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Volumn 38, Issue 10, 2012, Pages 1262-1269

In vitro digestion kinetics of excipients for lipid-based drug delivery and introduction of a relative lipolysis half life

Author keywords

Biorelevant test; Kinetic model; Lipid formulations; Lipolysis; Lipolysis degree; Pharmaceutical additives

Indexed keywords

CAPRYOL; CREMOPHOR; DIACYLGLYCEROL; DRUG ADDITIVE; EXCIPIENT; GELUCIRE; IMWITOR; LAUROGLYCOL; LIPID; MEDIUM CHAIN TRIACYLGLYCEROL; MIGLYOL; MONOACYLGLYCEROL; OCTANOIN; PEGLICOL 5 OLEATE; POLYSORBATE 80; TRIACYLGLYCEROL; UNCLASSIFIED DRUG;

EID: 84866241046     PISSN: 03639045     EISSN: 15205762     Source Type: Journal    
DOI: 10.3109/03639045.2011.645834     Document Type: Article
Times cited : (20)

References (31)
  • 1
    • 78649654159 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrins: Basic science and product development
    • Loftsson T, Brewster ME. (2010). Pharmaceutical applications of cyclodextrins: basic science and product development. J Pharm Pharmacol, 62:1607-1621.
    • (2010) J Pharm Pharmacol , vol.62 , pp. 1607-1621
    • Loftsson, T.1    Brewster, M.E.2
  • 2
    • 4544383493 scopus 로고    scopus 로고
    • Nanosuspensions in drug delivery
    • DOI 10.1038/nrd1494
    • Rabinow BE. (2004). Nanosuspensions in drug delivery. Nat Rev Drug Discov, 3:785-796. (Pubitemid 39242830)
    • (2004) Nature Reviews Drug Discovery , vol.3 , Issue.9 , pp. 785-796
    • Rabinow, B.E.1
  • 3
    • 0031853979 scopus 로고    scopus 로고
    • Interactions of griseofulvin with cyclodextrins in solid binary systems
    • DOI 10.1021/js970233x
    • Veiga MD, Díaz PJ, Ahsan F. (1998). Interactions of griseofulvin with cyclodextrins in solid binary systems. J Pharm Sci, 87: 891-900. (Pubitemid 28319422)
    • (1998) Journal of Pharmaceutical Sciences , vol.87 , Issue.7 , pp. 891-900
    • Veiga, M.D.1    Diaz, P.J.2    Ahsan, F.3
  • 4
    • 0033805858 scopus 로고    scopus 로고
    • Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
    • Pouton CW. (2000). Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems. Eur J Pharm Sci, 11 Suppl 2:S93-S98.
    • (2000) Eur J Pharm Sci , vol.11 , Issue.SUPPL. 2
    • Pouton, C.W.1
  • 5
    • 77955842200 scopus 로고    scopus 로고
    • Effects of non-ionic surfactants on in vitro triglyceride digestion and their susceptibility to digestion by pancreatic enzymes
    • Christiansen A, Backensfeld T, Weitschies W. (2010). Effects of non-ionic surfactants on in vitro triglyceride digestion and their susceptibility to digestion by pancreatic enzymes. Eur J Pharm Sci, 41:376-382.
    • (2010) Eur J Pharm Sci , vol.41 , pp. 376-382
    • Christiansen, A.1    Backensfeld, T.2    Weitschies, W.3
  • 6
    • 0035984949 scopus 로고    scopus 로고
    • Lipid-based formulations for intestinal lymphatic delivery
    • DOI 10.1016/S0928-0987(02)00051-9, PII S0928098702000519
    • O'Driscoll CM. (2002). Lipid-based formulations for intestinal lymphatic delivery. Eur J Pharm Sci, 15:405-415. (Pubitemid 34567104)
    • (2002) European Journal of Pharmaceutical Sciences , vol.15 , Issue.5 , pp. 405-415
    • O'Driscoll, C.M.1
  • 7
    • 79952224749 scopus 로고    scopus 로고
    • Oral self-emulsifying drug delivery systems, from biopharmaceutical to technical formulation aspects
    • Kuentz M. (2011). Oral self-emulsifying drug delivery systems, from biopharmaceutical to technical formulation aspects. J Drug Deliv Sci Technol, 21:17-26.
