Movatterモバイル変換


[0]ホーム

URL:


US2826532A - Process of stabilizing polyvinyl pyrrolidone-iodine compositions - Google Patents

Process of stabilizing polyvinyl pyrrolidone-iodine compositions
Download PDF

Info

Publication number
US2826532A
US2826532AUS457777AUS45777754AUS2826532AUS 2826532 AUS2826532 AUS 2826532AUS 457777 AUS457777 AUS 457777AUS 45777754 AUS45777754 AUS 45777754AUS 2826532 AUS2826532 AUS 2826532A
Authority
US
United States
Prior art keywords
iodine
polyvinyl pyrrolidone
available
composition
solution
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.)
Expired - Lifetime
Application number
US457777A
Inventor
William A Hosmer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GAF Chemicals Corp
Original Assignee
General Aniline and Film Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US282458Aexternal-prioritypatent/US2706701A/en
Application filed by General Aniline and Film CorpfiledCriticalGeneral Aniline and Film Corp
Priority to US457777ApriorityCriticalpatent/US2826532A/en
Application grantedgrantedCritical
Publication of US2826532ApublicationCriticalpatent/US2826532A/en
Anticipated expirationlegal-statusCritical
Expired - Lifetimelegal-statusCriticalCurrent

Links

Classifications

Definitions

Landscapes

Description

PROCESS OF STABILIZING POLYVINYL PYRROLI- DONE-IODINE COMPOSITIONS William A. Hosmer, Pittsiield, Mass., assignor to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application September 22, 1954 Serial No. 457,777
1 Claim. (Cl. 16770) This invention relates to a process of stabilizing a dry powdered adduct of iodine and polymeric 1-vinyl-2- pyrrolidone (hereinafter referred to as polyvinyl pyrrolidone) whereby a stable composition is obtained which when dissolved in water will not change its pH and maintain a constant available iodine content.
In the copending application of Herman A. Shelanski, Serial No. 135,519, filed December 28, 1949, now abandonded, there is disclosed a novel composition of polyvinyl pyrrolidone and iodine which has been found to be of substantial value for many applications in which advantage is taken of the bactericidal activity of the iodine but in which the irritating, sensitizing, and toxic properties of the iodine are substantially overcome. As disclosed in this application, this novel iodine-polyvinyl pyrrolidone composition may be prepared by adding a solution of iodine, such as Lugols solution or tincture of iodine to an aqueous solution of polyvinyl pyrrolidone followed by dessication in a suitable dryer.
To improve on the method of preparing the foregoing novel iodine-polyvinyl pyrrolidone composition, there is disclosed in the copending application of Hans Beller and W. A. Hosmer, Serial No. 282,458, filed April 15, 1952, now U. S. Patent 2,706,701, a process whereby dry elemental iodine is mixed with dry powdered polyvinyl pyrrolidone. The iodine and powdered polymer is mixed until a homogeneous powder is obtained, the mixing being carried out in materials which are not attacked by iodine so as to avoid the introduction of metal ions into the finished composition. This mixing is effected by grinding the iodine and polyvinyl pyrrolidone in a mortar and pestle or more advantageously in a suitable mechanical mixer such as a ball mill. The time of mixing varies only with the efficiency thereof, as the combination of the polyvinyl pyrrolidone with iodine on its surface is rapid, in fact, such combination will occur to some extent on dropping iodine crystals on the dry powdered polymer.
On completion of the mixing there is obtained a compound in a physical state similar to the polymer alone but which contains varying proportions of available iodine (as distinguished from free iodine), iodide ion, and bound iodine. A distinction between these forms may be made on an analytical basis, available iodine being determined directly by dissolving a sample of the product in water and titrating with 0.1-N sodium thiosulfate solution using starch as an indicator. The amount of iodine present as iodide ion is determined by reducing the iodine compound in solution with l-N sodium acid sulfite, adding enough to make the solution colorless, then adding 0.1-N silver nitrate and enough nitric acid to make the solution acidic and back-titrating with ammonium thiocyanate. The iodide ion is the difierence between this figure and the available iodine as determined above. The total iodine may be determined by combustion methods such as that formulated by Hallett in Scotts Standard Method of Chemical Analysis, bound iodine then being determined by subtracting the sum of available iodine and iodide ion from the total iodine as determined above.
The product thus obtained may have an available iodine content ranging from 845% and an iodide ion content from 0.98 to 5.6%. With any given sample of polyvinyl pyrrolidone, the iodine present as available iodine and iodide ion may vary somewhat. On standing, the amount of available iodine slightly decreases while the amount of iodide ion increases. in order to obtain a stable product, Hans Beller et al. referred to above found that a product in which the ratio of available iodine to iodide ion is substantially 2:1 is readily and rapidly obtained by heating the dry blended material in the order of -490 C. Further details regarding this process may be obtained by reference to their patent, the contents of which are incorporated herein by reference, especially, the various iodine-polyvinyl pyrrolidone compositions as prepared in accordance with their Examples 1 to V1 inclusive.
