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Title:
【発明の名称】微粒子に適した経口配布系
Document Type and Number:
Japanese Patent JP3296817
Kind Code:
B2
Abstract:
PCT No. PCT/AU92/00141 Sec. 371 Date Nov. 30, 1992 Sec. 102(e) Date Nov. 30, 1992 PCT Filed Apr. 2, 1992 PCT Pub. No. WO92/17167 PCT Pub. Date Oct. 15, 1992There are disclosed complexes and compositions for oral delivery of a substance or substances to the circulation or lymphatic drainage system of a host. The complexes of the invention comprise a microparticle coupled to at least one carrier, the carrier being capable of enabling the complex to be transported to the circulation or lymphatic drainage system via the mucosal epithelium of the host, and the microparticle entrapping or encapsulating, or being capable of entrapping or encapsulating, the substance(s). Examples of suitable carriers are mucosal binding proteins, bacterial adhesins, viral adhesins, toxin binding subunits, lectins, Vitamin B12 and analogues or derivatives of Vitamin B12 possessing binding activity to Castle's intrinsic factor.

Inventors:
Russell-Jones, Gregory John
Westwood, Stephen William
Application Number:
JP50746492A
Publication Date:
July 02, 2002
Filing Date:
April 02, 1992
Export Citation:
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Assignee:
Biotech Australia Pty Limited
International Classes:
A61K9/16; A61K9/50; A61K9/51; A61K9/52; A61K47/24; A61K47/42; A61K47/46; A61K47/48; (IPC1-7): A61K9/50
Other References:
【文献】国際公開91/289(WO,A1)
【文献】国際公開90/4963(WO,A1)
Attorney, Agent or Firm:
Tadashi Hagino (1 person outside)