Functionalized media and methods of making and using therefor

Abstract

Methods, compositions, devices and kits are provided herein for separating, scavenging, capturing or identifying a metal from a target using a medium or scaffold with a selenium-containing functional group. The medium or the scaffold including the selenium-containing functional group has affinity and specificity to metal ions or compounds having one or more metals, and efficiently separates, recovers, and scavenges of the metals from a target such as a sample, solution, suspension, or mixture.

Claims

1. A method for recovering, removing, or scavenging a metal from a target, the method comprising: contacting the target containing the metal with a medium or a scaffold comprising a selenium-containing functional group which is linked to the medium by a sulfur-containing functional group selected from a thiol or a thiolate, whereby the selenium-containing functional group specifically binds to the metal and separates the metal from at least one remaining component in the target; and, separating the medium or the scaffold from the target, wherein the target is a material selected from the group comprising of: an aqueous material, a reaction mixture, a complex material, and a biological sample.

2. The method according to claim 1, wherein the metal is selected from the group comprising of: a toxic metal, a composite metal, a high value metal, a transition metal, a lanthanide metal, and an actinide metal, for example the metal is at least one selected from the group of: scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, yttrium, zirconium, niobium, molybdenum, technetium, ruthenium, rhodium, palladium, silver, cadmium, hafnium, tantalum, tungsten, rhenium, osmium, iridium, platinum, gold, mercury, actinium, rutherfordium, dubnium, seaborgium, bohrium, hassium, meitnerium, darmstadtium, and roentgenium.

3. The method according to claim 1, wherein the medium or the scaffold comprises silica or is covalently linked or immobilized to the selenium-containing functional group by at least one spacer wherein the spacer is selected from the group consisting of: (C.sub.1-C.sub.18)alkyl, (C.sub.1-C.sub.8)alkoxy, (C.sub.1-C.sub.8)heteroalkyl, (C.sub.6-C.sub.10)aryl, (C.sub.1-C.sub.9)heteroaryl, and (C.sub.6-C.sub.10)aryl(C.sub.1-C.sub.6)alkyl.

4. The method according to claim 1, wherein contacting further comprises at least one step selected from the group of: stirring, sonicating, and filtering.

5. The method according to claim 1, wherein, after contacting, the method further comprises washing or drying a resulting solid.

6. The method according to claim 1, wherein the contacting comprises adding at least one solvent selected from the group consisting of: chloroform, dichloromethane, ethyl acetate, diethyl ether, acetic acid, hexane, toluene, ethanol, acetone, methanol, tetrahydrofuran, dimethyl sulfoxide, acetonitrile, and a combination thereof.

7. The method according to claim 1, wherein prior to contacting, the method comprises reacting a selenium benzyl ester with at least one silane selected from the group comprising of: 3-mercaptopropyltrimethoxysilane, 3-hydroxypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, n-butyltrimethoxysilane, and 3-cyanopropyltrimethoxysilane to form the resulting selenium containing functional group.

8. The method according to claim 1, wherein the medium comprises an activated silica gel or the medium is selected from the group consisting of: silica, silica gel, an activated silica gel, alumina, polystyrene, agarose, modified polymeric resin, cellulose, magnesium silicate, dextran, and starch.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a drawing showing methods for preparing chromatographic media having a selenium-functional group.

(2) FIG. 1 panel A is a drawing of a chemical reaction for synthesizing a propylselenol trimethoxysilane. The chemical reaction shows reacting a bromopropyltrimethoxysilane with potassium selenocyanate (KSeCN) in acetone, and then sodium borohydride (NaBH.sub.4) in ethanol to yield a selenol silane.

(3) FIG. 1 panel B is a drawing of a chemical reaction for synthesizing a benzylesterselenol trimethoxysilane. The chemical reaction involves reacting 3-hydroxypropyltrimethoxysilane with a selenium benzyl ester under acidic conditions to yield a selenol silane with an aromatic ring.

(4) FIG. 2 is a drawing showing a system for recovering a metal from a target using a selenium-functionalized medium. The system involves contacting the target having a metal with a selenium functionalized medium (i.e., medium including a selenium-containing functional group) that specifically binds to the metal; separating the metal from the target having at least one remaining non-metal component; and recovering the metal from the medium and/or recovering the target including the at least one remaining non-metal component.

(5) FIG. 3 is a drawing of a chemical reaction for synthesizing a selenoether functionalized silica material. The chemical reaction includes mixing a dimethyldiselenide with sodium borohydride, and adding the mixture in ethanol to a halogen-functionalized 3-propyl functionalized silica or silicon atom (X=chloride, Cl; bromide, Br; or iodide, I) to produce the selenoether functionalized silica material.

(6) FIG. 4 is a drawing of a chemical reaction for synthesizing a benzylesterselenol functionalized silica material. The reaction is a nucleophilic substitution that reacts a potassium selenium cyanide to a halogenated 1-(chloromethyl)-4-propylbenzene functionalized silica or silicon atom.

DETAILED DESCRIPTION

(7) Use of ion-exchange resins for the removal of metal ions from aqueous solutions is commercially wide spread especially in water softening applications and for the removal of toxic products from effluents. Processing of radioactive wastes, the purification of rare earth metals and the analysis of geological samples are other important activities that involve removal of metal ions. The high cost of available resins and the lack of resin selectivity are major obstacles to separation of metals (Hodgkin et al., U.S. Pat. No. 4,762,556 issued Aug. 9, 1988). Metal catalyzed reactions are commonly used in the manufacture of active pharmaceutical ingredients and fine chemicals, and steps are taken to remove metals from reaction mixtures (Crudden, C. M. 2005 J. Am. Chem. Soc. 127 (28): 10045-10050; Welsh, C. J. 2005 Org. Process Res. Dev. 9: 198-205; and Welch, C. J. 2008 Org. Process Res. Dev. 12: 81-87). The regulatory limits for metal content are becoming increasingly more stringent, for example, United States and European government regulations require candidate drugs and reaction mixtures to have very low concentration levels for many metal ions, e.g., palladium, platinum, copper, mercury, silver and lead. For example the regulations in many cases require metals to be present at amounts of parts per million or parts per billion.

(8) Selective chelating resins have become available commercially, for example resins containing imidodiacetic acid, ethylenediaminetetraacetic acid (EDTA), or picolylamine have been used (Meadow et al., U.S. Pat. No. 5,262,018 issued Nov. 16, 1993; Hosea et al., U.S. Pat. No. 5,108,615 issued Apr. 28, 1992; and Darnall et al., U.S. Pat. No. 5,178,746 issued Jan. 12, 1993). However, these resins are only marginally selective for a particular heavy metal ion and require complex procedures to effect practical separations in commercial situations.

(9) Scavenging of high value metals such as gold has always been of interest for commercial and analytical reasons and many resin systems have been designed to accomplish this. A common polymer used has been the Srafion NMRR resin (Ayalon Water Conditioning Co. Ltd., Haifa, Israel) which has an aromatic sulphaguanidine structure. Although this polymer has good capacity for gold in acidic solutions (greater than five millimoles per gram) it absorbs most other heavy metals as well (Geen, T. E. et al. 1970 Anal. Chem. 42: 1749-1753). Another commonly used analytical resin has been the iminodiacetic acid chelating resin. Although the iminodiacetic resins can be used relatively selectively in some cases, the resins adsorb many other metals as well (L. L. Sundberg 1975 Anal. Chem., 47, 2037-2046). Thus, the possibility for these resins for selectively binding metals is limited.