    • (2011) J Drug Deliv Sci Technol , vol.21 , pp. 17-26
    • Kuentz, M.1
  • 8
    • 5644294406 scopus 로고    scopus 로고
    • Solubilisation of poorly water-soluble drugs during in vitro lipolysis of medium- and long-chain triacylglycerols
    • DOI 10.1016/j.ejps.2004.08.003, PII S0928098704002003
    • Christensen JOø, Schultz K, Mollgaard B, Kristensen HG, Mullertz A. (2004). Solubilisation of poorly water-soluble drugs during in vitro lipolysis of medium- and long-chain triacylglycerols. Eur J Pharm Sci, 23:287-296. (Pubitemid 39369884)
    • (2004) European Journal of Pharmaceutical Sciences , vol.23 , Issue.3 , pp. 287-296
    • Christensen, J.O.1    Schultz, K.2    Mollgaard, B.3    Kristensen, H.G.4    Mullertz, A.5
  • 9
    • 34250867442 scopus 로고    scopus 로고
    • The effect of different lipid based formulations on the oral absorption of lipophilic drugs: The ability of in vitro lipolysis and consecutive ex vivo intestinal permeability data to predict in vivo bioavailability in rats
    • DOI 10.1016/j.ejpb.2007.01.017, PII S0939641107000227
    • Dahan A, Hoffman A. (2007). The effect of different lipid based formulations on the oral absorption of lipophilic drugs: the ability of in vitro lipolysis and consecutive ex vivo intestinal permeability data to predict in vivo bioavailability in rats. Eur J Pharm Biopharm, 67:96-105. (Pubitemid 46991342)
    • (2007) European Journal of Pharmaceutics and Biopharmaceutics , vol.67 , Issue.1 , pp. 96-105
    • Dahan, A.1    Hoffman, A.2
  • 10
    • 1242292226 scopus 로고    scopus 로고
    • Drug Solubilization Behavior during in Vitro Digestion of Simple Triglyceride Lipid Solution Formulations
    • DOI 10.1023/B:PHAM.0000016282.77887.1f
    • Kaukonen AM, Boyd BJ, Porter CJ, Charman WN. (2004). Drug solubilization behavior during in vitro digestion of simple triglyceride lipid solution formulations. Pharm Res, 21:245-253. (Pubitemid 38221969)
    • (2004) Pharmaceutical Research , vol.21 , Issue.2 , pp. 245-253
    • Kaukonen, A.M.1    Boyd, B.J.2    Porter, C.J.H.3    Charman, W.N.4
  • 11
    • 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
    • Porter CJ, Kaukonen AM, Taillardat-Bertschinger A, Boyd BJ, O'Connor JM, Edwards GA et al. (2004). Use of in vitro lipid digestion data to explain the in vivo performance of triglyceridebased oral lipid formulations of poorly water-soluble drugs: studies with halofantrine. J Pharm Sci, 93:1110-1121. (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
  • 13
    • 67650034409 scopus 로고    scopus 로고
    • In vitro gastrointestinal lipolysis of four formulations of piroxicam and cinnarizine with the self emulsifying excipients Labrasol and Gelucire 44/14
    • Fernandez S, Chevrier S, Ritter N, Mahler B, Demarne F, Carrière F et al. (2009). In vitro gastrointestinal lipolysis of four formulations of piroxicam and cinnarizine with the self emulsifying excipients Labrasol and Gelucire 44/14. Pharm Res, 26:1901-1910.
    • (2009) Pharm Res , vol.26 , pp. 1901-1910
    • Fernandez, S.1    Chevrier, S.2    Ritter, N.3    Mahler, B.4    Demarne, F.5    Carrière, F.6
  • 14
    • 0023724835 scopus 로고
    • In vitro model for ciclosporin intestinal absorption in lipid vesicles
    • DOI 10.1023/A:1015987223407
    • Reymond JP, Sucker H. (1988). In vitro model for ciclosporin intestinal absorption in lipid vehicles. Pharm Res, 5:673-676. (Pubitemid 18263617)
    • (1988) Pharmaceutical Research , vol.5 , Issue.10 , pp. 673-676
