HPLC Analysis and In Vitro and In Silico Evaluation of the Biological Activity of Polyphenolic Components Separated with Solvents of Various Polarities from IHelichrysum italicum/I

Helichrysum italicum has piqued the interest of many researchers in recent years, mostly for its essential oil, but increasingly for its polyphenolic content as well. In the current study, we examine the polyphenolic composition of H. italicum grown in Bulgaria. The polyphenolic complex was fraction...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2023-08, Vol.28 (17)
Hauptverfasser: Bojilov, Dimitar, Manolov, Stanimir, Ahmed, Sezan, Dagnon, Soleya, Ivanov, Iliyan, Marc, Gabriel, Oniga, Smaranda, Oniga, Ovidiu, Nedialkov, Paraskev, Mollova, Silviya
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container_issue 17
container_start_page
container_title Molecules (Basel, Switzerland)
container_volume 28
creator Bojilov, Dimitar
Manolov, Stanimir
Ahmed, Sezan
Dagnon, Soleya
Ivanov, Iliyan
Marc, Gabriel
Oniga, Smaranda
Oniga, Ovidiu
Nedialkov, Paraskev
Mollova, Silviya
description Helichrysum italicum has piqued the interest of many researchers in recent years, mostly for its essential oil, but increasingly for its polyphenolic content as well. In the current study, we examine the polyphenolic composition of H. italicum grown in Bulgaria. The polyphenolic complex was fractionated with solvents of various polarities, including hexane, chloroform, ethyl acetate, and butanol, in order to assess the biological impact of the components. HPLC-PDA and UHPLC-MS/MS were used to examine all fractions. The green coffee fingerprint profile was employed as a “surrogate standard” in the polyphenolic components detection approach. From the UHPLC-MS/MS analysis, we identified 60 components of the polyphenolic complex such as quercetin 3-O-glucuronide, quercetin acetyl-glycoside, isorhamnetin acetyl-glycoside, isorhamnetin caffeoyl-glycoside, quercetin caffeoyl-malonyl-glycoside, isorhamnetin coumaroyl-glycoside, coumaroyl-caffeoylquinic acid, and diCQA-acetyl-derivative were first reported in the composition of H. italicum. The biological activity of the fractions was evaluated in vitro and in silico, which included the fight against oxidative stress (hydrogen peroxide scavenging activity (HPSA), hydroxyl radical scavenging activity (HRSA), metal-chelating activity (MChA)) and nitrosative (nitric oxide scavenging activity) (NOSA)), in vitro anti-inflammatory, and anti-arthritic activity. Results are presented as IC[sub.50] ± SD μg/mL. The analysis showed that the EtOAc fraction was characterized by highest HPSA (57.12 ± 1.14 μg/mL), HRSA (92.23 ± 1.10 μg/mL), MChA (5.60 ± 0.17 μg/mL), and NOSA (89.81 ± 2.09 μg/mL), while the hexane and chloroform fractions showed significantly higher in vitro anti-inflammatory activity (30.48 ± 2.33 μg/mL, 62.50 ± 1.69 μg/mL) compared to the standard ibuprofen. All three fractions showed potential anti-arthritic activity (102.93 ± 8.62 μg/mL, 108.92 ± 4.42 μg/mL, 84.19 ± 3.89 μg/mL).
