Title:  Adhesive drug delivery composition

United States Patent:  6,355,276

Assignee:  West Pharmacuetical Services Drug Delivery & Clinical (Nottingham, GB)

Filed:  April 28, 1994

Foreign Application Priority Data:  Nov 08, 1988[GB] (8826116);  Nov 03, 1989[WO] (PCT/GB89/01317).

Adhesive material from the fimbriae (esp. Type 1) of bacteria or synthetic analogues or fragments thereof is combined with a drug to provide for attachment to the gut of a mammal, thereby prolonging the transit time of the drug through the gut. The 28 kDa polypeptide from E. coli Type 1 fimbriae is the preferred adhesive material ("adhesin"). The drug is presented in a carrier such as albumin, a polylactide/glycolide copolymer or alginate microcapsules. The adhesin may be incorporated in the carrier during preparation thereof, adsorbed onto the carrier after preparation, or covalently linked thereto, for example with carbodiimide.

Description of the Invention

The present invention relates to a drug delivery composition and more particularly to a drug delivery composition for administration via the gastrointestinal tract.

The gastrointestinal (G.I.) tract is one of the major routes for the administration of pharmacological agents. Drugs are normally well absorbed from the intestines, and dosage forms such as capsules, tablets and suspensions are well accepted by the general population. In recent years there has been a tendency towards the development of controlled release dosage forms that will provide therapy over an extended period of time. Normally this would be once a day and it is believed that such a change in dosage regimen will reduce adverse reactions and side effects and also improve patient compliance.

The design and evaluation of controlled release dosage forms must, however, take into account the properties of the gastrointestinal tract, including the rapid transit of material through the small intestine, which is the important site for absorption for certain drugs. Recent work by Davis and others at Nottingham University has shown that this transit time can be of the order of 3 hours or less. Thus the disadvantage of very long release times, for example 24 hours, is that the drug could have passed through the small intestine before being released and therefore its curative property could be effectively nullified.

A considerable advantage can be gained if the dosage form is held in the small intestine so that it will be well absorbed into the systemic circulation over a long period of time.

Recently, work has been done into investigating the use of synthetic polymers that may have muco- or bio-adhesive properties, for example those disclosed in WO 85/02092, such as cross-linked acrylic acid and methacrylic acid polymers. The problem with the use of synthetic polymers lies in the mode of action of such materials and in particular whether it is intended to attach dosage forms to the mucus, which should easily slough off, or to attach dosage forms to the glycocalyx or directly to the cell surface of the enterocyte. Various in vitro tests conducted with excised portions of stomach and oesophagus are not considered to be realistic in terms of in vivo environmental conditions and transit phenomena.

It is an object of preferred aspects of the present invention to provide a drug delivery system for use in the gastrointestinal tract which obviates the above disadvantages and maintains the drug in the G.I. tract, for example in the small intestine, for a prolonged period thereby allowing the drug to be released at a desired rate over this prolonged period. By extending the period, the drug can if required be released more slowly, which may lead to less severe adverse reactions and side effects.

The present invention therefore provides a drug delivery system, preferably including a plurality of particles containing active drug material, each of the particles preferably having a size of 20 microns of less, and incorporating on the outer surface of at least some of the particles a bioadhesive material derived from a bacterium such that in use the bioadhesive material will adhere to the small intestine of the gut.

The term "drug" is used herein to include any pharmacologically active compound or antigen-comprising material.

The term "bioadhesive" is used to denote a material which adheres to the gut wall. The bioadhesive derived from a bacterium may be isolated therefrom or may be a synthetically prepared version thereof, or an analogue or fragment of such material.

Such bioadhesive materials have been previously proposed for use in medicine in WO 88/07078, but only as immobilising materials for binding biological material to a carrier, for example binding a blood clotting agent to a carrier substance. There was no suggestion that the bioadhesives could be used to direct medicaments to the gut wall.

The micro-organisms from which the adhesive material is derived or to which it corresponds will generally be those found in the G.I. tract, especially the (small) intestine, of the mammal being treated. Such micro-organisms include E. coli, Klebsiella spp. and Salmonella spp.

Preferably, the bioadhesive material is obtained from Escherichia coli, especially a human G.I. tract infesting strain thereof, or corresponds to such material.

In the small intestine certain bacterial flora are found to adhere extremely well. Escherichia coli, for example, adheres via surface proteins called fimbriae (pili). E. coli strains express the following fimbrial types:

(a) Type 1 or `common` fimbriae whose adhesive properties are inhibited by mannose (mannose-sensitive fimbriae).

(b) P fimbriae (mannose-resistant).

(c) Colonisation factor antigens (CFAI and CFAII) which are mannose-resistant.

The present invention is concerned particularly with class (a). These materials, when purified, can be identified by the ability to haemagglutinate guinea-pig erythrocytes in the absence but not in the presence of .alpha.-methylmannoside. In the case of Type 1 fimbriae from E. coli, the presence of a 17 kDa sub-unit protein may be detected on sodium dodecyl sulphate polyacrylamide gel electrophoresis after denaturation of fimbriae by saturated guanidine HCl. In other organisms, such as Klebsiella spp. the corresponding sub-unit may be slightly larger or smaller. Finally, Type 1 fimbriae material from a given organism would be expected to react in Dot and Western Immunoblots with a polyclonal antiserum raised against the Type 1 fimbriae from the same organism. The various test methods for all three of these tests are standard.

