Method and device for enhancing transdermal agent flux

• US 20050031676A1
• Filed: 08/03/2004
• Published: 02/10/2005
• Est. Priority Date: 08/04/2003
• Status: Abandoned Application

• Current Assignee: ALZA Corporation (Johnson & Johnson)
• Original Assignee: ALZA Corporation (Johnson & Johnson)
• Inventors: Wong, Patrick S.L., Daddona, Peter
• Application Number:
  US10/910,889
• Publication Number:
  US 20050031676A1
• Time in Patent Office: Days
• US Class Current: 424/448
• CPC Class Codes: A61B 10/0064 for taking sweat or sebum samples measuring sweat production A61B5/4266
• CPC Class Codes: A61B 17/205 Vaccinating by means of needles or other puncturing devices
• CPC Class Codes: A61B 2010/0009 Testing for drug or alcohol abuse
• CPC Class Codes: A61M 2037/003 having a lumen
• CPC Class Codes: A61M 2037/0053 Methods for producing microneedles
• CPC Class Codes: A61M 37/0015 by using microneedles
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

A porous microprojection member for insertion into biological tissue surrounded by interstitial fluid having a wall that includes interior and exterior surfaces, the exterior surface substantially enclosing the interior surface; and a biocompatible coating disposed on the interior surface, the microprojection member being adapted to substantially restrict contact of the coating with the tissue during insertion of the microprojection member into the tissue, the microprojection member having sufficient porosity to allow migration of the interstitial fluid through the wall of the microprojection member.

Claims

1. A microprojection for insertion into a biological surface, comprising:

a microprojection member having interior and exterior surfaces, said exterior surface substantially enclosing said interior surface; and

a biocompatible coating disposed on said interior surface,

said microprojection member being adapted to substantially restrict contact of said coating with the body surface during insertion of said microprojection member into the body surface.

2. The microprojection of claim 1, wherein said microprojection member includes a substantially longitudinal slit.

3. The microprojection of claim 1, wherein said microprojection member includes a plurality of perforations that extend through said exterior and interior surfaces.

4. The microprojection of claim 1, wherein said microprojection member is constructed out of a material selected from the group consisting of stainless steel, titanium, nickel titanium alloys and like biocompatible materials.

5. The microprojection of claim 1, wherein said microprojection member is constructed out of a non-conductive material.

6. The microprojection of claim 1, wherein said microprojection member is coated with a non-conductive material.

7. The microprojection of claim 1, wherein said microprojection member has a length less than approximately 1000 microns.

8. The microprojection of claim 1, wherein said biocompatible coating is produced by applying a coating formulation on said microprojection member.

9. The microprojection of claim 8, wherein said coating formulation includes at least one biologically active agent selected from the group consisting of a hormone releasing hormone (LHRH), LHRH analog, vasopressin, desmopressin, corticotropin (ACTH), an ACTH analog, calcitonin, vasopressin, deamino [Val4, D-Arg8] arginine vasopressin, interferon alpha, interferon beta, interferon gamma, erythropoietin (EPO), granulocyte macrophage colony stimulating factor (GM-CSF), granulocyte colony stimulating factor (G-CSF), interleukin-10 (IL-10), glucagon, growth hormone releasing factor (GHRF), insulin, insulinotropin, calcitonin, octreotide, endorphin, TRN, NT-36 (chemical name:

