메뉴 건너뛰기




Volumn 2, Issue SUPPL. 1, 2010, Pages 37-42

Newer approches to self emulsifying drug delivery system

Author keywords

Biopharmaceutical classification; Dosage form; Excipients; Self emulsification

Indexed keywords

ABACAVIR; ALLOPURINOL; ARTEMETHER; BIPERIDEN; CARBAMAZEPINE; CHLORAMPHENICOL; CIMETIDINE; DAPSONE; DIAZEPAM; DICLOFENAC; EFAVIRENZ; ETHAMBUTOL; FLUOROURACIL; FUROSEMIDE; HALOPERIDOL; HYDRALAZINE; IBUPROFEN; INDINAVIR; LIPOSOME; MACROGOL STEARATE; MICROCRYSTALLINE CELLULOSE; MICROSPHERE; NIMESULIDE; PACLITAXEL; PHENYTOIN; PROGESTERONE; SOLID LIPID NANOPARTICLE; UBIQUINONE; UNINDEXED DRUG; VINPOCETINE;

EID: 77953425034     PISSN: None     EISSN: 09751491     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (28)

References (45)
  • 1
    • 0006421460 scopus 로고
    • The design of dosage forms
    • Aulton M.E, eds, Churchill Livingstone, Edinburgh;
    • York P, The design of dosage forms, In: Aulton M.E. (eds.), Pharmaceutics The science of dosage form design. Churchill Livingstone, Edinburgh; 1988. p 1-13.
    • (1988) Pharmaceutics The science of dosage form design , pp. 1-13
    • York, P.1
  • 2
    • 0032509855 scopus 로고    scopus 로고
    • Improvement of dissolution characteristics and bioavailability of poorly water-soluble drugs by novel cogrinding method using water-soluble polymer
    • Sugimoto M, Okagaki T, Narisawa S, Koida Y, and Nakajima K. Improvement of dissolution characteristics and bioavailability of poorly water-soluble drugs by novel cogrinding method using water-soluble polymer. Int. J. Pharma, 1998; 160: 11-19.
    • (1998) Int. J. Pharma , vol.160 , pp. 11-19
    • Sugimoto, M.1    Okagaki, T.2    Narisawa, S.3    Koida, Y.4    Nakajima, K.5
  • 3
    • 0031725929 scopus 로고    scopus 로고
    • Investigation of formulation approaches to improve the dissolution of SB-210661, a poorly water soluble 5- lipooxygenase inhibitor
    • Perng CH, Kearney AS, Patel K, Palepu NR, Zuber G. Investigation of formulation approaches to improve the dissolution of SB-210661, a poorly water soluble 5- lipooxygenase inhibitor. Int. J. Pharma, 1998; 176: 31-38.
    • (1998) Int. J. Pharma , vol.176 , pp. 31-38
    • Perng, C.H.1    Kearney, A.S.2    Patel, K.3    Palepu, N.R.4    Zuber, G.5
  • 5
    • 0022366625 scopus 로고
    • Self-emulsifying drug delivery system; assessment of the efficiency of emulsification
    • Pouton CW, Self-emulsifying drug delivery system; assessment of the efficiency of emulsification. Int. J. Pharm. 1985; 27: 335-348.
    • (1985) Int. J. Pharm , vol.27 , pp. 335-348
    • Pouton, C.W.1
  • 7
    • 0035984949 scopus 로고    scopus 로고
    • Lipid based formulation for intestinal lymphatic delivery
    • O'Driscoll CM. Lipid based formulation for intestinal lymphatic delivery. Eur. J. Pharm. Sci. 2002; 15: 405-415.
    • (2002) Eur. J. Pharm. Sci , vol.15 , pp. 405-415
    • O'Driscoll, C.M.1
  • 8
    • 0026586447 scopus 로고
    • Self-emulsifying drug delivery system: Formulation and biopharmaceutical evaluation of an investigational lipophilic compound
    • Charman SA, Charman WN, Rogge MC, Wilson TD, Dutko FJ, Pouton C W. Self-emulsifying drug delivery system: formulation and biopharmaceutical evaluation of an investigational lipophilic compound. Pharm. Res. 1992; 9: 87-93.
