U.S. patent number 5,300,564 [Application Number 07/637,873] was granted by the patent office on 1994-04-05 for doped sol-gel glasses for obtaining chemical interactions.
This patent grant is currently assigned to YISSUM, Research Development Company of the Hebrew University of. Invention is credited to David Avnir, Sergei Braun, Michael Ottolenghi, Rivka Zusman.
United States Patent |
5,300,564 |
Avnir , et al. |
April 5, 1994 |
**Please see images for:
( Certificate of Correction ) ( Reexamination Certificate
) ** |
Doped sol-gel glasses for obtaining chemical interactions
Abstract
A method is proposed of obtaining a chemical interaction between
at least one reagent trapped in sol-gel glass by doping it with the
reagent, and diffusible solutes or components in an adjacent liquid
or gas phase. The reagents, the solutes or the components can be
any organic or inorganic compounds or materials of biological
origin including enzymes. The doped sol-gel glass in various forms
may be useful as analytical test, chromatographic medium, sensor,
catalyst or biocatalyst, electrode or enzyme electrode, or other
detection device.
Inventors: |
Avnir; David (Jerusalem,
IL), Ottolenghi; Michael (Jerusalem, IL),
Braun; Sergei (Jerusalem, IL), Zusman; Rivka
(Jerusalem, IL) |
Assignee: |
YISSUM, Research Development
Company of the Hebrew University of (Jerusalem,
IL)
|
Family
ID: |
11060831 |
Appl.
No.: |
07/637,873 |
Filed: |
January 8, 1991 |
Foreign Application Priority Data
Current U.S.
Class: |
525/54.1;
435/175; 501/12; 436/183; 436/8; 435/174; 435/176; 501/32;
422/400 |
Current CPC
Class: |
B01J
20/283 (20130101); C12N 11/14 (20130101); G01N
33/552 (20130101); C12P 1/00 (20130101); G01N
33/5436 (20130101); B01J 20/291 (20130101); G01N
33/84 (20130101); G01N 31/22 (20130101); G01N
33/6869 (20130101); C03C 4/0007 (20130101); Y10T
428/2989 (20150115); Y02P 20/588 (20151101); B01J
2220/54 (20130101); Y10T 436/10 (20150115); Y10S
530/811 (20130101); Y10S 514/965 (20130101); Y02P
20/50 (20151101); G01N 30/92 (20130101); G01N
30/02 (20130101); G01N 2030/484 (20130101); Y10S
514/944 (20130101); G01N 30/02 (20130101); B01D
15/422 (20130101) |
Current International
Class: |
C03C
4/00 (20060101); C03C 4/00 (20060101); C12P
1/00 (20060101); C12P 1/00 (20060101); B01J
20/281 (20060101); B01J 20/281 (20060101); B01J
20/283 (20060101); B01J 20/283 (20060101); B01J
20/291 (20060101); B01J 20/291 (20060101); G01N
33/84 (20060101); G01N 33/84 (20060101); G01N
33/543 (20060101); G01N 33/543 (20060101); C12N
11/14 (20060101); C12N 11/14 (20060101); C12N
11/00 (20060101); C12N 11/00 (20060101); G01N
31/22 (20060101); G01N 31/22 (20060101); G01N
33/551 (20060101); G01N 33/551 (20060101); G01N
33/68 (20060101); G01N 33/68 (20060101); G01N
33/552 (20060101); G01N 33/552 (20060101); G01N
30/92 (20060101); G01N 30/92 (20060101); G01N
30/00 (20060101); G01N 30/00 (20060101); G01N
30/02 (20060101); G01N 30/02 (20060101); C86 ();
B01D 053/00 (); G01N 021/00 (); G01N 033/00 () |
Field of
Search: |
;525/54.1 ;514/2,21
;530/402,403,405,408,409,811 ;435/174,175,176 ;501/12,32 ;55/386
;436/8,183 ;422/55,56,57 |
References Cited
[Referenced By]
U.S. Patent Documents
Other References
"Water Consumption During the Early Stages of the Sol-Gel
Tetramethylorthosilicate Polymerization As Probed by Excited State
Proton Transfer", Journal of Non-Crystalline Solids, 99 (1988),
379-386. .
"Structural Changes Along the Sol-Gel-Xerogel Transition in Silica
As Probed by Pyrene Excited-State Emission", Langmuir 1986, 2,
717-722. .
"The Nature of the Silica Cage As Reflected by Spectral Changes and
Enhanced Photostability of Trapped Rhodamine 6G", J. Phys. Chem.
1984, 88, 5956-5959. .
"Production of L-Aspartic Acid By Microbial Cells Entrapped in
Polyacrylamide Gels", Methods of Enzymology 44 (XLIV) (1976)
739-746. .
"Inorganic Gels for Immobilization of Biocatalysts: Inclusion of
Invertase-active Whole Cells of Yeast . . . ", Journal of Molecular
Catalysis, 57 (1989) L13-L16..
|
Primary Examiner: Nutter; Nathan M.
