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Volumn 51, Issue 1, 2014, Pages 204-210

Investigating the correlation between in vivo absorption and in vitro release of fenofibrate from lipid matrix particles in biorelevant medium

Author keywords

Absorption; Fenofibrate; In vitro lipolysis; Lipid matrix particle; Particle size

Indexed keywords

CLOFIBRIC ACID; DRUG CARRIER; FENOFIBRATE; LIPID; LIPID MATRIX PARTICLE; PANCREATIN; UNCLASSIFIED DRUG;

EID: 84886545604     PISSN: 09280987     EISSN: 18790720     Source Type: Journal    
DOI: 10.1016/j.ejps.2013.09.022     Document Type: Article
Times cited : (38)

References (33)
  • 1
    • 84885081422 scopus 로고    scopus 로고
    • Biopharmaceutical classification of poorly soluble drugs with respect to "enabling formulations"
    • S.T. Buckley, K.J. Frank, G. Fricker, and M. Brandl Biopharmaceutical classification of poorly soluble drugs with respect to "enabling formulations" Eur. J. Pharm. Sci. 50 2013 8 16
    • (2013) Eur. J. Pharm. Sci. , vol.50 , pp. 8-16
    • Buckley, S.T.1    Frank, K.J.2    Fricker, G.3    Brandl, M.4
  • 3
    • 67349097388 scopus 로고    scopus 로고
    • Enhanced bioavailability of the poorly water-soluble drug fenofibrate by using liposomes containing a bile salt
    • Y. Chen, Y. Lu, J. Chen, J. Lai, J. Sun, F. Hu, and W. Wu Enhanced bioavailability of the poorly water-soluble drug fenofibrate by using liposomes containing a bile salt Int. J. Pharm. 376 2009 153 160
    • (2009) Int. J. Pharm. , vol.376 , pp. 153-160
    • Chen, Y.1    Lu, Y.2    Chen, J.3    Lai, J.4    Sun, J.5    Hu, F.6    Wu, W.7
  • 4
    • 39149091886 scopus 로고    scopus 로고
    • Evaluation of the impact of surfactant digestion on the bioavailability of danazol after oral administration of lipidic self-emulsifying formulations to dogs
    • DOI 10.1002/jps.21246
    • J.F. Cuiné, C.L. McEvoy, W.N. Charman, C.W. Pouton, G.A. Edwards, H. Benameur, and C.J.H. Porter Evaluation of the impact of surfactant digestion on the bioavailability of danazol after oral administration of lipidic self-emulsifying formulations to dogs J. Pharm. Sci. 97 2008 995 1012 (Pubitemid 351293898)
    • (2008) Journal of Pharmaceutical Sciences , vol.97 , Issue.2 , pp. 995-1012
    • Cuine, J.F.1    Mcevoy, C.L.2    Charman, W.N.3    Pouton, C.W.4    Edwards, G.A.5    Benameur, H.6    Porter, C.J.H.7
  • 5
    • 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
    • A. Dahan, and A. Hoffman 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 129 2008 1 10
    • (2008) J. Control. Release , vol.129 , pp. 1-10
    • Dahan, A.1    Hoffman, A.2
  • 6
    • 80051869434 scopus 로고    scopus 로고
    • Formulation and evaluation of solid lipid nanoparticles of ramipril
    • P. Ekambaram, and H.S. Abdul Formulation and evaluation of solid lipid nanoparticles of ramipril J. Young Pharm. 3 2011 216 220
    • (2011) J. Young Pharm. , vol.3 , pp. 216-220
    • Ekambaram, P.1    Abdul, H.S.2
  • 8
    • 34547863131 scopus 로고    scopus 로고
    • Pharmacokinetic evaluation of oral fenofibrate nanosuspensions and SLN in comparison to conventional suspensions of micronized drug
    • DOI 10.1016/j.addr.2007.04.005, PII S0169409X07000397, Lipid Nanoparticles: Recent Advances
    • A. Hanafy, H. Spahn-Langguth, G. Vergnault, P. Grenier, M. Tubic Grozdanis, T. Lenhardt, and P. Langguth Pharmacokinetic evaluation of oral fenofibrate nanosuspensions and SLN in comparison to conventional suspensions of micronized drug Adv. Drug Deliv. Rev. 59 2007 419 426 (Pubitemid 47260709)
    • (2007) Advanced Drug Delivery Reviews , vol.59 , Issue.6 , pp. 419-426
    • Hanafy, A.1    Spahn-Langguth, H.2    Vergnault, G.3    Grenier, P.4    Tubic Grozdanis, M.5    Lenhardt, T.6    Langguth, P.7
  • 9
    • 84884154027 scopus 로고    scopus 로고
    • Bile salts and their importance for drug absorption
