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Biotech: Calcium Reagents-biochemistry
Principle of Measurement
1. Arsenazo III Method (Most widely used in modern analyzers)
How it works:
-
Calcium ions react with Arsenazo III dye to form a blue-purple complex.
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The intensity of the color is measured photometrically at 650–660 nm.
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Highly specific for calcium with minimal interference from magnesium.
Advantages:
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Excellent stability
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Strong absorbance
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High specificity and precision
2. o-Cresolphthalein Complexone (OCPC) Method
How it works:
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Calcium forms a purple-red complex with o-cresolphthalein complexone in alkaline conditions.
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Read photometrically at 570–580 nm.
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Common in semi-auto chemistry analyzers.
Advantages:
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Reliable and widely established
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Suitable for manual and automated systems
Reagent Components
Arsenazo III Reagents May Contain:
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Arsenazo III dye
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Buffer (MES or other suitable buffers)
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Stabilizers
-
Surfactants
-
Preservatives
OCPC Reagents May Contain:
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o-Cresolphthalein complexone
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Alkaline buffer (e.g., 8-hydroxyquinoline to remove magnesium interference)
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Dye stabilizer
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Surfactants
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Preservatives
Packaging Format
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Single liquid reagent (most common)
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Two-reagent system (R1 + R2)
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Ready-to-use liquid stable bottles
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Analyzer-specific reagent cartridges
Common volumes: 25 ml, 50 ml, 100 ml, 250 ml or more.
Sample Types
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Serum
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Plasma (heparinized samples preferred)
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Urine (dilution may be needed)
Biotech: Chloride Reagents-biochemistry
Measurement Methods & Reagents
1. Ion-Selective Electrode (ISE) Method (Most common in modern analyzers)
Reagents include:
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Reference (internal standard) solution
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Electrode electrolyte solution
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Conditioning solution
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Cleaning solution
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Calibrators (Low and High Chloride)
Principle:
A chloride-selective membrane develops an electrical potential proportional to chloride concentration.
ISE systems require stable calibration solutions and maintenance reagents.
2. Mercuric Thiocyanate Colorimetric Method
How it works:
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Chloride reacts with mercuric ions, forming mercuric chloride.
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Released thiocyanate ions form a red-colored complex with ferric ions.
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The color intensity is measured photometrically at 480–520 nm.
Reagents contain:
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Mercuric thiocyanate
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Ferric nitrate or ferric ammonium sulfate
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Buffer system
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Surfactants and stabilizers
Advantages:
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Reliable for automated chemistry analyzers
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High precision
3. Colorimetric TPTZ Method (Less common)
Chloride displaces iron from a complex; the released iron reacts with TPTZ dye to form a measurable color.
Packaging Formats
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Single-liquid reagent
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Two-reagent kits (R1 buffer + R2 color reagent)
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ISE-specific reagent packs
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Ready-to-use liquid stable formulations
Typical volumes: 25 ml, 50 ml, 100 ml, 250 ml.
Biotech: Creatinine Reagents
1. Jaffe Method (Most Common)
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Based on the reaction between creatinine and picric acid in an alkaline medium.
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Produces an orange-red complex.
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Absorbance is measured photometrically, usually at 505–520 nm.
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Some kits include compensated Jaffe formulations to reduce interference from glucose, ketones, and proteins.
2. Enzymatic Method
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Uses a sequence of enzyme reactions (creatininase, creatinase, sarcosine oxidase, peroxidase).
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Produces a colored dye measurable at 550–570 nm.
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Higher specificity than Jaffe, minimal interference.
Reagent Components
Depending on the method, creatinine reagent kits may include:
For Jaffe Method
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Alkaline buffer
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Picric acid
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Stabilizers
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Surfactants
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Preservatives
For Enzymatic Method
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Enzyme mixture (creatininase, creatinase, sarcosine oxidase)
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Chromogenic dye reagents
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Phosphate or Good’s buffer
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Activators
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Preservatives
Packaging Format
Most creatinine reagent kits are provided as:
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Two-reagent system (R1 buffer + R2 working reagent)
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Ready-to-use liquid formulations
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Optional standards or calibrators
Common sizes: 25 ml, 50 ml, 100 ml, 250 ml, or analyzer-specific cartridges.
Sample Type
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Serum
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Plasma (heparin, EDTA)
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Urine (often diluted before analysis)
Biotech: GGT / Gamma GT Reagent-biochemistry
Principle of the Test
Most GGT reagents use the Szasz kinetic method, which involves:
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Substrate:
γ-glutamyl-p-nitroanilide
This compound contains a gamma-glutamyl group. -
Enzymatic Reaction:
GGT in the sample transfers the gamma-glutamyl group to an acceptor (often glycylglycine). -
Product Formation:
The reaction releases p-nitroaniline, which has a strong yellow color. -
Measurement:
The analyzer measures the increase in absorbance at 405 nm.
The rate of color formation is directly proportional to the GGT activity.