Attorney, Agent or Firm: Lowe, Price, LeBlanc &
Becker
Claims
We claim:
1. A method for obtaining an interaction between a reagent and a
component, comprising (a) trapping a reagent in an inorganic
sol-gel porous glass formed by polymerization of at least one metal
alkoxide, semi-metal alkoxide, metal ester or semi-metal ester, the
reagent being trapped in the sol-gel glass by conducting the
polymerization in the presence of the reagent, the reagent being
reactive after preparation of the sol-gel glass, and the sol-gel
glass providing a solid support for the reagent, the polymerization
including a gelling step conducted at not greater than room
temperature and a drying step conducted at not greater than
45.degree. C.; and (b) interacting the reagent trapped in the
sol-gel glass with a component which is in a liquid or gas phase in
pores of the sol-gel glass and which is reactive with the reagent
in the pores of the sol-gel glass.
2. A method according to claim 1, wherein the reagent is selected
from the group consisting of organic compounds, stable organic
radicals, organometallic compounds, and a material of biological
origin.
3. A method according to claim 1, wherein the component is selected
from the group consisting of organic compounds, stable organic
radicals, organometallic compounds, and a material of biological
origin.
4. A method according to claim 1, wherein the reagent is a pH
indicator.
5. A method according to claim 1, wherein the component is a
compound containing an ion selected from the group consisting of
Fe.sup.2+, Al.sup.3+, Co.sup.2+, Ni.sup.2+, and Cu.sup.2+.
6. A method according to claim 1, wherein the sol-gel glass is in
the shape of a rod, a sieve or a thin film.
7. A method according to claim 1, wherein the component is selected
from the group consisting of chlorides, nitrates, sulfates,
phosphate, herbicides, insecticides, inorganic ions and organic
pollutants.
8. A method according to claim 1, wherein the component is at least
one enzyme in a liquid phase, and the reagent is selected from the
group consisting of immunoglobulins and antigens.
9. A method according to claim 1, wherein the reagent is an enzyme
and the component is selected from the group consisting of
immunoglobulins and antigens.
10. A method according to claim 8, wherein the enzyme is of
microbial, animal or plant origin.
11. A method according to claim 9, wherein the enzyme is of
microbial, animal or plant origin.
12. A method according to claim 8, wherein the enzyme is a
hydrolase.
13. A method according to claim 9, wherein the enzyme is a
hydrolase.
14. A method according to claim 12, wherein the hydrolase is
selected from the group consisting of trypsin, alkaline
phosphatase, acid phosphatase, chitinase, lipase, lactase,
aminoacylase, penicillin and cephalosporin acylase.
15. A method according to claim 13, wherein the hydrolase is
selected from the group consisting of trypsin, alkaline
phosphatase, acid phosphatase, chitinase, lipase, lactase,
aminoacylase, penicillin and cephalosporin acylase.
16. A method according to claim 8, wherein the enzyme is a
lyase.
17. A method according to claim 9, wherein the enzyme is a
lyase.
18. A method according to claim 15, wherein the lyase is
aspartase.
19. A method according to claim 16, wherein the lyase is
aspartase.
20. A method according to claim 8, wherein the enzyme is an
oxidoreductase.
21. A method according to claim 9, wherein the enzyme is an
oxidoreductase.
22. A method according to claim 20, wherein the enzyme is selected
from the group consisting of peroxidase and glucose oxidase.
23. A method according to claim 21, wherein the enzyme is selected
from the group consisting of peroxidase and glucose oxidase.
24. A method according to claim 1, wherein the reagent is an
antibody and the component is an antigen of the antibody.
25. A method according to claim 1, wherein the component is an
antibody and the reagent is an antigen of the antibody.
26. A method according to claim 1, wherein the component is a
compound containing a metal ion.
Description
The present invention relates to a method for obtaining an
interaction between at least one reagent in a solid support and
diffusible solutes or components in an adjacent liquid or gas
phase, wherein the reagent's are trapped in sol-gel glass
(hereinafter also referred to as doped sol-gel glass) which
provides the solid support to the reagent.
The method according to the present invention can be applied to a
variety of interactions between the doped sol gel glasses and
reagent in an adjacent liquid or gas phase. The present invention
can be useful in a myriad of applications for quantitative or
qualitative analyses, for extraction or separation of solutes from
liquid solutions, and for many other applications. For example, the
above method can be useful for detection of ions by chemical
interaction between the ions in an aqueous phase and reagents
trapped in the "sol-gel" glass, or vice versa, via characteristic
"color test" reactions, or other routine detection methods. Another
example is utilization of the above method for qualitative or
quantitative analyses of pollutants.
