US20050245484A1 - Lubricious germicidal ophthalmic solutions - Google Patents
Lubricious germicidal ophthalmic solutions Download PDFInfo
- 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
- Authority
- US
- United States
- Prior art keywords
- solution
- monographed
- active substances
- pharmacologically active
- anionic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 230000002070 germicidal effect Effects 0.000 title claims abstract description 16
- 239000002997 ophthalmic solution Substances 0.000 title claims abstract description 6
- 239000003974 emollient agent Substances 0.000 claims abstract description 13
- 125000000129 anionic group Chemical group 0.000 claims abstract description 11
- 239000000243 solution Substances 0.000 claims description 26
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 10
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 229920000136 polysorbate Polymers 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 239000013543 active substance Substances 0.000 claims description 8
- 229920006318 anionic polymer Polymers 0.000 claims description 8
- -1 polyethylene Polymers 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- 229950008882 polysorbate Drugs 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 229960000686 benzalkonium chloride Drugs 0.000 claims description 6
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims description 6
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 5
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical group [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 3
- 239000000872 buffer Substances 0.000 claims description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 3
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims description 3
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- 235000010443 alginic acid Nutrition 0.000 claims description 2
- 239000000783 alginic acid Substances 0.000 claims description 2
- 229920000615 alginic acid Polymers 0.000 claims description 2
- 229960001126 alginic acid Drugs 0.000 claims description 2
- 150000004781 alginic acids Chemical class 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- 229920006321 anionic cellulose Polymers 0.000 claims description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims 4
- 229940054534 ophthalmic solution Drugs 0.000 claims 1
- 125000002091 cationic group Chemical group 0.000 abstract description 4
- 238000001556 precipitation Methods 0.000 abstract description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
- 229920001213 Polysorbate 20 Polymers 0.000 description 4
- 229910021538 borax Inorganic materials 0.000 description 4
- WYWIFABBXFUGLM-UHFFFAOYSA-N oxymetazoline Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C)=C1CC1=NCCN1 WYWIFABBXFUGLM-UHFFFAOYSA-N 0.000 description 4
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 4
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 4
- 229940068977 polysorbate 20 Drugs 0.000 description 4
- 235000010339 sodium tetraborate Nutrition 0.000 description 4
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 description 3
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 229960001528 oxymetazoline Drugs 0.000 description 3
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 3
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 3
- 229920000053 polysorbate 80 Polymers 0.000 description 3
- 229940068968 polysorbate 80 Drugs 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 2
- CNIIGCLFLJGOGP-UHFFFAOYSA-N 2-(1-naphthalenylmethyl)-4,5-dihydro-1H-imidazole Chemical compound C=1C=CC2=CC=CC=C2C=1CC1=NCCN1 CNIIGCLFLJGOGP-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- HUCJFAOMUPXHDK-UHFFFAOYSA-N Xylometazoline Chemical compound CC1=CC(C(C)(C)C)=CC(C)=C1CC1=NCCN1 HUCJFAOMUPXHDK-UHFFFAOYSA-N 0.000 description 2
- 230000007794 irritation Effects 0.000 description 2
- 229940068965 polysorbates Drugs 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BJORNXNYWNIWEY-UHFFFAOYSA-N tetrahydrozoline hydrochloride Chemical compound Cl.N1CCN=C1C1C2=CC=CC=C2CCC1 BJORNXNYWNIWEY-UHFFFAOYSA-N 0.000 description 2
- BYJAVTDNIXVSPW-UHFFFAOYSA-N tetryzoline Chemical compound N1CCN=C1C1C2=CC=CC=C2CCC1 BYJAVTDNIXVSPW-UHFFFAOYSA-N 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001219 Polysorbate 40 Polymers 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- FZQSLXQPHPOTHG-UHFFFAOYSA-N [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 Chemical compound [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 FZQSLXQPHPOTHG-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229960002179 ephedrine Drugs 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229960005016 naphazoline Drugs 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- SONNWYBIRXJNDC-VIFPVBQESA-N phenylephrine Chemical compound CNC[C@H](O)C1=CC=CC(O)=C1 SONNWYBIRXJNDC-VIFPVBQESA-N 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 235000010483 polyoxyethylene sorbitan monopalmitate Nutrition 0.000 description 1
- 239000000249 polyoxyethylene sorbitan monopalmitate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 229940101027 polysorbate 40 Drugs 0.000 description 1
- 229940113124 polysorbate 60 Drugs 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 229940069328 povidone Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 235000011071 sorbitan monopalmitate Nutrition 0.000 description 1
- 239000001570 sorbitan monopalmitate Substances 0.000 description 1
- 229940031953 sorbitan monopalmitate Drugs 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 229960000337 tetryzoline Drugs 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 239000005526 vasoconstrictor agent Substances 0.000 description 1
- 229960000833 xylometazoline Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/14—Quaternary ammonium compounds, e.g. edrophonium, choline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic 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.