The iodine-polyvinyl pyrrolidone compositions prepared in accordance with the aforestated application form aqueous solutions which contain iodine having a very high germicidal activity. The iodine-polyvinyl pyrrolidone composition in aqueous solution has a high acid reaction near a pH of 2, which in some instances, such as, for intravenous use or application on sensitive tissue necessitates the adjustment of such solution to near neutrality. Solutions so adjusted by alkaline agents, especially sodium bicarbonate have a tendency to lose their available iodine activity quite rapidly because of the shift of the hydrolysis equation to the right under increasingly alkaline conditions.
When aqueous solutions of iodine-polyvinyl pyrrolidone compositions are prepared and the pH adjusted to neutrality by the addition of sodium bicarbonate, the available iodine content decreases and the available iodide ion increases upon storage within a few weeks, thus posing a serious problem when shipping such solutions to hospitals and physicians. From the time the actual solution is made at the dispensing plant and the time at which it arrives in the hospital or physicians oflice, which may require several weeks, the solution loses potency in the available iodine content.
I have discovered that the tendency of the iodine-polyvinyl pyrrolidone composition to lose its available iodine content when prepared in aqueous solution. can be very readily overcome by blending 16 to 20 parts by weight of sodium bicarbonate per parts by weight of the iodine-polyvinyl pyrrolidone composition having an available iodine content from 8 to 15% and an available iodide ion content from 0.98 to 5.6% for a period of time ranging from 6 to 36 hours. The resulting product is stable and will readily dissolve in water to form essentially neutral solutions (having a pH range from 6.6 to 6.9). By this procedure, the iodine-polyvinyl pyrrolidone composition is made in a more available and readily useful form for injections and use on mucous tissue.
It is indeed wholly surprising and unexpected that the reaction indicated by the above equation has been found not to occur in the solid state when sodium bicarbonate is blended with the iodine-polyvinyl pyrrolidone composition even though moisture may be present either in the sodium bicarbonate or the iodine polyvinyl pyrrolidone composition, or both. More surprising is the fact that the solid mixture of iodine-polyvinyl pyrrolidone composition and sodium bicarbonate has the same stability as the dry iodine-polyvinyl pyrrolidone composition alone.
The following example will serve to illustrate how the stabilized iodinepolyvinyl pyrrolidone composition may be prepared in accordance with the present invention. It is to be understood, however, that this example is merely Example I To 100 parts of iodine-polyvinyl pyrrolidone composition (made by dry-blending 83.2 parts of polyvinyl pyrrolidone having a K value of 30 and 16.8 parts of iodine for 24 hours, followed by 24 hours of heating at 93 C.) there were added 10 parts of anhydrous sodium bicarbonate. The mixture was blended for 24 hours in a rotating glass vessel to insure uniformity. The product was made up as a 1% aqueous solution and had a pH of 6.7 to 6.9. In aging the dry product for six weeks at 100 F. no change in pH was observed, and no change in the available iodine and iodide ion content was noted.
For comparison a 1% aqueous solution of the iodinepolyvinyl pyrrolidone composition utilized above, i. e. prior to blending with sodium bicarbonate (having a pH of 2) and adjusted by the addition of anhydrous sodium bicarbonate to a pH of 6.6 to 6.7, the amount of bicarbonate added was not calculated, but made with vigorous stirring with the pH metered electrodes immersed in the solution. In aging this solution at 100 F. for six weeks, the pH increased from 6.6 to 7.4 and the available iodine content decreased from 11.84 to 11.3%, and the iodide content increased from 3.9 to 4.51%.
By blending sodium bicarbonate with the iodine-polyvinyl pyrrolidone composition, the resulting blend may be packaged as one stable unit and immediately utilized without further compounding. This expedient saves a considerable amount of money in packaging and shipping.
I claim:
The method of forming an aqueous iodine-polyvinylpyrrolidone composition which is stable with respect to a change in pH and loss in available iodine content, which comprises blending anhydrous sodium bicarbonate with dry iodine-polyvinyl-pyrrolidone composition until a uniform mixture is obtained, and dissolving the said mixture in water.
References Cited in the file of this patent UNITED STATES PATENTS OTHER REFERENCES Chemical Week, 69:25, Dec. 22, 1951, p. 19.
C and E N (Chem. and Eng. News), Feb. 19, 1951,
p. 664, New Iodine Compound.
Ridge et al.: Control of pH in Bleaching, Textile Manufacturer, July 1942, p. 282.
US457777A1952-04-151954-09-22Process of stabilizing polyvinyl pyrrolidone-iodine compositionsExpired - LifetimeUS2826532A (en)

