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US20050245484A1 - Lubricious germicidal ophthalmic solutions - Google Patents

Lubricious germicidal ophthalmic solutions Download PDF

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Publication number
US20050245484A1
US20050245484A1 US10/947,003 US94700304A US2005245484A1 US 20050245484 A1 US20050245484 A1 US 20050245484A1 US 94700304 A US94700304 A US 94700304A US 2005245484 A1 US2005245484 A1 US 2005245484A1
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United States
Prior art keywords
solution
monographed
active substances
pharmacologically active
anionic
Prior art date
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Abandoned
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US10/947,003
Inventor
Leonard Mackles
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Individual
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Individual
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Priority to US10/947,003 priority Critical patent/US20050245484A1/en
Priority to CA 2502992 priority patent/CA2502992A1/en
Publication of US20050245484A1 publication Critical patent/US20050245484A1/en
Abandoned legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/14Quaternary ammonium compounds, e.g. edrophonium, choline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/716Glucans
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents

Definitions

  • This class of solutions is used at a pH between 7 and 8 and consists essentially of from about 0.1 to about 4.0% by weight of an anionic polymeric demulcent; from about 0.005 to about 1.0% by weight of a quaternary germicide and from about 0.1 to about 1.0% by weight of a polysorbate surfactant.
  • said anionic polymeric component is selected from the group consisting of anionic cellulose derivatives, anionic polymers derived from acrylic acid, anionic polymers derived from methacrylic acid, anionic polymers derived from alginic acid, anionic polymers derived from amino acids and mixtures thereof.
  • anionic cellulose derivatives anionic polymers derived from acrylic acid, anionic polymers derived from methacrylic acid, anionic polymers derived from alginic acid, anionic polymers derived from amino acids and mixtures thereof.
  • it is carboxymethyl cellulose and most preferably sodium carboxymethylcellulose (hereinafter CMC).
  • the most suitable quaternary germicide is benzalkonium chloride, preferably used at a concentration of 0.10 to 0.010%.
  • this germicide could not be used with CMC as their reaction caused precipitate formation.
  • the presence of a polysorbate surfactant in the solution prior to the addition of the germicide prevents such precipitation.
  • the polysorbate acts as an ameliorating agent to lessen the irritation potential of the cationic quaternary germicide.
  • the invention also includes the process of preparing the novel solutions of the present invention.
  • the process comprises the steps of:
  • an anionic polymeric demulcent from about 0.005 to about 0.1% by weight of a quaternary germicide and from about 0.1 to about 1.0% by weight of a polysorbate surfactant.
  • a polysorbate surfactant Preferably it is a carboxymethyl cellulose, most preferably sodium carboxymethylcellulose, USP (hereinafter CMC).
  • Useful polysorbates include Polysorbate 20 (polyethylene 20 sorbitan monolaurate), Polysorbate 40 (polyethylene 20 sorbitan monopalmitate), Polysorbate 60 (polyethylene 20 sorbitan monostearate), and Polysorbate 80 (polyethylene 20 sorbitan monooleate).
  • the preferred polysorbates are Polysorbate 20 and Polysorbate 80 at 0.10 to 1.00% by weight of the total solution and most preferably 0.20 to 0.60% by weight.
  • Buffers useful in adjusting and maintaining pH include acetic acid, hydrochloric acid, phosphoric acid, potassium bicarbonate, potassium tetraborate, potassium hydroxide, potassium carbonate, potassium citrate, potassium phosphate, sodium acetate, sodium bicarbonate, sodium biphosphate, sodium borate, sodium carbonate, sodium citrate, sodium hydroxide and sodium phosphate.
  • Any monographed active which is soluble in the solutions may be used. These include ophthalmic vasoconstrictors such as ephedrine HCI, naphazoline HCI, phenylephrine HCI, tetrahydrozoline HCI, oxymetazoline HCI, xylometazoline HCI and the like as well as other monographed actives such as antihistamines.
  • ophthalmic vasoconstrictors such as ephedrine HCI, naphazoline HCI, phenylephrine HCI, tetrahydrozoline HCI, oxymetazoline HCI, xylometazoline HCI and the like as well as other monographed actives such as antihistamines.
  • the CMC can be used in combination with other monographed polymers such as povidone, hydroxymethyl cellulose, hydroxypropyl cellulose and the like.
  • other polyols that may be used are polyvinyl alcohol, glycerin, propylene glycol, polyethylene glycol and the like.
  • benzalkonium chloride suitably about 0.01 to about 0.10% but preferably about 0.01 to about 0.015% by weight of the total solution, may be used as a preservative which may be potentiated by EDTA.
  • the natural pH of ophthalmic tears is 7.4. It is important that the pH of the solutions of the system be held at a pH of between 7.0 and 8.0 in order to avoid damage to the eye.
  • the system is also very useful in products for contact lens wearers. It will refresh and moisten the lenses and help to remove particulate matter that may cause irritation and discomfort.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Ophthalmology & Optometry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Preparation (AREA)

Abstract

A novel class of lubricious ophthalmic solutions is formulated to permit the use of a recognized class of demulcents; namely, anionic polymeric demulcents in the presence of a cationic quaternary germicide wherein no precipitation of said germicide occurs.