Landscapes
- 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
- This application is a continuation in part of applicant's application Ser. No. 10/835,449 filed Apr. 29, 2004
- 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.
- 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.
- 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.
-
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.
-
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.
-
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).
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)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/835,449 Continuation-In-Part US7022740B2 (en) | 2004-04-29 | 2004-04-29 | Lubricious ophthalmic solutions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20050245484A1 true US20050245484A1 (en) | 2005-11-03 |
Family
ID=35187890
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/835,449 Expired - Fee Related US7022740B2 (en) | 2004-04-29 | 2004-04-29 | Lubricious ophthalmic solutions |
| US10/947,003 Abandoned US20050245484A1 (en) | 2004-04-29 | 2004-09-22 | Lubricious germicidal ophthalmic solutions |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/835,449 Expired - Fee Related US7022740B2 (en) | 2004-04-29 | 2004-04-29 | Lubricious ophthalmic solutions |
Country Status (2)
| Country | Link |
|---|---|
| US (2) | US7022740B2 (en) |
| CA (1) | CA2503331A1 (en) |
Cited By (3)
| 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 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4425345A (en) * | 1980-08-01 | 1984-01-10 | Smith And Nephew Associated Companies Limited | Pharmaceutical composition containing triamterene |
| US5505953A (en) * | 1992-05-06 | 1996-04-09 | Alcon Laboratories, Inc. | Use of borate-polyol complexes in ophthalmic compositions |
| US20020071874A1 (en) * | 2000-07-14 | 2002-06-13 | Allergan Sales, Inc. | Compositions containing therapeutically active components having enhanced solubility |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3697575A (en) | 1969-12-22 | 1972-10-10 | Basf Ag | Boric acid esters of 2-vinylthioethanol |
| JPS51146758A (en) | 1975-05-28 | 1976-12-16 | Sando Iron Works Co Ltd | Process for treating a drain water containing polyvinyl alcohol |
| JPS6056176B2 (en) | 1978-05-19 | 1985-12-09 | 日本合成化学工業株式会社 | Method for modifying polyvinyl alcohol |
| DE3000839A1 (en) | 1980-01-11 | 1981-07-16 | Hoechst Ag, 6000 Frankfurt | METHOD FOR PRODUCING A POLYVINYL ALCOHOL COUPLEX COMPOUND AND THE POLYVINYL ALCOHOL COMPLEX COMPOUNDS PRODUCED THEREOF |
| JPS61236886A (en) | 1985-04-12 | 1986-10-22 | Fuji Photo Film Co Ltd | Apparatus for recording and reading radiation image information |
| US5290774A (en) | 1989-08-03 | 1994-03-01 | Eisai Co., Ltd. | Photostabilizing method for ophthalmic solutions and the resulting ophthalmic solutions therefrom |
| DE4016979A1 (en) | 1990-05-25 | 1991-11-28 | Hoechst Ag | THICKENER SYSTEM FOR WATER-CONTAINING MIXTURES |
| AU3926093A (en) | 1992-03-18 | 1993-10-21 | Coopervision Pharmaceuticals, Inc. | Verapamil HC1 formulation and other ophthalmic solutions with buffer system for ocular administration |
| DE69333850T3 (en) | 1992-05-06 | 2011-03-17 | Alcon Laboratories, Inc., Fort Worth | APPLICATION OF BORAL-POLYOL COMPLEXES FOR OPHTHALMIC DRUG COMPOSITIONS |
| CN1101364A (en) | 1993-10-06 | 1995-04-12 | 黎思幸 | Surface modifier for polyvinyl alcohol coating and its preparation |
| TW274516B (en) | 1993-11-12 | 1996-04-21 | Ciba Geigy Ag | |
| WO1998025649A1 (en) | 1996-12-13 | 1998-06-18 | Alcon Laboratories, Inc. | Use of low molecular weight amino alcohols in ophthalmic compositions |
