Crystalline lanthanum-carboxylate coordination polymers and their use

Abstract

The present invention relates in a first aspect to a method of preparing a crystalline lanthanum-carboxylate coordination polymer and the crystalline lanthanum-carboxylate coordination polymer obtained or obtainable by the method. In another aspect of the present invention, also provides a method of detecting a target nucleic acid sequence in a sample.

Claims

1. A method of preparing a crystalline lanthanum-carboxylate coordination polymer, that method comprises steps of: (i) preparing a mixture comprising lanthanum ions and a pyridyl ligand which pyridyl ligand is a quaternized carboxylate pyridyl ligand and optionally subjecting the mixture to conditions under which a precipitate is formed and separating the precipitate; wherein the pyridyl ligand has a structure of Formula (V): ##STR00026## wherein X is Br, Cl, or I; (ii) subjecting the mixture of step (i) or the precipitate of step (i) to conditions under which crystals of the lanthanum-carboxylate coordination polymer are formed; (iii) separating the crystals of the lanthanum-carboxylate coordination polymer from the mixture.

2. The method of claim 1, wherein step (i) comprises steps of: a) preparing a first pre-mixture comprising mixing the pyridyl ligand and a solvent; b) preparing a second pre-mixture comprising mixing a lanthanum salt and a solvent; c) adding the second pre-mixture to the first pre-mixture.

3. The method of claim 2, wherein the lanthanum salt is a hydrate of La(NO.sub.3).sub.3 and wherein both of the solvent in step a) and the solvent in step b) independently comprise an aliphatic alcohol, water or a mixture thereof.

4. The method of claim 1 comprising steps of: (i) preparing a mixture comprising lanthanum ions and a pyridyl ligand which pyridyl ligand is a quaternized carboxylate pyridyl ligand and subjecting the mixture to conditions under which a precipitate is formed and separating the precipitate; (ii) subjecting the precipitate of step (i) to conditions under which crystals of the lanthanum-carboxylate coordination polymer are formed; (iii) separating the crystals of the lanthanum-carboxylate coordination polymer from the mixture; and wherein step (ii) comprises steps of: a) adding a solvent, which solvent comprises water to the precipitate at a temperature of between about 20 C. and about 30 C.; b) allowing the mixture after step a) to stand at a temperature between about 20 C. and about 30 C. for at least about 72 hours for forming crystals of the lanthanum-carboxylate coordination polymer.

5. The method of claim 4, wherein subjecting the mixture to conditions under which a precipitate is formed in step (i) comprises stirring the mixture for between about 15 min and about 60 min for forming the precipitate and the precipitate is separated by filtration, and wherein step (i) further comprises a step of purifying the precipitate by washing with a washing solvent comprising an aliphatic alcohol.

6. The method of claim 1 comprising steps of: (i) preparing a mixture comprising lanthanum ions and a pyridyl ligand which pyridyl ligand is a quaternized carboxylate pyridyl ligand; (ii) subjecting the mixture of step (i) to conditions under which crystals of the lanthanum-carboxylate coordination polymer are formed; (iii) separating the crystals of the lanthanum-carboxylate coordination polymer from the mixture; wherein step (ii) comprises steps of: a) stirring the mixture at a temperature of at least about 80 C. for about 15 min to about 60 min; b) filtering the mixture for obtaining a filtrate and a residue; c) allowing the filtrate to stand at a temperature of between 20 C. and 30 C. for at least about 72 hours for forming crystals of the lanthanum-carboxylate coordination polymer.

7. The method of claim 1, wherein step (iii) comprises steps of: a) separating the crystals from the mixture; b) purifying the crystals; c) drying the crystals.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

(2) FIGS. 1A, 1b, and 1C shows powder X-ray diffraction (PXRD) patterns of compounds 1 and 2 showing agreement among the simulated, as-synthesized and of the compounds immersed in H.sub.2O for 48 h and the weight loss of compounds 1 and 2 in percentage in a thermogravimetric analysis. FIG. 1A shows the PXRD pattern of compound 1. FIG. 1B shows the PXRD pattern of compound 2. FIG. 1C shows the weight loss of compounds 1 and 2 under various temperatures.

(3) FIGS. 2A, 2B, 2C, and 2D illustrate the coordination environment (La(1) (FIG. 2A), La(2) (FIG. 2C)) and coordination geometry (La(1) (FIG. 2B), La(2) (FIG. 2D)) of La(III) ions in compound 1. Only carboxylate groups and La(III) ions (FIGS. 2A and 2C) or only oxygen atoms and La(III) ions were kept for clarity. Color codes: La(1) (dark red), La(3) (teal), O (red), C (black).

(4) FIG. 3A illustrates the linking of the Cmdcp ligand in the asymmetric unit to four La(III) centers in a different fashion. Color codes: La(1) (dark red), La(2) (teal), La(3) (blue), O(red), C (black).

(5) FIG. 3B illustrates the 3D structure of compound 1 viewed down the c axis and the free H.sub.2O was omitted for clarity. Color codes: La (green), O(red), C (black).

(6) FIG. 4 shows the one-dimensional chain of La(III) units with only the La(III) ions, bridging carboxylate moieties containing ligands and coordination water molecules shown for clarity. Color codes: La (teal), O(red), N (blue), C (black).

(7) FIGS. 5A and 5B illustrate the structure of compound 2 showing the 2D plane structure and the plicated net while imagining Cbdcp ligands as the netting twine. Color codes: La (teal), O(red), N (blue), C (black).

(8) FIGS. 6A and 6B show fluorescence spectra of P-DNA (50 nM) incubated with compound 1 or 2 with varying concentrations. Inset: plot of the fluorescence intensity at 518 nm versus the concentrations of the compounds. FIG. 6A shows the fluorescence spectra of P-DNA incubated with compound 1. FIG. 6B shows fluorescence spectra of P-DNA incubated with compound 2.

(9) FIGS. 7A and 7B show the fluorescence quenching efficiency of the P-DNA (50 nM) by compounds 1, 2, La(NO.sub.3).sub.3, H.sub.3CbdcpBr, and H.sub.3CmdcpBr at varying concentrations and at the fixed concentration of 50 M in 100 M Tris-HCl buffer (pH 7.4) at room temperature. FIG. 7A shows the fluorescence quenching efficiency of the P-DNA by compounds 1, 2, La(NO.sub.3).sub.3, H.sub.3CbdcpBr, and H.sub.3CmdcpBr at varying concentrations. FIG. 7B shows the fluorescence quenching efficiency of the P-DNA (50 nM) by compounds 1, 2, La(NO.sub.3).sub.3, H.sub.3CbdcpBr, and H.sub.3CmdcpBr at the fixed concentration.

(10) FIGS. 8A and 8B show the fluorescence intensity of P-DNA@1 (50 nM/45 M) or P-DNA@2 (50 nM/40 M) in the presence of target SUDV RNA sequences T.sub.20 (25 nM) of varying incubation time. Insets: plots of fluorescence intensity at 518 nm versus the incubation time for target SUDV RNA sequences T.sub.20. FIG. 8A shows the fluorescence intensity of P-DNA@1. FIG. 8B shows the fluorescence intensity of P-DNA@2.

