IMPROVED PHARMACOKINETICS AND CHOLECYSTOKININ-2 RECEPTOR (CCK2R) TARGETING FOR DIAGNOSIS AND THERAPY
20210388025 · 2021-12-16
Inventors
Cpc classification
C07K14/705
CHEMISTRY; METALLURGY
A61K51/088
HUMAN NECESSITIES
A61P35/00
HUMAN NECESSITIES
International classification
Abstract
The present invention provides valuable peptidomimetics for therapeutic and diagnostic purposes as well as compositions, methods, uses and kits based on these peptidomimetics. In particular, the peptidomimetics of the present invention are incorporated by CCK2R expressing cells, for instance, cancer cells. This allows, for instance, to selectively destroy cancer cells or to selectively image cancer cells that express CCK2R.
Claims
1. A peptidomimetic comprising an amino acid polymer with the sequence TABLE-US-00008 (SEQ ID NO: 3) X.sup.1-X.sup.2-Asp-X.sup.3, wherein X.sup.1 is a hydrophobic amino acid, such as Phe or Trp, X.sup.2 is a hydrophobic amino acid with structural similarity to Met, such as Leu or Nle, X.sup.3 is an unnatural hydrophobic amino acid with structural similarity to Phe, such as 1Nal and 2Nal, and wherein the peptidomimetic comprises 5 to 50 amino acids.
2. The peptidomimetic of claim 1, wherein the peptidomimetic comprises an amino acid polymer with the sequence TABLE-US-00009 (SEQ ID NO: 4) X.sup.4-X.sup.5-X.sup.6-X.sup.7-X.sup.1-X.sup.2-Asp-X.sup.3, and wherein X.sup.4 is Leu, another hydrophobic amino acid, such as Pro, or a proteinogenic charged amino acid, X.sup.5 is Ala, beta-Ala, Tyr or Pro, X.sup.6 is Tyr, Pro, Phe, Met or a hydrophobic amino acid with structural similarity to Met, such as Nle, and X.sup.7 is Gly, Thr, Ser, Ala, beta-Ala or Pro.
3. The peptidomimetic of claim 1, wherein at least one of the bonds (—) between X.sup.4 and X.sup.5, X.sup.5 and X.sup.6, X.sup.6 and X.sup.7, X.sup.7 and X.sup.1, X.sup.1 and X.sup.2, X.sup.2 and Asp, and Asp and X.sup.3 is an isopeptide bond or a pseudopeptide bond, such as —CONCHS—, —NHCO— or —CH.sub.2NH—.
4. The peptidomimetic of claim 1, wherein the peptidomimetic comprises 8 to 13 amino acids.
5. The peptidomimetic of claim 1, wherein the peptidomimetic comprises a reporter group or a cytotoxic group.
6. The peptidomimetic of claim 5, wherein the reporter group or cytotoxic group is coordinated by a chelator that is comprised by the peptidomimetic, or wherein the reporter group or cytotoxic group is part of a prosthetic group that is comprised by the peptidomimetic.
7. The peptidomimetic of claim 5, wherein the reporter group or cytotoxic group is a radionuclide.
8. A method of producing the peptidomimetic of claim 1, comprising synthesizing the amino acid polymer.
9. A pharmaceutical or diagnostic composition comprising the peptidomimetic of claim 1.
10. A method of delivering a reporter group or a cytotoxic group to a cell, comprising contacting a cell with the peptidomimetic of claim 1, wherein the peptidomimetic comprises a reporter group or a cytotoxic group, thereby delivering the reporter group or the cytotoxic group to the cell.
11. A method of imaging cells, wherein the method comprises the steps of a) contacting a cell with the peptidomimetic of claim 1, wherein the peptidomimetic comprises a reporter group, and b) visualizing the reporter group that is in contact with the cell.
12. The method of claim 11, wherein contacting comprises administering the peptidomimetic to a patient.
13. (canceled)
14. A method of treating a patient that suffers from a disease that involves the expression of CCK2R, comprising administering the peptidomimetic of claim 1 to the patient.
15. A method of diagnosing cancer in a patient, wherein the method comprises the steps of a) contacting a cancer cell of the patient with the peptidomimetic of claim 1, wherein the peptidomimetic comprises a reporter group, and b) visualizing the reporter group that is in contact with the cancer cell.
16. The method of claim 12, wherein the patient has cancer.
17. The method of claim 14, wherein the disease that involves expression of CCK2R is a cancer that expresses CCK2R on the surface of cancer cells.
18. The method of claim 14, wherein the disease that involves expression of CCK2R is thyroid cancer, lung cancer, gastrointestinal stromal tumors, tumors of the nervous system, stromal ovarian cancer, gastrointestinal cancer, neuroendocrine tumors, gastroenteropancreatic tumors, neuroblastoma, tumors of the reproductive system, insulinomas, vipomas, bronchial carcinoids, ileal carcinoids, leiomyosarcomas, leiomyomas, and/or granulosa cell tumors.
19. The method of claim 15, wherein the cancer is a cancer that expresses CCK2R on the surface of cancer cells.
20. The method of claim 15, wherein the cancer is thyroid cancer, lung cancer, gastrointestinal stromal tumors, tumors of the nervous system, stromal ovarian cancer, gastrointestinal cancer, neuroendocrine tumors, gastroenteropancreatic tumors, neuroblastoma, tumors of the reproductive system, insulinomas, vipomas, bronchial carcinoids, ileal carcinoids, leiomyosarcomas, leiomyomas, and/or granulosa cell tumors.
21. The method of claim 16, wherein the cancer is a cancer that expresses CCK2R on the surface of cancer cells.
Description
BRIEF DESCRIPTION OF DRAWINGS
[0021] The invention will be described in more detail in the following section and illustrated in accompanying figures showing in:
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
DETAILED DESCRIPTION OF THE INVENTION
[0028] All publications, including but not limited to patents, patent applications and scientific publications, cited in this description are herein incorporated by reference for all purposes as if each individual publication were specifically and individually indicated to be incorporated by reference.
[0029] The use of the term “comprising” as well as other grammatical forms such as “comprises” and “comprised” is not limiting. The terms “comprising”, “comprises” and “comprised” should be understood as referring to an open-ended description of an embodiment of the present invention that may, but does not have to, include additional technical features in addition to the explicitly stated technical features. In the same sense the term “involving” as well as other respective grammatical forms such as “involves” and “involved” is not limiting. The same applies for the term “including” and other grammatical forms such as “includes” and “included”. Section headings throughout the description are for organizational purposes only. In particular, they are not intended as limiting for various embodiments described therein, and it is to be understood that embodiments (and features therein) described under one subheading may be freely combined with embodiments (and features therein) described under another subheading. Further, the terms “comprising”, “involving” and “including”, and any grammatical forms thereof, are not to be interpreted to exclusively refer to embodiments that include additional features to those explicitly recited. These terms equally refer to embodiments that consist of only those features that are explicitly mentioned.
[0030] As used herein, the term “peptidomimetic”, “peptide analogue” or “peptide derivative” or “peptide conjugate” refers to a compound that comprises a polymer of two or more amino acids that comprises at least one unnatural amino acid, pseudopeptide bond or chemical moiety that is different from an amino acid, such as a reporter group or a cytotoxic group, including also a chelator, a prosthetic group, a linker or a pharmacokinetic modifier. A peptidomimetic as defined herein generally mimics a biological activity of a natural peptide. In the present case the peptidomimetics of the present invention mimic the ability, in the sense of having the ability, of the natural CCK2R ligands, such as gastrin, to bind to CCK2R.
[0031] As used herein, the term “amino acid polymer” refers to a polymer of two or more amino acids.
[0032] The term “peptide” refers to a polymer of two or more proteinogenic amino acids in L-form that are connected by amide bonds.
[0033] The term “amino acid” as used herein refers to a compound that contains in its monomeric state at least an amine (—NH.sub.2) and a carboxyl (—COOH) functional group. If bonded to another amino acid through a peptide bond, the amine or carboxyl group of the amino acid will from an amide group —CONH— with an amine or carboxyl group of the other amino acid. If an amino acid is conjugated to another amino acid through a pseudopeptide bond, as described below, the amine or carboxyl group may be replaced by other chemical moieties depending on the nature of the pseudopeptide bond. Preferably, the term “amino acid” as used herein refers to alpha- or beta-amino acids. As used herein the term “amino acid” includes the proteinogenic amino acids alanine (Ala); arginine (Arg); asparagine (Asn); aspartic acid (Asp); cysteine (Cys); glutamine (Gin); glutamic acid (Glu); glycine (Gly); histidine (His); isoleucine (Ile): leucine (Leu); lysine (Lys); methionine (Met); phenylalanine (Phe); proline (Pro); serine (Ser); threonine (Thr); tryptophan (Trp); tyrosine (Tyr); valine (Val) and selenocysteine (Sec). The term “amino acid” as used herein also includes unnatural amino acids.
[0034] “Unnatural amino acids” in the sense of the present application are non-proteinogenic amino acids that occur naturally or are chemically synthesized, for example, norleucine (Nle), methoxinine, homopropargylglycin, ornithine, norvaline, homoserine, and other amino acid analogues such as those described in Liu C C, Schultz P G, Annu Rev Biochem 2010, 79: 413-444 and Liu D R, Schultz P G, Proc Natl Acad Sci USA 1999, 96: 4780-4785. An unnatural amino acid, as used herein, may be, for instance, a proteinogenic amino acid in D-form, for instance, DGlu. Additional contemplated unnatural amino acids are para-, ortho- or meta-substituted phenylalanine, such as para-ethynylphenylalanine, 4-Cl-phenylalanine (Cpa), 4-amino-phenylalanine, and 4-NO.sub.2-phenylalanine, homoprolin, homoalanine, beta-alanine, 1-naphthylalanine (1Nal), 2-naphtylalanine (2Nal), p-benzoyl-phenylalanine (Bpa), biphenylalanine (Bip), homophenylalanine (hPhe), homopropargylglycine (Hpg), azidohomoalanine (Aha), cyclohexylalanine (Cha), aminohexanoic acid (Ahx), 2-aminobutanoic acid (Abu), azidonorleucine (Ani), tert-leucine (Tle), 4-amino-carbamoyl-phenylalanine (Aph(Cbm)), 4-amino-hydroorotyl-phenylalanine (Aph(Hor)), S-Acetamidomethyl-L-cysteine (Cys(Acm)), 3-benzothienylalanine, 4-amino-3-hydroxy-6-methylheptanoic acid (Sta). Some of these unnatural amino acids have been explored already for somatostatin and bombesin analogues (Fani M et al., J Nucl Med 2011, 52: 1110-1118; Ginj Metal., Proc Natl Acad Sci USA 2006, 103: 16436-16441; Ginj Metal., Clin Cancer Res 2005, 11: 1136-1145; Mansi R, J Med Chem 2015, 58: 682-691).
[0035] As used herein, the term “hydrophobic amino acid” refers to amino acids that have a net zero charge at physiological pH (about pH 7.4). Hydrophobic amino acids can be proteinogenic hydrophobic amino acids or unnatural hydrophobic amino acids. Proteinogenic hydrophobic amino acids are for example serine, threonine, cysteine, selenocysteine, glycine, proline, alanine, valine, isoleucine, leucine, methionine, phenylalanine, tyrosine or tryptophan. Preferred proteinogenic hydrophobic amino acids are proline, isoleucine, leucine, phenylalanine, tyrosine and tryptophan. Unnatural hydrophobic amino acids are, for example, norleucine (Nle), methoxinine, tert-leucine (Tle), 1-naphthylalanine (1Nal), 2-naphtylalanine (2Nal), 3-benzothienylalanine, p-benzoyl-phenylalanine (Bpa), biphenylalanine (Bip), homophenylalanine (hPhe), homopropargylglycine (Hpg), azidohomoalanine (Aha), cyclohexylalanine (Cha), aminohexanoic acid (Ahx), 2-aminobutanoic acid (Abu), azidonorleucine (Anl), 2-aminooctynoic acid (Aoa), norvaline (Nva), para-ethynylphenylalanine, 4-Cl-phenylalanine, homoproline and homoalanine.