    • (1992) Pharm. Res , vol.9 , pp. 87-93
    • Charman, S.A.1    Charman, W.N.2    Rogge, M.C.3    Wilson, T.D.4    Dutko, F.J.5    Pouton, C.W.6
  • 9
    • 0028194817 scopus 로고
    • Self- emulsifying Drug Delivery systems (SEDDS) with polyglycolized glycerides for improving in-vitro dissolution and oral absorption of lipophilic drugs
    • Shah NH, Carvajal M T, Patel CI, Infiled M H, Malick AW. Self- emulsifying Drug Delivery systems (SEDDS) with polyglycolized glycerides for improving in-vitro dissolution and oral absorption of lipophilic drugs. Int. J. Pharm. 1994; 106: 15-23.
    • (1994) Int. J. Pharm , vol.106 , pp. 15-23
    • Shah, N.H.1    Carvajal, M.T.2    Patel, C.I.3    Infiled, M.H.4    Malick, A.W.5
  • 10
    • 0032103706 scopus 로고    scopus 로고
    • Formulation Design and bioavailability assessment of lipidic self-emulsifying formulation of halofantrine
    • Khoo S M, Humberstone A J, Porter CJH, Edward GA, Charman WN. Formulation Design and bioavailability assessment of lipidic self-emulsifying formulation of halofantrine. Int. J. Pharm. 1998; 167: 155-164.
    • (1998) Int. J. Pharm , vol.167 , pp. 155-164
    • Khoo, S.M.1    Humberstone, A.J.2    Porter, C.J.H.3    Edward, G.A.4    Charman, W.N.5
  • 11
    • 0028948839 scopus 로고
    • Therotical basis for a biopharmaceutical classification: The correlation of invitro drug product dissolution and in vivo bioavailability
    • Amidon GL, Lennernas H, Shah VP, Crison JRA. Therotical basis for a biopharmaceutical classification: The correlation of invitro drug product dissolution and in vivo bioavailability. Pharm Res, 1995; 12: 413-420.
    • (1995) Pharm Res , vol.12 , pp. 413-420
    • Amidon, G.L.1    Lennernas, H.2    Shah, V.P.3    Crison, J.R.A.4
  • 12
    • 77953459871 scopus 로고    scopus 로고
    • European Patent EP 1 886 667 A1 Microemulsified Drug Formulation
    • European Patent EP 1 886 667 A1 (Microemulsified Drug Formulation).
  • 13
    • 13544270954 scopus 로고    scopus 로고
    • Self-emulsifying pellets prepared by wet granulation in high-shear mixer: Influence of formulation variables and preliminary study on the in vitro absorption
    • Franceschinis E, Voinovich D, Grassi M, Perissutti Filipovic- Grcic BJ, Martinac A, Meriani-Merlo F. Self-emulsifying pellets prepared by wet granulation in high-shear mixer: influence of formulation variables and preliminary study on the in vitro absorption. Int. J. Pharm. 2005; 291: 87-97.
    • (2005) Int. J. Pharm , vol.291 , pp. 87-97
    • Franceschinis, E.1    Voinovich, D.2    Grassi, M.3    Perissutti4    Filipovic- Grcic, B.J.5    Martinac, A.6    Meriani-Merlo, F.7
  • 14
    • 0034889914 scopus 로고    scopus 로고
    • The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture
    • Newton M, Petersson J, Podczeck F, Clarke A, Booth S. The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture. J. Pharm. Sci. 2000; 90: 987-995.
    • (2000) J. Pharm. Sci , vol.90 , pp. 987-995
    • Newton, M.1    Petersson, J.2    Podczeck, F.3    Clarke, A.4    Booth, S.5
  • 16
    • 0016296842 scopus 로고
    • Measurement of "spontaneity" of self emulsifiable oils
    • Groves MJ, Mustafa RMA. Measurement of "spontaneity" of self emulsifiable oils. J. Pharm Pharmacol. 1974; 26: 671-688.