(11) FIGS. 9A and 9B show the fluorescence spectra of the P-DNA@compound system (50 nM/45 M for P-DNA@1 and 50 nM/40 M for P-DNA@2) incubated with T.sub.20 of varying concentrations. Inset: plot of the fluorescence intensity at 518 nm versus the concentrations of T.sub.20. FIG. 9A shows the fluorescence intensity of P-DNA@1. FIG. 9B shows the fluorescence intensity of P-DNA@2.

(12) FIGS. 10A, 10B, 10C, and 10D show the fluorescence recovery of P-DNA@1 (50 nM/45 M) or P-DNA@2 (50 nM/40 M) systems by target T.sub.20, T.sub.30, T.sub.40, T.sub.1, T.sub.2 and T.sub.40A at the fixed concentration of 50 nM or at varying concentrations. FIG. 10A shows the fluorescence recovery of P-DNA@1 systems by target T.sub.20, T.sub.30, T.sub.40, T.sub.1, T.sub.2 and T.sub.40A at the fixed concentration. FIG. 10B shows the fluorescence recovery of P-DNA@1 systems by target T.sub.20, T.sub.30, T.sub.40, T.sub.1, T.sub.2 and T.sub.40A at varying concentrations. FIG. 10C shows the fluorescence recovery of P-DNA@2 systems by target T.sub.20, T.sub.30, T.sub.40, T.sub.1, T.sub.2 and T.sub.40A at the fixed concentration. FIG. 10D shows the fluorescence recovery of P-DNA@2 systems by target T.sub.20, T.sub.30, T.sub.40, T.sub.1, T.sub.2 and T.sub.40A at varying concentrations.

(13) FIGS. 11A and 11B show the fluorescence anisotropy changes of P-DNA (P) P-DNA@T.sub.20 (P@T.sub.20, 50 nM/50 nM) before and after the addition of compound 1 (45 M) or 2 (40 M). FIG. 11A refers to compound 1. FIG. 11B refers to compound 2.

(14) FIGS. 12A and 12B refer to a gel electrophoresis of P-DNA (P, 50 nM), P-DNA@T.sub.20 (P@T.sub.20, 50 nM/50 nM) before and after the addition of compound 1 (45 M) or 2 (40 M). FIG. 12A refers to compound 1. FIG. 12B refers to compound 2.

DETAILED DESCRIPTION OF THE INVENTION

(15) Unless otherwise defined, all technical terms used herein have the same meaning as commonly understood by one skilled in the art to which the invention belongs.

(16) As used herein, comprising means including the following elements but not excluding others. Essentially consisting of means that the material consists of the respective element along with usually and unavoidable impurities such as side products and components usually resulting from the respective preparation or method for obtaining the material such as traces of further components or solvents. The expression that a material is a certain element as used herein such as that a solvent is water or the like means that the material essentially consists of said element. As used herein, the forms a, an, and the, are intended to include the singular and plural forms unless the context clearly indicates otherwise.

(17) The present invention provides a method of preparing a crystalline lanthanum-carboxylate coordination polymer.

(18) Said term lanthanum-carboxylate coordination polymer refers to a compound comprising and in particular essentially consisting of repeating lanthanum-carboxylate coordination entities. A coordination entity possesses a lanthanum ion bound to other atoms or groups of components referenced as ligands. The term ligands refers to the components with groups or atoms bound to the lanthanum ion, thereby the lanthanum ion usually occupies a central position in said coordination entity. The term carboxylate as used herein indicates that the ligands have one or more carboxylic acid moieties and are preferably bound to the lanthanum ion through one or more of their carboxylic acid moieties.

(19) Preferably, the crystalline lanthanum-carboxylate coordination polymer comprises and in particular essentially consists of repeating coordination entities extending in two dimensions forming a 2D coordination structure, i.e. the coordination polymer comprises and in particular is a 2D coordination polymer, or extending in three dimensions forming a 3D structure, i.e. the coordination polymer comprises and in particular is a 3D coordination polymer.

(20) The expression essentially consisting of in relation to the crystalline lanthanum-carboxylate coordination polymer does not exclude that further ions such as NO.sub.3.sup. ions from the preparation process or water molecules are still present in the coordination polymer.

(21) The lanthanum-carboxylate coordination polymer prepared according to the method of the present invention is crystalline, which shall mean that the atoms or molecules are substantially organized in a structure known as a crystal. Said term is generally used in the art for any structure of ions, molecules, or atoms that are held together in an ordered arrangement. A crystalline structure is one of two types of structural ordering of atoms, ions or molecules the other being the amorphous structure which is irregular and lacks an orderly arrangement of structural units. Whether a compound is crystalline and the respective crystal system can, for example, be confirmed by means of X-ray diffraction. Preferably, the crystalline lanthanum-carboxylate coordination polymer comprises and in particular essentially consists of crystals possessing monoclinic or hexagonal space groups.

(22) The method of the present invention comprises steps of:

(23) (i) preparing a mixture comprising lanthanum ions and a pyridyl ligand which pyridyl ligand is a quaternized carboxylate pyridyl ligand and optionally subjecting the mixture to conditions under which a precipitate is formed and separating the precipitate;

(24) (ii) subjecting the mixture of step (i) or the precipitate of step (i) to conditions under which crystals of the lanthanum-carboxylate coordination polymer are formed;

(25) (iii) separating the crystals of the lanthanum-carboxylate coordination polymer from the mixture.

(26) The lanthanum in the crystalline lanthanum-carboxylate coordination polymer is preferably of the oxidation state +3.

(27) The feature that the mixture comprises the pyridyl ligand as used herein is to be understood to cover any protonated or deprotonated form of said pyridyl ligand due to the presence of further components in the mixture added, for example, for dissolving it.

(28) The term pyridyl ligand as used herein generally refers to a ligand comprising at least one optionally substituted pyridine ring.

(29) The pyridyl ligand is a pyridyl ligand which has one or more carboxylic acid moieties, which means herein one or more free carboxylic acid functions. More preferably, the pyridyl ligand is a pyridyl ligand which has two or more and in particular which has three carboxylic acid moieties, i.e. three free carboxylic acid functions.

(30) The one or more, in particular three, carboxylic acid moieties are directly or indirectly attached to the at least one pyridine ring. The term quaternized as used herein means that the pyridyl ligand has at least one quaternary ammonium salt group, i.e. at least one positively charged moiety comprising a nitrogen atom, which nitrogen atom binds to carbon atoms via four covalent bonds. In particular, the pyridyl ligand is a zwitterionic quaternized carboxylate pyridyl ligand, i.e. is a molecule with both positive and negative charges.

(31) The first pyridyl ligand preferably has a structure of Formula (I):

(32) ##STR00006##
wherein X is a halogen, in particular selected from Cl, Br or I and most preferably Br. Two of R.sup.1 to R.sup.5 area group of Formula (II):

(33) ##STR00007##
m is an integer and selected from 0, 1 or 2, in particular m is selected from 0 or 1 and most preferably m is 0, e. the carboxylic acid moieties are directly attached to carbon atoms of the pyridine ring. The other of R.sup.1 to R.sup.5 are hydrogen. Preferably, R.sup.2 and R.sup.4 are a group of Formula (II) each and R.sup.1, R.sup.3 and R.sup.5 are hydrogen.

