Patent · US9446226B2 · B2 · US
Drug-delivering composite structures
- (11) Publication number
- US9446226B2
- (21) Application number
- 11/634,910
- (22) Filing date
- 2006-12-07
- (30) Priority date
- 2005-12-07
- (43) Publication date
- 2016-09-20
- (45) Date of grant
- 2016-09-20
- (51) IPC
- B32B 27/04; A61K 9/70; A61M 31/00; D06M 16/00
- (52) CPC
- A61K Preparations for medical, dental or toiletry purposes: 9/0024, 31/337, 38/44, 47/34, 9/0092, 9/19, 9/70
- A61M Devices for introducing media into, or onto, the body; devices for transducing body media or for taking media from the body; devices for producing or ending sleep or stupor {}: 31/002
- C12Y Enzymes: 111/01007
- D06M Treatment, not provided for elsewhere in class D06, of fibres, threads, yarns, fabrics, feathers or fibrous goods made from such materials: 16/00
- Y10T Technical subjects covered by former us classification: 442/2525
- (73) Assignee
- Ramot at Tel Aviv University Ltd
- (72) Inventors
- Meital Zilberman
- (54) Title
- Drug-delivering composite structures
- (57) Abstract
Composite structures composed of a fibril core and a polymeric coat and designed capable of encapsulating both hydrophobic and hydrophilic bioactive agents while retaining the activity of these agents are disclosed. Further disclosed are processes of preparing such composite structures, and medical devices and disposable articles made therefrom.
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Claims (24)
- A composite structure comprising a fibril core and a polymeric porous coat coating at least a part of said fibril core, said fibril core being a fiber characterized by a tensile strength of at least 200 MPa, said coat comprising at least one hydrophilic, amphiphilic or amphipathic bioactive agent encapsulated therein and/or applied thereon, wherein: said coat has a microstructure of a freeze-dried water-in-oil emulsion, said emulsion comprises, prior to freeze-drying, a dispersed aqueous solution and a continuous organic solution, said organic solution containing at least one second polymer and said aqueous solution containing said at least one bioactive agent, and a ratio of said organic solution and said aqueous solution is at least 8:1 and/or a concentration of said at least one second polymer ranges from 10 weight-to-volume percentages to 25 weight-to-volume percentages; and wherein a plurality of droplets of said dispersed aqueous solution freeze-dry to form microscopic capsules encapsulating said bioactive agent in a solid form of said continuous organic solution, in a form of a plurality of discrete pores randomly dispersed within said polymeric porous coat, wherein said microstructure is characterized by said plurality of discrete pores.
- The composite structure of claim 1, wherein an activity of said at least one bioactive agent is at least partially retained.
- The composite structure of claim 1, wherein said coat is capable of releasing said bioactive agent in a pre-determined release rate.
- The composite structure of claim 2, wherein said at least one bioactive agent is selected from a group consisting of a macro-biomolecule and a small organic molecule.
- The composite structure of claim 1, wherein said polymeric coat is characterized by an average pore diameter that ranges from about 1 nm to about 1 mm.
- The composite structure of claim 1, wherein said polymeric coat is characterized by a pore density that ranges from about 50% of void volume per coat volume to about 95% of void volume per coat volume.
- The composite structure of claim 1, wherein a thickness of said polymeric coat ranges from about 1 μm to about 2000 μm.
- The composite structure of claim 1, wherein said coat is biodegradable.
- The composite structure of claim 1, wherein a diameter of said fibril core ranges from about 1 μm to about 1 cm.
- The composite structure of claim 1, wherein said coat further comprises at least one additional agent.
- The composite structure of claim 1, wherein said core comprises at least one bioactive agent encapsulated therein.
- A fibrous composition-of-matter comprising the composite structure of claim 1.
- A process of preparing the composite structure of claim 1, the process comprising: contacting said fiber and said emulsion to thereby obtain said fiber having a layer of said emulsion applied on at least a part thereof; and freeze-drying said fiber having said layer applied thereon so as to solidify said emulsion, thereby obtaining the composite structure.
- The process of claim 13, further comprising, prior to said contacting: spinning at least one first polymer, to thereby obtain a crude fiber; and drawing said crude fiber, to thereby obtain said fiber.
- The process of claim 13, wherein said emulsion is prepared by: dissolving said at least one second polymer in an organic solvent to thereby obtain said organic solution; contacting said organic solution and said aqueous solution to thereby obtain a mixture; and emulsifying said mixture to thereby obtain said emulsion.
- The process of claim 15, wherein a concentration of said bioactive agent in said aqueous solution ranges from about 1 weight percentage to about 20 weight percentages.
- A medical device comprising the composite structure of claim 1.
- A medical device comprising the fibrous composition-of-matter of claim 12.
- An article-of-manufacture comprising the composite structure of claim 1.
- A method of predicting release rate of a bioactive agent from the composite structure of claim 1, the method comprising: solving a diffusion equation so as to obtain the concentration distribution of the bioactive agent in the biodegradable polymeric coat as a function of time; integrating said concentration distribution over a volume of said biodegradable polymeric coat so as to obtain an integrated bioactive agent mass as a function of time; and using said integrated bioactive agent mass for predicting the release rate of the bioactive agent.