(10) Many commercially available metal scavengers are produced by cross-linking polystyrene or another polymer, which is expensive. Large scale commercial applications, in which gold would advantageously be recovered by burning off the resin, involve costs that are prohibitive. In these cases a common anion exchange resin such as Amberlite IRA 400 (Dow Chemical; Center Midland, Mich.) is used to recover metals or metal halides. See Venkat et al., U.S. Pat. No. 6,379,556 issued Apr. 30, 2002. These materials are generally not selective, consequently recovery of pure gold from them requires a complex series of selective elutions to remove other metals (Burstall, F. H. et al. 1953 lnd. Eng. Chem. 45: 1648-1658). The capacity of these resins is also not very high, being about one to two millimoles of gold per gram of resin. More selective weak base resins have been produced, however capacity of these is much lower and the resins suffer from interference from sulphur-containing anions (Aveston, J et al. 1958 Journal of Applied Chemistry 8: 77-86). Combinations of weak and strong base resins have also been tried with no significant advantage (Aveston, J. et al. 1958 Journal of the Chemical Society 231-239).

(11) The compositions, methods, kits and devices herein contain a medium that has a selenium atom or selenium-containing functional group that effectively binds to metal and metal compounds. Without being limited by any particular theory or mechanism of action, it is here envisioned that the systems, methods, compositions and kits described herein having a medium with a selenium atom are more effective at binding and/or scavenging a metal than a sulfur atom. The metal is effectively attracted or bound to the selenium atom and does not leach from the stationary phase of the medium into the mobile phase of the solvents. Thus, the compositions, methods, kits and devices herein create a substantially permanent, reusable chromatographic medium for methods to calibrate, discriminate and separate metals from a broad variety of different samples, compounds and analytes having a metal atom and related materials. For example, the sample, compound or the analyte contacted with the selenium-containing functional group, and the sample contains any of a toxic metal, a composite metal, a high value metal, a transition metal, a lanthanide metal, or an actinide metal. In various embodiments, the metal is a catalyst such as a platinum. In various embodiments, the metal is at least one selected from the group of: scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, yttrium, zirconium, niobium, molybdenum, technetium, ruthenium, rhodium, palladium, silver, cadmium, hafnium, tantalum, tungsten, rhenium, osmium, iridium, platinum, gold, mercury, actinium, rutherfordium, dubnium, seaborgium, bohrium, hassium, meitnerium, darmstadtium, and roentgenium.

(12) Methods and compositions which are media that remove or scavenge metals from a target such as an aqueous solution or a reaction mixture are shown in Examples herein. In various embodiments the chromatographic media described herein are used for many kinds of liquid chromatographic methods including conventional liquid chromatography, HPLC, thin layer chromatography (TLC). An HPLC column described herein is composed of a selenium-containing functional group stationary phase and is used for the separation of metals from samples. The columns containing the media described herein can be repeatedly used for this type of separation, and are shown to maintain the same retention times for these metals. The selenol chromatographic media can be repeatedly tested over a period of time, and show no loss of metal-retention and no change of retention times. The separation is thus highly reproducible and highly stable. The media including the selenium-containing functional group can be safely stored at temperatures below, at or above room temperature with no appreciable physical signs of decomposition or degradation, such as a change in coloration, smell or complexion.

(13) An aspect of the invention provides a chromatographic medium that includes a selenium-containing functional group (e.g. a selenoate) covalently linked or attached to the medium, such that the selenium-containing functional group specifically binds to an atom of a transition metal, by which the chromatographic medium has affinity and specificity to bind a compound, mixture, solution or material having the metal. The phrase selenolate chromatographic medium is used interchangeably herein with the phrase selenium chromatographic medium.

(14) Thiol-functionalized silica gel has not previously been prepared for chromatographic purposes, but has been used for scavenging metal ions from aqueous solutions (Wasiak, W. 1987 Chromatographia 23: 423-426; Huang et al., PCT/US2011/46810 filed Aug. 5, 2011, each of which is incorporated by reference herein in its entirety). Several manufacturers supply thiol-functionalized silica gel (for example, Silicycle; Quebec, Canada). Most manufacturers do not use chromatographic grade silica gel to reduce the cost of production, hence directly purchased thiol-functionalized silica gel may not meet the requirement for liquid chromatography.

(15) Methods of preparation in the Examples herein used high grade chromatographic silica gel, on which modifications were performed including selenol- and propyl-selenol-functionalization. Selenium content in products was carefully monitored to develop at an optimal condition for making selenium-functionalized silica gel. Methods and procedures of use of the media were developed herein to quantitatively bond metal ions (e.g., platinum) onto the selenium-functionalized silica gel. The metal ion was observed to be bonded onto the selenium to form a stable metal-selenium complex so that effective chromatographic separations was successfully performed.

(16) Materials and methods herein involve covalently bonding selenium atoms and/or selenium functional groups to a medium or scaffold (e.g., silica gel), to obtain a chromatographic medium for effective separation of metals from at least one other component, compounds or molecules present in a target sample. Organoselenium compounds in various embodiments form a more stable complex with metals (e.g., silver (I)) in reactions and biological processes than organosulfur compounds (Pettit, L. D. et. al 1967 Chem. Commun. 1179-1180 and Wessjohann, L. A. et al. 2007 Biol. Chem., vol. 388: 997-1006, each of which is incorporated herein by reference in its entirety). Methods are provided herein for producing selenium chromatographic media for separating and identifying metals. Systems, compositions, devices, methods and kits using chromatographic functionalized media are provided herein.

(17) Without being limited by any particular theory or mechanism of action, it is here envisioned that the systems, methods, compositions and kits described herein having a medium or scaffold with a selenium bound to an electron-donating moiety are effective to bind and/or scavenge a metal. In various embodiments, the selenium includes a selenium atom or a selenium functional group, e.g., a selenol. In various embodiments, a composition containing the selenium is used as a capture medium for effectively binding to and capturing a metal.

(18) In various embodiments, the organoselenium functionalized medium or scaffold described herein includes a functional group and/or a substituent that is bound to the selenium. In various embodiments, the functional group and/or the substituent is an electron-donating moiety that enhances binding of the selenium to a metal. In various embodiments, the electron donating moiety includes: a hydrogen, a halogen, a hydroxyl, an amino, an alkyl, an alkoxy, an thioalkyl, an alkylamino, an imine, an amide, a phosphate, a phosphine, a carbonyl, a carboxyl, a silyl, an ether (e.g., a thioether), a sulfonyl, or a ketone. In various embodiments, the alkoxy includes an alkyether or an alcohol. For example, the selenium functionalized medium or scaffold includes a selenoether, or a homolog or analog thereof. The selenoether moiety includes in various embodiments a central selenium atom connected to two alkyl substituents. In various embodiments, at least one of the alkyl substituent is an sp3 (tetrahedral) hybridized carbon atom. The selenoether functionalized medium or scaffold effectively binds or scavenges the metal.