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In the current study, we examine the polyphenolic composition of H. italicum grown in Bulgaria. The polyphenolic complex was fractionated with solvents of various polarities, including hexane, chloroform, ethyl acetate, and butanol, in order to assess the biological impact of the components. HPLC-PDA and UHPLC-MS/MS were used to examine all fractions. The green coffee fingerprint profile was employed as a “surrogate standard” in the polyphenolic components detection approach. From the UHPLC-MS/MS analysis, we identified 60 components of the polyphenolic complex such as quercetin 3-O-glucuronide, quercetin acetyl-glycoside, isorhamnetin acetyl-glycoside, isorhamnetin caffeoyl-glycoside, quercetin caffeoyl-malonyl-glycoside, isorhamnetin coumaroyl-glycoside, coumaroyl-caffeoylquinic acid, and diCQA-acetyl-derivative were first reported in the composition of H. italicum. The biological activity of the fractions was evaluated in vitro and in silico, which included the fight against oxidative stress (hydrogen peroxide scavenging activity (HPSA), hydroxyl radical scavenging activity (HRSA), metal-chelating activity (MChA)) and nitrosative (nitric oxide scavenging activity) (NOSA)), in vitro anti-inflammatory, and anti-arthritic activity. Results are presented as IC[sub.50] ± SD μg/mL. The analysis showed that the EtOAc fraction was characterized by highest HPSA (57.12 ± 1.14 μg/mL), HRSA (92.23 ± 1.10 μg/mL), MChA (5.60 ± 0.17 μg/mL), and NOSA (89.81 ± 2.09 μg/mL), while the hexane and chloroform fractions showed significantly higher in vitro anti-inflammatory activity (30.48 ± 2.33 μg/mL, 62.50 ± 1.69 μg/mL) compared to the standard ibuprofen. 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The biological activity of the fractions was evaluated in vitro and in silico, which included the fight against oxidative stress (hydrogen peroxide scavenging activity (HPSA), hydroxyl radical scavenging activity (HRSA), metal-chelating activity (MChA)) and nitrosative (nitric oxide scavenging activity) (NOSA)), in vitro anti-inflammatory, and anti-arthritic activity. Results are presented as IC[sub.50] ± SD μg/mL. The analysis showed that the EtOAc fraction was characterized by highest HPSA (57.12 ± 1.14 μg/mL), HRSA (92.23 ± 1.10 μg/mL), MChA (5.60 ± 0.17 μg/mL), and NOSA (89.81 ± 2.09 μg/mL), while the hexane and chloroform fractions showed significantly higher in vitro anti-inflammatory activity (30.48 ± 2.33 μg/mL, 62.50 ± 1.69 μg/mL) compared to the standard ibuprofen. All three fractions showed potential anti-arthritic activity (102.93 ± 8.62 μg/mL, 108.92 ± 4.42 μg/mL, 84.19 ± 3.89 μg/mL).</description><subject>Analysis</subject><subject>High performance liquid chromatography</subject><subject>Medicinal plants</subject><subject>Medicine, Botanic</subject><subject>Medicine, Herbal</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptUMtuwjAQjKpWKqX9gN4s9QzETmLHR4poiYRUJBBX5Dgb4sqxUexQ8V_9wJo-JA7VHnZmdmYOG0WPOB4nCY8nrdUgew2O5JhRzPOraIBTEo-SOOXXF_g2unPuPY4JTnE2iD4Xq-UMTY3QJ6ccEqZChUFb5Tv7R9ZKK2nR_Ch0L7yyBtka-QbQs7La7pUUGk2lV0flT-fTyurToQFjQwzNbHuwBox3aA0H0QkPFfpQvkFrq4_feohsRads787RgLwCh-rOtqhYQChpupPrW6S8CKRvJ8V9dFML7eDhdw-jzct8M1uMlm-vxWy6HO0p4yNalnVKKVRE0JiXMkkJ54wIRvOKVTUjMqtBMMAUCw6lxFmWcCAxKSHHeUmSYfT0U7sXGnbK1NZ3QrbKyd2U0ZRQllIeXON_XGEqaMPfDNQq6BeBL8sxhwo</recordid><startdate>20230801</startdate><enddate>20230801</enddate><creator>Bojilov, Dimitar</creator><creator>Manolov, Stanimir</creator><creator>Ahmed, Sezan</creator><creator>Dagnon, Soleya</creator><creator>Ivanov, Iliyan</creator><creator>Marc, Gabriel</creator><creator>Oniga, Smaranda</creator><creator>Oniga, Ovidiu</creator><creator>Nedialkov, Paraskev</creator><creator>Mollova, Silviya</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20230801</creationdate><title>HPLC Analysis and In Vitro and In Silico Evaluation of the Biological Activity of Polyphenolic Components Separated with Solvents of Various Polarities from IHelichrysum italicum/I</title><author>Bojilov, Dimitar ; Manolov, Stanimir ; Ahmed, Sezan ; Dagnon, Soleya ; Ivanov, Iliyan ; Marc, Gabriel ; Oniga, Smaranda ; Oniga, Ovidiu ; Nedialkov, Paraskev ; Mollova, Silviya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g679-6bbf466ed2a609bc3429972a768d7df72c5fea7e161a9ebc15539e202be818b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Analysis</topic><topic>High performance liquid chromatography</topic><topic>Medicinal plants</topic><topic>Medicine, Botanic</topic><topic>Medicine, Herbal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bojilov, Dimitar</creatorcontrib><creatorcontrib>Manolov, Stanimir</creatorcontrib><creatorcontrib>Ahmed, Sezan</creatorcontrib><creatorcontrib>Dagnon, Soleya</creatorcontrib><creatorcontrib>Ivanov, Iliyan</creatorcontrib><creatorcontrib>Marc, Gabriel</creatorcontrib><creatorcontrib>Oniga, Smaranda</creatorcontrib><creatorcontrib>Oniga, Ovidiu</creatorcontrib><creatorcontrib>Nedialkov, Paraskev</creatorcontrib><creatorcontrib>Mollova, Silviya</creatorcontrib><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bojilov, Dimitar</au><au>Manolov, Stanimir</au><au>Ahmed, Sezan</au><au>Dagnon, Soleya</au><au>Ivanov, Iliyan</au><au>Marc, Gabriel</au><au>Oniga, Smaranda</au><au>Oniga, Ovidiu</au><au>Nedialkov, Paraskev</au><au>Mollova, Silviya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HPLC Analysis and In Vitro and In Silico Evaluation of the Biological Activity of Polyphenolic Components Separated with Solvents of Various Polarities from IHelichrysum italicum/I</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><date>2023-08-01</date><risdate>2023</risdate><volume>28</volume><issue>17</issue><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>Helichrysum italicum has piqued the interest of many researchers in recent years, mostly for its essential oil, but increasingly for its polyphenolic content as well. In the current study, we examine the polyphenolic composition of H. italicum grown in Bulgaria. The polyphenolic complex was fractionated with solvents of various polarities, including hexane, chloroform, ethyl acetate, and butanol, in order to assess the biological impact of the components. HPLC-PDA and UHPLC-MS/MS were used to examine all fractions. The green coffee fingerprint profile was employed as a “surrogate standard” in the polyphenolic components detection approach. From the UHPLC-MS/MS analysis, we identified 60 components of the polyphenolic complex such as quercetin 3-O-glucuronide, quercetin acetyl-glycoside, isorhamnetin acetyl-glycoside, isorhamnetin caffeoyl-glycoside, quercetin caffeoyl-malonyl-glycoside, isorhamnetin coumaroyl-glycoside, coumaroyl-caffeoylquinic acid, and diCQA-acetyl-derivative were first reported in the composition of H. italicum. The biological activity of the fractions was evaluated in vitro and in silico, which included the fight against oxidative stress (hydrogen peroxide scavenging activity (HPSA), hydroxyl radical scavenging activity (HRSA), metal-chelating activity (MChA)) and nitrosative (nitric oxide scavenging activity) (NOSA)), in vitro anti-inflammatory, and anti-arthritic activity. Results are presented as IC[sub.50] ± SD μg/mL. The analysis showed that the EtOAc fraction was characterized by highest HPSA (57.12 ± 1.14 μg/mL), HRSA (92.23 ± 1.10 μg/mL), MChA (5.60 ± 0.17 μg/mL), and NOSA (89.81 ± 2.09 μg/mL), while the hexane and chloroform fractions showed significantly higher in vitro anti-inflammatory activity (30.48 ± 2.33 μg/mL, 62.50 ± 1.69 μg/mL) compared to the standard ibuprofen. All three fractions showed potential anti-arthritic activity (102.93 ± 8.62 μg/mL, 108.92 ± 4.42 μg/mL, 84.19 ± 3.89 μg/mL).</abstract><pub>MDPI AG</pub><doi>10.3390/molecules28176198</doi></addata></record>
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subjects Analysis
High performance liquid chromatography
Medicinal plants
Medicine, Botanic
Medicine, Herbal
title HPLC Analysis and In Vitro and In Silico Evaluation of the Biological Activity of Polyphenolic Components Separated with Solvents of Various Polarities from IHelichrysum italicum/I
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