Use of inorganic aerogels in pharmacy

Details Use of inorganic aerogels in pharmacy Use of inorganic aerogels in pharmacy

1997-09-22

2001-08-28

Azpuru, Carlos A. (Department: 2165)

Drug, bio-affecting and body treating compositions

Preparations characterized by special physical form

C424S421000, C424S422000, C424S691000, C424S724000

Reexamination Certificate

active

06280744

ABSTRACT:

The invention relates to the use of inorganic aerogels as an auxiliary and/or excipient for pharmaceutical active compounds and/or preparations.
Aerogels, in particular those having porosities of over 60% and densities of under 0.6 g/cm
3
, have an extremely low thermal conductivity and are therefore used as a heat-insulating material as described, for example, in EP-A-0 171 722. Moreover, the use of aerogels for Cerenkov detectors on the basis of their refractive index, which is very low for solids, is known. Furthermore, on account of the particular acoustic impedance of the aerogels a possible use as matching impedance means, for example in the ultrasonic field, is described in the literature.
Aerogels in the wider sense, i.e. in the sense of “gel with air as a dispersant”, are prepared by drying a suitable gel. The term “aerogel” in this sense includes aerogels in the narrower sense, xerogels and cryogels. A dried gel is designated as an aerogel in the narrower sense here if the liquid of the gel is removed to the greatest possible extent at temperatures above the critical temperature and starting from pressures above the critical pressure. If the liquid of the gel, however, is removed subcritically, for example with formation of a liquid/vapor boundary phase, then the resulting gel is designated as a xerogel.
When using the term aerogels in the present application, we are dealing with aerogels in the wider sense, i.e. in the sense of “gel with air as a dispersant”.
Moreover, the aerogels can be basically subdivided into inorganic and organic aerogels.
Inorganic aerogels have been known since 1931 (S. S. Kistler, Nature 1931, 127, 741). Since then, aerogels have been prepared from all sorts of starting materials. It was possible here to prepare, for example, SiO
2
, Al
2
O
3
, TiO
2
, ZrO
2
, SnO
2
, Li
2
O, CeO
2
and V
2
O
5
aerogels, and mixtures of these (H. D. Gesser, P. C. Goswami, Chem. Rev. 1989, 89, 756 ff). For some years, organic aerogels made of all sorts of starting materials, such as, for example, from melamine formaldehyde, have also been known (R. W. Pekala, J. Mater, Sci. 1989, 24, 3221).
Inorganic aerogels can be prepared here in all sorts of different ways.
For example SiO
2
aerogels can be prepared by acidic hydrolysis and condensation of tetraethyl orthosilicate in ethanol. In this process a gel results which can be dried with retention of the structure by supercritical drying. Preparation processes based on this drying technique are known, for example, from EP-A-0 396 076 or WO 92/03378.
An alternative is offered by a process for the subcritical drying of SiO
2
gels if these are reacted with a chlorine-containing silylating agent before drying. The SiO
2
gel can be obtained here, for example, by acidic hydrolysis of tetralkoxysilanes in a suitable organic solvent by means of water. After replacement of the solvent by a suitable organic solvent, the gel obtained is reacted in a further step with a silylating agent. The SiO
2
gel resulting here can then be dried in the air from an organic solvent. Aerogels with densities of under 0.4 g/cm
3
and porosities of over 60% can thus be achieved.
The preparation process based on this drying technique is described in detail in WO 94/25149.
The gels described above can moreover be treated with tetraalkoxysilanes and aged before drying in the alcoholic-aqueous solution in order to increase the gel network strength, e.g. as disclosed in WO 92/20623.
Furthermore, the SiO
2
gel can also be prepared on the basis of waterglass. The preparation process based on this technique is known from DE-A-43 42 548.
German patent application 19502453.2 moreover describes the use of chlorine-free silylating agents.
The aerogels obtained by supercritical drying are, depending on the process specifically used, hydrophilic or, in the short term, hydrophobic. In the long-term, however, they are hydrophilic.
This can be avoided by a hydrophobization step during the supercritical drying. Such a process is known from EP-A-0 396 076.
Due to their preparation process (silylation before drying), subcritically dried aerogels are permanently hydrophobic.
The use of colloidal silica in therapeutic copper compositions is known, for example, from U.S. Pat. No. 4,123,511.
The use of organic aerogels in medicine is likewise known (WO 95/01165).
It was an object of the present invention to search for novel applications for aerogels.
It has now surprisingly been found that inorganic aerogels are suitable as an auxiliary and/or excipient for pharmaceutical active compounds and/or preparations.
An inorganic aerogel is to be understood in the present application as meaning an aerogel which was prepared based on inorganic materials.
The term “aerogels based on inorganic materials” in particular also includes those aerogels which have been modified, for example, by silylation.
Aerogels mainly comprising SiO
2
, Al
2
O
3
, TiO
2
, ZrO
2
or mixtures thereof are preferred. Depending on use, these can have hydrophilic and/or hydrophobic surface groups (e.g. OH, OR, R). The preparation of aerogels having hydrophilic and/or hydrophobic surface groups can be carried out here by all processes known to the person skilled in the art. Hydrophilic or hydrophobic SiO
2
-containing aerogels, in particular SiO
2
aerogels, are particularly preferred.
Moreover, it has surprisingly been found that by the choice of a suitable hydrophilic or hydrophobic aerogel appropriate substances with which the aerogel has been loaded can be released in accelerated or delayed form. Furthermore, aerogels can be employed as dispersants for dispersions of solid, liquid or gaseous substances in solid or liquid media. Moreover, hydrophilic or hydrophobic aerogels loaded with hydrophilic and/or hydrophobic substances can be incorporated without problems in hydrophilic and/or hydrophobic, liquid, semisolid or solid media, in particular in order, with the aid of hydrophilic aerogels, to introduce hydrophobic (i.e. lipophilic) substances into liquid and/or semisolid hydrophilic dispersion media, and with the aid of hydrophobic aerogels to introduce hydrophilic substances into liquid, hydrophobic dispersion media. Hydrophobic aerogels, for example, float on hydrophilic, aqueous media, by means of which pharmaceutical excipient systems which float on gastric juice are possible. Furthermore, it is also possible to convert liquid, hydrophilic or hydrophobic substances into solid, freely flowable powders or granules. Problem-free processing, for example to give tablets, capsules or suppositories, is thus possible. Furthermore, with appropriate aerogels the preparation of lotions, creams and gels with and without a peeling effect is also possible. Substances within the meaning of these applications are substances which can be used in pharmacy, e.g. pharmaceuticals, aromatic substances and flavorings.
The invention is described in greater detail in the following with the aid of working examples, without being restricted thereby.


REFERENCES:
patent: 4123511 (1978-10-01), Heintze
patent: 4185088 (1980-01-01), Wagener
patent: 4411885 (1983-10-01), Barels
patent: 4859709 (1989-08-01), Rawlins
patent: 4954327 (1990-09-01), Blount
patent: 5409902 (1995-04-01), Carson et al.
patent: 5670138 (1997-09-01), Venema et al.
patent: 5830480 (1998-11-01), Ducheyne et al.
patent: 1302895 (1992-06-01), None
patent: 26 52 163 (1978-01-01), None
patent: 0163178 (1985-12-01), None
patent: 0255000 (1988-02-01), None
patent: 1572718 (1980-07-01), None
patent: WO 95/01165 (1995-01-01), None
Database WPI, AN 94-089171; 1994.

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