(34) L is a linking group selected from an alkyl group, an aralkyl group, an alkaryl group, an alkarylalkyl group or an aryl.

(35) The term alkyl group as used herein refers to saturated, straight-chain or branched hydrocarbons which may, for example, contain between 1 and 20 carbon atoms such as 1 to

(36) ##STR00008##
5 carbon atoms. In particular, the alkyl group has a structure of with n being an integer and selected from 0, 1, 2 or 3.

(37) An aralkyl group means an aryl with an alkyl substituent, and the term alkaryl refers to an alkyl group with an aryl as substituent. An alkarylalkyl group means an alkyl group substituted with an aryl which aryl is substituted with an alkyl.

(38) The term aryl as used herein, refers to an aromatic mono- or polycyclic ring system, of which all the ring atoms are carbon, and which ring system has a maximum number of double bonds, in particular a delocalized, conjugated 7-electron system. A preferred aryl is benzene (or phenyl).

(39) L is preferably selected from

(40) ##STR00009##
with n and n being an integer and independently selected from 0, 1, 2 or 3.

(41) Further preferred, L is selected from

(42) ##STR00010##
with n and n being an integer and independently selected from 0, 1, 2 or 3. n is more preferably selected from 1 or 2, in particular it is 1. n is more preferably selected from 0 or 1 and is in particular 0, i.e. the carboxylic acid moiety is directly attached to the benzene ring.

(43) L is most preferably selected from

(44) ##STR00011##
with n being 1 or

(45) ##STR00012##
with n being 1 and n being 0.

(46) The pyridyl ligand has more preferably a structure of Formula (III):

(47) ##STR00013##
with X and L being as defined above.

(48) In particular embodiments of the present invention, the pyridyl ligand has a structure of Formula (IV):

(49) ##STR00014##
with X being as defined as above, in particular being Br.

(50) In alternative embodiments of the present invention, the pyridyl ligand has a structure of Formula (V):

(51) ##STR00015##
with X being as defined as above, in particular being Br.

(52) Step (i) preferably comprises steps of: a) preparing a first pre-mixture comprising mixing the pyridyl ligand and a solvent; b) preparing a second pre-mixture comprising mixing a lanthanum salt and a solvent; c) adding the second pre-mixture to the first pre-mixture.
The pyridyl ligand can be in form of a powder.

(53) The solvent in step a) and step b) preferably comprises an aliphatic alcohol, water or a mixture of both. The term aliphatic alcohol as used herein means an aliphatic hydrocarbon, preferably a branched or straight chain alkane, wherein at least one hydrogen atom of the aliphatic hydrocarbon is substituted with a hydroxyl group, preferably one hydrogen atom is substituted with a hydroxyl group referenced as monohydric aliphatic alcohol. More preferably, the aliphatic alcohol is a monohydric aliphatic alcohol, still more preferably a monohydric alcohol with 1 to 3 carbon atoms, further preferably with 1 to 2 carbon atoms. More preferably, the aliphatic alcohol is methanol. The solvent in step a) and step b) most preferably essentially consists of methanol or water.

(54) Step a) preferably further comprises a step of adjusting the pH to a pH of between about 5 and about 7, more preferably to a pH of about 6. The pH is preferably adjusted by adding a base. The base is preferably an alkali hydroxide. Alkali hydroxides are a class of chemical compounds which are composed of an alkali metal cation, i.e. one of lithium (Li), sodium (Na), potassium (K), rubidium (Rb), caesium (Cs), and the hydroxide anion (HO). In particular, the alkali metal cation is K or Na. More preferably, the base is NaOH, i.e. sodium hydroxide such as 0.1 M NaOH. In such embodiments, the first pre-mixture comprises the pyridyl ligand, the solvent of step a) and NaOH.

(55) The lanthanum salt is preferably a salt of lanthanum of the oxidation state +3, in particular it is a hydrate of La(NO.sub.3).sub.3, in particular the hexahydrate. Thus, the lanthanum salt is most preferably La(NO.sub.3).sub.36 H.sub.2O.

(56) In especially preferred embodiments, both solvents in step a) and step b) essentially consist of methanol or water.

(57) The first pre-mixture can be prepared by suspending the pyridyl ligand in the solvent or by dissolving it in the solvent. The pyridyl ligand in step a) is preferably used in a molar ratio compared to the lanthanum salt in step b) of more than about 1:1 to about 2:1, in particular of about 1.5:1.

(58) The mixture prepared in step (i) is preferably a solution, i.e. a homogeneous mixture comprising the lanthanum ions and the pyridyl ligand in the solvents from step a) and b) and optionally the base.

(59) In preferred embodiments of the present invention, the method comprises steps of:

(60) (i) preparing a mixture comprising lanthanum ions and a pyridyl ligand which pyridyl ligand is a quaternized carboxylate pyridyl ligand and subjecting the mixture to conditions under which a precipitate is formed and separating the precipitate;

(61) (ii) subjecting the precipitate of step (i) to conditions under which crystals of the lanthanum-carboxylate coordination polymer are formed;

(62) (iii) separating the crystals of the lanthanum-carboxylate coordination polymer from the mixture.

(63) Step (i) in such embodiments preferably comprises steps of:

(64) a) preparing a first pre-mixture comprising mixing the pyridyl ligand which preferably has a structure of Formula (IV):

(65) ##STR00016##
with X as defined above, preferably X is Br, and a solvent which preferably essentially consists of methanol; in particular further comprising a step of adjusting the pH to a pH of about 6 by adding NaOH such as 0.1 M NaOH;

(66) b) preparing a second pre-mixture comprising mixing a lanthanum salt which is preferably La(NO.sub.3).sub.36 H.sub.2O and a solvent, which preferably essentially consists of methanol;

(67) c) adding the second pre-mixture to the first pre-mixture;

(68) d) subjecting the mixture to conditions under which a precipitate is formed and separating the precipitate.

(69) Step d) in particular further comprises stirring the mixture after step c) for between about 15 min and about 60 min, in particular for about 30 min, for forming the precipitate and separating the precipitate preferably by filtration. Preferably, step d) further comprises a step of purifying the precipitate in particular by washing with a washing solvent comprising an aliphatic alcohol, most preferably the washing solvent essentially consists of methanol.

(70) Step (ii) in such embodiments preferably comprises steps of:

(71) a) adding a solvent, which solvent preferably comprises and in particular essentially consists of water to the precipitate at a temperature of between about 20 C. and about 30 C., in particular at a temperature of about 252 C.;

(72) b) allowing the mixture after step a) to stand at a temperature between about 20 C. and about 30 C., in particular at a temperature of about 252 C., for at least about 72 hours and most preferably for about 14 days for forming crystals of the lanthanum-carboxylate coordination polymer.

