MXPA97000853A - Composition lubricant, sterile, hygienic parauna manual den - Google Patents
Composition lubricant, sterile, hygienic parauna manual denInfo
- Publication number
- MXPA97000853A MXPA97000853A MXPA/A/1997/000853A MX9700853A MXPA97000853A MX PA97000853 A MXPA97000853 A MX PA97000853A MX 9700853 A MX9700853 A MX 9700853A MX PA97000853 A MXPA97000853 A MX PA97000853A
- Authority
- MX
- Mexico
- Prior art keywords
- demand
- piece
- composition
- volume
- approximately
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 54
- 239000000314 lubricant Substances 0.000 title claims abstract description 32
- 238000004659 sterilization and disinfection Methods 0.000 claims abstract description 44
- 230000001954 sterilising Effects 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 38
- 239000002775 capsule Substances 0.000 claims abstract description 13
- 238000005260 corrosion Methods 0.000 claims abstract description 13
- 239000002480 mineral oil Substances 0.000 claims abstract description 13
- 235000010446 mineral oil Nutrition 0.000 claims abstract description 13
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 12
- 239000003112 inhibitor Substances 0.000 claims abstract description 11
- 239000007788 liquid Substances 0.000 claims abstract description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 10
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 8
- 238000010438 heat treatment Methods 0.000 claims abstract description 7
- 230000002633 protecting Effects 0.000 claims abstract description 6
- 239000008174 sterile solution Substances 0.000 claims abstract description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims abstract 2
- 230000001050 lubricating Effects 0.000 claims description 7
- 235000013305 food Nutrition 0.000 claims description 5
- 239000000243 solution Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000000717 retained Effects 0.000 abstract description 2
- 239000003623 enhancer Substances 0.000 description 7
- 230000002708 enhancing Effects 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 238000011109 contamination Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 2
- 230000003115 biocidal Effects 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K 2qpq Chemical group [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 206010000565 Acquired immunodeficiency syndrome Diseases 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 210000002445 Nipples Anatomy 0.000 description 1
- 241000282890 Sus Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 230000002378 acidificating Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229920002892 amber Polymers 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000001580 bacterial Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 201000009910 diseases by infectious agent Diseases 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drugs Drugs 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 101700049451 lppL Proteins 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 231100000647 material safety data sheet Toxicity 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000008019 pharmaceutical lubricant Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001681 protective Effects 0.000 description 1
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 1
- 229960002026 pyrithione Drugs 0.000 description 1
- 230000002829 reduced Effects 0.000 description 1
- 230000003014 reinforcing Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000003612 virological Effects 0.000 description 1
Abstract
About 1/2 cc of a sterile composition (5) exhausted in the supply line (11) air impeller rotor a dental handpiece (10) while the lower handpiece is retained, protects and lubricates bearings handpiece and turbine during the subsequent autoclave sterilization process. An additional dose inserted into the hole of the cavity cutter after the autoclave process also lubricates the handpiece and inhibits the rust that forms in the bearings of the handpiece and the turbine during use. The pre-sterilization dose and post-sterilization dose of measured quantities can be packaged separately in available capsules (20, 30). The composition (5) is manufactured by heating the mixture to about 10% of sterile bulk volume of a sterile solution Power-Up NNL-690, which is a lubricant in the boundary layer of liquid hydrocarbon and corrosion inhibitor, with 90% by volume of pharmaceutical grade mineral oil
Description
PIECE BY THE DENTAL HAND the HYGIENIC PHARMACEUTICAL STERILIZATION
