Plasma levels of glyceryl trinitrate and dinitrates during application of three strengths of a new glyceryl trinitrate transdermal patch

被引:0
|
作者
Santoro, A
Rovati, LC
Follet, M
Setnikar, I
Caplain, H
Gualano, V
机构
[1] Rotta Res Lab SpA, Dept Clin Pharmacol, I-20052 Monza, Italy
[2] Rotta Res Lab SpA, Dept Regulatory Affairs, I-20052 Monza, Italy
[3] Rottapharm SARL, Pharm Responsable, Paris, France
[4] Aster, Paris, France
[5] Cephac Res Ctr, St Benoit, France
来源
ARZNEIMITTELFORSCHUNG-DRUG RESEARCH | 2000年 / 50卷 / 09期
关键词
CAS; 55-63-0; 621-65-8; 623-87-0; Epinitril; (R); pharmacokinetics; volunteers; glyceryl dinitrates; glyceryl trinitrate; transdermal patch;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The pharmacokinetic characteristics and the bioavailability of glyceryl trinitrate (GTN, CAS 55-63-0) and of its main metabolities 1,2-glyceryl dinitrate (1,2-GDN, CAS 621-65-8) and 1,3-glyceryl dinitrate (1,3-GDN, CAS 623-87-0) during a single 74-h application of three strengths of a newly developed GTN transdermal patch (Epinitril (R)) were investigated. The three strengths coded in this paper EPI-5, EPI-10 and EPI-15 have a nominal release rate of GTN of 5, 10 and 15 mg, respectively, in 24 h. The study was an open, randomized balanced cross-over study on 18 healthy male volunteers, to whom the patches were applied for 24 h to the antero-lateral part of the thorax in three periods, separated by an at least 3-day wash-out. Blood samples were collected before administration, during the 24-h patch application and 1, 3 and 6 h after patch removal. Assayed in plasma were GTN, 1,2-GDN and 1,3-GDN using validated GC/MS methods with stable isotope labeled internal standards (N-15(3)-GTN, N-15(2)-1,2-GDN, and N-15(2)-1,3-GDN). GTN and its two metabolites reached the plateau already 3 h after application of the patches and remained on extended and fairly constant levels during the whole 24-h application. The plasma levels of the three nitrates were proportional to the strengths of the patches. The plasma levels of 1,2-GDN were about 6 times higher than those of GTN. The plasma levels of 1,3-GDN were similar to those of GTN. Upon removal of the patches the concentrations of the three nitrates fell to negligible values within 3 h, an important property when an intermittent GTN therapy is needed in order to avoid tolerance to the drug. The patches were well tolerated at the application site. For their good tolerability, small size and transparency, the new GTN patches are very patient friendly, a quality that improves compliance with the therapeutic regimen.
引用
收藏
页码:786 / 794
页数:9
相关论文
共 50 条
  • [21] Prevention of Radial Artery Spasm With Transdermal Glyceryl Trinitrate Patches
    Economou, Fotios I.
    Doundoulakis, Ioannis
    Kalamakidou, Iliada
    Koliastasis, Leonidas
    Soulaidopoulos, Stergios
    Samara, Myrto
    Dimitriadis, Kyriakos
    Papazisis, Georgios
    Tsiachris, Dimitris
    Tsioufis, Konstantinos
    JACC-CARDIOVASCULAR INTERVENTIONS, 2023, 16 (03) : 365 - 367
  • [22] EFFECT OF TRANSDERMAL GLYCERYL TRINITRATE ON THE SURVIVAL OF PERIPHERAL INTRAVENOUS INFUSIONS
    KHAWAJA, HT
    CAMPBELL, MJ
    WEAVER, PC
    BRITISH JOURNAL OF SURGERY, 1988, 75 (06) : 614 - 614
  • [23] EXPOSURE TO GLYCERYL TRINITRATE DURING GUN POWDER PRODUCTION - PLASMA GLYCERYL TRINITRATE CONCENTRATION, ELIMINATION KINETICS, AND DISCOMFORT AMONG PRODUCTION WORKERS
    GJESDAL, K
    BILLE, S
    BREDESEN, JE
    BJORGE, E
    HALVORSEN, B
    LANGSETH, K
    LUNDE, PKM
    SIVERTSSEN, E
    BRITISH JOURNAL OF INDUSTRIAL MEDICINE, 1985, 42 (01): : 27 - 31
  • [24] Transdermal delivery of glyceryl trinitrate: clinical applications in acute stroke
    Appleton, Jason P.
    Krishnan, Kailash
    Bath, Philip M.
    EXPERT OPINION ON DRUG DELIVERY, 2020, 17 (03) : 297 - 303
  • [25] Therapeutic Potential of Transdermal Glyceryl Trinitrate in the Management of Acute Stroke
    Jason P. Appleton
    Nikola Sprigg
    Philip M. Bath
    CNS Drugs, 2017, 31 : 1 - 9
  • [26] Effects of AOT micellar systems on the transdermal permeation of glyceryl trinitrate
    Varshney, M
    Khanna, T
    Changez, M
    COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 13 (01) : 1 - 11
  • [27] BIOAVAILABILITY OF GLYCERYL TRINITRATE AFTER SUBLINGUAL APPLICATION
    RIETBROCK, N
    HERLING, C
    MUCK, B
    ARZNEIMITTEL-FORSCHUNG/DRUG RESEARCH, 1989, 39-1 (02): : 267 - 269
  • [28] Therapeutic Potential of Transdermal Glyceryl Trinitrate in the Management of Acute Stroke
    Appleton, Jason P.
    Sprigg, Nikola
    Bath, Philip M.
    CNS DRUGS, 2017, 31 (01) : 1 - 9
  • [29] The studies on the new metabolic process of glyceryl trinitrate
    Tian, YP
    Zhang, YD
    Wang, DQ
    Song, SZ
    Jiang, H
    Dong, J
    FREE RADICAL BIOLOGY AND MEDICINE, 2004, 36 : S149 - S149
  • [30] Human maternal and fetal plasma glyceryl trinitrate concentrations
    Bustard, MA
    Ryan, G
    Seaward, G
    Saleniak, ME
    Smith, GN
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2003, 189 (06) : 1777 - 1778