(19) Selenoethers are commonly used to prepare olefinically unsaturated compounds, and have been used as polymeric catalysts for Mizoroki-Heck chemical reactions (Mizoroki, T. et al. 1971 Bull. Chem. Soc. Jap. 44 (2): 581; Heck, R. F. et al. 1972 J. Org. Chem. 37 (14): 2320-2322; Krou, U.S. Pat. No. 4,601,860 issued Jul. 22, 1986; Chung et al., U.S. patent publication number 20050119497 published Jun. 2, 2005; Heyda, international patent publication number WO/2007/073765 published Jul. 5, 2007, each of which is incorporated by reference in its entirety). For example, a poly--methylselenopropylsiloxane catalyst was synthesized by immobilizing chloropropyltriethoxysilane on silica, and reacting the silica with sodium methylselenolate and then with palladium chloride. The selenoether silica is a heterogeneous catalyst for carbonylation of aryl halides (Mingzhonga, C. et al. 2002 Reactive & Functional Polymers. 50:191-195).

(20) A selenolate-functionalized silica gel was synthesized and used in Examples herein to effectively separate metals from solutions, suspensions and mixtures. The attachment between the metal and the selenolate-functionalized silica was observed to be extremely stable, a feature which reduces or even eliminates the possibility of metal leaching.

(21) The effectiveness of the selenolate-functionalized silica to bind to metals such as platinum and silver is shown in Examples herein. It is envisioned that in addition to these metals, other metals such as transition metals are bound and separated using the chromatographic media herein. For example gold (Au), cadmium (Cd), zinc (Zn), cobalt (Co), titanium (Ti), nickel (Ni), palladium (Pd), and lead (Pb) can be bound using the methods described herein. These and other metals demonstrate different chemical properties and degrees of affinity to the selenolate-functionalized media.

(22) The methods and resulting chromatographic media containing an appropriate choice of a selenium-functional group are further customized as useful for separating different metals and metal mixtures found in nature such as biological samples and environmental samples. The selenium-containing media are used individually or as a plurality of selenium-containing media (or with unmodified media), mixed in appropriate ratios to obtain a variety of affinity, separatory and retentive properties appropriate to the type of metal in a sample. The amount of selenium reacted to the stationary phase support medium, for example, silica gel, is optimized to afford the greatest extent of separation of the desired metal class or classes, for example a toxic metal, a composite metal, a high value metal, a transition metal, a lanthanide metal, and an actinide metal. In various embodiments compositions or chromatographic media containing selenium-functional groups (e.g., a selenol) is effective to scavenge or remove scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, yttrium, zirconium, niobium, molybdenum, technetium, ruthenium, rhodium, palladium, silver, cadmium, hafnium, tantalum, tungsten, rhenium, osmium, iridium, platinum, gold, mercury, actinium, rutherfordium, dubnium, seaborgium, bohrium, hassium, meitnerium, darmstadtium, or roentgenium.

(23) The alkyl-selenium-silica gel medium provided herein was observed in Examples herein to have effectively separated a wide range of otherwise difficult to separate metals from organic molecules and their derivatives and analogs, including for example sterols, polyaromatic hydrocarbons, triglycerides, alkenes (olefins), alkanes, and alkenones, and inorganic compounds. The metal in various embodiments is scavenged, i.e. is removed from a reaction mixture, such that the metal removed is used as a catalyst to increase the rate of a reaction and to selectively produce a desired product. For example, the catalyst includes a metal catalyst for synthetic organic chemistry research and fine chemical production. For example, the catalyst is at least one of: a palladium for example palladium (II) acetate and allylchloro[1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium(II); a nickel for example bis(1,5-cyclooctadiene)nickel and dichloro[1,1-bis(diphenylphosphino)ferrocene]nickel(II); a rhodium for example chloro(1,5-cyclooctadiene)rhodium(I) dimer; a ruthenium for example carbonylchlorohydridotris(triphenylphosphine)ruthenium(II) and 1-hydroxytetraphenylcyclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)--hydrotetracarbonyldiruthenium(II); a gold for example chloro[2-(di-t-butylphosphino)biphenyl]gold(I) and methyl(triphenylphosphine)gold(I); and a copper for example copper(II) trifluoromethanesulfonate and tetrakis(acetonitrile)copper(I) hexafluorophosphate. For example, the metal catalyst is used in a reaction such as a hydrogenation, a rearrangement, a carbonylation, an animation, an oxidation, a hydroboration, an epoxidation, a decarboxylation, a decarbonylation, a cyclization, a carbon-heteratom formation, or a carbon-carbon bond formation reaction (Fu, G. 2008 Acc. Chem. Res. 41: 1555-1564; Marion, N. et al. 2008 Acc. Chem. Res. 41: 1440-1449; Kantchev, E et al. 2007 Chem. Int. Ed. 6: 2768-2813; Martin, R. et al. 2008 Acc. Chem. Res. 41: 1461-1473; Knowles, J. P. et al. 2007 Org. Biomol. Chem. 5: 31-44; Falciola, C. A. et al. 2008 Eur. J. Org. Chem. 22: 3765-3780; Miyaura, N. 2002 Top. Curr. Chem. 219: 11-59; Espinet, P. et al. 2004 Chem. Int. Ed. 43: 4704-4734; Fugami, K. et al. 2002 Top. Curr. Chem. 219: 87-130; Valente, C. et al. 2012 Chem. Int. Ed. 51: 3314-3332; Knochel, P. et al. 2001 J. Org. Chem. 7: 1261-1277; Chincilla, R. et al. 2011 Chem. Soc. Rev. 40: 5084-5121; Surry, D. S. et al. 2011 Chem. Sci. 2: 27-50; Hartwig, J. F. 2008 Acc. Chem. Res. 41: 1534-1544; Evano, G. et al. 2008 Chem Rev. 108: 3054-3131; Negishi, E. (editor) Handbook on Organopalladium Chemistry for Organic Synthesis, volume 1, 2003 John Wiley & Sons; 3424 pages; and Hoff, R. et al. (editors) Handbook of Transition Metal Polymerization Catalysts, 1.sup.st edition, Wiley Publishing, 575 pages, each of which is incorporated by reference herein in its entirety).

(24) The medical field is increasingly interested in determining the number and kinds of molecules such as metals found in patient biological samples. Heavy metals may enter the body in food, water, or air, or by absorption through the skin. Once in the body, they compete with and displace essential minerals such as zinc, copper, magnesium, and calcium, and interfere with organ system function. People may contact heavy metals in industrial work, pharmaceutical manufacturing, and agriculture. Metal contamination (e.g., lead, cobalt, cadmium, arsenic, mercury, and thallium) of the environment has been observed to be widespread, and requires assays for monitoring extent of these metals in various parts of the environment and in subjects. Metals have been found to damage reproductive, renal, cardiovascular, and nervous systems, and many procedures have been developed to concentrate and analyze metals in serum and urine samples from mammals.

(25) The compositions provided herein include at least one selenium-functional group, and are used in various embodiments as a component in a device or system to remove, bind, and/or concentrate the metals from or in these samples, such that, these metals subsequently can be identified and analyzed using techniques such as HPLC-MS.