LUBRICANT BACKGROUND OF THE INVENTION 1. FIELD OF THE INVENTION The present invention generally relates to a sterile, pharmaceutical composition inserted in a piece prior by the dental hand to and after sterilization lubricating moving parts and inhibiting piece corrosion by hand, and , more particularly, to the process of sterilizing things if instrumented inserting the prior of the compositions to sterilization system. a. Previous Piece Lubricant by Hand and Processes It is well known that a piece by the dental hand has to be lubricated to maintain its effectiveness and prevent premature failure periodically. The rotor or turbine in the piece by hand is supported on bearings that are subjected to severe use due to the wide range of speeds and torque loads involved by drilling teeth. Typically, the bearings are lubricated by adding oil in a variety of ways, such as from a large nipple connected to the rotor drive line of the aerial feed that intermittently drops oil into the intake air stream where the oil is atomized and then carried to the entrained of the rotor in the air of the entrance. In a method discovered in Sugai U.S. Patent 4,218,216 an improved system employed a small oiler inserted into the airline food line that has a spring loaded check valve surmounted by atmospheric food pressure to allow oil to escape into the feed air, atomized and continuously lubricates the rotor bearings . However, with the AIDS attack and the need for increased sterilization, such a system did not work during system sterilization and offered no protection against cross contamination. Through 1991, as he discovered in Feldman U.S. Patent 5,131,845, it was favorably recommended that the piece by hand frequently be sterilized, and sterilization of the piece by hand among the patients was becoming a recommended procedure. However, increased sterilization required more frequent lubrication. It was known to lubricate the piece by hand both before and after sterilization. However, the initial lubricants used pre-sterilization and post-sterilization were generally the same products as was prior previously available to the need for increased sterilization. These products did not survive the heat of the system's own sterilization process and were in effective. Piece failures by hand increased and were replaced at a unit cost of approximately $ 150.00 US While that Feldman developed an improved method of inserting oil into the rotor ride aerial food line using a capable to tighten sealed capsule containing lubricant la and its system prevented the transmission of the material from the bacterial and beyond to the patient the viral and the dentist, of the art of no of the advance of the compositions of the lubricant in ways Of which no development could only withstand the cycle of the sterilization system, but also protect the piece by hand during the sterilization cycle by retaining and / or reinforcing its limit that lubricates the characteristics of and anti-corrosion Feldman merely discovered that his shell 10 was filled with an extremely light, dental quality, FDA approved, lubricating oil that was required for the piece by hand and was widely used in the art. Feldman 7: 21-24. b. Industrial Product Condoms It was also known to add ingredients, such as, an anion selected from the group consisting of the sulfate, the acetate and citrate groups, an acidic industrial products to inhibit micro-degradation in stories and products that son the result of the growth of micro-organisms that can cause biological odors, the corrosion deterioration of y. Pear U.S. Patent 4,920,107. In an improvement to Nelson U.S. Patent 5,283,005, the efficacy of the biocidal of such additives was reinforced by mixing a known condom (pyrithione, used in lubricant) with a known antibiotic (lipopeptide, for treating superficial infections) to inhibit bacteria and fungi notably from forming in the composition itself when used exclusively or in combination with an inert carrier, such as water, liquid hydrocarbons, ethanol, isopropanol, or the like. 2: 63-67. There was no discovery or suggestion of the composition of the present invention however, that the discovered compositions were sterile or could be used as a pre-sterilization lubricant for a piece by the dental hand, or that the lubricating limit or the protective quality of the compositions was reinforced. c. Theory of Limit Lubricant The general theory of how a limit lubricant works are well known. When the surfaces warn us when rolling or sliding contact, particles of se se form of what combines of use against the lubricant to form an eutectic film (new) The point of one of has material of the lowest fusion that the original material) which can resist high charges and can become the sacrificial layer that is carried away and removed instead of being under (rotor / carrying) the material, thus, reducing friction. It is an object of the present invention to provide a new, low friction coefficient, lubricant composition and process that allow insertion of the composition in the rotor ride the prior of the air inlet to the system sterilization cycle, or after , or both, and what remains effective during the sterilization cycle system and after this to provide improved protection of the piece by hand against corrosion, substantially reduced utilization rates and substantially improved resistance leading to that by extending the service life of the piece by the hand significantly. It is an extensive objective of the present invention to provide a new sterile composition and process that reduces the risk of cross-contamination of viruses and bacteria. 