[0036] A “hydrophobic amino acid with structural similarity to Met” as used herein is a hydrophobic amino acid as defined above that has a similar molecular geometry as and/or is a bioisostere of Met. In particular, in the context of the present invention, an unnatural hydrophobic amino acid with structural similarity to Met can be inserted at position X.sup.2 and/or position X.sup.6 while maintaining sufficient cellular uptake of the peptidomimetic. Sufficient cellular uptake of the peptidomimetic is maintained, if the cellular uptake of the peptidomimetic is at least about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, or about 95% of the total activity in an assay as described in Example 5. A “hydrophobic amino acid with structural similarity to Met” as used herein may be a proteinogenic hydrophobic amino acid or an unnatural hydrophobic amino acid, preferably Nle or Leu.
[0037] An “unnatural hydrophobic amino acid with structural similarity to Phe” as used herein is an unnatural hydrophobic amino acid as defined above that has a similar molecular geometry as and/or is a bioisostere of Phe. In particular, in the context of the present invention, an unnatural hydrophobic amino acid with structural similarity to Phe can be inserted at position X.sup.3 while maintaining sufficient cellular uptake of the peptidomimetic. Sufficient cellular uptake of the peptidomimetic is maintained, if the cellular uptake of the peptidomimetic is at least about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, or about 95% of the total activity in an assay as described in Example 5. Preferably, an “unnatural hydrophobic amino acid with structural similarity to Phe” as used herein is 1Nal or 2Nal.
[0038] In some embodiments the peptidomimetics of the present invention have a cellular uptake (i.e. binding to the cell membrane and internalization into the cells) to a degree of at least about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, or about 95% of the total activity in an assay as described in Example 5.
[0039] In some embodiments the peptidomimetics of the present invention specifically bind to CCK2R. The binding affinity of the peptidomimetics of the invention can be at least about 2%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, or about 100% of the binding affinity of CCK8, minigastrin or pentagastrin for CCK2R. In some embodiments of the present invention the binding affinity of the peptidomimetics can even be higher than the binding affinity of CCK8, minigastrin or pentagastrin for CCK2R, for example, at least about 110%, about 120%, about 130%, about 140%, about 150%, about 160%, about 170%, about 180%, about 190%, about 200%, about 500%, about 1000%, about 1500%, or about 2000% of the binding affinity of CCK8, minigastrin or pentagastrin for CCK2R in an assay as described in Example 4. Specific binding to CCK2R in the context of the present invention means binding of the peptidomimetic of the present invention to CCK2R that can be displaced with a cognate ligand of CCK2R, such as gastrin, or a radiolabelled variant of a cognate ligand, such as [.sup.125I]Tyr.sup.12-labelled gastrin-I. The half maximal inhibitory concentration (IC50) is a measure of this specific binding as explained above and can be obtained from an assay as described in Example 4.
[0040] Binding affinity according to the present invention is determined by measuring the half maximal inhibitory concentration (IC50), wherein binding affinity and IC50 value have an inverse relationship, meaning that binding affinity increases with decreasing IC50 value and binding affinity decreases with increasing IC50 value. Therefore, a binding affinity of about 50% means that the IC50 value is about twice as high as the IC50 value of CCK8, minigastrin or pentagastrin for CCK2R.
[0041] The term “charged amino acid” as used herein includes amino acids that have non-zero net charge at a physiological pH of about 7.4 and includes proteinogenic and unnatural amino acids, for instance, the proteinogenic amino acids Arg, Lys, His, Glu, and Asp.
[0042] The structure of the peptidomimetic is indicated in the three letter amino acid code known to the person skilled in the art, starting with the N-terminus (amino terminus) of the peptidomimetic on the left and ending with the C-terminus of the peptidomimetic on the right. For example, the tetra peptidomimetic or peptide “X.sup.4-X.sup.5-X.sup.6-X.sup.7” (SEQ ID NO:5), consisting of four amino acids X.sup.4, X.sup.5, X.sup.6 and X.sup.7, has amino acid X.sup.4 at the N-terminus and amino acid X.sup.7 at the C-terminus. A hyphen, “-”, indicates a chemical bond between two individual amino acids, for instance, X.sup.4 and X.sup.5.
[0043] The chemical bond that connects two amino acids of the peptidomimetic of the present invention may be a peptide bond, i.e., an amide bond (—CONH—). A peptide bond as used herein can be formed between an amino group attached to the alpha carbon of one amino acid and the carboxyl group attached to the alpha carbon of another amino acid. A peptide bond may also form between an amino group and a carboxyl group, one of which is not attached to the alpha carbon of the amino acid, but to the side chain of the amino acid (isopeptide bond), for example the amino group in the side chain of lysine. The chemical bond may also be a pseudopeptide bond. In preferred embodiments, the chemical bond that connects two amino acids of the peptidomimetic is an amide bond.
[0044] The term “pseudopeptide bond” as used herein refers to a bond that connects two amino acids and is not an amide bond (—CONH—). A pseudopeptide bond may also be included in the amidated C-terminus. Any pseudopeptide bond known in the art is contemplated in the context of the present invention, for instance, —CH.sub.2NH—, —CONRCH.sub.2—, —CONCH— (the latter also referred to as N-Me), or —CONR—, wherein R is alkyl, preferably methyl, ethyl, n-propyl, isopropyl, n-butyl, s-butyl, isobutyl, t-butyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1-methyl-2-methylpropyl, 2,2-dimethylpropyl, or 1-ethylpropyl.
[0045] Herein, the identity of the chemical bond between two amino acids may be indicated in parentheses or square brackets in between the amino acids that are connected through the bond, for instance, X.sup.4-(N-Me)X.sup.5. In this case, the two amino acids X.sup.4 and X.sup.5 are connected by a pseudopeptide bond of the structure —CONCH—, wherein the amide nitrogen is methylated. The following spellings, exemplarily given for two amino acids X.sup.4 and X.sup.5 and the pseudopeptide bond N-Me, are interchangeably used herein to indicate the nature of the pseudopeptide bond: “X.sup.4-(N-Me)-X.sup.5”, “X.sup.4-(N-Me)X.sup.5” and “X.sup.4(N-Me)-X.sup.5”. Alkylester, alkylether and urea bonds are also contemplated as pseudopeptide bonds. Other pseudopeptide bonds such as 1,2,3-triazoles (Mascarin A et al., Bioconjug Chem 2015, 26: 2143-2152) or other amide bond bioisosters, which have shown to stabilize peptidomimetics and improve tumour targeting are also contemplated.
[0046] In some embodiments the presence of a pseudopeptide bond is indicated by the term “psi”, as commonly used in the art. For instance, X.sup.4-psi[CH.sub.2NH]-X.sup.5 indicates that the two amino acids X.sup.4 and X.sup.5 are connected via the pseudopeptide bond —CH.sub.2NH—. In some embodiments the pseudopeptide bond can be -psi[CH.sub.2—NH—CO—NH]-, -psi[CH.sub.2—NH]-, -psi[CH.sub.2—CH.sub.2]—, -psi[CS—NH]- or -psi[Tz]-.
[0047] Further preferred pseudopeptide bonds are: —COO—, —COS—, —COCH.sub.2—, —CSNH—, —CH.sub.2CH.sub.2—, —CHCH—, —CC—, —NHCO—, —CH.sub.2S—, —CH.sub.2—NH—CO—NH— and —CH.sub.2O—.
[0048] In the context of the present invention L- and D-amino acids are equally contemplated. Any amino acid of the present invention may be present in L- or D-form unless otherwise stated.
[0049] The L-from is indicated by reciting a “L” directly before the name of the amino acid, the D-form is indicated by reciting a “D” directly before the name of the amino acid. For instance, “DGlu” refers to the D-form of the amino acid glutamate and “LGlu” refers to the L-form of the amino acid glutamate. In preferred embodiments, the enantiomeric form of one, more or all of the amino acids of the peptidomimetic is the L-form. For instance, if the nomenclature encompasses both enantiomeric forms, for example, as is the case in “-Asp-”, then the preferred enantiomeric form is the L-form (as in “-LAsp-”).
[0050] Cyclized forms of the peptidomimetic of the present invention are also contemplated, for example, the peptidomimetic may be cyclized by linking the N-terminus with the C-terminus, the N-terminus or side chain of the N-terminal amino acid with an amino acid side chain, or the C-terminus or side chain of the C-terminal amino acid with an amino acid side chain or two side chains of two different amino acids.
[0051] In some embodiments of the present invention the N-terminus is conjugated to a linker, spacer, chelator or prosthetic group and the C-terminus is amidated.
[0052] The term “chelator” is used as in the art and refers to organic compounds that are able to chelate metal ions.
[0053] The term “prosthetic group” also referred to as bifunctional labelling agent, is used as in the art and refers to a small organic molecule that can be easily radiolabelled, for example with a radionuclide, and conjugated to a biomolecule, such as an amino acid polymer, before or after radiolabelling, and is not a chelator. Generally, prosthetic groups are conjugated to amines, thiols or carboxylic acid functions present in the biomolecule. Also conjugation via click chemistry is contemplated.
[0054] In preferred embodiments of the present invention the C-terminus (carboxy terminus) of the peptidomimetic is modified to, for example, reduce proteolytic degradation, increase shelf life, and/or improve cellular uptake. The C-terminus may be for example amidated with an —NR′R″ group, wherein R′ and R″ are independently hydrogen or a substituted or non-substituted alkyl as defined herein. In some embodiments R′ and R″ are independently ethyl, propyl, butyl, pentyl or hexyl. In some preferred embodiments the peptidomimetics of the present invention are amidated at the C-terminus with a —NH.sub.2 group. The C-terminus can also be modified with an ester of the type —C(O)OR′″, wherein R′″ can be a substituted or non-substituted alkyl as defined herein, for instance, ethyl, propyl, butyl, pentyl or hexyl.
[0055] The term “alkyl” as used herein refers to a straight-chain or branched saturated aliphatic hydrocarbon with 1 to 20 (C1-C20), preferably 1 to 15 (C1-C15), more preferably 1 to 10 (C1-C10), and most preferably 1 to 5 (C1-05) carbon atoms. For example, “alkyl” may refer to methyl, ethyl, n-propyl, isopropyl, n-butyl, s-butyl, isobutyl, t-butyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1-methyl-2-methylpropyl, 2,2-dimethylpropyl, and 1-ethylpropyl.
[0056] The “alkyl” group may be substituted with, for example, halogens, such as fluorine, chlorine and bromine, amines, such as a primary amine (—NH.sub.2), primary amide, hydroxyl (—OH), further oxygen-, sulfur- or nitrogen-containing functional groups, heterocycles, or aryl substituents, such as phenyl and napthyl.
[0057] In a preferred embodiment (embodiment A), the enantiomeric form of Asp in X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) of the peptidomimetic is the L-form (X.sup.1—X.sup.2-LAsp-X.sup.3; SEQ ID NO:3).
[0058] In another preferred embodiment (embodiment B), the bond between X.sup.2 and Asp of X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) is not —CONCH— (N-Me, NMe).
[0059] In a further preferred embodiment (embodiment C), the bond between X.sup.2 and Asp of X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) is an amide bond.