N-[[(s)-4-oxo-2-azetidinyl]carbonyl]-L-histidyl-L-prolinamide), liprecin, aANF, bMSH, somatostatin, bradykinin, somatotropin, platelet-derived growth factor releasing factor, chymopapain, cholecystokinin, chorionic gonadotropin, epoprostenol, hirulog, interferon, interleukin, menotropins, oxytocin, streptokinase, tissue plasminogen activator, urokinase, ANP, ANP clearance inhibitor, angiotensin II antagonist, antidiuretic hormone agonist, bradykinn antagonist, ceredase, CSI, calcitonin gene related peptide (CGRP), enkephalins, FAB fragment, IgE peptide suppressor, IGF-1, neurotrophic factor, colony stimulating factor, parathyroid hormone and agonist, parathyroid hormone antagonist, prostaglandin antagonist, pentigetide, protein C, protein S, renin inhibitor, thymosin alpha-1, thrombolytic, TNF, vasopressin antagonist analog, alpha-1 antitrypsin (recombinant), TGF-beta, fondaparinux, ardeparin, dalteparin, defibrotide, enoxaparin, hirudin, nadroparin, reviparin, tinzaparin, pentosan polysulfate, oligonucleotide and oligonucleotide derivatives, alendronic acid, clodronic acid, etidronic acid, ibandronic acid, incadronic acid, pamidronic acid, risedronic acid, tiludronic acid, zoledronic acid, argatroban, RWJ 445167, and RWJ-671818.

10. The microprojection of claim 8, wherein said coating formulation includes at least one vaccine selected from the group consisting of flu vaccine, Lyme disease vaccine, rabies vaccine, measles vaccine, mumps vaccine, chicken pox vaccine, small pox vaccine, hepatitis vaccine, pertussis vaccine, diphtheria vaccine, recombinant protein vaccine, DNA vaccine and therapeutic cancer vaccine.

11. The microprojection of claim 8, wherein said coating formulation includes at least one buffer selected from the group consisting of ascorbic acid, citric acid, succinic acid, glycolic acid, gluconic acid, glucuronic acid, lactic acid, malic acid, pyruvic acid, tartaric acid, tartronic acid, fumaric acid, maleic acid, phosphoric acid, tricarballylic acid, malonic acid, adipic acid, citraconic acid, glutaratic acid, itaconic acid, mesaconic acid, citramalic acid, dimethylolpropionic acid, tiglic acid, glyceric acid, methacrylic acid, isocrotonic acid, crotonic acid, angelic acid, hydracrylic acid, aspartic acid, glutamic acid, glycine and mixtures thereof.

12. The microprojection of claim 8, wherein said coating formulation includes at least one surfactant selected from the group consisting of sodium lauroamphoacetate, sodium dodecyl sulfate (SDS), cetylpyridinium chloride (CPC), dodecyltrimethyl ammonium chloride (TMAC), benzalkonium, chloride, polysorbates and other sorbitan derivatives.

13. The microprojection of claim 8, wherein said coating formulation includes at least one polymeric material selected from the group consisting of hydroxyethylcellulose (HEC), hydroxypropylmethylcellulose (HPMC), hydroxypropycellulose (HPC), methylcellulose (MC), hydroxyethylmethylcellulose (HEMC) and ethylhydroxy-ethylcellulose (EHEC).

14. The microprojection of claim 8, wherein said coating formulation includes at least one hydrophilic polymer selected from the group consisting of hyroxyethyl starch, dextran, poly(vinyl alcohol), poly(ethylene oxide), poly(2-hydroxyethylmethacrylate), poly(n-vinyl pyrolidone), polyethylene glycol and mixtures thereof.

15. The microprojection of claim 8, wherein said coating formulation includes at least one biocompatible carrier selected from the group consisting of human albumin, bioengineered human albumin, polyglutamic acid, polyaspartic acid, polyhistidine, pentosan polysulfate, polyamino acids, sucrose, trehalose, melezitose, raffinose and stachyose.

16. The microprojection of claim 8, wherein said coating formulation includes at least one stabilizing agent selected from the group consisting of a reducing sugar, non-reducing sugar and polysaccharide.

17. The microprojection of claim 16, wherein said non-reducing sugar is selected from the group consisting of sucrose, trehalose, stachyose and raffinose.

18. The microprojection of claim 16, wherein said polysaccharide is selected from the group consisting of dextran, soluble starch, dextrin and insulin.

19. The microprojection of claim 16, wherein said reducing sugar is selected from the group consisting of apiose, arabinose, lyxose, ribose, xylose, digitoxose, fucose, quercitol, quinovose, rhamnose, allose, altrose, fructose, galactose, glucose, gulose, hamamelose, idose, mannose, tagatose, primeverose, vicianose, rutinose, scillabiose, cellobiose, gentiobiose, lactose, lactulose, maltose, melibiose, sophorose and turanose.

