics study. J Phys Chem B 2010; 28: 9220-9230.
    • (2010) J Phys Chem B , vol.28 , pp. 9220-9230
    • Ouyang, D.F.1
  • 24
    • 79958818504 scopus 로고    scopus 로고
    • Preparation, characterization, pharmacokinetics, and bioactivity of honokiol-in-hydroxypropyl-β-cyclodextrin-in-liposome
    • Wang X, et al. Preparation, characterization, pharmacokinetics, and bioactivity of honokiol-in-hydroxypropyl-β-cyclodextrin-in-liposome. J Pharm Sci 2011; 8: 3357-3364.
    • (2011) J Pharm Sci , vol.8 , pp. 3357-3364
    • Wang, X.1
  • 25
    • 33645020487 scopus 로고    scopus 로고
    • Betamethasone-in-cyclodextrin-in-liposome: The effect of cyclodextrins on encapsulation efficiency and release kinetics
    • Piel G, et al. Betamethasone-in-cyclodextrin-in-liposome: the effect of cyclodextrins on encapsulation efficiency and release kinetics. Int J Pharm 2006; 1-2: 75-82.
    • (2006) Int J Pharm , vol.12 , pp. 75-82
    • Piel, G.1
  • 26
    • 1042269559 scopus 로고    scopus 로고
    • Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine
    • Kostewicz ES, et al. Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine. J Pharm Pharmacol 2004; 1: 43-51.
    • (2004) J Pharm Pharmacol , vol.1 , pp. 43-51
    • Kostewicz, E.S.1
  • 27
    • 59649096972 scopus 로고    scopus 로고
    • Solubilisation of dipalmitoylphosphatidylcholine bilayers by sodium taurocholate: A model to study the stability of liposomes in the gastrointestinal tract and their mechanism of interaction with a model bile salt
    • Andrieux K, et al. Solubilisation of dipalmitoylphosphatidylcholine bilayers by sodium taurocholate: a model to study the stability of liposomes in the gastrointestinal tract and their mechanism of interaction with a model bile salt. Eur J Pharm Biopharm 2009; 2: 346-355.
    • (2009) Eur J Pharm Biopharm , vol.2 , pp. 346-355
    • Andrieux, K.1
  • 28
    • 48149088784 scopus 로고    scopus 로고
    • Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice
    • Lu JL, et al. Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice. Eur J Pharm Biopharm 2008; 3: 899-907.
    • (2008) Eur J Pharm Biopharm , vol.3 , pp. 899-907
    • Lu, J.L.1
  • 29
    • 62749095208 scopus 로고    scopus 로고
    • Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems
    • Cui J, et al. Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems. Int J Pharm 2009; 1-2: 148-155.
    • (2009) Int J Pharm , vol.12 , pp. 148-155
    • Cui, J.1
  • 30
    • 4344561085 scopus 로고    scopus 로고
    • Insertion and partition of sodium taurocholate into egg phosphatidylcholine vesicles
    • Karine A, et al. Insertion and partition of sodium taurocholate into egg phosphatidylcholine vesicles. Pharm Res 2004; 8: 1505-1516.
    • (2004) Pharm Res , vol.8 , pp. 1505-1516
    • Karine, A.1
  • 31
    • 0036278164 scopus 로고    scopus 로고
    • Tacrolimus is a class ?Low-solubility high-permeability drug: The effect of P-glycoprotein efflux on regional permeability of tacrolimus in rats
    • Shigeki T, et al. Tacrolimus is a class ?Low-solubility high-permeability drug: the effect of P-glycoprotein efflux on regional permeability of tacrolimus in rats. J Pharm Sci 2001; 91: 719-729.
    • (2001) J Pharm Sci , vol.91 , pp. 719-729
    • Shigeki, T.1
  • 32
    • 0038340961 scopus 로고    scopus 로고
    • The site-specific transport and metabolism of tacrolimus in rat small intestine
    • Tamura S, et al. The site-specific transport and metabolism of tacrolimus in rat small intestine. J Pharmacol Exp Ther 2003; 1: 310-316.
    • (2003) J Pharmacol Exp Ther , vol.1 , pp. 310-316
    • Tamura, S.1
  • 33
    • 49549091093 scopus 로고    scopus 로고
    • A novel nanocapsule delivery system to overcome intestinal degradation and drug transport limited absorption of P-glycoprotein substrate drugs
    • Nassar T, et al. A novel nanocapsule delivery system to overcome intestinal degradation and drug transport limited absorption of P-glycoprotein substrate drugs. Pharm Res 2008; 9: 2019-2029.
    • (2008) Pharm Res , vol.9 , pp. 2019-2029
    • Nassar, T.1
  • 34
    • 57049168640 scopus 로고    scopus 로고
    • Novel double coated nanocapsules for intestinal delivery and enhanced oral bioavailability of tacrolimus, a P-gp substrate drug
    • Nassar T, et al. Novel double coated nanocapsules for intestinal delivery and enhanced oral bioavailability of tacrolimus, a P-gp substrate drug. J Control Release 2009; 1: 77-84.
