Validated LC coupled to ESI-MS/MS analysis for fentanyl in human plasma and UV analysis in applied reservoir transdermal patches using a simple and rapid procedure

被引:16
作者
Takashina, Y. [1 ]
Naito, T. [1 ]
Mino, Y. [1 ,2 ]
Kagawa, Y. [2 ]
Kawakami, J. [1 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Hosp Pharm, Higashi Ku, Hamamatsu, Shizuoka 4313192, Japan
[2] Univ Shizuoka, Fac Pharmaceut Sci, Dept Clin Pharmaceut & Pharm Practice, Suruga Ku, Shizuoka 4228526, Japan
关键词
absorption rate; clinical application; drug reservoir; fentanyl; plasma concentration; transdermal therapeutic system; CANCER PAIN PATIENTS; MASS-SPECTROMETRY; HUMAN URINE; PHARMACOKINETICS; NORFENTANYL; ABSORPTION; OPIOIDS; TRIAL;
D O I
10.1111/j.1365-2710.2009.01033.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
P>Background and objectives: Fentanyl has been used for cancer pain in transdermal formulation. The aim of the present study was to establish an analytical method for fentanyl in human plasma and in an applied transdermal reservoir patch (Reservoir-TTS), as well as for therapeutic monitoring of fentanyl in cancer patients. Method: Electro-spray ionization mass spectrometric (ESI-MS/MS) analysis followed solid phase extraction (SPE) from human plasma and drug reservoir extraction from an applied Reservoir-TTS. Each separation was completed within 9 min using an ODS column (particle size, 3 mu m, 2 center dot 0 mm i.d. x 75 mm) with 25% acetonitrile containing 5 mm ammonium acetate at pH 3 center dot 5. In the ESI-MS/MS analysis, the calibration curve for fentanyl was linear over a concentration range of 0 center dot 05-7 center dot 2 ng/mL in human plasma. The extraction efficiency of fentanyl in the human plasma was more than 95%. The intra- and interassay precision and accuracy were within 7% and 97 center dot 3-101 center dot 2%, respectively. The lower LOQ for fentanyl was 0 center dot 05 ng/mL in the human plasma. The extraction of the 25 mu g/h and 50 mu g/h Reservoir-TTS gave reproducible recoveries of 88 center dot 3% and 90 center dot 9%, respectively. The plasma concentration of fentanyl showed large interindividual variation in 31 patients with cancer pain. Conclusion: The method described is simple, accurate, and reproducible, and should be helpful for the therapeutic monitoring of fentanyl in cancer patients.
引用
收藏
页码:523 / 529
页数:7
相关论文
共 27 条
  • [21] Inter- and intraindividual variabilities in pharmacokinetics of fentanyl after repeated 72-hour transdermal applications in cancer pain patients
    Solassol, I
    Bressolle, F
    Caumette, L
    Garcia, F
    Poujol, S
    Culine, W
    Pinguet, F
    [J]. THERAPEUTIC DRUG MONITORING, 2005, 27 (04) : 491 - 498
  • [22] Identification of fentanyl, alfentanil, sufentanil, remifentanil and their major metabolites in human urine by liquid chromatography/tandem mass spectrometry for doping control purposes
    Thevis, M
    Geyer, H
    Bahr, D
    Schänzer, W
    [J]. EUROPEAN JOURNAL OF MASS SPECTROMETRY, 2005, 11 (04) : 419 - 427
  • [23] Perioperative pharmacokinetics of transdermal fentanyl in elderly and young adult patients
    Thompson, JP
    Bower, S
    Liddle, AM
    Rowbotham, DJ
    [J]. BRITISH JOURNAL OF ANAESTHESIA, 1998, 81 (02) : 152 - 154
  • [24] US FDA, 2001, GUID IND BIOAN METH
  • [25] Validated GC-MS analysis for the determination of residual fentanyl in applied Durogesic® reservoir and Durogesic® D-Trans® matrix transdermal fentanyl patches
    Van Nimmen, Nadine F. J.
    Veulemans, Hendrik A. F.
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 846 (1-2): : 264 - 272
  • [26] ABSORPTION CHARACTERISTICS OF TRANSDERMALLY ADMINISTERED FENTANYL
    VARVEL, JR
    SHAFER, SL
    HWANG, SS
    COEN, PA
    STANSKI, DR
    [J]. ANESTHESIOLOGY, 1989, 70 (06) : 928 - 934
  • [27] Physicians' knowledge of transdermal fentanyl
    Welsh, J
    Reid, A
    Graham, J
    Curto, J
    MacLeod, K
    O'Neill, C
    [J]. PALLIATIVE MEDICINE, 2005, 19 (01) : 9 - 16