Corresponding author: Alona Savych ( alonasavych@gmail.com ) Academic editor: Plamen Peikov
© 2021 Alona Savych, Roksolana Basaraba, Nataliіa Muzyka, Pavlina Ilashchuk.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Savych A, Basaraba R, Muzyka N, Ilashchuk P (2021) Analysis of fatty acid composition content in the plant components of antidiabetic herbal mixture by GC-MS. Pharmacia 68(2): 433-439. https://doi.org/10.3897/pharmacia.68.e66693
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Medical plants and their combinations due to the wide range of biologically active substances can influence on various links of the pathogenetic mechanism of development of diabetes mellitus and its complications. One of such combinations is an anidiabetic herbal mixture (Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots) with established hypoglycemic, hypolipidemic, antioxidant, hepatoprotective, pancreatoprotective activity in previous pharmacological study in vivo. Thus, the aim of this study was to identify and establish the fatty acid content in the plant components of antidiabetic herbal mixture. Fatty acids were separated by validated method of of gas chromatography-mass spectrometry after conversion into methyl esters. The result showed that Urtica dioica L. leaf and Vaccinium myrtillus L. leaf contain 12 fatty acids (8 saturated, 2 monounsaturated and 2 polyunsaturated), Rosa majalis L. fruits and Taraxacum officinale L. roots – 13 fatty acids (9 saturated, 2 monounsaturated and 2 polyunsaturated) and Mentha piperita L. herb – 14 fatty acids (10 saturated, 2 monounsaturated and 2 polyunsaturated). The predominant long-chain carboxylic acids in all plant raw materials were unsaturated fatty acids, their content was 55.3% in Urtica dioica L. leaf, 64.7% in Rosa majalis L. fruits, 60.5% in Vaccinium myrtillus L. leaf, 64.3% in Mentha piperita L. herb and 51.7% in Taraxacum officinale L. roots. This indicates the feasibility of including each component in the antidiabetic herbal mixture in order to form anticholesterolemic, anti-inflammatory, immunomodulatory and neuroprotective activity, due to the high content of omega-3, omega-6 and omega-9 fatty acids.
diabetes mellitus, herbal mixture, GC-MS, fatty acids, Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots
Diabetes mellitus is one of WHO’s priorities matters, which requires immediate solutions, as the epidemiological situation is alarming – the number of patients is growing each year, leading to increased disability and mortality due to the development of diabetic angiopathies (
Modern pharmacotherapy increasingly takes into account the centuries-old experience of folk medicine with the use of phytopreparations as monotherapy and in combination with synthetic drugs. This is quite justified, because phytotherapy has a number of advantages over traditional therapy with synthetic drugs, namely, it is low-toxic, has a mild pharmacological effect and can be used for a long period of time without significant side effects and combines well with synthetic drugs (
One of such combinations is an anidiabetic herbal mixture (Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots) with established hypoglycemic, hypolipidemic, antioxidant, hepatoprotective, pancreatoprotective activity in pharmacological study in vivo (
Biologically active substances of plant origin have a wide range of pharmacological action and a variety of mechanisms of influencing on the development of diabetes and its complication (
The aim of this study was to identify and to establish the fatty acid content in Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots as the plant components of antidiabetic herbal mixture.
It was used the herbal raw materials of Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots harvested from June to October 2020 in Ternopil region and Charpathians (Vaccinium myrtillus L. leaf) (Ukraine) during the study. The raw materials were then dried, crushed and stored according to the general GACP requirements (
All herbal raw materials used in the study were the components of antidiabetic herbal mixture with established hypoglycemic, hypolipidemic, antioxidant, hepatoprotective, pancreatoprotective activity in pharmacological study in vivo (
All applied reagents were of analytical grade (≥ 99% purity). Standard carboxylic acids were purchased from Sigma-Aldrich Chemical Co. (St. Louis, MO, USA). Water used in the studies was produced by MilliQ Gradient water deionizaton system (Millipore, Bedford, MA, USA). Methanol, toluene, sulfuric acid and heptane were purchased from Sigma-Aldrich Chemical Co. (St. Louis, MO, USA).