20. The microprojection of claim 8, wherein said coating formulation includes at least one vasoconstrictor selected from the group consisting of amidephrine, cafaminol, cyclopentamine, deoxyepinephrine, epinephrine, felypressin, indanazoline, metizoline, midodrine, naphazoline, nordefrin, octodrine, ornipressin, oxymethazoline, phenylephrine, phenylethanolamine, phenylpropanolamine, propylhexedrine, pseudoephedrine, tetrahydrozoline, tramazoline, tuaminoheptane, tymazoline, vasopressin, xylometazoline and the mixtures thereof.

21. The microprojection of claim 8, wherein said coating formulation includes at least one pathway patentency modulator selected from the group consisting of an osmotic agent, zwitterionic compound and anti-inflammatory agent.

22. The microprojection of claim 21, wherein said anti-inflammatory agent is selected from the group consisting of betamethasone 21-phosphate disodium salt, triamcinolone acetonide 21-disodium phosphate, hydrocortamate hydrochloride, hydrocortisone 21-phosphate disodium salt, methylprednisolone 21-phosphate disodium salt, methylprednisolone 21-succinaate sodium salt, paramethasone disodium phosphate and prednisolone 21-succinate sodium salt.

23. The microprojection of claim 21, wherein said pathway patentency modulator comprises an anticoagulants selected from the group consisting of citric acid, citrate salts, dextrin sulfate sodium, aspirin and EDTA.

24. The microprojection of claim 8, wherein said coating formulation includes at least one solubilising/complexing agent selected from the group consisting of Alpha-Cyclodextrin, Beta-Cyclodextrin, Gamma-Cyclodextrin, glucosyl-alpha-Cyclodextrin, maltosyl-alpha-Cyclodextrin, glucosyl-beta-Cyclodextrin, maltosyl-beta-Cyclodextrin, hydroxypropyl beta-cyclodextrin, 2-hydroxypropyl-beta-Cyclodextrin, 2-hydroxypropyl-gamma-Cyclodextrin, hydroxyethyl-beta-Cyclodextrin, methyl-beta-Cyclodextrin, sulfobutylether-alpha-cyclodextrin, sulfobutylether-beta-cyclodextrin, and sulfobutylether-gamma-cyclodextrin. Most preferred solubilising/complexing agents are beta-cyclodextrin, hydroxypropyl beta-cyclodextrin, 2-hydroxypropyl-beta-Cyclodextrin and sulfobutylether7 beta-cyclodextrin.

25. The microprojection of claim 8, wherein said coating formulation has a viscosity less than approximately 500 centipoise and greater than 3 centipose.

26. The microprojection of claim 1, wherein said coating has a thickness less than 100 microns.

27. A microprojection for insertion into biological tissue, the tissue being surrounded by interstitial fluid, the microprojection comprising:

a porous microprojection member having a wall that includes interior and exterior surfaces, said exterior surface substantially enclosing said interior surface; and

a biocompatible coating disposed on said interior surface, said microprojection member being adapted to substantially restrict contact of said coating with the biological tissue during insertion of said microprojection member into the tissue, said microprojection member having sufficient porosity to allow migration of the interstitial fluid through said wall of said microprojection member.

28. The microprojection of claim 27, wherein said microprojection member is constructed out of a ceramic material.

29. The microprojection of claim 27, wherein said microprojection member has a closed tip and includes a plurality of perforations that extend through said exterior and interior surfaces.

30. The microprojection of claim 29, wherein said microprojection member includes at least one opening disposed proximate said closed tip.

31. The microprojection of claim 27, wherein said microprojection member has a length less than approximately 1000 microns.

32. The microprojection of claim 27, wherein said biocompatible coating is produced by applying a coating formulation on said microprojection member.

