메뉴 건너뛰기




Volumn 5, Issue 3, 2004, Pages

Formulation design and optimization of mouth dissolve tablets of nimesulide using vacuum drying technique

Author keywords

Camphor factorial design; Contour plot; Mouth dissolve tablet; Nimesulide

Indexed keywords

CAMPHOR; CROSPOVIDONE; LACTOSE; NIMESULIDE; POVIDONE; NONSTEROID ANTIINFLAMMATORY AGENT; PHARMACEUTICAL VEHICLES AND ADDITIVES; SULFONAMIDE;

EID: 23144440783     PISSN: 15309932     EISSN: 15309932     Source Type: Journal    
DOI: 10.1208/pt050336     Document Type: Article
Times cited : (229)

References (19)
  • 2
    • 0029959685 scopus 로고    scopus 로고
    • Preparation and evaluation of a compressed tablet rapidly disintegrating in oral cavity
    • Bi Y, Sunada H, Yonezawa Y, Dayo K, Otsuka A, Iida K. Preparation and evaluation of a compressed tablet rapidly disintegrating in oral cavity. Chem Pharm Bull (Tokyo). 1996;44:2121-2127.
    • (1996) Chem. Pharm. Bull. (Tokyo) , vol.44 , pp. 2121-2127
    • Bi, Y.1    Sunada, H.2    Yonezawa, Y.3    Dayo, K.4    Otsuka, A.5    Iida, K.6
  • 3
    • 0030815948 scopus 로고    scopus 로고
    • Formulation and production of rapidly disintegrating tablets by lyophilization using hydrochlorthiazide as a model drug
    • Corveleyn S, Remon JP. Formulation and production of rapidly disintegrating tablets by lyophilization using hydrochlorthiazide as a model drug. Int J Pharm. 1997;152:215-225.
    • (1997) Int. J. Pharm. , vol.152 , pp. 215-225
    • Corveleyn, S.1    Remon, J.P.2
  • 4
    • 33544470567 scopus 로고    scopus 로고
    • Freeze-dried rapidly disintegrating tablets
    • January 4
    • Remon JP, Corveleyn S. Freeze-dried rapidly disintegrating tablets. US patent 6 010 719. January 4, 2000.
    • (2000) US Patent 6 010 719
    • Remon, J.P.1    Corveleyn, S.2
  • 7
    • 0343273029 scopus 로고    scopus 로고
    • Rapidly soluble oral dosage forms, method of making same, and composition thereof
    • June 9
    • Roser BJ, Blair J. Rapidly soluble oral dosage forms, method of making same, and composition thereof. US patent 5 762 961. June 9, 1998.
    • (1998) US Patent 5 762 961
    • Roser, B.J.1    Blair, J.2
  • 8
    • 0026656034 scopus 로고
    • Prostaglandins, NSAIDs and cytoprotection
    • Wallace JL. Prostaglandins, NSAIDs and cytoprotection. Gastroenterol Clin. North Am. 1992;21:631-641.
    • (1992) Gastroenterol. Clin. North Am. , vol.21 , pp. 631-641
    • Wallace, J.L.1
  • 9
    • 0034078135 scopus 로고    scopus 로고
    • Nimesulide: Some pharmaceutical and pharmacological aspects and update
    • Singla AK, Chawla M, Singh A. Nimesulide: some pharmaceutical and pharmacological aspects and update. J Pharm Pharmacol. 2000;52:467-486.
    • (2000) J. Pharm. Pharmacol. , vol.52 , pp. 467-486
    • Singla, A.K.1    Chawla, M.2    Singh, A.3
  • 10
    • 0027988621 scopus 로고
    • The anti-inflammatory drug nimesulide inhibits neutrophil adherence to and migrations across monolayers of cytokine-activated endothelial cells
    • Dapino P, Ottonello L, Dallegri F. The anti-inflammatory drug nimesulide inhibits neutrophil adherence to and migrations across monolayers of cytokine-activated endothelial cells. Respiration. 1994;61:336-341.
    • (1994) Respiration , vol.61 , pp. 336-341
    • Dapino, P.1    Ottonello, L.2    Dallegri, F.3
  • 11
    • 0030910347 scopus 로고    scopus 로고
    • Study of the influence of both cyclodextrin and L-lysine on the aqueous solubility of Nimesulide: Isolation and characterization of nimesulide L-lysine-cyclodextrin complexes
