Ophthalmic and contact lens solutions containing simple saccharides as preservative enhancers

Information

  • Patent Grant
  • 9913474
  • Patent Number
    9,913,474
  • Date Filed
    Wednesday, September 28, 2016
    8 years ago
  • Date Issued
    Tuesday, March 13, 2018
    6 years ago
Abstract
The present invention relates to an ophthalmic solution comprising 0.00001 to 10.0 weight percent of a simple saccharide, at least 0.00001 weight percent of a preservative, and not more than about 0.2 percent by weight chloride. The simple saccharide is chosen from the group consisting of: inositol; mannitol; sorbitol; sucrose; dextrose; glycerin; propylene glycol; ribose; triose; tetrose; erythrose; threose; pentose; arabinose; ribulose; xylose; xylulose; lyxose; hexose; allose; altrose; fructose; galactose; glucose; gulose; idose; mannose; sorbose; talose; tagatose; adlose; ketose; heptose; sedoheptulose; monosaccharides; disaccharides; sugar alcohols; xylitol; and polyol.
Description
FIELD OF THE INVENTION

The present invention relates to the field of ophthalmic solutions and their uses. In particular the invention relates to contact lens cleaning solutions, contact lens rinsing and storing solutions, solutions to deliver active pharmaceutical agents to the eye, solutions for disinfecting ophthalmic devices and the like.


BACKGROUND

The present invention relates to the field of ophthalmic solutions and especially to the aspects of preservative efficacy and comfort after prolonged use. These ophthalmic solutions have been used for some period of time and are available as over the counter products. Solutions that are used in direct contact with corneal tissue such as the delivery of an active pharmaceutical agent to the eye, or indirectly, such as the cleaning, conditioning or storage of devices that will come in contact with corneal tissue, such as contact lenses, there is a need to ensure that these solution do not introduce sources of bacterial or other microbial infection. Thus preservatives are included to reduce the viability of microbes in the solution and to lessen the chance of contamination of the solution by the user since many of the solutions are bought, opened, used, sealed and then reused.


State of the art preservative agents include polyhexamethylene biguanide (PHMB), POLYQUAD™, chlorhexidine and benzalkonium chloride, and the like, all of which at some concentration irritate corneal tissue and lead to user discomfort. Therefore, a solution that employs a given amount of a preservative agent, but which is made more effective by addition of an agent that is not a preservative agent would be desired.


SUMMARY OF THE INVENTION

The present invention relates to improved ophthalmic solutions that employ inositol and other simple saccharides in order to more effectively preserve solutions and to reduce the degree to which cationic preservatives will deposit on contact lenses. Ophthalmic solutions are here understood to include contact lens treatment solutions, such as cleaners, soaking solutions, conditioning solutions and lens storage solutions, as well as wetting solutions and in-eye solutions for treatment of eye conditions.


More specifically, the invention relates to an ophthalmic solution comprising 0.00001 to 10.0 weight percent of a simple saccharide, at least 0.00001 weight percent of a preservative, and not more than about 0.2 percent by weight chloride. The simple saccharide may be chosen from the group consisting of: inositol; mannitol; sorbitol; sucrose; dextrose; glycerin; propylene glycol; ribose; triose; tetrose; erythrose; threose; pentose; arabinose; ribulose; xylose; xylulose; lyxose; hexose; allose; altrose; fructose; galactose; glucose; gulose; idose; mannose; sorbose; talose; tagatose; adlose; ketose; heptose; sedoheptulose; monosaccharides; disaccharides; sugar alcohols; xylitol; and polyol.


The solutions specifically described herein have 0.00001 to about 10.0 percent of simple saccharides in combination with other active ingredients useful in ophthalmic solutions such as buffers, preservatives, surfactants, and antimicrobial agents, and with a low chloride concentration, not more than about 0.2 percent by weight. It has been found, surprisingly that inositol, and other sugars including mannitol, sorbitol, sucrose, dextrose, glycerin and propylene glycol, effectively increase the antibacterial effect of preservatives in low salt (low chloride) conditions.