The method can be applied as well for medical diagnostic purposes
e.g. for detecting inorganic ions or small organic molecules in
blood, urine and other body liquids. Another example, according to
the present invention, .is a chemical interaction between a
substrate or antigen in the liquid phase and an enzyme or antibody
trapped in the "sol-gel" glass.
For centuries, inorganic glasses have been prepared by high
temperature melting methods. This has imposed a major limitation
upon the technological application of glasses: additives were
restricted to thermally stable inorganic materials, while
precluding the incorporation of labile organic molecules.
A recent major development in material science has been the
preparation of inorganic (silica) glasses through the low
temperature "sol-gel" synthesis as disclosed by (Brinker, C. J.,
Scherer, G. W., Sol-Gel Science, Academic Press, San Diego (1990).
An amorphous bond network of the glassy material is prepared by the
room-temperature polymerization of suitable monomers, usually metal
alkoxides, according to schemes such as:
in which water is consumed by
and released by
By sol-gel glass one also means the product obtained by a
polymerization of metal alkoxide mixtures which bear both
hydrolyzable and nonhydrolyzable substituents. The monomers may
also comprise metal esters, semi-metal esters, or semi-metal
alkoxides, with preferred metals or semi-metals comprising Si, Al,
Ti or Pb.
The result of the polymerization is a transparent porous solid
(xerogel) with surface areas of up to hundreds of square meters per
gram of product and having narrow pores (0.5-500 nm).
The low-temperature glass synthesis allows doping of inorganic
(silica or other) glasses, with essentially any organic molecule.
This possibility was used for trapping of photoactive molecules by
adding the compound to the starting mixture at the onset of
polymerization (Avnir, D., Levy D., Reisfeld, R., J. Phys. Chem.
88, 5956 (1984)). The compound remained permanently trapped, i.e.
non-leachable system have been obtained. These doped sol-gel
glasses have been used as photoactive materials, such as:
(a) Dye laser materials;
(b) Thin-film optical filters;
(c) Fluorescent solar collectors;
(d) Photochromic and phosphorescent glasses.
The interaction between the optical properties of trapped molecules
and their environment was employed for monitoring the progress of
the glass formation sequence:
monomer.fwdarw.oligomer.fwdarw.sol.fwdarw.gel.fwdarw.xerogel. This
allowed to study of the evolution of such parameters as porosity,
water content and degree of (cage) polarity (Kaufman, V. R., Avnir,
D., Structural changes Along the Sol-Gel-Xerogel Transitions,
Langmuir 2, 717 (1986); Kaufman, V. R., Avnir, D., Pines-Rojanski,
D., Huppert, D., Water Consumption During the Early Stages of the
Sol-Gel Polymerization, J. Non-Cryst. Solids 99, 379 (1988)).
Sol-gel glasses demonstrate several technologically attractive
properties:
(a) the ability to isolate a single doping molecule in an
individual cage, even at high concentrations of additive, thus
avoiding interfering side photophysical processes and interactions
with impurities or photodecomposition products;
(b) thermal and photochemical stability as well as transparency in
the U.V. range above 250 nm; and
(c) lack of leaching of the trapped compound, simplicity of
preparation, and easy technological manipulation allowing
production in any desired geometry, including films.
Surprisingly, it was found that molecules trapped in sol gel
glasses, may interact with diffusible solutes or components in an
adjacent liquid or gas phase in the pore space. This finding opened
a new wide range of applications of doped sol-gel glasses as solid
media for chemical interactions.
The present invention relates to a method for obtaining an
interaction between one or more reagents in a solid support and at
least diffusible solute or component in an adjacent liquid or gas
phase, wherein the reagent is trapped in the sol-gel glass which
serves as the solid support. Said reagent can be any organic
organometallic, or inorganic compound, or any biological material
capable of being trapped in the sol-gel glass.
The diffusible solute or components can be any organic compound,
stable organic radical, organometallic compound, or inorganic
compound or biological material capable to interact with the
trapped reagents.
The interaction between the reagent in the solid support and the
diffusible solute in the liquid phase or a component in the gas
phase can be a chemical interaction such as for analytical tests or
chemical reactions. The method according to the present invention
can be a specific color test reaction, N.M.R. or E.S.R. analysis,
analysis via emission or absorption, luminescence, fluorescence,
phosphorescence tests or electrochemical tests. The analytical
reagent can be a pH indicator, redox reagents or an ion complexant
or the like.
The chemical interaction according to the present invention can
take place between anions or cations in a liquid or gas phase and
reagent trapped in the sol gel glass or vice versa. For example the
interaction may take place between metal ions and a specific
reagents via a characteristic colour-test reaction, as in: (1) the
determination of Fe.sup.+2 cation with o-phenanthrolin, (2) the
determination of Co.sup.+2 with 1-nitroso-2-naphtol, (3) the
determination of Ni.sup.+2 wherein the reagent is dimethylglyoxime,
(4) the determination of SO.sub.4.sup.-2 anion wherein the reagent
is sodium rhodizonate and BaF.sub.2, or benzoinoxime, (5) the
detection of H.sup.+ is one of many examples for a pH sensors. The
analytical test can be carried out by dipping the doped sol gel
glass in the solution and observing the resulting color change.