(73) In alternative preferred embodiments of the present invention, the method comprises steps of:

(74) (i) preparing a mixture comprising lanthanum ions and a pyridyl ligand which pyridyl ligand is a quaternized carboxylate pyridyl ligand;

(75) (ii) subjecting the mixture of step (i) to conditions under which crystals of the lanthanum-carboxylate coordination polymer are formed;

(76) (iii) separating the crystals of the lanthanum-carboxylate coordination polymer from the mixture;

(77) wherein step (i) preferably comprises steps of:

(78) a) preparing a first pre-mixture comprising mixing the pyridyl ligand which preferably has a structure of Formula (V):

(79) ##STR00017##
with X as defined above, preferably X is Br, and a solvent which preferably essentially consists of water; in particular further comprising a step of adjusting the pH to a pH of about 6 by adding NaOH such as 0.1 M NaOH;

(80) b) preparing a second pre-mixture comprising mixing a lanthanum salt which is preferably La(NO.sub.3).sub.36 H.sub.2O and a solvent, which preferably essentially consists of water;

(81) c) adding the second pre-mixture to the first pre-mixture.

(82) Step (ii) preferably comprises steps of:

(83) a) stirring the mixture at a temperature of at least about 80 C., further preferred at about 100 C. for about 15 min to about 60 min, further preferred for about 30 min;

(84) b) filtering the mixture for obtaining a filtrate and a residue;

(85) c) allowing the filtrate to stand at a temperature of between 20 C. and 30 C., further preferred at a temperature of about 252 C., for at least about 72 hours, further preferred for at least about 20 days and in particular for about 28 days to about 31 days for forming crystals of the lanthanum-carboxylate coordination polymer.

(86) The method of the present invention further comprises a step (iii) of separating the crystals of the lanthanum-carboxylate coordination polymer. Said step (iii) preferably comprises steps of:

(87) a) separating the crystals from the mixture;

(88) b) purifying the crystals;

(89) c) drying the crystals, preferably by drying the crystals in vacuo.

(90) Preferably, purifying the crystals in step b) comprises and in particular is carried out by means of washing the crystals with a washing solvent. The washing solvent preferably comprises an aliphatic alcohol, in particular a monohydric alcohol, more preferably a monohydric alcohol with 1 to 3 carbon atoms, most preferably methanol. In particular embodiments of the present invention, the washing solvent essentially consists of methanol.

(91) The present invention in particular encompasses the following preferred embodiments A and B of the method of the present invention:

(92) Embodiment A: The first pyridyl ligand used in step (i) is of Formula (IV):

(93) ##STR00018##
with X being Br, i.e. is N-carboxymethyl-3,5-dicarboxyl-pyridinium bromide (H.sub.3CmdcpBr) and the lanthanum salt is La(NO.sub.3).sub.36 H.sub.2O, wherein the pyridyl ligand is used in a molar ratio to the lanthanum salt of about 1.5:1. In such embodiment, the crystalline lanthanum-carboxylate coordination polymer preferably comprises and in particular essentially consists of repeating coordination entities extending in three dimensions, i.e. is a 3D coordination polymer, preferably comprising and in particular essentially consisting of asymmetric units with the formula [La.sub.4(Cmdcp).sub.6(H.sub.2O).sub.9], i.e. which crystalline lanthanum-carboxylate coordination polymer can in embodiments be described as {[La.sub.4(Cmdcp).sub.6(H.sub.2O).sub.9]}.sub.n (also referenced as compound 1). As used herein, asymmetric unit means the minimal set of atomic coordinates that can be used to generate the entire repetition in a crystal.

(94) Embodiment B: The first pyridyl ligand used in step (i) is of Formula (V):

(95) ##STR00019##
with X being Br, i.e. is N-(4-carboxybenzyl)-3,5-dicarboxyl-pyridinium bromide (H.sub.3CbdcpBr) and the lanthanum salt is La(NO.sub.3).sub.36 H.sub.2O, wherein the pyridyl ligand is used in a molar ratio to the lanthanum salt of about 1.5:1. In such embodiment, the crystalline lanthanum-carboxylate coordination polymer preferably comprises and in particular essentially consists of repeating coordination entities extending in two dimensions, i.e. is a 2D coordination polymer, preferably comprising and in particular essentially consisting of asymmetric units with the formula [La.sub.2(Cbdcp).sub.3(H.sub.2O).sub.10], i.e. which crystalline lanthanum-carboxylate coordination polymer can in embodiments be described as {[La.sub.2(Cbdcp).sub.3(H.sub.2O).sub.10]}.sub.n (also referenced as compound 2).

(96) The present invention further provides a crystalline lanthanum-carboxylate coordination polymer obtained or obtainable by the method described above. In one embodiment of the present invention, the present invention provides a lanthanum-carboxylate coordination polymer obtained by the method described above. In another embodiment of the present invention, the present invention provides a crystalline lanthanum-carboxylate coordination polymer obtainable by the method described above. The crystalline lanthanum-carboxylate coordination polymer preferably comprises and more preferably essentially consists of crystals with a monoclinic or hexagonal space group.

(97) The crystalline lanthanum-carboxylate coordination polymer in preferred embodiments of the present invention is a coordination polymer extending through repeating coordination entities in two or three dimensions, i.e. more preferably is a 2D or 3D coordination polymer.

(98) The crystalline lanthanum-carboxylate coordination polymer is in preferred embodiments obtained or obtainable by the method described above in which the first pyridyl ligand in step (i) has a structure of Formula (IV):

(99) ##STR00020##
with X being Br, which crystalline lanthanum-carboxylate coordination polymer is according to embodiment A above and can be described by the formula {[La.sub.4(Cmdcp).sub.6(H.sub.2O).sub.9]}.sub.n, i.e. is compound 1.

(100) The crystalline lanthanum-carboxylate coordination polymer is in alternative preferred embodiments obtained or obtainable by the method described above in which the first pyridyl ligand in step (i) has a structure of Formula (V):

(101) ##STR00021##
with X being Br, which crystalline lanthanum-carboxylate coordination polymer is according to embodiment B described above and can be described by the formula {[La.sub.2(Cbdcp).sub.3(H.sub.2O).sub.10]}.sub.n, i.e. is compound 2.

(102) The present invention in a third aspect provides a method of detecting a target nucleic acid sequence in a sample. The sample is from a subject such as a mammal, preferably a human and can comprise, for example, blood.

(103) The method of the present invention of detecting a target nucleic acid sequence in a sample comprises steps of:

(104) (i) preparing a mixture of a crystalline lanthanum-carboxylate coordination polymer obtained or obtainable with the preparation method described above and an oligonucleotide probe having a nucleic acid sequence at least partially complementary to said target nucleic acid sequence and being labeled with a fluorescent;

(105) (ii) incubating the mixture with the sample;

(106) (iii) measuring the fluorescence after step (ii);

(107) (iv) determining the presence and/or amount of the target nucleic acid sequence in the sample based on the fluorescence determined in step (iii).

(108) The crystalline lanthanum-carboxylate coordination polymer used in step (i) is preferably obtained or obtainable by the method described above in which the first pyridyl ligand in step (i) has a structure of Formula (IV):

(109) ##STR00022##
which crystalline lanthanum-carboxylate coordination polymer is according to embodiment A above and can be described by the formula {[La.sub.4(Cmdcp).sub.6(H.sub.2O).sub.9]}.sub.n, i.e. is more preferably compound 1.

(110) The crystalline lanthanum-carboxylate coordination polymer used in step (i) is in alternative preferred embodiments obtained or obtainable by the method described above in which the first pyridyl ligand in step (i) has a structure of Formula (V):

(111) ##STR00023##
which crystalline lanthanum-carboxylate coordination polymer is according to embodiment B above and can be described by the formula {[La.sub.2(Cbdcp).sub.3(H.sub.2O).sub.10]}.sub.n, i.e. is more preferably compound 2.