(26) Without being limited by any particular theory or mechanism of action, it is here envisioned that systems, methods, compositions and kits described herein using selenium-containing functional groups to effectively bind to and scavenge metal ions and compounds from aqueous solutions and reactions mixtures are useful in systems for analysis of other molecules which are of interest in medicine and environmental areas including carbohydrates, nucleic acids and proteins, and monomeric components such as sugars, amino acids, lipids, and include also synthetic polymers and monomeric components. The chromatographic compositions, methods, kits, and devices herein are useful for purification, isolation, and analysis of wide range of organic molecules and inorganic molecules remaining after metals are selectively removed.

(27) The medium in various embodiments includes at least one selected from the group consisting of: silica, silica gel, alumina, polystyrene, agarose, modified polymeric resin, polymer fiber, cellulose, magnesium silicate, dextran, and starch. In a related embodiment, the medium is a substrate or nanoparticle that allows presentation of the selenium-containing functional group to selectively bind to the metal. In various embodiments, the medium includes at least one polymer that enhances a surface property of the medium. For example, the at least one polymer reduces non-specific binding of the selenium-containing functional group to non-metal components of the target. In a related embodiment, the polymer strengthens the medium against pressures encountered during binding of the metal to the selenium-containing functional group of the composition. See Grant et al., U.S. Pat. No. 7,335,306 issued Feb. 26, 2008; Sherrington et al., U.S. Pat. No. 7,332,086 issued Feb. 19, 2008; Burch et al., U.S. Pat. No. 7,250,388 issued Jul. 31, 2007; and Van Ness et al., U.S. Pat. No. 5,667,976 issued Sep. 16, 1997. In various embodiments, the medium or scaffold is cross-linked. See Kakodkar et al., U.S. Pat. No. 5,087,359 issued Feb. 11, 1992.

(28) In various embodiments, the selenium-containing functional group is linked to the medium by at least one spacer selected from the group of: a sulfur-containing functional group: (C.sub.1-C.sub.30)alkyl, (C.sub.1-C.sub.30)alkynyl, (C.sub.3-C.sub.12)carbocyclyl, (C.sub.1-C.sub.30)alkoxy, (C.sub.1-C.sub.30)heteroalkyl, (C.sub.6-C.sub.30)aryl, (C.sub.1-C.sub.30)heteroaryl, and (C.sub.6-C.sub.30)aryl(C.sub.1-C.sub.30)alkyl. For example, the selenium-containing functional group is linked to the medium by at least one spacer selected from the group consisting of: a sulfur-containing functional group: (C.sub.1-C.sub.18)alkyl, (C.sub.1-C.sub.18)alkoxy, (C.sub.1-C.sub.18)heteroalkyl, (C.sub.6-C.sub.10)aryl, (C.sub.1-C.sub.9)heteroaryl, and (C.sub.6-C.sub.10)aryl(C.sub.1-C.sub.6)alkyl. For example, the spacer includes a carbocycle, a perhaloalkyl, an alkenyl, a heterocyclyl, a heteroaryl, a heteroaralkyl, a substituted amino (e.g., mono-substituted and di-substituted), a sulfonyl, a sulfinyl, an acyl, a boronyl, a propyl group, or a benzyl group. In various embodiments, the medium and/or the spacer comprises at least one protecting group.

(29) The composition in various embodiments fours an analytical component of a chromatography system selected from: normal phase, reversed-phase, liquid, planar, column, flush, flash, thin layer, high performance liquid, gas, and solid phase extraction chromatography. The composition in a related embodiment forms a component of a dialysis system. In a related embodiment, the composition is used in an organic chemistry reaction scheme to remove the metal from a reagent and/or a product. For example, the composition is used to scavenge, recover, or remove a platinum catalyst or a rhodium catalyst. In various embodiments, the metal is a high value metal used in organic chemistry synthesis or cell culture processing.

(30) Structural characteristics of organic molecules and inorganic molecules differ in affinities and specificities of binding to alkyl-selenium-metal chromatographic media provided herein compared to metals. The selenium-containing media described herein retain the metals and do not bind other molecules remaining in a suspension, solution, mixture or material. Hence methods herein involve affinity separations that selectively bind metals and recover the metals from wash solutions the target molecules or compounds at different times relative to the metals. Thus, in certain embodiments the selenium-containing functional group media are used to bind and remove metal impurities and other undesired metals found in natural samples and synthetic mixtures, and to recover these metals if further desired.

(31) The chromatographic materials provided in examples herein are useful for a variety of products, and have wide application in different areas of organic chemistry such as environmental and pharmaceutical areas both for analytical and preparative chromatography. The selenium chromatographic media are useful in dialysis systems, solid phase extraction tubes, and in HPLC columns. For example, the dialysis system is a sterile system, and is used in hemodialysis, hemofiltration, hemodiafiltration, or peritoneal dialysis.

(32) In hemodialysis and hemofiltration, blood from a subject is impelled to flow at a slow rate through a special filter that removes wastes and extra fluids. The filtered (i.e., clean) blood is then returned to the subject. Removal of the harmful wastes and extra salt and fluids from the blood helps to control blood pressure and to keep the proper balance of electrolytes such as potassium and sodium in the body (Handbook Of Dialysis, 4th edition, 2007, editors John T. Daugirdas, Peter Gerard Blake, Todd S. Ing, Lippincott Williams & Wilkins pages 1-774; Alam U.S. Pat. No. 8,012,350 issued Sep. 6, 2011; and Beiriger, U.S. Pat. No. 8,425,780 issued Apr. 23, 2013, each of which is incorporated by reference herein in its entirety). The dialysis system in various embodiments herein includes a device for delivering extracorporeal blood to a hemodialyzer, blood filter or dialysis assembly that uses a dialysis solution (dialysate) including at least one pump to filter and purify the blood of the subject. The dialysis system monitors and/or controls blood-flow rate, arterial pressure, venous pressure, and provides anticoagulant delivery. In various embodiments, an isotonic replacement fluid is added to the blood to replace fluid volume and electrolytes. In various embodiments, at least one therapeutic agent or replacement electrolyte is added to the blood after detoxification using the media provided herein, and prior to being re-introduced to the subject. The system in various embodiments further includes a user/machine interface operably connected to the system for delivering extracorporeal blood (Connell et al. U.S. Pat. No. 7,318,892 issued Jan. 15, 2008).

(33) The selenium chromatographic media described in Examples herein are useful in peritoneal dialysis systems for treating subjects having conditions such as severe chronic kidney disease. Peritoneal dialysis in various embodiments uses a dialysis solution, also called dialysate, which is infused into a subject's peritoneal cavity using a device, e.g., a catheter or a syringe. In various embodiments, the dialysate is contacted to the peritoneal membrane of the peritoneal cavity (Ding et al., U.S. Pat. No. 8,404,091 issued Mar. 26, 2013). Waste, toxins and excess water pass from the patient's bloodstream, through the peritoneal membrane, and into the dialysate due to diffusion and osmosis, i.e., an osmotic gradient occurs across the membrane. The spent dialysate is drained from the subject in various embodiments, removing waste, toxins and excess water (Hopping et al., U.S. Pat. No. 8,403,880 issued Mar. 26, 2013).

