메뉴 건너뛰기




Volumn 12, Issue 1, 2007, Pages 21-33

Physicochemical characterization and dissolution study of solid dispersions of lovastatin with polyethylene glycol 4000 and polyvinylpyrrolidone K30

Author keywords

Dissolution; Lovstatin; Polyethylene glycol; Polyvinylpyrrolidone; Solid dispersion; Solubility

Indexed keywords

MACROGOL 4000; MEVINOLIN; POVIDONE; EXCIPIENT; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; MACROGOL DERIVATIVE;

EID: 34249652404     PISSN: 10837450     EISSN: 10979867     Source Type: Journal    
DOI: 10.1080/10837450601166510     Document Type: Article
Times cited : (58)

References (28)
  • 1
    • 0015124656 scopus 로고
    • Pharmaceutical applications of solid dispersion systems
    • Chiou, W.L.; Riegalman, S.. Pharmaceutical applications of solid dispersion systems. J. Pharm. Sci. 1971, 60, 1281-1302.
    • (1971) J. Pharm. Sci , vol.60 , pp. 1281-1302
    • Chiou, W.L.1    Riegalman, S.2
  • 2
    • 0032885450 scopus 로고    scopus 로고
    • Solid dispersions of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs
    • Serajuddin, A.T.M. Solid dispersions of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs. J. Pharma. Sci. 1999, 88, 1058-1066.
    • (1999) J. Pharma. Sci , vol.88 , pp. 1058-1066
    • Serajuddin, A.T.M.1
  • 3
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • Leuner, C.; Dressman, J. Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. 2000, 50, 47-60.
    • (2000) Eur. J. Pharm. Biopharm , vol.50 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 4
    • 85008071016 scopus 로고
    • Studies on absorption of eutectic mixtures. I. A comparison of the behaviour of eutectic mixture of sulfathiazole and that of ordinary sulfathiazole in man
    • Sekiguchi, K.; Obi, N. Studies on absorption of eutectic mixtures. I. A comparison of the behaviour of eutectic mixture of sulfathiazole and that of ordinary sulfathiazole in man. Chem. Pharm. Bull. 1961, 9, 866-872.
    • (1961) Chem. Pharm. Bull , vol.9 , pp. 866-872
    • Sekiguchi, K.1    Obi, N.2
  • 5
    • 0028340095 scopus 로고
    • Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000
    • Margarit, M.V.; Rodríguez, I.C.; Cerezo, A. Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000. Int. J. Pharm. 1994, 108, 101-107.
    • (1994) Int. J. Pharm , vol.108 , pp. 101-107
    • Margarit, M.V.1    Rodríguez, I.C.2    Cerezo, A.3
  • 6
    • 0033020439 scopus 로고    scopus 로고
    • Thermal behavior and dissolution properties of naproxen from binary and ternary solid dispersions
    • Mura, P.; Faucci, M.T.; Manderioli, A.; Bramanti, G.; Parrini, P. Thermal behavior and dissolution properties of naproxen from binary and ternary solid dispersions. Drug Dev. Ind. Pharm. 1999, 25, 257-264.
    • (1999) Drug Dev. Ind. Pharm , vol.25 , pp. 257-264
    • Mura, P.1    Faucci, M.T.2    Manderioli, A.3    Bramanti, G.4    Parrini, P.5
  • 7
    • 0033943041 scopus 로고    scopus 로고
    • Characterization and evaluation of tenoxicam coprecipitates
    • El-Gazayerly, O.N. Characterization and evaluation of tenoxicam coprecipitates. Drug Dev. Ind. Pharm. 2000, 26, 925-930.
    • (2000) Drug Dev. Ind. Pharm , vol.26 , pp. 925-930
    • El-Gazayerly, O.N.1
  • 8
    • 0033928655 scopus 로고    scopus 로고
    • Enhancement of dissolution and bioavailability of piroxicam in solid dispersions systems
    • Ryh-Nam, P.; Jing-Huey C.; Russel, R.C. Enhancement of dissolution and bioavailability of piroxicam in solid dispersions systems, Drug Dev. Ind. Pharm. 2000, 26, 989-994.