(112) The crystalline lanthanum-carboxylate coordination polymer used in step (i) of the method of detecting a target nucleic acid sequence preferably comprises and in particular essentially consists of compound 1, compound 2 or mixtures thereof. Such compounds proved to allow for an exceptional interaction with the oligonucleotide probe and quenching efficiency. The inventors further found that such crystalline lanthanum-carboxylate coordination polymers provide an exceptional quenching efficiency and a particularly high selectivity and specificity with detection limits as low as 112 and 67 pM when using an oligonucleotide probe of SEQ. ID. NO:1 and Sudan virus RNA (SUDV RNA) as target nucleic acid sequence.

(113) The target nucleic acid sequence can be of DNA or RNA, in particular viral RNA such as from Ebolavirus, in particular from Sudan virus such as SUDV RNA comprising or in particular consisting of a sequence having SEQ. ID. NO:2, NO:3 or NO:4, more preferably consisting of SEQ. ID. NO:2. Said part of the SUDV RNA includes nucleotide sequences very specific for the Sudan virus.

(114) The term oligonucleotide probe as known in the art refers to a short single-stranded sequence of nucleotides that are synthesized to match a specific region of target DNA or RNA used as a molecular probe to detect said sequence. Said oligonucleotide probe is labeled with a fluorescent, more preferably FAM (fluorescein) is attached to the oligonucleotide probe. The oligonucleotide probe is preferably made up of 10 to 25 nucleotides and more preferably comprises a sequence of SEQ. ID. NO: 1, most preferably it is a FAM-labeled ss-DNA sequence comprising or consisting of SEQ. ID. NO:1.

(115) The incubation in step (ii) of the method of detecting a target nucleic acid sequence may be carried out for at least about 10 min such as by oscillating the mixture.

(116) The wavelength for determining the fluorescence in step (iii) of the method of detecting a target nucleic acid sequence depends on the fluorescent. The skilled person is able to determine the respective absorption and emission wavelength.

(117) Step (iv) of the method of detecting a target nucleic acid sequence may further comprise a step of comparing the fluorescence with at least one reference value such as the fluorescence of a reference sample without the target nucleic acid sequence or at least one reference sample with a predetermined amount of target nucleic acid sequence.

(118) The inventors found that in step (i) the crystalline lanthanum-carboxylate coordination polymer can non-covalently bind to the oligonucleotide probe, in particular strongly absorb the oligonucleotide probe resulting and thereby quench the fluorescence of said oligonucleotide probe via a photo-induced electron transfer process. The oligonucleotide probe in step (ii) can then bind to the target nucleic acid sequence in the sample leading to a fluorescence regeneration.

(119) Hence, the method and the crystalline lanthanum-carboxylate coordination polymer can in particular be used in the diagnosis of Ebolavirus such as Sudan virus infections.

(120) Still further, a kit is provided with the present invention comprising:

(121) (i) a crystalline lanthanum-carboxylate coordination polymer obtained or obtainable with the preparation method described above;

(122) (ii) an oligonucleotide probe having a nucleic acid sequence complementary to a target nucleic acid sequence and being labeled with a fluorescent, in particular a FAM-labeled oligonucleotide probe of SEQ. ID. NO:1.

(123) The crystalline lanthanum-carboxylate coordination polymer in the kit is preferably obtained or obtainable by the preparation method described above in which the first pyridyl ligand in step (i) of the preparation method has a structure of Formula (IV):

(124) ##STR00024##
which crystalline lanthanum-carboxylate coordination polymer is according to embodiment A above and can be described by the formula {[La.sub.4(Cmdcp).sub.6(H.sub.2O).sub.9]}.sub.n, i.e. is more preferably compound 1.

(125) The crystalline lanthanum-carboxylate coordination polymer in the kit is in alternative preferred embodiments obtained or obtainable by the method described above in which the first pyridyl ligand in step (i) has a structure of Formula (V):

(126) ##STR00025##
which crystalline lanthanum-carboxylate coordination polymer is according to embodiment B above and can be described by the formula {[La.sub.2(Cbdcp).sub.3(H.sub.2O).sub.10]}.sub.n, i.e. is more preferably compound 2.

(127) In a further aspect, the present invention refers to the use of the crystalline lanthanum-carboxylate coordination polymer obtained or obtainable by the preparation method as described above or the kit in the diagnosis of viral infectious diseases, preferably of Ebolavirus, in particular Sudan virus infections. More specifically, the present invention refers to the use of the crystalline lanthanum-carboxylate coordination polymer or the kit for detecting the presence and/or the amount of a target nucleic acid in a sample from a subject such as a human, in particular Sudan virus RNA preferably comprising or consisting of SEQ. ID. NO:2, NO:3 or NO:4.

EXAMPLE 1

Methods of Preparing Crystalline Lanthanum-Carboxylate Coordination Polymers of the Present Invention

Method of Preparing {[La4(Cmdcp)6(H2O)9]}n (Compound 1)

(128) Powder of H.sub.3CmdcpBr (45.8 mg, 0.15 mmol) was suspended in methanol (15 mL), and the pH was adjusted to 6.0 with 0.1 M NaOH solution to give clear solution. Then, a solution of La(NO.sub.3).sub.3. 6H.sub.2O (43.3 mg, 0.1 mmol) in methanol (1.5 mL) was added and stirred for 30 min. The formed white precipitate was collected by filtration and washed with methanol (5 mL), then re-dissolved in H.sub.2O (30 mL) at room temperature to give a clear colorless solution. After standing at ambient temperature for about two weeks, the needle crystals of compound 1 were formed (44 mg, 86%). Anal. Calcd. for C.sub.54H.sub.48N.sub.6O.sub.45La.sub.4. 2H.sub.2O (compound 1.2H.sub.2O): C, 30.98, H, 2.49, N, 4.02. Found: C, 30.85, H, 2.39, N, 3.98%. IR (KBr disc) v 3424 (s), 2355 (w), 1649 (s), 1612 (s), 1384 (s), 1238 (w), 1178 (w), 774 (w), 724 (m), 623 (m), 526 (m).

Method of Preparing {[La2(Cbdcp)3(H2O)10]}n (Compound 2)

(129) A solution of H.sub.3CbdcpBr (114.6 mg, 0.3 mmol) in H.sub.2O (50 mL) was adjusted to pH 6.0 with 0.1 M NaOH solution. Then, a solution of La(NO.sub.3).sub.3. 6H.sub.2O (86.6 mg, 0.2 mmol) in H.sub.2O (50 mL) was added. The resulting mixture was stirred at 100 C. for 0.5 h to give a clear solution. The resulting colorless solution was filtered, then cooled to room temperature and allowed to stand for one month to give the block crystals of compound 2 (107 mg, 80%). Anal. Calcd. for C.sub.45H.sub.47N.sub.3O.sub.28La.sub.2.2H.sub.2O: C, 38.84, H, 3.69, N, 3.02. Found: C, 39.10, H, 3.54, N, 2.93%. IR (KBr disc) v 3393 (s), 3068 (s), 1649 (s), 1608 (s), 1596 (s), 1542 (s), 1402 (w), 1370 (w), 1226 (w), 1164 (w), 1016 (w), 924 (w), 856 (w), 768 (m), 720 (m).