The above method can be useful for the analysis of ore contents in
soil, sea water, and rocks (e.g. uranium).
The sol gel glass according to the present invention can be in any
shape suitable for the test. For example it can have the shape of
rods, discs, cubes, sieves, powder, or thin films coating
conventional glass plates or any other inert solid support. Thus,
an electrochemical test according to the invention can be performed
by preparing electrodes coated with doped sol gel glass layers.
These electrodes may be used for clinical, analytical or industrial
purpose, or as biosensors.
It should be emphasized that the method according to the invention
can be useful for qualitative and for quantitative analysis.
The method according to the present invention can be applied to
detection and analysis of pollutants in soil, in aquatic
environments and characteristic water sources (including waste,
industrial and municipal sources, lakes and swimming pools) in
food, drugs, or in the air. The method may be applied to
qualitative or quantitative analysis of pollutants. The pollutants
may be for example chlorides, nitrates, phosphates, herbicides,
insecticides, inorganic ions and pollutants of organic origin.
Detection devices according to this invention can be utilized as a
part of continuous monitoring systems.
The present invention can be utilized for extracting or separating
molecular solutes from liquid solutions. The doped sol gel glasses
can be used according to the present invention for all
chromatographic purposes, including liquid, gas and thin layer
chromatography. The extraction or separation is performed by
passing the solution through columns made from appropriately doped
sol gel material. The thin layer chromatography according to this
invention can be performed on conventional glass plates, paper or
other inert solid support coated with doped sol-gel glass
layers.
Medical diagnostics is another application of the present
invention. For example, detection of inorganic ions, small organic
molecules and other components in blood, urine and other body
liquids can be made. The invention can be applied also to the
fractionation of body fluids.
The present invention relates, as well, to a method for preparation
of bioactive materials (biocatalysts) by entrapment of enzymes in
forming sol-gel glass, which, following polycondensation of
suitable monomers, serves as a solid matrix, bonding the enzyme and
conveying to it mechanical, chemical and thermal stabilities.
The method, according to the present invention, can be applied to a
variety Of enzymes or enzyme systems, including co-immobilization
of co-factors, organic and inorganic ligands, mono- and polyclonal
antibodies, and their detection systems.
The method according to the present invention can be useful in a
variety of applications, such as: (a) biochemical reactions and
other bioconversions in organic and inorganic solvent solutions,
(b) detection or qualitative determination of organic and inorganic
molecules, which are substrates of the immobilized enzymes, or
inhibitors, or modifiers of enzyme activity, (c) construction of
bioelectronic detection devices, including construction of enzymes
electrodes and biosensors.
Commercial applications of enzymes require successful
immobilization. Immobilization allows reuse of an enzyme, protects
it from harsh external conditions, from microbial contamination,
and prolongs its useful lifetime. There are probably as many
immobilization methods as there are enzymes. This proliferation of
techniques reflects the complexity of the biological material and
the variety of its uses. Simple inexpensive general techniques,
resulting in stable and active enzyme catalyst are still in great
demand (Kennedy, J. F. and White, C. A. in "Handbook of Enzyme
Biotechnology" (Wiseman, A. ed.), Ellis Horwood Ltd, Chichester,
pp. 147-207 (1985)).
An ideal enzyme catalyst should be bound to a mechanically and
chemically stable, highly porous carrier. The bond linking the
enzyme to the support is required to be stable under the catalyst
application conditions to prevent leaching. The strong binding
forces also have stabilizing effects on enzyme activity (Martinek,
K. and Mozhaev, V. V. Adv. Enzymol. 57, 179, (1985)). The desired
immobilization procedure should be simple, mild (non-denaturing)
and generally applicable.
Enzymes covalently immobilized on controlled-pore glass beads offer
an almost ideal solution to the problems of the support and of the
binding force. However the preparation of catalyst by this
immobilization technique is neither simple nor generally
applicable. The beads are costly, require tedious chemical
derivatization procedures, and lack stability due to the continuous
leaching of silica during prolonged usage (Kennedy, J. F. and
White, C. A. in "Handbook of Enzyme Biotechnology" (Wiseman, A.
ed.), Ellis Horwood Ltd, Chichester, pp. 380-420 (1985)).
The most generally applicable immobilization procedure is a simple
entrapment of the enzyme in a forming gel of natural or synthetic
polymers. The main shortcoming of this technique is the loss of the
enzyme by leakage through a nonuniform net of polymer molecules.
Rather weak interactions between the enzyme and the matrix result
in a relatively nonrestricted diffusional movement of polypeptide
chains. This can be of a benefit, whereas conformational
transitions are required for successful catalysis. Otherwise, this
diffusional freedom of motion can negatively affect immobilized
enzyme stability.