The preservatives that are specifically useful are include polyhexamethylene biguanide (PHMB), POLYQUAD™, chlorhexidne, and benzalkonium chloride, as well as other cationic preservatives that may prove useful in the present invention as well. The cationic preservatives are used at effective amounts as preservatives, and in the instance of PHMB from 0.0001 percent by weight to higher levels of about 0.01 weight percent. Specifically, the cationic polymeric preservative includes polymeric biguanides such as polymeric hexamethylene biguanides (PHMB), and combinations thereof. Such cationic polymeric biguanides, and water-soluble salts thereof, having the following formula:




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wherein Z is an organic divalent bridging group which may be the same or different throughout the polymer, n is on average at least 3, preferably on average 5 to 20, and X1 and X2 are




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One preferred group of water-soluble polymeric biguanides will have number average molecular weights of at least 1,000 and more preferably will have number average molecular weights from 1,000 to 50,000. Suitable water-soluble salts of the free bases include, but are not limited to hydrochloride, borate, acetate, gluconate, sulfonate, tartrate and citrate salts.


The above-disclosed biguanides and methods of preparation are described in the literature. For example, U.S. Pat. No. 3,428,576 describes the preparation of polymeric biguanides from a diamine and salts thereof and a diamine salt of dicyanimide.


Most preferred are the polymeric hexamethylene biguanides, commercially available, for example, as the hydrochloride salt from Avecia (Wilmington, Del.) under the trademark COSMOCIL™ CQ. Such polymers and water-soluble salts are referred to as polyhexamethylene (PHMB) or polyaminopropyl biguanide (PAPB). The term polyhexamethylene biguanide, as used herein, is meant to encompass one or more biguanides have the following formula:




embedded image



wherein Z, X1 and X2 are as defined above and n is from 1 to 500.


Depending on the manner in which the biguanides are prepared, the predominant compound falling within the above formula may have different X1 and X2 groups or the same groups, with lesser amounts of other compounds within the formula. Such compounds are known and are disclosed in U.S. Pat. No. 4,758,595 and British Patent 1,432,345, which patents are hereby incorporated. Preferably, the water-soluble salts are compounds where n has an average value of 2 to 15, most preferably 3 to 12.


It was found that an unexpected preservative efficacy was displayed when inositol was used in conjunction with the cationic preservative. The other components of the solution are used at levels known to those skilled in the art in order to improve the wearability of lenses and when used directly in the eye, to provide increased resistance to infection. Inositol used in ophthalmic solutions increases preservative efficacy in certain formulations, provides increased resistance to infection in corneal tissue, in certain formulations, and improves the quality of tears in certain formulations.


The formulations may also include buffers such as phosphate, bicarbonate, citrate, borate, ACES, acetate, BES, BICINE, BIS, BIS-Tris, BIS-Tris Propane, bicarbonate, histidine, HEPES, Tris, HEPPS, imidazole, MES, MOPS, PIPES, TAPS, TES, glycine, tiomethamine, and Tricine.


Surfactants that might be employed include polysorbate surfactants, polyoxyethylene surfactants, phosphonates, saponins and polyethoxylated castor oils, but preferably the polyethoxylated castor oils. These surfactants are commercially available. The polyethoxylated castor oils are sold by BASF under the trademark CREMOPHOR®.


Inositol, mannitol, sorbitol, sucrose, dextrose, glycerin, propylene glycol and the other agents used in the present invention are all commercially available, and well enough understood to be formulated into products within the scope of the invention by those skilled in the art.


The solutions of the present invention may contain other additives including but not limited to buffers, tonicity agents, demulcents, wetting agents, preservatives, sequestering agents (chelating agents), surface active agents, and enzymes.