(130) Compounds 1 and 2 were synthesized in 86% and 80% yields from the reaction of La(NO.sub.3).sub.3. 6H.sub.2O with deprotonated pyridinium carboxylate. Compounds 1 and 2 are moisture and water stable. The powder X-ray diffraction (PXRD) pattern of the fresh powder of 1 and 2 immersed in H.sub.2O for 48 h, are in agreement with those of the simulated, indicating theirs bulky phase purity and water stability (FIGS. 1A and 1B). Thermogravimetric analysis (TGA) indicates that the as-synthesized samples of 1 and 2 are stable up to ca. 300 C. (FIG. 1C).

EXAMPLE 2

X-Ray Crystal Structure Determinations of the Obtained Crystalline Lanthanum-Carboxylate Coordination Polymers

(131) Crystallographic measurement was made on a Bruker APEX II diffractometer by using graphite-monochromated Mo K (=0.71073 ) irradiation for compounds 1 and 2. The data were corrected for Lorentz and polarization effects with the SMART suite of programs and for absorption effects with SADABS (Sheldrick G M. SADABS, program for empirical absorption correction of area detector data. University of Gttingen, Germany, 1996). The structure was solved by direct methods and refined on F.sup.2 by full-matrix least-squares techniques with SHELXTL-97 program (Sheldrick G M. SHELXS-97 and SHELXL-97, Programs for the Solution and Refinement of Crystal Structures. University of Gttingen, Germany, 1997). In compound 1, the location of the hydrogen atoms on the coordinated waters were suggested by Calc-OH program in WinGX suite, their OH distances were further restrained to OH=0.85 and thermal parameters constrained to U.sub.iso(H)=1.2U.sub.eq(O) (Farrugia, L. J., J. Appl. Crystallogr., 1999, 32, 837). While for compound 2, the hydrogen atoms on the coordinated water solvates were not located. In both 1 and 2, a large amount of spatially delocalized electron density in the lattice was found but acceptable refinement results could not be obtained for this electron density. The solvent contribution was then modeled using SQUEEZE in the Platon program suite (Spek, A. L., J. Appl. Crystallogr., 2003, 36, 7). Crystallographic data have been deposited with the Cambridge Crystallographic Data Center as supplementary publication numbers 1486699 and 1486700. A summary of the key crystallographic data for 1 and 2 is given in Table 1.

(132) TABLE-US-00001 TABLE 1 Crystallographic data for compounds 1 and 2 compounds 1 2 Molecular formula C.sub.54H.sub.48N.sub.6O.sub.45La.sub.4 C.sub.45H.sub.27N.sub.3O.sub.28La.sub.2 Formula weight 2056.62 1335.52 Crystal system hexagonal monoclinic Space group P-31c C2/c a () 14.9964 (13) 16.6409 (16) b () 14.9964 (13) 21.445 (2) c () 23.100 (2) 37.803 (4) () 90.00 90.00 () 90.00 21.445 (2) () 120.00 90.00 V (.sup.3) 4499.0 (7) 13297 (2) Z 2 8 T/K 296 (2) 153 (2) D.sub.calc (g .Math. cm) 1.518 1.163 (Mo-K) 0.71073 0.71073 (cm.sup.1) 1.948 0.892 Total reflections 50116 65088 Unique reflections 50116 17489 No. observations 43659 16940 No. parameters 163 866 R.sup.a 0.0404 0.0390 wR.sup.b 0.1063 0.1002 GOF.sup.c 1.043 1.029 .sub.max (e .sup.3) 2.221 0.665 .sub.min (e .sup.3) 2.943 0.374 .sup.aR.sub.1 = ||F.sub.o| |F.sub.c||/|F.sub.o|. .sup.bwR.sub.2 = {[w(F.sub.o.sup.2 F.sub.c.sup.2).sup.2]/[w(F.sub.o.sup.2).sup.2]}.sup.1/2. .sup.cGOF = {[w(F.sub.o.sup.2 F.sub.c.sup.2).sup.2]/(n p)}.sup.1/2, where n is the number of reflections and p is total number of parameters refined

Crystal Structure of {[La4(Cmdcp)6(H2O)9]}n (Compound 1)

(133) Compound 1 crystallizes in hexagonal space group P3.sub.1c and its asymmetric unit contains one Cmdcp ligand, two coordinated water molecules and three individual La atoms, in which La1 and La3 atoms are located at the center of hexagonal axis, while La2 at triad axis. As shown in FIG. 2A to 2D, La1 and La3 are nine-coordinated while La2 has a rare coordination number of twelve. Among these three La ions, La1 (FIG. 2A) and La3 are associated by nine oxygen atoms from six monodentate methyl carboxylate of six different Cmdcp ligands and three water molecules, thereby forming a monocapped square-antiprism coordination geometry (FIG. 2B). The coordination number of La2 is fulfilled by six chelating benzylcarboxylates of six different Cmdcp ligands (FIG. 2C), thereby giving an icosahedron coordination geometry (FIG. 2D).

(134) In compound 1, the Cmdcp ligand in the asymmetric unit is coordinated to four La atoms through two monodentate carboxylate groups, and one chelating meanwhile acting as -carboxylate group. Each La atom extends to other eleven La atoms through six Cmdcp ligands in three directions, thereby forming 3D channels. It's worth mentioning that the edges of the channels are decorated with quaternary ammonium groups from ligands as shown in blue in FIG. 3B.

(135) The 3D supramolecular structure possesses large circular channels that are occupied with guest water molecules. The guest molecules were highly disordered in the channel and hence, the SQUEEZE was applied to refine the guest-free structure (Spek, A. L., Acta. Crystallogr. D. Biol. Crystallogr., 2009, 65, 148). The approximate diameter of the circular channel, calculated considering the van der Waals surface, is 15.0 . The potential solvent-accessible void in guest-free turns out to be 1421 , which is 32% of the unit cell volume (Spek, A. L., J. Appl. Crystallogr., 2003, 36, 7).

Crystal Structure of {[La2(Cbdcp)3(H2O)10]}n (Compound 2)

(136) Compound 2 crystallizes in monoclinic space group C2/c and the asymmetric unit consists of one [La.sub.2(Cbdcp).sub.3(H.sub.2O).sub.10] molecule. The La centers are linked by a pair of -COO groups and a single -COO group alternatively in a [doublesingle].sub.n chain fashion (FIG. 4). Each La center is further coordinated to one monodentate carboxylate from one Cbdcp ligand. The other carboxylate of this Cbdcp ligand is connected to the neighboring chain as the single -COO group, thereby forming a 2D structure in the ac plane (FIG. 5). The remaining carboxylates are free and deprotonated to balance the positive charge of the pyridinum cations and La(III) centers. In compound 2, each La(III) has a monocapped square-antiprism coordination geometry with the coordination of nine oxygen atoms from three -COO carboxylate groups, one monodentate carboxylate groups and five water molecules.