Several properties of the sol-gel glasses make them especially
attractive as possible enzyme catalyst supports: (a) the ability to
entrap large amounts of additives; (b) the thermal and chemical
stability of the matrix; (c) simplicity of preparation with no need
of covalent modification; (d) easy technological manipulation and
production in any desired geometry, including thin films.
Recently, aggregates of whole Yeast cells trapped in thin layers of
SiO.sub.2 gels deposited on glass sheets were demonstrated to
possess invertase activity. Thin films with cell-free invertase
preparation were devoid of activity (Carturan, G., Campostrini, R.,
Dire, S., Scardi V. and de Alteriis, E. J. Mol. Cat., 57, L13,
(1989)).
The present invention relates therefore also to a method for
obtaining bioactive materials based on enzyme molecules trapped
within the porous structure of a sol-gel glass. The entrapment is
achieved by the addition of a cell-free enzyme to a mixture of
monomer or monomers at the onset of polycondensation. In addition
to the enzyme and monomer, the mixture should contain additives
ensuring (1) highly porous nature of the forming glass providing
minimal diffusional limitations to the binding of the substrate at
the catalytic site and to the removal of the product, (2) the
stability of the enzyme during the polymerization and its tight
binding preventing leaching of the enzyme.
Unexpectedly, we have found (1) that proteins can be trapped within
the matrix of a forming sol-gel, (2) that several cell-free
enzymes, belonging to various classes: hydrolases, oxidoreductases,
lyases and the like, can be effectively entrapped in such composite
bioactive sol-gel glasses, while retaining high enzymatic activity,
and (3) that strong binding forces retain the enzyme in the matrix,
thus producing a considerable stabilizing effect.
The sol-gel immobilized enzymes may be used as biosensors for
hormonal tests or for any industrial purposes, including diagnostic
and synthetic purposes. Said enzymes can be doped in sol gel glass
layers coated on electrodes for probing any substrate. The
enzymatic interaction according to the present invention can be
applied also to radioactive tests and also for enzymatic column
chromatography (crushed powder sol gel glasses may be used as
support for enzymatic column chromatography).
The sol gel glass can be applied, according to the present
invention, as active specific membranes allowing selective
incorporation of the trapped molecules or ions or any other
species.
The abovementioned applications are examples only and do not intend
in any way to limit the scope of the invention.
The present invention relates also to the application of doped sol
gel glasses according to this invention as well as for the
preparation of sol gel glasses and doped sol gel glasses for such
applications.
When prepared as a thin film, the width of the sol gel glass may be
from molecular monolayers up to macroscopic layers. The thin film
can be part of a multi-layered array of thin films. The glasses may
be supported on an electrode or optical support.
The unique transparency of "sol gel" glasses in the range above 250
nm, makes them highly applicable to quantitative spectrophotometric
and spectrofluorimetric tests. Trapping of host molecules is
relatively simple and does not require specific synthetic methods
such as those associated with covalent linking of reagents to solid
supports. Moreover, inherent properties of sol gel glasses such as
high surface area, the wide range of available pore sizes and the
thin film technology, make them highly attractive for potential
applications as solid supports for a variety of reagents.
BRIEF DESCRIPTION OF THE DRAWING
The FIGURE drawing shows various sol-gel glasses with a reagent
trapped therein, both before and after reaction with a component in
a liquid phase.
EXAMPLES
A. Preparation of Doped "Sol-Gel" Glasses
The polycondensation of alkoxysilane is associated with gelation of
the sol, which after drying is densified by a mild heat treatment
to form a glass. The properties of the final glass are determined
by the chemical and physical conditions during the process of
preparation. They depend upon the ratio metal (e.g.
silane)/alcohol/water, the alkoxide pH, the presence of a catalyst,
the temperature, the drying time and the amounts of organic
additives, such as surface active agents.
Pore size and surface area are controlled by addition of acid or
base (see Scherer and Brinker, 1990, cited above). Addition of NaF
to the starting tetramethoxysilane (TMOS) solution leads to an
increase in average pore size.
1. A standard mixture for preparation of doped "sol-gel" glasses
contained TMOS (5 ml) H.sub.2 O (2.4 ml) and methanol (6. ml). The
appropriate catalyst and the desired reagent were added in the
required amounts (water or methanol solutions). Gels were formed
within several minutes (base-catalyzed) or several hours
(acid-catalyzed). Gelation was carried out at room temperature in
glass bottles covered with aluminium foil. The gels were then
transferred to an incubator and kept at 37.degree.-45.degree. C.
The samples were used after they reached a constant weight (about
two weeks). The above procedure yields glass in any desired
shape(rods, disks etc.).
