메뉴 건너뛰기




Volumn 107, Issue , 2015, Pages 394-402

Reversibly changing a painkiller structure: A hot topic for a cold case-Ibuprofen lysine salt

Author keywords

DSC; Phase transition; Polymorphism; Thermodiffractometry; XRPD

Indexed keywords

IBUPROFEN LYSINE; IBUPROFEN; LYSINE;

EID: 84922327137     PISSN: 07317085     EISSN: 1873264X     Source Type: Journal    
DOI: 10.1016/j.jpba.2015.01.028     Document Type: Article
Times cited : (9)

References (20)
  • 1
    • 0031886547 scopus 로고    scopus 로고
    • Clinical pharmacokinetics of ibuprofen. The first 30 years
    • Davies N.M. Clinical pharmacokinetics of ibuprofen. The first 30 years. Clin. Pharmacokinet. 1998, 34:101-154.
    • (1998) Clin. Pharmacokinet. , vol.34 , pp. 101-154
    • Davies, N.M.1
  • 2
    • 0030953302 scopus 로고    scopus 로고
    • Effects of ibuprofen enantiomers and its coenzyme A thioesters on human prostaglandin endoperoxide synthases
    • Neupert W., Brugger R., Euchenhofer C., Brune K., Geisslinger G. Effects of ibuprofen enantiomers and its coenzyme A thioesters on human prostaglandin endoperoxide synthases. Br. J. Pharmacol. 1997, 122:487-492.
    • (1997) Br. J. Pharmacol. , vol.122 , pp. 487-492
    • Neupert, W.1    Brugger, R.2    Euchenhofer, C.3    Brune, K.4    Geisslinger, G.5
  • 3
    • 0024390397 scopus 로고
    • Therapeutically relevant differences in the pharmacokinetical and pharmaceutical behavior of ibuprofen lysinate as compared to ibuprofen acid
    • Geisslinger G., Dietzel K., Bezler H., Nuernberg B., Brune K. Therapeutically relevant differences in the pharmacokinetical and pharmaceutical behavior of ibuprofen lysinate as compared to ibuprofen acid. Int. J. Clin. Pharmacol. Ther. Toxicol. 1989, 2(7):324-328.
    • (1989) Int. J. Clin. Pharmacol. Ther. Toxicol. , vol.2 , Issue.7 , pp. 324-328
    • Geisslinger, G.1    Dietzel, K.2    Bezler, H.3    Nuernberg, B.4    Brune, K.5
  • 4
    • 0021234249 scopus 로고
    • Solubility-dissolution relationship for ibuprofen, fenbufen and their sodium salts in acid medium
    • Fini A., Zecchi V., Rodriguez L., Tartarini A. Solubility-dissolution relationship for ibuprofen, fenbufen and their sodium salts in acid medium. Pharm. Acta Helv. 1984, 59:106-108.
    • (1984) Pharm. Acta Helv. , vol.59 , pp. 106-108
    • Fini, A.1    Zecchi, V.2    Rodriguez, L.3    Tartarini, A.4
  • 7
    • 30744447963 scopus 로고    scopus 로고
    • Similarity in structures of racemic and enantiomeric ibuprofen sodium dihydrates
    • Zhang Y., Grant D.J.W. Similarity in structures of racemic and enantiomeric ibuprofen sodium dihydrates. Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 2005, 61:435-438.
    • (2005) Acta Crystallogr., Sect. C: Cryst. Struct. Commun. , vol.61 , pp. 435-438
    • Zhang, Y.1    Grant, D.J.W.2
  • 9
    • 84922291915 scopus 로고    scopus 로고
    • Bruker AXS, Karlsruhe, Germany
    • Coelho A.A. TOPAS-R, v3.0. 2005, Bruker AXS, Karlsruhe, Germany.
    • (2005) TOPAS-R, v3.0.
    • Coelho, A.A.1
  • 11
    • 0026852338 scopus 로고
    • A fundamental parameters approach to X-ray line-profile fitting
    • Cheary R.W., Coelho A. A fundamental parameters approach to X-ray line-profile fitting. J. Appl. Crystallogr. 1992, 25:109-121.
    • (1992) J. Appl. Crystallogr. , vol.25 , pp. 109-121
    • Cheary, R.W.1    Coelho, A.2
  • 13
    • 0026370416 scopus 로고
    • Detection and characterization of polymorphism in the pharmaceutical industry
    • McCauley J.A. Detection and characterization of polymorphism in the pharmaceutical industry. Am. Inst. Chem. Eng. Symp. Ser. 1991, 87:58-63.
    • (1991) Am. Inst. Chem. Eng. Symp. Ser. , vol.87 , pp. 58-63
    • McCauley, J.A.1
  • 16
    • 35548972070 scopus 로고    scopus 로고
    • The thermodynamic dissociation constants of four non-steroidal anti-inflammatory drugs by the least-squares nonlinear regression of multiwavelength spectrophotometric pH-titration data
    • Melouna M., Bordovska S., Galla L. The thermodynamic dissociation constants of four non-steroidal anti-inflammatory drugs by the least-squares nonlinear regression of multiwavelength spectrophotometric pH-titration data. J. Pharm. Biomed. Anal. 2007, 45:552-564.
    • (2007) J. Pharm. Biomed. Anal. , vol.45 , pp. 552-564
    • Melouna, M.1    Bordovska, S.2    Galla, L.3
  • 17
    • 84922310138 scopus 로고    scopus 로고
    • STRAIN.
    • Y. Ohashi, STRAIN. http://www.cryst.ehu.es/cryst/strain.html.
    • Ohashi, Y.1
  • 19
    • 33645749447 scopus 로고    scopus 로고
    • Wintensor Ein WIN95/98/NT Programm zum Darstellen tensorieller Eigenschaften
    • Kaminsky W. Wintensor Ein WIN95/98/NT Programm zum Darstellen tensorieller Eigenschaften. Z. Kristallogr. Suppl. 2000, 17:51.
    • (2000) Z. Kristallogr. Suppl. , vol.17 , pp. 51
    • Kaminsky, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.