MINIGASTRIN DERIVATES, IN PARTICULAR FOR USE IN CCK2 RECEPTOR POSITIVE TUMOUR DIAGNOSIS AND/OR TREATMENT

Abstract

It is therefore the objective of the present invention to provide minigastrin derivates which further improve the accumulation in CCK-2 receptor positive tumours by simultaneously very low accumulation in other organs, e.g. the kidneys. This objective is achieved according to the present invention by a minigastrin derivate having the formula: X-Z-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH.sub.2 (Y), wherein at least one of the connecting or terminal amide bonds between, before or after the amino acids of the sequence Z, Ala, Tyr, Gly, Trp, Met, Asp, Phe and NH.sub.2 or Y (C-terminal) is replaced by a 1,4-disubstituted or a 1,5-disubstituted 1,2,3-triazole, while X stands for a chemical group attached to the peptide for the purpose of diagnostic and/or therapeutic intervention at CCK-2 receptor relevant diseases, Y stands for C-terminal modifications of the peptide, such as amide, primary and secondary amides, free carboxylic acids and carboxylic ester derivatives including but not limited to amides and esters derived from linear or branched alkyl-,alkenyl-, alkynyl- aromatic-, and heterocyclic alcohols, and Z stands for a linker or DGlu* wherein DGlu* stands for a chain of DGlu having 1 to 6 repetitions (-DGlu-to-DGlu-DGlu-DGlu-DGlu-DGlu-DGlu-). These minigastrin derivates have a high specific internalization, excellent IC.sub.50 values and sufficient plasma stability.

Claims

1-10. (canceled)

11. A minigastrin derivate having the formula:
X-Z-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH2  (Y), wherein at least one of the connecting or terminal amide bonds between, before or after the amino acids of the sequence Z, Ala, Tyr, Gly, Trp, Met, Asp, Phe and NH2 or Y (C-terminal) is replaced by a 1,4-disubstituted or a 1,5-disubstituted 1,2,3-triazole, while X stands for a chemical group attached to the peptide for the purpose of diagnostic and/or therapeutic intervention at CCK-2 receptor relevant diseases, Y stands for C-terminal modifications of the peptide, and Z stands for a linker or DGlu* wherein DGlu* stands for a chain of DGlu* having 1 to 6 repetitions (-DGlu-to-DGlu-DGlu-DGlu-DGlu-DGlu-DGlu-).

12. The minigastrin derivate according to claim 11, wherein methionine is replaced by norleucine.

13. The minigastrin derivate according to claim 12, wherein methionine is replaced by norleucine to give minigastrin derivate [Nle15]-MG11 having one DGlu only and/or to give a minigastrin derivate PP-F11N.

14. The minigastrin derivate according to claim 13, wherein PP-F11N and [Nle15]-MG11 are defined as: DOTA-DGlu-DGlu-DGlu-DGlu-DGlu-DGlu-Ala-Tyr-Gly-Trp-Nle-Asp-Phe-NH2 and DOTA-DGlu-Ala-Tyr-Gly-Trp-Nle-Asp-Phe-NH2 resp.

15. The minigastrin derivate according to claim 14, wherein DOTA-DGlu-DGlu-DGlu-DGlu-DGlu-DGlu-Ala-Tyr-Gly-Trp-Nle-Asp-Phe-NH2 is labelled with 177Lu or DOTA-DGlu-Ala-Tyr-Gly-Trp-Nle-Asp-Phe-NH2 is labelled with 177Lu.

16. The minigastrin derivate according to claim 11, wherein X represents a radionuclide comprising a chelator for radiometals.

17. The minigastrin derivate according to claim 16, wherein the chelator for radiometals is selected from the group consisting of DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid), NOTA, NOTAGA, CHX-A″-DTPA and TCMC.

18. The minigastrin derivate according to claim 16, wherein the radionuclide is selected from the group consisting of 177Lu, 90Y, X11In, Ga-68/67, Tc-99m, Cu-64/67, Ac-225, Bi-213, Pb-212 and Th-227.

19. The minigastrin derivate according to claim 11, wherein X represents an optically active chemical compound.

20. The minigastrin derivate according to claim 11, wherein X represents a chemotherapeutic active compound or any other therapeutic active compound.

21. The minigastrin derivate according to claim 20, wherein X represents a tyrosine kinase inhibitor or an immunogenic active compound.

22. The minigastrin derivate according to claim 11, wherein X represents a nanoparticle or a liposome which has a diagnostic function or which has therapeutic function by itself or is loaded with an active compound.

