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Volumn 72, Issue 1, 2010, Pages 92-100

Characterization of indomethacin release from polyethylene glycol tablet fabricated with mold technique

Author keywords

Indomethacin; Mold tablet; Polyethylene glycol; Release; Xanthan gum

Indexed keywords

EUDRAGIT; INDOMETACIN; MACROGOL 4000; PHOSPHATE; XANTHAN;

EID: 77951668379     PISSN: 0250474X     EISSN: 19983743     Source Type: Journal    
DOI: 10.4103/0250-474X.62255     Document Type: Article
Times cited : (18)

References (36)
  • 1
    • 0025610778 scopus 로고
    • Polyethylene glycols and drug release
    • Craig DG. Polyethylene glycols and drug release. Drug Develop Ind Pharm 1990;16:2501-2526
    • (1990) Drug Develop Ind Pharm , vol.16 , pp. 2501-2526
    • Craig, D.G.1
  • 2
    • 15044361802 scopus 로고    scopus 로고
    • Preparation, characterization, and tableting of a solid dispersion of indomethacin with crospovidone
    • DOI 10.1016/j.ijpharm.2004.12.018
    • Fujii M, Okada H, Shibata Y, Teramachi H, Kondoh M, Watanabe Y. Preparation, characterization, and tableting of a solid dispersion of indomethacin with crospovidone. Int J Pharm 2005;293:145-153 (Pubitemid 40381088)
    • (2005) International Journal of Pharmaceutics , vol.293 , Issue.1-2 , pp. 145-153
    • Fujii, M.1    Okada, H.2    Shibata, Y.3    Teramachi, H.4    Kondoh, M.5    Watanabe, Y.6
  • 3
    • 0033021347 scopus 로고    scopus 로고
    • Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000
    • Trapani G, Franco M, Latrofa A, Pantaleo MR, Provenzano MR, Sanna E, et al. Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000. Int J Pharm 1999;184:121-130
    • (1999) Int J Pharm , vol.184 , pp. 121-130
    • Trapani, G.1    Franco, M.2    Latrofa, A.3    Pantaleo, M.R.4    Provenzano, M.R.5    Sanna, E.6
  • 4
    • 71049122247 scopus 로고    scopus 로고
    • Phase characterization of indomethacin in binary solid dispersions with PVP VA64 or Myrj 52
    • Wang X, Armasa HN, Blaton H, Michoel A, Van dan Mooter G. Phase characterization of indomethacin in binary solid dispersions with PVP VA64 or Myrj 52. Int J Pharm 2007;123:163-169
    • (2007) Int J Pharm , vol.123 , pp. 163-169
    • Wang, X.1    Armasa, H.N.2    Blaton, H.3    Michoel, A.4    Van Dan Mooter, G.5
  • 6
    • 37549059974 scopus 로고    scopus 로고
    • Development of prednisolone: Polyethylene glycol 6000 fast-release tablets from solid dispersions: Solid-state characterization, dissolution behavior, and formulation parameters
    • Article 108 [last accessed on 2009 Jan 4]
    • Leonardi D, Barrera MG, Lamas MC, Salomon CJ. Development of prednisolone: polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters. AAPS PharmSciTech 2007;8(4) Article 108 (http://www. aapspharmscitech.org) [last accessed on 2009 Jan 4].
    • (2007) AAPS PharmSciTech , vol.8 , pp. 4
    • Leonardi, D.1    Barrera, M.G.2    Lamas, M.C.3    Salomon, C.J.4
  • 7
    • 34248535178 scopus 로고    scopus 로고
    • Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water-soluble carriers
    • Ahuja N, Katare O P, Singh B. Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water-soluble carriers. Eur J Pharm Biopharm 2007;65:26-38.
    • (2007) Eur J Pharm Biopharm , vol.65 , pp. 26-38
    • Ahuja, N.1    Katare, O.P.2    Singh, B.3
  • 8
    • 71049130325 scopus 로고    scopus 로고