EXAMPLE 3

Sensing Properties of Compounds 1 and 2 Towards Sudan Virus RNA

General Procedures

(137) IR spectra were recorded on a Nicolet MagNa-IR 550 infrared spectrometer. Elemental analyses for C, H, and N were performed on an EA1110 CHNS elemental analyzer. Thermogravimetric analysis (TGA) was performed on a SDTA851 thermogravimetric analyzer at a heating rate of 10 C. min.sup.1 under a nitrogen gas flow in an Al.sub.2O.sub.3 pan. Powder X-ray diffraction (PXRD) spectra were recorded with a Rigaku D/max-2200/PC. The X-ray generated from a sealed Cu tube was mono-chromated by a graphite crystal and collimated by a 0.5 mm MONOCAP (CuK=1.54178 ). The tube voltage and current were 40 kV and 40 mA, respectively. Fluorescence spectra and fluorescence anisotropy were measured on an LS55 spectrofluorimeter. Zeta potential measurement was carried out on a NanoZS90 zetasizer.

(138) The DNA sequences were purchased from Sangon Inc. (Shanghai, China) and the RNA sequences were purchased from TaKaRa. (Dalian, China). The sequences are given in Table 2.

(139) All the samples were dissolved in 100 M Tris-HCl buffer solution (pH 7.4, 100 mM NaCl, 5 mM MgCl.sub.2). DNA was stored at 4 C. and RNA was stored at 80 C. for use. The ligands of H.sub.3CmdcpBr and H.sub.3CbdcpBr were synthesized according to the known method (Chen, M. et al., Dalton. Trans., 2015, 44, 13369; Chen, J. X. et al., Inorg. Chem., 2014, 53, 7446). All the other reagents and solvents were obtained from commercial sources and used without further purification. All the instruments used for the detection of Sudan virus RNA sequences were sterilized in an autoclavable container.

(140) TABLE-US-00002 TABLE2 DNAandRNAsequencesusedinthepresentinvention comprises SEQ.ID.NO. Sequence oligonucleotide FAM- FAM-5-TTAAAAAGTTTGTCCTCATC-3 probe/probeDNA labeledSEQ.ID. (P-DNA) NO:1 Complementary SEQ.ID. 5-GAUGAGGACAAACUUUUUAA-3 targetSUDV NO:2 5- RNAs SEQ.ID. UCUUCCGUUUGAUGAGGACAAACUUUUUAA-3 T.sub.20 NO:3 5-AUGAUGGUGAUCUUCCGUUUGAUGAGGAC T.sub.30 SEQ.ID. AAACUUUUUAA-3 T.sub.40 NO:4 Onebasepair SEQ.ID. 5-GAUGAGGACACACUUUUUAA-3 mutatedfor NO:5 complementary targetRNA(T.sub.1) Scramblednon- SEQ.ID. 5-GGCAAUCAGCUGGACACAUG-3 specificRNA(T.sub.2) NO:6

(141) Sudan Virus RNA Sequence Detection Experiments

(142) The fluorescence measurements were performed at room temperature with both excitation and emission slit width 10.0 nm. The fluorescence intensity at 518 nm with excitation at 480 nm was used for quantitative analysis.

(143) Firstly, fluorescence quenching experiments of probe DNA (P-DNA) by compounds 1, 2, H.sub.3CmdcpBr, H.sub.3CbdcpBr and La(NO.sub.3).sub.3 were performed by keeping the concentrations of P-DNA constant, while gradually increasing the concentrations of each compound.

(144) Specifically, to a solution of P-DNA (50 nM) in 100 M Tris-HCl (pH 7.4, 100 mM NaCl, 5 mM MgCl.sub.2) were added aliquots of a solution of each compound containing P-DNA (50 nM) in the same buffer and oscillated. The corresponding fluorescence spectra were measured until saturation was observed. The quenching efficiency (Q.sub.E%) was calculated according to Eq. (1).
Q.sub.E%=(1F.sub.M/F.sub.0)100%(1)
wherein F.sub.M and F.sub.0 are fluorescence intensities at 518 nm in the presence and absence of each compound, respectively.

(145) Secondly, fluorescence recovery experiments were conducted at room temperature by adding target SUDV RNA sequences of varying concentrations to the above saturated P-DNA@compound solution. The oscillation time was 30 min for P-DNA@1 and 18 min for P-DNA@2 until saturation of fluorescence recovery was observed. Fluorescence recovery efficiency was calculated according to Eq. (2).
R.sub.E=F.sub.T/F.sub.M1(2)
wherein F.sub.T and F.sub.M are the fluorescence intensities at 518 nm in the presence and the absence of target RNA, respectively.

Sensing Properties of Compounds 1 and 2

(146) As discussed above, with cationic metal centers and the conjugated 7-electrons in compounds 1 or 2, they can interact with aromatic nucleotide bases in the FAM-labeled, negatively charged P-DNA (on-state) to quench the FAM fluorescence (off-state) via photoinduced electron transfer (PET) (Daly, B. et al., Chem. Soc. Rev., 2015, 44, 4203; Atchison, J. et al., Chem. Commun., 2015, 51, 16832). The interactions of compounds 1 and 2 with FAM-labeled SEQ. ID. NO: 1, a complementary sequence of SUDV RNA, have further been evaluated. As shown in FIG. 6, the quenching efficiency of 1 and 2 are 70% and 57%, with saturated concentrations of 45 M and 40 M, respectively. Thus, both compounds 1 and 2 can quench the photoluminescence of the P-DNA due to the formation of P-DNA@1 or P-DNA@2 systems, i.e. P-DNA interacts with compounds 1 or 2 referenced herein as P-DNA@1 or P-DNA@2 systems. The results show that compound 1 has a higher quenching efficiency than compound 2. The inventors assume that this might be due to the exposure of positively charged quaternary ammonium centers at the edge of the channels of compound 1 that provide stronger electrostatic interaction with P-DNA. To verify such hypothesis, the binding affinity of compounds 1 and 2 has been calculated toward P-DNA. The binding constant is calculated via the following double logarithm Eq. (3) wherein F.sub.o and F are the fluorescence intensities at 518 nm in the absence and presence of MOF, K.sub.b is the binding constant and n is the number of binding sites (Zhang, G. W. et al., Spectrochim. Acta. A. Mol. Biomol. Spectrosc., 2010, 76, 410). The binding constants between compounds 1 or 2 and P-DNA are 3.010.sup.4 M.sup.1 and 1.510.sup.4 M.sup.1, respectively, which are in coincidence with their quenching efficiency.

