Pharmaceutical composition of nanoparticles
View Patent ↗The invention discloses a pharmaceutical composition of bioactive nanoparticles composed of chitosan, poly-glutamic acid, and a bioactive agent for oral delivery. The chitosan-based nanoparticles are characterized with a positive surface charge and enhanced permeability for drug delivery.
1. A method of delivering a bioactive agent to an intestinal tract that bypasses gastric fluid of an animal subject, the method comprising steps of (1) encapsulating said bioactive agent in nanoparticles, thus forming bioactive agent loaded nanoparticles; and (2) delivering said bioactive agent loaded nanoparticles to the intestinal tract via a conduit, wherein the conduit is selected from the group consisting of an endoscope, a syringe, a catheter, a tube, a channel, a pipe, and a duct, wherein said nanoparticles consist of a shell portion that is dominated by positively charged chitosan, and a core portion comprising said positively charged chitosan, a negatively charged substrate, and said bioactive agent.
2. The method according to claim 1 , wherein said nanoparticles consist of a shell portion that is dominated by positively charged chitosan, and a core portion comprising said positively charged chitosan, a negatively charged substrate, and said bioactive agent.
3. The method according to claim 1 , wherein said chitosan is N-trimethyl chitosan, EDTA-chitosan, low molecular weight chitosan, pegylated chitosan (PEG-chitosan), mono-N-carboxymethyl chitosan, N-palmitoyl chitosan (NPCS), chitosan derivatives, or combinations thereof.
4. The method according to claim 1 , wherein said bioactive agent is a pegylated bioactive agent.
5. The method according to claim 1 , wherein said nanoparticles are freeze-dried, thereby said nanoparticles being in a powder form.
6. The method according to claim 1 , wherein said nanoparticles are mixed with a cryoprotectant and then freeze-dried, thereby said nanoparticles being in a powder form.
7. The method according to claim 6 , wherein said cryoprotectant is selected from the group consisting of trehalose, hexan-1,2,3,4,5,6-hexyl, mannitol, dimethyl sulfoxide, ethylene glycol, glycol, 2-methyl-2,4-pentanediol, propylene, sucrose, and combinations thereof.
8. The method according to claim 1 , wherein said nanoparticics are encapsulated in a capsule.
9. The method according to claim 8 , wherein said capsule is made of methyl cellulose selected from the group consisting of hydroxypropyl methyl cellulose (HPMC), carboxymethyl cellulose, hydroxyethyl methyl cellulose (HEMC), and methyl cellulose derivatives.
10. The method according to claim 8 , wherein said capsule is treated with an enteric coating.
11. The method according to claim 8 , wherein said capsule further comprises a pharmaceutically acceptable carrier, diluent, excipient, desiccant, solubilizer, bubbling agent, or emulsifier.
12. The method according to claim 8 , wherein said capsule further comprises at least one absorption enhancer.
13. The method according to claim 12 , wherein said absorption enhancer is selected from the group consisting of bile salts, surfactants, medium-chain fatty acids, phosphate esters, chitosan, and chitosan derivatives.
14. The method according to claim 8 , wherein said capsule further comprises a second type of nanoparticles.
15. The method according to claim 1 , wherein said nanoparticles are treated with an enteric coating.
16. The method according to claim 1 , wherein said, negatively charged substrate is polyglutamic acid (PGA) selected from the group consisting of PGA-complexone conjugate, γ-PGA, α-PGA, derivatives of PGA, and salts of PGA.
17. The method according to claim 1 , wherein said bioactive agent is protein or a peptide.
18. The method according to claim 1 , wherein said bioactive agent is an anti-inflammatory drug, an anti-epileptic drug, an antibiotic, a growth hormone, a human growth hormone, a human growth hormone analog, or an Alzheimer's antagonist.
19. The method according to claim 1 , wherein said bioactive agent is an anti-diabetic drug.
20. The method according to claim 19 , wherein said anti-diabetic drug is selected from the group consisting of insulin, an insulin analog, GLP-1, a GLP-1 analog, an insulin sensitizer, an insulin secretagogue, an inhibitor of dipeptidyl peptidase 4, metformin, alpha-glucosidase inhibitors, amylin analog, sodium-glucose co-transporter type 2 (SGLT2) inhibitors, benfluorex, tolrestat, and combinations thereof.