2. SUMMARY OF INVENTION Part I below is a brief summary of the invention to achieve the foregoing and other benefits and advantages in accordance with the purpose of the present invention as included and broadly described herein. One aspect of the present invention is a piece lubricant by the dental hand that includes a composition of about 90% by volume of a liquid hydrocarbon and about 10% by volume of a limit lubricant and corrosion inhibitor. This composition is made by mixing approximately 10% by volume of a solution of NNL-690 with approximately 90% by volume of a pharmaceutical quality mineral oil. Preferably, the NNL-690 solution is substantially heated to about 250 ° F for about one hour or until sterile and the final composition is preferably further heated to about 225 ° F for about one hour or until sterile and completely mixed. An extensive aspect of the present invention is the process of sterilizing a piece by the dental hand having a rotor supported at a pressure and a buzz hole adapted to receive and sustain a buzz lubricating the piece rotor by hand and carrying inserting an amount predetermined of the composition mentioned in the rotor handled aerial food line while vertically holding the piece upside down by hand, and, then, sterilization system of the piece by hand in a sealed plastic bag. An extensive aspect of the invention is protecting the piece by hand in use by inserting a predetermined amount of the composition mentioned in the hole of the invention. buzzing before each use or during use. DESCRIPTION OF THE DRAWINGS Fig. IA are a perspective view of a piece by the hand of the previous art. Fig. IB are a perspective view of a capsule available from the prior art in which the composition of the present invention can conveniently be packaged. Fig. IC are a perspective view of the capsule of Fig. IB with the head highlighted. Fig. 2 is a front elevation of the piece by hand and Fig. IA held vertically upside down and showing the Fig. 1C capsule containing the composition of the present invention to be squeezed to insert a moderate dosage of the composition into the passage of air intake of piece prior by hand to sterilization. Fig. 3 is an elevation of the top of Fig. 2. Fig. 4 is a front perspective of the piece by the hand of Fig. A right side held to and slightly at an angle and showing the capsule of Fig. containing of the invention present of the one of inserting of for of pressing itself, after the sterilization of the, the moderate of quantity of one of the composition in the hole of buzz of the head of the piece by the hand that lodges the turbine, and both of the turbine of the the and the chock that they hold the buzz. Fig. 5 is a correct lateral elevation of Fig. 4. DETAILED DESCRIPTION OF THE PREFERRED INCARNATION The composition of the present invention is a specially formulated, mineral based, hygienic, pharmaceutical lubricant. It can be packaged individually before use for sterilization of the piece by hand without risk of contamination by the lubricant itself. It can be packaged individually for use after sterilizing the piece by hand without risk of contamination by the lubricant itself. The pre-sterilization package contains a moderate amount of about 1/2 c.c.p., enough for one application. The post-sterilization package contains a pre-moderate antity of approximately ten (10) applications of approximately 2 each drop. Composition 5 of the present invention comprises a mixture of refined petroleum liquid hydrocarbons including approximately 90% by volume of a fully refined, pharmaceutical quality, non-sterile, white oil to which has been added and completely mixed approximately 10% Through volume of a fully refined, ignite, mineral based oil, amber in color, as a limit lubricant enhancer and corrosion inhibitor. Composition 5 is manufactured for the applicant by Petroleum Products of America of Scottsdale, Arizona and sold under the STERI-LUBE ™ applicant brand. The mineral oil used in the meetings of the invention present the requirements of the United States Pharmacopeia XXII, as well as the requirements of Food and Drug Administration by 21 C.F.R. 172,878. The limit lubricant and corrosion inhibitor enhancer of the present invention is a non-sterile petroleum product known only to the applicant by the Power-Up ™ designation NNL-690, made and sold by Power-to-Distribution, Inc. of 6173-6 SE Callejeros, Calgary, AB, Canada T2H1L9 '("Power-Up"). Power-Up has retained the specific composition of NNL-690 as a trade secret. However, the product is commercially available to any