23. The minigastrin derivate according to claim 22, wherein X represents a nanoparticle or a liposome which is optically active or functions as an MRI contrast agent)

24. The minigastrin derivate according to claim 11, wherein Y represents an amide, primary or secondary amide, free carboxylic acid, or carboxylic ester derivative group.

25. The minigastrin derivate according to claim 24, wherein Y represents an amide or ester group derived from linear or branched alkyl-, alkenyl-, alkynyl- aromatic-, or heterocyclic alcohols.

Description

[0019] Preferred embodiments of the present invention are hereinafter described in more detail with respect to the attached drawings which depict in:

[0020] FIG. 1 the specific internalisation of [Nle.sup.15]-MG11 in its derivated forms according to the termed triazole-scan;

[0021] FIG. 2 the half maximal inhibitory concentration IC.sub.50 of [Nle.sup.15]-MG11 in its derivated forms according to the termed triazole-scan;

[0022] FIG. 3 the plasma stability of [Nle.sup.15]-MG11 in its derivated forms according to the termed triazole-scan;

[0023] FIG. 4 the summary of the results shown in FIGS. 1 to 3;

[0024] FIG. 5 a comparison of PP-F11N and the [Nle.sup.15]-MG11 derivate DOTA[Nle.sup.15, Tyr.sup.12-(Tz)-Gly.sup.13]-MG11; and

[0025] FIG. 6 principally the triazole scan with DOTA[Nle.sup.15]-MG11.

[0026] FIG. 7 the total internalisation of the Bis-TZMG from Table 2

[0027] FIG. 8 the half maximal inhibitory concentration IC.sub.50 of the Bis-TZMG from Table 2

[0028] FIG. 9 the plasma stability of the Bis-TZMG from Table 2

[0029] FIG. 10 in vitro characteristics of two mono-substituted triazolominigastrin vs. an analogue bearing both mutations showing additional improvement.

[0030] FIG. 11 the total internalisation of PPF11N and its derivated forms according to Table 3

[0031] FIG. 12 the half maximal inhibitory concentration IC.sub.50 of PPF11N in its derivated forms according to Table 3

[0032] FIG. 13 the plasma stability of PPF11N in its derivated forms according to Table 3

[0033] [Nle.sup.15]-MG11 is a truncated analogue of minigastrin, a regulatory peptide with high affinity and specificity towards the cholecystokinin 2 receptor (CCK2R) which is overexpressed in various types of cancer. The N-terminal conjugation of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) allows for radiolabelling of the peptide with metallic radionuclides (e.g., .sup.177Lu) and subsequent use for in vivo tumour imaging and peptide receptor radionuclide therapy.

[0034] A drawback of using MG11 as a tumour-targeting vector is its low tumour uptake due to fast enzymatic degradation which results in a biological half-life of only a few minutes. The systematic replacement of single amide bonds in the peptide sequence by stable 1,4-disubstituted or 1,5-disubstituted 1,2,3-triazoles, termed a triazole-scan, leads to an improved proteolytic stability and tumour targeting properties. To prove the general utility of this new methodology, a triazole-scan was performed with DOTA[Nle.sup.15]-MG11 by a solid phase approach employing a combination of SPPS and the Copper(I)-catalysed azide-alkyne cycloaddition (CuAAC for 1,4-disubstituted 1,2,3-triazoles) as this systematically shown in FIG. 6. The introduction of 1,5-disubstituted 1,2,3-triazoles is analogous but employing the Ruthenium-catalysed azide-alkyne cycloaddition (RuAAC).

[0035] The following examples discuss the synthesis of radiolabelled triazolopeptidomimetics and the evaluation of their physiochemical properties. Receptor affinities (IC.sub.50), tumour cell internalisation rates, and plasma stabilities of the peptide conjugates were investigated in vitro. First results of in vivo studies with xenografted mice have been achieved. The ultimate goal of this project is to identify an analogue of DOTA[Nle.sup.15]-MG11 or PPF11N with maintained or improved biological activity or superior resistance to enzymatic degradation leading to improved uptake in tumours.

[0036] The building blocks for CuAAC and triazolopeptides have been prepared by adapted procedures reported in literature by Valdere et al. and Mascarin et al.

