Abstract

Six aristolochic acids were identified in the Chilean species Aristolochia chilensis using high-performance liquid chromatography coupled to a diode array detector (HPLC-DAD) and subsequent confirmation with mass spectrometry (MS). The fractions of each signal were collected and injected directly into an Orbitrap mass detector model Q Exactive Focus (Thermo Scientific). The acids extraction was done with 0.10–0.50 g of lyophilized and pulverized sample and concentrated in Soxhlet extraction equipment. The liquid-liquid separations and a subsequent solid phase extraction (SPE) C18 were performed using 100 µL of the extract that contains the aristolochic acids present in the Aristolochia chilensis plant. The HPLC conditions used a single mobile phase acetonitrile : water (1 : 1) acidified with 0.1% acetic acid and an isocratic elution to 1 mL·min−1. The column InertSustain C18 250 × 4.6 mm and 3 µm was used, the injection volume was 20 µL, and the time of run was reduced to 15 min. Calibration curves were constructed with r 2 being 0.9997. The quantification limit for AAI was 0.138 ± 0.010 µg/mL, and for AAII, it was 0.558 ± 0.042 µg/mL.

Highlights

  • The aristolochic acids (AAs) are derivatives of nitrophenanthrene present in plants of the genus Asarum spp.and Aristolochia spp. [1]

  • The use of a single mobile phase has improved the performance of chromatography

  • 0.042 μg/mL were determined for AA I and AA II, respectively

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Summary

Introduction

The aristolochic acids (AAs) are derivatives of nitrophenanthrene present in plants of the genus Asarum spp.and Aristolochia spp. [1]. The aristolochic acids (AAs) are derivatives of nitrophenanthrene present in plants of the genus Asarum spp. and Aristolochia spp. Despite the high variety of these acids, only seven have been described for Aristolochia chilensis [3, 5], focused in the AAI and AAII. These acids are responsible for their mutagenic and carcinogenic nature [3, 6]. The aristolochic acids can be detected and quantified by using HPLC-MS [4, 7, 8], IR, and NMR [9], but those are expensive methods. In the case of IR and NMR, they require a considerable quantity of the pure compound, which is very difficult to obtain when we have a small quantity of biomass

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