Other aspects include adding to the solution from 0.001 to 1 weight percent chelating agent (preferably disodium EDTA) and/or additional microbicide, (preferably 0.00001 to 0.1 or 0.00001 to 0.01) weight percent polyhexamethylene biquanide (PHMB, N-alkyl-2-pyrrolidone, chlorhexidine, polyquaternium-1, hexetidine, bronopol, alexidine, low concentrations of hydrogen peroxide, and ophthalmologically acceptable salts thereof.


Ophthalmologically acceptable chelating agents useful in the present invention include amino carboxylic acid compounds or water-soluble salts thereof, including ethylenediaminetetraacetic acid, nitrilotriacetic acid, diethylenetriamine pentaacetic acid, hyd roxyethylethylenediaminetriacetic acid, 1,2-diaminocyclohexanetetraacetic acid, ethylene glycol bis (beta-aminoethyl ether) in N, N, N′, N′ tetraacetic acid (EGTA), aminodiacetic acid and hydroxyethylamino diacetic acid. These acids can be used in the form of their water soluble salts, particularly their alkali metal salts. Especially preferred chelating agents are the di-, tri- and tetra-sodium salts of ethylenediaminetetraacetic acid (EDTA), most preferably disodium EDTA (Disodium Edetate).


Other chelating agents such as citrates and polyphosphates can also be used in the present invention. The citrates which can be used in the present invention include citric acid and its mono-, di-, and tri-alkaline metal salts. The polyphosphates which can be used include pyrophosphates, triphosphates, tetraphosphates, trimetaphosphates, tetrametaphosphates, as well as more highly condensed phosphates in the form of the neutral or acidic alkali metal salts such as the sodium and potassium salts as well as the ammonium salt.


The pH of the solutions should be adjusted to be compatible with the eye and the contact lens, such as between 6.0 to 8.0, preferably between 6.8 to 7.8 or between 7.0 to 7.6. Significant deviations from neutral (pH 7.3) will cause changes in the physical parameters (i.e. diameter) in some contact lenses. Low pH (pH less than 5.5) can cause burning and stinging of the eyes, while very low or very high pH (less than 3.0 or greater than 10) can cause ocular damage.


The additional preservatives employed in the present invention are known, such as polyhexamethylene biguanide, N-alkyl-2-pyrrolidone, chlorhexidine, polyhexamethylenebiguanide, alexidine, polyquaternium-1, hexetidine, bronopol and a very low concentration of hydrogen peroxide, e.g., 30 to 200 ppm.


The solutions of the invention are compatible with both rigid gas permeable and hydrophilic contact lenses during storage, cleaning, wetting, soaking, rinsing and disinfection.


A typical aqueous solution of the present invention may contain additional ingredients which would not affect the basic and novel characteristics of the active ingredients described earlier, such as tonicity agents, surfactants and viscosity inducing agents, which may aid in either the lens cleaning or in providing lubrication to the eye. Suitable tonicity agents include sodium chloride, potassium chloride, glycerol or mixtures thereof. The tonicity of the solution is typically adjusted to approximately 240 milliosmoles per kilogram solution (mOsm/kg) to render the solution compatible with ocular tissue and with hydrophilic contact lenses. In one embodiment, the solution contains 0.01 to 0.2 weight percent sodium chloride. The important factor is to keep the concentrations of such additives to a degree no greater than that would supply a chloride concentration of no greater than about 0.2 mole percent.


Suitable viscosity inducing agents can include lecithin or the cellulose derivatives such as hydroxymethytcellulose, hydroxypropylcellulose, hydroxypropyl methylcellulose (HPMC), and methylcellulose in amounts similar to those for surfactants, above.







