Antioxidant, Tyrosinase, α-Glucosidase, and Elastase Enzyme Inhibition Activities of Optimized Unripe Ajwa Date Pulp ( Phoenix dactylifera ) Extracts by Response Surface Methodology
The Ajwa date ( L., Arecaceae family) is a popular edible fruit consumed all over the world. The profiling of the polyphenolic compounds of optimized unripe Ajwa date pulp (URADP) extracts is scarce. The aim of this study was to extract polyphenols from URADP as effectively as possible by using resp...
Gespeichert in:
Veröffentlicht in: | International journal of molecular sciences 2023-02, Vol.24 (4), p.3396 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 4 |
container_start_page | 3396 |
container_title | International journal of molecular sciences |
container_volume | 24 |
creator | Alshammari, Fanar Alam, Md Badrul Song, Bo-Rim Lee, Sang-Han |
description | The Ajwa date (
L., Arecaceae family) is a popular edible fruit consumed all over the world. The profiling of the polyphenolic compounds of optimized unripe Ajwa date pulp (URADP) extracts is scarce. The aim of this study was to extract polyphenols from URADP as effectively as possible by using response surface methodology (RSM). A central composite design (CCD) was used to optimize the extraction conditions with respect to ethanol concentration, extraction time, and temperature and to achieve the maximum amount of polyphenolic compounds. High-resolution mass spectrometry was used to identify the URADP's polyphenolic compounds. The DPPH-, ABTS-radical scavenging, α-glucosidase, elastase and tyrosinase enzyme inhibition of optimized extracts of URADP was also evaluated. According to RSM, the highest amounts of TPC (24.25 ± 1.02 mgGAE/g) and TFC (23.98 ± 0.65 mgCAE/g) were obtained at 52% ethanol, 81 min time, and 63 °C. Seventy (70) secondary metabolites, including phenolic, flavonoids, fatty acids, and sugar, were discovered using high-resolution mass spectrometry. In addition, twelve (12) new phytoconstituents were identified for the first time in this plant. Optimized URADP extract showed inhibition of DPPH-radical (IC
= 87.56 mg/mL), ABTS-radical (IC
= 172.36 mg/mL), α-glucosidase (IC
= 221.59 mg/mL), elastase (IC
= 372.25 mg/mL) and tyrosinase (IC
= 59.53 mg/mL) enzymes. The results revealed a significant amount of phytoconstituents, making it an excellent contender for the pharmaceutical and food industries. |
doi_str_mv | 10.3390/ijms24043396 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9966286</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A751924175</galeid><sourcerecordid>A751924175</sourcerecordid><originalsourceid>FETCH-LOGICAL-c479t-eeb5a635afe5bbd8afbb9fe692b689a8582212dd505ad50efe8c897e49b4aa3</originalsourceid><addsrcrecordid>eNptUk1v1DAQjRCItgs3zsgSl1baFMeJk_iCFJWlVCpqRcvZcuLxrleJHWKnbPqvuPAz-E14aSlbhCzZ88Zvnj0fUfQqwcdpyvBbve4cyXAWQP4k2k8yQmKM8-Lpjr0XHTi3xpikhLLn0V6al2lWYrof_aiM13ajpTB-jq6nwTpthIM5-vk9Pm3HJmD5Gwsj0aIVzgeEFuZ26gCdmZWudRAwqGq8vgkmOGQVuui97vQtSPTFDLoHVK2_CfReeECXY9ujQ3S5smD0BknR-KnVCgaBjtBi44fgcKie0GdwvTXhsatxUKIB9An8ykrb2uX0InqmROvg5f05i64-LK5PPsbnF6dnJ9V53GQF8zFATUWeUqGA1rUshaprpiBnpM5LJkpaEpIQKSmmImygoGxKVkDG6kyIdBa9u1Ptx7oD2YAJv2t5P-hODBO3QvPHN0av-NLecMbynJR5EDi8Fxjs1xGc5512DbStMGBHx0lRYlywbWNm0Zt_qGs7DiYkF1gFo2lOC_yXtRQtcG2U3dZrK8qrgiaMZElBA-v4P6ywJHS6sQaUDv5HAfO7gCb03w2gHnJMMN9OGd-dskB_vVuXB_KfsUp_ATBA0c8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2779536570</pqid></control><display><type>article</type><title>Antioxidant, Tyrosinase, α-Glucosidase, and Elastase Enzyme Inhibition Activities of Optimized Unripe Ajwa Date Pulp ( Phoenix dactylifera ) Extracts by Response Surface Methodology</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>PubMed Central</source><creator>Alshammari, Fanar ; Alam, Md Badrul ; Song, Bo-Rim ; Lee, Sang-Han</creator><creatorcontrib>Alshammari, Fanar ; Alam, Md Badrul ; Song, Bo-Rim ; Lee, Sang-Han</creatorcontrib><description>The Ajwa date (