(34) In vivo microdialysis sampling, during which little or no fluid is removed from or introduced into the system, involves implanting a tubular dialysis membrane at the site of interest then continuously perfusing the interior of the membrane with a solution similar in composition to the body fluid at that site. The dialysate containing chemicals, ions, molecules or metals which diffuse through the membrane are collected and analyzed using electrophoresis, immunoblotting, ELISA, chromatography (e.g., HPLC and size-exclusion chromatography), mass spectrometry, or absorbance (Kissinger, U.S. Pat. No. 5,706,806 issued Jan. 13, 1998). For example, capillary electrophoresis is a technique used to analyze biological mixtures as a small volume of the sample in a capillary tube interior is required (Liao et al., U.S. Pat. No. 5,766,435 issued Jun. 16, 1998). Separations on extremely small volumes, and at high speeds are performed.

(35) In various embodiments, a therapeutic agent added to blood after detoxification using dialysis, e.g., peritoneal dialysis. The therapeutic agent is added to the filtered fluid (e.g., blood) prior to re-introduction to the subject. In various embodiments, the therapeutic agent is selected from the group consisting of: anti-bacterial agent, anti-fungal agent, growth factors, anti-inflammatory agents, vasopressor agents including but not limited to nitric oxide and calcium channel blockers, collagenase inhibitors, topical steroids, matrix metalloproteinase inhibitors, ascorbates, angiotensin II, angiotensin III, calreticulin, tetracyclines, fibronectin, collagen, thrombospondin, transforming growth factors (TGF), keratinocyte growth factor (KGF), fibroblast growth factor (FGF), insulin-like growth factors (IGFs), IGF binding proteins (IGFBPs), epidermal growth factor (EGF), platelet derived growth factor (PDGF), neu differentiation factor (NDF), hepatocyte growth factor (HGF), vascular endothelial growth factor (VEGF), heparin-binding EGF (HBEGF), thrombospondins, von Willebrand Factor-C, heparin and heparin sulfates, and hyaluronic acid. See Toole et al. U.S. Pat. No. 5,902,795 issued May 11, 1999, which is incorporated by reference herein in its entirety.

(36) The therapeutic agent in various embodiments includes an anti-cancer or anti-tumor agent selected from the group of: alkylating agents, such as mechlorethamine, cyclophosphamide, melphalan, uracil mustard, chlorambucil, busulfan, carmustine, lomustine, semustine, streptozoticin, and decrabazine; antimetabolites, such as methotrexate, fluorouracil, fluorodeoxyuridine, cytarabine, azarabine, idoxuridine, mercaptopurine, azathioprine, thioguanine, and adenine arabinoside; natural product derivatives, such as irinotecan hydrochloride, vinblastine, vincristine, dactinomycin, daunorubicin, doxorubicin, mithramycin, taxanes (e.g., paclitaxel) bleomycin, etoposide, teniposide, and mitomycin C; and miscellaneous agents, such as hydroxyurea, procarbezine, mititane, and cisplatinum. See Brown et al. U.S. publication number 20050267069 published Dec. 1, 2005, which is incorporated by reference herein in its entirety.

(37) In other embodiments, the therapeutic agent is a cell, a compound, a composition, biological or the like that potentiates, stabilizes or synergizes the effects of the modulator or another molecule or compound on a cell or tissue. In some embodiments, the drug may include without limitation anti-tumor, anti-viral, antibacterial, anti-mycobacterial, anti-fungal, anti-proliferative or anti-apoptotic agents. Drugs that are included in the compositions of the invention are well known in the art. See for example, Goodman & Gilman's The Pharmacological Basis of Therapeutics, 9th Ed., Hardman, et al., eds., McGraw-Hill, 1996, the contents of which are herein incorporated by reference herein.

(38) Chromatographic media with a selenium-functional group provided herein are used in conjunction with various mass spectrometry methods such as electrospray ionization-mass spectrometry, for increased sensitivity for characterizing biomolecules, for example proteins and oligonucleotides as well as other high molecular weight compounds. Collisional induced dissociation methods have provided information on amino acid and nucleotide sequence and sites of damage or modification. Mass spectrometry has been more recently used for analysis of non-covalent complexes including oligonucleotide duplexes, quadruplexes, and DNA-protein complexes, and probing the higher order structure of proteins (Smith et al., U.S. Pat. No. 5,954,959 issued Sep. 21, 1999). Biological fluids contained in the extracellular spaces of living tissue, such as in the brain, other organs or subdermal tissue, often are sampled for research or diagnostic purposes. If sufficient fluid is available, it may be simply withdrawn and analyzed directly. However, in many embodiments, only small amounts of fluid are available and sampling is performed by indirect methods such as an ELISA, e.g., indirect fluorescent antibody (IFA) test. Thus, compositions and methods described herein are used for sensitive characterization of metals and biomolecules.

(39) Solid phase extraction tubes (SPE) tubes are used widely in various embodiments for rapid, manual or automated separation of metals and/or metal classes for example metals having different atomic masses. The media provided herein are suitable for HPLC columns and are useful for chromatographic resolution of organic compounds and to separate metals in the sample. Resolution and speed of normal-phase and reversed-phase HPLC are improved by use of the media prepared by methods herein compared to prior normal-phase media that afford only limited separation of metals from organic products and inorganic products. Compositions and methods using SPE tubes having a selenium-functionalized media are used to separate metals and other molecules.

(40) Chromatography is characterized by differing relative polarities of the mobile (liquid) and stationary (packing material) phases. Normal-phase chromatography involves a polar stationary phase, such as silanol on silica, and a relatively non-polar mobile phase, e.g., hexane and dichloromethane. Reversed-phase chromatography involves a non-polar stationary phase, often a hydrocarbon, and the mobile phase is relatively polar, e.g., water, methanol or acetonitrile. Generally in normal-phase chromatography, the least polar sample component is eluted first because it is most soluble in the non-polar mobile phase. Conversely, in reversed-phase chromatography, the most polar sample component is eluted first because it is most soluble in the polar mobile phase.

(41) A selenol functionalized silica gel is used herein for reversed-phase chromatography separations. The procedures for making C.sub.18 reversed-phase silica gel include imbedding the silver onto the silica gel thiol (3% to 5% surface coverage), and then covering the silica gel surface with C.sub.18 alkyl chain molecules. More than 90% of pharmaceutical chromatographic separations are performed using reserved-phase chromatography. Selenium functionalized silica gels as described herein have a major application in reversed-phase chromatography and thin layer chromatography.

(42) The term spacer, as used herein refers to a chemical moiety used in chemistry synthesis to influence chemical properties, for example reaction conditions, molecule stability, steric hindrance, and hydrophobicity. A spacer for example is a single atom (e.g., a carbon or heteroatom) or an functional group (e.g., an alkyl group) situated between a plurality of atoms or functional groups, such that the carbons atoms create additional space between the plurality of atoms or functional groups, thus reducing repulsive interaction (i.e., steric hindrance) between the plurality of atoms and functions groups. The term spacer is used herein interchangeably with the term linker.

