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Volumn 160, Issue 1, 2012, Pages 25-32

In vitro and in vivo performance of novel supersaturated self-nanoemulsifying drug delivery systems (super-SNEDDS)

Author keywords

Amorphous; Bioavailability; Precipitation; SNEDDS; Supersaturation

Indexed keywords

BIOAVAILABILITY; COSOLVENTS; DRIVING FORCES; DRUG CONCENTRATION; DRUG DELIVERY SYSTEM; ENHANCED ABSORPTION; EQUILIBRIUM SOLUBILITIES; HALOFANTRINE; IN-VITRO; IN-VIVO; LONG CHAINS; POORLY WATER-SOLUBLE DRUGS; PREDICTIVITY; SNEDDS; SOLUBILISATION; SOYBEAN OIL;

EID: 84861529172     PISSN: 01683659     EISSN: 18734995     Source Type: Journal    
DOI: 10.1016/j.jconrel.2012.02.027     Document Type: Article
Times cited : (181)

References (39)
  • 1
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • C.A. Lipinski, F. Lombardo, B.W. Dominy, and P.J. Feeney Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Deliv. Rev. 23 1997 3 25
    • (1997) Adv. Drug Deliv. Rev. , vol.23 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 3
    • 68349160715 scopus 로고    scopus 로고
    • Lipid - An emerging platform for oral delivery of drugs with poor bioavailability
    • S. Chakraborty, D. Shukla, B. Mishra, and S. Singh Lipid - an emerging platform for oral delivery of drugs with poor bioavailability Eur. J. Pharm. Biopharm. 73 2009 1 70
    • (2009) Eur. J. Pharm. Biopharm. , vol.73 , pp. 1-70
    • Chakraborty, S.1    Shukla, D.2    Mishra, B.3    Singh, S.4
  • 4
    • 0029562489 scopus 로고
    • Lipid microemulsions for Improving drug dissolution and oral absorption: Physical and biopharmaceutical aspects
    • P.P. Constantinides Lipid microemulsions for Improving drug dissolution and oral absorption: physical and biopharmaceutical aspects Pharm. Res. 12 1995 1561 1572
    • (1995) Pharm. Res. , vol.12 , pp. 1561-1572
    • Constantinides, P.P.1
  • 5
    • 34548049221 scopus 로고    scopus 로고
    • Oral lipid-based formulations
    • D.H. Hauss Oral lipid-based formulations Adv. Drug Deliv. Rev. 59 2007 667 676
    • (2007) Adv. Drug Deliv. Rev. , vol.59 , pp. 667-676
    • Hauss, D.H.1
  • 6
    • 0031125683 scopus 로고    scopus 로고
    • Charman, lipid-based vehicles for the oral delivery of poorly water soluble drugs
    • W.N. Humberstone Charman, lipid-based vehicles for the oral delivery of poorly water soluble drugs Adv. Drug Deliv. Rev. 25 1997 103 128
    • (1997) Adv. Drug Deliv. Rev. , vol.25 , pp. 103-128
    • Humberstone, W.N.1
  • 7
    • 39149092022 scopus 로고    scopus 로고
    • Enhancing intenstinal drug solubilisation using lipid-based delivery systems
    • C.J.H. Porter, C.W. Pouton, J.F. Cuine, and W.N. Charman Enhancing intenstinal drug solubilisation using lipid-based delivery systems Adv. Drug Deliv. Rev. 60 2008 673 691
    • (2008) Adv. Drug Deliv. Rev. , vol.60 , pp. 673-691
    • Porter, C.J.H.1    Pouton, C.W.2    Cuine, J.F.3    Charman, W.N.4
  • 8
    • 33847394968 scopus 로고    scopus 로고
    • Lipids and lipid-based formulations: Optimizing the oral delivery of lipophilic drugs
    • C.J.H. 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
    • (2007) Nat. Rev. Drug Discov. , vol.6 , pp. 231-248
    • Porter, C.J.H.1    Trevaskis, N.L.2    Charman, W.N.3
  • 9
    • 34247536339 scopus 로고    scopus 로고