EXAMPLE 1

An example of a formulation containing low salt, a buffer and cationic preservative follows:
















Log


Preservative



Reduction
Buffer
Preservative
Enhancer
Wetting Agent







2.27
none
PHMB
None
None




0.0001%


3.85
Bis-Tris
PRMB
None
CREMOPHOR ®RH 40



Propane 0.2%
0.0001%


4.00
Bis-Tris
PHMB
propylene
CREMOPHOR ®RH 40



Propane 0.2%
0.0001%
glycol 3%


4.40
Bis-Tris
PHMB
sorbitol 5%
CREMOPHOR ®RH 40



Propane 0.2%
0.0001%


4.40
Bis-Tris
PHMB
inositol 5%
CREMOPHOR ®RH 40



Propane 0.2%
0.0001%


2.98
OPTI-FREE ®



Express


0.68
Ciba SOLO-



CARE ®


2.99
B&L RENU ®



MULTIPLUS



MPS ®









Column 1 shows the reduction of C. albicans at 2 hours using a typical antibacterial test. The data shows improved activity over the preservative alone; improved activity over the buffer control without sugar additive and improved activity over commercially available products


EXAMPLE 2











Data Table










Log





Reduction
Buffer
Preservative
Additive





2.53
None
PHMB 0.0001%
none


1.34
Bis-Tris
PHMB 0.0001%
sodium chloride 0.5%



Propane 0.2%


3.42
Bis-Tris
PHMB 0.0001%
glycerin 0.5%



Propane 0.2%


2.73
Bis-Tris
PHMB 0.0001%
propylene glycol 05%



Propane 0.2%


1.13
Bis-Tris
PHMB 0.0001%
potassium chloride 0.5%



Propane 0.2%


3.92
Bis-Tris
PHMB 0.0001%
sorbitol 0.5%



Propane 0.2%


3.23
Bis-Tris
PHMB 0.0001%
mannitol 0.5%



Propane 0.2%


3.06
Bis-Tris
PHMB 0.0001%
inositol 0.5%



Propane 0.2%


3.72
Bis-Tris
PHMB 0.0001%
dextrose 0.5%



Propane 0.2%









This data shows that the antimicrobial activity of buffer with the sugar or glycol is greater than the preservative alone and that decreased activity at 0.5% sodium chloride or 0.5% potassium chloride solutions occurs as well. Thus the surprising effect of the sugar derived preservative enhancers is displayed and the effects relationship to chloride concentration is demonstrated.


EXAMPLE 3

Solutions with a cationic polymeric preservative (PHMB) sodium chloride and glycerin and a buffer were made as shown in the following table and the preservative efficacy was measured.
















Log


Sodium



Reduction
Buffer
Preservative
Chloride
Glycerin







1.69
none
PHMB 0.0001%
none
none


1.74
none
PHMB 0.0001%
0.1%
none


1.46
none
PHMB 0.0001%
0.2%
none


0.86
none
PHMB 0.0001%
0.4%
none


0.49
none
PHMB 0.0001%
0.5%
none


2.44
Bis-Tris
PHMB 0.0001%
none
none



Propane 0.2%


1.89
Bis-Tris
PHMB 0.0001%
0.1%
none



Propane 0.2%


1.54
Bis-Tris
PHMB 0.0001%
0.2%
none



Propane 0.2%


0.98
Bis-Tris
PHMB 0.0001%
0.4%
none



Propane 0.2%


0.89
Bis-Tris
PHMB 0.0001%
0.5%
none



Propane 0.2%


2.46
Bis-Tris
PHMB 0.0001%
none
0.20%



Propane 0.2%


2.41
Bis-Tris
PHMB 0.0001%
none
0.50%



Propane 0.2%









The above date illustrates the effect of sodium chloride on preservative efficacy and the effect of glycerin in improving preservative efficacy in low salt solutions.


EXAMPLE 4

Solutions were made according to methods described supra with sodium phosphate as the buffer.















Log





Reduction
Buffer
Preservative
Tonicity Agent







0.79
Sodium Phosphate 0.2%
PHMB 0.0001%
none


0.33
Sodium Phosphate 0.2%
PHMB 0.0001%
Sodium





Chloride 0.7%









This data illustrates the problem with sodium chloride is independent of buffer type.


EXAMPLE 5

Solutions were formulated with sodium chloride, sorbitol and sucrose and then lenses were immersed in the resultant solutions and chlorohexidine gluconate was added. The lenses were exposed for 3 hours and the amount of the chlorohexidine deposited on the lens was measured.