Priority Applications (1)

Application NumberPriority DateFiling DateTitle
US457777AUS2826532A (en)1952-04-151954-09-22Process of stabilizing polyvinyl pyrrolidone-iodine compositions

Applications Claiming Priority (2)

Application NumberPriority DateFiling DateTitle
US282458AUS2706701A (en)1952-04-151952-04-15Process for the preparation of iodinepolyvinylpyrrolidone by dry mixing
US457777AUS2826532A (en)1952-04-151954-09-22Process of stabilizing polyvinyl pyrrolidone-iodine compositions

Publications (1)

Publication NumberPublication Date
US2826532Atrue US2826532A (en)1958-03-11

Family

ID=26961460

Family Applications (1)

Application NumberTitlePriority DateFiling Date
US457777AExpired - LifetimeUS2826532A (en)1952-04-151954-09-22Process of stabilizing polyvinyl pyrrolidone-iodine compositions

Country Status (1)

CountryLink
US (1)US2826532A (en)

Cited By (56)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3028300A (en)*1960-09-131962-04-03West Laboratories IncGermicidal compositions and methods for preparing the same
US3620773A (en)*1969-04-031971-11-16Robert P GabrielMethod for treating harvested nonchlorophylleous produce
US3898326A (en)*1973-05-141975-08-05West Laboratories IncPolyvinylpyrrolidone-iodide compositions and polyvinylpyrrolidone-iodide-iodine complexes prepared therefrom
US4094967A (en)*1976-10-221978-06-13Allor FoundationIodine-polyvinylpyrrolidone solid product and method of preparation
US4200710A (en)*1978-04-281980-04-29Basf AktiengesellschaftPreparation of polyvinylpyrrolidone-iodine
US4235884A (en)*1978-03-171980-11-25Nicolas SalkinMethod for the preparation of stable aqueous solutions of complexes of polyvinylpyrrolidone and of halogens and the solutions obtained thereby
US4320114A (en)*1975-09-101982-03-16Basf AktiengesellschaftManufacture of aqueous polyvinylpyrrolidone-iodine solutions
US4401651A (en)*1979-04-181983-08-30Knutson Richard AWound-healing compositions containing povidone-iodine
US4402937A (en)*1979-10-181983-09-06Basf AktiengesellschaftPreparation of PVP-iodine
US4408001A (en)*1981-04-061983-10-04The Dow Chemical CompanyDegeneration inhibited sanitizing complexes
US4481167A (en)*1980-04-111984-11-06The Dow Chemical CompanySanitizing complexes of polyoxazolines or polyoxazines and polyhalide anions
US4844898A (en)*1986-09-021989-07-04Kowa Co., Ltd.Wound-healing preparations
US5709851A (en)*1990-03-211998-01-20Euro-Celtique, S.A.Pharmaceutical iodine compositions with reduced irritancy
US5753699A (en)*1997-01-101998-05-19Medlogic Global CorporationMethods for treating non-suturable, superficial wounds by use of cyanoacrylate ester compositions comprising an antimicrobial agent
WO1999020107A1 (en)*1997-10-211999-04-29West Agro, Inc.Improved iodine antimicrobial compositions containing nonionic surfactants and halogen anions
US6090397A (en)*1997-11-032000-07-18Medlogic Global CorporationKits containing cyanoacrylate compositions comprising an antimicrobial agent
US6475502B1 (en)1997-11-032002-11-05Flowers Park Ltd.Kits containing cyanoacrylate compositions comprising an antimicrobial agent
US20040074847A1 (en)*2002-10-162004-04-22Jaquess Percy A.Stable N-bromo-2-pyrrolidone and methods to make the same
US6811771B1 (en)1999-04-272004-11-02Ebara CorporationBactericidal organic polymeric material
US20040230309A1 (en)*2003-02-142004-11-18Depuy Spine, Inc.In-situ formed intervertebral fusion device and method
US6852233B1 (en)1999-04-272005-02-08Ebara CorporationMetal-collecting apparatus and method for elution and recovery of metal from metal-collecting material
US20080172032A1 (en)*2007-01-112008-07-17James Pitzer GillsMethod for preventing tissue damage associated with irrigation of tissue with an antimicrobial solution
CN102093279A (en)*2011-01-072011-06-15上海宇昂化工科技发展有限公司High-stability nonionic N-vinyl butyrate lactam iodine and preparation method thereof