General Procedures A: Synthesis of Weinreb Amides

[0037] ##STR00001##

[0038] The corresponding Fmoc- or Boc-protected amino acid (1 equiv.) was dissolved in CH.sub.2Cl.sub.2 (0.1 M) and DIPEA (2.5 equiv.) and BOP (1 equiv.) were added. The solution was stirred for 15 min, N,O-dimethylhydroxylamine (1.2 equiv.) was added and the reaction was stirred for 12-14 h at rt. The solution was diluted with CH.sub.2Cl.sub.2, washed with 0.1 M HCl (3×), saturated aq. NaHCO.sub.3 (3×) and water (3×). The organic phase was dried over MgSO.sub.4, filtered, and the solvent was removed under reduced pressure. The desired Weinreb amide was isolated by flash chromatography on silica gel.

General Procedures B: Synthesis of α-Amino Alcohols

[0039] ##STR00002##

[0040] For amino acids with a protected carboxylic acid in their side chain, the corresponding Fmoc-protected amino acid (1 equiv.) was dissolved in anhydrous THF (0.2 M) under Argon and cooled to 0° C. (ice bath). N-Methylmorpholine (1.1 equiv.) and isobutyl chloroformate (1.05 equiv.) were added and the reaction was stirred for 15 min at 0° C. Completion of the reaction was monitored by TLC. The white suspension was added dropwise to a precooled suspension of NaBH.sub.4 (2 equiv.) in THF/MeOH (3:1, or pure THF) at −78° C. (dry ice, acetone) and stirred for 20 min. Upon completion of the reduction, residual hydrides were quenched by aq. 10% acetic acid and the solution was concentrated under reduced pressure. The residue was extracted with ethylacetate (3×), and the organic layer was washed with aq. sat. NaHCO.sub.3 (2×) and water (1×). The organic layer was dried over Na.sub.2SO.sub.4, filtered and the solvent was removed under reduced pressure. The desired α-amino alcohol was isolated by flash chromatography on silica gel.

General Procedures C: Synthesis of α-Amino Alkynes5

[0041] C.1 Synthesis of α-Amino Alkynes from Boc-Protected Weinreb Amides

##STR00003##

[0042] The corresponding Weinreb amide (1 equiv.) was placed in a flame dried flask under argon and dissolved in anhydrous CH.sub.2Cl.sub.2 (0.1 M). The solution was cooled to −78° C. (dry ice/acetone bath) and 1 M DIBAL-H in toluene was added dropwise (3 equiv.). After 1 h of stirring, the reaction was checked for completion by TLC. If the reaction was not finished, 1 M DIBAL-H in toluene (1 equiv.) was added and the reaction was stirred again for 1 h at −78° C. After consumption of the starting material, the excess hydride was quenched by slow addition of anhydrous MeOH and the reaction was allowed to warm to 0° C. (ice/water bath). K.sub.2CO.sub.3 (3 equiv.), dimethyl-(1-diazo-2-oxopropyl)phosphonate (2 equiv.) and anhydrous MeOH were added and the reaction mixture was stirred for 12-14 h at rt. A saturated solution of Rochelle's salt was added and the mixture was stirred for 30 min. The solution was diluted with water and CH.sub.2Cl.sub.2 and the aqueous phase was extracted with CH.sub.2Cl.sub.2 (3×). The combined organic phases were dried over Na.sub.2SO.sub.4, filtered, and the solvent was removed under reduced pressure. The desired alkyne was isolated by flash chromatography on silica gel.

C.2 Synthesis of α-Amino Alkynes from Fmoc-Protected Weinreb Amides

##STR00004##

[0043] The corresponding Weinreb amide (1 equiv.) was placed in a flame dried flask under argon and dissolved in anhydrous CH.sub.2Cl.sub.2 (0.1 M). The solution was cooled to −78° C. (dry ice/acetone bath) and 1 M DIBAL-H in toluene was added dropwise (3 equiv.). After 1 h of stirring, the reaction was checked for completion by TLC. If the reaction was not finished, 1 M DIBAL-H in toluene (1 equiv.) was added and the reaction was stirred again for 1H at −78° C. After consumption of the starting material, the excess hydride was quenched by slow addition of anhydrous MeOH and the reaction was allowed to warm to 0° C. (ice/water bath). K.sub.2CO.sub.3 (3 equiv.), dimethyl-(1-diazo-2-oxopropyl)phosphonate (2 equiv.) and anhydrous MeOH were added and the reaction mixture was stirred for 12-14 h at RT. A saturated solution of Rochelle's salt was added and the mixture was stirred for 30 min. The solution was diluted with water and CH.sub.2Cl.sub.2 and the aqueous phase was extracted with CH.sub.2Cl.sub.2 (3×). The combined organic phases were dried over Na.sub.2SO.sub.4, filtered, and the solvent was removed under reduced pressure. If cleavage of the Fmoc protecting group was detected by TLC, the crude mixture was dissolved in CH.sub.2Cl.sub.2 (0.1 M according to initial scale). DIPEA (2.5 equiv.) and Fmoc-OSu (2 equiv.) were added and the reaction was stirred for 12-14 h at rt. The reaction mixture was then diluted with CH.sub.2Cl.sub.2 and water. The aqueous phase was extracted with CH.sub.2Cl.sub.2 three times. The combined organic phases were dried over Na.sub.2SO.sub.4, filtered, and the solvent was removed under reduced pressure. The desired alkyne was isolated by flash chromatography on silica gel.