Method: HPLC analysis for chlorhexidine gluconate






    • 3.0 mL solution exposed to ½ lens


      Matrix: 1 ppm CHG/0.2% Bis-Tris Propane/0.1% CREMOPHOR® RH 40


      Lens: Freshlook ColorBlends (45% phemfilcon A, 55% water) Wesley Jess




















Additive
μg CHG per lens
% Decrease









None
4.0
67.3%



Sodium Chloride
3.6
59.3%



Sorbitol
3.0
50.7%



Sucrose
1.3
21.4%










This test shows that the sugars used in the test have an ability to decrease the extent of preservative binding for of cationic preservatives when properly formulated. Both sorbitol and sucrose solutions demonstrated efficacy in reducing preservative deposition.


EXAMPLE 6

The following experiment demonstrates the effect of chloride concentration on the antimicrobial effectiveness of PHMB preservative solutions.

















Log



Addi-



Reduction
Buffer
Preservative
NaCI
tive
Effect







1.05
Bis-Tris 0.2%
PHMB 0.0001%
None
none
54%


1.47
Bis-Tris 0.2%
PHMB 0.0001%
None
None
75%


0.77
Bis-Tris 0.2%
PHMB 0.0001%
0.70%
None
39%


2.36
Bis-Tris
PHMB 0.0001%
None
None
123% 



Propane 0.2%


2.32
Bis-Tris
PHMB 0.0001%
None
None
119% 



Propane 0.2%


0.91
Bis-Tris
PHMB 0.0001%
0.70%
None
47%



Propane 0.2%


1.27
Tricine 0.2%
PHMB 0.0001%
None
None
65%


1.31
Tricine 0.2%
PHMB 0.0001%
None
None
67%


0.62
Tricine 0.2%
PHMB 0.0001%
0.70%
none
32%









EXAMPLE 7

Formulations containing inositol (Spectrum) were prepared in a 0.2% phosphate buffer. The solutions were made isotonic with sodium chloride and preserved with polyhexamethylene biquanide at 0.0001%. The pH was adjusted to 7.2 with either 1 N sodium hydroxide or 1 N hydrochloric acid. The in vitro microbicidal activity of the solutions was determined by exposing C. albicans to 10 ml of each solution at room temperature for 4 hours. Subsequently, an aliquot of each solution was serial diluted onto agar plates and incubated for 48 hours at elevated temperatures. At the conclusion of the incubation period the plates are examined for the development of colonies. The log reduction was determined based on a comparison to the inoculum control. The following table provides the results of the in vitro studies.
















Additive
4 hour log reduction









Inositol (0.5%)
1.1



Buffer control
0.8










The solution containing inositol showed an improvement in the activity against C. albicans as compared to the buffer control.


EXAMPLE 8

Formulation Preserved Solution for rinsing, storage, reconstituting enzyme tablets. A formulation was prepared by dissolving Tricine, Allantoin, Inositol, Disodium edetate, and Polyoxyl 40 Hydrogenated Castor Oil in 80% of the water volume. The pH of the solution was adjusted to 7.3 with 1 N sodium hydroxide. The tonicity of the solution was adjusted with sodium chloride and polyhexamethylene biguanide was added. The solution was diluted to volume with water.















Constituent
Supplier
% Weight/Volume
Amount



















Purified water

to 80%
40
mL


Tricine
Spectrum
1.0%
0.500
g


Allantoin
Spectrum
0.25%
0.125
g


Inositol
Spectrum
0.1%
0.050
g


Edetate Disodium
Spectrum
0.055%
0.0275
g










Polyoxyl 40
CREMOPHOR ® RH
0.1%
0.5 mL of 10%











Hydrogenated Castor
40 from BASF Co.