WO2012003326A1 (en)2010-07-022012-01-05Wright Medical Technology, Inc.Composition comprising calcium phosphate and sulfate powders and tri - calcium phosphate particles used in the treatment of degenerative bone conditions
WO2015089373A1 (en)2013-12-132015-06-18Wright Medical Technology, Inc.Multiphasic bone graft substitute material
US9320614B2 (en)2006-07-312016-04-26DePuy Synthes Products, Inc.Spinal fusion implant
US9801725B2 (en)2009-12-092017-10-31DePuy Synthes Products, Inc.Aspirating implants and method of bony regeneration
WO2019046844A1 (en)2017-09-022019-03-07Iview Therapeutics, Inc.In situ gel-forming pharmaceutical compositions and uses thereof for sinus diseases
US10238500B2 (en)2002-06-272019-03-26DePuy Synthes Products, Inc.Intervertebral disc
US10888433B2 (en)2016-12-142021-01-12DePuy Synthes Products, Inc.Intervertebral implant inserter and related methods
US10940016B2 (en)2017-07-052021-03-09Medos International SarlExpandable intervertebral fusion cage
US10966840B2 (en)2010-06-242021-04-06DePuy Synthes Products, Inc.Enhanced cage insertion assembly
US10973652B2 (en)2007-06-262021-04-13DePuy Synthes Products, Inc.Highly lordosed fusion cage
WO2021155165A1 (en)2020-01-312021-08-05Wright Medical Technology, Inc.Improved bone graft substitute formulation
US11273050B2 (en)2006-12-072022-03-15DePuy Synthes Products, Inc.Intervertebral implant
US11344424B2 (en)2017-06-142022-05-31Medos International SarlExpandable intervertebral implant and related methods
US11426286B2 (en)2020-03-062022-08-30Eit Emerging Implant Technologies GmbhExpandable intervertebral implant
US11426290B2 (en)2015-03-062022-08-30DePuy Synthes Products, Inc.Expandable intervertebral implant, system, kit and method
US11446155B2 (en)2017-05-082022-09-20Medos International SarlExpandable cage
US11446156B2 (en)2018-10-252022-09-20Medos International SarlExpandable intervertebral implant, inserter instrument, and related methods
US11452607B2 (en)2010-10-112022-09-27DePuy Synthes Products, Inc.Expandable interspinous process spacer implant
US11497619B2 (en)2013-03-072022-11-15DePuy Synthes Products, Inc.Intervertebral implant
US11510788B2 (en)2016-06-282022-11-29Eit Emerging Implant Technologies GmbhExpandable, angularly adjustable intervertebral cages
US11596522B2 (en)2016-06-282023-03-07Eit Emerging Implant Technologies GmbhExpandable and angularly adjustable intervertebral cages with articulating joint
US11602438B2 (en)2008-04-052023-03-14DePuy Synthes Products, Inc.Expandable intervertebral implant
US11607321B2 (en)2009-12-102023-03-21DePuy Synthes Products, Inc.Bellows-like expandable interbody fusion cage
US11612491B2 (en)2009-03-302023-03-28DePuy Synthes Products, Inc.Zero profile spinal fusion cage
US11612493B2 (en)2003-06-302023-03-28DePuy Synthes Products, Inc.Intervertebral implant with conformable endplate
US11654033B2 (en)2010-06-292023-05-23DePuy Synthes Products, Inc.Distractible intervertebral implant
US11737881B2 (en)2008-01-172023-08-29DePuy Synthes Products, Inc.Expandable intervertebral implant and associated method of manufacturing the same
US11752009B2 (en)2021-04-062023-09-12Medos International SarlExpandable intervertebral fusion cage
US11850160B2 (en)2021-03-262023-12-26Medos International SarlExpandable lordotic intervertebral fusion cage
US11911287B2 (en)2010-06-242024-02-27DePuy Synthes Products, Inc.Lateral spondylolisthesis reduction cage
USRE49973E1 (en)2013-02-282024-05-21DePuy Synthes Products, Inc.Expandable intervertebral implant, system, kit and method
US12090064B2 (en)2022-03-012024-09-17Medos International SarlStabilization members for expandable intervertebral implants, and related systems and methods
US12440346B2 (en)2023-03-312025-10-14DePuy Synthes Products, Inc.Expandable intervertebral implant

