Miniature device for aqueous and non-aqueous solubility measurements during drug discovery

被引:40
作者
Chen, XQ [1 ]
Venkatesh, S
机构
[1] Bristol Myers Squibb Pharmaceut Res Inst, Pharmaceut Candidate Optimizat, Pharmaceut Discovery, Princeton, NJ 08543 USA
[2] Bristol Myers Squibb Pharmaceut Res Inst, Pharmaceut Candidate Optimizat, Pharmaceut Discovery, Wallingford, CT 06492 USA
关键词
drug discovery; equilibrium; microscale; miniature; physicochemical properties; solubility;
D O I
10.1023/B:PHAM.0000045225.76650.53
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. A miniature device was developed for the measurement of aqueous and non-aqueous equilibrium solubility during drug discovery. The solubility values obtained using the miniature device were compared to those obtained using the conventional shake-flask method. Methods. The aqueous solubility of six structurally diverse compounds, the solubility of carbamazepine in various cosolvent systems, and the pH-solubility profile of saquinavir were determined using the miniature device. The device contains a multichannel cartridge pump and a Tygon tubing that is mounted on the pump with two ends linked by a syringe filter. The drug slurry was filled into the tubing and circulated inside, continually passing through the syringe filter. At the end of the experiment, the filtrate was collected and analyzed directly by High-Pressure Liquid Chromatography ( HPLC). The solubility was also determined by the shake-flask method. Results. The solubility values determined by the miniature device were in good agreement with those measured by the conventional shake-flask method. Conclusions. The miniature device provides a unique way of testing aqueous and non-aqueous equilibrium solubility in a microscale setting. With approximate to1 mg of compound, it is possible to determine the entire pH-solubility profile. The device is useful for solubility screening during lead optimization and candidate selection in early drug discovery, when compound supply is limited. It can also be used for screening solubility in non-aqueous systems to select vehicles for preclinical in vivo studies.
引用
收藏
页码:1758 / 1761
页数:4
相关论文
共 12 条
[1]   pH-metric solubility. 2: Correlation between the acid-base titration and the saturation shake-flask solubility-pH methods [J].
Avdeef, A ;
Berger, CM ;
Brownell, C .
PHARMACEUTICAL RESEARCH, 2000, 17 (01) :85-89
[2]   A high-throughput screening method for the determination of aqueous drug solubility using laser nephelometry in microtiter plates [J].
Bevan, CD ;
Lloyd, RS .
ANALYTICAL CHEMISTRY, 2000, 72 (08) :1781-1787
[3]   Micro-scale measurement of the mechanical properties of compressed pharmaceutical powders. 2: The dynamic moduli of microcrystalline cellulose [J].
Hancock, BC ;
Dalton, CR ;
Clas, SD .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 228 (1-2) :139-145
[4]   MICROSCALE DETERMINATION OF DISSOCIATION-CONSTANTS OF MULTIVALENT PHARMACEUTICALS BY CAPILLARY ELECTROPHORESIS [J].
ISHIHAMA, Y ;
ODA, Y ;
ASAKAWA, N .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 83 (10) :1500-1507
[5]   An integrated process for measuring the physicochemical properties of drug candidates in a preclinical discovery environment [J].
Kibbey, CE ;
Poole, SK ;
Robinson, B ;
Jackson, JD ;
Durham, D .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (08) :1164-1175
[6]   Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings [J].
Lipinski, CA ;
Lombardo, F ;
Dominy, BW ;
Feeney, PJ .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 23 (1-3) :3-25
[7]   Solubility measurement using differential scanning calorimetry [J].
Mohan, R ;
Lorenz, H ;
Myerson, AS .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2002, 41 (19) :4854-4862
[8]   Microscale titrimetric and spectrophotometric methods for determination of ionization constants and partition coefficients of new drug candidates [J].
Morgan, ME ;
Liu, K ;
Anderson, BD .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (02) :238-245
[9]  
Pan L, 2001, J PHARM SCI, V90, P521, DOI 10.1002/1520-6017(200104)90:4<521::AID-JPS1009>3.0.CO
[10]  
2-B