2. An alternative technique of preparing sol-gel glasses is based
on thin-layer coating of conventional glass supports. A
characteristic procedure for the preparation of such thin layers
began with a mixture containing methanolic or ethanolic solution of
dopant (85 ml), TMOS (10 ml), Triton X-100 (3 g) and 0.03N HCL or
0.01N NaOH (3 ml). After mixing the solution was allowed to stand
for 30 min at 25.degree.-35.degree. C. and was then used for
coating. Coating was performed by dipping a glass plate into the
solution, followed by drying for several minutes at room
temperature to provide a porous coating layer (0.25-0.5 .mu.m).
B. Representative Examples of Reactivity of Reagents Trapped in
Sol-Gel Glasses
1. Tests were carried out by the immersion for 5 min of an
appropriately doped sol-glass in aqueous solutions containing ions
or molecules to be detected. With reference to FIG. 1, arrows
denote transitions from the reagent-doped glass to the same glass
after immersion in the tested solution. The doped glasses represent
four classes of reactions: (a) a glass-trapped organic reagent with
an inorganic cation to be determined in the solution; (b) same with
inorganic anions; (c) a glass doped with an inorganic ion, testing
a solution containing an organic molecule (reversal of a & b);
(d) glass doped with a pH indicator.
Representative examples of color tests are shown in FIG. 1. Top
(left to right): a) Glass doped with 1,10-phenanthrolin after
immersion in: b) 10.sup.-5 M Fe.sup.2+ solution, c) 10.sup.-4 M
Fe.sup.2+, d) 10.sup.-2 M Fe.sup.2+. Glass was prepared in the
presence of the reagent (0.005%) and 5.times.10.sup.-3 M NaOH as
catalyst in the starting aqueous solution.
Middle: Doped glasses (top) and some glasses after immersion in
solutions containing several ions:
a) Reagent for A1.sup.3+ was quinalyzarin
(1,2,5,8-tetrahydroxyanthraquinone). To the starting solution (see
above) 2 drops of a solution with the following composition were
added: 18 cc methanol containing 0.01 g of the reagent, 2 cc
pyridine and two drops of 0.1N NH.sub.4 OH. b) Reagent for
Co.sup.2+ was nitroso naphthol. Starting solution contained 0.25%
of the reagent and 3 drops of 0.1N HCI as catalyst. c) Reagent for
Ni.sup.2+ was dimethylglyoxime (starting solution, contained 0.25%
of the reagent and 3 drops of 0.1N NH.sub.4 OH as catalyst. d)
Reagent for the SO.sub.4.sup.2- anion was sodium rhodizonate and
BaF.sub.2.
Starting solution contained 0.25% sodium rhodizonate,
3.5.times.10.sup.-3 g. BaF.sub.2 and 3.times.10.sup.-3 N NaOH.
Bottom left: Glass doped with Fe.sup.2+ (top, yellow) after
immersion in a solution containing o-phenanthrolin (bottom, red).
The glass, prepared in the presence of an acid catalyst (a few
drops of concentrated HCL), was used before complete drying
(container was capped after 3 days).
Bottom right: Two different reagents for the determination of
Cu.sup.2+ (top: glass with reagent, bottom: same after immersion in
Cu.sup.2+ solution). Left: Rubeanic acid as a reagent. Starting
solution contained 0.15% of the reagent and 0.25% sodium tartaric
in the presence of 0.01N NaOH. Right: Benzoinoxime (Cupron) as
reagent. Starting solution contained 0.25% of the reagent with one
drop of concentrated HCL. After 3 minutes 3 drops of concentrated
NH.sub.4 OH were added.
C. Representative Examples of Bioprocesses Involving Proteins
1. Preparation of sol-gel immobilized enzymes.
Enzyme solutions (0.2 ml, 10 mg/ml) in non-buffered water, which
may contain various additives were mixed in the at 4.degree. C.
with either methanol or polyethylene glycol (PEG 400). The
concentrations of additives (such as e.g. NaF, NaOH, HCl), the
volumes of methanol and PEG 400 were as indicated in the examples
below. Tetra-methoxy silane (TMOS, 1 ml) was then added. The tubes
containing the reaction mixture were transferred to a shaking water
bath at 8.degree. C. The bath was allowed to reach the room
temperature during 2-3 h. In samples containing PEG 400, the
polymerization was completed in about 3 h. All the liquid remaining
on the top of sol-gel was then removed by suction. In
methanol-containing mixtures gelation took place in about 4-5 h.
The polymerized sol was allowed to dry for a week at 30.degree.
C.
2. Retention of protein by the sol-gel glass.
All the glasses prepared according to example C1 were ground to a
size of about 60-100 mesh and packed in 2 ml-columns. The columns
were eluted with 0 5M NH.sub.4 HCO.sub.3 (250 ml), followed by
water (250 ml). This cycle was repeated twice. All washing
solutions were collected, concentrated by freeze-drying, and
assayed for protein content and for respective enzyme activity. It
was found that neither significant enzyme activity nor protein
could be detected in the eluates.