Citations (4)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US1557266A (en)*1922-12-271925-10-13Us Ind Alcohol CoComposition adapted to generate free iodine
US1841694A (en)*1930-05-161932-01-19Eimer & AmendTherapeutic iodine solution
US2386252A (en)*1942-02-211945-10-09Mendelsohn MajerAntiseptic composition
US2706701A (en)*1952-04-151955-04-19Gen Aniline & Film CorpProcess for the preparation of iodinepolyvinylpyrrolidone by dry mixing

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US1557266A (en)*1922-12-271925-10-13Us Ind Alcohol CoComposition adapted to generate free iodine
US1841694A (en)*1930-05-161932-01-19Eimer & AmendTherapeutic iodine solution
US2386252A (en)*1942-02-211945-10-09Mendelsohn MajerAntiseptic composition
US2706701A (en)*1952-04-151955-04-19Gen Aniline & Film CorpProcess for the preparation of iodinepolyvinylpyrrolidone by dry mixing

Cited By (116)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3028300A (en)*1960-09-131962-04-03West Laboratories IncGermicidal compositions and methods for preparing the same
US3620773A (en)*1969-04-031971-11-16Robert P GabrielMethod for treating harvested nonchlorophylleous produce
US3898326A (en)*1973-05-141975-08-05West Laboratories IncPolyvinylpyrrolidone-iodide compositions and polyvinylpyrrolidone-iodide-iodine complexes prepared therefrom
US4320114A (en)*1975-09-101982-03-16Basf AktiengesellschaftManufacture of aqueous polyvinylpyrrolidone-iodine solutions
US4094967A (en)*1976-10-221978-06-13Allor FoundationIodine-polyvinylpyrrolidone solid product and method of preparation
US4235884A (en)*1978-03-171980-11-25Nicolas SalkinMethod for the preparation of stable aqueous solutions of complexes of polyvinylpyrrolidone and of halogens and the solutions obtained thereby
US4200710A (en)*1978-04-281980-04-29Basf AktiengesellschaftPreparation of polyvinylpyrrolidone-iodine
US4401651A (en)*1979-04-181983-08-30Knutson Richard AWound-healing compositions containing povidone-iodine
US4402937A (en)*1979-10-181983-09-06Basf AktiengesellschaftPreparation of PVP-iodine
US4481167A (en)*1980-04-111984-11-06The Dow Chemical CompanySanitizing complexes of polyoxazolines or polyoxazines and polyhalide anions
US4408001A (en)*1981-04-061983-10-04The Dow Chemical CompanyDegeneration inhibited sanitizing complexes
US4844898A (en)*1986-09-021989-07-04Kowa Co., Ltd.Wound-healing preparations
US5709851A (en)*1990-03-211998-01-20Euro-Celtique, S.A.Pharmaceutical iodine compositions with reduced irritancy
US5753699A (en)*1997-01-101998-05-19Medlogic Global CorporationMethods for treating non-suturable, superficial wounds by use of cyanoacrylate ester compositions comprising an antimicrobial agent
WO1999020107A1 (en)*1997-10-211999-04-29West Agro, Inc.Improved iodine antimicrobial compositions containing nonionic surfactants and halogen anions
US5916581A (en)*1997-10-211999-06-29West Agro, Inc.Iodine antimicrobial compositions containing nonionic surfactants and halogen anions
US6090397A (en)*1997-11-032000-07-18Medlogic Global CorporationKits containing cyanoacrylate compositions comprising an antimicrobial agent
US6475502B1 (en)1997-11-032002-11-05Flowers Park Ltd.Kits containing cyanoacrylate compositions comprising an antimicrobial agent
US6811771B1 (en)1999-04-272004-11-02Ebara CorporationBactericidal organic polymeric material
US6852233B1 (en)1999-04-272005-02-08Ebara CorporationMetal-collecting apparatus and method for elution and recovery of metal from metal-collecting material
US10238500B2 (en)2002-06-272019-03-26DePuy Synthes Products, Inc.Intervertebral disc
US20040074847A1 (en)*2002-10-162004-04-22Jaquess Percy A.Stable N-bromo-2-pyrrolidone and methods to make the same
US11207187B2 (en)2003-02-142021-12-28DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9730803B2 (en)2003-02-142017-08-15DePuy Synthes Products, Inc.Method of in-situ formation of an intervertebral fusion device
US10376372B2 (en)2003-02-142019-08-13DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US11096794B2 (en)2003-02-142021-08-24DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10786361B2 (en)2003-02-142020-09-29DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10639164B2 (en)2003-02-142020-05-05DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US20040230309A1 (en)*2003-02-142004-11-18Depuy Spine, Inc.In-situ formed intervertebral fusion device and method
