Evaluation of the feasibility and use of a prototype remote drug delivery capsule (RDDC) for non-invasive regional drug absorption studies in the GI tract of man and beagle dog

被引:24
作者
Parr, AF
Sandefer, EP
Wissel, P
McCartney, M
McClain, C
Ryo, UY
Digenis, GA [1 ]
机构
[1] Univ Kentucky, Coll Pharm, Lexington, KY 40536 USA
[2] Glaxo Wellcome Inc, Res Triangle Pk, NC 27709 USA
[3] Res Triangle Inst, Res Triangle Pk, NC 27709 USA
[4] Univ Kentucky, Albert B Chandler Med Ctr, Lexington, KY 40536 USA
关键词
regional drug absorption; gamma scintigraphy; remote control capsule; non-invasive;
D O I
10.1023/A:1018884510163
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. Evaluate a prototype Remote Drug Delivery Capsule (RDDC) For use in beagle dogs and human volunteers For non-invasive drug absorption studies in different regions of the gastrointestinal tract. Methods. The device was dual radiolabeled and GI transit of the RDDC was monitored by gamma scintigraphy. Beagles were used initially to demonstrate the functional utility of the device where a solution of ranitidine hydrochloride (150 mg) was non-invasively delivered to the stomach, proximal small intestine and distal small intestine. A subsequent first time in human study enrolled twelve healthy male volunteers where the intended site of release was the stomach, early small bower, distal small bowel or colon. Results. Preliminary studies conducted in beagles indicated that the RDDC operated successfully and the onset of ranitidine serum levels were dependent on the time of capsule activation and site of drug release. Results from the human study showed that all twelve subjects swallowed the device with no discomfort. Mean gastric emptying of the RDDC was 1.50 +/- 1.28 h (range = 0.25 to 4.25 h), and total small intestine transit was 4.79 +/- 1.82 h (range = 2.00 to 8.25 h). The capsule was retrieved from the feces at 30.25 +/- 15.21 h (range = 14.12 to 74.25 h) and there were no reported adverse events. The prototype RDDC operated successfully in nine of the twelve human volunteers and the cause for the three failures was attributed to mechanical failure while the electronics assembly performed favorably. Conclusions, This prototype remote control capsule was shown to be well tolerated and functional to use in human volunteers as well as beagles. The application of the device coupled with gamma scintigraphy has the potential to be a valuable and rapid method to non-invasively evaluate regional drug absorption in the gastrointestinal tract under conditions that are both pharmaceutically and physiologically meaningful.
引用
收藏
页码:266 / 271
页数:6
相关论文
共 27 条
  • [1] Intestinal drug absorption and metabolism in cell cultures: Caco-2 and beyond
    Artursson, P
    Borchardt, RT
    [J]. PHARMACEUTICAL RESEARCH, 1997, 14 (12) : 1655 - 1658
  • [2] THE USE OF CULTURED EPITHELIAL AND ENDOTHELIAL-CELLS FOR DRUG TRANSPORT AND METABOLISM STUDIES
    AUDUS, KL
    BARTEL, RL
    HIDALGO, IJ
    BORCHARDT, RT
    [J]. PHARMACEUTICAL RESEARCH, 1990, 7 (05) : 435 - 451
  • [3] DIFFERENTIAL ABSORPTION OF AMOXICILLIN FROM THE HUMAN SMALL AND LARGE-INTESTINE
    BARR, WH
    ZOLA, EM
    CANDLER, EL
    HWANG, SM
    TENDOLKAR, AV
    SHAMBUREK, R
    PARKER, B
    HILTY, MD
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1994, 56 (03) : 279 - 285
  • [4] Investigation of nifedipine absorption in different regions of the human gastrointestinal (GI) tract after simultaneous administration of C-13- and C-12-nifedipine
    Bode, H
    Brendel, E
    Ahr, G
    Fuhr, U
    Harder, S
    Staib, AH
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 50 (03) : 195 - 201
  • [5] CASPER RA, 1992, Patent No. 5170801
  • [6] CASPER RA, 1992, Patent No. 5167626
  • [7] SITE-DIFFERENTIAL GASTROINTESTINAL ABSORPTION OF BENAZEPRIL HYDROCHLORIDE IN HEALTHY-VOLUNTEERS
    CHAN, KKH
    BUCH, A
    GLAZER, RD
    JOHN, VA
    BARR, WH
    [J]. PHARMACEUTICAL RESEARCH, 1994, 11 (03) : 432 - 437
  • [8] TRANSIT OF PHARMACEUTICAL DOSAGE FORMS THROUGH THE SMALL-INTESTINE
    DAVIS, SS
    HARDY, JG
    FARA, JW
    [J]. GUT, 1986, 27 (08) : 886 - 892
  • [9] DIGENIS GA, 1991, CRIT REV THER DRUG, V7, P309
  • [10] Doll Walter J., 1997, Pharmaceutical Research (New York), V14, pS654