FLUORESCENT IMMUNOASSAYS AND FLUORESCENT COMPOUNDS AND TRACERS THEREFORE
BACKGROUND OF THE INVENTION
This invention was made in part under United States Government Contract No. N00014-81-C-0619 and the United States Government has a non-exclusive, non- transferable, irrevocable, paid-up license to practice or have practiced for or on behalf of the United States, this invention throughout the world.
The present invention relates to fluorescence compounds and resultant tracers utilized as reagents in fluorescent immunoassay procedures to detect the presence of and/or quantify analytes in a mixture; even analytes that are present only in very low concentrations. In particular, the invention has relevance for the determination of constituents present in biological fluids such as blood serum, plasma, spinal fluid, urine, amniotic fluid, and the like and other fluids such as milk and water, or even solid materials such as wastes that can be solubilized. Such measurements are important for the practice of public health medi¬ cine as well as human and veterinary medicine. In addition, the determination of therapeutic drug levels and the presence of drugs of abuse in fluids is very valuable.
The determination of analytes which are pre-
sent only in very low concentrations has been a pervasive problem in analysis. The introduction of radioimmunoassays in 1956 enormously expanded the capabilities of clinical laboratories because of the great sensitivity and selectivity of such radioimmunoassays, making possible the quan¬ tification of many analytes that could not easily be determined by other methods. They have been used to identify and quantify metabolites, hor- mones, drugs, and other biologically important substances both for purposes of diagnosis, and for purposes of assessing and following the effec¬ tiveness of medical treatment.
One type of immunoassay involves the com- petitive binding of an unknown quantity of analyte in the sample to be analyzed, with a known quan¬ tity of analyte labeled by a tracer added to the reaction mixture, for a limited number of receptor-binding sites on specific antibodies that combine with labeled and unlabeled analyte.
The use of radioactive tracers in immunoassays requires special licensing and special precautions in handling to minimize health hazards and con¬ tamination. Federal and state regulations that
must be followed in handling radioactive materials frequently impose an added burden in terms of time and effort required to perform the tests and to dispose of the used radioactive materials. Standard curves constantly change owing to the decay of radioactivity and radiodecomposition of the constituent reagents. There are considerable batch-to-batch differences in manufacture. Furthermore, counters for the measurement of radioactivity are large, expensive, cumbersome, and do not lend themselves to automation. Owing to these and other problems, immunoassays utilizing fluorescent tracers are gradually displacing the older assays using radioactive tracers. However, only certain molecules exhibit the property of fluorescence to a significant extent. A fluorescent molecule will absorb a photon of light and utilize the energy to move an electron from the ground state to an oribtal with a higher energy level. This process is known as
"excitation" and occurs at specific wave lengths of light. After a short interval of time; of the order of nanoseconds, the excited electron falls back into the ground state and emits a photon of
light. Some energy is lost in the process and the photon of emitted light is shifted toward the red part of the spectrum with respect to the wave length of exciting light. The difference between wave lengths of exciting light and emitting light is known as the "Stokes shift".
The most commonly used fluorescent tracer in immunoassays is fluorescein. In the case of fluorescein, maximum excitation occurs when it is illuminated with light of wave length 496 n . The maximum emitted light occurs at a wave length of 516 nm. Thus, the Stokes shift is 20 nm. A number of other fluorescent tracers are known in the art and have been used in immunoassays, but these fluorescent tracers have Stokes shifts of less than 35 nm. The use of tracers with Stokes shifts shorter than 35 nm presents a number of problems that limit fluorescence measurements. First, fluorescence measurements are limited by light scattering which causes part of the exci¬ tation light to be detected in the emission chan¬ nel. In practice, light scattering interference is reduced by placing band pass optical inter¬ ference filters in both the excitation and emission channels. The -greater the separation
between the wave length of maximum excitation and the wave length of maximum emission, and therefore of the band pass filters, the more effective such interference filters will be, and the more effec- tive will be the minimization of light scattering background, an advantage not possible with tracers having Stokes shifts of 35 nm or below.