(43) The phrase selenium-containing functional group, as used herein refers to a molecule or compound which has a molecular or compound structure that contains a selenium atom or selenium atom moiety. The selenium atom or moiety for example may have been attached by reaction with a functional group such as selenide, a selenol, or a selenolate.

(44) The phrase sulfur-containing functional group, as used herein refers to a molecule or compound which has a molecular or compound structure that contains a sulfur atom or sulfur atom moiety. The sulfur atom or moiety for example may have been attached by reaction with a functional group such as a thiol, a sulfide, and a disulfide. An exemplary sulfur-containing functional group is a thiol, however other sulfur containing functional groups are within the scope of the composition of the chromatographic media provided herein.

(45) The term derivative, as used herein refers to a chemically related form of a molecule or a compound having an additional substituent, for example, a different functional group or atom attached to an atom of the molecule.

(46) The term analog, as used herein refers to a chemically related form of a molecule or a compound having a different configuration, for example, an isomer, or a D-configuration rather than an L-configuration, or an molecule with the approximate size and shape of the molecule, or a molecule with modification to the atoms that are involved in a chemical bond, including for example to confer resistance to or to facilitate degradation, cleavage, addition, removal, and substitution.

(47) The term target, as used herein refers to a sample and its components, including a mixture, compound, solution, a colloid, suspension, gel, slurry, or solid having been exposed for containing or suspected of containing a metal or a plurality of metals. The selenium-containing media described herein is used to remove or scavenge the metal or plurality of the metals from the target. The media specifically bind to the metal and leave the remaining component(s) of the target within the sample. In various embodiments the target is a reaction mixture includes a catalyst. For example, the catalyst is a metal or metal compound. In a related embodiment, the target is a sample, mixture, compound, solution, suspension, gel, slurry, or solid at risk for exposure to or containing a metal or a plurality of metals. For example, the target is a biological sample from a subject having indicia/symptoms of metal poisoning.

(48) In various embodiments, the target includes a polycyclic aromatic hydrocarbon, an alkene, an alkenone, a triglyceride, a monoglyceride, a diglyceride, a wax ester, a steryl ester, a phthalate, a sterol, a steroid, a terpene, a terpenoid, a triterpernoid, a fatty acid, a lipid including a phospholipid and other complex lipid molecules, an oil, a sugar, an oligosaccharide, a polysaccharide, a carbohydrate, a protein, an amino acid, a fossil fuel, a natural or synthetic organic compound of pharmaceutical use, a petroleum-derived compound, a coal-derived compound, and a combination thereof found in a biological sample or an environmental sample.

(49) The target in various embodiments includes a biological sample, for example from a subject such as a human or animal. In various embodiments the biological sample is at least one of: an excretion or a secretion such as tears, saliva, urine, feces, perspiration, blood, lymph, serum, plasma, cerebrospinal fluid, bile, semen, vaginal fluid, breast milk, and amniotic fluids.

(50) For example the biological sample is from a plant, bacteria or archea, and is obtained by further separating techniques such as for example by solvent extraction. The target in various embodiments is an environmental sample for example: soil; water such as samples taken from a river, a glacier, an ocean and a lake; sediment; algal deposits; oil deposits; and fossil deposits including coal and tar, and atmospheric aerosols.

(51) Scavenging as used herein refers to any salvaging, cleaning, or removing of a metal from an area, a solution, or a material. In certain embodiments scavenging involves, after contacting a target, further extracting, salvaging or separating a high value metal (e.g., gold and/or silver) from the target so as to recover the metal for further use. Alternatively, scavenging involves removing an unwanted metal from the target such that the target without the metal may be used. For example, scavenging in certain embodiments involves removing toxic metals, unwanted by-product metals, or catalyst metals from the target, such as from a pharmaceutical composition, a container, an aqueous layer, an organic layer, and a drinking-water source. In certain embodiments, the target includes an aqueous solution, suspension, or complex mixture. Scavenging includes without limitation removal of toxic metals from a patient by combining the media provided herein with standard blood dialysis procedures.

(52) Aqueous solution as used herein pertains to or relates to a sample that is wholly or partially being dissolved in water. For example, the percent water in the aqueous solution is at least about 10%, at least about 20%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 90%, at least about 95%, or at least about 99% water. For example the aqueous solution is a water sample in need of determination of presence of one or more metals, or the aqueous solution is a previously used treatment fluid such as processing or cleaning water that is in need of treatment for compliance or disposal.

(53) In various embodiments, the selenium-containing functional group is linked to the medium or the scaffold by at least one spacer selected from the group of: a sulfur-containing functional group: (C.sub.1-C.sub.30)alkyl, (C.sub.1-C.sub.30)alkynyl, (C.sub.3-C.sub.12)carbocyclyl, (C.sub.1-C.sub.30)alkoxy, (C.sub.1-C.sub.30)heteroalkyl, (C.sub.6-C.sub.30)aryl, (C.sub.1-C.sub.30)heteroaryl, and (C.sub.6-C.sub.30)aryl(C.sub.1-C.sub.30)alkyl. For example, the selenium-containing functional group is linked to the medium by at least one spacer selected from the group consisting of: a sulfur-containing functional group: (C.sub.1-C.sub.18)alkyl, (C.sub.1-C.sub.18)alkoxy, (C.sub.1-C.sub.18)heteroalkyl, (C.sub.6-C.sub.10)aryl, (C.sub.1-C.sub.9)heteroaryl, and (C.sub.6-C.sub.10)aryl(C.sub.1-C.sub.6)alkyl. For example, the spacer includes a carbocycle, a perhaloalkyl, an alkenyl, a heterocyclyl, a heteroaryl, a heteroaralkyl, a substituted amino (e.g., di-substituted and tri-substituted), a sulfonyl, a sulfinyl, an acyl, a boronyl, a propyl group, or a benzyl group. In various embodiments, the medium and/or the spacer comprises at least one protecting group. See Handbook of Chemistry and Physics, 94.sup.th edition, 2013; editor W. M. Haynes, Taylor and Francis Group Publishing, Boulder Colo.; Organic Chemistry, 1999, editor Thomas Sorrell, University Science Books, Sausalito; March's Advanced Organic Chemistry, 5th edition, 2001, editors Michael B. Smith et al., John Wiley & Sons, Inc., New York; Comprehensive Organic Transformations, 1989, author Richard C. Larock, VCH Publishers Inc., New York, N.Y.; and Modern Methods of Organic Synthesis, 4th Edition, 2004, authors William Carruthers et al., Cambridge University Press, Cambridge, UK, each of which is incorporated by reference herein in its entirety.

(54) Examples herein show methods of preparing selenolate silica gels having a variety of linkers or spacers for attachment of the selenium functional group to the silica gel, for example a propyl (three carbons) group separating the silicon from the selenium respectively. The length of the aliphatic carbon chain alters the affinity properties of the silica. Accordingly, different functionalized silica gels are synthesized in examples herein by using as starting materials each of several different carbon spacer lengths, e.g., spacers having from 1 to 20 carbons. Possible spacers include alkyl and aryl structures and include heteroatoms and functional groups bonded to the carbon chains, for example oxygen, nitrogen, phosphorus, nitrile groups, di-thiol groups, thioester groups, carbonyl groups, and hydroxyl groups.