Fatty acid composition of herbal raw materials was studied by gas chromatography-mass spectrometry (GC-MS). Chromatographic separation was performed on a gas chromato-mass spectrometric system model 6890N/5973inert (Agilent Technologies, USA) using a capillary column HP-5 ms (30 m × 0.25 mm × 0.25 mkm, Agilent Technologies, USA). Evaporator temperature was 250 °C, the interface temperature – 280 °C. Separation was performed in the mode of temperature programming from 60 to 320 °C at a speed of 7 deg/min. Samples of 1 μL were administered in a 1:50 flow divider mode. Detection was held in the SCAN mode in the range of (38–400 m/z). Carrier gas flow rate through a column was 1.0 mL/min (
Samples of herbal raw materials were grinded into a powder by laboratory mill and about 0.5 g (accurately mass) were selected and placed into a glass vial. Then 3.3 mL of reacting mixture (methanol: toluene: sulfuric acid (44:20:2 v/v)) with 1.7 mL of internal standard solution (undecanoic acid in heptane solution) was added. The obtained samples were standed at 80 °C for 2 hours, refrigerated and centrifuged for 10 minutes at 5000 rpm. It was taken 0.5 mL of the upper heptane phase, which containing methyl esters of fatty acids (
Identification of methyl esters of fatty acids was performed by comparing of retention time (tR) of the mixture of standard and using the NIST 05 and WILEY 2007 mass spectrum library in combination with programs for identification of AMDIS.
Quantitative content (X, mg/kg) was determined by the method of internal standards according to the formula:
where S1 –peak area of the studied substance;
m1 – mass of the internal standard injected into the sample, mg;
Sx – peak area of the standard;
m – sample of raw materials, mg.
The method was validated for linearity, limit of detection (LOD), limit of quantitation (LOQ) and precision. Linearity was performed by injecting a series of standard solutions of fatty acids methyl esters (0.1–10.0 mg/100 g) with a threefold derivatization procedure and a single injection for each reference standard. The mean value and standard deviation, as well as regression analysis were calculated using Microsoft Excel software package 2016 (USA). The values for LOD and LOQ were calculated based on the data obtained during linearity testing in the low concentration range of the working in the test solution, using the following formulas: LOD = 3.3 * s / Slope; LOQ = 10 * s / Slope. Linearity testing was repeated with the same samples after a complete restart of the system with removement and re-installation of the column. Repeatability precision was determined by five-fold injection of the same sample in a row. For the resulting relative peak area of the quantifier ions the relative standard deviation (RSD) was calculated. To determine intra-day precision, five standard preparations of each reference standard of fatty acids methyl esters with the same concentration were single injected and the resulting relative peak areas were used to calculate the RSD. Inter-day precision for the day of sample preparation and the two following days was specified by injecting five standard sample of each reference standard preparations once each on all three days. The RSD of the samples on that day together with the previous samples were calculated as above (
According to the results of the GC-MS analysis, it was identified 12 fatty acids, in particular 8 saturated, 2 monounsaturated and 2 polyunsaturated in Urtica dioica L. leaf (Fig.
The results of the quantitative study showed that the predominant saturated fatty acid component in all test samples was palmitic acid. It was mostly found in Rosa majalis L. fruits (4.73±0.05 mg/g) and in Urtica dioica L. leaf (4.48±0.07 mg/g). In all samples of plant raw materials were found two monounsaturated fatty acids – predominant oleic and palmitoleic. Oleic acid, which is part of omega-9, was found in the largest amount in Vaccinium myrtillus L. leaf (0.81±0.02 mg/g), in Rosa majalis L. fruits (0.69±0.02 mg/g) and in Taraxacum officinale L. roots (0.61±0.02 mg/g). As for polyunsaturated fatty acids, two of them – linoleic and linolenic, were also identified in all five plant components of the antidiabetic herbal mixture. Linoleic acid, which is part of omega-6, was present in fairly large quantities in the studied objects, but in the largest – in Urtica dioica L. leaf (5.22±0.06 mg/g). As for another polyunsaturated acid, namely linolenic, which belongs to the class of omega-3, its highest content was found in Rosa majalis L. fruits (7.07±0.08 mg/g) (Table
The results of the GC-MS analysis of fatty acids content in the plant components of antidiabetic herbal mixture.