    • R. Holm, A. Müllertz, and H. Mu Bile salts and their importance for drug absorption Int. J. Pharm. 453 2013 44 55
    • (2013) Int. J. Pharm. , vol.453 , pp. 44-55
    • Holm, R.1    Müllertz, A.2    Mu, H.3
  • 10
    • 10044223246 scopus 로고    scopus 로고
    • Solid lipid nanoparticles (SLNs) to improve oral bioavailability of poorly soluble drugs
    • DOI 10.1211/0022357044959
    • L. Hu, X. Tang, and F. Cui Solid lipid nanoparticles (SLNs) to improve oral bioavailability of poorly soluble drugs J. Pharm. Pharmacol. 56 2004 1527 1535 (Pubitemid 39601993)
    • (2004) Journal of Pharmacy and Pharmacology , vol.56 , Issue.12 , pp. 1527-1535
    • Hu, L.1    Tang, X.2    Cui, F.3
  • 11
    • 80054692198 scopus 로고    scopus 로고
    • Design of fenofibrate microemulsion for improved bioavailability
    • L. Hu, H. Wu, F. Niu, C. Yan, X. Yang, and Y. Jia Design of fenofibrate microemulsion for improved bioavailability Int. J. Pharm. 420 2011 251 255
    • (2011) Int. J. Pharm. , vol.420 , pp. 251-255
    • Hu, L.1    Wu, H.2    Niu, F.3    Yan, C.4    Yang, X.5    Jia, Y.6
  • 12
    • 79851474101 scopus 로고    scopus 로고
    • Design and evaluation of self-nanoemulsifying drug delivery system of flutamide
    • J.B. Jeevana, and K. Sreelakshmi Design and evaluation of self-nanoemulsifying drug delivery system of flutamide J. Young Pharm. 3 2011 4 8
    • (2011) J. Young Pharm. , vol.3 , pp. 4-8
    • Jeevana, J.B.1    Sreelakshmi, K.2
  • 13
    • 80052265520 scopus 로고    scopus 로고
    • In vitro lipolysis models as a tool for the characterization of oral lipid and surfactant based drug delivery systems
    • A.T. Larsen, P. Sassene, and A. Mullertz In vitro lipolysis models as a tool for the characterization of oral lipid and surfactant based drug delivery systems Int. J. Pharm. 417 2011 245 255
    • (2011) Int. J. Pharm. , vol.417 , pp. 245-255
    • Larsen, A.T.1    Sassene, P.2    Mullertz, A.3
  • 14
    • 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. Methods 44 2000 235 249 (Pubitemid 32239479)
    • (2000) Journal of Pharmacological and Toxicological Methods , vol.44 , Issue.1 , pp. 235-249
    • Lipinski, C.A.1
  • 15
    • 70349238697 scopus 로고    scopus 로고
    • Design of lipid-based formulations for oral administration of poorly water-soluble drugs: Precipitation of drug after dispersion of formulations in aqueous solution
    • K. Mohsin, M.A. Long, and C.W. Pouton Design of lipid-based formulations for oral administration of poorly water-soluble drugs: Precipitation of drug after dispersion of formulations in aqueous solution J. Pharm. Sci. 98 2009 3582 3595
    • (2009) J. Pharm. Sci. , vol.98 , pp. 3582-3595
    • Mohsin, K.1    Long, M.A.2    Pouton, C.W.3
  • 16
    • 84884160665 scopus 로고    scopus 로고
    • Lipid-based formulations for oral administration of poorly water-soluble drugs
    • H. Mu, R. Holm, and A. Müllertz Lipid-based formulations for oral administration of poorly water-soluble drugs Int. J. Pharm. 453 2013 215 224
    • (2013) Int. J. Pharm. , vol.453 , pp. 215-224
    • Mu, H.1    Holm, R.2    Müllertz, A.3
  • 17
    • 57349171371 scopus 로고    scopus 로고
    • Lipid nanoparticles with a solid matrix (SLN, NLC, LDC) for oral drug delivery
    • M. Muchow, P. Maincent, and R.H. Müller Lipid nanoparticles with a solid matrix (SLN, NLC, LDC) for oral drug delivery Drug Dev. Ind. Pharm. 34 2008 1394 1405
    • (2008) Drug Dev. Ind. Pharm. , vol.34 , pp. 1394-1405
    • Muchow, M.1    Maincent, P.2    Müller, R.H.3
  • 18
    • 0038032150 scopus 로고    scopus 로고
    • Solid lipid nanoparticles (SLN) for controlled drug delivery - A review of the state of the art
    • DOI 10.1016/S0939-6411(00)00087-4, PII S0939641100000874
    • R. Müller, K. Mäder, and S. Gohla Solid lipid nanoparticles (SLN) for controlled drug delivery - a review of the state of the art Eur. J. Pharm. Biopharm. 50 2000 161 177 (Pubitemid 30326695)
