CA1140051A - Emploi comme agents fonctionnels de conservation de complexes d'acide borique - Google Patents

Emploi comme agents fonctionnels de conservation de complexes d'acide borique

Info

Publication number: CA1140051A
Authority: CA; Canada
Prior art keywords: boric acid; complex; urine; samples; bacteria
Prior art date: 1978-02-24
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

Application number

CA000321844A

Other languages

English (en)

Inventor

Tore L.I. Carolusson

Gerhard O. Hentschel

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.)

OPUS CHEMICAL AB

Original Assignee

OPUS CHEMICAL AB

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.)

1978-02-24

Filing date

1979-02-16

Publication date

1983-01-25

1979-02-16 Application filed by OPUS CHEMICAL AB filed Critical OPUS CHEMICAL AB

1983-01-25 Application granted granted Critical

1983-01-25 Publication of CA1140051A publication Critical patent/CA1140051A/fr

Status Expired legal-status Critical Current

Links

KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 title claims abstract description 95
238000004321 preservation Methods 0.000 title claims description 14
239000003795 chemical substances by application Substances 0.000 title description 7
239000004327 boric acid Substances 0.000 claims abstract description 85
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 54
238000000034 method Methods 0.000 claims abstract description 36
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
239000007795 chemical reaction product Substances 0.000 claims abstract description 17
239000000203 mixture Substances 0.000 claims abstract description 16
-1 polyoxy Polymers 0.000 claims abstract description 10
239000005715 Fructose Substances 0.000 claims abstract description 9
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims abstract description 9
229930091371 Fructose Natural products 0.000 claims abstract description 9
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims abstract description 8
229930195725 Mannitol Natural products 0.000 claims abstract description 8
239000000594 mannitol Substances 0.000 claims abstract description 8
235000010355 mannitol Nutrition 0.000 claims abstract description 8
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims abstract description 7
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims abstract description 7
239000000600 sorbitol Substances 0.000 claims abstract description 7
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims abstract description 4
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 4
235000013772 propylene glycol Nutrition 0.000 claims abstract description 4
230000000087 stabilizing effect Effects 0.000 claims abstract description 4
239000003381 stabilizer Substances 0.000 claims abstract 2
210000002700 urine Anatomy 0.000 claims description 58
239000000654 additive Substances 0.000 claims description 15
RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 claims description 12
229960000907 methylthioninium chloride Drugs 0.000 claims description 12
238000006243 chemical reaction Methods 0.000 claims description 11
230000000996 additive effect Effects 0.000 claims description 7
238000004040 coloring Methods 0.000 claims 3
239000000126 substance Substances 0.000 claims 2
241000894006 Bacteria Species 0.000 abstract description 42
150000001875 compounds Chemical class 0.000 abstract description 17
238000002360 preparation method Methods 0.000 abstract description 2
229960002645 boric acid Drugs 0.000 description 65
235000010338 boric acid Nutrition 0.000 description 65
238000012360 testing method Methods 0.000 description 23
239000000523 sample Substances 0.000 description 14
239000000243 solution Substances 0.000 description 14
230000032258 transport Effects 0.000 description 13
230000000721 bacterilogical effect Effects 0.000 description 9
239000000047 product Substances 0.000 description 9
238000005057 refrigeration Methods 0.000 description 9
239000003755 preservative agent Substances 0.000 description 8
230000002335 preservative effect Effects 0.000 description 7
241000588748 Klebsiella Species 0.000 description 6
239000002253 acid Substances 0.000 description 6
241000588769 Proteus <enterobacteria> Species 0.000 description 5
PEEKVIHQOHJITP-UHFFFAOYSA-N boric acid;propane-1,2,3-triol Chemical compound OB(O)O.OCC(O)CO PEEKVIHQOHJITP-UHFFFAOYSA-N 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000000843 powder Substances 0.000 description 5
241000589516 Pseudomonas Species 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
239000003086 colorant Substances 0.000 description 4
229940093476 ethylene glycol Drugs 0.000 description 4
238000011002 quantification Methods 0.000 description 4
238000005070 sampling Methods 0.000 description 4
230000006641 stabilisation Effects 0.000 description 4
238000011105 stabilization Methods 0.000 description 4
229920001817 Agar Polymers 0.000 description 3
241000588724 Escherichia coli Species 0.000 description 3
239000008272 agar Substances 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000000376 reactant Substances 0.000 description 3
241000790917 Dioxys <bee> Species 0.000 description 2
241000219470 Mirabilis Species 0.000 description 2
241000589517 Pseudomonas aeruginosa Species 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
238000013100 final test Methods 0.000 description 2
230000008014 freezing Effects 0.000 description 2
238000007710 freezing Methods 0.000 description 2
208000015181 infectious disease Diseases 0.000 description 2
238000009533 lab test Methods 0.000 description 2
238000005259 measurement Methods 0.000 description 2
238000011160 research Methods 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
244000293889 Bombax malabaricum Species 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
241000375722 Cyperus eriocauloides Species 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
208000012868 Overgrowth Diseases 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
241000191963 Staphylococcus epidermidis Species 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
238000005576 amination reaction Methods 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
239000006161 blood agar Substances 0.000 description 1
125000005619 boric acid group Chemical group 0.000 description 1
RERVRRLGFUNERS-UHFFFAOYSA-N boron;propane-1,2,3-triol Chemical compound [B].OCC(O)CO RERVRRLGFUNERS-UHFFFAOYSA-N 0.000 description 1
208000037516 chromosome inversion disease Diseases 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
230000000875 corresponding effect Effects 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
230000000881 depressing effect Effects 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
239000002609 medium Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
235000020200 pasteurised milk Nutrition 0.000 description 1
239000013610 patient sample Substances 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000008279 sol Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000004448 titration Methods 0.000 description 1
208000019206 urinary tract infection Diseases 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Investigating Or Analysing Biological Materials (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Chemical And Physical Treatments For Wood And The Like (AREA)
Ceramic Products (AREA)
Amplifiers (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CA000321844A 1978-02-24 1979-02-16 Emploi comme agents fonctionnels de conservation de complexes d'acide borique Expired CA1140051A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
SE7802147A SE419346B (sv)	1978-02-24	1978-02-24	Forfarande for stabilisering av bakteriologiska prover
SE7802147-4		1978-02-24

