Formulating insulin for oral administration:: Preparation of hyaluronan-insulin complex

被引:14
作者
Jederstrom, G
Andersson, A
Gråsjö, J
Sjöholm, I
机构
[1] Uppsala Univ, Biomed Ctr, Dept Pharm, SE-75123 Uppsala, Sweden
[2] Uppsala Univ, Biomed Ctr, Dept Med Cell Biol, SE-75123 Uppsala, Sweden
关键词
hyaluronan-insulin complex; glucose-lowering activity; insulin; hyaluronan; insulin formulation;
D O I
10.1023/B:PHAM.0000048195.69304.ff
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. To investigate the behaviour of peptides and hyaluronan in strong acid solutions containing electrolytes in the preparation of a new formulation of insulin, hyaluronan-insulin complex, and to evaluate the in vivo oral activity of the formulation. Methods. Individual processing parameters in the preparation of the insulin complex were first refined, and two formulations were subsequently investigated. The chemical structure, particle size and hydrophilic/hydrophobic properties of the insulin complex in these formulations were studied using light scattering techniques, amino acid analysis, atomic force microscopy and cryo-transmission electron microscopy. The in vivo activity of oral hyaluronan-insulin complex was then evaluated by measuring the decrease in blood glucose concentrations in streptozotocin diabetic rats. Results. Five of seven batches of the two insulin complex formulations fit the baseline criteria for approval of the new formulation. The formulation consists of a transparent aqua sol containing a solid hydrophobic phase as precipitate. Glucose-lowering activity was demonstrated after oral administration of the insulin complex to diabetic rats. Conclusion. A new insulin formulation, a hyaluronan-insulin complex, has been developed and oral activity has been demonstrated.
引用
收藏
页码:2040 / 2047
页数:8
相关论文
共 25 条
  • [1] Cryo transmission electron microscopy of liposomes and related structures
    Almgren, M
    Edwards, K
    Karlsson, G
    [J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2000, 174 (1-2) : 3 - 21
  • [2] ATTWOOD D., 2002, PHARM SCI DOSAGE FOR, V2nd, DOI 10.1360/zd-2013-43-6-1064
  • [3] STRUCTURE OF INSULIN IN 4-ZINC INSULIN
    BENTLEY, G
    DODSON, E
    DODSON, G
    HODGKIN, D
    MERCOLA, D
    [J]. NATURE, 1976, 261 (5556) : 166 - 168
  • [4] BERGKVIST M, 2002, ORIENTATION CONFORMA, P62
  • [5] Berne R., 1976, DYNAMIC LIGHT SCATTE
  • [6] Brange J, 1987, GALENICS INSULIN PHY
  • [7] Exploiting M cells for drug and vaccine delivery
    Clark, MA
    Jepson, MA
    Hirst, BH
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2001, 50 (1-2) : 81 - 106
  • [8] PHYSIOLOGICAL FUNCTION OF CONNECTIVE-TISSUE POLYSACCHARIDES
    COMPER, WD
    LAURENT, TC
    [J]. PHYSIOLOGICAL REVIEWS, 1978, 58 (01) : 255 - 315
  • [9] PHENOL STABILIZES MORE HELIX IN A NEW SYMMETRICAL ZINC INSULIN HEXAMER
    DEREWENDA, U
    DEREWENDA, Z
    DODSON, EJ
    DODSON, GG
    REYNOLDS, CD
    SMITH, GD
    SPARKS, C
    SWENSON, D
    [J]. NATURE, 1989, 338 (6216) : 594 - 596
  • [10] DIRECT MEASUREMENT OF MOLECULAR ATTRACTION BETWEEN SOLIDS SEPARATED BY A NARROW GAP
    DERJAGUIN, BV
    [J]. QUARTERLY REVIEWS, 1956, 10 (03): : 295 - &