- The method of claim 20, wherein said diffusion equation comprises a time-dependent diffusion coefficient.
- The method of claim 21, wherein said time-dependent diffusion coefficient comprises a constant term which is proportional to a porosity characterizing the polymeric coat.
- The method of claim 22, wherein said constant term is proportional to the ratio of said porosity to a tortuosity characterizing the polymeric coat.
- The method of claim 21, wherein said time-dependent diffusion coefficient comprises a degradation profile characterizing the polymeric coat.
Description
The present invention relates to the field of material science and, more particularly, to novel composite structures which can be used for delivering therapeutic agents.
Organ and tissue failure or loss is one of the most frequent and devastating problems still challenging human health care. Tissue regeneration is a new discipline where living cells, being, for example, autologous, allogenic, or xenogenic cells, are used to replace cells lost as a result of injury, disease or birth defect in a living subject.
Tissue regeneration typically involves the preparation of delicate polymeric structures that serve as biodegradable scaffolds incorporating bioactive molecules and/or cells. Such biodegradable scaffolds are often further utilized for in vitro studies of tissues, cells, bioactive agents and the interactions therebetween.
An efficient scaffold for tissue regeneration is typically made of biodegradable structural elements, preferably fibers, in which biologically active molecules can be incorporated and be controllably released over time.
Fibrillar biodegradable scaffolds are ideal particularly when thin, delicate structures are needed, for example in nerve regeneration applications. They can also be used to build implants and other medical devices that combine drug release with other functions, such as mechanical support for a regenerating tissue or as stents.
Citations (40)
- US4525340A
- US4814184A
- US5232648A
- US5824048A
- US6045908A
- US5948020A
- US6485737B1
- US6420027B2
- US6441267B1
- WO2001010421A1
- US6596296B1
- US6858222B2
- US20050106211A1
- CN1378554A
- WO2001029061A1
- WO2002043799A1
- EP1308180A1
- US6984393B2
- US6645622B2
- US6881726B2
- JP2005523332A
- WO2003090684A2
- EP1518517A2
- US20050037133A1
- US20050079199A1
- WO2004098503A2
- JP2004357986A
- US20040249450A1
- US20040253185A1
- WO2004112746A1
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- WO2005065843A1
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- JP2007517647A
- WO2007066339A1
- US20080071355A1
- US20080103584A1
- WO2009150650A2
- US20160082161A1
Record as JSON
{
"publication_number": "US9446226B2",
"country": "US",
"kind": "B2",
"title": "Drug-delivering composite structures",
"abstract": "Composite structures composed of a fibril core and a polymeric coat and designed capable of encapsulating both hydrophobic and hydrophilic bioactive agents while retaining the activity of these agents are disclosed. Further disclosed are processes of preparing such composite structures, and medical devices and disposable articles made therefrom.",
"claims": [
"1. A composite structure comprising a fibril core and a polymeric porous coat coating at least a part of said fibril core, said fibril core being a fiber characterized by a tensile strength of at least 200 MPa, said coat comprising at least one hydrophilic, amphiphilic or amphipathic bioactive agent encapsulated therein and/or applied thereon, wherein: said coat has a microstructure of a freeze-dried water-in-oil emulsion, said emulsion comprises, prior to freeze-drying, a dispersed aqueous solution and a continuous organic solution, said organic solution containing at least one second polymer and said aqueous solution containing said at least one bioactive agent, and a ratio of said organic solution and said aqueous solution is at least 8:1 and/or a concentration of said at least one second polymer ranges from 10 weight-to-volume percentages to 25 weight-to-volume percentages; and wherein a plurality of droplets of said dispersed aqueous solution freeze-dry to form microscopic capsules encapsulating said bioactive agent in a solid form of said continuous organic solution, in a form of a plurality of discrete pores randomly dispersed within said polymeric porous coat, wherein said microstructure is characterized by said plurality of discrete pores.",
"2. The composite structure of claim 1, wherein an activity of said at least one bioactive agent is at least partially retained.",
"3. The composite structure of claim 1, wherein said coat is capable of releasing said bioactive agent in a pre-determined release rate.",
"4. The composite structure of claim 2, wherein said at least one bioactive agent is selected from a group consisting of a macro-biomolecule and a small organic molecule.",
"5. The composite structure of claim 1, wherein said polymeric coat is characterized by an average pore diameter that ranges from about 1 nm to about 1 mm.",
"6. The composite structure of claim 1, wherein said polymeric coat is characterized by a pore density that ranges from about 50% of void volume per coat volume to about 95% of void volume per coat volume.",
"7. The composite structure of claim 1, wherein a thickness of said polymeric coat ranges from about 1 μm to about 2000 μm.",
"8. The composite structure of claim 1, wherein said coat is biodegradable.",
"9. The composite structure of claim 1, wherein a diameter of said fibril core ranges from about 1 μm to about 1 cm.",
