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Volumn 98, Issue 3, 2009, Pages 1129-1135

Thermodynamics of cosolvent action: Phenacetin, salicylic acid and probenecid

Author keywords

Acid; Cosolvent action; Enthalpy entropy compensation; Phenacetin; Probenecid; Salicylic; Solubility; Solution thermodynamics; Solvent mixtures

Indexed keywords

ACETIC ACID ETHYL ESTER; ALCOHOL; PHENACETIN; PROBENECID; SALICYLIC ACID;

EID: 62849119057     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.21497     Document Type: Article
Times cited : (26)

References (15)
  • 1
    • 0020666212 scopus 로고
    • Enthalpy-entropy compensation analysis of pharmaceuticals, biochemical and biological systems
    • Tomlinson E. 1983. Enthalpy-entropy compensation analysis of pharmaceuticals, biochemical and biological systems. Int J Pharm 13:115-144.
    • (1983) Int J Pharm , vol.13 , pp. 115-144
    • Tomlinson, E.1
  • 2
    • 0028393186 scopus 로고
    • Binding geometry, stoichiometry, and thermodynamics of cyclamate-oligosaccharide (cyclodextrin) inclusion complex formation with chlorogenic acid, the major substrate of apple polyphenol oxidase
    • Irwin PL, Pfeiffer PE, Doner LW, Sapers GM, Brewster GN, Hicks KB. 1994. Binding geometry, stoichiometry, and thermodynamics of cyclamate-oligosaccharide (cyclodextrin) inclusion complex formation with chlorogenic acid, the major substrate of apple polyphenol oxidase. Carbohydr Res 256:13-27.
    • (1994) Carbohydr Res , vol.256 , pp. 13-27
    • Irwin, P.L.1    Pfeiffer, P.E.2    Doner, L.W.3    Sapers, G.M.4    Brewster, G.N.5    Hicks, K.B.6
  • 3
    • 0025343507 scopus 로고
    • Strength of molecular complexation of apolar solutes in water and in organic solvents is predictable by linear free energy relationships: A general model for solvation effects on apolar binding
    • Smithrud DB, Diederich F. 1990. Strength of molecular complexation of apolar solutes in water and in organic solvents is predictable by linear free energy relationships: A general model for solvation effects on apolar binding. J Am Chem Soc 112:339-343.
    • (1990) J Am Chem Soc , vol.112 , pp. 339-343
    • Smithrud, D.B.1    Diederich, F.2
  • 4
    • 0025123357 scopus 로고
    • Microcalorimetry study for the binding of ionic drugs to human erythrocytes and the ghost membranes
    • Aki H, Yamamoto M. 1990. Microcalorimetry study for the binding of ionic drugs to human erythrocytes and the ghost membranes. J Pharm Pharmacol 42:637-641.
    • (1990) J Pharm Pharmacol , vol.42 , pp. 637-641
    • Aki, H.1    Yamamoto, M.2
  • 6
    • 33847798413 scopus 로고
    • Enthalpyentropy compensation. 2. Separation of the chemical from the statistical effect
    • Krug RR, Hunter WG, Grieger RA. 1976. Enthalpyentropy compensation. 2. Separation of the chemical from the statistical effect. J Phys Chem 80:2341-2351.
    • (1976) J Phys Chem , vol.80 , pp. 2341-2351
    • Krug, R.R.1    Hunter, W.G.2    Grieger, R.A.3
  • 7
    • 0028207026 scopus 로고
    • Thermodynamics of transfer of indocarbocyanides from gel to fluid phases of phospholipids bilayers
    • Spink CH, Clouser D, O'Neil J. 1994. Thermodynamics of transfer of indocarbocyanides from gel to fluid phases of phospholipids bilayers. Biochim Biophys Acta 1191:164-172.
    • (1994) Biochim Biophys Acta , vol.1191 , pp. 164-172
    • Spink, C.H.1    Clouser, D.2    O'Neil, J.3
  • 8
    • 0029836768 scopus 로고    scopus 로고
    • Nonlinear enthalpy-entropy compensation for the solubility of phenacetin in dioxane-water mixtures
    • Bustamante C, Bustamante P. 1996. Nonlinear enthalpy-entropy compensation for the solubility of phenacetin in dioxane-water mixtures. J Pharm Sci 85:1109-1111.
    • (1996) J Pharm Sci , vol.85 , pp. 1109-1111
    • Bustamante, C.1    Bustamante, P.2
  • 9
    • 0031774542 scopus 로고    scopus 로고
    • Enthalpy-entropy compensation for the solubility of drugs in solvent mixtures: Paracetamol, acetanilide, and nalidixic acid in dioxane-water
    • Bustamante P, Romero S, Peña MA, Escalera B, Reíllo A. 1998. Enthalpy-entropy compensation for the solubility of drugs in solvent mixtures: Paracetamol, acetanilide, and nalidixic acid in dioxane-water. J Pharm Sci 87:1590-1596.
    • (1998) J Pharm Sci , vol.87 , pp. 1590-1596
    • Bustamante, P.1    Romero, S.2    Peña, M.A.3    Escalera, B.4    Reíllo, A.5
  • 10
    • 0036285086 scopus 로고    scopus 로고
    • Thermodynamic origin of the solubility profile of drugs showing one or two maxima against the polarity of aqueous and non-aqueous mixtures: Niflumic acid and caffeine
    • Bustamante P, Navarro J, Romero S, Escalera B. 2002. Thermodynamic origin of the solubility profile of drugs showing one or two maxima against the polarity of aqueous and non-aqueous mixtures: Niflumic acid and caffeine. J Pharm Sci 91:874-883.
    • (2002) J Pharm Sci , vol.91 , pp. 874-883
    • Bustamante, P.1    Navarro, J.2    Romero, S.3    Escalera, B.4
  • 11
    • 35748930860 scopus 로고    scopus 로고
    • Thermodynamic study of the solubility of ibuprofen and naproxen in some ethanol + propylene glycol mixtures
    • Pacheco D, Manrique Y, Martínez F. 2007. Thermodynamic study of the solubility of ibuprofen and naproxen in some ethanol + propylene glycol mixtures. Fluid Phase Equilibria 262:23-31.
    • (2007) Fluid Phase Equilibria , vol.262 , pp. 23-31
    • Pacheco, D.1    Manrique, Y.2    Martínez, F.3
  • 14
    • 0027211738 scopus 로고
    • A modification of the extended Hildebrand approach to predict the solubility of structurally related drugs in solvent mixtures
    • Bustamante P, Escalera B, Martin A, Selles E. 1993. A modification of the extended Hildebrand approach to predict the solubility of structurally related drugs in solvent mixtures. J Pharm Pharmacol 45:253-257.
    • (1993) J Pharm Pharmacol , vol.45 , pp. 253-257
    • Bustamante, P.1    Escalera, B.2    Martin, A.3    Selles, E.4
  • 15
    • 33747354139 scopus 로고    scopus 로고
    • Solubility parameter of drugs for predicting the solubility profile type within a wide polarity range in solvent mixtures
    • Peña MA, Reíllo A, Escalera B, Bustamante P. 2006. Solubility parameter of drugs for predicting the solubility profile type within a wide polarity range in solvent mixtures. Int J Pharm 321:155-161.
    • (2006) Int J Pharm , vol.321 , pp. 155-161
    • Peña, M.A.1    Reíllo, A.2    Escalera, B.3    Bustamante, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.