Also, serum and other biological fluids are intrinsically fluorescent. Almost all of the intrinsic fluorescence of biological fluids show Stokes shifts of less than 35 nm. Thus, utiliza¬ tion of fluorescent tracers with Stokes shifts of 35 nm or shorter allows more interference by the intrinsic fluorescence of serum and other biologi- cal fluids as well as other fluids to be tested. Another limiting factor in fluorescence measurements of solutions is elastic Raman light scattering. In the case of aqueous solutions, Raman scattering occurs at approximately 300 wave numbers on either side of the frequency of the exciting light. Raman scattering is a problem with fluorescent tracers with small Stokes shifts.
Certain polycyclic compounds, in particular pyrene and chrysene compounds, have been shown to have relatively large Stokes shifts in purely
biochemical and cell biology research experiments. For example, 1-pyreneisothiocyanate is relatively nonfluorescent but reacts with the amine groups of antibodies to form conjugates with excitation maxima of approximately 386 nm and emission maxima of 470 nm giving a Stokes shift of 84 nm. Similarly 6-chrysenemaleimide is a relatively nonfluorescent compound which forms adducts with the sulfhydryl groups of various compounds to form fluorescent products with an excitation maximum of 360 nm and an emission maximum of 400 nm. 8-Hydroxypyrene-l,3,6-trisulfonic acid has been used as a pH indicator having an excitation maxi¬ mum of 450 nm and an emission maximum of 515 nm giving a Stokes shift of 65 nm. The various reports describing the use of such reactive pyrene or chrysene compounds fail to teach or suggest their use in immunoassay testing; whether fluorescence intensity or fluorescence polariza- tion is measured.
SUMMARY OF THE INVENTION The present invention overcomes the noted problems of prior fluorescent compounds and tra¬ cers -made therefrom in immunoassays and provides tracers having large Stokes shifts thereby
enabling fluorescent assays of greater sensitivity with minimization of light scattering background, of interference by intrinsic fluorescence of the fluid being test, and of Raman light scattering.
Briefly, the present invention comprises a polycyclic hydrocarbon
in which A is 0, N, or S; R is H, a substituted or unsubstitued Ci - Cβ alkyl group, a substituted or unsubstituted C2 - Cβ ester group, or a substi¬ tuted aryl group; Y is H or SO3Z wherein Z is H or a halide, with at least one Y being SO3Z and Z is a halide; R' is H, Y or A-R; and n is 0 or 1 with at least one n equal to 1.
The invention also comprises the tracers and iramunoassay as hereinafter set forth.
DETAILED DESCRIPTION The terms "ligand" and analyte" are used interchangeably herein and refer to consti¬ tuents of fluids or dissolved materials? par- ticularly biological fluids whose presence and/or concentration is to be measured. Antibodies that specifically bind to ligands can be raised in ani¬ mals and such antisera isolated and purified by standard techniques well-known to those skilled in this art, or highly specific monclonal antibodies can be selected and produced by again standard techniques. The ligands that can be identified and/or quantified by the assays of the present invention vary over a wide range of molecular weight and include, inter alia, such represen¬ tative compounds as theophyllin, dilantin, pheno- barbital, carbamazepine, gentamycin, streptomycin, amikacin, tobramycin, thyroxine, digoxin, digi- toxin, procainamide, lidocaine, quinidine, pri i- done, propranolol, morphine, codeine, heroin, hormones, and the like.