US9333091B2 (en)2003-02-142016-05-10DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10583013B2 (en)2003-02-142020-03-10DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9439777B2 (en)2003-02-142016-09-13DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9439776B2 (en)2003-02-142016-09-13DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10575959B2 (en)2003-02-142020-03-03DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9724207B2 (en)2003-02-142017-08-08DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US11432938B2 (en)2003-02-142022-09-06DePuy Synthes Products, Inc.In-situ intervertebral fusion device and method
US10555817B2 (en)2003-02-142020-02-11DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9788963B2 (en)2003-02-142017-10-17DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10492918B2 (en)2003-02-142019-12-03DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9801729B2 (en)2003-02-142017-10-31DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9808351B2 (en)2003-02-142017-11-07DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9814589B2 (en)2003-02-142017-11-14DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9814590B2 (en)2003-02-142017-11-14DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10433971B2 (en)2003-02-142019-10-08DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US9925060B2 (en)2003-02-142018-03-27DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10420651B2 (en)2003-02-142019-09-24DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10085843B2 (en)2003-02-142018-10-02DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US10405986B2 (en)2003-02-142019-09-10DePuy Synthes Products, Inc.In-situ formed intervertebral fusion device and method
US11612493B2 (en)2003-06-302023-03-28DePuy Synthes Products, Inc.Intervertebral implant with conformable endplate
US9320614B2 (en)2006-07-312016-04-26DePuy Synthes Products, Inc.Spinal fusion implant
US9737413B2 (en)2006-07-312017-08-22DePuy Synthes Products, Inc.Spinal fusion implant
US10695191B2 (en)2006-07-312020-06-30DePuy Synthes Products, Inc.Spinal fusion implant
US10010428B2 (en)2006-07-312018-07-03DePuy Synthes Products, Inc.Spinal fusion implant
US9387091B2 (en)2006-07-312016-07-12DePuy Synthes Products, Inc.Spinal fusion implant
US9713538B2 (en)2006-07-312017-07-25DePuy Synthes Products, Inc.Spinal fusion implant
US11273050B2 (en)2006-12-072022-03-15DePuy Synthes Products, Inc.Intervertebral implant
US11660206B2 (en)2006-12-072023-05-30DePuy Synthes Products, Inc.Intervertebral implant
US11642229B2 (en)2006-12-072023-05-09DePuy Synthes Products, Inc.Intervertebral implant
US11432942B2 (en)2006-12-072022-09-06DePuy Synthes Products, Inc.Intervertebral implant
US11497618B2 (en)2006-12-072022-11-15DePuy Synthes Products, Inc.Intervertebral implant
US11712345B2 (en)2006-12-072023-08-01DePuy Synthes Products, Inc.Intervertebral implant
US20080172032A1 (en)*2007-01-112008-07-17James Pitzer GillsMethod for preventing tissue damage associated with irrigation of tissue with an antimicrobial solution
US11622868B2 (en)2007-06-262023-04-11DePuy Synthes Products, Inc.Highly lordosed fusion cage
US10973652B2 (en)2007-06-262021-04-13DePuy Synthes Products, Inc.Highly lordosed fusion cage
US11737881B2 (en)2008-01-172023-08-29DePuy Synthes Products, Inc.Expandable intervertebral implant and associated method of manufacturing the same
US12011361B2 (en)2008-04-052024-06-18DePuy Synthes Products, Inc.Expandable intervertebral implant
US11602438B2 (en)2008-04-052023-03-14DePuy Synthes Products, Inc.Expandable intervertebral implant
US11712341B2 (en)2008-04-052023-08-01DePuy Synthes Products, Inc.Expandable intervertebral implant
US11712342B2 (en)2008-04-052023-08-01DePuy Synthes Products, Inc.Expandable intervertebral implant
US12023255B2 (en)2008-04-052024-07-02DePuy Synthes Products, Inc.Expandable inter vertebral implant
US11707359B2 (en)2008-04-052023-07-25DePuy Synthes Products, Inc.Expandable intervertebral implant
US11701234B2 (en)2008-04-052023-07-18DePuy Synthes Products, Inc.Expandable intervertebral implant
US11617655B2 (en)2008-04-052023-04-04DePuy Synthes Products, Inc.Expandable intervertebral implant
US11612491B2 (en)2009-03-302023-03-28DePuy Synthes Products, Inc.Zero profile spinal fusion cage
US12097124B2 (en)2009-03-302024-09-24DePuy Synthes Products, Inc.Zero profile spinal fusion cage
US10342662B2 (en)2009-12-092019-07-09DePuy Synthes Products, Inc.Aspirating implants and method of bony regeneration
US9801725B2 (en)2009-12-092017-10-31DePuy Synthes Products, Inc.Aspirating implants and method of bony regeneration