    • Solid dispersion matrix tablet comprising indomethacin-PEG-HPMC fabricated with fusion and mold technique
    • Mesnukul A, Yodkhum K, Phaechamud T. Solid dispersion matrix tablet comprising indomethacin-PEG-HPMC fabricated with fusion and mold technique. Indian J Pharm Sci 2009;71:413-420
    • (2009) Indian J Pharm Sci , vol.71 , pp. 413-420
    • Mesnukul, A.1    Yodkhum, K.2    Phaechamud, T.3
  • 9
    • 0141692120 scopus 로고    scopus 로고
    • Macromolecular properties of xanthan gum
    • S. Dumitriu New York: Marcel Dekker
    • Stokke BT, Christensen BE, Smidsrod O. Macromolecular properties of xanthan gum. In S. Dumitriu, Polysaccharides. New York: Marcel Dekker; 1998, pp. 433-472
    • (1998) Polysaccharides , pp. 433-472
    • Stokke, B.T.1    Christensen, B.E.2    Smidsrod, O.3
  • 11
    • 0037222706 scopus 로고    scopus 로고
    • Release of pentoxifylline from xanthan matrix
    • El-Gazayerly ON. Release of pentoxifylline from xanthan matrix. Drug Develop Ind Pharm 2003;29:241-246
    • (2003) Drug Develop Ind Pharm , vol.29 , pp. 241-246
    • El-Gazayerly, O.N.1
  • 13
    • 23244439570 scopus 로고    scopus 로고
    • Development of a simple method for the preparation of a silica gel based controlled delivery system with a high drug content
    • Ohta KM, Fuji M, Takei T, Chikazawa M. Development of a simple method for the preparation of a silica gel based controlled delivery system with a high drug content. Eur J Pharm Sci 2005;26:87-96.
    • (2005) Eur J Pharm Sci , vol.26 , pp. 87-96
    • Ohta, K.M.1    Fuji, M.2    Takei, T.3    Chikazawa, M.4
  • 14
    • 43249101732 scopus 로고    scopus 로고
    • Effect of calcium ions on the gelling and drug release characteristics of xanthan matrix tablets
    • Baumgartner S, Pavli M, Kristl J. Effect of calcium ions on the gelling and drug release characteristics of xanthan matrix tablets. Eur J Pharm Biopharm 2008;69:698-707.
    • (2008) Eur J Pharm Biopharm , vol.69 , pp. 698-707
    • Baumgartner, S.1    Pavli, M.2    Kristl, J.3
  • 15
    • 0032581116 scopus 로고    scopus 로고
    • In vivo evaluation of xanthan gum as a potential excipient for oral controlled-release matrix tablet formulation
    • Talukdar MM, Van den Mooter P, Augustijns T, Tjandra-Maga G. In vivo evaluation of xanthan gum as a potential excipient for oral controlled-release matrix tablet formulation. Int J Pharm 1998;169:105-113
    • (1998) Int J Pharm , vol.169 , pp. 105-113
    • Talukdar, M.M.1    Van Den Mooter, P.2    Augustijns, T.3    Tjandra-Maga, G.4
  • 16
    • 0029968703 scopus 로고    scopus 로고
    • Prediction of physical properties of a novel polysaccharide controlled release system. i
    • Tobyn MJ, Staniforth JN, Baichwal AR, McCall TW. Prediction of physical properties of a novel polysaccharide controlled release system. I. Int J Pharm 1996;128:113-120
    • (1996) Int J Pharm , vol.128 , pp. 113-120
    • Tobyn, M.J.1    Staniforth, J.N.2    Baichwal, A.R.3    McCall, T.W.4
  • 17
    • 23144462420 scopus 로고    scopus 로고
    • Formulation variables affecting drug release from xanthan gum matrices at laboratory scale and pilot scale
    • Billa N, Yuen KH. Formulation variables affecting drug release from xanthan gum matrices at laboratory scale and pilot scale. AAPS PharmSciTech 2000;4:120-127
    • (2000) AAPS PharmSciTech , vol.4 , pp. 120-127