C.3 Synthesis of α-Amino Alkynes from Fmoc-Protected α-Amino Alcohols

##STR00005##

[0044] DMSO (2.2 equiv.) was dissolved in anhydrous CH.sub.2Cl.sub.2 (1 M) and cooled to −45° C. (dry ice/MeCN bath) under Argon. Oxalyl dichloride (1.2 equiv.) was added dropwise at −45° C. under development of gas. The solution was stirred for 5 min, before the corresponding Fmoc-protected α-amino alcohol (1 equiv., 0.13 M in CH.sub.2Cl.sub.2) was added dropwise at −45° C. and stirred for 30 min. DIPEA (3 equiv.) was added, the reaction was warmed to −20° C. (NaCl/ice bath) and monitored by TLC until completion. The solution was then diluted with CH.sub.2Cl.sub.2 and the organic layer was extracted with water, 1 M NaHSO.sub.4 and water. The combined organic phases were dried over Na.sub.2SO.sub.4, filtered, and the solvent was removed under reduced pressure. The crude reaction workup was subsequently dissolved in anhydrous MeOH (0.1 M according to initial yield), K.sub.2CO.sub.3 (3 equiv.) and dimethyl-(1-diazo-2-oxopropyl)phosphonate (2 equiv.) were added and the reaction mixture was stirred for 12-14 h at RT. The reaction mixture was diluted with water and the aqueous phase was extracted with CH.sub.2Cl.sub.2 three times. The combined organic phases were dried over Na.sub.2SO.sub.4, filtered, and the solvent was removed under reduced pressure. If cleavage of the Fmoc protecting group was detected by TLC, the crude mixture was dissolved in CH.sub.2Cl.sub.2 (0.1 M according to initial scale). DIPEA (2.5 equiv.) and Fmoc-OSu (2 equiv.) were added and the reaction was stirred for 12-14 h at rt. The reaction mixture was then diluted with CH.sub.2Cl.sub.2 and water. The aqueous phase was extracted with CH.sub.2Cl.sub.2 three times. The combined organic phases were dried over Na.sub.2SO.sub.4, filtered, and the solvent was removed under reduced pressure. The desired alkyne was isolated by flash chromatography on silica gel.

[0045] General Procedure D for the Determination of the Optical Purity of α-Amino Alkyne Building Blocks: Synthesis of Dipeptides from α-Amino Alkynes

D.1 Synthesis of Dipeptides from Boc-Protected α-Amino Alkynes

##STR00006##

[0046] The corresponding α-amino alkyne (1 equiv.) was dissolved in a solution of CH.sub.2Cl.sub.2/TFA/H.sub.2O (75:20:5) (0.05M) and the reaction was stirred for 15-30 min. after completion of the reaction, the solvent was removed under reduced pressure. Residual amounts of water and TFA were removed by co-evaporation with toluene. The residue was dissolved in CH.sub.2Cl.sub.2 (0.1 M) and PG-Ala-OH (2 equiv., PG=Boc or Fmoc), (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP, 2 equiv.) and DIPEA (5 equiv.) were added. The reaction was stirred at rt and monitored by TLC until completion. The solvent was removed from the crude mixture under reduced pressure and the desired dipeptide was isolated by flash chromatography on silica gel.

D.2 Synthesis of Dipeptides from Fmoc-Protected α-Amino Alkynes

##STR00007##

[0047] The corresponding α-amino alkyne (1 equiv.) was dissolved in 25% piperidine in DMF (0.05 M) and the reaction was stirred for 15-30 min at rt. Ice-cold H.sub.2O was added to the reaction mixture and it was extracted with EtOAc (3×). The combined organic fractions were dried over MgSO.sub.4, filtered, and the solvent was removed under reduced pressure. The residue was dissolved in CH.sub.2Cl.sub.2 (0.1 M) and Fmoc-Ala-OH (2 equiv.), BOP (2 equiv.) and DIPEA (5 equiv.) were added. The reaction was stirred at rt and monitored by TLC until completion. The solvent was removed from the crude mixture under reduced pressure and the desired dipeptide was isolated by flash chromatography on silica gel.