    • Morphological observations on a lipid-based drug delivery system during in vitro digestion
    • D.G. Fatouros, B. Bergenstahl, and A. Müllertz Morphological observations on a lipid-based drug delivery system during in vitro digestion Eur. J. Pharm. Sci. 31 2007 85 94
    • (2007) Eur. J. Pharm. Sci. , vol.31 , pp. 85-94
    • Fatouros, D.G.1    Bergenstahl, B.2    Müllertz, A.3
  • 10
    • 58549106999 scopus 로고    scopus 로고
    • Colloidal structures in media simulating intestinal fed state conditions with and without lipolysis products
    • D.G. Fatouros, I. Walrand, B. Bergenstahl, and A. Müllertz Colloidal structures in media simulating intestinal fed state conditions with and without lipolysis products Pharm. Res. 26 2008 361 374
    • (2008) Pharm. Res. , vol.26 , pp. 361-374
    • Fatouros, D.G.1    Walrand, I.2    Bergenstahl, B.3    Müllertz, A.4
  • 12
    • 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
    • J.F. Cuiné, C.L. Claire, 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
    • (2008) J. Pharm. Sci. , vol.97 , pp. 995-1012
    • Cuiné, J.F.1    Claire, C.L.2    McEvoy, L.3    Charman, W.N.4    Pouton, C.W.5    Edwards, G.A.6    Benameur, H.7    Porter, C.J.H.8
  • 13
    • 5644294406 scopus 로고    scopus 로고
    • Solubilisation of poorly water-soluble drugs during in vitro lipolysis of medium- and long-chain triacylglycerols
    • J. Christensen, K. Schultz, B. Mollgard, H.G. Kristensen, and A. Müllertz Solubilisation of poorly water-soluble drugs during in vitro lipolysis of medium- and long-chain triacylglycerols Eur. J. Pharm. Sci. 23 2004 287 296
    • (2004) Eur. J. Pharm. Sci. , vol.23 , pp. 287-296
    • Christensen, J.1    Schultz, K.2    Mollgard, B.3    Kristensen, H.G.4    Müllertz, A.5
  • 14
    • 1242292226 scopus 로고    scopus 로고
    • Drug solubilization behavior during in vitro digestion of simple triglyceride lipid solution formulations
    • A.M. Kaukonen, B.J. Boyd, C.J.H. Porter, and W.N. Charman Drug solubilization behavior during in vitro digestion of simple triglyceride lipid solution formulations Pharm. Res. 21 2004 245 253
    • (2004) Pharm. Res. , vol.21 , pp. 245-253
    • Kaukonen, A.M.1    Boyd, B.J.2    Porter, C.J.H.3    Charman, W.N.4
  • 15
    • 59849110173 scopus 로고    scopus 로고
    • Characterization and optimization of AMG 517 supersaturatable self-emulsifying drug delivery system (S-SEDDS) for improved oral absorption
    • P. Gao, A. Akrami, F. Alvarez, J. Hu, L. Li, C. Ma, and S. Surapaneni Characterization and optimization of AMG 517 supersaturatable self-emulsifying drug delivery system (S-SEDDS) for improved oral absorption J. Pharm. Sci. 98 2009 516 528
    • (2009) J. Pharm. Sci. , vol.98 , pp. 516-528
    • Gao, P.1    Akrami, A.2    Alvarez, F.3    Hu, J.4    Li, L.5    Ma, C.6    Surapaneni, S.7
  • 16
    • 0344012523 scopus 로고    scopus 로고
    • Development of a supersaturable SEDDS (S-SEDDS) formulation of paclitaxel with improved oral bioavailability
    • P. Gao, B.D. Rush, W.P. Pfund, T. Huang, J.M. Bauer, W. Morozowich, M.-S. Kuo, and M.J. Hageman Development of a supersaturable SEDDS (S-SEDDS) formulation of paclitaxel with improved oral bioavailability J. Pharm. Sci. 92 2003 2386 2398
    • (2003) J. Pharm. Sci. , vol.92 , pp. 2386-2398
    • Gao, P.1    Rush, B.D.2    Pfund, W.P.3    Huang, T.4    Bauer, J.M.5    Morozowich, W.6    Kuo, M.-S.7    Hageman, M.J.8
