Pharmaceutical compositions of water soluble peptides with poor solubility in isotonic conditions and methods for their use
The present invention provides compositions comprising water soluble peptides with poor solubility in isotonic solutions which exhibit enhanced bioavailability with reduced adverse effects including injection site reactions. Methods are also disclosed for using such compositions for the treatment of diseases including, but not limited to, cancer, type 2 diabetes, acromegaly, metabolic disorders, endocrine disorders, exocrine tumors, and hormone-related tumors. Methods to reduce adverse injection site reactions and improve bioavailability are also disclosed.
1. A pharmaceutical composition comprising:
veldoreotide or a pharmaceutically acceptable salt thereof;
an excipient selected from hydroxypropyl-β-cyclodextrin (HPBCD) or dextrose; and
a polymeric microsphere, wherein veldoreotide or the pharmaceutically acceptable salt thereof and the excipient are encapsulated in the polymeric microsphere; and wherein the surface area of the polymeric microsphere is from about 7 m 2 /g to about 12 m 2 /g.
2. The pharmaceutical composition of claim 1 , wherein the polymeric microsphere comprises poly(lactic-co-glycolic acid) (PLGA).
3. The pharmaceutical composition of claim 1 , wherein the excipient is dextrose.
4. The pharmaceutical composition of claim 3 , wherein the amount of dextrose is from about 0.1 weight % to about 1.0 weight % based on the total weight of the polymeric microsphere.
5. The pharmaceutical composition of claim 1 , wherein the diameter of the polymeric microsphere is from about 10 microns to about 100 microns.
6. A process for manufacturing polymeric microspheres comprising the steps of:
(i) mixing an excipient comprising a cyclic polysaccharide or dextrose or a combination thereof, and veldoreotide or a pharmaceutically acceptable salt thereof in water to form a first aqueous mixture;
(ii) mixing a polymer in organic solvent to form a polymeric solution;
(iii) mixing the first aqueous mixture in the polymeric solution to form a first dispersion mixture comprising a water-in-oil primary emulsion;
(iv) mixing polyvinyl alcohol (PVA) in phosphate buffered saline or in saline to form a second aqueous mixture;
(v) mixing the primary emulsion in the second aqueous mixture of PVA to form a water-in-oil-in-water double emulsion thereby providing a secondary dispersion mixture; and
(vi) allowing the organic solvent in the secondary dispersion mixture to evaporate to form polymeric microspheres comprising veldoreotide or pharmaceutically acceptable salt thereof.
7. The process of claim 6 , wherein the excipient is dextrose and the mass ratio of dextrose to veldoreotide or pharmaceutically acceptable salt thereof is from 1:4 to 1:16.
8. The process of claim 6 , wherein the excipient is dextrose and the mass ratio of dextrose to veldoreotide or pharmaceutically acceptable salt thereof is from 1:6 to 1:10.
9. The process of claim 6 , wherein the excipient is dextrose and the mass ratio of dextrose to veldoreotide or pharmaceutically acceptable salt thereof is 1:8.
10. The process of claim 6 , wherein the pharmaceutically acceptable salt of veldoreotide is veldoreotide acetate.
11. The process of claim 6 , wherein the polymeric solution comprises poly(lactic-co-glycolic acid) (PLGA).
12. The pharmaceutical composition of claim 1 , wherein the microsphere comprises a plurality of internal voids separated by thin interstitial boundaries.