No. | tR | Common name of fatty acid | Chemical nomen-clature | Quantitative content of fatty acids methyl esters, mg/g | |||||
---|---|---|---|---|---|---|---|---|---|
Urtica dioica L. leaf | Rosa majalis L. fruits | Vaccinium myrtillus L. leaf | Mentha piperita L. herb | Taraxacum officinale L. roots | |||||
Saturated acids | |||||||||
1. | 2.66 | Capric (decanoic) | C 10:0 | - | - | - | 0.06±0.01 | - | |
2. | 3.74 | Undecylic (undecanoic) | C 11:0 | Internal standart | |||||
3. | 5.42 | Lauric (dodecanoic) | С 12:0 | - | - | - | 0.21±0.01 | 0.08±0.01 | |
4. | 9.78 | Myristic (tetradecanoic) | С 14:0 | 0.11±0.01 | 0.21±0.01 | - | 0.08±0.01 | 0.31±0.02 | |
5. | 14.04 | Pentadecylic (pentadecanoic) | С 15:0 | 0.07±0.01 | 0.07±0.01 | 0.12±0.01 | 0.08±0.01 | 0.16±0.01 | |
6. | 14.57 | Palmitic (hexadecanoic) | С 16:0 | 4.48±0.07 | 4.73±0.05 | 2.34±0.04 | 2.71±0.03 | 3.84±0.07 | |
7. | 16.03 | Margaric (heptadecanoic) | С 17:0 | 0.26±0.01 | 0.16±0.02 | - | - | 0.29±0.02 | |
8. | 19.15 | Stearic (octadecanoic) | С 18:0 | 0.76±0.02 | 0.52±0.02 | 0.28±0.01 | 0.25±0.01 | 0.85±0.03 | |
9. | 23.42 | Arachidic (eicosanoic) | С 20:0 | 0.18±0.01 | 0.13±0.01 | 0.27±0.01 | 0.12±0.01 | 0.31±0.01 | |
10. | 27.38 | Behenic (docosanoic) | С 22:0 | 0.31±0.01 | 0.10±0.01 | 0.54±0.03 | 0.18±0.02 | 0.37±0.02 | |
11. | 29.03 | Tricosylic (tricosanoic) | С 23:0 | - | - | 0.22±0.01 | - | - | |
12. | 31.06 | Lignoceric (tetracosanoic) | С 24:0 | 0.57±0.01 | 0.39±0.02 | 0.51±0.04 | 0.28±0.02 | 0.65±0.03 | |
13. | 32.38 | Pentacosylic (pentacosanoic) | С 25:0 | - | - | - | 0.19±0.01 | - | |
14. | 33.41 | Cerotic (hexacosanoic) | С 26:0 | - | 0.08±0.01 | 0.11±0.01 | - | - | |
Monounsaturated acids | |||||||||
15. | 18.67 | Oleic (octadecenoic, ω-9) | C 18:1 | 0.36±0.01 | 0.69±0.02 | 0.81±0.02 | 0.48±0.01 | 0.61±0.02 | |
16. | 14.04 | Palmitoleic acid (hexadecenoic, ω-7) | C 16:1 | 0.10±0.01 | 0.39±0.03 | 0.57±0.02 | 0.29±0.01 | 0.29±0.01 | |
Polyunsaturated acids | |||||||||
17. | 18.41 | Linoleic (octadecadienic, ω-6) | С 18:2 | 5.22±0.06 | 3.67±0.06 | 3.39±0.05 | 3.73±0.05 | 2.96±0.04 | |
18. | 18.56 | Linolenic (octadecatrienic, ω-3) | С 18:3 | 2.67±0.04 | 7.07±0.08 | 1.91±0.04 | 2.98±0.02 | 3.49±0.04 | |
The amount of saturated fatty acids | 6.74 | 6.39 | 4.39 | 4.16 | 6.86 | ||||
The amount of unsaturated fatty acids | 8.35 | 11.72 | 6.68 | 7.48 | 7.35 | ||||
Total | 15.09 | 18.11 | 11.07 | 11.64 | 14.21 |
According to the chromatographic study, it was determined that the total content of fatty acids in Urtica dioica L. leaf was 15.09 mg/g, in Rosa majalis L. fruits was 18.11 mg/g, in Vaccinium myrtillus L. leaf was 11.07 mg/g, in Mentha piperita L. herb was 11.64 mg/g and in Taraxacum officinale L. roots was 14.21 mg/g. The predominant fatty acids in all plant raw materials were unsaturated fatty acids and their content was 55.3% in Urtica dioica L. leaf, 64.7% in Rosa majalis L. fruits, 60.5% in Vaccinium myrtillus L. leaf, 64.3% in Mentha piperita L. herb and 51.7% in Taraxacum officinale L. roots (Table
