Nanoparticle containing prostaglandin I
There is provided a beraprost sodium-containing nanoparticle that contains beraprost sodium among other prostaglandin I 2 (prostacyclin) derivatives, which are therapeutic agents for pulmonary hypertension. The beraprost sodium-containing nanoparticle is obtained by making beraprost sodium hydrophobic using a metal ion and allowing the hydrophobic beraprost sodium to react with poly-L-lactic acid or a poly(L-lactic acid/glycolic acid) copolymer, and a poly-DL- or L-lactic acid-polyethylene glycol block copolymer or a poly(DL- or L-lactic acid/glycolic acid)-polyethylene glycol block copolymer. The beraprost sodium-containing nanoparticle excels in sustained release of an active ingredient, reduces a side effect, and furthermore, has an excellent drug retention in the blood. Therefore, the beraprost sodium-containing nanoparticle is quite outstanding particularly regarding the sustainability of the medicinal effect.
1. A beraprost sodium-containing nanoparticle for treatment of pulmonary hypertension obtained by:
(a) converting beraprost sodium represented by the following formula (I):
to a hydrophobicized beraprost sodium using a metal ion; and
(b) allowing the hydrophobicized beraprost sodium to react with poly-L-lactic acid or a poly(L-lactic acid/glycolic acid) copolymer, and a poly-DL- or L-lactic acid-polyethylene glycol block copolymer or a poly(DL- or L-lactic acid/glycolic acid)-polyethylene glycol block copolymer to obtain a beraprost sodium-containing nanoparticle.
2. The beraprost sodium-containing nanoparticle for treatment of pulmonary hypertension according to claim 1 , in which a basic low molecular weight compound is further mixed with the obtained hydrophobicized beraprost sodium.
3. The beraprost sodium-containing nanoparticle for treatment of pulmonary hypertension according to claim 1 , wherein the particle has a diameter of 20 to 300 nm.
4. The beraprost sodium-containing nanoparticle for treatment of pulmonary hypertension according to claim 1 , wherein the metal ion is one or two or more of an iron ion, a zinc ion, a copper ion, a magnesium ion, a calcium ion, a nickel ion, a beryllium ion, a manganese ion, or a cobalt ion.
5. The beraprost sodium-containing nanoparticle for treatment of pulmonary hypertension according to claim 1 , wherein a weight average molecular weight of the poly-DL- or L-lactic acid-polyethylene glycol block copolymer or the poly(DL- or L-lactic acid/glycolic acid)-polyethylene glycol block copolymer is 3,000 to 30,000.
6. The beraprost sodium-containing nanoparticle for treatment of pulmonary hypertension according to claim 2 , wherein the basic low molecular weight compound is one or two or more selected from the group consisting of: (dimethylamino)pyridine, pyridine, piperidine, pyrimidine, pyrazine, pyridazine, quinoline, quinuclidine, isoquinoline, bis(dimethylamino)naphthalene, naphthylamine, morpholine, amantadine, aniline, spermine, spermidine, hexamethylenediamine, putrescine, cadaverine, phenethylamine, histamine, diazabicyclooctane, diisopropylethylamine, monoethanolamine, diethanolamine, triethanolamine, ethylamine, diethylamine, triethylamine, methylamine, dimethylamine, trimethylamine, triethylenediamine, diethylenetriamine, ethylenediamine, and trimethylenediamine.
7. A pharmaceutical preparation for treatment of pulmonary hypertension comprising a beraprost sodium-containing nanoparticle, wherein the beraprost sodium-containing nanoparticle is obtained by:
(a) converting beraprost sodium represented by the following formula (I):
to a hydrophobicized beraprost sodium using a metal ion; and
(b) allowing the hydrophobicized beraprost sodium to react with poly-L-lactic acid or a poly(L-lactic acid/glycolic acid) copolymer, and a poly-DL- or L-lactic acid-polyethylene glycol block copolymer or a poly(DL- or L-lactic acid/glycolic acid)-polyethylene glycol block copolymer to obtain a beraprost sodium-containing nanoparticle.
8. The pharmaceutical preparation for treatment of pulmonary hypertension comprising the beraprost sodium-containing nanoparticle recited in claim 7 , in which a basic low molecular weight compound is mixed with the obtained hydrophobicized beraprost sodium.