US11607321B2 (en)2009-12-102023-03-21DePuy Synthes Products, Inc.Bellows-like expandable interbody fusion cage
US10966840B2 (en)2010-06-242021-04-06DePuy Synthes Products, Inc.Enhanced cage insertion assembly
US11872139B2 (en)2010-06-242024-01-16DePuy Synthes Products, Inc.Enhanced cage insertion assembly
US11911287B2 (en)2010-06-242024-02-27DePuy Synthes Products, Inc.Lateral spondylolisthesis reduction cage
US12318304B2 (en)2010-06-242025-06-03DePuy Synthes Products, Inc.Lateral spondylolisthesis reduction cage
US11654033B2 (en)2010-06-292023-05-23DePuy Synthes Products, Inc.Distractible intervertebral implant
EP4186534A1 (en)2010-07-022023-05-31Agnovos Healthcare, LLCMethods of treating degenerative bone conditions
WO2012003326A1 (en)2010-07-022012-01-05Wright Medical Technology, Inc.Composition comprising calcium phosphate and sulfate powders and tri - calcium phosphate particles used in the treatment of degenerative bone conditions
EP2987507A1 (en)2010-07-022016-02-24Agnovos Healthcare, LLCMethods of treating degenerative bone conditions
US11452607B2 (en)2010-10-112022-09-27DePuy Synthes Products, Inc.Expandable interspinous process spacer implant
CN102093279B (en)*2011-01-072012-05-23上海宇昂化工科技发展有限公司High-stability nonionic N-vinyl butyrolactam iodine and related preparation method
CN102093279A (en)*2011-01-072011-06-15上海宇昂化工科技发展有限公司High-stability nonionic N-vinyl butyrate lactam iodine and preparation method thereof
USRE49973E1 (en)2013-02-282024-05-21DePuy Synthes Products, Inc.Expandable intervertebral implant, system, kit and method
US11497619B2 (en)2013-03-072022-11-15DePuy Synthes Products, Inc.Intervertebral implant
US11850164B2 (en)2013-03-072023-12-26DePuy Synthes Products, Inc.Intervertebral implant
EP3269399A1 (en)2013-12-132018-01-17Agnovos Healthcare, LLCMultiphasic bone graft substitute material
WO2015089373A1 (en)2013-12-132015-06-18Wright Medical Technology, Inc.Multiphasic bone graft substitute material
US11426290B2 (en)2015-03-062022-08-30DePuy Synthes Products, Inc.Expandable intervertebral implant, system, kit and method
US11596522B2 (en)2016-06-282023-03-07Eit Emerging Implant Technologies GmbhExpandable and angularly adjustable intervertebral cages with articulating joint
US12433757B2 (en)2016-06-282025-10-07Eit Emerging Implant Technologies GmbhExpandable, angularly adjustable and articulating intervertebral cages
US12390343B2 (en)2016-06-282025-08-19Eit Emerging Implant Technologies GmbhExpandable, angularly adjustable intervertebral cages
US11596523B2 (en)2016-06-282023-03-07Eit Emerging Implant Technologies GmbhExpandable and angularly adjustable articulating intervertebral cages
US11510788B2 (en)2016-06-282022-11-29Eit Emerging Implant Technologies GmbhExpandable, angularly adjustable intervertebral cages
US10888433B2 (en)2016-12-142021-01-12DePuy Synthes Products, Inc.Intervertebral implant inserter and related methods
US12427031B2 (en)2017-05-082025-09-30Medos International SarlExpandable cage
US11446155B2 (en)2017-05-082022-09-20Medos International SarlExpandable cage
US11344424B2 (en)2017-06-142022-05-31Medos International SarlExpandable intervertebral implant and related methods
US10940016B2 (en)2017-07-052021-03-09Medos International SarlExpandable intervertebral fusion cage
WO2019046844A1 (en)2017-09-022019-03-07Iview Therapeutics, Inc.In situ gel-forming pharmaceutical compositions and uses thereof for sinus diseases
US11446156B2 (en)2018-10-252022-09-20Medos International SarlExpandable intervertebral implant, inserter instrument, and related methods
EP4467169A2 (en)2020-01-312024-11-27Wright Medical Technology, Inc.Improved bone graft substitute formulation
WO2021155165A1 (en)2020-01-312021-08-05Wright Medical Technology, Inc.Improved bone graft substitute formulation
US11806245B2 (en)2020-03-062023-11-07Eit Emerging Implant Technologies GmbhExpandable intervertebral implant
US11426286B2 (en)2020-03-062022-08-30Eit Emerging Implant Technologies GmbhExpandable intervertebral implant
US11850160B2 (en)2021-03-262023-12-26Medos International SarlExpandable lordotic intervertebral fusion cage
US12023258B2 (en)2021-04-062024-07-02Medos International SarlExpandable intervertebral fusion cage
US11752009B2 (en)2021-04-062023-09-12Medos International SarlExpandable intervertebral fusion cage
US12090064B2 (en)2022-03-012024-09-17Medos International SarlStabilization members for expandable intervertebral implants, and related systems and methods
US12440346B2 (en)2023-03-312025-10-14DePuy Synthes Products, Inc.Expandable intervertebral implant