    • Billa, N.1    Yuen, K.H.2
  • 18
    • 33846581961 scopus 로고
    • Xanthan alginate composite gel beads: Molecular interaction and in vitro characterization
    • Walker M, Wells J. Xanthan alginate composite gel beads: Molecular interaction and in vitro characterization. Int J Pharm 1982;331:61-71.
    • (1982) Int J Pharm , vol.331 , pp. 61-71
    • Walker, M.1    Wells, J.2
  • 19
    • 1242338845 scopus 로고    scopus 로고
    • Prediction of drug release from HPMC matrices: Effect of physicochemical properties of drug and polymer concentration
    • Fu XC, Wang GP, Liang WQ, Chow MS. Prediction of drug release from HPMC matrices: effect of physicochemical properties of drug and polymer concentration. J Control Release 2004;95:209-216
    • (2004) J Control Release , vol.95 , pp. 209-216
    • Fu, X.C.1    Wang, G.P.2    Liang, W.Q.3    Chow, M.S.4
  • 20
    • 0037366973 scopus 로고    scopus 로고
    • Coating polymers for colon specific drug delivery: A comparative in vitro evaluation
    • Sinha VR, Kumria R. Coating polymers for colon specific drug delivery: A comparative in vitro evaluation. Acta Pharm Sci 2003;53:41-47
    • (2003) Acta Pharm Sci , vol.53 , pp. 41-47
    • Sinha, V.R.1    Kumria, R.2
  • 21
    • 0037163898 scopus 로고    scopus 로고
    • Studies on the properties of Celluclast/Eudragit L-100 conjugate
    • Dourado F, Bastos M, Mota M, Gama FM. Studies on the properties of Celluclast/Eudragit L-100 conjugate. J Biotechnol 2002;99:121-131
    • (2002) J Biotechnol , vol.99 , pp. 121-131
    • Dourado, F.1    Bastos, M.2    Mota, M.3    Gama, F.M.4
  • 24
    • 0032700381 scopus 로고    scopus 로고
    • Development and evaluation of a multiple-unit oral sustained release dosage form for S(+)-ibuprofen: Preparation and release kinetics
    • Cox PL, Khan KA, Munday DL, Sujja-areevath J. Development and evaluation of a multiple-unit oral sustained release dosage form for S(+)-ibuprofen: preparation and release kinetics. Int J Pharm 1999;193:73-84.
    • (1999) Int J Pharm , vol.193 , pp. 73-84
    • Cox, P.L.1    Khan, K.A.2    Munday, D.L.3    Sujja-Areevath, J.4
  • 26
    • 0034212876 scopus 로고    scopus 로고
    • Swellable matrices for controlled drug delivery: Gel-layer behaviour, mechanisms and optimal performance
    • Colombo P, Bettini R, Santi P, Peppas NA. Swellable matrices for controlled drug delivery: gel-layer behaviour, mechanisms and optimal performance. Pharm Sci Tech Today 2000;6:32-38.
    • (2000) Pharm Sci Tech Today , vol.6 , pp. 32-38
    • Colombo, P.1    Bettini, R.2    Santi, P.3    Peppas, N.A.4
  • 27
    • 33745172447 scopus 로고    scopus 로고
    • Design and evaluation of xanthan gum-based sustained release matrix tablet of diclofenac sodium
    • Yeole PG, Galgatte UC, Babla IB, Nakhat PD. Design and evaluation of xanthan gum-based sustained release matrix tablet of diclofenac sodium. Indian J Pharm Sci 2006;68:185-189
    • (2006) Indian J Pharm Sci , vol.68 , pp. 185-189
    • Yeole, P.G.1    Galgatte, U.C.2    Babla, I.B.3    Nakhat, P.D.4
  • 28
    • 0037082716 scopus 로고    scopus 로고
    • Dissolution behaviour of hydrophilic matrix tablets containing two different polyethylene oxides (PEOs) for the controlled release of a water-soluble drug