    • (2000) European Journal of Pharmaceutics and Biopharmaceutics , vol.50 , Issue.1 , pp. 161-177
    • Muller, R.H.1    Mader, K.2    Gohla, S.3
  • 19
    • 2242472082 scopus 로고    scopus 로고
    • Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) in cosmetic and dermatological preparations
    • R.H. Müller, M. Radtke, and S.A. Wissing Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) in cosmetic and dermatological preparations Adv. Drug Del. Rev. 54 2002 S131 S155
    • (2002) Adv. Drug Del. Rev. , vol.54
    • Müller, R.H.1    Radtke, M.2    Wissing, S.A.3
  • 20
    • 39849097998 scopus 로고    scopus 로고
    • Cyclosporine-loaded solid lipid nanoparticles (SLN): Drug-lipid physicochemical interactions and characterization of drug incorporation
    • DOI 10.1016/j.ejpb.2007.07.006, PII S0939641107002603
    • R.H. Müller, S.A. Runge, V. Ravelli, A.F. Thunemann, W. Mehnert, and E.B. Souto Cyclosporine-loaded solid lipid nanoparticles (SLN): drug-lipid physicochemical interactions and characterization of drug incorporation Eur. J. Pharm. Biopharm. 68 2008 535 544 (Pubitemid 351318197)
    • (2008) European Journal of Pharmaceutics and Biopharmaceutics , vol.68 , Issue.3 , pp. 535-544
    • Muller, R.H.1    Runge, S.A.2    Ravelli, V.3    Thunemann, A.F.4    Mehnert, W.5    Souto, E.B.6
  • 21
    • 0042383291 scopus 로고    scopus 로고
    • Improvement of cefpodoxime proxetil oral absorption in rats by an oil-in-water submicron emulsion
    • DOI 10.1016/S0378-5173(03)00365-X
    • G. Nicolaos, S. Crauste-Manciet, R. Farinotti, and D. Brossard Improvement of cefpodoxime proxetil oral absorption in rats by an oil-in-water submicron emulsion Int. J. Pharm. 263 2003 165 171 (Pubitemid 37087943)
    • (2003) International Journal of Pharmaceutics , vol.263 , Issue.1-2 , pp. 165-171
    • Nicolaos, G.1    Crauste-Manciet, S.2    Farinotti, R.3    Brossard, D.4
  • 22
    • 33847394968 scopus 로고    scopus 로고
    • Lipids and lipid-based formulations: Optimizing the oral delivery of lipophilic drugs
    • DOI 10.1038/nrd2197, PII NRD2197
    • C.J. Porter, N.L. Trevaskis, and W.N. Charman Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs Nat. Rev. Drug Discov. 6 2007 231 248 (Pubitemid 46344627)
    • (2007) Nature Reviews Drug Discovery , vol.6 , Issue.3 , pp. 231-248
    • Porter, C.J.H.1    Trevaskis, N.L.2    Charman, W.N.3
  • 23
    • 1942498896 scopus 로고    scopus 로고
    • Use of in Vitro Lipid Digestion Data to Explain the in Vivo Performance of Triglyceride-Based Oral Lipid Formulations of Poorly Water-Soluble Drugs: Studies with Halofantrine
    • DOI 10.1002/jps.20039
    • C.J.H. Porter, A.M. Kaukonen, A. Taillardat-Bertschinger, B.J. Boyd, J.M. O'Connor, G.A. Edwards, and W.N. Charman Use of in vitro lipid digestion data to explain the in vivo performance of triglyceride-based oral lipid formulations of poorly water-soluble drugs: studies with halofantrine J. Pharm. Sci. 93 2004 1110 1121 (Pubitemid 38529685)
    • (2004) Journal of Pharmaceutical Sciences , vol.93 , Issue.5 , pp. 1110-1121
    • Porter, C.J.H.1    Kaukonen, A.M.2    Taillardat-Bertschinger, A.3    Boyd, B.J.4    O'Connor, J.M.5    Edwards, G.A.6    Charman, W.N.7
  • 24
    • 84875878549 scopus 로고    scopus 로고
    • Optimization of self nanoemulsifying drug delivery system for poorly water-soluble drug using response surface methodology
    • S. Ren, H. Mu, F. Alchaer, A. Chtatou, and A. Mullertz Optimization of self nanoemulsifying drug delivery system for poorly water-soluble drug using response surface methodology Drug Dev. Ind. Pharm. 39 2013 799 806
    • (2013) Drug Dev. Ind. Pharm. , vol.39 , pp. 799-806
    • Ren, S.1    Mu, H.2    Alchaer, F.3    Chtatou, A.4    Mullertz, A.5
  • 25
    • 79952586373 scopus 로고    scopus 로고
    • Development of a novel method for fabrication of solid lipid nanoparticles: Using high shear homogenization and ultrasonication