(55) In various embodiments, the composition containing the selenium-containing functional group is disposable. Alternatively, the composition is re-usable. In various embodiments, the composition containing the selenium-containing functional group bound to the metal is treated to remove the bound metal. In various embodiments, the method involves applying a fluid or material that disrupts a complex or binding between the metal and the selenium functional group. For example the fluid or material includes at least one of an acid or an oxidizing agent. See Rosenberg et al., U.S. patent publication number 20040000523 published Jan. 1, 2004.

(56) In various embodiments, removing the metal includes drying or heating the medium or the scaffold. In various embodiments, removing includes directing wavelengths of energy (e.g., microwaves and radiation) to the medium or the scaffold, or a using magnetic material (e.g., beads). In various embodiments, removing includes separating by size the metal and/or the other components of the target. In various embodiments, removing includes applying a flow of a fluid (e.g., a gas or a liquid). See Vladimir, U.S. Pat. No. 8,123,041 issued Feb. 28, 2012; Vorpahl, U.S. Pat. No. 5,770,388 issued Jun. 23, 1998; and Bai et al., U.S. patent publication number 20120272791 published Nov. 1, 2012, each of which is incorporated by reference herein in its entirety.

(57) In various embodiments, after removing the metal, the composition is treated (i.e., regenerated or recharged), such that the composition can be re-used. For example regenerating or recharging the composition includes filtering, screening, heating, or drying. See Fortier et al., U.S. Pat. No. 6,248,683 issued Jun. 19, 2001.

(58) In various embodiments of the method, the metal is a catalyst, and the method includes after removing, regenerating the metal catalyst. For example, the regenerating the metal catalyst includes using an adsorption medium or a complexing agent, for example an organo-complexing agent. In various embodiments, the complexing agent is selected from the group consisting of: an aliphatic and/or aromatic mono, di, and/or tribasic carboxylic acid, a polyacrylate, a polymethacrylate, a polyvinybenzoate, a polyvinylsulfate, a polyvinyl sulfonate, a polybiphenol carbonate, a polybenizimidazole, a polyvinylpyrrolidone, a polypyridine, an ethylene diaminc, a propylene diaminc, a diethylenetriamine, a triethylenetctraamine, a diethylenetriamine pentaccetic acid (DTPA), a N-Qiydroxyethyl)-ethylenediaminetriacctic acid (HEDTA), an amino tri(methylanephosphonic acid) (ATMP), a 1-Hydroxy-1,1-diphosphonic acid (HEDP), a diethylenetriamine penta (methylphosphonic) acid, or a salt or combination thereof. See Zhou et al., U.S. Pat. No. 6,908,873 issued Jun. 21, 2005; and Sechrist, U.S. Pat. No. 6,790,802 issued Sep. 14, 2004. In general, the method described herein includes in various embodiments, after removing, analyzing for presence of the metal in the remaining material using instrumental analysis. See Skoog et al. 2006 Principles of Instrumental Analysis (sixth edition) Brooks Cole Publishing chapter 28.

(59) In various embodiments, analyzing involves at least one technique or measurement selected from: spectrometry, absorbance, transmittance, and spectroscopy. For example, analyzing involves atomic absorption spectrometry, inductively coupled plasma mass spectrometry, anodic stripping voltammetry, X-ray fluorescence spectrometry, and microprobes. See Bannon, D. I. et al. 2001 Clin. Chem. 47 (9): 1703-1704; Liu, H. W. et al. 1999 Spectrochim. Acta, Part B 54 (9): 1367-1375; Yang, W. R. et al. 2003 Analyst 128 (6): 712-718; Baldo, M. A. et al. 2004 Electroanalysis 16 (5): 360-366; Eksperiandova, L. P. et al. 2002 X-ray Spectrom. 31 (3): 259-263; Arai, Y. et al. 2003 Environ. Sci. Technol. 37 (18): 4083-4090; Burdette, S. C. et al. 2003 J. Am. Chem. Soc. 2003, 125 (7), 1778-1787. Wu, X. Q. et al. 2000 Biotechnol. Prog. 16 (3): 513-516; Darwish, I. A. et al. 2002 Anal. Chem. 74 (1): 52-58; Godwin, H. 2000 J. Am. Chem. Soc. 122 (1): 174-175; Yang, W. R. et al. 2001 Chem. Commun. 19: 1982-1983; Shults, M. D. 2003 J. Am. Chem. Soc. 125 (35): 10591-10597; Mlynarz, P. et al. 2002 New J. Chem. 26 (2): 264-268; Shetty, R. S. et al. 2001 Abstr. Pap. Am. Chem. S. 221: U92-U92; Lu, Y. et al. 2003 Biosens. Bioelectron. 18 (5-6): 529-540; and Chinowsky, T. M. et al. 1996 Sens. Actuators B 35 (1-3): 37-43, each of which is incorporated by reference herein in its entirety.

(60) Compositions, methods and kits are described herein for removing, recovering and/or scavenging a metal using a selenium-containing functional group attached or covalently linked to a medium, scaffold, or bead. In certain embodiments, the medium which may be considered to be a scaffold, or a bead, or a silica, for example as shown in FIG. 1 panels A-B and FIGS. 3-4.

(61) The following examples and claims are illustrative and are not meant to be further limiting. Those skilled in the art will recognize or be able to ascertain using no more than routine experimentation, numerous equivalents to the specific procedures described herein. Such equivalents are within the scope of the present invention and claims. The contents of all references including issued patents, published patent applications and non-patent literature references cited in this application are hereby incorporated by reference herein in their entireties.

Examples

Example 1

Synthesis of a Propylselenol Trimethoxysilane

(62) Organoselenium compounds form a more stable complex with silver (I) than organosulfur compounds (Pettit et. al. 1967 Chem. Commun. 1179-1180; and Kreif et al. 1985 Tetrahedron. 41(21): 4793-4812). Methods for preparing an organoselenium compound bound to silica surface that binds more effectively to metals than organosulfur compounds are illustrated in the Examples herein.

(63) A 3-bromopropyltrimethoxysilane was reacted with potassium selenocyanate (KSeCN) in acetone and then reacted with sodium borohydride (NaBH.sub.4) in ethanol to yield a propylselenol trimethoxysilane (FIG. 1 panel A).

(64) The reactions shown in FIG. 1 panel A were performed by combining 3-bromopropyl functionalized silica (5.0 grams; g) and dimethylformamide (DMF; 30 milliliters) in a 250 mL three-necked flask fitted with a mechanical stirrer and a condenser. The solution was heated to 80 C. under an argon gas flow. Potassium selenium cyanide (1.42 g; approximately 1.4 molar equivalents) dissolved in DMF (30 milliliters; mL) was added slowly to the flask. The solution was stirred for four hours at 80 C. The resulting 3-seleniumcyanide-propyl functionalized silica was filtered using a vacuum filtration apparatus and was washed using three washes each of DMF and then methanol sequentially (50 mL per wash). The 3-seleniumcyanide-propyl functionalized silica was placed in a two-necked flask containing anhydrous dry ethanol (50 mL) and a mechanical stirrer. The silica was stirred and cooled to 0 C. Sodium borohydride (0.37 g; approximately molar 1.5 equivalents) in 30 mL of ethanol was added slowly to the flask and the solution was stirred for one hour at 0 C. The solution equilibrated to room temperature for one hour, and the solution was hydrolyzed three times using 10% aqueous hydrochloric acid solutions (15 mL each). The resulting 3-selenopropyl silica was filtered using a vacuum filter flask and was washed with water and ethanol sequentially (three washes each; 50 mL per wash). Elemental analysis of the reaction product shown in FIG. 1 panel A showed that the nitrogen content was not detected.