    • (1974) J. Pharm Pharmacol , vol.26 , pp. 671-688
    • Groves, M.J.1    Mustafa, R.M.A.2
  • 18
    • 0343487750 scopus 로고    scopus 로고
    • Formulation of self-emulsifying drug delivery system
    • Pouton CW. Formulation of self-emulsifying drug delivery system. Adv. Drug Del. Rev. 1997; 25: 47-58.
    • (1997) Adv. Drug Del. Rev , vol.25 , pp. 47-58
    • Pouton, C.W.1
  • 19
    • 77953436905 scopus 로고    scopus 로고
    • Non-aqueous compositions for oral delivery of insoluble bioactive agents
    • US Pat 20070190080
    • Friedman D, Non-aqueous compositions for oral delivery of insoluble bioactive agents. US Pat 20070190080
    • Friedman, D.1
  • 20
    • 0016255066 scopus 로고
    • Fatty acid binding protein in the small intestine; indentification, isolation and evidence for its role in cellular fatty acid transport
    • Ockner RK, Manning JM, Fatty acid binding protein in the small intestine; indentification, isolation and evidence for its role in cellular fatty acid transport. Journal. Clinical Invest. 1974; 54: 326-338.
    • (1974) Journal. Clinical Invest , vol.54 , pp. 326-338
    • Ockner, R.K.1    Manning, J.M.2
  • 21
    • 0013882158 scopus 로고
    • Absorption of medium and long chain triglycerides: Factors influencing their hydrolysis and transport. Journal of
    • Greenberger NJ, Rodgers JB, Isselbacher KJ. Absorption of medium and long chain triglycerides: factors influencing their hydrolysis and transport. Journal of. Clinical Invest. 1966; 45: 217-227.
    • (1966) Clinical Invest , vol.45 , pp. 217-227
    • Greenberger, N.J.1    Rodgers, J.B.2    Isselbacher, K.J.3
  • 22
    • 0343051915 scopus 로고    scopus 로고
    • Uptake of drug into the intestinal lymphatic after oral administration
    • Porter CJH, Charman WN, Uptake of drug into the intestinal lymphatic after oral administration. Adv. Drug Del. Rev. 1997; 25: 71-89.
    • (1997) Adv. Drug Del. Rev , vol.25 , pp. 71-89
    • Porter, C.J.H.1    Charman, W.N.2
  • 23
    • 0023126917 scopus 로고
    • Lipid Vehicles for intestinal lymphatic drug transport
    • Cheema M, Palin K., Davis SS. Lipid Vehicles for intestinal lymphatic drug transport. J. Pharm Pharmacol. 1987; 39: 55-56.
    • (1987) J. Pharm Pharmacol , vol.39 , pp. 55-56
    • Cheema, M.1    Palin, K.2    Davis, S.S.3
  • 24
    • 0343907176 scopus 로고    scopus 로고
    • Structure and function of gastro- intestinal lipase
    • Embleton JK, Pouton CW. Structure and function of gastro- intestinal lipase, Adv. Drug Del. Rev. 1997; 25:15-32.
    • (1997) Adv. Drug Del. Rev , vol.25 , pp. 15-32
    • Embleton, J.K.1    Pouton, C.W.2
  • 27
    • 20444508016 scopus 로고    scopus 로고
    • Oral solid gentamicin preparation using emulsifier and adsorbent
    • Ito YKT, Ishida M, Tawa R, Shibata N, Takada K Oral solid gentamicin preparation using emulsifier and adsorbent. J. Cont. Rel. 2005; 105: 23-31.