Key Reagent Components
The GGT reagent typically contains:
✔ γ-glutamyl-p-nitroanilide
The chromogenic substrate used in the Szasz method.
✔ Glycylglycine (or similar acceptor)
Accepts the gamma-glutamyl group during the reaction.
✔ Buffers
Maintain optimal pH (usually alkaline, around pH 8.2–8.4).
✔ Stabilizers & Preservatives
Ensure reagent stability and long shelf life.
✔ Detergents / Surfactants
Help maintain reagent clarity and enhance reaction performance.
Biotech: High-Density Lipoprotein (HDL) biochemistry
Features / Components
Depending on the method (commonly direct enzymatic method), HDL reagent typically contains:
1. Detergents / Selective Chemicals
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These selectively mask or inactivate non-HDL lipoproteins (VLDL, LDL, chylomicrons), allowing accurate measurement of HDL only.
2. Enzymes
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Cholesterol esterase (CHE): Converts HDL-cholesterol esters into free cholesterol.
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Cholesterol oxidase (CHOD): Converts free cholesterol into cholest-4-en-3-one and hydrogen peroxide.
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Peroxidase (POD): Reacts with hydrogen peroxide to form a measurable colored compound.
3. Chromogenic Substrates
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Color-forming agents (e.g., 4-Aminoantipyrine) produce a detectable color reaction measured photometrically.
4. Buffers
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Maintain optimal pH for enzyme activity.
5. Stabilizers & Preservatives
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Ensure long shelf life and consistent performance.
Biotech: High-Density Lipoprotein cholesterol reagent-biochemistry
🔬 HDL Chemistry Reagents (Clinical Chemistry / Lipid Panel)
HDL reagents are used to quantify High-Density Lipoprotein cholesterol in serum or plasma as part of a lipid profile. In semi-automated systems (bench-top analyzers, open systems, manual/semi-auto photometric readers), the reagents must be:
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Stable at 2–8°C
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Compatible with open-channel analyzers
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Ready-to-use or with simple reconstitution
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Optimized for endpoint or two-reagent homogeneous methods
Biotech: Phosphorus Reagents-biochemistry
Principle of Measurement
1. UV Phosphomolybdate Method (Most modern analyzers)
How it works:
-
Inorganic phosphate reacts with ammonium molybdate in an acidic medium.
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Forms a phosphomolybdate complex.
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The complex is measured photometrically in the UV range (usually 340 nm).
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The absorbance is directly proportional to phosphate concentration.
Advantages:
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Fast and highly specific
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Suitable for fully automated analyzers
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Minimal interference
2. Reduced Phosphomolybdate Method (Colorimetric)
How it works:
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Phosphomolybdate complex is formed.
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The complex is reduced to a blue-colored compound (“molybdenum blue”).
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Measured at 600–700 nm, depending on dye.
Advantages:
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Strong color intensity
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Stable reaction for manual or semi-automatic systems
Reagent Components
Phosphorus reagent kits typically include:
R1 (Acid/Molybdate reagent)
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Ammonium molybdate
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Sulfuric acid or perchloric acid
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Stabilizers
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Surfactants
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Preservatives
R2 (Reducing reagent) (if applicable)
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Reducing agents (e.g., ascorbic acid, stannous chloride)
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Dye stabilizers
Some kits are single-reagent formulations.
Packaging Formats
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Liquid-stable ready-to-use reagents
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Two-reagent systems (R1 + R2)
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Analyzer-specific cartridges
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Optional calibrators and controls
Common volumes: 25 ml, 50 ml, 100 ml, 250 ml.
Biotech: Potassium Reagents-biochemistry
Measurement Methods & Corresponding Reagents
1. Ion-Selective Electrode (ISE) Method (Most common in modern analyzers)
Reagents include:
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Internal standard (reference solution)
-
Electrolyte solution for K⁺ electrode balance
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Conditioning solution
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Electrode cleaning solution
-
Calibrators (Low & High K⁺)
Principle:
Potassium-selective membranes generate an electrical potential when exposed to K⁺ ions.
The potential difference is proportional to potassium concentration.
ISE is fast, accurate, and ideal for automated analyzers.
2. Turbidimetric/Colorimetric Tetraphenylboron Method
How it works:
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Potassium reacts with sodium tetraphenylboron.
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Forms a turbid or cloudy precipitate.
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The degree of turbidity is measured photometrically at 510–550 nm.
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Intensity correlates with potassium concentration.
Reagents contain:
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Sodium tetraphenylboron
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Buffer solution
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Surfactants
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Stabilizers
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Preservatives
Used in: Semi-auto analyzers and manual systems.
Packaging Formats
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Single-liquid reagent bottles
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Multi-solution electrolyte packs (for ISE analyzers)
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Ready-to-use liquid stable reagents
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Analyzer-specific cartridges
Typical sizes: 25 ml, 50 ml, 100 ml, 250 ml.