3. Entrapment of trypsin in sol-gel glasses.
Trypsin (E.C. 3.4.21.4, from bovine pancreas, 11,000 U/mg) was
supplied by RAD Chemicals, Rehovot, Israel. Trypsin entrapped in
sol-gel was prepared as described in example C1. Assays were
performed on the washed glasses at 25.degree. C. at pH 8 using
N-benzoyl-L-arginine-4-nitroanilide (3.3 mM) as the substrate. The
concentration of NaF in the enzyme solution and the addition of
methanol or PEG 400 (ml per ml TMOS) as well as the enzymatic
activity of the glass catalyst (expressed in per cent of trypsin
activity initially added to the condensation mixture) are shown in
the following Table:
______________________________________ Trypsin Activity (percent of
initial) MeOH (ml/ml TMOS) PEG (ml/ml TMOS) NaF (mM) 0.6 0.2 0.4
0.6 ______________________________________ 0 0.1 11.4 33.0 33.6 1
0.6 16.9 24.7 29.7 10 1.9 10.0 18.2 23.6 100 2.8 4.1 21.6 17.5
______________________________________
4. Entrapment of acid phosphatase in sol-gel glasses.
Acid phosphatase (E.C. 3.1.3.2, from wheat germ, 0.45 U/mg) was
purchased from Sigma. The acid phosphatase-containing sol-gel
glasses were prepared as described in the example C1. The assays
were performed on the washed glasses at 25.degree. C. at pH 5.6
using p-nitrophenyl phosphate (6 mM) as the substrate. The activity
yield, calculated in percents of enzyme activity used initially for
the preparation of glasses, is shown in the following Table:
______________________________________ NaF, mM 1.0 3.0 10.0 SOLVENT
ACID PHOSPHATASE YIELD, % ______________________________________
Methanol 0.6 ml/ml 1.9 -- 39.2 PEG 400, 0.2 ml/ml 46.6 56.4 21.1
PEG 400, 0.4 ml/ml 39.8 41.0 46.7
______________________________________
5. Thermal stability of immobilized acid phosphatase in different
sol-gel glasses.
The acid phosphatase-containing sol-gel glasses (example C4) were
incubated at 70.degree. C. in citrate buffer (pH 5.6, 0.1M) for
various periods of time (up to 5 min). The activity of acid
phosphatase was determined, as described in the legend to Table 1.
The half-life time was calculated assuming the 1st order
inactivation kinetics. The half-life time of the soluble enzyme at
the same conditions was below 0.1 min.
______________________________________ NaF, mM 1.0 3.0 10.0 SOLVENT
HALF-LIFE TIMES AT 70.degree. C., min
______________________________________ Methanol 0.6 ml/ml -- -- 3.9
PEG 400, 0.2 ml/ml 3.3 3.3 12.0 PEG 400, 0.4 ml/ml 3.2 3.1 3.5
______________________________________
6. Entrapment of peroxidase in sol-gel glasses.
Peroxidase (E.C. 1.11.1.7, from horseradish, 200 U/mg) was obtained
from Sigma. Sol-gels doped with peroxidase were prepared as shown
in the example C1. All the glasses prepared with the addition of
PEG 400 were active, although it was not possible to determine the
extent of their activity quantitatively, since the dye formed by
oxidation of several substrates was adsorbed strongly in the glass.
Semi-quantitative comparison of the dye stain shortly after the
addition of the assay mixture indicated improved activity yields at
higher concentrations of PEG 400. In contrast to trypsin and
catalase, sol-gel glasses made at elevated concentrations of NaF
were more active. Glasses prepared in methanol-containing mixtures
were devoid of peroxidase activity.
7. Entrapment of trypsin in sol-gel glasses.
Trypsin solution (1.0 ml, 2 mg/ml) in non-buffered water was mixed
with either 20 mM NaF (0.1 ml) or the same volume of water, and
with one of the following: (1) methanol, (2) polyethylene glycol
solution (PEG 6000, 20% w/vol in water), or (3) glycerol solution
(75% w/vol in water). The mixture was cooled to 4.degree. C.
Tetra-methoxy silane (TMOS, 1 ml) was then added. The tubes
containing the reaction mixture were transferred to a shaking water
bath and allowed to reach the room temperature. The polymerized sol
was allowed to dry for a week at 30.degree. C. The resulting
glasses were treated as described (example C2). Trypsin activity of
the trypsin-doped sol-gel glasses expressed as the yield of
activity used for the preparation of the catalyst is presented in
the following Table.