[0060] In a preferred embodiment (embodiment D), the bond between X.sup.1 and X.sup.2 of X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) is —CONCH— (N-Me, NMe).
[0061] In a preferred embodiment (embodiment E), X.sup.2 is Nle.
[0062] Particularly preferred are embodiments (embodiment F), wherein the bond between X.sup.1 and X.sup.2 of X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) is —CONCH— (N-Me, NMe) and X.sup.2 is Nle.
[0063] In a preferred embodiment (embodiment G), the bond between X.sup.1 and X.sup.2 of X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) is —CONCH— (N-Me, NMe), X.sup.2 is Nle and X.sup.3 is 1Nal or 2Nal, preferably 1Nal.
[0064] In another preferred embodiment (embodiment H) one or more of the amino acid residues in X.sup.4-X.sup.5-X.sup.6-X.sup.7 (SEQ ID NO:5) is Pro.
[0065] Particularly preferred are combinations of embodiment G with embodiments A, B, C or H.
[0066] The present invention encompasses peptidomimetics that are combinations of embodiments A-H, in particular, combinations of all embodiments A-H. These embodiments may be combined with any of the preceding or subsequent embodiments. In particular, any disclosed peptidomimetic that encompasses the sequence X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) may be combined with embodiments A-H, or any combinations thereof.
[0067] Particularly preferred are embodiments, wherein X.sup.1—X.sup.2-Asp-X.sup.3 (SEQ ID NO:3) is X.sup.1-(N-Me)Nle-(CONH)-LAsp-X.sup.3 (SEQ ID NO:3), and wherein X.sup.3 is 1Nal or 2Nal.
[0068] In a preferred embodiment of the present invention, the peptidomimetic comprises an amino acid polymer with the sequence X.sup.4-X.sup.5-X.sup.6-X.sup.7-X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:4). Preferably, the peptidomimetic comprises this polymer at the C-terminus of the peptidomimetic. More preferably, as mentioned above, the C-terminus of the peptidomimetic is amidated with a —NH.sub.2 group. X.sup.4 is Leu or another hydrophobic amino acid such as Pro or any proteinogenic charged amino acid, such as Arg, Asp, Lys, His and Glu. X.sup.5 is Ala, beta-Ala, Tyr or Pro. X.sup.6 is Tyr, Pro, Phe, Met or a hydrophobic unnatural amino acid with structural similarities to Met, such as Nle. X.sup.7 is Gly, Thr, Ser, Ala, beta-Ala or Pro. Amino acids X.sup.1, X.sup.2 and X.sup.3 are as defined herein. Any combination that results from the above or below mentioned embodiments of amino acids X.sup.4, X.sup.5, X.sup.6, X.sup.7, X.sup.1, X.sup.2, and X.sup.3 is equally contemplated in the context of the present invention.
[0069] The peptidomimetic of the present invention comprises 5 to 50 amino acids. The term “comprises 5 to 50 amino acids” as used herein means that the peptidomimetic does not have more than 50 amino acids and not less than 5 amino acids. In addition, the comprising language (“comprising”) means that the peptidomimetic may contain further components, such as a chelator, a prosthetic group, a linker, a spacer, a pharmacokinetic modifier, a reporter group or cytotoxic group, that are not explicitly recited.
[0070] In some embodiments the peptidomimetic comprises not more than 45, 40, 35, 30, 25, 20, 15 or 13 amino acids. Particularly preferred are peptidomimetics that comprise 5 to 15 amino acids. More preferred are peptidomimetics that comprise 8 to 13 amino acids. In some embodiments of the present invention, the peptidomimetic comprises at least 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 amino acids. Any range that results from a combination of the above mentioned maximal and minimal numbers of amino acids that are comprised by the peptidomimetic is also contemplated in the context of the present invention, for instance, in some embodiments the peptidomimetic comprises 8 to 35, 8 to 25 or 8 to 20 amino acids. Equally contemplated are the above-mentioned ranges wherein both the upper and the lower endpoint of the range is excluded, both the upper and the lower endpoint of the range is included, wherein the lower endpoint is included and the upper endpoint is excluded, or wherein the lower endpoint is excluded and the upper endpoint is included. This interpretation applies to all ranges recited in the present application.
[0071] In some preferred embodiments of the present invention, the peptidomimetic comprises 8 to 13 amino acids, X.sup.1 is Trp, X.sup.2 is Nle, and X.sup.3 is 1Nal or 2Nal. In even more preferred embodiments of the present invention, the peptidomimetic comprises 8 to 13 amino acids, X.sup.1 is Trp, X.sup.2 is Nle, X.sup.3 is 1Nal or 2Nal, the bond between X.sup.1 and X.sup.2 is —CONCH.sub.3—, and the C-terminus is amidated with a —NH.sub.2 group. In a further preferred embodiment, the peptidomimetic comprises 8 to 13 amino acids, X.sup.1 is Trp, X.sup.2 is Nle, X.sup.3 is 1Nal or 2Nal, the bond between X.sup.1 and X.sup.2 is —CONCH.sub.3—, Asp in X.sup.1-X.sup.2-Asp-X.sup.3 is in the L-form, the bond between X.sup.2 and Asp is an amide bond (—CONH—) and the C-terminus is amidated with a —NH.sub.2 group Preferably, these and all other peptidomimetics mentioned herein are modified at the N-terminus with the chelator DOTA or HYNIC.
[0072] In some embodiments of the present invention X.sup.1 is a hydrophobic amino acid. Preferably, X.sup.1 is Phe or Trp. Most preferably, X.sup.1 is Trp.
[0073] In some embodiments of the present invention X.sup.2 is a hydrophobic amino acid with structural similarity to Met. Preferably, X.sup.2 is Leu or Nle. Most preferably, X.sup.2 is Nle.
[0074] In some embodiments of the present invention X.sup.3 is an unnatural hydrophobic amino acid with structural similarity to Phe. Preferably, X.sup.3 is 1Nal or 2Nal. Most preferably, X.sup.3 is 1Nal.
[0075] In some embodiments of the present invention X.sup.4 is Leu or another hydrophobic amino acid such as Pro or a proteinogenic charged amino acid. Preferably, X.sup.4 is Leu, Arg, Asp, Asn, Lys, His or Glu. Preferably, X.sup.4 is an amino acid in D form. Most preferably, X.sup.4 is DGlu or DLys, in particular DGlu.
[0076] In some embodiments of the present invention X.sup.5 is Ala, beta-Ala, Tyr or Pro. Preferably, X.sup.5 is Ala, Tyr or Pro.
[0077] In some embodiments of the present invention X.sup.6 is Tyr, Pro, Phe, Met, or a hydrophobic amino acid with structural similarity to Met, such as Leu or Nle. Preferably, X.sup.6 is Tyr or Pro.
[0078] In some embodiments of the present invention X.sup.7 is Gly, Thr, Ser, Ala, beta-Ala or Pro. Preferably, X.sup.7 is Gly or Pro.
[0079] The following tables list particularly preferred embodiments of the present invention. Particularly preferred are peptidomimetics that comprise or consist of amino acid polymers with the sequences listed in Table 1. In preferred embodiments of the present invention the amino acid polymer listed in Table 1 is located at the C-terminus of the peptidomimetic, preferably the C-terminus is amidated.
TABLE-US-00001 TABLE 1 DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-2Nal DGlu-Pro-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DLys-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-Tyr-Pro-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-(N-Me)X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-psi[CH.sub.2NH.sub.2] DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-psi[CH.sub.2NH]-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-psi[CH.sub.2NH]Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-Trp-psi[CH.sub.2NH]-Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-Trp-psi[CH.sub.2NH]-Nle-Asp-(N-Me)X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-psi[CH.sub.2NH]-Trp-psi[CH.sub.2NH]-Nle- psi[CH.sub.2NH]-Asp-psi[CH.sub.2NH]-X.sup.3 DGlu-X.sup.5-psi[CH.sub.2NH]-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-psi[CH.sub.2NH]-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-psi[CH.sub.2NH]-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-Trp-psi[CH.sub.2NH]-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-(N-Me)Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Thr-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Ser-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-Gly-DPhe-(N-Me)Nle-Asp-X.sup.3 DGlu-X.sup.5-X.sup.6-DGly-Phe-(N-Me)Nle-Asp-X.sup.3 DGlu-(DGlu).sub.5-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DGlu-(Glu).sub.5-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DAsp-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DGlu-Ala-Tyr-Pro-Trp-(N-Me)Nle-Asp-X.sup.3 Pro-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 (SEQ ID NO: 6) Leu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 (SEQ ID NO: 7) X.sup.4-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 (SEQ ID NO: 8) DGlu-X.sup.5-X.sup.6-X.sup.7-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-Ala-Tyr-Gly-(N-Me)Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-Ala-(N-Me)Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-(N-Me)Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 (N-Me)DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3 DGlu-Ala-Tyr-Gly-DTrp-(N-Me)Nle-Asp-X.sup.3
[0080] Equally contemplated are peptidomimetics that comprise at least the 4 most C-terminal amino acids of the amino acid polymer sequences of Table 1 and which comprise 5 to 50 amino acids, preferably 8 to 13 amino acids.
[0081] In some embodiments of the present invention the peptidomimetic comprises a chelator. In some embodiments the chelator is DOTA or HYNIC. Table 2, shown below, illustrates some preferred embodiments of the present invention. In some embodiments of the present invention, the peptidomimetic may comprise one of the structures as shown in Table 2, or may consist of one of the structures as shown in Table 2.
TABLE-US-00002 TABLE 2 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 HYNIC-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-Pro-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DLys-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-Tyr-Pro-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-Ala-Tyr-Pro-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-Ala-Tyr-(N-Me)Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-Ala-Tyr-Gly-DTrp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NR′R″ (R′ and R″ = alkyl as defined herein) DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-(N-Me)X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-psi[CH.sub.2NH.sub.2] DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-psi[CH.sub.2NH]-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-psi[CH.sub.2NH]Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-psi[CH.sub.2NH]-Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-psi[CH.sub.2NH]-Nle-Asp-(N-Me)X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-psi[CH.sub.2NH]-Trp-psi[CH.sub.2NH]-Nle-psi[CH.sub.2NH]-Asp-psi[CH.sub.2NH]- X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-psi[CH.sub.2NH]-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-psi[CH.sub.2NH]-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-psi[CH.sub.2NH]-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-Trp-psi[CH.sub.2NH]-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-(N-Me)Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Thr-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Ser-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-Gly-DPhe-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-X.sup.5-X.sup.6-DGly-Phe-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-(DGlu).sub.5-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DGlu-(Glu).sub.5-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-DAsp-Tyr-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-X.sup.4-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 9) DOTA-X.sup.4-X.sup.5-Tyr-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 10) DOTA-X.sup.4-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 11) DOTA-X.sup.4-X.sup.5-X.sup.6-X.sup.7-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 12) DOTA-X.sup.4-X.sup.5-X.sup.6-X.sup.7-(N-Me)Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 13) DOTA-X.sup.4-X.sup.5-X.sup.6-(N-Me)Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 14) DOTA-DGlu-X.sup.5-(N-Me)X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 DOTA-X.sup.4-(N-Me)X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 15) DOTA-(N-Me)X.sup.4-X.sup.5-X.sup.6-Gly-Trp-(N-Me)Nle-Asp-X.sup.3-NH.sub.2 (SEQ ID NO: 16)
[0082] X.sup.3 as recited in Table 1 or 2 is as used herein, preferably 1Nal or 2Nal, most preferably 1Nal.
