Colloidal suspension of nanoparticles based on an amphiphilic copolymer
View Patent ↗An aqueous suspension, stable in physiological medium, of nanoparticles for delivering active principles such as insulin. The delivery particles are based on a three-block copolymer: polyethylene glycol/hydrophilic polyaminoacid/hydrophobic polyaminoacid. These three-block copolymers can be associated with an active principle without denaturing it, and perform a controlled and long-term release of the active principle in vivo, and thus provide the active principle with a very prolonged release. Also disclosed is a powder form solid from which are derived the delivery particles, the preparation of the powder-form solid, a suspension of delivery particles based on the three-block copolymer, and pharmaceutical specialties obtainable from the delivery particles filled with active principle.
1. A colloidal suspension comprising submicronic particles, wherein the particles:
comprise at least one amphiphilic copolymer comprising at least one block of hydrophilic polyalkylene glycol polymer and at least one linear, α-peptide-linked copolyamino acid comprising at least one block of hydrophilic amino acid monomers with one or more ionizable chains which are at least partially ionized and having an absolute length of greater than or equal to 5 IAA monomers and a block of hydrophobic amino acid monomers having an absolute length of greater than or equal to 5 OAA monomers, wherein the copolyamino acid has a block structure;
are individualized supramolecular arrangements;
are in a nondissolved state;
will spontaneously associate with at least one active principle by adsorption, and without the aid of organic solvents or surfactants, when at least one active principle is added to the colloidal suspension; and release of the at least one active principle is in either or both a sustained manner or a delayed manner.
2. The colloidal suspension of claim 1 , wherein the at least one block of hydrophilic polyalkylene glycol polymer has an absolute length of greater than or equal to 5 monomers.
3. The colloidal suspension of claim 1 , wherein the particles comprise at least one amphiphilic copolymer comprising a linear triblock of polyethylene glycol, at least one block of hydrophilic amino acid monomers with one or more ionizable chains and having an absolute length of greater than or equal to 5 IAA monomers, and a block of hydrophobic amino acid monomers having an absolute length of greater than or equal to 5 OAA monomers.
4. The colloidal suspension of claim 3 , wherein the at least one amphiphilic copolymer comprises a linear triblock of polyethylene glycol, glutamate in the at least one block of hydrophilic amino acid monomers, and leucine as the hydrophobic amino acid monomer.
5. The colloidal suspension of claim 1 , wherein the particles have a mean size of between 10 and 500 nm.
6. The colloidal suspension of claim 1 , wherein the suspension is aqueous and stable.
7. The colloidal suspension of claim 1 , wherein the suspension further comprises at least one active principle.
8. The colloidal suspension of claim 7 , wherein the at least one active principle is a vaccine, a protein, a peptide, a polysaccharide, a nucleic acid, an anticancer chemotherapeutic, or a mixture thereof.
9. The colloidal suspension of claim 7 , wherein the at least one active principle is a hemoglobin, a cytochrome, an albumin, an interferon, an antigen, an antibody, erythropoietin, insulin, a growth hormone, factor VIII, factor IX, an interleukin, a hematopoiesis-stimulating factor, heparin, RNA, a DNA, an anthracycline, a taxoid, or a mixture thereof.
10. A process for preparing the colloidal suspension of claim 7 , comprising contacting the colloidal suspension of claim 1 with a liquid phase containing the at least one active principle, to thereby obtain a colloidal suspension of particles further comprising at least one active principle.
11. A process for preparing the colloidal suspension of claim 7 , comprising contacting the colloidal suspension of claim 1 with a solid phase containing the at least one active principle, to thereby obtain a colloidal suspension of particles further comprising the at least one active principle.
12. A pulverulent solid comprising submicronic particles, wherein the pulverulent solid is produced by removing liquid from the colloidal suspension of claim 1 , to thereby produce a pulverulent solid comprising submicronic particles.