L., Arecaceae family) is a popular edible fruit consumed all over the world. The profiling of the polyphenolic compounds of optimized unripe Ajwa date pulp (URADP) extracts is scarce. The aim of this study was to extract polyphenols from URADP as effectively as possible by using response surface methodology (RSM). A central composite design (CCD) was used to optimize the extraction conditions with respect to ethanol concentration, extraction time, and temperature and to achieve the maximum amount of polyphenolic compounds. High-resolution mass spectrometry was used to identify the URADP's polyphenolic compounds. The DPPH-, ABTS-radical scavenging, α-glucosidase, elastase and tyrosinase enzyme inhibition of optimized extracts of URADP was also evaluated. According to RSM, the highest amounts of TPC (24.25 ± 1.02 mgGAE/g) and TFC (23.98 ± 0.65 mgCAE/g) were obtained at 52% ethanol, 81 min time, and 63 °C. Seventy (70) secondary metabolites, including phenolic, flavonoids, fatty acids, and sugar, were discovered using high-resolution mass spectrometry. In addition, twelve (12) new phytoconstituents were identified for the first time in this plant. Optimized URADP extract showed inhibition of DPPH-radical (IC
= 87.56 mg/mL), ABTS-radical (IC
= 172.36 mg/mL), α-glucosidase (IC
= 221.59 mg/mL), elastase (IC
= 372.25 mg/mL) and tyrosinase (IC
= 59.53 mg/mL) enzymes. The results revealed a significant amount of phytoconstituents, making it an excellent contender for the pharmaceutical and food industries.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms24043396</identifier><identifier>PMID: 36834805</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>alpha-Glucosidases - metabolism ; Analysis ; Antioxidants ; Antioxidants - pharmacology ; Design optimization ; Diabetes ; Elastase ; Enzymes ; Ethanol ; Flavonoids ; Food industry ; Glucosidase ; Health aspects ; High resolution ; Hydrolases ; Independent variables ; Mass spectrometry ; Mass spectroscopy ; Metabolites ; Methods ; Monophenol Monooxygenase - metabolism ; Neutrophils ; Optimization ; Pancreatic Elastase - metabolism ; Phenols ; Phoeniceae - chemistry ; Phoenix dactylifera ; Plant extracts ; Plant Extracts - pharmacology ; Polyphenols ; Pulmonary fibrosis ; Reproducibility ; Response surface methodology ; Scavenging ; Secondary metabolites ; Statistical methods ; Statistical significance ; Tyrosinase ; α-Glucosidase</subject><ispartof>International journal of molecular sciences, 2023-02, Vol.24 (4), p.3396</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-eeb5a635afe5bbd8afbb9fe692b689a8582212dd505ad50efe8c897e49b4aa3</citedby><cites>FETCH-LOGICAL-c479t-eeb5a635afe5bbd8afbb9fe692b689a8582212dd505ad50efe8c897e49b4aa3</cites><orcidid>0000-0002-8509-6827 ; 0000-0002-2343-7315 ; 0000-0002-7418-3650</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966286/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966286/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36834805$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alshammari, Fanar</creatorcontrib><creatorcontrib>Alam, Md Badrul</creatorcontrib><creatorcontrib>Song, Bo-Rim</creatorcontrib><creatorcontrib>Lee, Sang-Han</creatorcontrib><title>Antioxidant, Tyrosinase, α-Glucosidase, and Elastase Enzyme Inhibition Activities of Optimized Unripe Ajwa Date Pulp ( Phoenix dactylifera ) Extracts by Response Surface Methodology</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>The Ajwa date (
L., Arecaceae family) is a popular edible fruit consumed all over the world. The profiling of the polyphenolic compounds of optimized unripe Ajwa date pulp (URADP) extracts is scarce. The aim of this study was to extract polyphenols from URADP as effectively as possible by using response surface methodology (RSM). A central composite design (CCD) was used to optimize the extraction conditions with respect to ethanol concentration, extraction time, and temperature and to achieve the maximum amount of polyphenolic compounds. High-resolution mass spectrometry was used to identify the URADP's polyphenolic compounds. The DPPH-, ABTS-radical scavenging, α-glucosidase, elastase and tyrosinase enzyme inhibition of optimized extracts of URADP was also evaluated. According to RSM, the highest amounts of TPC (24.25 ± 1.02 mgGAE/g) and TFC (23.98 ± 0.65 mgCAE/g) were obtained at 52% ethanol, 81 min time, and 63 °C. Seventy (70) secondary metabolites, including phenolic, flavonoids, fatty acids, and sugar, were discovered using high-resolution mass spectrometry. In addition, twelve (12) new phytoconstituents were identified for the first time in this plant. Optimized URADP extract showed inhibition of DPPH-radical (IC
= 87.56 mg/mL), ABTS-radical (IC