    • Reymond, J.-P.1    Sucker, H.2
  • 15
    • 0036159895 scopus 로고    scopus 로고
    • Evaluation of the in-vitro digestion profiles of long and medium chain glycerides and the phase behaviour of their lipolytic products
    • DOI 10.1211/0022357021771896
    • Sek L, Porter CJ, Kaukonen AM, Charman WN. (2002). Evaluation of the in-vitro digestion profiles of long and medium chain glycerides and the phase behaviour of their lipolytic products. J Pharm Pharmacol, 54:29-41. (Pubitemid 34116220)
    • (2002) Journal of Pharmacy and Pharmacology , vol.54 , Issue.1 , pp. 29-41
    • Sek, L.1    Porter, C.J.H.2    Kaukonen, A.M.3    Charman, W.N.4
  • 16
    • 0034898463 scopus 로고    scopus 로고
    • A dynamic in vitro lipolysis model. I. Controlling the rate of lipolysis by continuous addition of calcium
    • DOI 10.1016/S0928-0987(01)00169-5, PII S0928098701001695
    • Zangenberg NH, Müllertz A, Kristensen HG, Hovgaard L. (2001). A dynamic in vitro lipolysis model. I. Controlling the rate of lipolysis by continuous addition of calcium. Eur J Pharm Sci, 14:115-122. (Pubitemid 32737533)
    • (2001) European Journal of Pharmaceutical Sciences , vol.14 , Issue.2 , pp. 115-122
    • Zangenberg, N.H.1    Mullertz, A.2    Kristensen, H.G.3    Hovgaard, L.4
  • 17
    • 34247489694 scopus 로고    scopus 로고
    • Correlation between digestion of the lipid phase of smedds and release of the anti-HIV drug UC 781 and the anti-mycotic drug enilconazole from smedds
    • DOI 10.1016/j.ejpb.2006.10.005, PII S0939641106002761
    • Goddeeris C, Coacci J, Van den Mooter G. (2007). Correlation between digestion of the lipid phase of smedds and release of the anti-HIV drug UC 781 and the anti-mycotic drug enilconazole from smedds. Eur J Pharm Biopharm, 66:173-181. (Pubitemid 46654766)
    • (2007) European Journal of Pharmaceutics and Biopharmaceutics , vol.66 , Issue.2 , pp. 173-181
    • Goddeeris, C.1    Coacci, J.2    Van Den Mooter, G.3
  • 19
    • 0001097080 scopus 로고    scopus 로고
    • Interfacial and temporal organization of lipolysis
    • Panaiotov I, Ivanova M, Verger R. (1997). Interfacial and temporal organization of lipolysis. Curr Opin Colloid In, 2:517-525.
    • (1997) Curr Opin Colloid in , vol.2 , pp. 517-525
    • Panaiotov, I.1    Ivanova, M.2    Verger, R.3
  • 20
  • 22
    • 2242464517 scopus 로고
    • New parameters for simulating progress curves of the lipase reaction
    • Kosugi Y, Suzuki H. (1983). New parameters for simulating progress curves of the lipase reaction. J Ferment Technol, 61:287-294.
    • (1983) J Ferment Technol , vol.61 , pp. 287-294
    • Kosugi, Y.1    Suzuki, H.2
  • 23
    • 0031893209 scopus 로고    scopus 로고
    • Kinetics of lipase-catalyzed hydrolysis of palm oil in lecithin/izooctane reversed micelles
    • DOI 10.1007/s002530051167
    • Knezevic ZD, Siler-Marinkovic SS, Mojovic LV. (1998). Kinetics of lipase-catalyzed hydrolysis of palm oil in lecithin/isooctane reversed micelles. Appl Microbiol Biotechnol, 49:267-271. (Pubitemid 28172639)
    • (1998) Applied Microbiology and Biotechnology , vol.49 , Issue.3 , pp. 267-271
    • Knezevic, Z.D.1    Siler-Marinkovic, S.S.2    Mojovic, L.V.3
  • 24
    • 0343907176 scopus 로고    scopus 로고
    • Structure and function of gastrointestinal lipases
    • Embleton JK, Pouton CW. (1997). Structure and function of gastrointestinal lipases. Adv Drug Del Rev, 25:15-32.
    • (1997) Adv Drug Del Rev , vol.25 , pp. 15-32