Description

    RELATED APPLICATIONS
  • This application is a continuation in part of applicant's application Ser. No. 10/835,449 filed Apr. 29, 2004
  • FIELD OF THE INVENTION
  • Discussion of the Prior Art
  • The use of ophthalmic solutions for the relief of many eye conditions is well known in the art. The problem with many of these solutions is that while they are pH compatible with tears, their level of lubricity or slipperiness is less than would be desirable. Thus many advantages of such solutions and the pharmacologically active substances which they may carry are not optimized. A further legal issue which must be met, at least in the United States of America is that the Food and Drug administration has set forth a list of substances which can be used in such non-prescription solutions and no others are permissible. Thus any invention in this art must be limited to the use of “monographed” components.
  • In order to provide lubricity to ophthalmic solutions, a demulcent must be added. A number of these have been “monographed” by the FDA. Unfortunately, some exhibit incompatibility with quaternary preservatives. Thus solutions containing them must be marketed in a single dose applicator to avoid the possibility of infection by an already opened container. This increases the expense and inconvenience to the consumer. Thus the ability to incorporate preservatives into solutions of such demulcents meets a long felt need.
  • SUMMARY OF THE INVENTION
  • There is provided a novel class of lubricious ophthalmic solutions which is formulated to permit the use of a recognized class of demulcents; namely, anionic polymeric demulcents in the presence of a cationic quaternary germicide wherein no precipitation of said germicide occurs.
  • This class of solutions is used at a pH between 7 and 8 and consists essentially of from about 0.1 to about 4.0% by weight of an anionic polymeric demulcent; from about 0.005 to about 1.0% by weight of a quaternary germicide and from about 0.1 to about 1.0% by weight of a polysorbate surfactant.
  • Suitably, said anionic polymeric component is selected from the group consisting of anionic cellulose derivatives, anionic polymers derived from acrylic acid, anionic polymers derived from methacrylic acid, anionic polymers derived from alginic acid, anionic polymers derived from amino acids and mixtures thereof. Preferably it is carboxymethyl cellulose and most preferably sodium carboxymethylcellulose (hereinafter CMC).
  • The most suitable quaternary germicide is benzalkonium chloride, preferably used at a concentration of 0.10 to 0.010%. Heretofore this germicide could not be used with CMC as their reaction caused precipitate formation. It is the surprising finding of this invention that the presence of a polysorbate surfactant in the solution prior to the addition of the germicide prevents such precipitation. In addition to preventing the precipitation of the cationic quaternary germicide, the polysorbate acts as an ameliorating agent to lessen the irritation potential of the cationic quaternary germicide.
  • It will be understood by those skilled in the art that to the foregoing groups and subgroups of components there may be added monographed pharmacologically inactive substances such as colorants and other nonionic demulcents.
  • The invention also includes the process of preparing the novel solutions of the present invention. The process comprises the steps of:
      • a.) dissolving the anionic polymeric demulcent in water;
      • b.) adding the polysorbate;
      • c.) adding the quaternary germicide;
      • d.) adjusting the pH to the desired range with various buffers and
      • e.) adding water to adjust the concentration to the desired range.
        This process is to be carried out in the foregoing sequence but is not limited thereto. The sequence of steps (b), (a), (c), (d) and (e) is also within the scope of the invention since the results obtained are similar.
    DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Suitably there are employed about 0.1 to about 4.0% by weight of an anionic polymeric demulcent; from about 0.005 to about 0.1% by weight of a quaternary germicide and from about 0.1 to about 1.0% by weight of a polysorbate surfactant. Preferably it is a carboxymethyl cellulose, most preferably sodium carboxymethylcellulose, USP (hereinafter CMC).
  • Useful polysorbates include Polysorbate 20 (polyethylene 20 sorbitan monolaurate), Polysorbate 40 (polyethylene 20 sorbitan monopalmitate), Polysorbate 60 (polyethylene 20 sorbitan monostearate), and Polysorbate 80 (polyethylene 20 sorbitan monooleate). The preferred polysorbates are Polysorbate 20 and Polysorbate 80 at 0.10 to 1.00% by weight of the total solution and most preferably 0.20 to 0.60% by weight.
  • Buffers useful in adjusting and maintaining pH include acetic acid, hydrochloric acid, phosphoric acid, potassium bicarbonate, potassium tetraborate, potassium hydroxide, potassium carbonate, potassium citrate, potassium phosphate, sodium acetate, sodium bicarbonate, sodium biphosphate, sodium borate, sodium carbonate, sodium citrate, sodium hydroxide and sodium phosphate.
  • Any monographed active which is soluble in the solutions may be used. These include ophthalmic vasoconstrictors such as ephedrine HCI, naphazoline HCI, phenylephrine HCI, tetrahydrozoline HCI, oxymetazoline HCI, xylometazoline HCI and the like as well as other monographed actives such as antihistamines.
  • The CMC can be used in combination with other monographed polymers such as povidone, hydroxymethyl cellulose, hydroxypropyl cellulose and the like. In addition, other polyols that may be used are polyvinyl alcohol, glycerin, propylene glycol, polyethylene glycol and the like.
  • As stated above, benzalkonium chloride, suitably about 0.01 to about 0.10% but preferably about 0.01 to about 0.015% by weight of the total solution, may be used as a preservative which may be potentiated by EDTA.
  • The natural pH of ophthalmic tears is 7.4. It is important that the pH of the solutions of the system be held at a pH of between 7.0 and 8.0 in order to avoid damage to the eye.
  • The system is also very useful in products for contact lens wearers. It will refresh and moisten the lenses and help to remove particulate matter that may cause irritation and discomfort.
  • EXAMPLES Example # 1
  • Eye Care Lubricant %
    1. CMC, USP 1.00
    2. Polysorbate 20 0.50
    3. Benzalkonium Chloride 0.01
    4. Disodium EDTA 0.10
    5. Boric Acid 0.30
    6. Sodium Borate 0.20
    7. PEG 400 1.00
    8. Deionized Water 96.89
    100.00
  • Adjust the pH to 7.4 with hydrochloric acid or sodium hydroxide.
  • Procedure:
      • 1.) Mix #1 and #8 and heat to 70° C. until dissolved.
      • 2.) Add #2 to the batch and mix.
      • 3.) Add #'s 4, 5, 6 and 7 to the batch and mix.
      • 4.) Cool the batch to 50° C.; add #3 and cool the batch to room temperature.
      • 5.) Adjust the pH to 7.4 with sodium hydroxide or hydrochloric acid.
    Example #2
  • Eye Care Lubricant with
    Tetrahydrozoline HCl %
    1. CMC, USP 0.50
    2. Polysorbate 20 0.50
    3. Benzalkonium chloride 0.01
    4. Disodium EDTA 0.10
    5. Boric Acid 0.30
    6. Sodium Borate 0.20
    7. PEG 400 1.00
    8. Tetrahydrozoline HCl 0.05
    9. Deionized Water 97.34
    100.00
  • Adjust the pH to 7.4 with hydrochloric acid or sodium hydroxide.
  • Procedure:
      • 1.) Mix #1 and #9 and heat to 70° C. until dissolved.
      • 2.) Add #2 to the batch and mix.
      • 3.) Add #'s 4, 5, 6 and 7 to the batch and mix.
      • 4.) Cool the batch to 50° C.; add #8 and mix until dissolved.
      • 5.) Add #3 to the batch and cool the batch to room temperature.
      • 6.) Adjust the pH to 7.4 with sodium hydroxide or hydrochloric acid.
    Example #3
  • Eye Care Lubricant with
    Oxymetazoline HCl %
    1. CMC, USP 0.50
    2. Polysorbate 80 0.50
    3. Benzalkonium chloride 0.01
    4. Disodium EDTA 0.10
    5. Boric Acid 0.30
    6. Sodium Borate 0.20
    7. PEG 400 1.00
    8. Oxymetazoline HCl 0.05
    9. Deionized Water 97.34
    100.00
  • Adjust the pH to 7.4 with hydrochloric acid or sodium hydroxide.
  • Procedure:
  • See the procedure used in Example #2.