9. The pharmaceutical preparation for treatment of pulmonary hypertension comprising the beraprost sodium-containing nanoparticle recited in claim 7 , wherein the particle has a diameter of 20 to 300 nm.
10. The pharmaceutical preparation for treatment of pulmonary hypertension comprising the beraprost sodium-containing nanoparticle recited in claim 7 , wherein the metal ion is one or two or more of an iron ion, a zinc ion, a copper ion, a magnesium ion, a calcium ion, a nickel ion, a beryllium ion, a manganese ion, or a cobalt ion.
11. The pharmaceutical preparation for treatment of pulmonary hypertension comprising the beraprost sodium-containing nanoparticle recited in claim 7 , wherein a weight average molecular weight of the poly-DL- or L-lactic acid-polyethylene glycol block copolymer or the poly(DL- or L-lactic acid/glycolic acid)-polyethylene glycol block copolymer is 3,000 to 30,000.
12. The pharmaceutical preparation for treatment of pulmonary hypertension comprising the beraprost sodium-containing nanoparticle recited in claim 8 , wherein the basic low molecular weight compound is one or two or more selected from the group consisting of: (dimethylamino)pyridine, pyridine, piperidine, pyrimidine, pyrazine, pyridazine, quinoline, quinuclidine, isoquinoline, bis(dimethylamino)naphthalene, naphthylamine, morpholine, amantadine, aniline, spermine, spermidine, hexamethylenediamine, putrescine, cadaverine, phenethylamine, histamine, diazabicyclooctane, diisopropylethylamine, monoethanolamine, diethanolamine, triethanolamine, ethylamine, diethylamine, triethylamine, methylamine, dimethylamine, trimethylamine, triethylenediamine, diethylenetriamine, ethylenediamine, and trimethylenediamine.
13. A formulation for parenteral administration in a form of an intravenous injection formulation or a local injection formulation, wherein the formulation comprises a pharmaceutical preparation for treatment of pulmonary hypertension comprising a beraprost sodium-containing nanoparticle, wherein the beraprost sodium-containing nanoparticle is obtained by:
(a) converting beraprost sodium represented by the following formula (I):
to a hydrophobicized beraprost sodium using a metal ion; and
(b) allowing the hydrophobicized beraprost sodium to react with poly-L-lactic acid or a poly(L-lactic acid/glycolic acid) copolymer, and a poly-DL- or L-lactic acid-polyethylene glycol block copolymer or a poly(DL- or L-lactic acid/glycolic acid)-polyethylene glycol block copolymer to obtain a beraprost sodium-containing nanoparticle.
14. The formulation for parenteral administration recited in claim 13 , in which a basic low molecular weight compound is mixed with the obtained hydrophobicized beraprost sodium.
15. The formulation for parenteral administration recited in claim 13 , wherein the particle has a diameter of 20 to 300 nm.
16. The formulation for parenteral administration recited in claim 13 , wherein the metal ion is one or two or more of an iron ion, a zinc ion, a copper ion, a magnesium ion, a calcium ion, a nickel ion, a beryllium ion, a manganese ion, or a cobalt ion.
17. The formulation for parenteral administration recited in claim 13 , wherein a weight average molecular weight of the poly-DL- or L-lactic acid-polyethylene glycol block copolymer or the poly(DL- or L-lactic acid/glycolic acid)-polyethylene glycol block copolymer is 3,000 to 30,000.
18. The formulation for parenteral administration recited in claim 14 , wherein the basic low molecular weight compound is one or two or more selected from the group consisting of: (dimethylamino)pyridine, pyridine, piperidine, pyrimidine, pyrazine, pyridazine, quinoline, quinuclidine, isoquinoline, bis(dimethylamino)naphthalene, naphthylamine, morpholine, amantadine, aniline, spermine, spermidine, hexamethylenediamine, putrescine, cadaverine, phenethylamine, histamine, diazabicyclooctane, diisopropylethylamine, monoethanolamine, diethanolamine, triethanolamine, ethylamine, diethylamine, triethylamine, methylamine, dimethylamine, trimethylamine, triethylenediamine, diethylenetriamine, ethylenediamine, and trimethylenediamine.