🐟 Histamine in fish (HPLC)

Food Chemistry PN-EN ISO 19343

Determination of histamine in fish and fishery products by HPLC with dansyl chloride derivatization and UV detection. Mandatory test for Scombridae family fish.

Overview

Histamine is a biogenic amine formed from histidine decarboxylation by bacterial enzymes (histidine decarboxylase) in fish and fishery products during improper storage (too high temperature). Histamine poisoning (scombroid fish poisoning) manifests with headaches, urticaria, nausea, and diarrhea, and in severe cases — breathing difficulties and blood pressure drop.

EU regulations (EC Reg. 2073/2005) require histamine testing in fish from families with high histidine content (Scombridae — tuna, mackerel, bonito; Clupeidae — herring, sardine; Engraulidae — anchovy). Limits: 9 sample units, with m = 100 mg/kg (max average) and M = 200 mg/kg (no sample may exceed). For fish ripened in brine (fish sauces, anchovies): m = 200, M = 400 mg/kg.

ISO 19343 method is based on histamine extraction with perchloric acid, derivatization with dansyl chloride (5-(dimethylamino)naphthalene-1-sulfonyl chloride), separation on HPLC C18 column in reversed phase and UV detection at 254 nm. Dansyl derivatization is necessary because histamine has no strong chromophore for direct UV detection. Alternatively, OPA (o-phthalaldehyde) derivatization with fluorescence detection or direct LC-MS/MS is used.

Histamine is thermostable — it is not decomposed during cooking, frying, or preservation. Therefore, the only way of prevention is maintaining the cold chain from catch to consumer. Histamine testing is a key element of HACCP system in fish processing.

Method principle

Fish sample (10 g) is extracted with 0.4 mol/L perchloric acid by homogenization and centrifugation. Supernatant is cleaned and subjected to pre-column derivatization with dansyl chloride (dansyl-Cl) in alkaline environment (pH 9–10, carbonate buffer). Dansyl-Cl reacts with histamine amino groups, forming fluorescent/UV-absorbing dansyl-histamine derivative. Excess dansyl-Cl is removed by reaction with proline. Biogenic amine derivatives are separated on C18 HPLC column in acetonitrile/water gradient and detected by UV (254 nm). Histamine concentration is calculated from calibration curve using internal standard (1,7-diaminoheptane).

Applications

Key parameters

ParameterValue
AnalyteHistamine (2-[4-imidazolyl]ethylamine)
LOQ5–10 mg/kg
Calibration range10–500 mg/kg
EU limit (m)100 mg/kg (fresh fish), 200 mg/kg (fish sauces)
EU limit (M)200 mg/kg (fresh fish), 400 mg/kg (fish sauces)
DerivatizationDansyl chloride (pre-column) or OPA (post-column)

Standard

Standard number
PN-EN ISO 19343:2017
Title (PL)
Mikrobiologia łańcucha żywnościowego — Wykrywanie i oznaczanie ilościowe histaminy w rybach i przetworach rybnych — Metoda HPLC
Title (EN)
Microbiology of the food chain — Detection and quantification of histamine in fish and fishery products — HPLC method

Step-by-step procedure

1. Sample preparation

Homogenize fish sample. Weigh 10 g into 50 mL centrifuge tube.

⏱ Time: 5 min

2. Extraction

Add 20 mL 0.4 mol/L perchloric acid. Homogenize 2 min (Ultra-Turrax). Centrifuge 10 min at 3000 rcf.

⏱ Time: 15 min

3. Derivatization preparation

Take 1 mL supernatant into screw-cap tube. Add 200 µL internal standard solution (1,7-diaminoheptane).

⏱ Time: 5 min

4. Alkalization

Add 300 µL saturated NaHCO₃ and 200 µL 2 mol/L NaOH. Mix.

⏱ Time: 2 min

5. Dansyl-Cl derivatization

Add 2 mL dansyl chloride (10 mg/mL in acetone). Mix on vortex. Incubate 45 min at 40°C.

⏱ Time: 45 min • 🌡 Temperature: 40°C

6. Excess dansyl-Cl removal

Add 100 µL L-proline solution (100 mg/mL). Incubate 15 min at room temperature.

⏱ Time: 15 min

7. Derivative extraction

Add 2 mL toluene or ethyl acetate. Shake 1 min. Collect organic phase. Evaporate to dryness under N₂.

⏱ Time: 10 min

8. Sample reconstitution

Dissolve dry residue in 200 µL acetonitrile/water (60:40). Mix on vortex. Filter into HPLC vial.

⏱ Time: 5 min

9. HPLC analysis

Inject 20 µL onto C18 column. Gradient: 50→95% MeCN in 25 min. UV detection 254 nm. Flow 1 mL/min.

⏱ Time: 30 min

10. Quantification

Calculate histamine/IS peak area ratio. Read concentration from calibration curve. Include dilution.

⏱ Time: 10 min

11. Result interpretation

Compare with EU limits: n=9, c=2, m=100 mg/kg, M=200 mg/kg (fresh fish). No sample may exceed M.

⏱ Time: 5 min

12. Quality control

Every series: blank, spike (50 and 200 mg/kg), CRM (FAPAS). Recovery 80–110%, RSD < 15%. PT participation.

⏱ Time: 60 min

Required equipment and apparatus

EquipmentExampleIndicative price
HPLC system with UV/DAD detectorShimadzu Nexera + SPD-M40, Agilent 1260 + DAD, Waters Alliance + PDA120 000–300 000 PLN
HPLC C18 columnWaters Symmetry C18 (250 × 4.6 mm, 5 µm), Phenomenex Luna C181 500–3 000 PLN
HomogenizerIKA Ultra-Turrax T25, Kinematica Polytron PT 2500E5 000–15 000 PLN
Laboratory centrifugeHettich Rotina 380 R, Eppendorf 5810 R (≥3000 rcf)15 000–40 000 PLN
Water bath 40°CMemmert WNB 7, Julabo TW 123 000–8 000 PLN
Fume hood / fume cupboardFor work with dansyl chloride and perchloric acid15 000–40 000 PLN
Analytical balance 0.1 mgMettler Toledo ME204, Radwag AS 220.R28 000–20 000 PLN

Reagents, media and consumables

ReagentCASDetails
Histamine dihydrochloride (standard)56-92-8Calibration standard, certified CRM, 1 g
Dansyl chloride (dansyl-Cl)605-65-2Derivatizing reagent, 5-(dimethylamino)naphthalene-1-sulfonyl chloride, 1 g
Perchloric acid 0.4 mol/L7601-90-3Histamine extraction from sample, 500 mL
1,7-diaminoheptane (internal standard)646-19-5Internal standard IS, 5 g
Carbonate buffer pH 9–10Derivatization reaction environment (NaHCO₃/Na₂CO₃)
L-proline147-85-3Removing excess dansyl chloride after derivatization, 25 g
Acetonitrile HPLC grade75-05-8Mobile phase and solvent, 2.5 L
HPLC grade water (ultrapure)Mobile phase, Milli-Q system (18.2 MΩ·cm)

Health and safety (OHS)

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