buyer and can be obtained simply by notifying Power-Up to the previous situation. Prior to the present invention, it has been known to use NNL-690 as a limit lubricant enhancer to reduce friction in automotive devices. Preferably, the solution of the enhancer / inhibitor of the present invention is first heated to a temperature of about 250 degrees Fahrenheit for about one hour to sterilize it. The lubricant enhancer / inhibitor also used in the present invention obeys the Material Safety Data Sheet ("MSDS") specifications. The final lubricant composition 5 of the present invention is made by mixing 90% through volume the mineral oil with 10% by volume enhancer / enhancer and then heating the final mixture to a temperature of about 225 degrees Fahrenheit for about one hour sterilize it and ensure a complete mixing of the ingredients. The additional features of the final composition 5 of the present invention are as follows: 1. Color / odor: Clear - the pleasant order, abundant in nuts. 2. Specific gravity: <; 1.0 @ 15 Deg. C. 3. Vapor pressure: < .5mm 4. Evaporation rate: None @ 25 Deg. C. 5. Boiling point: > 230 Deg. C. 6. Rain point: > -9 Deg. C. 7. Flash point: 193. Deg. C; > 380 Deg. F. 8. Solubility in Water: Nothing. 9. pH: N / A. 10. Viscosity: 100 (SUS) WORKING EXAMPLE Take 5.5 gallons of NNL-690 and heat to 250 degrees F. for 1 hour. Mix the resulting liquid again with 49.5 gallons of mineral oil and heat at approximately 225 degrees F. for about 1 hour. The two steps of heating can be omitted if a final sterile composition is not required. Package and ship. The packaging of the invention is conventional. A pre-sterilization package, such as a capsule 20, can be sized to hold an amount of the final composition of the present invention sufficient to protect the piece by hand 10 during the sterilization process suitably, as, approximately 1 / 2 ccp.A la post-sterilization package, one of as 30 capsule, can be conveniently sized according to a 1 applicator capable of closing back from ccp which supports ten individual applications of approximately l / 10th c.c.p. each. l / 10th c.c.p. It is the equivalent of approximately 2 otes. The post-sterilization La capsule will be a vessel capable of closing as it is well known in the art once again. PROCESS OF USING The process of using the composition of the present invention is best understood with reference to the drawings. 1. Fig. 1. samples the piece by hand 10 of the previous art. The piece by the hand 10 is held erectly upside down as shown in Fig. 2. The cap of the capsule 20 containing the pre-sterilization system of sterile composition 5 is remote and the capsule is tightened to allow a dosage of about 1/2 ccp of the lubricant enter the main hole 11 aerial by hand 10. 2. Place the piece by hand 10 in a sterilization bag (not shown) and place the bag in a normal sterilization system (not shown). 3. Follow the sterilization instructions system.
in 4. When the system sterilization cycle is complete, remove the bag and piece by hand. 5. As seen in Fig. 2 hold the piece by hand 10 side of the right side and to an angle to expose access to the hole 12 hum and then the capsule grip 30 allowing two (2) drops of post-sterilization system of sterile solution 5 to enter the drilling hole 12 before the use of piece by hand 10. The above description of a preferred embodiment and best mode of the invention is known to the applicant at the time filing the application, and has been presented with the purpose of the illustration and description. It is not thought to be exhaustive or to limit the invention to the form of precision discovered, and obviously many modifications and variations are possible in light of previously teaching. The incarnation was chosen and described in order to better explain the principles of the invention and its practical application to enable others by or experienced in the art to better use the invention in several incarnations and with several modifications suited to the particular use contemplated. It is thought that the scope of the invention was defined by the demands added to this.
Claims (29)
1. The manufacturing process a piece lubricant by the dental hand characterized by the step of: mixing approximately 10% by volume of NNL-690 and approximately 90% by volume of a pharmaceutical grade mineral oil.
2. The process of demand 1 beyond characterized by the? Of: heating the mixture until sterile.
3. The process of demand 2 in which the heating step is characterized by the step of heating the mixture to approximately 225 ° F for approximately one hour.
4. The process of demand 3 beyond characterized by the step of: heating the NNL-690 to approximately 250 ° F for approximately a prior of the hour to the mixing step.
5. The demand process 1 in which the mixture is not characterized by more than about 10% by volume of NNL-690 and not less than about 90% by volume of mineral oil.