(147) To further explore the key contributing factors that cause the fluorescence quenching, the quenching efficiency of each individual component has been analyzed (H.sub.3CbdcpBr, H.sub.3CmdcpBr and La(NO.sub.3).sub.3) at varying concentrations. As shown in FIG. 7A to 7B, the quenching efficiency of La(NO.sub.3).sub.3, H.sub.3CbdcpBr and H.sub.3CmdcpBr are 79.8%, 8.3% and 7.5% with saturated concentrations of 60 M, 30 M and 30 M, indicating that La.sup.3+ ion plays a major factor in the quenching process.
log(F.sub.0F)/F=n log[compound]+log K.sub.b(3)

(148) In the P-DNA@1 or P-DNA@2 systems, addition of the relevant complementary target SUDV RNA sequences leads to stable DNA/RNA hybrid duplexes (Rauzan, B. et al., Biochemistry, 2013, 52, 765). The formation of hybrid duplex structures would keep the P-DNA away from the surface of compounds 1 and 2, leading to the fluorescence regeneration (on state). Thus, the sensing capability of P-DNA@1 and P-DNA@2 systems for SUDV RNA sequences was evaluated by the fluorescence regeneration induced by the addition of complementary SUDV RNA sequences (T.sub.20). The fluorescence intensity recovery was found to be time dependent. The fluorescence intensity increased with incubation time and remained unchanged when the incubation time was longer than 30 min for P-DNA@1 and 18 min for P-DNA@2 (FIGS. 8A and 8B) with lowest concentration of 25 nM of T.sub.20 for both systems. The longer recovery time of P-DNA@1 compared to that of P-DNA@2 is probably due to adsorption of the P-DNA by the pores of compound 1 which shields its re-combination with target RNA, and makes the hybridization more difficult. While for P-DNA@2, the flat surface of compound 2 lowers the steric hindrance and favors target-probe hybridization. In addition, the increased concentration of target SUDV RNA sequences led to a gradual increase in the fluorescence intensity until saturation was observed at the concentration of 50 nM for both P-DNA@1 and P-DNA@2 (FIGS. 9A and 9B). Under this condition, the fluorescence intensity of P-DNA@1 and P-DNA@2 shows good linear relationships with the concentration of target RNA (inset of FIGS. 9A and 9B) leading to detection limits of 112 M with RSD of 1.2% and 67 M with RSD of 1.1%, respectively.

(149) To investigate the specificity of P-DNA@1 and P-DNA@2 toward T.sub.20, two RNA sequences have been selected, including one base pair mutated RNA T.sub.1 (one A base of T.sub.20 was replaced with C) and non-specific T.sub.2 to hybridize with P-DNA in the two systems. As shown in FIG. 10A and FIG. 10C, the introduction of completely complementary target Sudan virus RNA T.sub.20 results in significant fluorescence enhancement with the recovery efficiency (R.sub.E) reaching 0.62 for P-DNA@1 and 0.78 for P-DNA@2. Under the same conditions, the R.sub.E is only 0.03 for T.sub.1 and 0.02 for T.sub.2 with P-DNA@1 system, 0.02 for T.sub.1 and 0.01 for T.sub.2 with P-DNA@2 system. In addition, the fluorescence recovery induced by T.sub.20 shows much higher concentration dependence than that by T.sub.1 and T.sub.2 (FIG. 10B and FIG. 10D). These results collectively point out that the formed sensing platforms are high selective towards the target SUDV RNA sequences.

(150) Sequence T.sub.20 is part of the complete Sudan virus genome (GenBank No. AF173836.1) that has 2926 nucleotides in length. Therefore, in order to further evaluate the application of P-DNA@1 or P-DNA@2 in the detection of SUDV RNA sequences, the length of target SUDV RNA sequences has been extended from 20 (T.sub.20) bases to 30 (T.sub.30) and 40 (T.sub.40) bases. As shown in FIG. 10A to 10D, introducing T.sub.20, T.sub.30 and T.sub.40 to both systems results in significant fluorescence enhancement with R.sub.E values being 0.62, 0.49 and 0.37 for P-DNA@1, 0.78, 0.63 and 0.50 for P-DNA@2. Under this condition, the detection limits are 112 pM for T.sub.20, 806 M for T.sub.30 and 1016 pM for T.sub.40 for the P-DNA@1 system, 67 M for T.sub.20, 83 pM for T.sub.30 and 92 M for T.sub.40 for the P-DNA@2 system. These observations suggest that the recovery efficiency decreases as the length of target RNA sequence increases. In addition, using one base-mutated target RNA T.sub.40A as interfered RNA sequences for T.sub.40 gives R.sub.E values as low as 0.01 for both systems.

(151) The above positive results confirm that P-DNA@1 and P-DNA@2 are highly efficient and exceptional selective sensing platforms for SUDV RNA sequences which may be rationalized from the unique structural features of compounds 1 and 2. The zeta potential of compounds 1 and 2 are +3.1 mV and 3.6 mV, indicating that they are positively charged (Hunter R J. Zeta potential in colloid science: principles and applications. Academic press, 2013). With the conjugated 7-electron system in the compounds and aromatic nucleotide bases in the probe DNA, compounds 1 and 2 can absorb P-DNA through electrostatic and 7-stacking interactions to form P-DNA@1 and P-DNA@2 hybrids (Acuna, G. P. et al., ACS. Nano., 2012, 6, 3189), and quench the fluorescence of the FAM via a PET process (Goldberg, J. M. et al., J. Am. Chem. Soc., 2013, 135, 18651). In the fluorescence recovery step, the channel size of compound 1 and the large surface of compound 2 may play a critical role in effectively distinguishing P-DNA from DNA/RNA duplex. The single-strand moiety of P-DNA having smaller cross-sectional area but larger conformational flexibility should be able to induced fit to enter the pore and closely interact with the surface of compound 1 through multiple non-covalent interactions (Frieden, E., J. Chem. Educ., 1975, 52, 754). Furthermore, compounds 1 and 2 may have less affinity for DNA/RNA duplex because of the absence of unpaired bases and its rigid conformation. Therefore, the competitive hybridization of T.sub.20 with the absorbed P-DNA would lead to the release of the FAM-labeled P-DNA from compounds 1 and 2 to form duplex DNA/RNA, resulting in the recovery of fluorescence. This is firstly supported by the changes of the fluorescence anisotropy (FA), a measure for the rotational motion-related factors of the P-DNAs, P-DNA@T.sub.20 (hybrid duplex) before and after the addition of compounds 1 and 2 (Cao, Y. C. et al., Science, 2002, 297, 1536). As shown in FIGS. 11A and 11B, the addition of 1 and 2 into the P-DNA leads to an increase in the fluorescence anisotropy by factors 0.25 and 0.21, whereas a negligible influence on the P-DNA@T.sub.20. This result reveals the exclusively stronger interaction of compounds 1 or 2 with the P-DNA than with hybrid duplex DNA/RNA. Secondly, agarose gel electrophoresis was carried out to further confirm this assertion. As shown in FIG. 12, P-DNA displayed one light band with a strong fluorescence. Such fluorescence is absent upon its incubation with compounds 1 and 2, suggesting that P-DNA can integrate with compounds 1 or 2 and the formed P-DNA@1 and P-DNA@2 systems are too large to pass through the gel (Guo, J. F. et al., RSC. Adv., 2014, 4, 9379). Once T.sub.20 was introduced into the hybrids, the mixture yields two light bands. One band represents the hybrid duplex DNA/RNA which possesses higher molecular weight and moved slower, while the other one represents the remaining excessive, un-hybridized T.sub.20. The identities of these two bands are verified by adding P-DNA to a solution containing excessive T.sub.20. In such case, a bright and slower band corresponding to the duplex, and a light and faster band corresponding to the remaining excessive T.sub.20, are observed (Liu, J. H. et al., Anal. Chem., 2013, 85, 1424). This experiment certificated that compounds 1 or 2 can distinguish P-DNA from hybrid duplex DNA/RNA and verified the proposed mechanism.