Oil










Sodium Hydroxide,

as required for pH
as required for pH


1N

adjustment to 7.3
adjustment to 7.3


Purified Water

to 98%
Dilute to 49 mL


Sodium Chloride
Fisher
As required for
As required for




tonicity adjustment
tonicity adjustment




285 mOsm
285 mOsm


Polyhexamethylene-
20% w/w solution
0.0001%
50 μL of 0.1%











biguanide HCl
available under the






mark COSMOCIL ™



CQ from Avecia










Purified Water

Balance to 100%
Dilute to 50 mL









This provides an example of a specific formulation of the present invention but does not fully illustrate the bounds or limits of the invention.

Claims
  • 1. A method for providing an ophthalmic solution to an eye, the method comprising: contacting the eye with a single-part solution comprising 0.00001 to 10.0 weight percent of a preservative enhancer chosen from the group consisting of: inositol; ribose; triose; tetrose; erythrose; threose; pentose; arabinose; ribulose; xylose; xylulose; lyxose; hexose; allose; altrose; fructose; galactose; glucose; gulose; idose; mannose; sorbose; talose; tagatose; adlose; ketose; heptose; sedoheptulose; and xylitol; at least 0.00001 weight percent of a preservative having a structure given by:
  • 2. The method as recited in claim 1, wherein the preservative is polyhexamethylene biguanide with a concentration between 0.1 and 100 parts per million.
  • 3. The method as recited in claim 1, wherein the preservative has a concentration between 0.1 and 100 parts per million.
  • 4. The method as recited in claim 1, wherein the single-part solution further comprises a physiologically compatible buffer.
  • 5. The method as recited in claim 4, wherein the physiologically compatible buffer is selected from a group consisting of: phosphate, bicarbonate, citrate, borate, ACES, acetate, BES, BICINE, BIS, BIS-Iris, BIS-Iris Propane, bicarbonate, histidine, HEPES, Iris, HEPPS, imidazole, MES, MOPS, PIPES, TAPS, TES, glycine, tromethamine, and Tricine.
  • 6. The method as recited in claim 1, wherein the single-part solution further comprises a wetting agent.
  • 7. The method as recited in claim 6, wherein the wetting agent is selected from a group consisting of: polysorbate surfactants, polyoxyethylene surfactants, polyethoxylated glycerides, phosphonates, saponins and polyethoxylated castor oils.
  • 8. The method as recited in claim 1, wherein the single-part solution further comprises a sequestering agent.
  • 9. The method as recited in claim 8, wherein the sequestering agent is selected from a group consisting of: ethylenediaminetetraacetic acid, phosphonates, citrate, gluconate, nitrilotriacetic acid, diethylenetriamine pentaacetic acid, hydroxyethylethylenediaminetriacetic acid, 1,2-diaminocyclohexanetetraacetic acid, ethylene glycol bis (beta-aminoethyl ether), tetraacetic acid (EGTA), aminodiacetic acid, hydroxyethylamino diacetic acid, tartarate, and water-soluble salts thereof.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. patent application Ser. No. 11/613,029 (filed Dec. 19, 2006) which is a continuation-in-part of U.S. patent application Ser. No. 10/544,151 (filed Aug. 1, 2005) which is a national stage entry of International Patent Application PCT/US01/46344 (filed Nov. 8, 2001) which claims the benefit of U.S. Provisional Patent Application 60/246,870 (filed Nov. 8, 2000). The content of each of these applications is hereby incorporated by reference.

US Referenced Citations (3)
Number Name Date Kind
6139646 Asgharian et al. Oct 2000 A
6162393 De Bruiju et al. Dec 2000 A
6617291 Smith Sep 2003 B1
Foreign Referenced Citations (5)
Number Date Country
0923950 Jun 1999 EP
10-108899 Apr 1998 JP
20000084052 Mar 2000 JP
WO0007634 Feb 2000 WO
WO0238161 May 2002 WO
Related Publications (1)
Number Date Country
20170013839 A1 Jan 2017 US
Provisional Applications (1)
Number Date Country
60246870 Nov 2000 US
Continuation in Parts (2)
Number Date Country
Parent 11613029 Dec 2006 US
Child 15278660 US
Parent 10544151 US
Child 11613029 US