General Procedures E: Manual Solid Phase Peptide Synthesis

[0048] The rink amide MBHA LL resin (ca. 100 mg, 0.03-0.04 mmol) was placed in a polypropylene syringe with a polyethylene frit and a Teflon tap and swollen repeatedly in CH.sub.2Cl.sub.2 and DMF. 20% piperidine in DMF was used to cleave the Fmoc protecting group (3×3 min, rt). For elongation of the sequence, the Fmoc-protected amino acids or DOTA-tris(tert-butyl ester) (2 equiv., 0.06 mmol), HATU (1.9 equiv., 0.057 mmol) and DIPEA (5 equiv., 0.15 mmol) in DMF (total 3 mL) were added to the resin. The suspension was shaken for 1 h at rt. The solvent was removed by filtration, and the resin was repeatedly washed with DMF and CH.sub.2Cl.sub.2. Completion of the reaction was monitored by the Kaiser test and the coupling was repeated if necessary.

General Procedure F: Introduction of the Azido Functionality on the N-Terminus of the Peptide on Solid Support

[0049] After cleavage of the Fmoc protecting group, the free N-terminal amine was treated with imidazole-1-sulfonyl azide hydrochloride (3 equiv., 0.09 mmol), DIPEA (9 equiv., 0.27 mmol) and a catalytic amount of CuSO.sub.4 (0.01 equiv., 0.03 μmol)7 in DMF (total 2 mL). The suspension was shaken for 1 h at rt. The solvent was removed by filtration, and the resin was repeatedly washed with a 0.5% solution of sodium diethyldithiocarbamate in DMF, DMF and CH.sub.2Cl.sub.2. Completion of the reaction was monitored by the Kaiser test and repeated if necessary.

General Procedure G: Solid Phase Copper(I)-Catalysed Cycloaddition (CuAAC)

[0050] The Fmoc-protected α-amino alkyne (2 equiv., 0.06 mmol), DIPEA (1 equiv., 0.03 mmol), tetrakis(acetonitrile)copper(I) hexafluorophosphate (0.5 equiv., 0.015 mmol) and tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]amine (TBTA, 0.5 equiv., 0.015 mmol) in DMF (2 mL) were added to the N-terminal azide functionality and the suspension was shaken for 12-14 h at rt. The solvent was removed by filtration, and the resin was repeatedly washed with a 0.5% solution of sodium diethyldithiocarbamate in DMF, DMF and CH.sub.2Cl.sub.2. Completion of the reaction was monitored by a colorimetric test for aliphatic azides.

General Procedure H: Solid Phase Ruthenium-Catalysed Cycloaddition (RuAAC)

[0051] The Fmoc-protected α-amino alkyne (2 equiv., 0.06 mmol) and (chloro(pentamethylcyclopentadienyl)(cyclooctadiene)ruthenium (CpRu(COD)Cl, 0.5 equiv.) in DMF (2 mL) were added to the N-terminal azide functionality under argon atmosphere and the suspension was shaken for 12-14 h at rt. The solvent was removed by filtration, and the resin was repeatedly washed with a 0.5% solution of sodium diethyldithiocarbamate in DMF, DMF and CH.sub.2Cl.sub.2. Completion of the reaction was monitored by a colorimetric test for aliphatic azides

General Procedure I: Cleavage and Purification of the Peptide Conjugates

[0052] After the final coupling of the N-terminal chelator DOTA-tris(tert-butyl ester), the conjugates were deprotected and cleaved from the resin using TFA/TIS/H.sub.2O/phenol (92.5/2.5/2.5/2.5, 6 mL) with agitation for 5 h at rt. The cleavage mixture was separated from the resin by filtration and a stream of nitrogen was applied for evaporation of the volatile components. The crude peptide was then precipitated by the addition of ice-cold diethyl ether (15 mL). After centrifugation (1800 rpm, 5 min) and two washing steps with ice-cold diethyl ether, the crude peptide conjugates were dissolved in 20% CH.sub.3CN in water (1 mg/mL) and purified by reverse phase semipreparative HPLC. Subsequent lyophilisation gave the final products as white powders.

