메뉴 건너뛰기




Volumn 315, Issue 1-2, 2006, Pages 110-121

Controlled release of a self-emulsifying formulation from a tablet dosage form: Stability assessment and optimization of some processing parameters

Author keywords

Coenzyme Q10; Controlled release; Face centered cubic design; Optimization; Self emulsified drug delivery system; Stability

Indexed keywords

DRUG CARRIER; LIPID; MAGNESIUM STEARATE; SILICATE; UBIDECARENONE;

EID: 33646383855     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2006.02.019     Document Type: Article
Times cited : (115)

References (39)
  • 1
    • 0020554053 scopus 로고
    • Influence of dispersion method on particle size and dissolution of griseofulvin silicon dioxide triturations
    • Abdallah H.Y., Khalafallah N., and Khalil S.A. Influence of dispersion method on particle size and dissolution of griseofulvin silicon dioxide triturations. Drug Dev. Ind. Pharm. 9 (1983) 795-808
    • (1983) Drug Dev. Ind. Pharm. , vol.9 , pp. 795-808
    • Abdallah, H.Y.1    Khalafallah, N.2    Khalil, S.A.3
  • 2
    • 0020461661 scopus 로고
    • Studies on direct compression of tablets. Part 4. Effect of particle size on the mechanical strength of tablets
    • Alderborn G., and Nystrom C. Studies on direct compression of tablets. Part 4. Effect of particle size on the mechanical strength of tablets. Acta Pharm. Suec. 19 (1982) 381-390
    • (1982) Acta Pharm. Suec. , vol.19 , pp. 381-390
    • Alderborn, G.1    Nystrom, C.2
  • 3
    • 33646379535 scopus 로고    scopus 로고
    • Oral solid dosage forms of lipid-based drug delivery systems
    • Cannon J.B. Oral solid dosage forms of lipid-based drug delivery systems. Am. Pharmaceut. Rev. 8 (2005) 108-115
    • (2005) Am. Pharmaceut. Rev. , vol.8 , pp. 108-115
    • Cannon, J.B.1
  • 4
    • 0000496231 scopus 로고
    • Evaluating flow properties of solids
    • Carr R.L. Evaluating flow properties of solids. Chem. Eng. 18 (1965) 163-168
    • (1965) Chem. Eng. , vol.18 , pp. 163-168
    • Carr, R.L.1
  • 6
    • 0026586447 scopus 로고
    • Self-emulsifying drug delivery systems: formulation and biopharmaceutic evaluation of an investigational lipophilic compound
    • Charman S.A., Charman W.N., Rogge M.C., Wilson T.D., Dukto F.J., and Pouton C.W. Self-emulsifying drug delivery systems: formulation and biopharmaceutic evaluation of an investigational lipophilic compound. Pharmaceut. Res. 9 (1992) 87-93
    • (1992) Pharmaceut. Res. , vol.9 , pp. 87-93
    • Charman, S.A.1    Charman, W.N.2    Rogge, M.C.3    Wilson, T.D.4    Dukto, F.J.5    Pouton, C.W.6
  • 7
    • 0027301116 scopus 로고
    • An investigation into the physico-chemical properties of self-emulsifying systems using low frequency dielectric spectroscopy, surface tension measurements and particle size analysis
    • Craig D.Q.M., Lievens H.S.R., Pitt K.G., and Storey D.E. An investigation into the physico-chemical properties of self-emulsifying systems using low frequency dielectric spectroscopy, surface tension measurements and particle size analysis. Int. J. Pharm. 96 (1993) 147-155
    • (1993) Int. J. Pharm. , vol.96 , pp. 147-155
    • Craig, D.Q.M.1    Lievens, H.S.R.2    Pitt, K.G.3    Storey, D.E.4
  • 8
    • 0029825871 scopus 로고    scopus 로고
    • Effects of polymer particle size, compaction pressure and hydrophilic polymers on drug release from matrices containing ethylcellulose
    • Dabbagh M.A., Ford J.L., Rubinstein M.H., and Hogan J.E. Effects of polymer particle size, compaction pressure and hydrophilic polymers on drug release from matrices containing ethylcellulose. Int. J. Pharm. 140 (1996) 85-95
    • (1996) Int. J. Pharm. , vol.140 , pp. 85-95
    • Dabbagh, M.A.1    Ford, J.L.2    Rubinstein, M.H.3    Hogan, J.E.4
  • 9
    • 78651231328 scopus 로고    scopus 로고
    • ® Sofcap™ for controlled release of non-aqueous liquid formulations
    • ® Sofcap™ for controlled release of non-aqueous liquid formulations. Drug Deliv. Technol. 2 (2002) 52-55