    • (2005) J. Cont. Rel , vol.105 , pp. 23-31
    • Ito, Y.K.T.1    Ishida, M.2    Tawa, R.3    Shibata, N.4    Takada, K.5
  • 28
    • 33646383855 scopus 로고    scopus 로고
    • Controlled release of a self-emulsifying formulation from a tablet dosage form: Stability assessment and optimization of some processing parameters
    • Nazzal S, Khan MA, Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters. Int. J. Pharm. 2006; 315: 110-121,
    • (2006) Int. J. Pharm , vol.315 , pp. 110-121
    • Nazzal, S.1    Khan, M.A.2
  • 29
    • 24644475058 scopus 로고    scopus 로고
    • Melt extrusion-based dosage forms: Excipients and processing conditions for pharmaceutical formulations
    • Verreck G. Brewster ME. Melt extrusion-based dosage forms: excipients and processing conditions for pharmaceutical formulations. Bull. Tech. Gattefosse, 2004; 97: 85-95.
    • (2004) Bull. Tech. Gattefosse , vol.97 , pp. 85-95
    • Verreck, G.1    Brewster, M.E.2
  • 32
    • 8444221211 scopus 로고    scopus 로고
    • Process characteristics and compaction of spray-dried emulsions containing a drug dissolved in lipid
    • Hansen T, Holm P, Schultz K. Process characteristics and compaction of spray-dried emulsions containing a drug dissolved in lipid. Int. J. Pharm. 2004; 287: 55-66.
    • (2004) Int. J. Pharm , vol.287 , pp. 55-66
    • Hansen, T.1    Holm, P.2    Schultz, K.3
  • 33
    • 33745847130 scopus 로고    scopus 로고
    • Improvement of bioavailability and photostability of amlodipine using redispersible dry emulsion
    • Jang DJ, Jeong EJ, Lee HM, Kim BC, Lim SJ, Kim CK. Improvement of bioavailability and photostability of amlodipine using redispersible dry emulsion. Eur. J. Pharm. Sci. 2006; 28: 405-411.
    • (2006) Eur. J. Pharm. Sci , vol.28 , pp. 405-411
    • Jang, D.J.1    Jeong, E.J.2    Lee, H.M.3    Kim, B.C.4    Lim, S.J.5    Kim, C.K.6
  • 34
    • 0037142237 scopus 로고    scopus 로고
    • Optimiztion of a self-nanoemulsified tablets dosage form of Ubiquinone using response surface methodology: Effect of formulation ingredients
    • Nazzal S, Nutan M, Palamakula Shah AR, Zaghloul AA, Khan MA, Optimiztion of a self-nanoemulsified tablets dosage form of Ubiquinone using response surface methodology: effect of formulation ingredients. Int. J. Pharm. 2002; 240: 103-114.
    • (2002) Int. J. Pharm , vol.240 , pp. 103-114
    • Nazzal, S.1    Nutan, M.2    Palamakula Shah, A.R.3    Zaghloul, A.A.4    Khan, M.A.5
  • 36
    • 2642540226 scopus 로고    scopus 로고
    • Comparative bioavailability study in Dogs of a self-emulsifying formulation of progesterone presented in a pellets and liquid form compared with an aqueous suspension of progesterone
    • Tuleu C. et al. Comparative bioavailability study in Dogs of a self-emulsifying formulation of progesterone presented in a pellets and liquid form compared with an aqueous suspension of progesterone. J. Pharm Sci, 2004; 93(6): 1495-1502.
    • (2004) J. Pharm Sci , vol.93 , Issue.6 , pp. 1495-1502
    • Tuleu, C.1
  • 37
    • 13544270954 scopus 로고    scopus 로고
    • Self-emulsifying pellets by wet granulation in high -shear mixer: Influence of formulation variables and preliminary study on the in vitro absorption
    • Franceschinis E, et al. Self-emulsifying pellets by wet granulation in high -shear mixer: influence of formulation variables and preliminary study on the in vitro absorption. Int. J. Pharm. 2005; 291: 87-97.
    • (2005) Int. J. Pharm , vol.291 , pp. 87-97
    • Franceschinis, E.1
  • 38
    • 33751518550 scopus 로고    scopus 로고
    • Controlled drug release from pellets containing water-insoluble drugs dissolved in a self-emulsifying system
    • Serratoni M, Newton M, Booth S, Clarke A. Controlled drug release from pellets containing water-insoluble drugs dissolved in a self-emulsifying system. Eur. J. Pharm. Biopharm. 2007; 65: 94-98.