Quantification of a ligand in a solution or Tnixture requires the preparation of a fluorescent- labeled ligand {tracer) that can be used to com- pete with unlabeled ligand for binding by a
specific antibody. The fluorescent compounds of the present invention can be bound to reactive a ino, reactive carboxyl, or other reactive substitutents present on the ligands or to ligand analogs possessing a reactive amino, reactive carboxyl reactive sulfhydryl, or other reactive groups to form suitable tracers. Some of the possible reactions that can be employed to link fluorescent tracers to ligands will be described below in the examples of embodiments of the inven¬ tion and other known techniques can also be used for this purpose. The tracers formed by reacting the instant pyrene or chrysene compounds having the formula
(
(Y)
in which A is 0, N, or S; R is H, a substituted or unsubstitued C^ - Cg alkyl group, a substituted or unsubstituted C2 - Cg ester group, or a substi¬ tuted aryl group; Y is H or SO3Z wherein Z is H or a halide, with at least ony Y being SO3Z and Z is a halide; R' is H, Y or A-R; and n is 0 or 1 with at least one n equal to 1.
The pyrenesulfonic acid or pyrenesulfonyl chloride compounds are preferred with specific preferred compounds being 8-acetoxy-l,3,6- pyrenetrisulfonyl chloride, 6-8-diacetoxy -1,3-pyrenedisulfonyl chloride, 8-ethoxy-l,3 ,6-pyrenetrisulfonyl chloride, 6,8-diethoxy-l,3-pyrenedisulfonyl chloride, and 8-succinylamino-l,3,6-pyrenetrisulfonic acid. As to the chrysene, 9-acetoxy-l,3,7-chrysenet- risulfonyl chloride is preferred, which form sulfonamides with reactive amino groups of a ligand or ligand analog. In general, such compounds can be synthesized from pyrene and chrysene by the conventional pro¬ cess of forming the tetrasulfonic acid derivati¬ ves using anhydrous sodium sulfate and concentrated sulfuric acid- The hydroxy or amino compounds are subsequently formed by reaction "with
aqueous sodium hydroxide or ammonia at elevated temperatures under pressure. Reactive fluorescent derivatives are the formed in one of two ways. The sulfonic acid groups are to be converted to sulfonyl chlorides, for example, by the use of thionyl chloride. Sulfonyl chloride derivates form adducts with reactive amino groups of ligands or ligand analog, for example. Alternatively, the ligand or ligand analog can be coupled to the -0-R, -N-R, or -S-R group.
In general, tracer adducts of ligands or ligand analogs with fluorescent moieties are formed by conventional procedures such as shown, for example, in U.S. Patents 3,996,345 or 4,420,568.
The pyrene and chrysene tracers of the present invention are o the forumla
i n which A is 0, N , or S ; R is H , a substituted or
unsubstitued C^ - Cg alkyl group, a substituted or unsubstituted C2 - Cg ester group, or a substituted aryl group; Y is H or SO3Z wherein Z is H or a halide, with at least one Y being SO3Z? R is H, Yr or A-R; and n 0 or 1 with at least one n equal to 1; L is a ligand or ligand-analog; and m is 0 or 1 with only one m being 1.
One group of-preferred fluorescent tracer com¬ pounds are based on pyrenesulfonic acids and pyrenesylfonyl chlorides. Pyrene and chrysene compounds generally have large Stokes shifts, greater than 35 nm and often as large as 50 to 70 nm. A particular advantages of hydroxy, ethoxy, acetoxy or similarly substituted pyrenesulfonic acids is that their excitation is in the blue- green part of the spectrum, rather than the near ultraviolet part of the spectrum characterstic of other pyrene or chysene compounds. Another advan¬ tage of these compounds is that they are readily soluble in water, rather than being hydrophobic like other pyrene and chrysene compounds.
Fluoroimmunoassays can be carried out in several different ways. It is preferable to use a homogeneous assay method in which the antibody bound ligand and tracer need not "be separated from
the free ligand and tracer prior to measuring the fluorescence. Because only one incubation and no washings are required such assays can be performed simply and rapidly. Particularly useful are fluorescence polarization immunoassays first described by Dandliker, .B. e al. , Immunochemistry 10, 219 (1973) and Spencer, et al. Clin. Chem. 19, 838-844 (1973). In such assays, the reaction mixture is excited with polarized light, and the polarization of the fluorescence emission is measured. The degree of polarization of the fluorescence emission depends upon the ratio of free tracer to tracer bound to antibody, and thus, the ratio in unknown samples can be determined by comparision to a standard curve. If owing to the high molecular weight of ligand, or to the low concentration of ligand, fluorescence polarization immunoassays are not sufficiently sensitive, another type of fluorescent immunoassay may be employed such as those reviewed by Hemmila in Clin. Chem. 31, 359 (1985).