Type 1 fimbrial material from E. coli has previously been isolated and shown to comprise polypeptides of molecular weights of about 14 kDa, 17 kDa and 28 kDa. See, for example, Hanson & Brinton, Nature 332, 265 (1988) and Hanson et al, J. Bact. 170(8), 3350 (1988). The 28 kDa polypeptide described therein is probably the same as the 29 kDa FimH polypeptide described by Abraham et al, (1988) Infect. & Immun. 56(5), 1023-1029. This latter paper suggests using FimH in a vaccine to confer immunity against E. coli binding, but does not suggest using FimH to bind a drug or antigen to the gut wall. The 17 kDa polypeptide is the major polypeptide. Since micro-organisms can adhere firmly in the gastrointestinal tract through this adhesion process (which may be through an interaction between the adhesive molecule ("adhesin") and sugar residues, eg mannosides, in the gastrointestinal tract) it is possible in accordance with the present invention to achieve similar adhesive effects by the isolation and purification of an individual adhesin polypeptide. When administered to rabbits the adhesin is seen to adhere to the gastrointestinal tract.

Alternatively, the larger bodies known as "fimbriosomes" may be used. These bodies are described in Abraham et al, Infect. & Immun. 56(5), 1023, (1988).

In the present invention adhesins and similar bioadhesive materials produced from micro-organisms are used to design and develop controlled release dosage forms with extended gastrointestinal residence. The delivery system preferably consists of small particles (a few microns in size) so that the adhesive is able to attach the particle to the wall of the gastrointestinal tract through sugar residue, lectin-mediated processes. The adhesins may be coated onto particles or covalently bound (grafted) onto the surface of the particle. A preferred adhesin is the bacterial adhesin obtained from E. coli, but there are many other adhesin-producing bacteria available, for example Pseudomonas aeruginosa.

It is also apparent that the adhesive characteristics of the fimbrial material do not necessarily reside in the complete fimbrial structure and that a suitably cleaved product or its synthetic equivalent comprising the correct sequence of amino acids demonstrates similar bioadhesive properties. The preparation of a peptide of this sort is described in Abraham & Beachey, J. Bact. 169(6), 2460, (1987). More specifically, the peptide consisted of residues 23-35 of E. coli Type 1 fimbrial protein namely VDAGTVDQTVQLGC (i.e. Val-Asp-Ala-Gly-Thr-Val-Asp-Gln-Thr-Val-Gln-Lys-Gly-Cys). Such a peptide may be made by conventional techniques.

Likewise, synthetic polymers with a similar structure to that of the adhesin will generally have the same effect in enhancing the interaction between the wall of the small intestine and administered colloidal particles. Purified adhesin materials or synthetic analogues may be used as macromolecular carriers where the drug is attached to the adhesin molecule directly and not necessarily within a microparticle.

The attachment of fimbriae to the surface of drug-containing particles may be by adsorption (hydrophobic region of peptide to hydrophobic surface of a suitable particle, for example polymeric microsphere, polystyrene, polymethylmethacrylate, polyalkylcyanoacry late, emulsion (triglyceride)), or by covalent attachment. Mechanisms for linking proteins to microspheres are given in Illum & Jones, Methods in Enzymology 112, 67-84 (1985).

Other ways of attaching the protein include modification of a particle surface by adsorption or covalent attachment of suitable linking groups to which the protein may be subsequently attached. Examples here include albumin, gelatin, dextran, alginate, polylactide/glycolide, polyhydroxy-butyrate, polyanhydride microspheres and liposomes.

Dry formulations are to be preferred but suspensions in a suitable vehicle (for example, polyethylene glycol or triglyceride oil) may also be used. An actual drug formulation preferably involves the preparation of a multiparticulate drug containing system (size preferably below 1 mm) such as a microsphere or microcapsule. Drug entrapment may be performed during preparation (e.g. emulsification, polymerisation) or after (remote loading).

The fimbrial material may be included in the particle preparation step (if it can be attached to the particle surface; proteins are good stabilizers of emulsions) or grafted onto the surface during a polymerization stage. Alternatively, the material may be attached by adsorption or covalent linkage after the particles have been prepared.

The concept is readily applicable to many, if not all, drugs given orally, including cephalosporins, chlorthiazide, isosorbide and frusemide (which are absorbed in the (upper) regions of the small intestines) and peptides which are intended for absorption in the colon, for example insulin, growth hormone, calcitonin, interferon and tumour necrosis factor.

Claim 1 of 17 Claims

What is claimed is:

1. A drug delivery composition for sustained release of a drug in the gastrointestinal tract comprising:

polymeric particles having a size of 20 microns or less, having incorporated therein

at least one drug, and

having bound to the outer surface of the particles a natural bioadhesive material present in a bacterium which adheres to the gut wall,

in combination with a carrier for administration to the gastrointestinal tract,

wherein the particles are bound to the gut surface by the bioadhesive material and result in sustained release of the drug to the gastrointestinal tract of said mammal.

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