[0053] Synthesis Results are shown in Table 1.

TABLE-US-00001 TABLE 1 Summary of synthesis scale, yields and purities of the novel triazolominigastrins Mwt scale yield purity (g/mol) (mmol) (%) (%) DOTA[Nle15]-MG11 1384.6 0.058 67.4 >99 DOTA[Nle15, Phe17-ψ[Tz]-H]-MG11 1409.5 0.0511 35.7 >99 DOTA[Nle15, Asp16-ψ[Tz]-Phe17]- 1409.5 0.0379 10.1 98.5 MG11 DOTA[Nle15, Nle15-ψ[Tz]-Asp16]- 1409.5 0.0399 76.3 >99 MG11 DOTA[Nle15, Trp14-ψ[Tz]-Nle15]- 1409.5 0.041 61.8 97 MG11 DOTA[Nle15, Gly13-ψ[Tz]-Trp14]- 1409.5 0.0324 12.5 98.6 MG11 DOTA[Nle15, Tyr12-ψ[Tz]-Gly13]- 1409.5 0.04101 13.9 >99 MG11 DOTA[Nle15, Ala11-ψ[Tz]-Tyr12]- 1409.5 0.0394 23.7 >99 MG11 DOTA[Nle15, DGlu10-ψ[Tz]-Ala11]- 1409.5 0.0403 12.5 >99 MG11

TABLE-US-00002 TABLE 2 Summary of synthesis scale, yields and purities of the novel triazolominigastrins bearing to amide-to-triazole modifications (bis-TZMG). Mwt scale yield purity (g/mol) (mmol) (%) (%) DOTA[Nle.sup.15, Tyr.sup.12-ψ[Tz]-Gly.sup.13- 1433.6 0.0466 11.6 97.0 Trp.sup.14-ψ[Tz]-Nle.sup.15]-MG11 (64) DOTA[Nle.sup.15, Tyr.sup.12-ψ[Tz]-Gly.sup.13- 1433.6 0.0506 10.8 98.2 ψ[Tz]-Trp.sup.14]MG11 (65) DOTA[Nle.sup.15, Ala.sup.11-ψ[Tz]-Tyr.sup.12, 1433.6 0.0507 25.0 >99 Trp.sup.14-ψ[Tz]-Nle.sup.15]MG11 (74) DOTA[Nle.sup.15, Ala.sup.11-ψ[Tz]-Tyr.sup.12- 1433.6 0.0495 5.9 97.3 ψ[Tz]-Gly.sup.13]MG11 (76) DOTA[Nle.sup.15, DGlu.sup.10-ψ[Tz]-Ala.sup.11- 1433.6 0.0528 10.1 97.9 Tyr.sup.12-ψ[Tz]-Gly.sup.13]MG11 (86) DOTA[Nle.sup.15, DGlu.sup.10-ψ[Tz]-Ala.sup.11- 1433.6 0.0506 10.6 97.8 ψ[Tz]-Tyr.sup.12]MG11 (87)

TABLE-US-00003 TABLE 3 Summary of synthesis scale, yields and purities of the novel triazole-derivatives of PPF11N (DOTA-(DGlu).sub.6-Ala-Tyr-Gly-Trp-Nle-Asp-Phe-NH.sub.2) Mwt scale yield purity (g/mol) (mmol) (%) (%) [Tyr-ψ[Tz]-Gly]-PPF11N 2055.1 0.0325 19.6 98.1 [Trp-ψ[Tz]-Nle]-PPF11N 2055.1 0.0334 20.9 >99

[0054] (Radio)Metal Labelling

[0055] Stock solutions were prepared by dissolving the reference substances (DOTA-[Nle15]-MG11 and DOTA-PP-F11-N) or the triazolominigastrins (1 mg, 750 nmol) in ammonium acetate buffer (50 μL, 0.5 M, pH 5.5) and addition of water to a final peptide concentration of 250 μM (approx. 0.3 mg/mL). For in vitro experiments, DOTA-functionalized compounds (1 nmol, 4 μL of 250 μM stock solution) were added to a mixture of aq. HCl (22.5 μL, 0.05 M, pH 1.3), ammonium acetate buffer (10 μL, 0.5 M, pH 5.5) and aq. sodium ascorbate (5 μL, 0.5 M). 20-25 MBq of 177LuCl3 (ca. 2.5 μL, in 0.04 M HCl, 20-25 MBq/nmol) were added and the mixtures were heated to 95° C. for 20 min in a heating block. After labelling, a 1 μL aliquot of the labelling mixture was added to aq. DTPA (200 μL, 25 μM) for quality control by γ-HPLC.