[0083] X.sup.4, X.sup.5, X.sup.6, and X.sup.7 as recited in Table 1 or 2 is as used herein, in particular, X.sup.4 is Leu or another hydrophobic amino acid such as Pro or any proteinogenic charged amino acid such as Arg, Asp, Lys, His and Glu, X.sup.5 is Ala, beta-Ala, Tyr or Pro, and X.sup.6 is Tyr, Pro, Phe, Met or a hydrophobic amino acid with structural similarity to Met, such as Leu or Nle, and X.sup.7 is Gly, Thr, Ser, Ala, beta-Ala or Pro.
[0084] It should be understood, that the peptidomimetics listed in Tables 1 and 2 are given by way of illustration and that combinations of the different modifications stated in Table 1 or 2 which are not explicitly disclosed are also contemplated. Preferred embodiments of Tables 1 and 2 are given in Table 3 below.
TABLE-US-00003 TABLE 3 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 HYNIC-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-2Nal-NH.sub.2 DOTA-DGlu-Pro-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-DLys-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-DGlu-Tyr-Pro-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-2Nal-NH.sub.2 DGlu-Pro-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DLys-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DGlu-Tyr-Pro-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp- (N-Me)1Nal-NH.sub.2 HYNIC-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp- (N-Me)1Nal-NH.sub.2 DOTA-DGlu-Ala-Tyr-Pro-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-(N-Me)1Nal-NH.sub.2 DGlu-Ala-Tyr-Pro-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2
[0085] In Tables 1-3, unless otherwise indicated, the individual amino acids are linked through amide bonds. Preferably, any amino acid shown in Tables 1-3 is in the L-form, for example, Asp in Tables 1-3 is preferably LAsp.
[0086] In some embodiments of the present invention the peptidomimetic comprises one of the structures as shown in Table 2 or 3, wherein the chelator DOTA or HYNIC coordinates a radionuclide, for example a metal radionuclide, such as .sup.225Ac, .sup.212Bi, .sup.213Bi, .sup.62Cu, .sup.64Cu, .sup.67Cu, .sup.69Cu, .sup.66Ga, .sup.67Ga, .sup.68Ga, .sup.111In, .sup.113mIn, .sup.177Lu, .sup.186Re, .sup.188Re, .sup.43Sc, .sup.44Sc, .sup.47Sc, .sup.155Tb, .sup.161Tb, .sup.99mTc, .sup.86Y, .sup.90Y, .sup.169Yb, .sup.175Yb.
[0087] In particularly preferred embodiments of the present invention, the peptidomimetic consists of the structures as shown in Table 2 or 3, wherein in addition to the information provided in Table 2 or 3 the DOTA chelator coordinates the radionuclide .sup.90Y, .sup.111In, .sup.68Ga or .sup.177Lu and the HYNIC chelator coordinates the radionuclide .sup.99mTc.
[0088] The peptidomimetics of the present invention may comprise a reporter group, a cytotoxic group, a photosensitizer, a linker and/or a pharmacokinetic modifier. Preferably, the peptidomimetics comprise a reporter group or a cytotoxic group.
[0089] Reporter Group
[0090] The term “reporter group” as used herein can be any material or chemical moiety capable of being detected either directly or indirectly in a method of imaging. Peptidomimetics that comprise a reporter group can therefore be used in methods of imaging, for instance, for diagnostic purposes. The term “reporter group” is interchangeably used with the terms “reporter agent” and “label”. The reporter group can be a material or chemical moiety that emits or may be caused to emit detectable radiation (e.g. by radioactive decay, fluorescence excitation, spin resonance excitation, etc.), affects local electromagnetic fields (e.g. paramagnetic, superparamagnetic, ferrimagnetic or ferromagnetic species), absorbs or scatters radiation energy (e.g. chromophores and fluorophores), particles (including liquid containing vesicles), heavy elements and compounds thereof, and moieties which generate a detectable substance, and others.
[0091] A wide range of materials and chemical moieties that are detectable by methods of imaging, for example diagnostic methods of imaging, such as computer tomography (CT), magnetic resonance imaging (MRI), scintigraphy, SPECT, PET, or other similar techniques, are known from the art and the reporter group will be selected according to the method of imaging to be used. Thus, for example, for ultrasound imaging an echogenic material, or a material capable of generating an echogenic material will normally be selected.
[0092] The reporter group may be a fluorophore. Fluorophores as defined herein are known in the art and available to the skilled person and include and are not limited to all the various members of the alexa family, bimane, bodipy, nitrobenzoxadiazole, dansyl, acrylodan, fluorescein, rhodamine, lanthanides, and members of the Cye3/Cye5 series (Filizola M, G Protein-Coupled Receptors in Drug Discovery, Humana Press, Springer Science+Business Media New York 2015). Preferred fluorophores are, for instance, near infrared dyes, such as, indocyanine green, IRDye 800CW, IRDye 650, LS-288, or Alexa Fluor dyes (for instance AF647, AF680 and AF488), fluorescein, cyanine and hemicyanine dyes, such as Dy488, Dy676 and Dy754. These fluorophores can be, for example, used in methods of imaging in the context of fluorescence microscopy or fluorescence guided endoscopy or surgery and optical imaging. The reporter group may also be a chemiluminescent dye.
[0093] The reporter group may also be a stable isotope or a chemical moiety comprising a stable isotope.
[0094] The reporter group may further be or contain a heavy atom (e.g. of atomic weight 38 or above), in particular for being detected by x-ray imaging. The reporter group may also be a non zero nuclear spin isotope (such as .sup.19F) or a material having unpaired electron spins and hence paramagnetic, superparamagnetic, ferrimagnetic or ferromagnetic properties, which is useful for magnetic resonance imaging. The reporter group can be a light scatterer (e.g. a coloured or uncoloured particle), a light absorber or a light emitter, which is useful for light imaging. For magnetometric imaging the reporter group will have detectable magnetic properties; for electrical impedance imaging the reporter group will affect electrical impedance. The reporter group can be a radionuclide or a chemical moiety comprising a radionuclide, which is useful for scintigraphy, SPECT, PET, or other similar techniques.
[0095] Examples of suitable reporter groups that can be used in the context of the present invention are widely known from the diagnostic imaging literature, e.g. magnetic iron oxide particles, X-ray contrast agent containing vesicles, chelated paramagnetic metals (such as Gd, Dy, Mn, Fe etc.). See for example U.S. Pat. No. 4,647,447, PCT/GB97/00067, U.S. Pat. Nos. 4,863,715, 4,770,183, WO96/09840, WO85/02772, WO92/17212, PCT/GB97/00459, EP-A-554213, U.S. Pat. No. 5,228,446, WO91/15243, WO93/05818, WO96/23524, WO96/17628, U.S. Pat. No. 5,387,080, WO95/26205, and GB9624918.0. See also WO 98/47541 (pages 63-66 and 70-86).
[0096] Particularly preferred as reporter group are chelated paramagnetic metal ions such as Gd, Dy, Fe, and Mn, especially when chelated by macrocyclic chelators.
[0097] The reporter group may be (1) a chelatable metal or polyatomic metal-containing ion (i.e. TcO, etc), where the metal is a high atomic number metal (e.g. atomic number greater than 37), a paramagnetic species (e.g. a transition metal or lanthanide), or a radioactive isotope, (2) a covalently bound non-metal species which is an unpaired electron site (e.g. an oxygen or carbon in a persistent free radical), a high atomic number non-metal, or a radioisotope, (3) a polyatomic cluster or crystal containing high atomic number atoms, displaying cooperative magnetic behavior (e.g. superparamagnetism, ferrimagnetism or ferromagnetism) or containing radionuclides, or (4) a chromophore (by which term species which are fluorescent or phosphorescent are included), e.g. an inorganic or organic structure, particularly a complexed metal ion or an organic group having an extensive delocalized electron system.
[0098] Examples of particular preferred reporter groups are described in more detail below.
[0099] Preferred reporter groups are, for instance, radionuclides, such as metal radionuclides, paramagnetic metal ions, fluorescent metal ions, heavy metal ions and cluster ions.
[0100] The radionuclide of the present invention can be selected, for example, from radioisotopes of C, N, O F, Na, P, Sc, Ti, Cr, Mn, Fe, Co, Cu, Zn, Ga, Ge, As, Se, Br, Rb, Sr, Y, Zr, Mo, Tc, Ru, Rh, Pd, Ag, In, Sn, Sb, Te, I, La, Ce, Pr, Pm, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Ta, W, Re, Os, Ir, Pt, Au, Hg, Tl, Pb, Bi, Po, At, Ra, Ac, Th, and Fm.
[0101] Preferred radionuclides include, but are not limited to radionuclides of metals, such as but not limited to .sup.225Ac, .sup.198Au, .sup.199Au, .sup.212Bi, .sup.213Bi, .sup.51Cr, .sup.62Cu, .sup.64Cu, .sup.67Cu, .sup.69Cu, .sup.159Dy, .sup.166Dy, .sup.66Ga, .sup.67Ga, .sup.68Ga, .sup.159Gd, .sup.166Ho, .sup.111In, .sup.113mIn, .sup.196Ir, .sup.177Lu, .sup.189mOs, .sup.203Pb, .sup.109Pd, .sup.149Pm, .sup.151Pm, .sup.142Pr, .sup.143Pr, .sup.186Re, .sup.188Re, .sup.97Ru, .sup.43Sc, .sup.44Sc, .sup.47Sc, .sup.153Sm, .sup.117mSn, .sup.121Sn, .sup.155Tb, .sup.161Tb, .sup.99mTc, .sup.127Te, .sup.167Tm, .sup.86Y, .sup.90Y, .sup.169Yb, .sup.175Yb, and .sup.89Zr. Preferred reporter groups are radionuclides of halogens, such as, but not limited to .sup.18F, .sup.131I, .sup.123I, .sup.124I, and .sup.125I.
[0102] Gamma and positron emitters for diagnostic applications include and are not limited to 11C, .sup.51Cr, .sup.62Cu, .sup.64Cu, .sup.52Fe, .sup.66Ga, .sup.67Ga, .sup.68Ga, .sup.123I, .sup.124I, .sup.125I, .sup.111In, .sup.113mIn, .sup.177Lu, .sup.24Na, .sup.203Pb, .sup.97Ru, .sup.43Sc, .sup.44Sc, .sup.152Tb, .sup.155Tb, .sup.94mTc, .sup.99mTc, .sup.167Tm, .sup.86Y, and .sup.89Zr.
[0103] Radionuclides with alpha and beta emission as well as Auger electron and internal conversion electron emission for therapeutic applications include and are not limited to .sup.225Ac, .sup.111Ag, .sup.77As, .sup.211At, .sup.198Au, .sup.199Au, .sup.212Bi, .sup.213Bi, .sup.77Br, .sup.58Co, .sup.51Cr, .sup.67Cu, .sup.152Dy, .sup.159Dy, .sup.165Dy, .sup.169Er, .sup.255Fm, .sup.67Ga, .sup.159Gd, .sup.195Hg, .sup.161Ho, .sup.166Ho, .sup.123I, .sup.125I, .sup.131I, .sup.111In, .sup.192Ir, .sup.194Ir, .sup.196Ir, .sup.177Lu, .sup.189mOs, .sup.32P, .sup.212Pb, .sup.109Pd, .sup.149Pm, .sup.142Pr, .sup.143Pr, .sup.223Ra, .sup.186Re, .sup.188Re, .sup.105Rh, .sup.119Sb, .sup.47Sc, .sup.153Sm, .sup.117mSn, .sup.121Sn, .sup.89Sr, .sup.149Tb, .sup.161Tb, .sup.99mTc, .sup.127Te, .sup.227Th, .sup.201Tl, and .sup.90Y. Preferred paramagnetic metal ions include and are not limited to ions of transition and lanthanide metals (e.g. metals having atomic numbers of 6 to 9, 21-29, 42, 43, 44, or 57-71), in particular ions of Cr, V, Mn, Fe, Co, Ni, Cu, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu, especially of Mn, Cr, Fe, Gd and Dy, more especially Gd.