The invention will be further described in connection with the following examples which was set forth for purposes of illustration only. EXAMPLE 1
A novel reactive fluorescent compound of great utility is 8-acetoxy-l,3,6-pyrenetrisulfonyl chloride which was synthesized as follows:
5 g 8-hydroxy-1,3,6-pyrenetrisulfonic acid (available from Eastman Koadk) were refluxed in 50 ml acetic anhydride for 1.5 hrs. A light yellow solid precipitated that was collected by filtra¬ tion, washed with ethylene chloride, and dried in a dessicator. 1.5 g of this material dissolved in 1 ml dimethylformamide was added to 10 ml thionyl chloride with constant stirring for 20 hrs in a fume hood. The mixture was then poured onto about 20 g crushed ice. After the vigorous reaction had subsided, the aqueous solution was transferred to a separatory funnel and extracted three times with 20 ml portions of chloroform. The organic layers were combined and dried over anhydrous magnesium sulfate. The clear orange solution was filtered and the volume reduced to 15 ml by evaporation. Hexane was added until cloudiness of the solution appeared. After storage at 2 degrees, golden brown crystals formed which were harvested. Yield = 31%. For steric reasons, only one molecule of ligand couples to each fluorescent probe molecule? the remaining two sulfonyl chloride groups are
hydrolyzed.
To formulate an assay for phenobarbital, the fluorescent compound was reacted with 2-aminophe- nobarbital to form a tracer. Excitation maximum of this tracer was at 455 nm and emission maximum at 520 nm (Stokes shift 65 nm) . The assay was performed as described by Dandliker, et al. , supra.
A standard solution serum to be tested or other unknown was diluted 1:400 in 0.15 M phosphate buffer, pH 7.5, containing 0.01% sodium azide and 0.01% bovine gamma globulin. To 0.5 ml diluted sample was added 20 1 phenobarbital tracer stock solution which contained 5 g/ml 2-aminop- henobarbital in the above buffer. The best antibody and optimum antibody dilution was determined by generating antibody titration curves upon adding increasing amounts of antibody to a constant amount of tracer and determining the polarization using a fluorescence polarimeter. The appropriate amount of antibody in 20 1/buffer was added to the reaction and the mixture incu¬ bated at room temperature for 3 min. The polari¬ zation was then measured. Figure 1 illustrates a typical standard curve. The polarization of unknown serum samples was
assessed in this manner and the concentration of phenobarbital calculated by comparison to the standard curve.
EXAMPLE 2 2.5g 1-nitropyrene was added with stirring over a period of 5 minutes to a mixture of 13g concentrated sulfuric acid and 3g anhydrous sodium sulfate at 60°C and stirred for an additional 15 min. breaking up the dark purple clumps that formed. Then 8 g fuming sulfuric acid was added over 30 min. at 60° with constant stirring. The whole mixture was added to 80g ice. An additional 60 ml water was added. After 18 hours the pH was adjusted to 5 and solution filtered. The aqueous phase containing 8-nitro-l,3,6-pyrenetrisulfonic acid was reduced with iron filings and acetic acid. The solution was filtered and 8-amino-l,3,6-pyrenetrisulfonic acid was precipi¬ tated by the addition of dilute HC1. To 2.5 g of this product dissolved in 10 ml dry dimethyl formamide was added 0.75g succinic anhydride and the mixture stirred for 4 hrs. at 50° in the dark. 20 ml water was added and the -mixture was slightly acidified and cooled on ice. The precipitate was collected and the product
purified on prepative thin layer silica gel.