[0056] For the labelling with non-radioactive 175Lu, the test compounds (25 nmol, 100 μL, 250 μM) were mixed with a 5-molar excess of aq. .sup.175LuCl.sub.3 (125 nmol, 12.5 μL, 10 mM), ammonium acetate (5 μL, 0.5 M, pH 5.5) and heated to 95° C. for 20 min in a heating block.

[0057] For in vivo experiments, DOTA-functionalized compounds were labelled with higher amount of .sup.177LuCl.sub.3 resulting in specific activities of 45-55 MBq/nmol and—after quality control—diluted with PBS to reach concentrations of 100 pmol/mL.

[0058] Cell Culture Human Medullary Thyroid Cancer cells (MZ-CRCl) expressing the CCK2R were grown in monolayers in Nunclon™ Delta treated cell culture flasks in humidified air at 5% CO.sub.2 and 37° C. The cells were maintained in the culture medium DMEM (high glucose (4.5 g/L)) supplemented with 20 mM L-Glutamine (L-Glu) and 10% FCS. The culture was passaged regularly at 80 to 90% confluency using a 0.25% trypsin 0.38% EDTA solution. Assays were conducted in the assay medium DMEM (high glucose) containing 0.1% BSA.

Cell Internalization Experiments

[0059] On the day prior to the experiment MZ-CRCl cells were placed in six-well plates (0.85.Math.106 cells/well) in cell culture medium and incubated overnight for attachment. On the day of the experiment, the medium was removed and the cells were washed twice with 1 mL PBS. The plates were put on ice for preparation. 0.9 mL of assay medium was dispensed to all wells except the ones for nonspecific binding. 0.2 pmol of 177Lu-labelled conjugates (100 μL, 2 nM in assay medium, ca. 4.2 kBq) were dispensed to all wells. For the determination of nonspecific binding, a 5000-fold excess of minigastrin (1 nmol, 100 μL, 10 μM in assay medium) was added to 0.8 mL of assay medium containing the .sup.177Lu labelled conjugates. The plates were incubated at 37° C. in 5% CO.sub.2 to allow binding and internalization. The process was stopped after 30, 60, 120 and 240 min by collection of the supernatant. The cells were washed twice with PBS (each 0.6 mL). The combined supernatants represent the free, unbound fraction of radioactivity. Membrane-bound activity was determined by incubating the cells with cold saline glycine buffer (0.6 mL, 0.05 M, pH 2.8) twice for 5 min at rt. The internalized fraction was isolated by two cycles of cell lysis with NaOH (each 0.6 mL, 1 M, 10 min, rt). The radioactivity of the fractions was measured by a COBRA-II gamma counter and is represented as percentage of total applied radioactivity dosage (n=3-5 in triplicates).

Receptor Affinity—IC50 Assays

[0060] On the day prior to the experiment MZ-CRCl cells were placed in six-well plates (0.85.Math.106 cells/well) in cell culture medium and incubated overnight for attachment. On the day of the experiment, the medium was removed and the cells were washed twice with 1 mL PBS. On ice, 0.8 mL of assay medium and the radiolabelled reference compound .sup.177Lu-DOTA-PP-F11N (0.2 pmol, 2 nM in assay medium, 100 μL, ca. 4.2 kBq) were dispensed to each well (final concentration in well=0.2 nM). .sup.175Lu-labelled test compounds were added to reach final well concentrations of 10.sup.−11 to 5.Math.10.sup.−6 M (100 μL of dilution series from 10.sup.−16 to 5.Math.10.sup.−5 M in assay medium). Total binding of 177Lu-DOTA-PP-F11N was identified by incubation of the cells without addition of test compounds. After incubation of the plates at 4° C. for 1 h, the supernatant was removed and cells were washed twice with 1 mL cold PBS. NaOH was added twice to all wells for cell lysis (0.6 mL, 1 M, 10 min, rt). The radioactivity associated with the lysed cells was determined by a COBRA-II gamma counter. 50% inhibitory concentrations (IC50) were calculated by normalized nonlinear regression with GraphPad Prism (n=3 in triplicates).