6. The process of demand 1 in which the NNL-690 are characterized by a liquid hydrocarbon limit lubricant and corrosion inhibitor.
7. A piece lubricant by the dental hand characterized by a mixture of 15L approximately 10% by volume of NNL-690 and approximately 90% by volume of a pharmaceutical grade mineral oil.
8. The demand lubricant 7 in which the solution is sterile.
9. The demand lubricant 7 in which the mixture is not characterized by more than about 10% by volume of NNL-690 and not less than about 90% by volume of mineral oil.
10. The demand lubricant 7 in which the NNL-690 is characterized by a limit of liquid hydrocarbon and corrosion inhibitor.
11. The product made by the demand process 1.
12. The product of demand 11 made by the process of demand 2.
13. The product of demand 12 made by the process of demand 3.
14. The product of demand 13 made by the process of demand 4.
15. The product of demand 11 made by the process of demand 5.
16. The product of demand 11 made by the process of demand 6.
17. The process of sterilizing a piece by the dental hand that have a rotor supported at a pressure and a buzz hole adapted to receive and sustain a buzzing characterized by the steps of: (a) lubricate the rotor and carrying of the piece by hand with a predetermined amount of a composition one comprises a solution of approximately 90% by volume of a liquid hydrocarbon and approximately 10% by volume of a limit lubricant and corrosion inhibitor, and (b) insert the piece by hand in a sealed bag and attach the bag to a cycle of sterilization. To sterilize the piece by hand.
18. The process of demand 17 in which the predetermined quantity is approximately 1/2 ccp
19. The process of demand 17 in which the step by lubricating further characterized by the step of inserting the composition in a rotor ride the food line aerial while vertically holding the piece up by hand.
20. The process of demand 17 in which the composition of the step lubricating further characterized by: the limit lubricant and the corrosion inhibitor is NNL-690, and the liquid hydrocarbon includes a pharmaceutical grade mineral oil.
21. The demand process 20 in which the composition is sterile.
22. The process of claim 21 further characterized by the step of: after completing the cycle of the sterilization system, inserting a predetermined amount I & of the composition in the buzz hole.
23. The demand process 20 in which the composition does not include more than about 10% by volume of NNL-690 and not less than about 90% by volume of the liquid hydrocarbon.
24. The process of claim 17 further characterized by the step of: after completing the cycle of sterilization system, inserting a predetermined amount of composition into the buzz hole.
25. The process of protecting a piece by the dental hand having a rotor supported at a pressure and a hole of zoomed tuned receiving and sustaining a buzz is characterized by the step of: lubricating the rotor and carrying the piece by hand with a predetermined amount of a composition comprising approximately 10% by volume of NNL-690 and Approximately 90% by volume of a pharmaceutical grade mineral oil.
26. The demand process 25 in which the composition is not characterized by more than about 10% NNL-690 and not less than about 90% mineral oil.
27. The claim process 26 in which the predetermined amount is approximately 2 drops.
28. The demand process 25 in which the composition is sterile.
29. The process of demand 25 in what the step lubricating / 4T 2 is further characterized by the step of inserting the composition 3 in the buzz hole. F, ABSTRACT ABOUT 1/2 c.c.p. of a sterile composition (5) dropped on the rotor ride the air feed line (11) of a piece by dental hand (10) while holding the piece by the upside down hand protects and lubricates the piece's headings by the hand and turbine during the process of sterilization of sterilization system of subsequent. An additional dosage inserted further into the buzz hole after the sterilization process system lubricates the piece by hand and inhibits rust from forming on the piece bearings by hand and turbine during use. Dosage of pre-sterilization and post-sterilization dosing of moderate amounts separately in available capsules can be packaged (20, 30). Composition (5) is made by heat mixing up to approximately 10% by volume of a sterile solution of Power-Up ™ NNL-690 which is a liquid hydrocarbon limit lubricant and corrosion inhibitor, with 90% by / olu in pharmaceutical grade mineral oil. DX-W ---- C - PCTAPP -M
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08283851 | 1994-08-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA97000853A true MXPA97000853A (en) | 2000-07-01 |
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