    • (2007) Eur. J. Pharm. Biopharm , vol.65 , pp. 94-98
    • Serratoni, M.1    Newton, M.2    Booth, S.3    Clarke, A.4
  • 39
    • 34247536269 scopus 로고    scopus 로고
    • Preparation and characterization of a self-emulsifying pellets formulation
    • Abdalla A, Mader K. Preparation and characterization of a self-emulsifying pellets formulation. Eur. J. Pharm Biopharm. 2007; 66: 220-226.
    • (2007) Eur. J. Pharm Biopharm , vol.66 , pp. 220-226
    • Abdalla, A.1    Mader, K.2
  • 40
    • 43249131737 scopus 로고    scopus 로고
    • Bi-layered self-emulsifying pellets prepared by co-extrusion and speronization: Influence of formulation variables and preliminary study on the in vivo absorption
    • Iosio T., et al. Bi-layered self-emulsifying pellets prepared by co-extrusion and speronization: Influence of formulation variables and preliminary study on the in vivo absorption. Eur.J. Pharm. Biopharm. 2008 ;69(2): 686-697.
    • (2008) Eur.J. Pharm. Biopharm , vol.69 , Issue.2 , pp. 686-697
    • Iosio, T.1
  • 41
    • 33645468795 scopus 로고    scopus 로고
    • Patil, P. and Paradkar, A Porous polystyrene beads as carriers for self emulsifying system containing loratadine. AAPS Pharm. Sci. Tech. 10.1208/ pt070128. 2006;
    • Patil, P. and Paradkar, A Porous polystyrene beads as carriers for self emulsifying system containing loratadine. AAPS Pharm. Sci. Tech. 10.1208/ pt070128. 2006;
  • 42
    • 11144249850 scopus 로고    scopus 로고
    • A novel formulation design about water-insoluble oily drug:preparation of zedoary turmeric oil microspheres with self emulsifying ability and evaluation in rabbits
    • You J, Fu-de Cui, Qing-po Li, X. Han, Ying-Wei Yu. A novel formulation design about water-insoluble oily drug:preparation of zedoary turmeric oil microspheres with self emulsifying ability and evaluation in rabbits. Int. J. Pharm. 2005; 288(2): 315-325.
    • (2005) Int. J. Pharm , vol.288 , Issue.2 , pp. 315-325
    • You, J.1    de Cui, F.2    po Li, Q.3    Han, X.4    Wei Yu, Y.5
  • 43
    • 26444465627 scopus 로고    scopus 로고
    • In vitro evaluation of drug release from self micro-emulsifying drug delivery systems using a biodegradable homo lipid from Capra hircus
    • Attama AA, Nkemnele MO. In vitro evaluation of drug release from self micro-emulsifying drug delivery systems using a biodegradable homo lipid from Capra hircus. Int. J. Pharm. 2005; 304: 4-10.
    • (2005) Int. J. Pharm , vol.304 , pp. 4-10
    • Attama, A.A.1    Nkemnele, M.O.2
  • 44
    • 34249674062 scopus 로고    scopus 로고
    • Preparation and evaluation of 5-FU/PLGA/gene nanoparticles
    • Hu YX. et al., Preparation and evaluation of 5-FU/PLGA/gene nanoparticles. Key Eng. Mat.2005; 288-289 147-150.
    • (2005) Key Eng. Mat
    • Hu, Y.X.1
  • 45
    • 51449104994 scopus 로고    scopus 로고
    • A novel nanoparticle formulation for sustained paclitaxel delivery. AAPS Pharm. Sci. Tech
    • 1208/s12249-008-9063-7
    • Trickler WJ. et al. A novel nanoparticle formulation for sustained paclitaxel delivery. AAPS Pharm. Sci. Tech., 2008;10 1208/s12249-008-9063-7.
    • (2008) , pp. 10
    • Trickler, W.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.