  • 17
    • 78049518013 scopus 로고    scopus 로고
    • Precipitation of a poorly soluble model drug during in vitro lipolysis: Characterization and dissolution of the precipitate
    • P.J. Sassene, M.M. Knopp, J.Z. Hesselkilde, V. Koradia, A. Larsen, T. Rades, and A. Müllertz Precipitation of a poorly soluble model drug during in vitro lipolysis: characterization and dissolution of the precipitate J. Pharm. Sci. 99 2010 4982 4991
    • (2010) J. Pharm. Sci. , vol.99 , pp. 4982-4991
    • Sassene, P.J.1    Knopp, M.M.2    Hesselkilde, J.Z.3    Koradia, V.4    Larsen, A.5    Rades, T.6    Müllertz, A.7
  • 18
    • 33847364354 scopus 로고    scopus 로고
    • Increasing the proportional content of surfactant (Cremophor EL) relative to lipid in self-emulsifying lipid-based formulations of danazol reduces oral bioavailability in beagle dogs
    • J.F. Cuiné, W.N. Charman, C.W. Pouton, G.A. Edwards, and C.J.H. Porter Increasing the proportional content of surfactant (Cremophor EL) relative to lipid in self-emulsifying lipid-based formulations of danazol reduces oral bioavailability in beagle dogs Pharm. Res. 24 2004 748 757
    • (2004) Pharm. Res. , vol.24 , pp. 748-757
    • Cuiné, J.F.1    Charman, W.N.2    Pouton, C.W.3    Edwards, G.A.4    Porter, C.J.H.5
  • 20
    • 2242472082 scopus 로고    scopus 로고
    • Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) in cosmetic and dermatological preparations
    • (Supplement)
    • 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 Deliv. Rev. 54 2002 S131 S155 (Supplement)
    • (2002) Adv. Drug Deliv. Rev. , vol.54
    • Müller, R.H.1    Radtke, M.2    Wissing, S.A.3
  • 21
    • 0030899727 scopus 로고    scopus 로고
    • The penetration of supersaturated solutions of piroxicam across silicone membranes and human skin in vitro
    • M.A. Pellett, S. Castellano, J. Hadgraft, and A.F. Davis The penetration of supersaturated solutions of piroxicam across silicone membranes and human skin in vitro J. Control. Release 46 1997 205 214
    • (1997) J. Control. Release , vol.46 , pp. 205-214
    • Pellett, M.A.1    Castellano, S.2    Hadgraft, J.3    Davis, A.F.4
  • 22
    • 0029926358 scopus 로고    scopus 로고
    • Lymphatic transport of halofantrine in the triple-cannulated anesthetized rat model: Effect of lipid vehicle dispersion
    • C.J.H. Porter, S.A. Charman, and W.N. Charman Lymphatic transport of halofantrine in the triple-cannulated anesthetized rat model: effect of lipid vehicle dispersion J. Pharm. Sci. 85 1996 351 356
    • (1996) J. Pharm. Sci. , vol.85 , pp. 351-356
    • Porter, C.J.H.1    Charman, S.A.2    Charman, W.N.3
  • 23
    • 0037371606 scopus 로고    scopus 로고
    • Separation and characterization of the colloidal phases produced on digestion of common formulation lipids and assessment of their impact on the apparent solubility of selected poorly water-soluble drugs
    • G.A. Kossena, B.J. Boyd, C.J.H. Porter, and W.N. Charman Separation and characterization of the colloidal phases produced on digestion of common formulation lipids and assessment of their impact on the apparent solubility of selected poorly water-soluble drugs J. Pharm. Sci. 92 2003 634 648
    • (2003) J. Pharm. Sci. , vol.92 , pp. 634-648
    • Kossena, G.A.1    Boyd, B.J.2    Porter, C.J.H.3    Charman, W.N.4