= 172.36 mg/mL), α-glucosidase (IC
= 221.59 mg/mL), elastase (IC
= 372.25 mg/mL) and tyrosinase (IC
= 59.53 mg/mL) enzymes. The results revealed a significant amount of phytoconstituents, making it an excellent contender for the pharmaceutical and food industries.</description><subject>alpha-Glucosidases - metabolism</subject><subject>Analysis</subject><subject>Antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Design optimization</subject><subject>Diabetes</subject><subject>Elastase</subject><subject>Enzymes</subject><subject>Ethanol</subject><subject>Flavonoids</subject><subject>Food industry</subject><subject>Glucosidase</subject><subject>Health aspects</subject><subject>High resolution</subject><subject>Hydrolases</subject><subject>Independent variables</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Metabolites</subject><subject>Methods</subject><subject>Monophenol Monooxygenase - metabolism</subject><subject>Neutrophils</subject><subject>Optimization</subject><subject>Pancreatic Elastase - metabolism</subject><subject>Phenols</subject><subject>Phoeniceae - chemistry</subject><subject>Phoenix dactylifera</subject><subject>Plant extracts</subject><subject>Plant Extracts - pharmacology</subject><subject>Polyphenols</subject><subject>Pulmonary fibrosis</subject><subject>Reproducibility</subject><subject>Response surface methodology</subject><subject>Scavenging</subject><subject>Secondary metabolites</subject><subject>Statistical methods</subject><subject>Statistical significance</subject><subject>Tyrosinase</subject><subject>α-Glucosidase</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptUk1v1DAQjRCItgs3zsgSl1baFMeJk_iCFJWlVCpqRcvZcuLxrleJHWKnbPqvuPAz-E14aSlbhCzZ88Zvnj0fUfQqwcdpyvBbve4cyXAWQP4k2k8yQmKM8-Lpjr0XHTi3xpikhLLn0V6al2lWYrof_aiM13ajpTB-jq6nwTpthIM5-vk9Pm3HJmD5Gwsj0aIVzgeEFuZ26gCdmZWudRAwqGq8vgkmOGQVuui97vQtSPTFDLoHVK2_CfReeECXY9ujQ3S5smD0BknR-KnVCgaBjtBi44fgcKie0GdwvTXhsatxUKIB9An8ykrb2uX0InqmROvg5f05i64-LK5PPsbnF6dnJ9V53GQF8zFATUWeUqGA1rUshaprpiBnpM5LJkpaEpIQKSmmImygoGxKVkDG6kyIdBa9u1Ptx7oD2YAJv2t5P-hODBO3QvPHN0av-NLecMbynJR5EDi8Fxjs1xGc5512DbStMGBHx0lRYlywbWNm0Zt_qGs7DiYkF1gFo2lOC_yXtRQtcG2U3dZrK8qrgiaMZElBA-v4P6ywJHS6sQaUDv5HAfO7gCb03w2gHnJMMN9OGd-dskB_vVuXB_KfsUp_ATBA0c8</recordid><startdate>20230208</startdate><enddate>20230208</enddate><creator>Alshammari, Fanar</creator><creator>Alam, Md Badrul</creator><creator>Song, Bo-Rim</creator><creator>Lee, Sang-Han</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8509-6827</orcidid><orcidid>https://orcid.org/0000-0002-2343-7315</orcidid><orcidid>https://orcid.org/0000-0002-7418-3650</orcidid></search><sort><creationdate>20230208</creationdate><title>Antioxidant, Tyrosinase, α-Glucosidase, and Elastase Enzyme Inhibition Activities of Optimized Unripe Ajwa Date Pulp ( Phoenix dactylifera ) Extracts by Response Surface Methodology</title><author>Alshammari, Fanar ; Alam, Md Badrul ; Song, Bo-Rim ; Lee, Sang-Han</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-eeb5a635afe5bbd8afbb9fe692b689a8582212dd505ad50efe8c897e49b4aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>alpha-Glucosidases - metabolism</topic><topic>Analysis</topic><topic>Antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>Design optimization</topic><topic>Diabetes</topic><topic>Elastase</topic><topic>Enzymes</topic><topic>Ethanol</topic><topic>Flavonoids</topic><topic>Food industry</topic><topic>Glucosidase</topic><topic>Health aspects</topic><topic>High resolution</topic><topic>Hydrolases</topic><topic>Independent variables</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Metabolites</topic><topic>Methods</topic><topic>Monophenol Monooxygenase - metabolism</topic><topic>Neutrophils</topic><topic>Optimization</topic><topic>Pancreatic Elastase - metabolism</topic><topic>Phenols</topic><topic>Phoeniceae - chemistry</topic><topic>Phoenix dactylifera</topic><topic>Plant extracts</topic><topic>Plant Extracts - pharmacology</topic><topic>Polyphenols</topic><topic>Pulmonary fibrosis</topic><topic>Reproducibility</topic><topic>Response surface methodology</topic><topic>Scavenging</topic><topic>Secondary metabolites</topic><topic>Statistical methods</topic><topic>Statistical significance</topic><topic>Tyrosinase</topic><topic>α-Glucosidase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alshammari, Fanar</creatorcontrib><creatorcontrib>Alam, Md