    • Maggi L, Segale L, Torre ML, Ochoa ME, Conte U. Dissolution behaviour of hydrophilic matrix tablets containing two different polyethylene oxides (PEOs) for the controlled release of a water-soluble drug. Dimensionality study. Biomater 2002;23:1113-1119
    • (2002) Dimensionality Study. Biomater , vol.23 , pp. 1113-1119
    • Maggi, L.1    Segale, L.2    Torre, M.L.3    Ochoa, M.E.4    Conte, U.5
  • 29
    • 0035844738 scopus 로고    scopus 로고
    • Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC)
    • Siepmann J, Peppas N. Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC). Adv Drug Del Rev 2001;48:139-157
    • (2001) Adv Drug Del Rev , vol.48 , pp. 139-157
    • Siepmann, J.1    Peppas, N.2
  • 30
    • 34547914143 scopus 로고    scopus 로고
    • Correlation between drug dissolution and polymer hydration: A study using texture analysis
    • Li H, Gu X. Correlation between drug dissolution and polymer hydration: A study using texture analysis. Int J Pharm 2007;342:18-25.
    • (2007) Int J Pharm , vol.342 , pp. 18-25
    • Li, H.1    Gu, X.2
  • 31
    • 0032411241 scopus 로고    scopus 로고
    • Non-steroidal induced benign structures of colon: A case report and review of the literature
    • Eis MJ, Watkins BM, Philip A, Welling RE. Non-steroidal induced benign structures of colon: a case report and review of the literature. Am J Gastroenterol 1998;93:120-121
    • (1998) Am J Gastroenterol , vol.93 , pp. 120-121
    • Eis, M.J.1    Watkins, B.M.2    Philip, A.3    Welling, R.E.4
  • 32
    • 0031573912 scopus 로고    scopus 로고
    • Dissolution mechanism and rate of solid dispersion particles of nifednipine with hydroxypropylmethylcellulose
    • Okimoto K, Miyake M, Ibuki R, Ohnishi N, Nakai T. Dissolution mechanism and rate of solid dispersion particles of nifednipine with hydroxypropylmethylcellulose. Int J Pharm 1997;159:85-93.
    • (1997) Int J Pharm , vol.159 , pp. 85-93
    • Okimoto, K.1    Miyake, M.2    Ibuki, R.3    Ohnishi, N.4    Nakai, T.5
  • 33
    • 0032997934 scopus 로고    scopus 로고
    • Improving the oral bioavailability of albendazole in rabbits by the solid dispersion technique
    • Kohri N, Yamayoshi Y, Xin H, Iseki K, Sato N, Toda S, Miyazaki K. Improving the oral bioavailability of albendazole in rabbits by the solid dispersion technique. J Pharm Pharmacol 1999;51:159-164
    • (1999) J Pharm Pharmacol , vol.51 , pp. 159-164
    • Kohri, N.1    Yamayoshi, Y.2    Xin, H.3    Iseki, K.4    Sato, N.5    Toda, S.6    Miyazaki, K.7
  • 35
    • 20644439328 scopus 로고    scopus 로고
    • Selection of excipients for extended release formulations of glipizide through drug-excipient compatibility testing
    • Verma RK, Garg S. Selection of excipients for extended release formulations of glipizide through drug-excipient compatibility testing. J Pharm Biomed Anal 2005;38:633-644
    • (2005) J Pharm Biomed Anal , vol.38 , pp. 633-644
    • Verma, R.K.1    Garg, S.2
  • 36
    • 44649197127 scopus 로고    scopus 로고
    • Drug release and swelling kinetics of directly compressed glipizide sustained-release matrices: Establishment of level A IVIVC
    • Sankalia JM, Sankalia MG, Mashru RC. Drug release and swelling kinetics of directly compressed glipizide sustained-release matrices: Establishment of level A IVIVC. J Control Release 2008;129:49-58.
    • (2008) J Control Release , vol.129 , pp. 49-58
    • Sankalia, J.M.1    Sankalia, M.G.2    Mashru, R.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.