Similar Documents

PublicationPublication DateTitle
US2826532A (en)Process of stabilizing polyvinyl pyrrolidone-iodine compositions
US2706701A (en)Process for the preparation of iodinepolyvinylpyrrolidone by dry mixing
US2900305A (en)Preparation of iodine polyvinylpyrrolidone adducts
US4170637A (en)Frosting bleach composition
US4025609A (en)Process for preparing stable sodium percarbonate
EP0203526B1 (en)Compounds in melted block form containing alkaline hydroxide and active chlorine for machine dish-washing, and process for their preparation
US5885620A (en)Stable glycerin iodine concentrate compositions
EP1117299A1 (en)Stable glycerin iodine concentrate compositions
US3992197A (en)Silver crystals and production thereof
US3981713A (en)Urea-zinc oxide composition and process
JPH0788236B2 (en) Glass composition for adding synthetic resin
US2807591A (en)Water-soluble gums of improved water solubility and method of producing same
GB2276546A (en)Iodophor preparation
NO117848B (en)
US2184053A (en)Stable compositions useful in the compounding of photographic developers
US3087853A (en)Water soluble compositions consisting essentially of iodine and a water soluble oxygen containing polymer
US2897114A (en)Fungicidal composition
USRE35795E (en)Method of making flowable alkaline thiosulfate/alkaline sulfite and the product thereof
US2962416A (en)Stabilizing agents for bordeaux mixture
US2729672A (en)Non-hygroscopic choline salts
US3024161A (en)Stable, dry bordeaux mixture
US376445A (en)Adhesive paste
JPH0475017B2 (en)
US3000783A (en)Process of stabilizing solutions of chloroprocaine and the like
CN107601929B (en)High-folding-degree cement and preparation method thereof

[8]ページ先頭

©2009-2025 Movatter.jp