    • (2002) Drug Deliv. Technol. , vol.2 , pp. 52-55
    • Dong, L.1    Shafi, K.2    Wong, P.3    Wan, J.4
  • 10
    • 0022677641 scopus 로고
    • Studies on direct compression of tablets XVII. Porosity-pressure curves for the characterization of volume reduction mechanisms in powder compression
    • Duberg M., and Nystrom C. Studies on direct compression of tablets XVII. Porosity-pressure curves for the characterization of volume reduction mechanisms in powder compression. Powder Technol. 46 (1986) 67-75
    • (1986) Powder Technol. , vol.46 , pp. 67-75
    • Duberg, M.1    Nystrom, C.2
  • 11
    • 0032498581 scopus 로고    scopus 로고
    • Physicochemical characterization and evaluation of a microemulsion system for oral delivery of cyclosporine A
    • Gao Z.G., Choi H.G., Shin H.J., Park K.M., Lim S.J., Hwang K.J., and Kim C.K. Physicochemical characterization and evaluation of a microemulsion system for oral delivery of cyclosporine A. Int. J. Pharm. 161 (1998) 75-86
    • (1998) Int. J. Pharm. , vol.161 , pp. 75-86
    • Gao, Z.G.1    Choi, H.G.2    Shin, H.J.3    Park, K.M.4    Lim, S.J.5    Hwang, K.J.6    Kim, C.K.7
  • 12
    • 0031399587 scopus 로고    scopus 로고
    • Controlled-release tablet matrices from carrageenans: compression and dissolution studies
    • Hariharan M., Wheatley T.A., and Price J.C. Controlled-release tablet matrices from carrageenans: compression and dissolution studies. Pharm. Dev. Technol. 2 (1997) 383-393
    • (1997) Pharm. Dev. Technol. , vol.2 , pp. 383-393
    • Hariharan, M.1    Wheatley, T.A.2    Price, J.C.3
  • 13
    • 23844442127 scopus 로고    scopus 로고
    • Self emulsifying drug delivery systems
    • Jannin V., and Chambin O. Self emulsifying drug delivery systems. STP Pharma Pratiques 15 (2005) 247-254
    • (2005) STP Pharma Pratiques , vol.15 , pp. 247-254
    • Jannin, V.1    Chambin, O.2
  • 14
    • 0022655984 scopus 로고
    • Investigation of the film formation of magnesium stearate by applying a flow through dissolution technique
    • Johansson M.E., and Nicklasson M. Investigation of the film formation of magnesium stearate by applying a flow through dissolution technique. J. Pharm. Pharmacol. 38 (1986) 51-54
    • (1986) J. Pharm. Pharmacol. , vol.38 , pp. 51-54
    • Johansson, M.E.1    Nicklasson, M.2
  • 15
    • 0020655017 scopus 로고
    • Effect of mixing time of magnesium stearate on the tableting properties of dried microcrystalline cellulose
    • Khan K.A., Musikabhumma P., and Rubinstein M.H. Effect of mixing time of magnesium stearate on the tableting properties of dried microcrystalline cellulose. Pharm. Acta Helv. 58 (1983) 109-111
    • (1983) Pharm. Acta Helv. , vol.58 , pp. 109-111
    • Khan, K.A.1    Musikabhumma, P.2    Rubinstein, M.H.3
  • 16
    • 0034948974 scopus 로고    scopus 로고
    • Once-a-day oral dosing regimen of cyclosporine A: combined therapy of cyclosporine A premicroemulsion concentrates and enteric coated solid-state premicroemulsion concentrates
    • Kim C., Shin H., Yang S., Kim J., and Oh Y. Once-a-day oral dosing regimen of cyclosporine A: combined therapy of cyclosporine A premicroemulsion concentrates and enteric coated solid-state premicroemulsion concentrates. Pharmaceut. Res. 18 (2001) 454-459
    • (2001) Pharmaceut. Res. , vol.18 , pp. 454-459
    • Kim, C.1    Shin, H.2    Yang, S.3    Kim, J.4    Oh, Y.5
  • 17
    • 0017344561 scopus 로고
    • Interaction of lubricants and colloidal silica during mixing with excipients. 2. Its effect on wettability and dissolution velocity
    • Lerk C.F., and Bolhuis G.K. Interaction of lubricants and colloidal silica during mixing with excipients. 2. Its effect on wettability and dissolution velocity. Pharm. Acta Helv. 52 (1977) 39-44
    • (1977) Pharm. Acta Helv. , vol.52 , pp. 39-44
    • Lerk, C.F.1    Bolhuis, G.K.2
  • 18
    • 0021349430 scopus 로고
    • Dissolution rates of corticoid solutions dispersed on silicas