  • 24
    • 0028919886 scopus 로고
    • A simplified liquid chromatography assay for the quantitation of halofantrine and desbutylhalofantrine in plasma and identification of a degradation product of desbutylhalofantrine formed under alkaline conditions
    • A.J. Humberstone, G.J. Currie, C.J.H. Porter, M.J. Scanlon, and W.N. Charman A simplified liquid chromatography assay for the quantitation of halofantrine and desbutylhalofantrine in plasma and identification of a degradation product of desbutylhalofantrine formed under alkaline conditions J. Pharm. Biomed. Anal. 13 1995 265 272
    • (1995) J. Pharm. Biomed. Anal. , vol.13 , pp. 265-272
    • Humberstone, A.J.1    Currie, G.J.2    Porter, C.J.H.3    Scanlon, M.J.4    Charman, W.N.5
  • 25
    • 84864323714 scopus 로고    scopus 로고
    • Influence of lipid composition and drug load on the in vitro performance of self-nanoemulsifying drug delivery systems (SNEDDS)
    • 10.1002/jps.23054
    • N. Thomas, A. Müllertz, A. Graf, and T. Rades Influence of lipid composition and drug load on the in vitro performance of self-nanoemulsifying drug delivery systems (SNEDDS) J. Pharm. Sci. 101 2012 1721 1731 10.1002/jps.23054
    • (2012) J. Pharm. Sci. , vol.101 , pp. 1721-1731
    • Thomas, N.1    Müllertz, A.2    Graf, A.3    Rades, T.4
  • 26
    • 0034898463 scopus 로고    scopus 로고
    • A dynamic in vitro lipolysis model: I. Controlling the rate of lipolysis by continuous addition of calcium
    • N.H. Zangenberg, A. Müllertz, H.G. Kristensen, and L. Hovgaard 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.H.1    Müllertz, A.2    Kristensen, H.G.3    Hovgaard, L.4
  • 28
    • 50449093858 scopus 로고    scopus 로고
    • Intestinal lymphatic transport of halofantrine in rats assessed using a chylomicron flow blocking approach: The influence of polysorbate 60 and 80
    • M.L. Lind, J. Jacobsen, R. Holm, and A. Müllertz Intestinal lymphatic transport of halofantrine in rats assessed using a chylomicron flow blocking approach: the influence of polysorbate 60 and 80 Eur. J. Pharm. Sci. 35 2008 211 218
    • (2008) Eur. J. Pharm. Sci. , vol.35 , pp. 211-218
    • Lind, M.L.1    Jacobsen, J.2    Holm, R.3    Müllertz, A.4
  • 29
    • 79952282344 scopus 로고    scopus 로고
    • A novel excipient, 1-perfluorohexyloctane shows limited utility for the oral delivery of poorly water-soluble drugs
    • R. Holm, E.B. Jorgensen, M. Harborg, R. Larsen, P. Holm, A. Müllertz, and J. Jacobsen A novel excipient, 1-perfluorohexyloctane shows limited utility for the oral delivery of poorly water-soluble drugs Eur. J. Pharm. Sci. 42 2011 416 422
    • (2011) Eur. J. Pharm. Sci. , vol.42 , pp. 416-422
    • Holm, R.1    Jorgensen, E.B.2    Harborg, M.3    Larsen, R.4    Holm, P.5    Müllertz, A.6    Jacobsen, J.7
  • 30
    • 0036744709 scopus 로고    scopus 로고
    • Structured triglyceride vehicles for oral delivery of halofantrine: Examination of intestinal lymphatic transport and bioavailability in conscious rats
    • R. Holm, C. Porter, A. Müllertz, H. Kristensen, and W. Charman Structured triglyceride vehicles for oral delivery of halofantrine: examination of intestinal lymphatic transport and bioavailability in conscious rats Pharm. Res. 19 2002 1354 1361
    • (2002) Pharm. Res. , vol.19 , pp. 1354-1361
    • Holm, R.1    Porter, C.2    Müllertz, A.3    Kristensen, H.4    Charman, W.5