Publications (1)

Publication Number	Publication Date
CA1140051A true CA1140051A (fr)	1983-01-25

Family

ID=20334100

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000321844A Expired CA1140051A (fr)	1978-02-24	1979-02-16	Emploi comme agents fonctionnels de conservation de complexes d'acide borique

Country Status (7)

Country	Link
CA (1)	CA1140051A (fr)
DE (1)	DE2906730C2 (fr)
DK (1)	DK80479A (fr)
FI (1)	FI63595C (fr)
GB (1)	GB2016446B (fr)
NO (1)	NO147054C (fr)
SE (1)	SE419346B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8800502D0 (en) *	1988-01-11	1988-02-10	Cerestar Holding Bv	Method of adding borax/boric acid to mixing/reaction-zone
US5505953A (en)	1992-05-06	1996-04-09	Alcon Laboratories, Inc.	Use of borate-polyol complexes in ophthalmic compositions
FR2731008B1 (fr) *	1995-02-24	1999-05-07	Dev Activites Chimiques Distri	Solution aqueuse boree, notamment pour l'adjuvantation de colle amylacee
WO2008131499A1 (fr) *	2007-04-26	2008-11-06	Realco Sa	Procédé de traitement de la cercosporiose du bananier et composition de traitement
US9102700B1 (en)	2014-08-29	2015-08-11	Vdf Futureceuticals, Inc.	Compositions and methods for borocarbohydrate complexes

1978
- 1978-02-24 SE SE7802147A patent/SE419346B/sv unknown
1979
- 1979-02-16 NO NO790518A patent/NO147054C/no unknown
- 1979-02-16 CA CA000321844A patent/CA1140051A/fr not_active Expired
- 1979-02-19 FI FI790541A patent/FI63595C/fi not_active IP Right Cessation
- 1979-02-21 DE DE2906730A patent/DE2906730C2/de not_active Expired
- 1979-02-21 GB GB7906062A patent/GB2016446B/en not_active Expired
- 1979-02-23 DK DK80479A patent/DK80479A/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
DE2906730C2 (de)	1982-04-22
FI790541A7 (fi)	1979-08-25
DK80479A (da)	1979-08-25
FI63595C (fi)	1983-07-11
FI63595B (fi)	1983-03-31
DE2906730A1 (de)	1979-09-06
GB2016446B (en)	1982-12-01
NO790518L (no)	1979-08-27
NO147054C (no)	1983-01-26
SE7802147L (sv)	1979-08-25
GB2016446A (en)	1979-09-26
SE419346B (sv)	1981-07-27
NO147054B (no)	1982-10-18

Legal Events

Date	Code	Title	Description
2000-01-25	MKEX	Expiry

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US4423043A (en)	1983-12-27	Aqueous liquid formulations for control of bacterial and protozoal diseases
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US2545431A (en)	1951-03-13	Method of killing weeds and the materials used therein
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FI63595C (fi)	1983-07-11	Foerfarande foer stabilisering av bakteriologiska prover i synnerhet urinprover
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