This fluorescent marker was utilized in an assay for thyroxine by forming an adduct with 3,5-dichloro-3• ,5'diiodothyroxine using dicyclo- hexylcarbodiimide. Excitation of the adduct tracer was 461 nm and the emission maximum was 524 nm (Stokes shift of 63 nm) . This fluorescent thyroxine tracer was utilized in a fluorescence polarization assay similar to that described above.
EXAMPLE 3 To a mixture of 6.5g concentrated sulfuric acid and 1.5g anhydrous sodium sulfate was added lOg pyrene with stirring at 60° for 15 min. After cooling to 50°, 4g fuming sulfuric acid was added in small portions over a 20 min. period. The dark reddish-black mass was cooled on ice. After standing for 2 hrs, it was broken up and dissolved in 70 ml water. After filtration, the product was precipitated by saturating the filtrate with NaCl. A mixture of 1.5g above product, 1.5g sodium hydroxide and 1.0 ml water was sealed in a glass pressure tube and heated at 155°C for 30 min; then at 165°C for 20 min.; and then at 170°C for 5 min. The thin slurry thickened during this procedure.
The resulting mass was dissolved in water and the excess alkali neutralized. After filtration, the supernatant was acidified with acetic acid which precipitated the 6,8-dihydroxy-l,3-pyrenedisulfonic acid product. The diacetoxy derivative was first formed by treatment with acetic anhydride, and then the disulfonyl chloride formed as described in Example 1. Fig. 2 illustrates a typical stan¬ dard curve. A tracer adduct was formed by reacting the
6,8-diacetoxy-l,3 pryrenedisulfonyl chloride with 8-aminoethyltheophyllin. The tracer adduct had an excitation maximum of 464 nm and an emission maxi¬ mum of 527 nm. The theophyllin tracer was uti- lized in a fluorescence polarization assay similar to that described in Example 1. The typical stan¬ dard curve is shown in Figure 2.
EXAMPLE 4 To a mixture of 6.5g concentrated sulfuric acid and 1.5g anhydrous sodium sulfate was added lOg chrysene with stirring at 60° for 15 min. After cooling to 50°, 4g fuming sulfuric acid was added in small portions over a 20 min period. The dark mass was cooled on ice. -After standing for 2 hrs it was broken up, and dissolved in 70 ml
water. After filtration, the product was precipi¬ tated by saturating the filtrate with NaCl.
The above product was mixed with 1.5g sodium hydroxide and 1.0 ml water, sealed in a glass pressure tube and heated at 155° for 30 min; then at 165° for 20 min; and then at 170° for 5 min. The pressure tube was cooled and the resulting mass was dissolved in water and then brought to pH 9.0 After filtration, the supernatant was aci- dified with formic acid which precipitated the 7,9-dihydroxy-l,3-chrysenedisulfonic acid. The diacetoxy derivative was first prepared by treat¬ ment with acetic anhydride, and then the disulfo- nyl chloride was formed by treatment with thionyl chloride as described in Example 1.
A tracer adduct was formed by reacting the 7,9-diacetoxy-l,3-chrysenedisulfonyl chloride with diphenyl glycine. The tracer adduct had an absorption maximum of 438 nm and an emission maxi- mum of 482 nm. The phenytoin tracer was utilized in a fluorescence polarization assay similar to that described in Example 1.
EXAMPLE 5 8-Acetoxy-1,3 f6-pyrenetrisulfonyl chloride was reacted with genta ycin to form a tracer adduct
that was utilized in a fluroescence polarization assay similar to that described in Example 1 using excitation light of 455 nm and measuring the fluorescence at 520 nm. The average intrasample correlation coefficients for six replications of 26 samples was 0.987. The average interassay correlation coefficiencts (n = 26) compared to commercially available gentamycin assays using a fluorescein based tracer was 0.966. While the invention has been described in con¬ nection with preferred embodiments, it is not intended to limit the scope of the invention to the particular form set forth, but on the contrary, it is intended to cover such alter- natives, modification, and equivalents as may be included within the spirit and scope of the inven¬ tion as defined by the appended claims.