[0104] In some embodiments of the present invention, the reporter group has no therapeutic effect, such as a cytotoxic effect, in particular when comprised by the peptidomimetic. In some embodiments, the reporter group does at least not have a cytotoxic effect to a degree that is therapeutically relevant. The skilled person is able to determine an administered dose/radioactivity dose of the reporter group that is sufficient for being detected, for instance in a method of imaging, but low enough for not having a therapeutic effect. Consequently, in some embodiments of the present invention, for instance, the method of imaging and any diagnostic uses or methods, a dose of the reporter group, in particular the radionuclide, is used that is sufficient for detection, but does not have a therapeutic effect. As used herein, reporter groups without therapeutic effect are referred to as “non-therapeutic reporter groups”. Thus, the present invention also relates to non-therapeutic embodiments of the above mentioned reporter groups. For example the invention includes non-therapeutic fluorophores, stable isotopes or chemical moieties comprising a stable isotope, heavy atoms, radionuclides, such as metal radionuclides, paramagnetic metal ions, fluorescent metal ions, heavy metal ions and cluster ions.
[0105] Preferred non-therapeutic reporter groups that are radionuclides, which can be used for imaging, are .sup.64Cu, .sup.67Ga, .sup.68Ga, .sup.123I, .sup.124I, .sup.125I, .sup.131I, .sup.111In, .sup.177Lu, .sup.203Pb, .sup.97Ru, .sup.44Sc, .sup.152Tb, .sup.155Tb, .sup.99mTc, .sup.167Tm, .sup.86Y, and .sup.89Zr.
[0106] Cytotoxic Group
[0107] In some embodiments, the peptidomimetic comprises a cytotoxic group. The term “cytotoxic group” as used herein refers to any material or chemical moiety that directly or indirectly causes the death of the cell to which the peptidomimetic that comprises the cytotoxic group is bound or by which it has been internalized.
[0108] The cytotoxic group can be, for example, a chemotherapeutic agent or a radionuclide. If the chemotherapeutic agent or radionuclide that is comprised by the peptidomimetic is internalized by a cell that expresses CCK2R, the CCK2R expressing cell is killed by the chemotherapeutic agent or radionuclide. In some embodiments, the cell to which the peptidomimetic is bound may also be killed without internalizing the peptidomimetic that comprises the cytotoxic group.
[0109] The chemotherapeutic agent can be selected from the group consisting of vinblastine monohydrazide, tubulysin B hydrazide, actinomycin, all-trans retinoic acid, azacitidine, bleomycin, bortezomib, carboplatin, capecitabine, cisplatin, chlorambucil, cyclophosphamide, cytarabine, daunorubicin, docetaxel, doxifluridine, doxorubicin, epirubicin, epothilone, etoposide, fluorouracil, gemcitabine, hydroxyurea, idarubicin, imatinib, irinotecan, mechlorethamine, mercaptopurine, methotrexate, mitoxantrone, oxaliplatin, paclitaxel, pemetrexed, teniposide, tioguanine, topotecan, indotecan, indimitecan, mertansine, emtansine, valrubicin, vemurafenib, vinblastine, vincristine, vindesine, and vinorelbine.
[0110] Preferred radionuclides that can be used as a cytotoxic group include metal and halogen radionuclides. The radionuclide of the present invention can be for example selected from radioisotopes of P, Sc, Cr, Mn, Fe, Co, Cu, Zn, Ga, As, Br, Sr, Y, Tc, Ru, Rh, Pd, Ag, In, Sn, Sb, Te, I, Pr, Pm, Sm, Gd, Tb, Y, Ho, Er, Lu, Ta, W, Re, Os, Ir, Au, Hg, Tl, Pb, Bi, Po, At, Ra, Ac, Th, and Fm. Preferred radionuclides include, but are not limited to, .sup.225Ac, .sup.111Ag, .sup.77As, .sup.211At, .sup.198Au, .sup.199Au, .sup.212Bi, .sup.213Bi, .sup.77Br, .sup.58Co, .sup.51Cr, .sup.67Cu, .sup.152Dy, .sup.159Dy, .sup.165Dy, .sup.169Er, .sup.255Fm, .sup.67Ga, .sup.159Gd, .sup.195Hg, .sup.161Ho, .sup.166Ho, .sup.123I, .sup.125I, .sup.131I, .sup.111In, .sup.192Ir, .sup.194Ir, .sup.196Ir, .sup.177Lu, .sup.189mOs, .sup.32P, .sup.212Pb, .sup.109Pd, .sup.149Pm, .sup.142Pr, .sup.143Pr, .sup.223Ra, .sup.186Re, .sup.188Re, .sup.105Rh, .sup.119Sb, .sup.47Sc, .sup.153Sm, .sup.117mSn, .sup.121Sn, .sup.89Sr, .sup.149Tb, .sup.161Tb, .sup.99mTc, .sup.127Te, .sup.227Th, .sup.201Tl, and .sup.90Y.
[0111] Photosensitizer
[0112] In some embodiments of the present invention the peptidomimetic comprises a photosensitizer.
[0113] As used herein the term “photosensitizer” refers to a material or chemical moiety that becomes toxic or releases toxic substances upon exposure to light such as singlet oxygen or other oxidizing radicals which are damaging to cellular material or biomolecules, including the membranes of cells and cell structures, and such cellular or membrane damage may eventually kill the cells. Photosensitizers as defined herein are known in the art and available to the skilled person. The cytotoxic effects of photosensitizers can be used in the treatment of various abnormalities or disorders, including neoplastic diseases. Such treatment is known as photodynamic therapy (PDT) and involves the administration of a photosensitizer to the affected area of the body, followed by exposure to activating light in order to activate the photosensitizer and convert them into cytotoxic form, whereby the affected cells are killed or their proliferative potential diminished.
[0114] Photosensitizers exert their effects by a variety of mechanisms, directly or indirectly. Thus for example, certain photosensitizers become directly toxic when activated by light, whereas other photosensitizers act to generate toxic species, e.g. oxidizing agents such as singlet oxygen or oxygen-derived free radicals, which are destructive to cellular material and biomolecules, such as lipids, proteins and nucleic acids, and ultimately kill cells.
[0115] In some embodiments the photosensitizer includes, for example, psoralens, porphyrins, chlorins and phthalocyanines. Porphyrin photosensitizers act indirectly by generation of toxic oxygen species and are particularly preferred. Porphyrins are naturally occurring precursors in the synthesis of heme. In particular, heme is produced when iron (Fe.sup.2+) is incorporated in protoporphyrin IX (PpIX) by the action of the enzyme ferrochelatase. PpIX is a highly potent photosensitizer. Further photosensitizer that can be used in the context of the present invention are aminolevulinic acid (ALA), silicon phthalocyanine Pc 4, m-tetrahydroxyphenylchlorin (mTHPC) and mono-L-aspartyl chlorin e6 (NPe6), porfimer sodium, verteporfin, temoporfin, methyl aminolevulinate, hexyl aminolevulinate, laserphyrin-PDT, BF-200 ALA, amphinex and azadipyrromethenes.
[0116] Linker
[0117] The peptidomimetic of the present invention comprises an amino acid polymer with a sequence as defined herein. The total number of amino acids comprised by the peptidomimetic is limited as defined herein. In addition to the amino acid polymer, the peptidomimetic of the present invention may comprise further components, such as a reporter group, a cytotoxic group, a photosensitizer, a chelator, a prosthetic group, a pharmacokinetic modifier, a linker, or a spacer. These individual components or chemical moieties may be directly connected to each other or to the amino acid polymer through a covalent, ionic or coordinated bond, for example, the reporter group or the cytotoxic group may be connected with a chelator through a coordinated bond.
[0118] Alternatively, the above-mentioned components may be indirectly connected to each other or to the amino acid polymer through a linker. The term “linker” as used herein refers to a chemical moiety that connects two individual chemical moieties. The terms “linker” or “spacer” are interchangeably used in the literature and herein to describe such a chemical moiety. The linker can be bound to the N-terminus of the amino acid polymer of the peptidomimetic, integrated within the amino acid sequence of the amino acid polymer of the peptidomimetic or conjugated to a side chain of an amino acid of the amino acid polymer of the peptidomimetic or another functional group and is usually used as a separator between the amino acid polymer of the peptidomimetic and the reporter agent or cytotoxic agent or as pharmacokinetic modifier influencing, for example, the hydrophilicity and pharmacokinetics of the peptidomimetic. For example, the reporter group, the cytotoxic group, the photosensitizer, the chelator, the prosthetic group or the pharmacokinetic modifier of the present invention may be connected with the amino acid polymer, for instance X.sup.4-X.sup.5-X.sup.6-X.sup.7-X.sup.1-X.sup.2-Asp-X.sup.3 (SEQ ID NO:4), through a linker. The linker can connect any of the above mentioned components to the N-terminus, the C-terminus or any side chain of the amino acid polymer of the peptidomimetic. In some embodiments, the linker may also connect the above mentioned components with each other, for instance, the linker may connect a pharmacokinetic modifier with the reporter group.
[0119] The linker may be an amino acid, such as Gly, Ala, Gln, Glu, His, all in L- or D-form, or an amino acid polymer consisting of one or more of these amino acids, or any other chemical moiety, such as polyethylene glycol or a carbohydrate, as well as aminohexanoyl or aminobenzoyl or piperidine moieties. In some embodiments the linker can be 6-aminohexanoic acid, 4-aminobutyric acid, 4-amino-1-carboxymethylpiperidine or urea or another chemical moiety that allows introducing a functional group in the peptidomimetic. In some embodiments the linker is a combination of the above mentioned linkers.
[0120] The linker can be used as a separator of the individual components of the peptidomimetic. The linker can also be used to form multimeric conjugates of multiple peptidomimetics or in combination with other ligands targeting for instance alternative receptors. The linker can further be used to bind multiple reporter groups or a combination of a reporter group and a cytotoxic group to the peptide. Such examples are given by the divalent gastrin peptidomimetic DOTA-Gly-Ser-Cys(succinimidopropionyl-Glu-Ala-Tyr-Gly-Trp-Nle-Asp-Phe-NH.sub.2)-Glu-Ala-Tyr-Gly-Trp-Nle-Asp-Phe-NH.sub.2 (DOTA-MGD5) (Sosabowski J K et al., J Nucl Med 2009, 50: 2082-2089) or by the dual-modality fluorescent and radiolabelled ligand DOTA-Lys(IRDye-650)-PEG4-[D-Phe.sup.6,Sta.sup.13]-bombesin(6-14)NH.sub.2 (HZ220) targeting the gastrin-releasing peptide receptor antagonist (Zhang H et al., J Nucl Med 2017, 58: 29-35). DOTA-MGD5 is a divalent MG analogue based on a maleimide-linker for which a high tumour uptake and low kidney retention has been shown in preclinical studies. The gastrin-releasing peptide receptor antagonist HZ220 targeting gastrin-releasing peptide (GRP) receptors is based on a bombesin analogue in which the two amines of a lysine are used to conjugate the chelator DOTA and the near-infrared fluorescent (NIRF) dye IRDye 650. For .sup.68Ga-labelled HZ220 a high tumour-to-background contrast could be achieved for both PET and optical imaging. A linker can also be used to introduce a cleavable group into the peptide sequence, releasing a part of the peptide conjugate, such as a peptide fragment, a cytotoxic or a reporter group. Such an example is given by cathepsin B cleavage sites (Naqvi S A et al., Cancer Biother Radiopharm 2010, 25: 89-95; Albericio F and Kruger H G, Future Med Chem 2012, 4: 1527-1231). Also a combination of linkers, such as the combination of glucose and 4-aminobenzoic acid in the bombesin derivative .sup.177Lu-DOTA-Lys(glucose)-4 aminobenzoic acid-BBS7-14 can be used (Lim J C et al, Nucl Med Biol 2015, 42:234-241.