33. The microprojection of claim 32, wherein said coating formulation includes at least one biologically active agent selected from the group consisting of a hormone releasing hormone (LHRH), LHRH analog, vasopressin, desmopressin, corticotropin (ACTH), an ACTH analog, calcitonin, vasopressin, deamino [Val4, D-Arg8] arginine vasopressin, interferon alpha, interferon beta, interferon gamma, erythropoietin (EPO), granulocyte macrophage colony stimulating factor (GM-CSF), granulocyte colony stimulating factor (G-CSF), interleukin-10 (IL-10), glucagon, growth hormone releasing factor (GHRF), insulin, insulinotropin, calcitonin, octreotide, endorphin, TRN, NT-36 (chemical name:

N-[[(s)-4-oxo-2-azetidinyl]carbonyl]-L-histidyl-L-prolinamide), liprecin, aANF, bMSH, somatostatin, bradykinin, somatotropin, platelet-derived growth factor releasing factor, chymopapain, cholecystokinin, chorionic gonadotropin, epoprostenol, hirulog, interferon, interleukin, menotropins, oxytocin, streptokinase, tissue plasminogen activator, urokinase, ANP, ANP clearance inhibitor, angiotensin II antagonist, antidiuretic hormone agonist, bradykinn antagonist, ceredase, CSI, calcitonin gene related peptide (CGRP), enkephalins, FAB fragment, IgE peptide suppressor, IGF-1, neurotrophic factor, colony stimulating factor, parathyroid hormone and agonist, parathyroid hormone antagonist, prostaglandin antagonist, pentigetide, protein C, protein S, renin inhibitor, thymosin alpha-1, thrombolytic, TNF, vasopressin antagonist analog, alpha-1 antitrypsin (recombinant), TGF-beta, fondaparinux, ardeparin, dalteparin, defibrotide, enoxaparin, hirudin, nadroparin, reviparin, tinzaparin, pentosan polysulfate, oligonucleotide and oligonucleotide derivatives, alendronic acid, clodronic acid, etidronic acid, ibandronic acid, incadronic acid, pamidronic acid, risedronic acid, tiludronic acid, zoledronic acid, argatroban, RWJ 445167, and RWJ-671818.

34. The microprojection of claim 32, wherein said coating formulation includes at least one vaccine selected from the group consisting of flu vaccine, Lyme disease vaccine, rabies vaccine, measles vaccine, mumps vaccine, chicken pox vaccine, small pox vaccine, hepatitis vaccine, pertussis vaccine, diphtheria vaccine, recombinant protein vaccine, DNA vaccine and therapeutic cancer vaccine.

35. The microprojection of claim 32, wherein said coating formulation includes at least one buffer selected from the group consisting of ascorbic acid, citric acid, succinic acid, glycolic acid, gluconic acid, glucuronic acid, lactic acid, malic acid, pyruvic acid, tartaric acid, tartronic acid, fumaric acid, maleic acid, phosphoric acid, tricarballylic acid, malonic acid, adipic acid, citraconic acid, glutaratic acid, itaconic acid, mesaconic acid, citramalic acid, dimethylolpropionic acid, tiglic acid, glyceric acid, methacrylic acid, isocrotonic acid, crotonic acid, angelic acid, hydracrylic acid, aspartic acid, glutamic acid, glycine and mixtures thereof.

36. The microprojection of claim 32, wherein said coating formulation includes at least one surfactant selected from the group consisting of sodium lauroamphoacetate, sodium dodecyl sulfate (SDS), cetylpyridinium chloride (CPC), dodecyltrimethyl ammonium chloride (TMAC), benzalkonium, chloride, polysorbates and other sorbitan derivatives.

37. The microprojection of claim 32, wherein said coating formulation includes at least one polymeric material selected from the group consisting of hydroxyethylcellulose (HEC), hydroxypropylmethylcellulose (HPMC), hydroxypropycellulose (HPC), methylcellulose (MC), hydroxyethylmethylcellulose (HEMC) and ethylhydroxy-ethylcellulose (EHEC).

38. The microprojection of claim 32, wherein said coating formulation includes at least one hydrophilic polymer selected from the group consisting of hyroxyethyl starch, dextran, poly(vinyl alcohol), poly(ethylene oxide), poly(2-hydroxyethylmethacrylate), poly(n-vinyl pyrolidone), polyethylene glycol and mixtures thereof.