"10. The composite structure of claim 1, wherein said coat further comprises at least one additional agent.",
"11. The composite structure of claim 1, wherein said core comprises at least one bioactive agent encapsulated therein.",
"12. A fibrous composition-of-matter comprising the composite structure of claim 1.",
"13. A process of preparing the composite structure of claim 1, the process comprising: contacting said fiber and said emulsion to thereby obtain said fiber having a layer of said emulsion applied on at least a part thereof; and freeze-drying said fiber having said layer applied thereon so as to solidify said emulsion, thereby obtaining the composite structure.",
"14. The process of claim 13, further comprising, prior to said contacting: spinning at least one first polymer, to thereby obtain a crude fiber; and drawing said crude fiber, to thereby obtain said fiber.",
"15. The process of claim 13, wherein said emulsion is prepared by: dissolving said at least one second polymer in an organic solvent to thereby obtain said organic solution; contacting said organic solution and said aqueous solution to thereby obtain a mixture; and emulsifying said mixture to thereby obtain said emulsion.",
"16. The process of claim 15, wherein a concentration of said bioactive agent in said aqueous solution ranges from about 1 weight percentage to about 20 weight percentages.",
"17. A medical device comprising the composite structure of claim 1.",
"18. A medical device comprising the fibrous composition-of-matter of claim 12.",
"19. An article-of-manufacture comprising the composite structure of claim 1.",
"20. A method of predicting release rate of a bioactive agent from the composite structure of claim 1, the method comprising: solving a diffusion equation so as to obtain the concentration distribution of the bioactive agent in the biodegradable polymeric coat as a function of time; integrating said concentration distribution over a volume of said biodegradable polymeric coat so as to obtain an integrated bioactive agent mass as a function of time; and using said integrated bioactive agent mass for predicting the release rate of the bioactive agent.",
"21. The method of claim 20, wherein said diffusion equation comprises a time-dependent diffusion coefficient.",
"22. The method of claim 21, wherein said time-dependent diffusion coefficient comprises a constant term which is proportional to a porosity characterizing the polymeric coat.",
"23. The method of claim 22, wherein said constant term is proportional to the ratio of said porosity to a tortuosity characterizing the polymeric coat.",
"24. The method of claim 21, wherein said time-dependent diffusion coefficient comprises a degradation profile characterizing the polymeric coat."
],
"description_excerpt": "The present invention relates to the field of material science and, more particularly, to novel composite structures which can be used for delivering therapeutic agents.\n\nOrgan and tissue failure or loss is one of the most frequent and devastating problems still challenging human health care. Tissue regeneration is a new discipline where living cells, being, for example, autologous, allogenic, or xenogenic cells, are used to replace cells lost as a result of injury, disease or birth defect in a living subject.\n\nTissue regeneration typically involves the preparation of delicate polymeric structures that serve as biodegradable scaffolds incorporating bioactive molecules and/or cells. Such biodegradable scaffolds are often further utilized for in vitro studies of tissues, cells, bioactive agents and the interactions therebetween.\n\nAn efficient scaffold for tissue regeneration is typically made of biodegradable structural elements, preferably fibers, in which biologically active molecules can be incorporated and be controllably released over time.\n\nFibrillar biodegradable scaffolds are ideal particularly when thin, delicate structures are needed, for example in nerve regeneration applications. They can also be used to build implants and other medical devices that combine drug release with other functions, such as mechanical support for a regenerating tissue or as stents.",
"cpc": [
"A61K 9/0024",
"A61K 31/337",
"A61K 38/44",
"A61K 47/34",
"A61K 9/0092",
"A61K 9/19",
"A61K 9/70",
"A61M 31/002",
"C12Y 111/01007",
"D06M 16/00",
"Y10T 442/2525"
],
"ipc": [
"B32B 27/04",
"A61K 9/70",
"A61M 31/00",
"D06M 16/00"
],
"assignees": [
"Ramot at Tel Aviv University Ltd"
],
"inventors": [
"Meital Zilberman"
],
"filing_date": "2006-12-07",
"publication_date": "2016-09-20",
"grant_date": "2016-09-20",
"priority_date": "2005-12-07",
"application_number": "US-63491006-A",
"family_id": "37781811",
"cited_by_count": 813,
"citations": [
"US4525340A",
"US4814184A",
"US5232648A",
"US5824048A",
"US6045908A",
"US5948020A",
"US6485737B1",
"US6420027B2",
"US6441267B1",
"WO2001010421A1",
"US6596296B1",
"US6858222B2",
"US20050106211A1",
"CN1378554A",
"WO2001029061A1",
"WO2002043799A1",
"EP1308180A1",
"US6984393B2",
"US6645622B2",
"US6881726B2",
"JP2005523332A",
"WO2003090684A2",
"EP1518517A2",
"US20050037133A1",
"US20050079199A1",
"WO2004098503A2",
"JP2004357986A",
"US20040249450A1",
"US20040253185A1",
"WO2004112746A1",
"US20050037052A1",
"US20050154451A1",
"WO2005065843A1",
"CA2549372A1",
"JP2007517647A",
"WO2007066339A1",
"US20080071355A1",
"US20080103584A1",
"WO2009150650A2",
"US20160082161A1"
]
}
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