Multifunctional nanoparticles for theragnosis

Patent metadata

Field	Value
Publication number	US-2021162077-A1
Application number	US-201917265790-A
Country	US
Kind code	A1
Filing date	Apr 12, 2019
Priority date	Apr 12, 2018
Publication date	Jun 3, 2021
Grant date	—

Abstract

The present invention relates to the field of medicine, particularly to functionalised nanoparticles (NP) for use in cancer therapy (treatment or diagnosis), to pharmaceutical compositions or nano devices comprising same, and also to a method for obtaining said functionalised nanoparticles. The nanoparticles described in the present invention can be used specifically to treat cancer efficiently, as same can selectively detect tumour cells.

First claim

1 . Method for producing functionalised polystyrene nanoparticles (NPs), preferably functionalised amino polystyrene NPs that can be bifunctionalised, comprising the following steps:
a) introducing the NPs in a suitable medium, preferably dimethylformamide (DMF), in which a PEG spacer (or any other suitable spacer) protected, preferably by Fmoc (fluorenylmethoxycarbonyl), preferably Fmoc-4,7,10-trioxa-1,13-tridecanediamine succinamic acid (Fmoc-PEG-OH), is either dissolved and activated in the medium or activated before being dissolved in the medium, for a period of time sufficient for coupling the PEG spacer protected with Fmoc, preferably Fmoc-PEG-OH, to the amino nanoparticles; b) optionally deprotecting the Fmoc group of the NPs of step a) and then adding one or more PEG spacers protected with Fmoc, preferably Fmoc-4,7,10-trioxa-1,13-tridecanediamine succinamic acid (Fmoc-PEG-OH), in the same manner as described in step a); c) deprotecting the Fmoc group of the NPs of step a) or b) and then adding one or more amino acids or the analogues thereof, preferably one or more lysines having the N-α-amino and N-ε groups thereof protected by orthogonal protecting groups such as Dde and Fmoc, preferably Fmoc-Lys (Dde); and d) optionally deprotecting the Fmoc group of the NPs of step c) and then adding one or more PEG spacers protected with Fmoc, preferably Fmoc-4,7,10-trioxa-1,13-tridecanediamine succinamic acid (Fmoc-PEG-OH), in the same manner as described in step a).

2 . Method for producing bifunctionalised polystyrene nanoparticles (NPs), preferably functionalised amino polystyrene NPs, comprising the steps according to claim 1 , wherein the nanoparticles are bifunctionalised by deprotecting the Fmoc and Dde groups and coupling two chemical groups, used for the bifunctionalisation of the NPs, respectively, to the Dde-bonded amino group of the lysine side chain before the deprotection step and to the Fmoc-bonded amino group before the deprotection step.

3 . Method for producing polystyrene nanoparticles (NPs), preferably functionalised amino polystyrene NPs, which can be trifunctionalised, comprising the steps according to claim 1 and an additional step comprising:
e) deprotecting the Fmoc group of the NPs of step d) or c) and then adding one or more amino acids or analogues orthogonally protected with Dde and Fmoc, preferably Fmoc-lysine (Dde).

4 . Method for producing trifunctionalised polystyrene nanoparticles (NPs), comprising the steps according to claim 3 , wherein the nanoparticles are trifunctionalised by deprotecting the Fmoc and Dde groups and bonding three chemical groups, used for the trifunctionalisation of the NPs, respectively, at least two amino groups of the lysine side chain, respectively, bonded to the Dde groups before the deprotection step and to the Fmoc group-bonded amino before the deprotection step.

5 . Method for producing polystyrene nanoparticles (NPs) or functionalised polystyrene NPs which can be trifunctionalised, wherein the trifunctionalisation of the NPs is performed by bonding to the NPs a chemical group comprising two PEG spacers that are orthogonally protected, preferably with Fmoc, preferably Fmoc-4,7,10-trioxa-1,13-tridecanediamine succinamic acid (Fmoc-PEG-OH), said spacers each having two units and two amino acids or analogues having the N-α-amino and N-ε groups thereof protected by orthogonal protecting groups such as Dde and Fmoc, preferably Fmoc-Lys (Dde).