39. The microprojection of claim 32, wherein said coating formulation includes at least one biocompatible carrier selected from the group consisting of human albumin, bioengineered human albumin, polyglutamic acid, polyaspartic acid, polyhistidine, pentosan polysulfate, polyamino acids, sucrose, trehalose, melezitose, raffinose and stachyose.

40. The microprojection of claim 32, wherein said coating formulation includes at least one stabilizing agent selected from the group consisting of a reducing sugar, non-reducing sugar and polysaccharide.

41. The microprojection of claim 32, wherein said non-reducing sugar is selected from the group consisting of sucrose, trehalose, stachyose and raffinose.

42. The microprojection of claim 32, wherein said polysaccharide is selected from the group consisting of dextran, soluble starch, dextrin and insulin.

43. The microprojection of claim 32, wherein said reducing sugar is selected from the group consisting of apiose, arab inose, lyxose, ribose, xylose, digitoxose, fucose, quercitol, quinovose, rhamnose, allose, altrose, fructose, galactose, glucose, gulose, hamamelose, idose, mannose, tagatose, primeverose, vicianose, rutinose, scillabiose, cellobiose, gentiobiose, lactose, lactulose, maltose, melibiose, sophorose and turanose.

44. The microprojection of claim 32, wherein said coating formulation includes at least one vasoconstrictor selected from the group consisting of amidephrine, cafaminol, cyclopentamine, deoxyepinephrine, epinephrine, felypressin, indanazoline, metizoline, midodrine, naphazoline, nordefrin, octodrine, omipressin, oxymethazoline, phenylephrine, phenylethanolamine, phenylpropanolamine, propylhexedrine, pseudoephedrine, tetrahydrozoline, tramazoline, tuaminoheptane, tymazoline, vasopressin, xylometazoline and the mixtures thereof.

45. The microprojection of claim 32, wherein said coating formulation includes at least one pathway patentency modulator selected from the group consisting of an osmotic agent, zwitterionic compound and anti-inflammatory agent.

46. The microprojection of claim 45, wherein said anti-inflammatory agent is selected from the group consisting of betamethasone 21-phosphate disodium salt, triamcinolone acetonide 21-disodium phosphate, hydrocortamate hydrochloride, hydrocortisone 21-phosphate disodium salt, methylprednisolone 21-phosphate disodium salt, methylprednisolone 21-succinaate sodium salt, paramethasone disodium phosphate and prednisolone 21-succinate sodium salt.

47. The microprojection of claim 45, wherein said pathway patentency modulator comprises an anticoagulant selected from the group consisting of citric acid, citrate salts, dextrin sulfate sodium, aspirin and EDTA.

48. The microprojection of claim 32, wherein said coating formulation includes at least one solubilising/complexing agent selected from the group consisting of Alpha-Cyclodextrin, Beta-Cyclodextrin, Gamma-Cyclodextrin, glucosyl-alpha-Cyclodextrin, maltosyl-alpha-Cyclodextrin, glucosyl-beta-Cyclodextrin, maltosyl-beta-Cyclodextrin, hydroxypropyl beta-cyclodextrin, 2-hydroxypropyl-beta-Cyclodextrin, 2-hydroxypropyl-gamma-Cyclodextrin, hydroxyethyl-beta-Cyclodextrin, methyl-beta-Cyclodextrin, sulfobutylether-alpha-cyclodextrin, sulfobutylether-beta-cyclodextrin, and sulfobutylether-gamma-cyclodextrin. Most preferred solubilising/complexing agents are beta-cyclodextrin, hydroxypropyl beta-cyclodextrin, 2-hydroxypropyl-beta-Cyclodextrin and sulfobutylether7 beta-cyclodextrin.

49. The microprojection of claim 32, wherein said coating formulation has a viscosity less than approximately 500 centipoise and greater than 3 centipose.

50. The microprojection of claim 27, wherein said coating has a thickness less than 100 microns.