    • (2009) J Control Release , vol.1 , pp. 77-84
    • Nassar, T.1
  • 35
    • 60849130683 scopus 로고    scopus 로고
    • In vivo evaluation of safety and efficacy of self-assembled nanoparticles for oral insulin delivery
    • Sonaje K, et al. In vivo evaluation of safety and efficacy of self-assembled nanoparticles for oral insulin delivery. Biomaterials 2009; 12: 2329-2339.
    • (2009) Biomaterials , vol.12 , pp. 2329-2339
    • Sonaje, K.1
  • 36
    • 67349154874 scopus 로고    scopus 로고
    • Bioadhesive properties and biodistribution of cyclodextrin- poly(anhydride) nanoparticles
    • Agüeros M, et al. Bioadhesive properties and biodistribution of cyclodextrin-poly(anhydride) nanoparticles. Eur J Pharm Sci 2009; 3-4: 231-240.
    • (2009) Eur J Pharm Sci , vol.34 , pp. 231-240
    • Agüeros, M.1
  • 37
    • 79551528343 scopus 로고    scopus 로고
    • In vitro and in vivo evaluation of WGA-carbopol modified liposomes as carriers for oral peptide delivery
    • Makhlof A, et al. In vitro and in vivo evaluation of WGA-carbopol modified liposomes as carriers for oral peptide delivery. Eur J Pharm Biopharm 2011; 2: 216-224.
    • (2011) Eur J Pharm Biopharm , vol.2 , pp. 216-224
    • Makhlof, A.1
  • 38
    • 38349112036 scopus 로고    scopus 로고
    • Improved intestinal absorption of calcitonin by mucoadhesive delivery of novel pectin-liposome nanocomplexes
    • Thirawong N, et al. Improved intestinal absorption of calcitonin by mucoadhesive delivery of novel pectin-liposome nanocomplexes. J Control Release 2008; 3: 236-245.
    • (2008) J Control Release , vol.3 , pp. 236-245
    • Thirawong, N.1
  • 39
    • 0037035977 scopus 로고    scopus 로고
    • Computer-aided molecular modeling techniques for predicting the stability of drug-cyclodextrin inclusion complexes in aqueous solutions
    • Maria Teresa F, et al. Computer-aided molecular modeling techniques for predicting the stability of drug-cyclodextrin inclusion complexes in aqueous solutions. Chem Phys Lett 2002; 358: 383-390.
    • (2002) Chem Phys Lett , vol.358 , pp. 383-390
    • Maria Teresa, F.1
  • 40
    • 84862833264 scopus 로고    scopus 로고
    • Liposomes containing glycocholate as potential oral insulin delivery systems: Preparation, in vitro characterization, and improved protection against enzymatic degradation
    • Niu M, et al. Liposomes containing glycocholate as potential oral insulin delivery systems: preparation, in vitro characterization, and improved protection against enzymatic degradation. Int J Nanomedicine 2011; 6: 1155-1166.
    • (2011) Int J Nanomedicine , vol.6 , pp. 1155-1166
    • Niu, M.1
  • 41
    • 79151473262 scopus 로고    scopus 로고
    • Stability of liposomes containing bio-enhancers and tetraether lipids in simulated gastro-intestinal fluids
    • Parmentier J, et al. Stability of liposomes containing bio-enhancers and tetraether lipids in simulated gastro-intestinal fluids. Int J Pharm 2011; 1-2: 210-217.
    • (2011) Int J Pharm , vol.12 , pp. 210-217
    • Parmentier, J.1
  • 42
    • 80155182416 scopus 로고    scopus 로고
    • Enhanced oral bioavailability of cyclosporine A by liposomes containing a bile salt
    • Guan P, et al. Enhanced oral bioavailability of cyclosporine A by liposomes containing a bile salt. Int J Nanomedicine 2011; 6: 965-974.
    • (2011) Int J Nanomedicine , vol.6 , pp. 965-974
    • Guan, P.1
  • 43
    • 23844462026 scopus 로고    scopus 로고
    • Role of clathrin- and caveolae-mediated endocytosis in gene transfer mediated by lipo- and polyplexes
    • Rejman J, et al. Role of clathrin- and caveolae-mediated endocytosis in gene transfer mediated by lipo- and polyplexes. Mol Ther 2005; 3: 468-474.
    • (2005) Mol Ther , vol.3 , pp. 468-474
    • Rejman, J.1
  • 44
    • 79952268655 scopus 로고    scopus 로고
    • Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus
    • Yang M, et al. Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus. Angew Chem Int Ed Engl 2011; 11: 2597-2600.
    • (2011) Angew Chem Int Ed Engl , vol.11 , pp. 2597-2600
    • Yang, M.1


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