Oral controlled release technology for peptides: Status and future prospects

被引:108
作者
Fix, JA
机构
[1] Alza Corporation, Palo Alto, CA 94303
关键词
oral drug delivery; peptide absorption; absorption enhancers; enzymatic degradation; chemical stability;
D O I
10.1023/A:1016008419367
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In spite of significant efforts in academic and commercial laboratories, major breakthroughs in oral peptide and protein formulation have not been achieved. The major barriers to developing oral formulations for peptides and proteins include poor intrinsic permeability,, lumenal and cellular enzymatic degradation, rapid clearance, and chemical and conformational stability. pharmaceutical approaches to address these barriers, which have been successful with traditional, small, organic drug molecules, have not readily translated into effective peptide and protein formulations. The success achieved by Sandoz with cyclosporin formulations remains one clear example of what can be achieved, although it is likely that effective oral formulations for peptides and proteins will remain highly compound specific. Although the challenges are significant, the potential therapeutic benefit remains high, particularly with the increasing identification of potential peptide and protein drag candidates emerging from the biotechnology arena. Successful formulations will most likely require a systematic and careful merger of formulation and design delivery systems which maximize the potential for absorption across the epithelial cell layer.
引用
收藏
页码:1760 / 1764
页数:5
相关论文
共 33 条
  • [1] STRUCTURAL SPECIFICITY OF MUCOSAL-CELL TRANSPORT AND METABOLISM OF PEPTIDE DRUGS - IMPLICATION FOR ORAL PEPTIDE DRUG DELIVERY
    BAI, JPF
    AMIDON, GL
    [J]. PHARMACEUTICAL RESEARCH, 1992, 9 (08) : 969 - 978
  • [2] TRANSEPITHELIAL TRANSPORT OF INSULIN .1. INSULIN DEGRADATION BY INSULIN-DEGRADING ENZYME IN SMALL-INTESTINAL EPITHELIUM
    BAI, JPF
    CHANG, LL
    [J]. PHARMACEUTICAL RESEARCH, 1995, 12 (08) : 1171 - 1175
  • [3] STARCH MICROSPHERES INDUCE PULSATILE DELIVERY OF DRUGS AND PEPTIDES ACROSS THE EPITHELIAL BARRIER BY REVERSIBLE SEPARATION OF THE TIGHT JUNCTIONS
    BJORK, E
    ISAKSSON, U
    EDMAN, P
    ARTURSSON, P
    [J]. JOURNAL OF DRUG TARGETING, 1995, 2 (06) : 501 - 507
  • [4] HYDROGELS FOR SITE-SPECIFIC DRUG DELIVERY TO THE COLON - INVITRO AND INVIVO DEGRADATION
    BRONDSTED, H
    KOPECEK, J
    [J]. PHARMACEUTICAL RESEARCH, 1992, 9 (12) : 1540 - 1545
  • [5] BUHLMAYER P, 1988, J MED CHEM, V31, P1839
  • [6] CITRIC-ACID AS AN ADJUVANT FOR TRANS-EPITHELIAL TRANSPORT
    CHO, MJ
    SCIESZKA, JF
    BURTON, PS
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 52 (01) : 79 - 81
  • [7] ENHANCED INTESTINAL-ABSORPTION OF AN RGD PEPTIDE FROM WATER-IN-OIL MICROEMULSIONS OF DIFFERENT COMPOSITION AND PARTICLE-SIZE
    CONSTANTINIDES, PP
    LANCASTER, CM
    MARCELLO, J
    CHIOSSONE, DC
    ORNER, D
    HIDALGO, I
    SMITH, PL
    SARKAHIAN, AB
    YIV, SH
    OWEN, AJ
    [J]. JOURNAL OF CONTROLLED RELEASE, 1995, 34 (02) : 109 - 116
  • [8] CONSTANTINIDES PP, 1993, P INT S CONTROLLED R, V20, P184
  • [9] ACYLCARNITINES - DRUG ABSORPTION-ENHANCING AGENTS IN THE GASTROINTESTINAL-TRACT
    FIX, JA
    ENGLE, K
    PORTER, PA
    LEPPERT, PS
    SELK, SJ
    GARDNER, CR
    ALEXANDER, J
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (03): : G332 - G340
  • [10] FIX JA, 1995, C FORM DRUG DEL ACS