  • 31
    • 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
    • C.J.H. Porter, and A.M. Kaukonen 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
    • (2004) J. Pharm. Sci. , vol.93 , pp. 1110-1121
    • Porter, C.J.H.1    Kaukonen, A.M.2
  • 32
    • 0034854134 scopus 로고    scopus 로고
    • Comparison of the lymphatic transport of halofantrine administered in disperse systems containing three different unsaturated fatty acids
    • R. Holm, A. Müllertz, G.P. Pedersen, and H.G. Kristensen Comparison of the lymphatic transport of halofantrine administered in disperse systems containing three different unsaturated fatty acids Pharm. Res. 18 2001 1299 1304
    • (2001) Pharm. Res. , vol.18 , pp. 1299-1304
    • Holm, R.1    Müllertz, A.2    Pedersen, G.P.3    Kristensen, H.G.4
  • 33
    • 0043122366 scopus 로고    scopus 로고
    • Intestinal lymphatic transport of halofantrine occurs after oral administration of a unit-dose lipid-based formulation to fasted dogs
    • S.-M. Khoo, D.M. Shackleford, C.J.H. Porter, and G.A. Edwards Intestinal lymphatic transport of halofantrine occurs after oral administration of a unit-dose lipid-based formulation to fasted dogs Pharm. Res. 20 2003 1460 1465
    • (2003) Pharm. Res. , vol.20 , pp. 1460-1465
    • Khoo, S.-M.1    Shackleford, D.M.2    Porter, C.J.H.3    Edwards, G.A.4
  • 35
    • 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 H. Amnon 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    Amnon, H.2
  • 36
    • 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. Müllertz 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    Müllertz, A.3
  • 37
    • 0029996464 scopus 로고    scopus 로고
    • A physicochemical basis for the effect of food on the absolute oral bioavailability of halofantrine
    • A.J. Humberstone, C.J.H. Porter, and W.N. Charman A physicochemical basis for the effect of food on the absolute oral bioavailability of halofantrine J. Pharm. Sci. 85 1996 525 529
    • (1996) J. Pharm. Sci. , vol.85 , pp. 525-529
    • Humberstone, A.J.1    Porter, C.J.H.2    Charman, W.N.3
  • 38
    • 33750592309 scopus 로고    scopus 로고
    • Use of a dynamic in vitro lipolysis model to rationalize oral formulation development for poor water soluble drugs: Correlation with in vivo data and the relationship to intra-enterocyte processes in rats
    • A. Dahan, and A. Hoffmann Use of a dynamic in vitro lipolysis model to rationalize oral formulation development for poor water soluble drugs: correlation with in vivo data and the relationship to intra-enterocyte processes in rats Pharm. Res. 23 2006 2165 2174
    • (2006) Pharm. Res. , vol.23 , pp. 2165-2174
    • Dahan, A.1    Hoffmann, A.2
  • 39
    • 57149136074 scopus 로고    scopus 로고
    • Lipid-based formulations for danazol containing a digestible surfactant, Labrafil M2125CS: In vivo bioavailability and dynamic in vitro lipolysis
    • A. Larsen, R. Holm, M. Pedersen, and A. Müllertz Lipid-based formulations for danazol containing a digestible surfactant, Labrafil M2125CS: in vivo bioavailability and dynamic in vitro lipolysis Pharm. Res. 25 2008 2769 2777
    • (2008) Pharm. Res. , vol.25 , pp. 2769-2777
    • Larsen, A.1    Holm, R.2    Pedersen, M.3    Müllertz, A.4


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