Blood Plasma Stability

[0061] The .sup.177Lu-labelled compounds were diluted with 0.9% NaCl to a concentration of 3.75 μM and incubated (375 pmol, 100 μL, 7.5-12 MBq) in nitrogen-flushed fresh human blood plasma (1.5 mL) at 37° C. At different time points (0.5, 1, 2, 4, 6 and 24 h) aliquots (75 μL) were taken and the proteins were precipitated in CH.sub.3CN (100 μL) and centrifuged (2 min, 14680 rpm, rt). The supernatant (75 μL) was diluted with water (75 μL) and analyzed by γ-HPLC. One phase decay nonlinear regression (A=A0*ek.sup.−kT) was used to calculate the half-lifes (t.sub.1/2) of the peptide conjugates with GraphPad Prism (n=2-3).

Log D Determination

[0062] The lipophilicity of the radiolabelled triazolopeptides (log D) was determined by the “shake flask method”. The radiolabelled conjugates (10 pmol, 10 μL, 1 μM in PBS, ca. 0.25 MBq) were added to a saturated 1:1 mixture of n-octanol/PBS (1 mL, pH 7.4) and shaken vigorously by vortex for 1 min. After centrifugation (3000 rpm, 10 min), 100 μL aliquots of both phases were taken and the radioactivity was measured in a gamma counter (n=2 in quadruplicates).

Biodistribution Studies in Xenografted Mice

[0063] All procedures were approved by the regional animal committee and were in accordance with international guidelines on the ethical use of animals. Six-week old female CD1 nu/nu mice (Charles River Laboratory, Germany) were inoculated with 5 Mio MZCRC cells. They were grown for 2 weeks until they had reached a size of 50-200 mm2. On the day of the experiment, they were injected with 10 pmol of the respective .sup.177Lu-labeled compound in 100 μl PBS (ca. 0.5 MBq) via the tail vein. The mice were sacrificed by CO.sub.2 suffocation 4 hours p.i., and the organs (blood, heart, lungs, spleen, kidneys, pancreas, stomach, intestines, liver, muscle, bone, tumour) were harvested by dissection, weighed and measured in a gamma counter (n=4).

[0064] For blocking experiments, the mice were injected with 100 mg of minigastrin (ca. 60′000 pmol, 6000 fold excess) in 100 μl PBS prior to the injection of the radiolabelled compounds (n=4). Tissue distribution data were calculated as percent injected activity per gram of tissue (% ID/g) and statistical analysis was performed with GraphPad Prism.

[0065] FIG. 1 illustrates the specific internalization for the the minigastrin derivate DOTA[Nle15]-MG11 as a reference and the derivated minigastrins having incorporated Tz (1,4-disubstituted 1,2,3-triazole) at different positions in the chain of the last six amino acides. DOTA[Nle15, Tyr.sup.12-(Tz)-Gly.sup.13]-MG11 shows a value of more than 50% of specific internalization after 120 minutes.

[0066] FIG. 2 illustrates the half maximal inhibitory concentration IC.sub.50 of [Nle.sup.15]-MG11 in its derivated forms according to the termed triazole-scan as compared to the reference minigastrin derivate DOTA[Nle15]-MG11. Accordingly, DOTA[Nle15, Tyr.sup.12-(Tz)-Gly.sup.13]-MG11 is the minigastrin derivate having the highest effectiveness in displacing the radiolabelled reference compound PP-F11-N.

[0067] FIG. 3 illustrates the plasma stability of [Nle.sup.15]-MG11 in its derivated forms according to the termed triazole-scan as compared to the reference minigastrin derivate DOTA[Nle15]-MG11. Most of the derivates behave similar to the reference derivate. DOTA[Nle15, Tyr.sup.12-(Tz)-Gly.sup.13]-MG11 has in this regard a lower stability but nevertheless more than 60% of the peptides remain stable for at least more than 2 hours which allows for a brought range of diagnostic and therapeutic applications. Therefore, as also illustrated in FIG. 4 in the summary of the results displayed in FIGS. 1 to 3, DOTA[Nle15, Tyr.sup.12-(Tz)-Gly.sup.13]-MG11 seems to be the best candidate for future diagnostic and therapeutic applications since the highest measured specific internalization and the lowest IC.sub.50 value compensate the slightly lower plasma half live.

[0068] In comparison to the minigastrin derivate PPF11N from WO 2015/067473 A1, the minigastrin derivate DOTA[Nle15, Tyr.sup.12-(Tz)-Gly.sup.13]-MG11 possesses a higher specific internalization at time spans in the range up to 120 min and therefore a higher effectiveness to “block” the addressed receptors (e.g. GPCRs).