Process for measuring endotoxin and apparatus used therefor

• US 4,740,460 A
• Filed: 06/26/1985
• Issued: 04/26/1988
• Est. Priority Date: 06/27/1984
• Status: Expired due to Term

• Current Assignee: WAKO Pure Chemical Industries Limited (Fujifilm Holdings Corporation)
• Original Assignee: WAKO Pure Chemical Industries Limited (Fujifilm Holdings Corporation)
• Inventors: Oishi, Haruki, Shiraishi, Hiromi, Hatayama, Yasumichi, Sakata, Yoshitsugu, Yanagisawa, Kazuya
• Primary Examiner(s): NOT, DEFINED
• Application Number:
  US06/748,805
• Time in Patent Office: 1,035 Days
• Field of Search: 436/502, 436/517, 436/805, 422/73, 73/64.1, 435/18
• US Class Current: 435/18
• CPC Class Codes: G01N 21/83 Turbidimetric titration
• CPC Class Codes: G01N 2201/0407 with multiple optical units, e.g. one per sample
• CPC Class Codes: G01N 33/50 Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing measuring or testing processes involving enzymes or microorganisms, compositions or test papers therefor; processes for forming such compositions, condition responsive control in microbiological or enzymological processes C12Q
• CPC Class Codes: G01N 33/579 involving limulus lysate
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

Endotoxin contents in samples can be determined qualitatively, or quantitatively, singly or in parallel, with high precision in a short time by a process comprising applying a light to each sample solution, measuring an initial transmitted light amount I₀ and a transmitted light amount at a time t, I(t), to give a ratio R(t)=I(t)/I₀, and judging a gelation point by a threshold value of R(t), or further obtaining a gelation time from the gelation point. An apparatus used therefor is also disclosed.

Claims

1. A process for measuring an endotoxin which comprises

mixing a sample with an endotoxin gelating reagent to give one or more sample solutions,

applying a light to each sample solution,

measuring a transmitted light amount at an initial stage I₀ and that after a reaction time t, I(t), in each sample solution to give a ratio R(t)=I(t)/I₀, and

judging a gelation point by the ratio R(t) reaching a certain value in the range of 75 to 97%.

2. A process according to claim 1, wherein the initial value I₀ is a maximum initial value I₀.max, an average initial value I₀.av, a minimum initial value I₀.min, or an initial value at a special point of time "ts" I₀.ts.

3. A process according to claim 1, which further comprises

obtaining a gelation time T_G from a time required for reaching the gelation point from the mixing of the sample and the endotoxin gelating reagent, and

determining the endotoxin content in the sample.

4. A process according to claim 3, wherein two or more sample solutions are used in parallel.

5. A process according to claim 3, wherein the initial value I₀ is a maximum initial value I₀.max, an average initial value I₀.av, a minimum initial value I₀.min, or an initial value at a special point of time "ts", I₀.ts.

6. An apparatus for measuring an endotoxin comprising

one or more optical systems each comprising a light source, a sample solution-holding vessel, and a means for detecting transmitted light amounts,

a constant temperature bath for maintaining the optical systems at a constant temperature and keeping the vessel still,

a means for correcting the sensitivity of the optical systems and for judging a gelation point by the ratio R(t)=I(t)/I₀, wherein I₀ is a transmitted light amount at an initial stage and I(t) is a transmitted light amount after a reaction time t, reaching a certain value in the range of 75 to 97%,

a means for instructing the initiation of measurement of transmitted light amounts connected to the means for correction and judgment, and

a timer for measuring the time passed from the initiation of measurement of transmitted light amounts for each optical system in parallel and independently and connected to the means for correction and judgement.

7. An apparatus according to claim 6, wherein the sample solution-holding vessel is a cuvette having an inner diameter of 6 to 12 mm.

8. An apparatus according to claim 6, wherein the means for instructing the initiation of measurement is a switch which can give the instruction to two or more sample solution-holding vessels independently.

9. An apparatus according to claim 6, wherein the means for correcting the sensitivity of the optical systems and for judging a gelation point comprises one or more devices having functions of

(a) starting the timer by the initiation of measurement instructed by the means for instructing the initiation of measurement,

(b) beginning to measure transmitted light amounts,

(c) measuring transmitted light amounts with the lapse of time,

(d) conducting the correction of the sensitivity of each optical system,

(e) judging a gelation point, and

(f) stopping the timer at the time of judging the gelation.

10. An apparatus according to claim 6, wherein the means for correcting the sensitivity of the optical systems and for judging a gelation point has a means for transferring data of transmitted light amounts or data of measured time to one or more outer computers.

11. An apparatus according to claim 6, which further comprises at least one device connected to the means for correcting the sensitivity of the optical systems and for judging a gelation point and selected from the group consisting of a measuring state display, a gelation judgement display, a gelation time display and a measuring time display.

12. An apparatus according to claim 11, which further comprises a printer connected to the means for correcting the sensitivity of the optical systems and for judging a gelation point.

13. A process for measuring an endotoxin which comprises

mixing a sample with an endotoxin gelating reagent to give two or more sample solutions,

applying a light to each sample solution,

measuring a transmitted light amount at an initial stage I₀ and that after a reaction time t, I(t), in each sample solution to give a ratio R(t)=I(t)/I₀, and

judging a gelation point by the ratio R(t) reaching a certain value,

obtaining a gelation time T_G from a time required for reaching the gelation point from the mixing of the sample and the endotoxin gelating reagent, and

determining the endotoxin contents in the samples in parallel.

14. A process according to claim 13, wherein the certain value of R(t) for judging the gelation point is in the range of 75 to 97%.

15. A process according to claim 13, wherein the sample is a liquid sample in an amount of 0.1 ml and the endotoxin gelating reagent is a Limulus amoebocyte lysate reagent in an amount of 0.1 ml.

16. A process according to claim 13, wherein the sample is a liquid sample in an amount of 0.2 ml and the endotoxin gelating reagent is a freeze-dried Limulus amoebocyte lysate reagent.

17. A process according to claim 13, wherein the transmitted light amount at an initial stage I₀ is a maximum initial value I₀.max.

18. A process according to claim 13, wherein the transmitted light amount at an initial stage I₀ is an average initial value I₀.av.

19. A process according to claim 13, wherein the transmitted light amount at an initial stage I₀ is a minimum initial value I₀.min.

20. A process according to claim 13, wherein the transmitted light amount at an initial stage I₀ is an initial value at a special point of time "ts", I₀.ts.

21. An apparatus for measuring an endotoxin comprising

a plurality of optical systems each comprising a light source, a sample solution-holding vessel, and a means for detecting transmitted light amounts, and conducting the measurement of a plurality of samples in parallel,

a constant temperature bath for maintaining the optical systems at a constant temperature and keeping the vessel still,

a means for correcting the sensitivity of the optical systems and for judging a gelation point,

a means for instructing the initiation of measurement of transmitted light amounts connected to the means for correction and judgement, and

a timer for measuring the time passed from the initiation of measurement of transmitted light amounts for each optical system in parallel and independently and connected to the means for correction and judgment.