The bioavailability of intranasal and smoked methamphetamine

被引:87
作者
Harris, DS [1 ]
Boxenbaum, H [1 ]
Everhart, ET [1 ]
Sequeira, G [1 ]
Mendelson, JE [1 ]
Jones, RT [1 ]
机构
[1] Univ Calif San Francisco, Langley Porter Psychiat Inst, Drug Dependence Res Ctr, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.clpt.2003.08.002
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Background. Patients in harm-reduction treatment programs are switching from intravenous to other routes of methamphetamine (INN, metamfetamine) administration to avoid risks associated with needle use. Relatively little has been reported about the bioavailability of methamphetamine when smoked or used intranasally. Methods. Eight experienced methamphetamine users were administered smoked or intranasal methamphetamine concurrently with an intravenous dose of deuterium-labeled methamphetamine. Plasma and urine concentrations were measured for calculation of bioavailability and other pharmacokinetic parameters by noncompartmental methods. Results. Methamphetamine was well absorbed after smoking or intranasal administration, with bioavailabilities of 79% after intranasal administration and 67% of the estimated delivered dose or 37.4% of the absolute (pipe) dose after smoking. Maximum methamphetamine concentrations occurred at 2.7 and 2.5 hours after intranasal and smoked doses. The elimination half-life was similar for intravenous (11.4 hours), intranasal (10.7 hours), and smoked (10.7 hours) methamphetamine. Clearance (272 mL . h(-1) . kg(-1)), steady-state volume of distribution (4.2 L/kg), and mean residence time (16 hours) of the intravenous dose were similar to previously reported values. Dextroamphetamine (INN, dexamfetamine) half-life (all routes) was 16.2 hours. Methamphetamine and dextroamphetamine renal clearances (all routes) were about 100 and 1100 mL . h(-1) . kg(-1), respectively. Conclusions. Intranasal and smoked methamphetamine are well absorbed. Although intranasal or smoked routes may decrease the risk of transmission of blood-borne diseases, exposure to methamphetamine and the possibility of drug-related complications remain substantial.
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页码:475 / 486
页数:12
相关论文
共 33 条
[1]
BECKETT AH, 1965, J PHARM PHARMACOL, V17, P109
[2]
Beebe D K, 1994, J Miss State Med Assoc, V35, P225
[3]
BEEBE DK, 1995, AM FAM PHYSICIAN, V51, P449
[4]
METABOLISM OF NICOTINE TO COTININE STUDIED BY A DUAL STABLE-ISOTOPE METHOD [J].
BENOWITZ, NL ;
JACOB, P .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1994, 56 (05) :483-493
[5]
CRITICAL EVALUATION OF THE POTENTIAL ERROR IN PHARMACOKINETIC STUDIES OF USING THE LINEAR TRAPEZOIDAL RULE METHOD FOR THE CALCULATION OF THE AREA UNDER THE PLASMA LEVEL TIME CURVE [J].
CHIOU, WL .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1978, 6 (06) :539-546
[6]
Cook C E, 1991, NIDA Res Monogr, V115, P6
[7]
COOK CE, 1993, DRUG METAB DISPOS, V21, P717
[8]
COOK CE, 1992, DRUG METAB DISPOS, V20, P856
[9]
DERLET RW, 1990, WESTERN J MED, V153, P625
[10]
Myocardial infarction after intranasal methamphetamine [J].
Farnsworth, TL ;
Brugger, CH ;
Malters, P .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 1997, 54 (05) :586-587