    • Liao C., and Jarowski C.I. Dissolution rates of corticoid solutions dispersed on silicas. J. Pharm. Sci. 73 (1984) 401-403
    • (1984) J. Pharm. Sci. , vol.73 , pp. 401-403
    • Liao, C.1    Jarowski, C.I.2
  • 19
    • 2342652446 scopus 로고    scopus 로고
    • Mathematical comparison of dissolution profiles
    • Moore J.W., and Flanner H.H. Mathematical comparison of dissolution profiles. Pharm. Technol. 20 (1996) 64-74
    • (1996) Pharm. Technol. , vol.20 , pp. 64-74
    • Moore, J.W.1    Flanner, H.H.2
  • 20
    • 0023742833 scopus 로고
    • Effect of mixing on the biopharmaceutical properties of sulfadiazine tablets
    • Morasso M.I., Salas J., and Arancibia A. Effect of mixing on the biopharmaceutical properties of sulfadiazine tablets. Farmaco Ed. Prat. 43 (1988) 177-188
    • (1988) Farmaco Ed. Prat. , vol.43 , pp. 177-188
    • Morasso, M.I.1    Salas, J.2    Arancibia, A.3
  • 22
    • 0141798535 scopus 로고    scopus 로고
    • Response surface methodology for the optimization of ubiquinone self-emulsified drug delivery system
    • (article 3)
    • Nazzal S., and Khan M.A. Response surface methodology for the optimization of ubiquinone self-emulsified drug delivery system. AAPS PharmSciTech. 3 (2002) (article 3)
    • (2002) AAPS PharmSciTech. , vol.3
    • Nazzal, S.1    Khan, M.A.2
  • 24
    • 0037142237 scopus 로고    scopus 로고
    • Optimization of a self-nanoemulsified tablet dosage form of ubiquinone using response surface methodology: effect of formulation ingredients
    • Nazzal S., Nutan M., Palamakula A., Shah R., Zaghloul A.A., and Khan M.A. Optimization of a self-nanoemulsified tablet dosage form of ubiquinone using response surface methodology: effect of formulation ingredients. Int. J. Pharm. 240 (2002) 103-114
    • (2002) Int. J. Pharm. , vol.240 , pp. 103-114
    • Nazzal, S.1    Nutan, M.2    Palamakula, A.3    Shah, R.4    Zaghloul, A.A.5    Khan, M.A.6
  • 25
    • 0037139412 scopus 로고    scopus 로고
    • Preparation and in-vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation
    • Nazzal S., Smalyukh I.I., Lavrentovich O.D., and Khan M.A. Preparation and in-vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation. Int. J. Pharm. 235 (2002) 247-265
    • (2002) Int. J. Pharm. , vol.235 , pp. 247-265
    • Nazzal, S.1    Smalyukh, I.I.2    Lavrentovich, O.D.3    Khan, M.A.4
  • 26
    • 0036338543 scopus 로고    scopus 로고
    • Effect of extra-granular microcrystalline cellulose on compaction, surface roughness and in-vitro dissolution of a self-nanoemulsified solid dosage form of ubiquinone
    • Nazzal S., Zaghloul A.A., and Khan M.A. Effect of extra-granular microcrystalline cellulose on compaction, surface roughness and in-vitro dissolution of a self-nanoemulsified solid dosage form of ubiquinone. Pharmaceut. Technol. 26 (2002) 86-98
    • (2002) Pharmaceut. Technol. , vol.26 , pp. 86-98
    • Nazzal, S.1    Zaghloul, A.A.2    Khan, M.A.3
  • 28
    • 0034889914 scopus 로고    scopus 로고
    • The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture
    • Newton R.M., Petterson J., Podczeck F., Clarke A., and Booth S. The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture. J. Pharm. Sci. 90 (2001) 987-995
    • (2001) J. Pharm. Sci. , vol.90 , pp. 987-995
    • Newton, R.M.1    Petterson, J.2    Podczeck, F.3    Clarke, A.4    Booth, S.5
  • 29
    • 0031725929 scopus 로고    scopus 로고
    • Investigation of formulation approaches to improve the dissolution of SB-210661, a poorly water soluble 5-lipoxygenase inhibitor
    • Perng C.H., Kearney A.S., Patel K., Palepu N.R., and Zuber G. Investigation of formulation approaches to improve the dissolution of SB-210661, a poorly water soluble 5-lipoxygenase inhibitor. Int. J. Pharm. 176 (1998) 31-38
    • (1998) Int. J. Pharm. , vol.176 , pp. 31-38
    • Perng, C.H.1    Kearney, A.S.2    Patel, K.3    Palepu, N.R.4    Zuber, G.5
  • 30
