Determination of a new polymer-bound paclitaxel derivative (PNU 166945), free paclitaxel and 7-epipaclitaxel in dog plasma and urine by reversed-phase high-performance liquid chromatography with UV detection

被引:17
作者
Fraier, D [1 ]
Cenacchi, V [1 ]
Frigerio, E [1 ]
机构
[1] Pharmacia & Upjohn Inc, Dept Metab & Pharmacokinet, I-20014 Milan, Italy
关键词
taxanes; paclitaxel; PNU; 166945;
D O I
10.1016/S0021-9673(97)01204-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and selective high-performance liquid chromatographic method for the determination of PNU 166945, a new polymer-bound paclitaxel derivative, free paclitaxel and 7-epipaclitaxel in dog plasma and urine has been developed. The method involves a solid-phase extraction of free paclitaxel and its possible degradation product 7-epipaclitaxel from plasma and urine, previously buffered with an equal volume of 0.05 M or 1 M KH2PO4 respectively, on 1-ml cyanopropyl columns. Cartridges elution was performed with the mobile phase, 0.05 M (pH 4.6) monobasic potassium phosphate-acetonitrile mixture (45:55, v/v). The samples were chromatographed on a reversed-phase octyl 4-mu m column with UV detection at 229 nm. The retention times of paclitaxel and 7-epipaclitaxel were about 14 and 22 min, respectively. Determination of total paclitaxel (free+polymer-bound) was performed after release of paclitaxel from the polymeric carrier by chemical hydrolysis at room temperature (22 degrees C) for 20 h. After addition of 0.5 mi of methanol-0.1 M KH2PO4 mixture (50:50, v/v, pH=7.5) to 0.5 mi of plasma or urine, paclitaxel was analysed as described above. PNU 166945 concentration was then determined by subtraction of free from total paclitaxel. The linearity, precision, accuracy and recovery of the method were evaluated. The limit of quantitation of the method was 5 ng/ml for biological fluid for paclitaxel and 7-epipaclitaxel and 20 ng/ml for PNU 166945 (as paclitaxel equivalent). (C) 1998 Elsevier Science B.V.
引用
收藏
页码:295 / 303
页数:9
相关论文
共 13 条
[1]   STABILITY PROBLEMS WITH TAXOL IN MOUSE PLASMA DURING ANALYSIS BY LIQUID-CHROMATOGRAPHY [J].
LESLIE, J ;
KUJAWA, JM ;
EDDINGTON, N ;
EGORIN, M ;
EISEMAN, J .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1993, 11 (11-12) :1349-1352
[2]  
LONGNECKER SM, 1987, CANCER TREAT REP, V71, P53
[3]  
Pesenti E., 1995, Proceedings of the American Association for Cancer Research Annual Meeting, V36, P307
[4]   ANALYSIS OF ANTICANCER DRUGS IN BIOLOGICAL-FLUIDS - DETERMINATION OF TAXOL WITH APPLICATION TO CLINICAL PHARMACOKINETICS [J].
RIZZO, J ;
RILEY, C ;
VONHOFF, D ;
KUHN, J ;
PHILLIPS, J ;
BROWN, T .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1990, 8 (02) :159-164
[5]   DRUG-THERAPY - PACLITAXEL (TAXOL) [J].
ROWINSKY, EK ;
DONEHOWER, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (15) :1004-1014
[6]   REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF TAXOL IN MOUSE PLASMA [J].
SHARMA, A ;
CONWAY, WD ;
STRAUBINGER, RM .
JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS, 1994, 655 (02) :315-319
[7]  
SONG D, 1995, J CHROMATOGR B, V663, P337
[8]   DETERMINATION OF PACLITAXEL AND METABOLITES IN MOUSE PLASMA, TISSUES, URINE AND FECES BY SEMIAUTOMATED REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
SPARREBOOM, A ;
VANTELLINGEN, O ;
NOOIJEN, WJ ;
BEIJNEN, JH .
JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS, 1995, 664 (02) :383-391
[9]  
Sparreboom A, 1996, CANCER RES, V56, P2112
[10]   PACLITAXEL - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND THERAPEUTIC POTENTIAL IN THE TREATMENT OF CANCER [J].
SPENCER, CM ;
FAULDS, D .
DRUGS, 1994, 48 (05) :794-847