______________________________________ TRYPSIN ACTIVITY, % of
initial ADDITIVES +NaF -NaF ______________________________________
Methanol 17.2 26.8 PEG 6000, 51.3 46.1 Glycerol 82.0 38.1
______________________________________
8. Entrapment of aspartase in sol-gel glasses.
Escherichia coli cells (ATCC 11303) were cultured as described
(Chibata, I, Tosa, T., and Sato, T. Meth. Enzymol. 44, 739-746
(1976)). Saline-washed cells (4 g wet weight) were suspended in
water (2ml) and disrupted by sonication. The homogenate was cleared
by centrifugation (10,000xg, 30 min, 4.degree. C.) and used for the
preparation of sol-gel glasses. The homogenate (0.5 ml) was mixed
with NaF solution (0.2 ml) at the concentrations indicated in the
Table below. Methanol (0.6 ml) or PEG 400 (0.2 ml) was then added
followed by TMOS (1 ml). All the additions were made at 4.degree.
C. The resulting sol was kept overnight at room temperature and
then washed with an excess of 50 mM phosphate buffer pH 7.
Aspartase activity was measured and expressed in .mu.moles/min/g
cells (wet weight). The results are presented in the Table. For
comparison the polyacrylamide gel-entrapped whole cells from the
same batch, prepared according to Chibata (1976), possessed
aspartase activity of 133 .mu.moles/min/g cells.
______________________________________ NaF Aspartase Activity,
.mu.mole/min/g cells solution MeOH (ml/ml TMOS) PEG (ml/ml TMOS) mM
0.6 0.2 ______________________________________ 0 105.0 79.0 1 15.8
127.7 100 64.5 39.8 ______________________________________
9. Preparation of protein-doped glasses by NaOH catalyzed
polycondensation. Immobilization of alkaline phosphatase.
A mixture of tetra-methoxy silane (TMOS, 5 ml), methanol (6 ml) and
1 mM NaOH in methanol (0.1 ml) was cooled to -20.degree. C. and
mixed with an ice-cold solution (0.9 ml) of alkaline phosphatase
(ALP, E.C. 3.1.3.1 from bovine intestinal mucosa, Type I-S, 8.5
U/mg, Sigma Chem. Co) containing 1.5 mg of the enzyme. A cloudy
mixture was allowed to reach room temperature under stirring. The
resulting viscous opaque material was kept for 10 days at
37.degree. C. During this time the glass formation was completed
and it reached a constant weight. The glass was ground and washed
as described in the example C2. The enzyme activity was determined
in NaOH-glycine buffer (40 mM, pH 9.5) at 25.degree. C. using
p-nitrophenyl phosphate as the substrate. The yield of the alkaline
phosphatase activity after immobilization was estimated at about
30%. The half-life time of the immobilized enzyme at 70.degree. C.
(pH 9.0) was 4.7 min, as compared to 2.6 min for the soluble ALP at
the same conditions.
10. Immobilization of chitinase
The glass trapped enzyme was prepared by adding 1.0 ml of the
enzyme chitinase (EC 3.2.1.14, cloned from Serracia marcensens and
expressed in E. coli, 200 units) in the phosphate buffer (10 mM, pH
6.3), to a solution obtained by stirring 3.0 ml methanol and 2.ml
TMOS for 15 minutes.
11. Antibody reactions
Interleukin-2 receptor (IL-2R) is the protein that mediates the
action of interleukin-2 (IL-2), an immune system growth hormone.
Levels of soluble IL-2R have been shown to be elevated in a number
of pathological conditions, and may thus be of significant
prognostic value. We have used an Anti-IL-2R monoclonal antibody,
trapped in a sol-gel glass, to determine IL- 2R, using a sandwich
immuno assay test (cell-free Interleukin-2 Receptor CK 1020, 96
Test kit, T Cell Sciences, Inc., Cambridge, Mass., U.S.A.).
Trapping of Anti-IL-2R monoclonal antibody in a "sol-gel" glass was
carried out with a starting solution composed of methanol (3 ml),
TMOS (2.5 ml), 6 mM phosphate buffered saline (PBS, 0.25 ml) and
Anti-IL-2R antibody (0.25 ml, from the kit). After stirring for 50
min. the sample was allowed to stand for 5 days at 27.degree.
C.
The resulting glass (4 mg, 0.4% of the total amount) was crushed
and washed three times with 350 .mu.l of the "washing solution"
from the kit (0.2 ml surfactant in 200 ml PBS). To this solution
100 .mu.l the "sample diluent" (buffered serum protein) and 50
.mu.l of the human IL-2R standard "solution" were added and mixed
for 15 sec, followed by covering and incubating for 2 hours at
37.degree. C. After three washings, 100ml peroxidase- conjugated
Anti-IL-2R antibody solution was added and incubated at 37.degree.
C. for 2 hours. After three washings with the "washing solution",
100 .mu.g of o-phenylenediamine dissolved in a "substrate diluent"
(buffered H.sub.2 O.sub.2) were added and incubated for 20 min at
room temperature. An absorbance OD.sub.490 =0.93 was recorded,
compared to OD.sub.490 =0.357 obtained with the above commercial
kit, with a similar amount of Anti-IL-2R monoclonal antibody
absorbed into polystyrene microtiter wells.
* * * * *