The results show that all plant components, such as Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots, of the antidiabetic herbal mixture have a high content of unsaturated fatty acids, which provide a number of pharmacological properties of this phytomixture. Unsaturated fatty acids belonging to the class of omega-3, omega-6 and omega-9 play have an important role in the human body, namely, provide cell membrane function, exhibit anticholesterolemic activity, converting cholesterol into cholic acids and removing them from the body, take involved in fat metabolism (
This phytochemical study is a confirmation of the fatty acid composition of the antidiabetic herbal mixture (Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots) as a whole, which was studied in previous research (
The analytical procedure has been validated to confirm its reliability. All the peaks of reference standards showed good linearity (R2 > 0.995) in a wide concentration range (0.1–10.0 mg/100 g). The results showed that the LODs and the LOQs of methyl esters of fatty acids were in the range of 0.01–0.07 mg/100 g and 0.03–0.22 mg/100 g, respectively, indicating that the sensitivity of the method was satisfactory. The repeatability of the subsequent derivatization and GC-measurement of five standard samples of each reference standard with the same concentration resulted in precision values for the derivatization procedure. For intra- and inter-day precision, the RSD was in a range of 1.57% to 6.26%, which is acceptable.
We identified and established the quantity content of fatty acid composition of Urtica dioica L. leaf, Rosa majalis L. fruits, Vaccinium myrtillus L. leaf, Mentha piperita L. herb and Taraxacum officinale L. roots, which are plant components of antidiabetic herbal mixture with hypoglycemic, hypolipidemic, antioxidant, hepatoprotective, pancreatoprotective activity and defined phytochemical composition by GC-MS method. The total content of fatty acids in Urtica dioica L. leaf was 15.09 mg/g, in Rosa majalis L. fruits was 18.11 mg/g, in Vaccinium myrtillus L. leaf was 11.07 mg/g, in Mentha piperita L. herb was 11.64 mg/g and in Taraxacum officinale L. roots was 14.21 mg/g. The predominant long-chain carboxylic acids in all plant raw materials were unsaturated fatty acids, their content was 55.3% in Urtica dioica L. leaf, 64.7% in Rosa majalis L. fruits, 60.5% in Vaccinium myrtillus L. leaf, 64.3% in Mentha piperita L. herb and 51.7% in Taraxacum officinale L. roots. This indicates the feasibility of including each component in the antidiabetic mixture in order to form anticholesterolemic, anti-inflammatory, immunomodulatory and neuroprotective activity, due to the high content of omega-3, omega-6 and omega-9 fatty acids.