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Volumn 100, Issue 7, 2011, Pages 2734-2743

Improved pharmacokinetics of AMG 517 through co-crystallization part 2: Analysis of 12 carboxylic acid co-crystals

Author keywords

Co crystals; Dissolution; Formulation; Pharmacokinetics; Solubility

Indexed keywords

CARBOXYLIC ACID; N [4 [6 [4 (TRIFLUOROMETHYL)PHENYL] 4 PYRIMIDINYLOXY]BENZOTHIAZOL 2 YL]ACETAMIDE; POVIDONE; SORBIC ACID;

EID: 79955594268     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.22502     Document Type: Article
Times cited : (27)

References (19)
  • 1
    • 77956387616 scopus 로고    scopus 로고
    • Improved pharmacokinetics of AMG 517 through co-crystallization. Part 1: Comparison of two acids with corresponding amide co-crystals
    • Stanton MK, Kelly RC, Colletti A, Kiang Y-H, Langley M, Munson EJ, Peterson ML, Roberts J, Wells M. 2010. Improved pharmacokinetics of AMG 517 through co-crystallization. Part 1: Comparison of two acids with corresponding amide co-crystals. J Pharm Sci 99(9):3769-3778.
    • (2010) J Pharm Sci , vol.99 , Issue.9 , pp. 3769-3778
    • Stanton, M.K.1    Kelly, R.C.2    Colletti, A.3    Kiang, Y.-H.4    Langley, M.5    Munson, E.J.6    Peterson, M.L.7    Roberts, J.8    Wells, M.9
  • 2
    • 85030591182 scopus 로고    scopus 로고
    • Preparation, solid state characterization, and single crystal structure analysis of N-(4-(6-(4-(trifluoromethyl)phenyl)pyrimidin-4-yloxy)benzo[d]thiasol-2-yl)acetamide crystal forms
    • DOI:10.1039/C1030CE00544D. In press.
    • Peterson ML, Stanton MK, Kelly RC, Staples R, Cheng A. 2010. Preparation, solid state characterization, and single crystal structure analysis of N-(4-(6-(4-(trifluoromethyl)phenyl)pyrimidin-4-yloxy)benzo[d]thiasol-2-yl)acetamide crystal forms. Cryst Eng Comm DOI:10.1039/C1030CE00544D. In press.
    • (2010) Cryst Eng Comm
    • Peterson, M.L.1    Stanton, M.K.2    Kelly, R.C.3    Staples, R.4    Cheng, A.5
  • 3
    • 53049103992 scopus 로고    scopus 로고
    • The co-crystal approach to improve the exposure of a water-insoluble compound: AMG 517 sorbic acid co-crystal characterization and pharmacokinetics
    • Bak A, Gore A, Yanez E, Stanton M, Tufekcic S, Syed R, Akrami A, Rose M, Surapaneni S, Bostick T, et al. 2008. The co-crystal approach to improve the exposure of a water-insoluble compound: AMG 517 sorbic acid co-crystal characterization and pharmacokinetics. J Pharm Sci 97(9):3942-3956.
    • (2008) J Pharm Sci , vol.97 , Issue.9 , pp. 3942-3956
    • Bak, A.1    Gore, A.2    Yanez, E.3    Stanton, M.4    Tufekcic, S.5    Syed, R.6    Akrami, A.7    Rose, M.8    Surapaneni, S.9    Bostick, T.10
  • 4
    • 85030589841 scopus 로고    scopus 로고
    • ACD, Inc. ACD/pKa DB v12.0. ACD/pKa DB v120. Toronto, Canada: ACD, Inc.
    • ACD, Inc. ACD/pKa DB v12.0. ACD/pKa DB v120. Toronto, Canada: ACD, Inc.
  • 5
    • 33947540867 scopus 로고    scopus 로고
    • Expanding the scope of crystal form evaluation in pharmaceutical science
    • Peterson ML, Hickey MB, Zaworotko MJ, Almarsson Ö. 2006. Expanding the scope of crystal form evaluation in pharmaceutical science. J Pharm Pharm Sci 9(3):317-326.
    • (2006) J Pharm Pharm Sci , vol.9 , Issue.3 , pp. 317-326
    • Peterson, M.L.1    Hickey, M.B.2    Zaworotko, M.J.3    Almarsson, O.4
  • 6
    • 61549111509 scopus 로고    scopus 로고
    • Physicochemical properties of pharmaceutical co-crystals: A case study of ten AMG 517 co-crystals
    • Stanton MK, Bak A. 2008. Physicochemical properties of pharmaceutical co-crystals: A case study of ten AMG 517 co-crystals. Cryst Growth Des 8(10):3856-3862.
    • (2008) Cryst Growth Des , vol.8 , Issue.10 , pp. 3856-3862
    • Stanton, M.K.1    Bak, A.2