6 . The method according to claim 3 , wherein a first spacer having two PEG units is coupled directly to the NPs; a first amino acid or analogue, preferably orthogonally protected lysine, is coupled directly to the amino group of the first PEG spacer; the second PEG spacer is coupled directly to the alpha-amino group of the first lysine group, and the second lysine group is coupled directly to the amino group of the second PEG spacer.

7 . Method for producing functionalised polystyrene nanoparticles (NPs) or amino-functionalised nanoparticles, comprising the steps according to any of claim 5 or 6 , wherein the nanoparticles are trifunctionalised by deprotecting the Fmoc and Dde groups and bonding three chemical groups, used for the trifunctionalisation of the NPs, respectively, at least two amino groups of the lysine side chain, respectively, bonded to the Dde groups before the deprotection step and to the Fmoc group-bonded amino before the deprotection step.

8 . Method according to any of the preceding claims, wherein the NPs are characterised by being cross-linked with divinylbenzene.

9 . Method according to any of claim 4 or 7 , wherein the nanoparticle is trifunctionalised with (a) at least one imaging agent (T), at least one bioactive molecule (D), and at least one ligand (L).

10 . Polystyrene or amino polystyrene nanoparticle trifunctionalised preferably with (a) at least one imaging agent (T), at least one bioactive molecule (D), and at least one ligand (L), wherein said nanoparticle is bonded to a chemical group moiety comprising two PEG spacers protected with Fmoc, preferably Fmoc-4,7,10-trioxa-1,13-tridecanediamine succinamic acid (Fmoc-PEG-OH), said spacers each having two units and two amino acids or analogues, preferably a lysine having the N-α-amino and N-ε groups thereof protected by orthogonal protecting groups such as Dde and Fmoc, preferably Fmoc-Lys (Dde).

11 . Nanoparticle according to claim 10 , wherein a first PEG spacer having two units is coupled directly to the NPs; a first lysine is bonded directly to the amino group of the first PEG spacer; the second PEG spacer is coupled directly to the alpha-amino group of the first lysine group, and the second lysine group is coupled directly to the amino group of the second PEG spacer.

12 . Nanoparticle according to any of claim 10 or 11 , wherein the size range of the nanoparticle is from 100 nm to 2000 nm, preferably about 200 nm.

13 . Nanoparticle according to any of claims 10 to 12 or obtained by means of the method according to claim 9 , wherein the bioactive molecule (D) is a therapeutic agent, a diagnostic agent, or a drug, preferably doxorubicin.

14 . Nanoparticle according to any of claims 10 to 13 or obtained by means of the method according to claim 9 , wherein the ligand (L) is a tumour-specific peptide or peptidomimetic, preferably a homing peptide RGD.

15 . Nanoparticle according to any of claims 10 to 14 or obtained by means of the method according to claim 9 , wherein the imaging agent (T) is a fluorophore, preferably a far-red cyanine derivative (Cy7).

16 . Nanodevice comprising a nanoparticle according to any of claims 10 to 15 .

17 . Nanoparticle according to any of claims 10 to 15 or nanodevice of claim 16 , for use in the treatment of cancer, the diagnosis of cancer, or in the control of the treatment of cancer.

18 . Nanoparticle obtained by means of the method according to claims 1 to 9 , for use in the treatment of cancer, the diagnosis of cancer, or in the control of the treatment of cancer.

19 . Pharmaceutical formulation comprising a nanoparticle obtained by means of the method according to claims 1 to 9 .

20 . Pharmaceutical formulation comprising the nanoparticle according to any of claims 10 to 15 .

Assignees

• Univ Granada

Inventors

• Sánchez Martín Rosario María
• Marchal Corrales Juan Antonio
• Díaz Mochón Juan José
• Cano Cortés Victoria
• Navarro Marchal Saúl Abenhamar
• RUIZ BLAS Maria Paz

Classifications

• A61K9/5138

  obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates · CPC title

• C08F8/30

  Introducing nitrogen atoms or nitrogen-containing groups · CPC title

• C08F12/28

  Amines · CPC title

• A61K47/6933 Primary

  the polymer being obtained by reactions only involving carbon to carbon, e.g. poly(meth)acrylate, polystyrene, polyvinylpyrrolidone or polyvinylalcohol · CPC title

• A61K47/60

  the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol · CPC title