Optical sensor system for determining pH values and ionic strengths

• US 5,922,612 A
• Filed: 01/02/1997
• Issued: 07/13/1999
• Est. Priority Date: 05/02/1994
• Status: Expired due to Fees

• Current Assignee: Ciba-Geigy Corporation (Novartis Ag)
• Original Assignee: Novartis Corporation (Novartis Ag)
• Inventors: Barnard, Steven, Blom, Nils, Berger, Joseph, Rouilly, Marizel, Alder, Alex
• Primary Examiner(s): Lipman, Bernard
• Assistant Examiner(s): SAROFIM, NABIL F
• Application Number:
  US08/737,034
• Time in Patent Office: 922 Days
• Field of Search: 526/248, 526/320, 436/163, 436/172
• US Class Current: 436/163
• CPC Class Codes: C07D 311/78 Ring systems having three or more relevant rings
• CPC Class Codes: C07D 311/90 with hydrocarbon radicals, substituted by amino radicals, directly attached in position 9
• CPC Class Codes: C08F 220/54 Amides , e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
• CPC Class Codes: C08F 291/00 Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
• CPC Class Codes: C09D 4/06 Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
• CPC Class Codes: G01N 31/221 for investigating pH value

Abstract

A method for the independent, reversible, optical determination of the pH value and the ionic strength of an aqueous sample with the aid of two different sensors in accordance with the fluorescence method, in which method two optical sensors, which are each composed of polymers of different structure but each contain the same fluorescent dye and which each consist of a coated material composed of

a) a carrier material, to which there is applied

b) at least one water-insoluble layer of a polymer comprising at least one hydrophilic monomer (A) from the group of substituted olefins, and

c) a proton-sensitive fluorescent dye which is bonded directly or via a bridge group to the spine of polymer b) or which is incorporated in polymer b),

are brought into contact with an aqueous test sample, irradiated with exciting light, the fluorescence is measured and the pH values and the ionic strengths are calculated from the measured fluorescence intensities with reference to calibration curves.

Claims

1. A method for the independent, reversible, optical determination of pH value and ionic strength of an aqueous sample, in which the method comprises contacting a first optical sensor and a second optical sensor with the aqueous sample, irradiating the optical sensors with exciting light to generate fluorescence, measuring the fluorescence generated, and calculating the pH value and the ionic strength from the measured fluorescence with reference to a standard calibration curve wherein the two optical sensors comprise,

a) a carrier material, to which there is applied

b) at least one water-insoluble layer of a polymer comprising at least one hydrophilic, substituted olefin monomer (A), wherein the first and second optical sensors have different polymers in layer b, and

c) a proton-sensitive fluorescent dye which is bonded directly or via a bridge group to the spine of the polymer of layer b) or which is incorporated in the polymer of layer b).

2. A method according to claim 1 wherein the carrier material of the optical sensors is transparent and is a glass or transparent polymer.

3. A method according to claim 1 wherein the carrier material is planar.

4. A method according to claim 1 wherein the polymers in layer b) comprise at least 20 mol % of monomer (A), based on the polymer.

5. A method according to claim 1 wherein the hydrophilic monomer (A) is an olefinic monomer corresponding to formula XX

6. A method according to claim 5 wherein the hydrophobic substituents are selected from C₁ -C₁₂ alkyl, C₁ -C₁₂ alkoxy, C₁ -C₁₂ haloalkyl, phenyl, halophenyl, C₁ -C₄ alkylphenyl, C₁ -C₄ alkoxyphenyl, carboxylic acid ester groups having a total of from 2 to 20 carbon atoms, --CN, F and Cl.

7. A method according to claim 5 wherein the hophilic radicals are selected from --OH, --O--(C₂ -C₁₂ alkylene)--OH, --C(O)--NH₂, --C(O)--NH--(C₂ -C₁₂ alkylene)--OH, --C(O)--N--(C₂ -C₁₂ alkylene)₂ --OH, --C(O)--NH--C₁ -C₁₂ alkyl, --C(O)--N--(C₁ -C₁₂ alkyl)₂, pyrrolidonyl and --C(O)--O--(C₂ -C₁₂ alkylene)--OH.

8. A method according to claim 1 wherein the thickness of layer b) is from 0.01 to 50 μ

m.

9. A method according to claim 1 wherein the difference in the ionic strength dependency of the sensors is at least 0.1, measured as the pK_a displacement between the calibration curves in buffer solutions of 0.1M and 0.3M ionic strength.

10. A method according to claim 1 wherein the polymers in layer b) are cross-linked.

11. A method according to claim 1 wherein the polymers in layer b) comprise at least 20 mol % of monomer (A) and, accordingly, at most 80 mol % of a hydrophobic comonomer (B), based on the polymer.

12. A method according to claim 1 wherein polymer b) comprises from 20 to 100 mol % of at least one structural unit of formula III ##STR17## and from 80 to 0 mol % of at least one structural unit of formula IV ##STR18## wherein R_a is hydrogen, C₁ -C₆ alkyl or --COOR_g and

R_g is hydrogen, C₁ -C₆ alkyl, C₁ -C₆ hydroxyalkyl or an alkali metal cation, for example Na.sup.⊕

or K.sup.⊕

,

R_b is pyrrolidonyl, --OH, C₂ -C₆ hydroxyalkoxy, --CONR₇ R₈ or --COOR₉, R₇ and R₈ are each independently of the other hydrogen, C₁ -C₆ alkyl or C₂ -C₆ hydroxyalkyl and

R₉ is hydrogen or C₁ -C₆ hydroxyalkyl,

R_c is hydrogen or C₁ -C₆ alkyl,

R_d is hydrogen, C₁ -C₆ alkyl, F or Cl,

R_e is hydrogen or C₁ -C₆ alkyl, or

R_e and R_f together are --CO--O--CO--, and

R_f is hydrogen, C₁ -C₆ alkyl, --CN, F or Cl.

13. A method according to claim 12 wherein the layer is composed of polymers having 100 mol % of structural units of formula III wherein R_a is hydrogen, R_c is hydrogen or methyl and R_b is pyrrolidonyl, --CONR₇ R₈ or --COOR₉, R₇ and R₈ are each independently of the other hydrogen, C₁ -C₆ alkyl or C₂ -C₆ hydroxyalkyl and R₉ is hydrogen or C₂ -C₆ hydroxyalkyl.

14. A method according to claim 1 wherein the layer of polymers comprises from 20 to 80 mol % of at least one structural unit of formula IIIa ##STR19## and from 80 to 20 mol % of at least one structural unit of formula IIIb ##STR20## wherein R_g and R_i are each independently of the other hydrogen or methyl, preferably hydrogen;

R_h is di(C₁ -C₆ alkyl)amino, preferably di(C₁ -C₄ alkyl)amino, and especially dimethylamino or diethylamino; and

R_j is amino, preferably mono(C₁ -C₆ alkyl)amino and especially mono(C₁ -C₆ alkyl)amino, for example tert-butylamino.

15. A method according to claim 1 wherein the hydrophilic polymers of layer b) are polymers comprising a polymerisate of at least one hydrophilic monomer (A) from the group of substituted olefins in which there is homogeneously distributed at least one carrier polymer comprising at least one hydrophilic monomer (A) from the group of substituted olefins that is identical to or different from the former.

16. A method according to claim 15 wherein the polymerisate is cross-linked and the carrier polymer is embedded in the polymer network.

17. A method according to claim 15 wherein the hydrophilic carrier polymer is a homo- or co-polymer of vinylpyrrolidone;

of a hydroxyalkyl acrylate or methacrylate;

of vinyl alcohol;

of a vinylhydroxyalkyl ether;

of an acrylamide or methacrylamide;

or of a hydroxyalkyl acrylamide or methacrylamide.

18. A method according to claim 15 wherein the carrier polymer is composed of monomer (A), and monomer (A) is simultaneously used together with that carrier polymer for the preparation of the membrane.

19. A method according to claim 15 wherein the hydrophilic carrier polymer is polyvinylpyrrolidone, a poly(C₂ -C₆ hydroxyalkyl) acrylate or methacrylate, for example polyhydroxyethyl methacrylate, polyhydroxypropyl methacrylate, polyhydroxybutyl methacrylate, polyhydroxyhexyl methacrylate, polyhydroxyethyl acrylate, polyhydroxypropyl acrylate, polyhydroxybutyl acrylate or polyhydroxyhexyl acrylate, a polyacrylamide or polymethacrylamide, mono(C₁ -C₆ alkyl)polyacrylamide or mono(C₁ -C₆ alkyl)polymethacrylamide, di(C₁ -C₆ alkyl)polyacrylamide or di(C₁ -C₆ alkyl)polymethacrylamide.