    • (2000) Drug Dev. Ind. Pharm , vol.26 , pp. 989-994
    • Ryh-Nam, P.1    Jing-Huey, C.2    Russel, R.C.3
  • 9
    • 0037074108 scopus 로고    scopus 로고
    • The mechanism of drug release from solid dispersion in water-soluble polymers
    • Craig, D.Q.M. The mechanism of drug release from solid dispersion in water-soluble polymers. Int. J. Pharm. 2002, 231, 131-144.
    • (2002) Int. J. Pharm , vol.231 , pp. 131-144
    • Craig, D.Q.M.1
  • 10
    • 0031423468 scopus 로고    scopus 로고
    • Spectroscopic characterization interactions between PVP and indomethacin in amorphous molecular dispersions
    • Taylor, L.S.; Zografi, G. Spectroscopic characterization interactions between PVP and indomethacin in amorphous molecular dispersions, Pharm. Res. 1997, 14, 1691-1698.
    • (1997) Pharm. Res , vol.14 , pp. 1691-1698
    • Taylor, L.S.1    Zografi, G.2
  • 12
    • 24144502380 scopus 로고    scopus 로고
    • Effects of water content in physical mixture and heating temperature on crystallinity of troglitazone-PVP K30 solid dispersions prepared by closed melting method
    • Susumu H.; Takeshi H.; Naho F.; Akira K.; Etsuo Y.; Katsuhide T. Effects of water content in physical mixture and heating temperature on crystallinity of troglitazone-PVP K30 solid dispersions prepared by closed melting method Int. J. Pharm. 2005, 302, 103-112.
    • (2005) Int. J. Pharm , vol.302 , pp. 103-112
    • Susumu, H.1    Takeshi, H.2    Naho, F.3    Akira, K.4    Etsuo, Y.5    Katsuhide, T.6
  • 13
    • 0036754188 scopus 로고    scopus 로고
    • Characterization and solubility study of solid dispersions of flunarizine and polyvinylpyrrolidone
    • Teresa, M. M.; Victoria, M. M.; Gloria E. S. Characterization and solubility study of solid dispersions of flunarizine and polyvinylpyrrolidone. Il Farmaco. 2002, 57, 723-727.
    • (2002) Il Farmaco , vol.57 , pp. 723-727
    • Teresa, M.M.1    Victoria, M.M.2    Gloria, E.S.3
  • 14
    • 0035964448 scopus 로고    scopus 로고
    • Dissolution properties and anticonvulsant activity of phenytoin-polyethylene glycol 6000 and -polyvinylpyrrolidone K-30 solid dispersions
    • Franco, M.; Trapani, G.; Latrofa, A.; Tullio, C.; Provenzano, M.R.; Serra, M.; Muggironi, M.; Biggio, G.; Liso, G. Dissolution properties and anticonvulsant activity of phenytoin-polyethylene glycol 6000 and -polyvinylpyrrolidone K-30 solid dispersions. Int. J. Pharm. 2001, 225, 63-73.
    • (2001) Int. J. Pharm , vol.225 , pp. 63-73
    • Franco, M.1    Trapani, G.2    Latrofa, A.3    Tullio, C.4    Provenzano, M.R.5    Serra, M.6    Muggironi, M.7    Biggio, G.8    Liso, G.9
  • 15
    • 0032513499 scopus 로고    scopus 로고
    • Kinget, R.. Physicochemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K30
    • Van den Mooter, G.; Augustijns, P.; Blaton, N.; Kinget, R.. Physicochemical characterization of solid dispersions of temazepam with polyethylene glycol 6000 and PVP K30. Int. J. Pharm. 1998, 164, 67-80.
    • (1998) Int. J. Pharm , vol.164 , pp. 67-80
    • Van den Mooter, G.1    Augustijns, P.2    Blaton, N.3
  • 16
    • 0032542788 scopus 로고    scopus 로고
    • X-ray powder diffraction determination of the relative amount of crystalline acetaminophen in solid dispersions with PVP
    • Melgardt, M.V.; Dale, E.W.; Jakkie, G.; Amol, K. X-ray powder diffraction determination of the relative amount of crystalline acetaminophen in solid dispersions with PVP. Int. J. Pharm. 1998, 163, 219-224.
    • (1998) Int. J. Pharm , vol.163 , pp. 219-224