[0121] As used herein, “pharmacokinetic modifier” means a chemical moiety that influences the pharmacokinetics of the peptidomimetic, such as the hydrophilicity, biodegradation, and clearance. For instance, the pharmacokinetic modifier may increase the half-life of the peptidomimetic in the blood stream.
[0122] The radiolabelled MG analogue DOTA-His-His-Glu-Aly-Tyr-Gly-Trp-Met-Asp-Phe-NH.sub.2 (SEQ ID NO:17) (Mather S J et al., J Nucl Med 2007, 48: 615-622) is derived from MG11 and includes two His residues in the N-terminal part of the peptide. The radiolabeled MG analogues DOTA-DGln-DGln-DGln-DGln-DGln-DGln-Aly-Tyr-Gly-Trp-Met-Asp-Phe-NH.sub.2, DOTA-DGln-DGln-DGln-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH.sub.2, DOTA-DGln-DGlu-DGln-DGlu-DGln-DGlu-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH.sub.2 and DOTA-DGlu-DGlu-DGlu-DGlu-DGlu-DGlu-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH.sub.2 are derived from MG0 and include different numbers of DGln and DGlu residues in the N-terminal part of the peptide (Laverman P et al., Eur J Nucl Med Mol Imaging 2011, 38: 1410-1416). The design of these novel peptide derivatives was based on the knowledge that the high renal uptake of MG0 is caused by the anionic pentaglutamate sequence in the structure. By the introduction of positively charged residues and D-amino acid residues the kidney uptake could be reduced with a concomitant improved tumour-to-kidney ratio. To obtain a high tumour-to-background contrast in imaging a rapid clearance of the radioligand from the circulation is desirable. Also other spacers with different polarities, including PEG or D-amino acids such as D-Ser and D-Gln, have been studied as pharmacokinetic modifiers for MG analogues in the attempt to increase the stability and tumour-to-kidney ratio of the radioligands (Kolenc-Peitl P et al., J Med Chem 2011, 54: 2602-2609). By introducing hydrophilic and uncharged spacers of different lengths favourable effects on serum stability, kidney uptake and tumour-to-kidney ratio could be observed.
[0123] Linkage of the Reporter Group and Cytotoxic Group
[0124] The peptidomimetic of the present invention may comprise a reporter group or a cytotoxic group or multiple reporter groups or cytotoxic groups. In some embodiments the peptidomimetic may also comprise a reporter group and a cytotoxic group. In some embodiments the reporter group, the cytotoxic group, or both, can be directly linked to the amino acid polymer of the peptidomimetic, for example, through a covalent bond. In other embodiments the reporter group, the cytotoxic group, or both, can be indirectly linked to the amino acid polymer of the peptidomimetic.
[0125] If the reporter group, or the cytotoxic group, or both, are indirectly linked to the amino acid polymer of the peptidomimetic, they are linked to the amino acid polymer through a linker or pharmacokinetic modifier as defined above, or through a chelator or a prosthetic group. For instance, reporter groups that are fluorophores are preferably covalently linked to the amino acid polymer of the peptidomimetic, either directly or through a linker or spacer, such as polyethylenglycol. On the other hand, radionuclides, such as metal radionuclides, and metal ions are preferably linked to the peptidomimetic via a chelator. Radionuclides of halogens are preferably linked to the peptidomimetic via a prosthetic group or via a functional group of a side chain of an amino acid.
[0126] The reporter group or cytotoxic group can be directly or indirectly linked to the amino acid polymer of the peptidomimetic via the N-terminus, C-terminus or via an amino acid side chain, for example lysine or cysteine or via a functional group of a linker or pharmacokinetic modifier. Preferably, the reporter group or cytotoxic group is linked to the amino acid polymer of the peptidomimetic via the N-terminus. In preferred embodiments of the present invention, the reporter group or cytotoxic group is linked to the N-terminus of the peptide through a chelator or prosthetic group. In particular, in some embodiments, radionuclides are linked to the amino acid polymer of the peptidomimetic via the N-terminus of the peptide. A linker may be additionally used to connect the chelator or prosthetic group to the N-terminus or a side chain of an amino acid in the peptide sequence. The reporter group, for instance, the radionuclide can be coordinated by the chelator or introduced into the prosthetic group before or after conjugation with the peptide conjugate.
[0127] Chelator and Prosthetic Group
[0128] For the introduction of the reporter group or cytotoxic group the peptidomimetic can comprise a chelator or a prosthetic group. The chelator or prosthetic group can be conjugated to the amino acid polymer of the peptidomimetic at the N-terminus, the C-terminus or at any amino acid side chain or functional group present in a linker or pharmacokinetic modifier. Preferably, the chelator or prosthetic group is conjugated to the amino acid polymer of the peptidomimetic at the N-terminus.
[0129] The introduction of the reporter group or cytotoxic group into the chelator or prosthetic group can be performed before or after conjugation of the chelator or prosthetic group with the amino acid polymer of the peptidomimetic.
[0130] In some embodiments the chelator coordinates a metal, for example a metal radionuclide as mentioned herein, as a reporter group or a cytotoxic group or the prosthetic group comprises a halogen, for example a halogen radionuclide as mentioned herein, as a reporter group or a cytotoxic group.
[0131] The chelator may contain different donor groups for metal complexation such as oxygen, nitrogen, sulphur, (carboxyl, phosphonate, hydroxamate, amine, thiol, thiocarboxylate or derivatives thereof) and comprises acyclic and macrocyclic chelators such as polyaminopolycarboxylic ligands.
[0132] In some embodiments the chelator is selected from the group consisting of diethylenetriaminopentaacetic acid (DTPA), ethylenediaminetetraacetic acid (EDTA), 1,4,7-triazacyclononane-1,4,7-tris[methylene(2-carboxyethyl)]phosphinic acid (TRAP), 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA), 1,4,7-triazacyclononane-1,4,7-triacetic acid (NOTA), 1,4,7-triazacyclononane-1,4-diiacetic acid (NODA), 1,4,8,11-tetraazacyclotetradecane-1,4,8,11-tetraacetic acid (TETA) as well as derivatives thereof such as DOTA or NOTA functionalized with a glutaric acid arm (DOTAGA, NOTAGA). Other chelators are also contemplated in particular chelators for chelating radiometals.
[0133] Further chelators that are contemplated, for example for chelating .sup.99mTc, include, but are not limited to, diamidedithiols (N.sub.2S.sub.2), triamidethiols (N.sub.3S), tetraamines (N.sub.4) and hydrazinonicotinic acid (HYNIC). HYNIC is usually used in combination with co-ligands to complete the coordination sphere of the metal, which include and are not limited to ethylendiamine-N,N′-diacetic acid (EDDA) and tricine. In some embodiments, using the organometallic aqua ion .sup.99mTc(CO).sub.3(H.sub.2O).sub.3, tricarbonyl complexes can be generated by exchanging water molecules with mono-, di- and tridentate chelators to form stable complexes including also the click-to-chelate methodology.
[0134] Further chelators, which are for example useful for labelling the peptidomimetics with .sup.68Ga, include, but are not limited to N,N′-bis[2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N′-diacetic acid (HBED-CC), siderophore-based ligands such as desferrioxamine, hydroxypyridinone ligands such as deferiprone and tris(hydroxypyridinone) (THP), and derivatives thereof.
[0135] Preferred prosthetic groups of the present invention are labelled with radionuclides of halogens such as iodine or fluorine, for example those mentioned herein. In some embodiments the prosthetic group will be selected from a group consisting of the Bolton-Hunter reagent, N-succinimidyl-5-(trialkylstannyl)-3-pyridinecarboxylates or N-succinimidyl-4-[.sup.131I]iodobenzoate ([.sup.131I]SIB) for radioiodination. In some embodiments the prosthetic group will be selected from a group comprising but not limited to 4-[.sup.18F]fluorophenacyl bromide, N-succinimidyl-4-[.sup.18F]fluorobenzoate ([.sup.18F]SFB), N-succinimidyl-4-([.sup.18F]fluoromethyl)benzoate, 4-[.sup.18F]fluorobenzaldehyde, 6-[.sup.18F]fluoronicotinic acid tetrafluorophenyl ester ([.sup.18F]F-Py-TFP), silicon-containing building blocks such as N-Succinimidyl 3-(di-tert-butyl[.sup.18F]fluorosilyl)benzoate ([.sup.18F]SiFB), carbohydrate-based prosthetic groups, such as [.sup.18F]fluoro-deoxyglucose, preferably 2-[.sup.18F]fluoro-2-deoxyglucose ([.sup.18F]FDG), and [.sup.18F]fluoro-deoxymannose, preferably [.sup.18F]2-fluoro-2-deoxymannose, or derivatives thereof, maleimide-based and heterocyclic methylsulfone-based .sup.18F-synthons, .sup.18F-labelled prosthetic groups such as .sup.18F-azides or .sup.18F-alkynes permitting labelling via click chemistry, .sup.18F-labelled organotrifluoroborates and [.sup.18F]fluoropyridines. In some embodiments a chelator-based labelling approach using aluminum-fluoride (Al.sup.18F) is applied for radiofluorination.
Further Aspects and Embodiments of the Invention
[0136] The present invention also relates to a method of producing the present peptidomimetics as described herein. Production of the present peptidomimetics is possible by standard organic chemistry methods and solid phase peptide synthesis methods available to the person skilled in the art. The method at least comprises synthesizing the amino acid polymer of the peptidomimetic (Behrendt R et al., J Pept Sci 2016, 22: 4-27; Jones J, Amino Acid and Peptide Synthesis, Oxford University Press, New York 2002; Goodman M, Toniolo C, Moroder L, Felix A, Houben-Weyl Methods of Organic Chemistry, Synthesis of Peptides and Peptidomimetics, workbench edition set, Thieme Medical Publishers, 2004).
[0137] The present invention further relates to pharmaceutical and diagnostic compositions comprising the peptidomimetic described herein. Pharmaceutical compositions according to the present invention can be used in the treatment of CCK2R related diseases, such as diseases that are characterized by CCK2R expression or overexpression. In some embodiments the pharmaceutical compositions of the present invention can be used in the treatment of cancer, in particular such cancers that are characterized by expression of CCK2R. In some embodiments of the present invention the pharmaceutical compositions of the present invention can be used to deliver a cytotoxic group, such as a chemotherapeutic agent or a radionuclide to CCK2R expressing tumour cells. Thus, pharmaceutical compositions of the present invention can be used for targeted cancer therapy.
[0138] The present invention also relates to a kit comprising one or more components of the present invention, for instance, the pharmaceutical or diagnostic composition according to the present invention or the peptidomimetic according to the present invention. The kit may further comprise an information leaflet that provides explanations how to prepare or use the peptidomimetic, pharmaceutical composition or diagnostic composition of the present invention. In one embodiment, the kit comprises the pharmaceutical or diagnostic composition of the present invention ready for use. In a further embodiment, the kit comprises two or more compositions that are sufficient to prepare the pharmaceutical or diagnostic composition, ready for use. For instance, in one embodiment, the kit may comprise a first composition comprising a peptidomimetic that comprises a chelator, and a second composition comprising a reporter or cytotoxic group. To prepare the final diagnostic or therapeutic composition, the skilled person would follow the information leaflet provided in the kit and combine the first and second composition to generate a ready to use diagnostic or therapeutic composition.