Example 2

Synthesis of a Benzylesterselenol Trimethoxysi Lane

(65) Methods for synthesizing a benzylesterselenol trimethoxysilane are shown in Examples herein. The synthesis involves reacting 3-hydroxypropyltrimethoxysilane with a selenium benzyl ester under acidic conditions to yield 3-hydroxypropyltrimethoxysilane, a selenol silane with an aromatic ring (FIG. 1 panel B).

(66) The reactions herein show multiple methods of preparing selenolate materials that effectively bind metals. The systems, methods, compositions and kits using selenium-containing functional groups effectively metal ions and compounds from a target (FIG. 2), for example the target includes an aqueous solution or a reaction mixture.

(67) Chromatographic media including the selenium-containing functional groups described herein are stable during storage at temperatures below or at room temperature, and in the light and are reusable. Transition metals including platinum, nickel, gold and silver in solutions and mixtures are bound to the selenium containing functional groups on the medium. Separation components including selenolate chromatographic material produce accurate, reproducible and reliable separations, products and data for small-scale assays and diagnostic kits.

Example 3

Synthesis of a Selenoether Functionalized Silica

(68) Methods for synthesizing a selenoether functionalized silica are shown in FIG. 3. A solution of dimethyldiselenide (1.04 g, 5.5 millimoles) in 50 mL of ethanol was prepared and stirred at room temperature under a nitrogen gas flow. An aliquot of sodium borohydride (0.43 g, 11 millimoles) was added drop-wise to the solution and stirred for three hours. An amount of 3-propylchloride functionalized silica gel (4.65 g) was added to the solution and the resulting slurry was refluxed for 24 hours. The slurry was cooled, filtered and washed five times with 20 mL distilled water then rinsed three times with 20 mL ethanol. The slurry was dried under vacuum.

Example 4

Synthesis of a Benzylesterselenol Functionalized Silica

(69) Methods are shown for synthesizing a silica having a benzyl moiety bound to a selenium functional group. Synthesis of a benzylesterselenol in FIG. 4 was performed by a nucleophilic substitution reaction. Potassium selenium cyanide was reacted with a halogenated 1-(halogen methyl)-4-propylbenzene functionalized silica.

(70) Without being limited by any particular theory or mechanism of action, it is here envisioned that a methylene spacer could be chemically inserted between the selenium and the benzene in various embodiments to produce a functionalized silica that is effective to bind to and scavenge metal.

Example 5

Separation and Scavenging of Metals Using Selenium-Containing Chromatographic Material

(71) The selenium-functionalized media described herein are tested to determine ability to effectively scavenging and capturing transition metals that are used as catalyst during drug synthesis. Palladium is a common catalyst used for drug synthesis, and has been detected in trace amounts in products based on small-molecule active pharmaceutical ingredients (API).

(72) The systems, methods, compositions and kits using the selenium-functionalized media described above are at least one order of magnitude more efficient on a weight basis, for recovering and extracting metals than thiol based silica gels. The selenium-functionalized media produces at least ten-fold less waste and is requires a ten-fold smaller volume, which is important for industrial metal scavenging facilities to process materials from a target material.

(73) Further separations and scavenging analyses are performed with the selenium-functionalized media to determine the ability to scavenge transition metals such as platinum at different concentrations and percentages from a target. The compositions, methods and kit using the selenium-functionalized media are used to recover, separate, and/or scavenge platinum and transitions metals such as silver, palladium, nickel and gold from organic chemistry reaction mixtures and samples.

Example 6

Detection of Metals in Biological Samples Using a Device with a Selenium-Containing Functional Group

(74) Point-of-care devices and methods are shown herein for detecting presence of toxic heavy metals in biological samples from subjects. See Principles and Practice of Point-of-Care Testing (1st edition), 2002, editor Gerald J. Kost, publisher Lippincott Williams & Wilkins, pages 1-672, which is incorporated by references herein in its entirety.

(75) A blinded study is performed using subjects from a population environmentally or industrially exposed to toxic heavy metals, and control subjects from a different population not exposed to the metals. Biological samples (i.e., urine and serum) are collected from the subjects and randomly assigned numbers such that subsequent testers using assay devices are unaware of presence or absence of the metals in samples, i.e., samples are analyzed by a double blind protocol.

(76) Assay devices are prepared containing a housing which contains nitrocellulose media allowing for capillary action by the biological samples, a sample application area, a detection area, and a control area. Each sample is tested using an individual assay device. The sample is added to a sample application area having a gold labeled anti-human antibody. The sample flows over the nitrocellulose media to the detection area. The detection area contains a composition including a selenium-containing functional group which reacts and/or binds with the metal to form a visible band or mark. Control samples from subjects not exposed to metal are also analyzed by the devices.

(77) The samples flows to a control area that is distal to detection the detection area, which identifies that the sample flowed through the test zone and thus is a control for the operation of the device. The control area in various embodiments includes an antibody that visibly detects a marker of the sample. The antibody in the control area binds to the marker that is bound to the gold-labeled anti-human antibody from the sample application area. For example, the antibody in the control area is an anti-human immunoglobulin produced by an animal host.

(78) Data show that the assay devices are effective for detecting extremely small quantities of a toxic metal in a biological sample. The devices that analyze metal-containing biologically samples specifically bind the metal and provide highly efficient selectivity and sensitivity compared to other analyzed devices.

Example 7

Removal of Toxic Metals Using a Selenium-Containing Dialysis System

(79) A dialysis system is used to determine whether the selenium-functionalized medium is effective to bind and remove metals from a biological sample circulating from and to a living subject. The system includes a needle for obtaining blood from the subject. The system includes monitors for calculated the subject's temperature, blood pressure and heart rate prior to, during and after the dialysis procedure (Handbook Of Dialysis, 4th edition, 2007, editors John T. Daugirdas et al., Lippincott Williams & Wilkins Publishing, pages 1-774, which is incorporated by reference herein in its entirety).

(80) The needle is connected to an inlet tube. The inlet tube transmits the samples from the needle to a proximal end of a dialysis assembly including a porous membrane and an atoxic selenium-functionalized media for binding a metal in the sample. The blood is introduced into the dialysis assembly using a pump lying between the needle and the dialysis assembly. A dialysis buffer is applied to the membrane with the selenium-functional group containing medium in the dialysis assembly and outside the membrane, to facilitate removal of metal contaminants and solutes that are at an undesirable concentration. The distal end of the dialysis assembly includes an outlet tube that takes the dialyzed blood from which the metal contaminants have been removed to be re-introduced into the subject.

(81) Data show that the dialysis assembly having the membrane and the selenium-functionalized media is effective for selectively removing toxic materials and metals, and excess water from the blood in subjects having conditions such as renal failure caused by uremia or acidemia.