Determination of perillaldehyde in perilla herbs using relative molar sensitivity to single-reference diphenyl sulfone

Perillaldehyde (PRL) is one of the essential oil components derived from perilla plants ( Perilla frutescens Britton) and is a characteristic compound of the traditional medicine “perilla herb (蘇葉)” listed in the The Japanese Pharmacopoeia, 17th edition (JP17). HPLC using an analytical standard of P...

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Veröffentlicht in:Journal of natural medicines 2019-06, Vol.73 (3), p.566-576
Hauptverfasser: Masumoto, Naoko, Nishizaki, Yuzo, Maruyama, Takeshi, Igarashi, Yasushi, Nakajima, Kaori, Yamazaki, Taichi, Kuroe, Miho, Numata, Masahiko, Ihara, Toshihide, Sugimoto, Naoki, Sato, Kyoko
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container_issue 3
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container_title Journal of natural medicines
container_volume 73
creator Masumoto, Naoko
Nishizaki, Yuzo
Maruyama, Takeshi
Igarashi, Yasushi
Nakajima, Kaori
Yamazaki, Taichi
Kuroe, Miho
Numata, Masahiko
Ihara, Toshihide
Sugimoto, Naoki
Sato, Kyoko
description Perillaldehyde (PRL) is one of the essential oil components derived from perilla plants ( Perilla frutescens Britton) and is a characteristic compound of the traditional medicine “perilla herb (蘇葉)” listed in the The Japanese Pharmacopoeia, 17th edition (JP17). HPLC using an analytical standard of PRL has been used to quantitatively determine the PRL content in perilla herb. However, PRL reagents have been reported to decompose easily. In this study, we utilized an alternative quantitative method using on a single reference with relative molar sensitivity ( RMS ) based on the results of experiments performed in two laboratories. It was possible to calculate the exact RMS using an offline combination of 1 H-quantitative NMR spectroscopy ( 1 H-qNMR) and an HPLC/photodiode array (PDA) detector (or an HPLC/variable-wavelength detector [VWD]). Using the RMS of PRL to the single-reference compound diphenyl sulfone (DFS), which is an inexpensive and stable compound, the PRL content in the perilla herb could be determined using HPLC/PDA or HPLC/VWD without the need for the analytical standard of PRL. There was no significant difference between the PRL contents of perilla herb determined using the method employing the single-reference DFS with RMS and using the JP17 assay, the calibration curve of which was generated using the analytical standard of PRL with adjusted purity measured by 1 H-qNMR. These results demonstrate that our proposed method using a single reference with RMS is suitable for quantitative assays of perilla herb and can be an alternative method for the current assay method defined in the JP17.
doi_str_mv 10.1007/s11418-019-01306-7
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HPLC using an analytical standard of PRL has been used to quantitatively determine the PRL content in perilla herb. However, PRL reagents have been reported to decompose easily. In this study, we utilized an alternative quantitative method using on a single reference with relative molar sensitivity ( RMS ) based on the results of experiments performed in two laboratories. It was possible to calculate the exact RMS using an offline combination of 1 H-quantitative NMR spectroscopy ( 1 H-qNMR) and an HPLC/photodiode array (PDA) detector (or an HPLC/variable-wavelength detector [VWD]). Using the RMS of PRL to the single-reference compound diphenyl sulfone (DFS), which is an inexpensive and stable compound, the PRL content in the perilla herb could be determined using HPLC/PDA or HPLC/VWD without the need for the analytical standard of PRL. There was no significant difference between the PRL contents of perilla herb determined using the method employing the single-reference DFS with RMS and using the JP17 assay, the calibration curve of which was generated using the analytical standard of PRL with adjusted purity measured by 1 H-qNMR. 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HPLC using an analytical standard of PRL has been used to quantitatively determine the PRL content in perilla herb. However, PRL reagents have been reported to decompose easily. In this study, we utilized an alternative quantitative method using on a single reference with relative molar sensitivity ( RMS ) based on the results of experiments performed in two laboratories. It was possible to calculate the exact RMS using an offline combination of 1 H-quantitative NMR spectroscopy ( 1 H-qNMR) and an HPLC/photodiode array (PDA) detector (or an HPLC/variable-wavelength detector [VWD]). Using the RMS of PRL to the single-reference compound diphenyl sulfone (DFS), which is an inexpensive and stable compound, the PRL content in the perilla herb could be determined using HPLC/PDA or HPLC/VWD without the need for the analytical standard of PRL. There was no significant difference between the PRL contents of perilla herb determined using the method employing the single-reference DFS with RMS and using the JP17 assay, the calibration curve of which was generated using the analytical standard of PRL with adjusted purity measured by 1 H-qNMR. 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subjects Biomedical and Life Sciences
Biomedicine
Chromatography, High Pressure Liquid - methods
Complementary & Alternative Medicine
Herbal medicine
Magnetic Resonance Spectroscopy
Medicinal Chemistry
Monoterpenes - analysis
Oils, Volatile - analysis
Organic chemicals
Original Paper
Perilla frutescens - chemistry
Pharmacology/Toxicology
Pharmacy
Phytochemicals
Plant Sciences
Sulfones - chemistry
Vegetable oils
title Determination of perillaldehyde in perilla herbs using relative molar sensitivity to single-reference diphenyl sulfone
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