[0139] Diagnostic compositions of the present invention can be used for diagnostic purposes. Diagnostic compositions of the present invention can be administered to the patient as part of the diagnostic process, for example, to allow imaging of CCK2R expressing cells or tissues, for example CCK2R expressing tumour cells. The diagnostic composition of the present invention can be used in methods of imaging, such as methods of imaging according to the present invention, for example methods of imaging tumour cells.
[0140] The present invention also relates to a use of the peptidomimetic of the present invention described herein for delivering a reporter group or a cytotoxic group as described herein to a cell. Preferably, the reporter group or cytotoxic group is delivered to a cell that expresses CCK2R, for example a cancer cell expressing CCK2R. The use of the present peptidomimetic can be in vivo or in vitro. For example, the peptidomimetic of the present invention can be used to deliver a reporter group or a cytotoxic group to a human or animal, for example a mammal, such as mouse, rat, rabbit, hamster or other mammals. In some embodiments of the present invention the peptidomimetic can be used to deliver a reporter group or a cytotoxic group to cells ex vivo, for example, immortalized or primary cell lines that are cultured in cell culture.
[0141] The present invention also relates to a method of imaging cells as described herein. The method of imaging cells described herein makes use of the peptidomimetic described herein. In some embodiments of the present invention, the method of imaging cells makes use of a non-therapeutic peptidomimetic as described herein. The present method of imaging cells may involve or can be based on established methods of imaging, such as computer tomography (CT), magnetic resonance imaging (MRI), scintigraphy, SPECT, PET, or other similar techniques. Based on the individual method of imaging that is used, the skilled person will select the proper reporter group. The present method of imaging cells can be carried out in vivo or in vitro. In some embodiments of the present invention contacting a cell with the peptidomimetic of the present invention involves administering the peptidomimetic described herein to a patient, for example a patient that suffers from cancer, for example a cancer that involves the expression of CCK2R. In some preferred embodiments the cell is a tumour cell. Thus, in some preferred embodiments a tumour cell is contacted with the peptidomimetic. In some preferred embodiments, the tumour cell expresses CCK2R.
[0142] In some embodiments, the present invention also relates to a method of treating a patient that suffers from a disease that involves the expression of CCK2R, for example a cancer that is characterized by the expression of CCK2R in the tumour cells. Such a method of treating a patient involves the administration of the peptidomimetic of the present invention to the patient.
[0143] In some embodiments, the present invention relates to the peptidomimetic described herein for use in therapy. In preferred embodiments of the present invention the peptidomimetic is for use in the treatment of cancer. Preferably, the cancer is a cancer that expresses CCK2R on the surface of tumour cells.
[0144] The peptidomimetic of the present invention is useful for the diagnostic workup and treatment of various types of cancer, for example: thyroid cancer such as medullary thyroid carcinomas (MTC), lung cancers such as small cell lung cancer (SCLC), gastrointestinal stromal tumours, tumours of the nervous system such as astrocytomas and meningiomas, stromal ovarian cancers, gastrointestinal cancers, neuroendocrine tumours, gastroenteropancreatic tumours, neuroblastomas, tumours of the reproductive system such as breast carcinomas, endometrial carcinomas, ovarian cancers and prostate carcinomas, insulinomas, vipomas, bronchial and ileal carcinoids, leiomyosarcomas, leiomyomas and granulosa cell tumours. In some preferred embodiments the above mentioned types of cancer express CCK2R.
EXAMPLES
Example 1: Synthesis of the Peptidomimetics of the Present Invention
[0145] The synthesis of the peptidomimetics of the present invention was performed using standard 9-fluorenylmethoxycarbonyl (Fmoc) chemistry.
[0146] The peptidomimetics were assembled on a Rink Amide MBHA resin (Novabiochem, Hohenbrunn, Germany) in N-methyl-2-pyrrolidone (NMP) using an excess of Fmoc-protected amino acid, 1-Hydroxy-7-azabenzotriazole (HOAt), and (2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) in alkaline medium. The reactive side chains of the amino acids were masked with appropriate protection groups. After assembling the desired amino acid sequence, coupling of Boc protected DOTA or HYNIC was performed followed by cleavage of the peptidomimetic from the resin with concomitant removal of acid-labile protecting groups. After HPLC purification and lyophilization the peptidomimetics were obtained in >20% yield with a chemical purity ≥95% as confirmed by RP-HPLC and MALDI-TOF MS. Radiolabelling of the inventive peptidomimitics with different radiometals was performed using standard radiolabelling protocols by dissolving the peptide in aqueous solution such as 25-50% ethanol and mixing the solution with an acidic solution such as hydrochloric acid containing the radiometal and a solution such as sodium acetate solution or ascorbic acid solution for pH adjustment and incubating the mixture at high temperature (90-95° C.) for approximately 30 min. Radiolabelling with the different radiometals resulted in high labelling yields and radiochemical purity. HPLC analysis of the peptidomimetics and of the radiolabelled derivatives was performed on a Dionex chromatography system consisting of a Dionex UltiMate 3000 Pump (Dionex, Gemering, Deutschland), UV detection at 280 nm (UltiMate 3000 variable UV-detector) and radiodetection (Gabi Star, Raytest, Straubenhardt, Germany) and using a Phenomenex Jupiter 4μ Proteo 90A 250×4.6 (C12) column and a flow rate of 1 mL/min together with a gradient system of water containing 0.1% TFA (solvent A) and acetonitrile containing 0.1% TFA (solvent B): 0-3 min 10% B, 3-18 min 10-55% B, 18-20 min 80% B, 20-21 min 10% B, 21-25 min 10%.
[0147] The following peptidomimetics (Table 4) were synthesized according to the above method:
TABLE-US-00004 TABLE 4 Name Structure DOTA-MGS5 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 HYNIC-MGS5 HYNIC-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-MGS5-2 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-2Nal-NH.sub.2 DOTA-MGS8 DOTA-DGlu-Pro-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-MGS9 DOTA-DLys-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-MGS10 DOTA-DGlu-Tyr-Pro-Gly-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-MGS11 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-(N-Me)1Nal-NH.sub.2 HYNIC-MGS11 HYNIC-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-(N-Me)1Nal-NH.sub.2 DOTA-MGS12 DOTA-DGlu-Ala-Tyr-Pro-Trp-(N-Me)Nle-Asp-1Nal-NH.sub.2 DOTA-MGS16 DOTA-DGlu-Ala-Tyr-Gly-Trp-(N-Me)Nle-Asp-Phe-NH.sub.2
Example 2: Peptidomimetics of the Present Invention have Increased Stability in Human Serum In Vitro
[0148] To characterise the radiolabelled peptidomimetics in vitro, the stability in human serum was studied. The peptidomimetics labelled with .sup.111In were incubated in fresh human serum at a concentration of 500-2000 pmol/mL at 37° C. for up to 24 h and the degradation was assessed by radio-HPLC. For this purpose human serum samples were precipitated with ACN, centrifuged at 2000 g for 2 min and diluted with water (1:1/v:v) prior to HPLC analysis on a Dionex chromatography system including radiodetection and UV detection equipped with a Phenomenex Jupiter Proteo C12 column (90 Å, 4 μm, 250×4.6 mm) column or a Bischoff Chromatography Nucleosil C18 column (120 Å, 5 μm, 250×4.6 mm) using different water/acetonitrile/0.1% TFA gradient systems. As shown in
Example 3: Peptidomimetics of the Present Invention Bind to Serum Proteins
[0149] Additionally, protein binding to serum proteins was investigated. For this purpose the .sup.111In-labelled peptidomimetics were incubated in duplicates in fresh human serum at 37° C. (500 pmol/mL) and analyzed after 4 and 24 h by Sephadex G-50 size-exclusion chromatography (GE Healthcare Illustra, Little Chalfont, UK). The percentage of protein binding was determined by measuring the column and the eluate in a 2480 Wizard 2 automatic gamma-counter (Perkin Elmer Life Sciences and Analytical Sciences, Turku, F). The results are summarized in Table 5.
TABLE-US-00005 TABLE 5 Percentage of Percentage of radioligand radioligand bound to serum bound to serum proteins after proteins after Peptidomimetic 4 h incubation 24 h incubation .sup.111In-DOTA-MG 1 1 10.1 ± 2.7% 6.25 ± 1.7% .sup.111In-DOTA-MGS1 20.0 ± 1.8% 28.8 ± 3.5% .sup.111In-DOTA-MGS4 8.9 ± 4.5% 11.9 ± 4.7% .sup.111In-DOTA-MGS5 41.0 ± 0.2% 44.3 ± 0.3% .sup.111In-DOTA-MGS5-2 31.7 ± 0.7% 34.6 ± 0.3% .sup.111In-DOTA-MGS8 44.5 ± 1.8% 52.8 ± 0.1% .sup.111In-DOTA-MGS9 26.6 ± 0.8% 27.8 ± 0.4% .sup.111In-DOTA-MGS10 56.7 ± 0.1% 53.4 ± 0.2% .sup.111In-DOTA-MGS11 31.9 ± 0.3% 39.8 ± 4.2% .sup.111In-DOTA-MGS12 41.2 ± 0.04% 45.9 ± 0.5% Protein binding of .sup.111In-labelled peptidomimetics determined after 4 and 24 h incubation in human serum in comparison with .sup.111In-DOTA-MG11,.sup.111In-DOTA-MGS1 and .sup.111In-DOTA-MGS4 (expressed as percentage of radioligand bound to serum proteins)
[0150] When compared with .sup.111In-DOTA-MG11 showing a protein binding of <10% after 24 h incubation, .sup.111In-DOTA-MGS4 showed a similar protein binding (˜12%). The radiolabelled peptidomimetics of the present invention showed a higher protein binding, as indicated in Table 5. .sup.111In-DOTA-MGS5-2, .sup.111In-DOTA-MGS9 and .sup.111In-DOTA-MGS11 showed an intermediate protein binding of ˜30%. With four peptidomimetics high protein binding was observed with values >40% for .sup.111In-DOTA-MGS5 and .sup.111In-DOTA-MGS12, and >50% for .sup.111In-DOTA-MGS8 and .sup.111In-DOTA-MGS10 after 24 h incubation.