  • 7
    • 65249188682 scopus 로고    scopus 로고
    • Drug substance and former structure property relationships in 15 diverse pharmaceutical co-crystals
    • Stanton MK, Tufekcic S, Morgan C, Bak A. 2009. Drug substance and former structure property relationships in 15 diverse pharmaceutical co-crystals. Cryst Growth Des 9(3):1344-1352.
    • (2009) Cryst Growth Des , vol.9 , Issue.3 , pp. 1344-1352
    • Stanton, M.K.1    Tufekcic, S.2    Morgan, C.3    Bak, A.4
  • 9
    • 67049169036 scopus 로고    scopus 로고
    • Developability assessment in pharmaceutical industry: An integrated group approach for selecting developable candidates
    • Saxena V, Panicucci R, Joshi Y, Garad S. 2009. Developability assessment in pharmaceutical industry: An integrated group approach for selecting developable candidates. J Pharm Sci 98(6):1962-1979.
    • (2009) J Pharm Sci , vol.98 , Issue.6 , pp. 1962-1979
    • Saxena, V.1    Panicucci, R.2    Joshi, Y.3    Garad, S.4
  • 11
    • 0017870960 scopus 로고
    • Fenoprofen: Drug form selection and preformulation stability studies
    • Hirsch CA, Messenger RJ, Brannon JL. 1978. Fenoprofen: Drug form selection and preformulation stability studies. J Pharm Sci 67(2):231-236.
    • (1978) J Pharm Sci , vol.67 , Issue.2 , pp. 231-236
    • Hirsch, C.A.1    Messenger, R.J.2    Brannon, J.L.3
  • 13
    • 0031757855 scopus 로고    scopus 로고
    • The relative bioavailability and in vivo-in vitro correlations for four marketed carbamazepine tablets
    • Meyer MC, Straughn AB, Mhatre RM, Shah VP, Williams RL, Lesko LJ. 1998. The relative bioavailability and in vivo-in vitro correlations for four marketed carbamazepine tablets. Pharm Res 15(11):1787-1791.
    • (1998) Pharm Res , vol.15 , Issue.11 , pp. 1787-1791
    • Meyer, M.C.1    Straughn, A.B.2    Mhatre, R.M.3    Shah, V.P.4    Williams, R.L.5    Lesko, L.J.6
  • 14
    • 0031913402 scopus 로고    scopus 로고
    • Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms
    • Dressman JB, Amidon GL, Reppas C, Shah VP. 1998. Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms. Pharm Res 15(1):11-22.
    • (1998) Pharm Res , vol.15 , Issue.1 , pp. 11-22
    • Dressman, J.B.1    Amidon, G.L.2    Reppas, C.3    Shah, V.P.4
  • 15
    • 34547560453 scopus 로고    scopus 로고
    • Novel vanilloid receptor-1 antagonists: 2. Structure-activity relationships of 4-oxopyrimidines leading to the selection of a clinical candidate
    • Doherty EM, Fotsch C, Bannon AW, Bo Y, Chen N, Dominguez C, Falsey J, Gavva NR, Katon J, Nixey T, et al. 2007. Novel vanilloid receptor-1 antagonists: 2. Structure-activity relationships of 4-oxopyrimidines leading to the selection of a clinical candidate. J Med Chem 50(15):3515-3527.
    • (2007) J Med Chem , vol.50 , Issue.15 , pp. 3515-3527
    • Doherty, E.M.1    Fotsch, C.2    Bannon, A.W.3    Bo, Y.4    Chen, N.5    Dominguez, C.6    Falsey, J.7    Gavva, N.R.8    Katon, J.9    Nixey, T.10
  • 17
    • 0027275566 scopus 로고
    • Physiological parameters in laboratory animals and humans
    • Davies B, Morris T. 1993. Physiological parameters in laboratory animals and humans. Pharm Res 10(7):1093-1095.
    • (1993) Pharm Res , vol.10 , Issue.7 , pp. 1093-1095
    • Davies, B.1    Morris, T.2
  • 18
    • 41549088444 scopus 로고    scopus 로고
    • Controlled flow-through dissolution methodology: A high performance system
    • Stevens LE, Missel PJ, Weiner AL. 2008. Controlled flow-through dissolution methodology: A high performance system. Pharm Dev Tech 13:135-153.
    • (2008) Pharm Dev Tech , vol.13 , pp. 135-153
    • Stevens, L.E.1    Missel, P.J.2    Weiner, A.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.