Sample Types
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Serum
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Plasma
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Urine (may require dilution)
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Whole blood (in ISE/blood gas analyzers)
Biotech: Sodium Reagents-biochemistry
1. Ion-Selective Electrode (ISE) Method
Most modern chemistry analyzers use ISE for sodium.
Reagents include:
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Reference solution / Internal standard
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Electrolyte solution for electrode stability
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Conditioning solution
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Cleaning solution
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Calibration solutions (Low & High Na⁺ standards)
Principle:
The sodium ISE membrane selectively binds Na⁺ ions, generating an electrical potential proportional to sodium concentration. Calibration solutions are crucial for accuracy.
2. Flame Photometry Method
Older or standalone electrolyte analyzers may use flame photometry.
Reagents include:
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Diluent
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Standard sodium solution
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Internal lithium standard (in some systems)
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Cleaning solutions
Principle:
Sodium emits light at a characteristic wavelength (589 nm) when introduced into a flame. The emitted intensity is proportional to concentration.
3. Colorimetric (Photometric) Method
Used in some semi-automatic chemistry analyzers when ISE is not available.
Reagents include:
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Ionophore-based chromogenic reagents
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Buffer solution
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Color-forming indicator dye
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Stabilizers and preservatives
Principle:
Sodium ions react with a specific ionophore dye to produce a measurable color change.
Reagent Format
Sodium reagent kits may include:
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Single bottle (for colorimetric systems)
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Multi-solution packs (ISE systems)
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Standards in sealed ampoules or bottles
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Ready-to-use liquid formulations
Sample Types
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Serum
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Plasma
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Urine (diluted appropriately)
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Whole blood (in ISE blood gas analyzers)
Biotech: Total Cholesterol Reagents-biochemistry
🔬 1. CHOD-PAP Method (Gold Standard)
Principle
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Cholesterol esterase converts cholesterol esters → free cholesterol
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Cholesterol oxidase converts cholesterol → cholest-4-en-3-one + H₂O₂
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Peroxidase (POD) uses H₂O₂ to produce a colored dye
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Common chromogens: 4-AAP, TOOS, DAOS, HDAOS
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Absorbance: measured at 500–550 nm depending on chromogen.
What the Reagents Contain
R1 (Buffer / Chromogen)
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Good’s buffer (e.g., PIPES, TES)
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Phenol or TOOS/DAOS derivatives
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Stabilizers & surfactants
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Preservatives
R2 (Enzyme Reagent)
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Cholesterol esterase
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Cholesterol oxidase
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Peroxidase
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Additional surfactants
Biotech: Triglycerides (TG) Reagents- biochemistry
🔬 1. Szasz Method (Standard for GGT)
Principle
GGT catalyzes the transfer of the γ-glutamyl group from a synthetic donor substrate to an acceptor molecule.
Reaction:
L-γ-glutamyl-3-carboxy-4-nitroanilide
-
Glycylglycine
→ 5-amino-2-nitrobenzoate (colored product) -
γ-glutamyl-glycylglycine
The rate of formation of 5-amino-2-nitrobenzoate is measured kinetically.
Measurement
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Absorbance: 405–410 nm
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Mode: Kinetic, multiple readings (rate method)
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Proportional to: GGT activity (U/L)
Biotech: Urea Reagents-biochemstry
Principle of Measurement
1. Urease–GLDH Method (Enzymatic UV)
(Most widely used, highly specific)
How it works:
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Urease enzyme hydrolyzes urea → ammonia + carbon dioxide.
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Ammonia reacts with α-ketoglutarate in the presence of GLDH (glutamate dehydrogenase).
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NADH is oxidized to NAD⁺, causing a decrease in absorbance at 340 nm.
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The rate of absorbance decrease is proportional to urea concentration.
Advantages:
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Very specific
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Minimal interference
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Ideal for automated chemistry analyzers
2. Berthelot (Indophenol) Colorimetric Method
(Common in semi-auto analyzers)
How it works:
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Urease converts urea to ammonia.
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Ammonia reacts with phenol and hypochlorite → blue indophenol dye.
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Absorbance measured at 580–600 nm.
Advantages:
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Stable color formation
-
Suitable for manual and semi-automatic systems
3. Diacetyl Monoxime (DAM) Method (Older method)
Forms a yellow complex; used mainly in research.
Reagent Components
Urease–GLDH Reagents May Contain:
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Urease enzyme
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GLDH enzyme
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NADH
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α-ketoglutarate
-
Buffer solution
-
Surfactants and stabilizers
-
Preservatives
Berthelot Reagents May Contain:
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Phenol
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Sodium nitroprusside
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Hypochlorite
-
Buffer solution
Packaging Formats
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Two-reagent systems (R1 buffer + R2 enzyme)
-
Single-reagent kits (less common)
-
Analyzer-specific liquid cartridges
Typical volumes: 25 ml, 50 ml, 100 ml, 250 ml.