    • Melgardt, M.V.1    Dale, E.W.2    Jakkie, G.3    Amol, K.4
  • 17
    • 0041177972 scopus 로고    scopus 로고
    • Study by DSC and HSM of the oxazepam PEG 6000 and oxazepam-D-mannitol systems: Application to the preparation of solid dispersions
    • Arias, M.J.; Moyano, J.R.; Gines, J.M. Study by DSC and HSM of the oxazepam PEG 6000 and oxazepam-D-mannitol systems: application to the preparation of solid dispersions. Thermochimica Acta. 1998, 321, 33-41.
    • (1998) Thermochimica Acta , vol.321 , pp. 33-41
    • Arias, M.J.1    Moyano, J.R.2    Gines, J.M.3
  • 19
    • 0024150625 scopus 로고    scopus 로고
    • Mechanism of action and biological profile of HMG CoA reductase inhibitors: A new therapeutic alternative
    • Slater, E.E.; MacDonald, J.S. Mechanism of action and biological profile of HMG CoA reductase inhibitors: A new therapeutic alternative. Drugs 1998, 36 (Suppl. 3), 72-82.
    • (1998) Drugs , vol.36 , Issue.SUPPL. 3 , pp. 72-82
    • Slater, E.E.1    MacDonald, J.S.2
  • 21
    • 0025989564 scopus 로고
    • Preparation, characterization and dissolution of ciprofloxacin/PEG 6000 binary systems
    • Frances, C.; Veiga, M.D.; Espanol, O.M.; Cadorniga, R. Preparation, characterization and dissolution of ciprofloxacin/PEG 6000 binary systems. Int. J. Pharm. 1991, 77, 193-198.
    • (1991) Int. J. Pharm , vol.77 , pp. 193-198
    • Frances, C.1    Veiga, M.D.2    Espanol, O.M.3    Cadorniga, R.4
  • 22
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • Christian, L.; Jennifer, D. Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. 2000, 50, 47-60.
    • (2000) Eur. J. Pharm. Biopharm , vol.50 , pp. 47-60
    • Christian, L.1    Jennifer, D.2
  • 23
    • 2342652446 scopus 로고    scopus 로고
    • Mathematical comparison of dissolution profiles
    • Moore, J.W.; Flanner, H. Mathematical comparison of dissolution profiles, Pharm. Technol. 1996, 20 (6), 64-74.
    • (1996) Pharm. Technol , vol.20 , Issue.6 , pp. 64-74
    • Moore, J.W.1    Flanner, H.2
  • 24
    • 0035990530 scopus 로고    scopus 로고
    • Barzegar-Jalali, M.; Maleki, N.; Garjani, A.; Khandar, A.A.; Haji-Hosseinloo, M.; Jabbari, R.C; Dasmalchi, S. Enhancement of dissolution rate and anti-inflammatory effects of piroxicam using solvent deposition technique. Drug Dev. Ind. Pharm. 2002, 28, 681-686.
    • Barzegar-Jalali, M.; Maleki, N.; Garjani, A.; Khandar, A.A.; Haji-Hosseinloo, M.; Jabbari, R.C; Dasmalchi, S. Enhancement of dissolution rate and anti-inflammatory effects of piroxicam using solvent deposition technique. Drug Dev. Ind. Pharm. 2002, 28, 681-686.
  • 25
    • 0035660775 scopus 로고    scopus 로고
    • Evaluation and selection of bio-relevant dissolution media for a poorly water soluble new chemical entity
    • Tang, L.; Khan, S.U.; Muhmmad, N.A. Evaluation and selection of bio-relevant dissolution media for a poorly water soluble new chemical entity. Pharm. Dev. Technol. 2001, 6, 531-540.
    • (2001) Pharm. Dev. Technol , vol.6 , pp. 531-540
    • Tang, L.1    Khan, S.U.2    Muhmmad, N.A.3
  • 26
    • 85056934683 scopus 로고    scopus 로고
    • Analysis of drug dissolution data
    • Dressman, J.B, Lennernäs, H. Eds. Marcel Dekker, Inc, New York
    • Reppas, C.; Nicolaides, E. Analysis of drug dissolution data. In Oral Drug Absorption Prediction and Assessment; Dressman, J.B.; Lennernäs, H. Eds. Marcel Dekker, Inc.: New York, 2000, 229-254.
    • (2000) Oral Drug Absorption Prediction and Assessment , pp. 229-254
    • Reppas, C.1    Nicolaides, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.