    • Embleton, J.K.1    Pouton, C.W.2
  • 25
    • 44749087279 scopus 로고    scopus 로고
    • Dissolution media simulating conditions in the proximal human gastrointestinal tract: An update
    • Jantratid E, Janssen N, Reppas C, Dressman JB. (2008). Dissolution media simulating conditions in the proximal human gastrointestinal tract: an update. Pharm Res, 25:1663-1676.
    • (2008) Pharm Res , vol.25 , pp. 1663-1676
    • Jantratid, E.1    Janssen, N.2    Reppas, C.3    Dressman, J.B.4
  • 26
    • 77950619099 scopus 로고    scopus 로고
    • Comparison of different in vitro tests to assess oral lipid-based formulations using a poorly soluble acidic drug
    • Arnold Y, Gonzalez RB, Versace H, Kuentz M. (2010). Comparison of different in vitro tests to assess oral lipid-based formulations using a poorly soluble acidic drug. J Drug Del Sci Tech, 20:143-148.
    • (2010) J Drug Del Sci Tech , vol.20 , pp. 143-148
    • Arnold, Y.1    Gonzalez, R.B.2    Versace, H.3    Kuentz, M.4
  • 27
    • 0020837232 scopus 로고
    • Studies on the detergent inhibition of pancreatic lipase activity
    • Gargouri Y, Julien R, Bois AG, Verger R, Sarda L. (1983). Studies on the detergent inhibition of pancreatic lipase activity. J Lipid Res, 24:1336-1342.
    • (1983) J Lipid Res , vol.24 , pp. 1336-1342
    • Gargouri, Y.1    Julien, R.2    Bois, A.G.3    Verger, R.4    Sarda, L.5
  • 28
    • 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
    • Cuiné JF, McEvoy CL, Charman WN, Pouton CW, Edwards GA, Benameur H, Porter CJH. (2007). 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, 993-1010.
    • (2007) J Pharm Sci , vol.97 , pp. 993-1010
    • Cuiné, 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
  • 29
    • 39049129258 scopus 로고    scopus 로고
    • In vitro lipid digestion models in design of drug delivery systems for enhancing oral bioavailability
    • DOI 10.1517/17425255.4.1.65
    • Fatouros DG, Mullertz A. (2008). In vitro lipid digestion models in design of drug delivery systems for enhancing oral bioavailability. Expert Opin Drug Metab Toxicol, 4:65-76. (Pubitemid 351234101)
    • (2008) Expert Opinion on Drug Metabolism and Toxicology , vol.4 , Issue.1 , pp. 65-76
    • Fatouros, D.G.1    Mullertz, A.2
  • 30
    • 79960751951 scopus 로고    scopus 로고
    • Real time evolution of liquid crystalline nanostructure during the digestion of formulation lipids using synchrotron small-angle X-ray scattering
    • Warren DB, Anby MU, Hawley A, Boyd BJ. (2011). Real time evolution of liquid crystalline nanostructure during the digestion of formulation lipids using synchrotron small-angle X-ray scattering. Langmuir, 27:9528-9534.
    • (2011) Langmuir , vol.27 , pp. 9528-9534
    • Warren, D.B.1    Anby, M.U.2    Hawley, A.3    Boyd, B.J.4
  • 31
    • 39549095134 scopus 로고    scopus 로고
    • Comparison between lipolysis and compendial dissolution as alternative techniques for the in vitro characterization of α-tocopherol self-emulsified drug delivery systems (SEDDS)
    • Ali H, Nazzal M, Zaghloul AA, Nazzal S. (2008). Comparison between lipolysis and compendial dissolution as alternative techniques for the in vitro characterization of α-tocopherol self-emulsified drug delivery systems (SEDDS). Int J Pharm, 352:104-114.
    • (2008) Int J Pharm , vol.352 , pp. 104-114
    • Ali, H.1    Nazzal, M.2    Zaghloul, A.A.3    Nazzal, S.4


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