Claims (17)

1. A lubricious aqueous ophthalmic solution having a pH between 7 and 8 consisting essentially of:
a.) from about 0.1-about 4.0% by weight of an anionic polymeric demulcent,
b.) from about 0.005-to about 0.1% by weight of a quaternary germicide,
c.) from about 0.1-to about 1.0% by weight of a polysorbate surfactant.
2. The solution of claim 1 wherein said anionic polymeric component is selected from the group consisting of anionic cellulose derivatives, anionic polymers derived from acrylic acid, anionic polymers derived from methacrylic acid, anionic polymers derived from alginic acid, anionic polymers derived from amino acids and mixtures thereof.
3. The solution of claim 1 wherein said anionic polymeric component comprises a carboxymethyl cellulose.
4. The solution of claim 1 wherein the anionic polymeric demulcent is sodium carboxymethylcellulose.
5. The solution of claim 1 wherein the quaternary germicide of is benzalkonium chloride at a concentration of 0.10-0.015%.
6. The solution of claim 1 wherein the polysorbate surfactant is selected from the group consisting of the monolaurate, monopalmitate, monostearate and monooleate of polyethylene sorbitan.
7. The solution of claim 1 wherein the polyethylene sorbitan is polyethylene sorbitan 20 or polyethylene sorbitan 80.
8. The solution of claim 1 further comprising monographed pharmacologically active substances.
9. The solution of claim 2 further comprising monographed pharmacologically active substances.
10. The solution of claim 3 further comprising monographed pharmacologically active substances.
11. The solution of claim 4 further comprising monographed pharmacologically active substances.
12. The solution of claim 5 further comprising monographed pharmacologically active substances.
13. The solution of claim 6 further comprising monographed pharmacologically active substances.
14. The solution of claim 7 further comprising monographed pharmacologically active substances.
15. A process of preparing a solution of claim 1 comprising the steps of
a) dissolving the anionic polymeric demulcent in water,
b) adding the polysorbate,
c) adding quaternary germicide,
d) adjusting the pH to the desired range with buffers,
e) adding water to adjust the concentration to the desired range.
16. The process of claim 15, wherein the steps are carried out in the sequence of (b), (a), (c), (d), (e).
17. The process of claim 15, wherein the order of the steps is (a), (b), (c), (d), (e).
US10/947,003 2004-04-29 2004-09-22 Lubricious germicidal ophthalmic solutions Abandoned US20050245484A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US10/947,003 US20050245484A1 (en) 2004-04-29 2004-09-22 Lubricious germicidal ophthalmic solutions
CA 2502992 CA2502992A1 (en) 2004-04-29 2005-03-30 Lubricious germicidal ophthalmic solutions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/835,449 US7022740B2 (en) 2004-04-29 2004-04-29 Lubricious ophthalmic solutions
US10/947,003 US20050245484A1 (en) 2004-04-29 2004-09-22 Lubricious germicidal ophthalmic solutions

Related Parent Applications (1)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100086512A1 (en) * 2008-10-02 2010-04-08 Rolf Schaefer Mucomimetic compositions and uses therefore
WO2012118704A1 (en) * 2011-03-03 2012-09-07 Voom, Llc Compositions and methods for non-surgical treatment of ptosis
RU2635521C2 (en) * 2011-08-04 2017-11-13 Омерос Корпорейшн Stable anti-inflammatory solutions for injection

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US20020071874A1 (en) * 2000-07-14 2002-06-13 Allergan Sales, Inc. Compositions containing therapeutically active components having enhanced solubility

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100086512A1 (en) * 2008-10-02 2010-04-08 Rolf Schaefer Mucomimetic compositions and uses therefore
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WO2012118704A1 (en) * 2011-03-03 2012-09-07 Voom, Llc Compositions and methods for non-surgical treatment of ptosis
US8357714B2 (en) 2011-03-03 2013-01-22 Voom, Llc Compositions and methods for non-surgical treatment of ptosis
US9018240B2 (en) 2011-03-03 2015-04-28 Voom, Llc Compositions and methods for non-surgical treatment of ptosis
US9867808B2 (en) 2011-03-03 2018-01-16 Voom, Llc Compositions and methods for non-surgical treatment of Ptosis
EP3653205A3 (en) * 2011-03-03 2020-08-26 Voom, LLC Oxymethazoline for topical ophthalmic administration and uses thereof
US10912765B2 (en) 2011-03-03 2021-02-09 Voom, Llc Compositions and methods for non-surgical treatment of ptosis
RU2635521C2 (en) * 2011-08-04 2017-11-13 Омерос Корпорейшн Stable anti-inflammatory solutions for injection

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Publication number Publication date
CA2503331A1 (en) 2005-10-29
US20050245618A1 (en) 2005-11-03
US7022740B2 (en) 2006-04-04

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