    • Piel G, Pirotte I, Delnevvile I, Neven P, Delattre L. Study of the influence of both cyclodextrin and L-lysine on the aqueous solubility of Nimesulide: isolation and characterization of nimesulide L-lysine-cyclodextrin complexes. J Pharm Sci. 1997;86:475-480.
    • (1997) J. Pharm. Sci. , vol.86 , pp. 475-480
    • Piel, G.1    Pirotte, I.2    Delnevvile, I.3    Neven, P.4    Delattre, L.5
  • 12
    • 0141576825 scopus 로고    scopus 로고
    • Physicochemical Characterization and dissolution properties of nimesulide-cyclodextrin binary systems
    • Nalluri BN, Chowdary KPR, Murthy KVR, Hayman AR, Becket G. Physicochemical Characterization and dissolution properties of nimesulide-cyclodextrin binary systems. AAPS PharmSciTech. 2003;4(1):E2.
    • (2003) AAPS PharmSciTech. , vol.4 , Issue.1
    • Nalluri, B.N.1    Chowdary, K.P.R.2    Murthy, K.V.R.3    Hayman, A.R.4    Becket, G.5
  • 13
    • 23144465464 scopus 로고    scopus 로고
    • Solubility enhancement of cox-2 inhibitors using various solvent systems
    • Seedher N, Bhatia S. Solubility enhancement of cox-2 inhibitors using various solvent systems. AAPS PharmSciTech. 2003;4(3):E33.
    • (2003) AAPS PharmSciTech. , vol.4 , Issue.3
    • Seedher, N.1    Bhatia, S.2
  • 14
    • 0004186239 scopus 로고
    • 2nd ed. New York, NY: Marcel Decker Inc
    • Bolton S. Pharmaceutical Statistics. 2nd ed. New York, NY: Marcel Decker Inc. 1990:234.
    • (1990) Pharmaceutical Statistics , pp. 234
    • Bolton, S.1
  • 15
    • 0000137328 scopus 로고
    • Experiment design, modeling and optimization strategies for product and process development
    • Libermann HA, Reiger MM, Banker GS, eds. New York, NY: Marcel Dekker Inc
    • Franz RM, Browne JE, Lewis AR. Experiment design, modeling and optimization strategies for product and process development. In: Libermann HA, Reiger MM, Banker GS, eds. Pharmaceutical Dosage Forms: Disperse Systems. Vol 1. New York, NY: Marcel Dekker Inc; 1988;427-519.
    • (1988) Pharmaceutical Dosage Forms: Disperse Systems , vol.1 , pp. 427-519
    • Franz, R.M.1    Browne, J.E.2    Lewis, A.R.3
  • 16
    • 0031006213 scopus 로고    scopus 로고
    • New method of preparing high porosity rapidly saliva soluble compressed tablets using mannitol with camphor, a subliming material
    • Koizumi K, Watanabe Y, Morita K, Utoguchi N, Matsumoto M. New method of preparing high porosity rapidly saliva soluble compressed tablets using mannitol with camphor, a subliming material. Int J Pharm. 1997;152:127-131.
    • (1997) Int. J. Pharm. , vol.152 , pp. 127-131
    • Koizumi, K.1    Watanabe, Y.2    Morita, K.3    Utoguchi, N.4    Matsumoto, M.5
  • 17
    • 0015535580 scopus 로고
    • A new tablet disintegrating agent: Cross-linked polyvinylpyrollidone
    • Kornblum S, Stoopak S. A new tablet disintegrating agent: cross-linked polyvinylpyrollidone. J Pharm Sci. 1973;62:43-49.
    • (1973) J. Pharm. Sci. , vol.62 , pp. 43-49
    • Kornblum, S.1    Stoopak, S.2
  • 18
    • 33544468078 scopus 로고    scopus 로고
    • Fast disintegrating solid formulations of anirectam
    • Japanese patent 11 13 662. May 15
    • Shasaku K. Fast disintegrating solid formulations of anirectam. Jpn Kokai Tokyo Koho. Japanese patent 11 13 662. May 15, 1999.
    • (1999) Jpn. Kokai Tokyo Koho
    • Shasaku, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.