Badrul</creatorcontrib><creatorcontrib>Song, Bo-Rim</creatorcontrib><creatorcontrib>Lee, Sang-Han</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alshammari, Fanar</au><au>Alam, Md Badrul</au><au>Song, Bo-Rim</au><au>Lee, Sang-Han</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant, Tyrosinase, α-Glucosidase, and Elastase Enzyme Inhibition Activities of Optimized Unripe Ajwa Date Pulp ( Phoenix dactylifera ) Extracts by Response Surface Methodology</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2023-02-08</date><risdate>2023</risdate><volume>24</volume><issue>4</issue><spage>3396</spage><pages>3396-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>The Ajwa date (
L., Arecaceae family) is a popular edible fruit consumed all over the world. The profiling of the polyphenolic compounds of optimized unripe Ajwa date pulp (URADP) extracts is scarce. The aim of this study was to extract polyphenols from URADP as effectively as possible by using response surface methodology (RSM). A central composite design (CCD) was used to optimize the extraction conditions with respect to ethanol concentration, extraction time, and temperature and to achieve the maximum amount of polyphenolic compounds. High-resolution mass spectrometry was used to identify the URADP's polyphenolic compounds. The DPPH-, ABTS-radical scavenging, α-glucosidase, elastase and tyrosinase enzyme inhibition of optimized extracts of URADP was also evaluated. According to RSM, the highest amounts of TPC (24.25 ± 1.02 mgGAE/g) and TFC (23.98 ± 0.65 mgCAE/g) were obtained at 52% ethanol, 81 min time, and 63 °C. Seventy (70) secondary metabolites, including phenolic, flavonoids, fatty acids, and sugar, were discovered using high-resolution mass spectrometry. In addition, twelve (12) new phytoconstituents were identified for the first time in this plant. Optimized URADP extract showed inhibition of DPPH-radical (IC
= 87.56 mg/mL), ABTS-radical (IC
= 172.36 mg/mL), α-glucosidase (IC
= 221.59 mg/mL), elastase (IC
= 372.25 mg/mL) and tyrosinase (IC
= 59.53 mg/mL) enzymes. The results revealed a significant amount of phytoconstituents, making it an excellent contender for the pharmaceutical and food industries.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36834805</pmid><doi>10.3390/ijms24043396</doi><orcidid>https://orcid.org/0000-0002-8509-6827</orcidid><orcidid>https://orcid.org/0000-0002-2343-7315</orcidid><orcidid>https://orcid.org/0000-0002-7418-3650</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2023-02, Vol.24 (4), p.3396 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9966286 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; MDPI - Multidisciplinary Digital Publishing Institute; PubMed Central |
subjects | alpha-Glucosidases - metabolism Analysis Antioxidants Antioxidants - pharmacology Design optimization Diabetes Elastase Enzymes Ethanol Flavonoids Food industry Glucosidase Health aspects High resolution Hydrolases Independent variables Mass spectrometry Mass spectroscopy Metabolites Methods Monophenol Monooxygenase - metabolism Neutrophils Optimization Pancreatic Elastase - metabolism Phenols Phoeniceae - chemistry Phoenix dactylifera Plant extracts Plant Extracts - pharmacology Polyphenols Pulmonary fibrosis Reproducibility Response surface methodology Scavenging Secondary metabolites Statistical methods Statistical significance Tyrosinase α-Glucosidase |
title | Antioxidant, Tyrosinase, α-Glucosidase, and Elastase Enzyme Inhibition Activities of Optimized Unripe Ajwa Date Pulp ( Phoenix dactylifera ) Extracts by Response Surface Methodology |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T18%3A43%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antioxidant,%20Tyrosinase,%20%CE%B1-Glucosidase,%20and%20Elastase%20Enzyme%20Inhibition%20Activities%20of%20Optimized%20Unripe%20Ajwa%20Date%20Pulp%20(%20Phoenix%20dactylifera%20)%20Extracts%20by%20Response%20Surface%20Methodology&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Alshammari,%20Fanar&rft.date=2023-02-08&rft.volume=24&rft.issue=4&rft.spage=3396&rft.pages=3396-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms24043396&rft_dat=%3Cgale_pubme%3EA751924175%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2779536570&rft_id=info:pmid/36834805&rft_galeid=A751924175&rfr_iscdi=true |