Comparative bioavailability of metoprolol tartrate after oral and transidermal administration in healthy male volunteers

被引:7
|
作者
Aqil, M. [1 ]
Ali, A.
Sultana, Y.
Saha, N.
机构
[1] Hamdard Univ, Fac Pharm, Dept Pharmaceut, New Delhi 110062, India
[2] Majeedia Hosp, Ranbaxy Clin Pharmacol Unit, New Delhi, India
关键词
D O I
10.2165/00044011-200727120-00005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and objective: Transdermal drug delivery systems (TDDSs) of metoprolol tartrate have been previously prepared and evaluated in vitro and in vivo in an animal model. This study compares the bioavailability of metoprolol tartrate from a TDDS with that from a conventional marketed tablet in healthy human volunteers. Methods: This was an open-label, balanced randomised, two-treatment, two-period crossover study with a washout period of I week. Volunteers were randomised (by means of a SAS software-generated randomisation schedule) to have a TDDS applied to their chest for 48 hours or to receive a 100mg conventional marketed tablet of metoprolol tartrate in period I. In period H, the volunteers received the other dosage form. Blood samples were collected through an indwelling cannula placed in the forearm vein of each subject. Metoprolol tartrate concentrations were quantified in plasma samples by a validated high-performance liquid chromatography method. Results: A 3-fold improvement in bioavailability was observed with the TDDS form over oral therapy as shown by the extent of absorption indicated by the mean area under the concentration-time curve from time zero to time t values for tablets (451.98 ng center dot h/mL) and TDDS (1552.66 ng center dot h/mL). Although the maximum plasma concentration was higher for the tablet form than the TDDS (77.67 +/- 23.33 vs 51.16 +/- 16.61 ng/mL), the variable absorption profile, which is a characteristic feature of oral therapy, was quite evident. Plasma metoprolol tartrate concentrations plummeted to therapeutically ineffective concentrations as early as 8 hours following oral administration. Conclusion: The TDDS developed in our laboratory produced therapeutically effective plasma concentrations for up to 48 hours, with a minimum of 26.09 ng/ mL and a maximum of 76.70 ng/mL, which is in good agreement with the therapeutic range (20-100 ng/mL) of metoprolol tartrate. It could be concluded that the TDDS meets the intended goal of 2-day management of hypertension with application of a single patch, obviating the inconvenience of frequent administration and thus improving patient compliance.
引用
收藏
页码:833 / 839
页数:7
相关论文
共 50 条
  • [31] Absolute oral bioavailability of rosuvastatin in healthy white adult male volunteers
    Martin, PD
    Warwick, MJ
    Dane, AL
    Brindley, C
    Short, T
    CLINICAL THERAPEUTICS, 2003, 25 (10) : 2553 - 2563
  • [32] Lack of effect of food on the oral bioavailability of irbesartan in healthy male volunteers
    Vachharajani, NN
    Shyu, WC
    Mantha, S
    Park, JS
    Greene, DS
    Barbhaiya, RH
    JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 38 (05): : 433 - 436
  • [33] Effect of Calcium Supplements on the Oral Bioavailability of Moxifloxacin in Healthy Male Volunteers
    Heino Stass
    Christoph Wandel
    Heinz Delesen
    Jan-Georg Möller
    Clinical Pharmacokinetics, 2001, 40 : 27 - 32
  • [34] Absolute bioavailability of midazolam after subcutaneous administration to healthy volunteers
    Pecking, M
    Montestruc, F
    Marquet, P
    Wodey, E
    Homery, MC
    Dostert, P
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 54 (04) : 357 - 362
  • [35] COMPARATIVE BIOAVAILABILITY STUDY OF 2 ORAL DOSAGE FORMS OF PIROXICAM IN HEALTHY INDIAN MALE-VOLUNTEERS
    DHANERIA, SP
    GARG, SK
    KUMAR, N
    SHARMA, PL
    DRUG INVESTIGATION, 1993, 6 (05): : 300 - 302
  • [36] Comparative bioavailability of two capsule formulations of ofloxacin in healthy volunteers after a single dose administration
    Oliveira, CF
    Dias, HB
    Ribeiro, W
    Poli, A
    Peixoto, AP
    Moraes, MEA
    Moraes, MO
    Bezerra, FAF
    Moreno, H
    Muscará, MN
    de Nucci, G
    CLINICAL RESEARCH AND REGULATORY AFFAIRS, 1999, 16 (1-2) : 29 - 40
  • [37] Comparative bioavailability of two ramipril formulations after single-dose administration in healthy volunteers
    Mendes, GD
    Sanfelice, ATD
    Borges, NCD
    Cavedal, LE
    Sverdloff, C
    Galuppo, MP
    Módolo, JH
    De Nucci, G
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2006, 44 (02) : 93 - 98
  • [38] Comparative bioavailability of two losartan formulations in healthy human volunteers after a single dose administration
    Oliveira, CH
    Silva, RM
    Santagada, V
    Caliendo, G
    Perissutti, E
    Galuppo, MP
    Rezende, VM
    Barrientos-Astigarraga, RE
    Mendes, GD
    De Nucci, G
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2006, 44 (03) : 142 - 148
  • [39] Comparative bioavailability of 4 amoxicillin formulations in healthy human volunteers after a single dose administration
    Oliveira, CH
    Abib, E
    Vannuchi, YB
    Sucupira, M
    Ilha, J
    De Nucci, G
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2001, 39 (04) : 167 - 172
  • [40] HPLC determination of amoxicillin comparative bioavailability in healthy volunteers after a single dose administration.
    de Abreu, LRP
    Ortiz, RAM
    de Castro, SC
    Pedrazzoli, J
    JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, 2003, 6 (02): : 223 - 230