| CN100408100C (en) | 1997-07-29 | 2008-08-06 | 阿尔康实验室公司 | Ophthalmic compositions comprising galactomannan polymers and borates |
-
2004
- 2004-04-29 US US10/835,449 patent/US7022740B2/en not_active Expired - Fee Related
- 2004-09-22 US US10/947,003 patent/US20050245484A1/en not_active Abandoned
-
2005
- 2005-03-30 CA CA002503331A patent/CA2503331A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4425345A (en) * | 1980-08-01 | 1984-01-10 | Smith And Nephew Associated Companies Limited | Pharmaceutical composition containing triamterene |
| US5505953A (en) * | 1992-05-06 | 1996-04-09 | Alcon Laboratories, Inc. | Use of borate-polyol complexes in ophthalmic compositions |
| US20020071874A1 (en) * | 2000-07-14 | 2002-06-13 | Allergan Sales, Inc. | Compositions containing therapeutically active components having enhanced solubility |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20100086512A1 (en) * | 2008-10-02 | 2010-04-08 | Rolf Schaefer | Mucomimetic compositions and uses therefore |
| WO2010038129A1 (en) | 2008-10-02 | 2010-04-08 | Chemisches Institut Schaefer Ag | Mucomimetic compositions and uses therefore |
| JP2012504594A (en) * | 2008-10-02 | 2012-02-23 | ヒェーミシェス・インスティトゥート・シェーファー・アクチェンゲゼルシャフト | Mucus-like composition and use thereof |
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2503331A1 (en) | 2005-10-29 |
| US20050245618A1 (en) | 2005-11-03 |
| US7022740B2 (en) | 2006-04-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US8299079B2 (en) | Preparations and methods for ameliorating or reducing presbyopia | |
| US20100298335A1 (en) | Preparations and Methods for Ameliorating or Reducing Presbyopia | |
| EP3045164B1 (en) | Aqueous pharmaceutical compositions containing borate-polyol complexes | |
| US20050266089A1 (en) | Contact lens and eye drop rewetter compositions and methods | |
| CN1479631A (en) | A reversible gel system for ocular drug delivery | |
| US20200129505A1 (en) | Topical Brimonidine Tartrate Ophthalmic Solution | |
| US9889088B2 (en) | Alpha-2 adrenergic agonist having long duration of intraocular pressure-lowering effect | |
| US7683039B2 (en) | Water soluble, randomly substituted partial N-, partial O-acetylated chitosan, preserving compositions containing chitosan, and processes for making thereof | |
| TW201105369A (en) | N-halamine formulations with enhanced antimicrobial activity | |
| EP0996442B1 (en) | Aqueous liquid pharmaceutical composition containing as main component benzopyran derivative | |
| US20050245484A1 (en) | Lubricious germicidal ophthalmic solutions | |
| US11337921B2 (en) | Multi-use torasemide composition | |
| EP2349251B1 (en) | Topical formulations with a tertiary amine oxide | |
| US20060148899A1 (en) | Ophthalmic compositions and methods of using the same | |
| CA2502992A1 (en) | Lubricious germicidal ophthalmic solutions | |
| US20210145861A1 (en) | Chitosan containing compositions and methods relating to same | |
| EP2419081B1 (en) | Aqueous ophthalmic compositions containing anionic therapeutic agents | |
| US20140275197A1 (en) | Alpha-2 adrenergic agonist for treating intraocular pressure and ocular diseases through intravitreal and intracameral routes | |
| CN110799188B (en) | Ophthalmic formulations based on tropicamide | |
| US20130210876A1 (en) | Alpha-2 adrenergic agonist having long duration of intraocular pressure-lowering effect | |
| US20080199537A1 (en) | Topical gatifloxacin formulations | |
| HK1186395A (en) | Ophthalmic composition for contact lens |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |