Product information

Diagnostic reagents

Additives for diagnostic reagents

NOF is developing Biolipidure® series and LIPIDURE®-SF series as additives for in vitro diagnostics.

Function of LIPIDURE®

As additives for diagnostics, Biolipidure® has multiple functions such as suppression of non-specific adsorption of protein, stabilization of protein, and sensitization, all of which are required for developing diagnostic reagents.

Basic function of Biolipidure®

The table below shows basic functions of Biolipidure® as additives for diagnostic reagents.
The Biolipidure® series has great variety of polymers having different physical properties, which is derived from rich variation of secondary monomers copolymerized with MPC.

Biolipidure® Side chain property Blocking effect Stabilizing effect Sensitizing effect Improvement of reproducibility and accuracy Solubilizing effect
100 series Hydrophilic    
200 series Hydrophobic
400 series Anion      
500 series Cation        
700 series Hydrogen bond        
800 series Hydrophilic
Hydrophobic
 
1000 series Hydrophobic
1200 series Hydrophobic  
1300 series Hydrophobic  

◎ : Best
○ : Good

Index

Products
-[Polymer type] Biolipidure® series
-[Zwitterionic surfactant type] LIPIDURE®-SF08
Basic properties of LIPIDURE®
-Blocking effect
-Protein-stabilization effect
-Sensitizing effect
Application of Biolipidure®
-Latex agglutination
-Immunochromatography
-ELISA / CLEIA

Products

[Polymer type] Biolipidure® series

Product nameCharacteristicsForm
Biolipidure®-103Hydrophilic side chain5 wt% aqueous solution
Biolipidure®-203Hydrophobic side chain5 wt% aqueous solution
Biolipidure®-206Hydrophobic side chain5 wt% aqueous solution
Biolipidure®-405Anionic side chain5 wt% aqueous solution
Biolipidure®-502Cationic side chain5 wt% aqueous solution
Biolipidure®-702Hydrogen bonding side chain5 wt% aqueous solution
Biolipidure®-802Hydrophobic/hydrogen bonding side chain5 wt% aqueous solution
Biolipidure®-1002Hydrophobic side chain5 wt% aqueous solution
Biolipidure®-1201Hydrophobic side chain5 wt% aqueous solution
Biolipidure®-1301Hydrophobic side chain5 wt% aqueous solution

[Zwitterionic surfactant type] LIPIDURE®-SF08

The LIPIDURE®-SF08 is a low molecule additive for diagnostic reagents.

Product nameCMC [wt%]Form
LIPIDURE®-SF080.15 wt% aqueous solution

Basic performance of Biolipidure®

Blocking effect

Biolipidure® suppresses non-specific adsorption of biomolecule. NOF provides a set of products that can coat the surface of plastic, metal or other various materials.
Biolipidure® consists of wholly synthesized polymers, so it is free from biohazardous risk and has little lot-to-lot variation, making Biolipidure® the best blocking agent for diagnostic reagents.

Example 1: Blocking microplates

After a microplate was treated with Biolipidure®, the amount of non-specific adsorption of enzyme-labeled antibody was measured. The amount of non-specific adsorption of enzyme-labeled antibody was significantly reduced, proving that Biolipidure® provides excellent blocking effect.

[Test procedure]

  1. 200 µL of LIPIDURE® (diluted 10-fold by PBS) was applied to a 96-well plate.
  2. The plate was aspirated and dried overnight.
  3. 100 µL of 24,000-fold diluted HRP-IgG was added.
  4. After 1 hr incubation at a room temperature, the plate was washed with PBS-T.
  5. TMB colorimetric substrate (KPL) was applied and the non-specific adsorption of HRP-IgG was measured.

Example 2: Blocking magnetic beads

After magnetic beads was treated with Biolipidure®, the amount of non-specific adsorption of enzyme-labeled antibody was measured.
The amount of non-specific adsorption of enzyme-labeled antibody was significantly reduced, showing that Biolipidure® provides excellent blocking effect.

RLU: Relative Light Unit

[Test procedure]

  1. 170µg/mL of magnetic beads suspension was added to the same amount of Biolipidure® diluted 5-fold by TBS.
  2. After 1 hr of incubation at a room temperature, the beads was washed with TBS.
  3. 10 ng of AP-IgG was added.
  4. After 1 hr of incubation at a room temperature, the beads was washed with TBS–T.
  5. Chemiluminescent substrate was applied and non-specific adsorption of AP-IgG was measured.

Example 3: Blocking magnetic beads (Antibody solution)

The same protein-blocking effect was also achieved when Biolipidure® was added to an antibody solution. Biolipidure® was added to a diluted solution of enzyme-labeled antibody, and the amount of non-specific adsorption to magnetic beads was measured.
The amount of non-specific adsorption of enzyme-labeled antibody was significantly reduced, proving that LIPIDURE® provides excellent blocking effect.
* Biolipidure® does not affect antibody titer.

RLU: Relative Light Unit

[Test procedure]

  1. 0.1 times volume of Biolipidure® added to 100 ng/mL of AP-IgG solution.
  2. 100 µL of the AP-IgG solution containing Biolipidure® was added to 8.6 µg of magnetic beads.
  3. After 1 hr of incubation at a room temperature, the beads was washed with TBS-T.
  4. Chemiluminescent substrate was applied and non-specific adsorption of AP-IgG was measured.

Protein-stabilization effect

Biolipidure® stabilizes proteins, probably because the interaction between Biolipidure® and proteins maintains the native state structure of the proteins.

Example 1: Stabilization of antibodies (Solid phase)

The stability of immobilized capture antibody was improved by treating the surface od the microplate by Biolipidure®. This treatment also reduces the non-specific adsorption of proteins applied subsequently.
After the capture-antibody-immobilized microplate was coated with Biolipidure® and stored at 25°C, the residual antibody titer was measured using ELISA (sandwich method).
By using Biolipidure®, the stability of antibody was improved, that is, alsmost 100% of antibody titer was maintained for more than 15 days.

Relative activity: Measured using activity of Day 0 as 100%.

[Test procedure]

  1. Anti-mouse IgG antibody (capture antibody) was immobilized on a microplate.
  2. After 1 hr of incubation at a room temperature, the plate was washed with PBS.
  3. 200 µL of LIPIDURE® diluted 10-fold by PBS was added.
  4. After 1 hr of incubation at a room temperature, the plate was washed with PBS.
  5. The microplate was stored at 25°C in desiccator.
  6. Mouse IgG (antigen) was added.
  7. After 1 hr of incubation at a room temperature, the plate was washed with PBS-T.
  8. HRP labeled anti-mouse IgG antibody was added.
  9. After 1 hr of incubation at a room temperature, the plate was washed with PBS-T.
  10. Colorimetric substrate (TMB) was added and the antibody titer of the capture antibody was measured.

Example 2: Stabilization of antibodies (Liquid phase)

LIPIDURE®-SF provides stabilization effect when added to a diluted solution of enzyme-labeled antibody.
LIPIDURE®-SF was added to a diluted solution of enzyme-labeled antibody and residual enzyme activity was measured after storage at 4°C.
By adding LIPIDURE®-SF, the stability of enzyme-labeled antibody was markedly improved and 100% of enzyme activity was maintained for 60 days.
* LIPIDURE®-SF does not affect antibody titer.

Relative activity: Measured using activity of Day 0 as 100%.

[Test procedure]

  1. 0.02 times volume of LIPIDURE®-SF08 was added to 10,000-fold diluted solution of enzyme-labeled antibody.
  2. The solution was stored at 4°C.
  3. The residual activity of labelled enzyme was measured with colorimetric substrate (TMB).

Sensitizing effect

BIOLIPIDURE® exhibits sensitizing effect in immunoassay systems such as latex agglutination or immunochromatography, most likely caused by the improved dispersion of latex particle or gold colloid.

Example 1: Sensitizing effect of Biolipidure® in latex agglutination test

Biolipidure® provides excellent sensitizing effect in latex agglutination test.

[Test procedure]

CRP: C-reactive protein)
(Detection was performed using an automated analyzer.)

Example 2: Sensitizing effect of Biolipidure® in lateral flow test (immunochromatography)

Biolipidure® provides excellent sensitizing effect in lateral flow test (immunochromatography).

[Test procedure]

(hCG: human chorionic gonadotropin)
(The immunochromatography kit is manufactured in our laboratory.)

Application examples using Biolipidure®

Latex agglutination test

Biolipidure® provides excellent sensitizing effect in latex agglutination test.

[Test procedure]

(CRP: C-reactive protein)
(Detection was performed using an automated analyzer.)

Lateral flow test (Immunochromatography)

Biolipidure®, especially Biolipidure-40X, provides improved sensitizing effect in lateral flow test (immunochromatography).

Dengue virus kit

[Test procedure]

Adenovirus kit

[Test procedure]

ELISA / CLEIA

Biolipidure® provides sensitizing effect in sandwich type Chemiluminescent Enzyme Immunoassay (CLEIA).

[Test procedure]

  1. Mouse anti-Human IgG antibody was immobilized on a microplate.
  2. After 1 hr of incubation at a room temperature, the plate was washed with TBS.
  3. Biolipidure® solution (0.1 times volume) was added.
  4. The plate was incubated for 1 hr at a room temperature.
  5. Human IgG (antigen) standard was added.
  6. After 1 hr of incubation at a room temperature, the plate was washed with TBS-T.
  7. AP labeled anti-Human IgG antibody was added.
  8. After 1 hr of incubation at a room temperature, the plate was washed with TBS-T.
  9. Chemiluminescent substrate was added and calibration curve for Human IgG concentration was prepared.

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