    • A. Sharma, M. Jindal, G. Aggarwal, and S. Jain Development of a novel method for fabrication of solid lipid nanoparticles: using high shear homogenization and ultrasonication Res. J. Pharm. Biol. Chem. Sci. 1 2010 265 274
    • (2010) Res. J. Pharm. Biol. Chem. Sci. , vol.1 , pp. 265-274
    • Sharma, A.1    Jindal, M.2    Aggarwal, G.3    Jain, S.4
  • 26
    • 77953283407 scopus 로고    scopus 로고
    • Lipid nanoparticles: Effect on bioavailability and pharmacokinetic changes
    • E.B. Souto, and R.H. Müller Lipid nanoparticles: effect on bioavailability and pharmacokinetic changes Handb. Exp. Pharmacol. 2010 115 141
    • (2010) Handb. Exp. Pharmacol. , pp. 115-141
    • Souto, E.B.1    Müller, R.H.2
  • 27
    • 80052757917 scopus 로고    scopus 로고
    • Formulation and characterization of lipid-based drug delivery system of raloxifene-microemulsion and self-microemulsifying drug delivery system
    • H. Thakkar, J. Nangesh, M. Parmar, and D. Patel Formulation and characterization of lipid-based drug delivery system of raloxifene-microemulsion and self-microemulsifying drug delivery system J. Pharm. Bioallied Sci. 3 2011 442 448
    • (2011) J. Pharm. Bioallied Sci. , vol.3 , pp. 442-448
    • Thakkar, H.1    Nangesh, J.2    Parmar, M.3    Patel, D.4
  • 28
    • 79960190356 scopus 로고    scopus 로고
    • Nanostructured lipid carrier versus solid lipid nanoparticles of simvastatin: Comparative analysis of characteristics, pharmacokinetics and tissue uptake
    • R. Tiwari, and K. Pathak Nanostructured lipid carrier versus solid lipid nanoparticles of simvastatin: comparative analysis of characteristics, pharmacokinetics and tissue uptake Int. J. Pharm. 415 2011 232 243
    • (2011) Int. J. Pharm. , vol.415 , pp. 232-243
    • Tiwari, R.1    Pathak, K.2
  • 29
    • 0030866983 scopus 로고    scopus 로고
    • Physicochemical characterization of lipid nanoparticles and evaluation of their drug loading capacity and sustained release potential
    • DOI 10.1016/S0168-3659(97)00046-1, PII S0168365997000461
    • K. Westesen, H. Bunjes, and M.H.J. Koch Physicochemical characterization of lipid nanoparticles and evaluation of their drug loading capacity and sustained release potential J. Control. Release 48 1997 223 236 (Pubitemid 27401980)
    • (1997) Journal of Controlled Release , vol.48 , Issue.2-3 , pp. 223-236
    • Westesen, K.1    Bunjes, H.2    Koch, M.H.J.3
  • 30
    • 80052830812 scopus 로고    scopus 로고
    • Preparation and evaluation of ofloxacin-loaded palmitic acid solid lipid nanoparticles
    • S. Xie, L. Zhu, Z. Dong, Y. Wang, X. Wang, and W. Zhou Preparation and evaluation of ofloxacin-loaded palmitic acid solid lipid nanoparticles Int. J. Nanomed. 6 2011 547 555
    • (2011) Int. J. Nanomed. , vol.6 , pp. 547-555
    • Xie, S.1    Zhu, L.2    Dong, Z.3    Wang, Y.4    Wang, X.5    Zhou, W.6
  • 32
    • 0034898463 scopus 로고    scopus 로고
    • A dynamic in vitro lipolysis model: I. Controlling the rate of lipolysis by continuous addition of calcium
    • N.M.A. Zangenberg, and H.H.L. Kristensen A dynamic in vitro lipolysis model: I. Controlling the rate of lipolysis by continuous addition of calcium Eur. J. Pharm. Sci. 14 2001 115 122
    • (2001) Eur. J. Pharm. Sci. , vol.14 , pp. 115-122
    • Zangenberg, N.M.A.1    Kristensen, H.H.L.2
  • 33
    • 0031960962 scopus 로고    scopus 로고
    • Solid lipid nanoparticles (SLN) for controlled drug delivery - Drug release and release mechanism
    • DOI 10.1016/S0939-6411(97)00150-1, PII S0939641197001501
    • A. Zur Mühlen, C. Schwarz, and W. Mehnert Solid lipid nanoparticles (SLN) for controlled drug delivery -Drug release and release mechanism Eur. J. Pharm. Biopharm. 45 1998 149 155 (Pubitemid 28167741)
    • (1998) European Journal of Pharmaceutics and Biopharmaceutics , vol.45 , Issue.2 , pp. 149-155
    • Zur Muhlen, A.1    Schwarz, C.2    Mehnert, W.3


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