20. A method according to claim 15 wherein the polymer of layer b) comprises at least one monomer (A) from the group:

vinylpyrrolidone, 2-hydroxyethyl methacrylate, 3-hydroxypropyl methacrylate, 4-hydroxybutyl acrylate, 5-hydroxypentyl acrylate, 6-hydroxyhexyl acrylate, acrylamide, N,N-dimethylacrylamide and tert-butylacrylamide, or a polymer obtainable by polymerisation in solution of a monomer (A) from the group;

vinylpyrrolidone, 2-hydroxyethyl methacrylate, 3-hydroxypropyl methacrylate, 4-hydroxybutyl acrylate, 5-hydroxypentyl acrylate, 6hydroxyhexyl acrylate and acrylamide, in the presence of a carrier polymer of a monomer (A) from the group consisting of vinylpyrrolidone, 2-hydroxyethyl methacrylate, 3-hydroxypropyl methacrylate, 4-hydroxybutyl acrylate and acrylamide.

21. A method according to claim 15 wherein the mixture ratio between monomer A and carrier polymer is from 5 to 95% by weight of carrier polymer, and from 95 to 5% by weight of monomer A, based on the total mixture of monomer and carrier polymer.

22. A method according to claim 1 wherein the polymers of layer b) are cross-linked with from 0.01 to 50 mol % of a cross-linking agent, based on the polymer.

23. A method according to claim 22 wherein the cross-linking agent is an acrylic or methacrylic acid ester or amide of a polyol or polyamine.

24. A method according to claim 1 wherein the fluorescent dye is present in an amount of from 0.01 to 10% by weight, based on the polymer.

25. A method according to claim 1 wherein the proton-sensitive fluorescent dye is selected from the group fluorescein, xanthenes and benzoxanthenes;

acridines;

acridones;

pyrenes and coumarins, which are optionally covalently bonded directly or via a bridge group to the polymer.

26. A method according to claim 1 wherein the bridge group of the fluorescent dye is the group --(CO)_s --NH--(C₂ -C₁₂ alkylene-O)_r --CO-- or --(CO)_s --O--(C₂ -Cl₂ alkylene-O)_r --CO-- or --C(O)--NH--(CH₂ CH₂ --O)₁ bis 6 --CH₂ C(O)--NH--, with the (CO)_s group or the NH group being bonded to the fluorescent dye and r and s each being 0 or 1.

27. A method according to claim 1 wherein the fluorescent dye is a dye of formula I, II or IIa ##STR21## wherein R₁ and R₂ are each independently of the other hydrogen, C₁ -C₄ alkyl, C₁ -C₄ alkoxy, C₁ -C₄ alkoxycarbonyl, C₁ -C₄ -alkyl-SO₂ or halogen, and either R₃ is hydrogen and R₄ is --NH--CO--, --CO--NH--(C₂ -C₁₂ alkylene-O)--CO--, --CO--NH--(C₂ -C₁₂ alkylene-NH)--CO-- or --C(O)--NH--(CH₂ CH₂ --O)₁ bis 6 --CH₂ C(O)--NH--, or R₃ is --NH--CO--, --CO--NH--(C₂ -C₁₂ alkylene-O)--CO--, --CO--NH--(C₂ -C₁₂ alkylene-NH)--CO-- or --C(O)--NH--(CH₂ CH₂ --O)₁ bis 6 --CH₂ C(O)--NH-- and R₄ is hydrogen;

or

wherein either R₅ is hydrogen and R₆ is --NH--C(O)--, --CO--NH--(C₂ -C₁₂ alkylene-O)--CO--, --CO--NH--(C₂ -C₁₂ alkylene-NH)--CO-- or --C(O)--NH--(CH₂ CH₂ --O)₁ bis 6 --CH₂ C(O)--NH--, or R₅ is --NH--C(O)--, --CO--NH--(C₂ -C₁₂ alkylene-O)--CO--, --CO--NH--(C₂ -C₁₂ alkylene-NH)--CO-- or --C(O)--NH--(CH₂ CH₂ --O)₁ bis 6 --CH₂ C(O)--NH--, and R₆ is hydrogen, in each case in free form or in salt form, or a C₁ -C₂₀ alkyl ester thereof.