Example 4: Peptidomimetics of the Present Invention have High Affinity for CCK2R
[0151] Affinity for CCK2R was studied in A431 human epidermoid carcinoma cells stably transfected with the plasmid pCR3.1 containing the full coding sequence for the human CCK2R (A431-CCK2R) kindly provided by Dr. Luigi Aloj (Aloj L et al., J Nucl Med 2004, 45: 485-494). The binding affinity was tested in a competition assay against [.sup.125I]Tyr.sup.12-gastrind in comparison with pentagastrin (Boc-β-Ala-Trp-Met-Asp-Phe-NH.sub.2; SEQ ID NO:18), DOTA-MG11, and PP-F11, a peptide analogue derived from MG0 by substitution of the penta-Glu sequence with five D-glutamic acid residues, as well as DOTA-MGS1 and DOTA-MGS4. Radioiodination of gastrin-1 was carried out using the chloramine-T method. Non-carrier-added [.sup.125I-Tyr.sup.12]gastrind was obtained by HPLC purification and stored in aliquots at −20° C. Binding assays were carried out in 96-well filter plates (MultiScreen.sub.HTS-FB, Merck Group, Darmstadt, Germany) pretreated with 10 mM TRIS/139 mM NaCl pH 7.4 (2×250 μl). For the assay a number of 200,000-400,000 A431-CCK2R cells per well was prepared in 35 mM HEPES buffer pH 7.4 containing 10 mM MgCl.sub.2, 14 μM bacitracin and 0.5% BSA (a hypotonic solution disturbing the integrity of the cell membranes). The cells were incubated in triplicates with increasing concentrations of the peptidomimetics (0.0003 to 10,000 nM, for example 0.001 to 1000 nM) and [.sup.125I-Tyr.sup.12]gastrin-I (20,000-60,000 cpm) for 1 h at RT. Incubation was interrupted by filtration of the medium and rapid rinsing with ice-cold 10 mM TRIS/139 mM NaCl pH 7.4 (2×200 μl) and the filters were counted in the gamma-counter. Half maximal inhibitory concentration (IC50) values were calculated following nonlinear regression with Origin software (Microcal Origin 6.1, Northampton, Mass.) and a representative assay was chosen for comparison. As shown in Table 6 a high binding affinity for the CCK2R with IC50 values in the low nanomolar range could be confirmed for all tested peptidomimetics.
TABLE-US-00006 TABLE 6 Tested CCK2R ligand IC50 [nM] pentagastrin 0.9 ± 0.3 DOTA-MG11 0.9 ± 0.5 PP-F11 0.4 ± 0.1 DOTA-MGS1 1.9 ± 0.2 DOTA-MGS4 1.2 ± 0.2 DOTA-MGS5 0.4 ± 0.2 HYNIC-MGS5 6.0 ± 1.5 DOTA-MGS5-2 1.6 ± 0.4 DOTA-MGS8 1.6 ± 0.2 DOTA-MGS9 1.8 ± 0.4 DOTA-MGS10 0.9 ± 0.2 Receptor binding of the inventive CCK2R targeting peptidomimetics in comparison with pentagastrin, DOTA-MG11, DOTA-MGS1 and DOTA-MGS4 on A431-CCK2R cells as analyzed by displacement with [.sup.125I]Tyr.sup.12-gastrind-I
Example 5: Peptidomimetics of the Present Invention Show Improved Cellular Internalization
[0152] These studies were carried out according to a previously published protocol (von Guggenberg E et al., Bioconjug Chem 2004, 15: 864-871) using 1.0 million of A431-CCK2R cells as well as the same cell line transfected with the empty vector alone (A431-mock) as a control. DMEM supplemented by 1% (v/v) fetal bovine serum was used as internalization medium and the non-specific cell uptake was studied in A431-mock cells instead of performing blocking studies. The cells were incubated in triplicates with 10,000-500,000 cpm, for example 10,000-30,000 cpm of radiolabelled peptidomimetic (corresponding to a final concentration of 0.4 nM and ˜600 fmol of total peptidomimetic in the assay) and incubated at 37° C. for 2 h. The internalized fraction in A431-CCK2R and A431-mock cells was expressed in relation to the total activity added (% of total). For each radiolabelled peptidomimetic the mean value of one representative assay performed in triplicates is represented. For .sup.111In-DOTA-MGS1 and .sup.111In-DOTA-MGS4 the mean value of the cell uptake obtained from two independent assays was considered.
[0153] The cellular internalization of different radiolabelled peptidomimetics of the present invention was compared to PP-F11 and PP-F11N. These two peptide derivatives are derived from MG0 by substitution of the penta-Glu sequence with five D-glutamic acid residues and additional substitution of Met with Nle in PP-F11N. In comparison with PP-F11 and PP-F11N labelled with .sup.111In and .sup.177Lu all radiolabelled peptidomimetics of the present invention show an increased cellular internalization. As shown in
[0154] Further cell uptake studies were performed with different DOTA and HYNIC conjugated peptidomimetics of the present invention to confirm the surprisingly high cell uptake also for radiolabelling with other radiometals. As shown in
Example 6: Peptidomimetics of the Present Invention Show Improved Biodistribution In Vivo
[0155] Biodistribution studies evaluating the tumour uptake of the radiolabelled inventive CCK2R targeting peptide analogues were performed in 7-week-old female athymic BALB/c nude mice (Charles River, Sulzfeld, Germany). All animal experiments were conducted in compliance with the Austrian animal protection laws and with the approval of the Austrian Ministry of Science. For the induction of tumour xenografts, A431-CCK2R and A431-mock cells were injected subcutaneously in the right and left flank respectively (2 million cells in 200 μl). When tumours had reached a size of approximately 0.2 ml biodistribution studies were carried out. Groups of 4 mice were injected intravenously via a lateral tail vein with the peptidomimetics of the present invention, labelled with .sup.111In (approximately 0.2 MBq and 0.02 nmol peptidomimetic), with .sup.68Ga (approximately 0.8 MBq and 0.02-0.03 nmol peptidomimetic), with .sup.177Lu (approximately 0.5 MBq and 0.02 nmol peptidomimetic) or with .sup.99mTc (approximately 0.3 MBq and 0.02 nmol peptidomimetic). After a time period of 1 or 4 h post-injection (p.i.) the animals were sacrificed by cervical dislocation, tumours and other tissues (blood, lung, heart, muscle, bone, spleen, intestine, liver, kidneys, stomach, pancreas) were removed, weighed, and their radioactivity measured in the gamma counter. Results were expressed as percentage of injected activity per gram tissue (% IA/g) and tumour to organ activity ratios were calculated from the activity measured in the dissected tissues. In
[0156] The exceptional combination of low uptake in blood and normal tissue combined with very high tumour uptake and tumour retention over time resulted in very favourable tumour to organ activity ratios, especially for the peptidomimetics DOTA-MGS5, DOTA-MGS5-2, DOTA-MGS8 and DOTA-MGS10. High tumour-to-kidney ratios in the order of .sup.111In-DOTA-MGS8 (11.6±3.0) >.sup.111In-DOTA-MGS10 (9.3±2.0) >.sup.111In-DOTA-MGS5 (6.4±0.6) >.sup.111In-DOTA-MGS5-2 (6.0±0.9) were observed.
[0157] When comparing the tumour-to-kidney ratio of the model peptidomimetic MGS5 radiolabelled with different radioisotopes a tumour-to-kidney ratio in the order of .sup.177Lu-DOTA-MGS5 (6.5±1.6) >.sup.111In-DOTA-MGS5 (6.4±0.6) >.sup.68Ga-DOTA-MGS5 (4.1±0.3) >.sup.99mTc-HYNIC-MGS5 (3.3±1.1) was reached. These impressing biodistribution properties remain unmatched in the literature. So far, similar improvements in the targeting profile of CCK2R targeting peptides have been achieved only by the co-administration of an enzyme inhibitor (Kaloudi A et al., Q J Nucl Med Mol Imaging 2015, 59: 287-302; Nock B A et al., J Nucl Med 2014, 55: 121-127). No similar report exists on a comparable improvement in tumour targeting by single injection of a radiolabelled CCK2R targeting peptide analogue alone. The peptidomimetics of the present invention therefore display outstanding properties. When comparing different .sup.111In-labelled peptide analogues in the same tumour model .sup.111In-DOTA-MG0 showed a tumour uptake of 9.9±2.0% ID/g and .sup.111In-DOTA-MG11 of 3.04±1.30% ID/g (Laverman Petal., Eur J Nucl Med Mol Imaging 2011, 38: 1410-1416). In the series of radioligands studied .sup.111In-PP-F11, a MG analogue with six D-Glu residues, showed the most favourable tumour retention (6.30±2.75% ID/g at 4 h p.i.) combined with a tumour-to-kidney ratio of 1.2±0.5. A similar tumour uptake has been reported also for .sup.177Lu-PP-F11 (6.70±0.60% IA/g) and .sup.177Lu-PP-F11N (6.90±0.80% IA/g) (Sauter A W et al., Eur J Nucl Med Mol Imaging 2016, 43: S238-S239).
[0158] The peptidomimetics of the present invention, in comparison, show a highly improved tumour uptake and tumour-to-kidney ratio, combining the positive features of MG0 (high tumour uptake) and MG11 (low kidney retention) and show a very favourable tumour to kidney ratio.
Example 7: Peptidomimetics of the Present Invention have Increased Stability In Vivo
[0159] To further characterise the stability of the radiolabelled peptidomimetics in vivo, metabolic studies were carried out in 5-6-week-old female BALB/c mice (Charles River, Sulzfeld, Germany) injected intravenously with the .sup.111In- and .sup.111Lu-labelled peptidomimetics. All animal experiments were conducted in compliance with the Austrian animal protection laws and with the approval of the Austrian Ministry of Science. To allow monitoring of the metabolites by radio-HPLC, mice were injected with a higher amount of radioactivity (5-15 MBq .sup.111In and 20-40 MBq .sup.177Lu, corresponding to 1-2 nmol total peptide) through a lateral tail vein and euthanized by cervical dislocation 10 or 30 min post injection (p.i.). A sample of blood was collected and the degradation was assessed by radio-HPLC. For this purpose blood samples were precipitated with ACN, centrifuged at 2000 g for 2 min and diluted with water (1:1/v:v) prior to HPLC analysis using a Dionex chromatography system including radiodetection and UV detection equipped with a Phenomenex Jupiter Proteo C12 column (90 Å, 4 μm, 250×4.6 mm) column or a Bischoff Chromatography Nucleosil C18 column (120 Å, 5 μm, 250×4.6 mm) using different water/acetonitrile/0.1% TFA gradient systems.
[0160] As shown in
[0161] For comparison, metabolic studies in vivo were carried out also with PP-F11 and PP-F11N labelled with Lu-177 (n=1).
TABLE-US-00007 PP-F11: DOTA-DGlu-DGlu-DGlu-DGlu-DGlu-DGlu-Ala-Tyr-Gly-Trp- Met-Asp-Phe-NH.sub.2 PP-F11N: DOTA-DGlu-DGlu-DGlu-DGlu-DGlu-DGlu-Ala-Tyr-Gly-Trp- Nle-Asp-Phe-NH.sub.2
[0162] All bonds (“-”) in PP-F11 and PP-F11N are amide bonds and all amino acids whose enantiomeric form is not expressly indicated are in the L-form.
[0163] These two peptide derivatives are derived from MG0 by substitution of the penta-Glu sequence with five D-glutamic acid residues and additional substitution of Met with Nle in PP-F11N. The two peptide conjugates were developed with the aim to improve the metabolic stability and pharmacokinetics and were first described in 2012 (Kroselj M et al., Eur J Nucl Med Mol Imaging 2012, 39: S533-S534 and WO 2015/067473 A1). For the same time point at 10 min p.i., a low enzymatic stability was confirmed for .sup.177Lu-PP-F11N with 22.3% intact radioligand present in the blood. At 30 min p.i. .sup.177Lu-PP-F11 and .sup.177Lu-PP-F11N showed values of 5.5 and 12.7%, respectively, and resulted to be almost completely degraded.
[0164] The peptidomimetics of the present invention therefore display a much higher stability against enzymatic degradation, as compared, for example, with PP-F11 and PP-F11N of the prior art. Surprisingly, the combination of substitutions in different positions, as according to the present invention, allows completely stabilizing the peptidomimetic.
[0165] Without being bound by any particular theory, it is currently believed that beside improved cellular uptake also the in vivo stability may contribute to the improved tumour uptake and retention. The extremely high tumour uptake and tumour retention as well as very favourable tumour-to-back-ground activity ratios, including kidneys, render the present peptidomimetics particularly useful for diagnostic and therapeutic uses in CCK2R relevant diseases, such as cancer.