    • 0033805858 scopus 로고    scopus 로고
    • Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
    • Pouton C.W. Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems. Eur. J. Pharm. Sci. (2000) S93-S98
    • (2000) Eur. J. Pharm. Sci.
    • Pouton, C.W.1
  • 31
    • 33646367098 scopus 로고
    • Effect of changes in compression pressure on dissolution of drugs from tablets
    • Rehula A., Rehulova M., and Muzik M. Effect of changes in compression pressure on dissolution of drugs from tablets. Folia Pharm. 8 (1985) 35-42
    • (1985) Folia Pharm. , vol.8 , pp. 35-42
    • Rehula, A.1    Rehulova, M.2    Muzik, M.3
  • 32
    • 0025963952 scopus 로고
    • Physicochemical aspects of drug release. Part 11. Tableting properties of solid dispersions, using xylitol as carrier material
    • Sjokvist E., and Nystrom C. Physicochemical aspects of drug release. Part 11. Tableting properties of solid dispersions, using xylitol as carrier material. Int. J. Pharm. 67 (1991) 139-153
    • (1991) Int. J. Pharm. , vol.67 , pp. 139-153
    • Sjokvist, E.1    Nystrom, C.2
  • 33
    • 0024392986 scopus 로고
    • Physicochemical aspects of drug release. Part 9. Investigation of some factors that impair dissolution of drugs from solid particulate dispersion systems
    • Sjokvist E., Nystrom C., and Alden M. Physicochemical aspects of drug release. Part 9. Investigation of some factors that impair dissolution of drugs from solid particulate dispersion systems. Int. J. Pharm. 54 (1989) 161-170
    • (1989) Int. J. Pharm. , vol.54 , pp. 161-170
    • Sjokvist, E.1    Nystrom, C.2    Alden, M.3
  • 34
    • 0026793126 scopus 로고
    • Powdered solution technology: principles and mechanism
    • Spireas S.S., Jarowski C.I., and Rohera B.D. Powdered solution technology: principles and mechanism. Pharm. Res. 9 (1992) 1351-1358
    • (1992) Pharm. Res. , vol.9 , pp. 1351-1358
    • Spireas, S.S.1    Jarowski, C.I.2    Rohera, B.D.3
  • 35
    • 0032543173 scopus 로고    scopus 로고
    • Enhancement of prednisolone dissolution properties using liquisolid compacts
    • Spireas S., and Sadu S. Enhancement of prednisolone dissolution properties using liquisolid compacts. Int. J. Pharm. 166 (1998) 177-188
    • (1998) Int. J. Pharm. , vol.166 , pp. 177-188
    • Spireas, S.1    Sadu, S.2
  • 36
    • 0035857733 scopus 로고    scopus 로고
    • Effect of initial particle size on the tableting properties of l-lysine monohydrochloride dihydrate powder
    • Sun C., and Grant D.J.W. Effect of initial particle size on the tableting properties of l-lysine monohydrochloride dihydrate powder. Int. J. Pharm. 215 (2001) 221-228
    • (2001) Int. J. Pharm. , vol.215 , pp. 221-228
    • Sun, C.1    Grant, D.J.W.2
  • 37
    • 0032830863 scopus 로고    scopus 로고
    • Reduction of tablet coloration at tableting for oily medicine (tocopheryl nicotinate)
    • Takashima Y., Yuasa H., Kanaya Y., Nomura I., and Shinozawa K. Reduction of tablet coloration at tableting for oily medicine (tocopheryl nicotinate). Int. J. Pharm. 187 (1999) 125-135
    • (1999) Int. J. Pharm. , vol.187 , pp. 125-135
    • Takashima, Y.1    Yuasa, H.2    Kanaya, Y.3    Nomura, I.4    Shinozawa, K.5
  • 38
    • 0025233671 scopus 로고
    • Drug-excipient interactions resulting from powder mixing. Part 5. Role of sodium lauryl sulfate
    • Wang L.H., and Chowhan Z.T. Drug-excipient interactions resulting from powder mixing. Part 5. Role of sodium lauryl sulfate. Int. J. Pharm. 60 (1990) 61-78
    • (1990) Int. J. Pharm. , vol.60 , pp. 61-78
    • Wang, L.H.1    Chowhan, Z.T.2
  • 39
    • 0018761797 scopus 로고
    • Effect of amorphous silicon dioxide on drug dissolution
    • Yang K.Y., Glemza R., and Jarowski C.I. Effect of amorphous silicon dioxide on drug dissolution. J. Pharm. Sci. 68 (1979) 560-565
    • (1979) J. Pharm. Sci. , vol.68 , pp. 560-565
    • Yang, K.Y.1    Glemza, R.2    Jarowski, C.I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.