Anti-allergic and Profilaggrin (ProFLG)-mRNA expression modulatory effects of sacran
•Sacran is a sulfated glucosaminoglycan-like polysaccharide extracted from river alga Aphanothece sacrum.•Topical sacran markedly upregulates filaggrin production in hapten-induced murine model of contact hypersensitivity.•Topical sacran alleviates skin lesions in dust-mite extracts (DME)-induced at...
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creator | Ngatu, Nlandu R. Motoyama, Keiichi Nishimura, Yasumitsu Okajima, Maiko Kaneko Hirota, Ryoji Higashi, Taishi Lee, Suni Arima, Hidetoshi Ikeda, Mitsunori Nojima, Sayumi Kaneko, Tatsuo |
description | •Sacran is a sulfated glucosaminoglycan-like polysaccharide extracted from river alga Aphanothece sacrum.•Topical sacran markedly upregulates filaggrin production in hapten-induced murine model of contact hypersensitivity.•Topical sacran alleviates skin lesions in dust-mite extracts (DME)-induced atopic dermatitis-like disease in NC/Nga mice.•Sacran might serve as a natural skin barrier enhancer and anti-allergic agent.
Atopic dermatitis (AD) is a skin disorder characterized by filaggrin (FLG) defect. We evaluated sacran’s effects on dust-mite extracts (DME)-induced AD-like disease and also its effect on profilaggrin (proFLG) in a murine model of 2,4-dinitroflurobenze (DNFB)-induced contact hypersensitivity. In the murine AD-like disease model, allergic NC/Nga mice (N=60) were randomly divided into five treatment groups of 12 animals each: 0.2% and 1%sacran; 0.1% Tacrolimus; Vaseline and buffer-treated controls. Blood samples were drawn and serum levels of representative Th-1, Th-2 and also Th-17 (IL-17A) cytokines were assayed by Cytometric Bead Array (CBA). In the contact hypersensitivity model, diseased NC/Nga mice (N=20) were divided into four groups of five mice each [0.05%sacran, 0.05% chondroitin sulfate (CS), 0.5% prednisolone (PD), non-treated control group] and were treated for 14days. Skin biopsies were performed for the measurement of proFLG-mRNA by real-time PCR. Sacran solutions and 0.1%Tacrolimus reduced disease severity, suppressed histological changes and decreased the serum Th-1 (IFN-γ, TNF-α, IL-2) and Th-2 (IL-4, IL-6, IL-10) cytokines in allergic mice (vs. controls). Additionally, a marked increase of proFLG-mRNA expression was observed in 0.05%sacran group (vs. control 0.05% CS and 0.5% PD groups). Thus, Sacran might be useful as a natural skin barrier enhancer and anti-allergic agent. |
doi_str_mv | 10.1016/j.ijbiomac.2017.05.049 |
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Atopic dermatitis (AD) is a skin disorder characterized by filaggrin (FLG) defect. We evaluated sacran’s effects on dust-mite extracts (DME)-induced AD-like disease and also its effect on profilaggrin (proFLG) in a murine model of 2,4-dinitroflurobenze (DNFB)-induced contact hypersensitivity. In the murine AD-like disease model, allergic NC/Nga mice (N=60) were randomly divided into five treatment groups of 12 animals each: 0.2% and 1%sacran; 0.1% Tacrolimus; Vaseline and buffer-treated controls. Blood samples were drawn and serum levels of representative Th-1, Th-2 and also Th-17 (IL-17A) cytokines were assayed by Cytometric Bead Array (CBA). In the contact hypersensitivity model, diseased NC/Nga mice (N=20) were divided into four groups of five mice each [0.05%sacran, 0.05% chondroitin sulfate (CS), 0.5% prednisolone (PD), non-treated control group] and were treated for 14days. Skin biopsies were performed for the measurement of proFLG-mRNA by real-time PCR. Sacran solutions and 0.1%Tacrolimus reduced disease severity, suppressed histological changes and decreased the serum Th-1 (IFN-γ, TNF-α, IL-2) and Th-2 (IL-4, IL-6, IL-10) cytokines in allergic mice (vs. controls). Additionally, a marked increase of proFLG-mRNA expression was observed in 0.05%sacran group (vs. control 0.05% CS and 0.5% PD groups). Thus, Sacran might be useful as a natural skin barrier enhancer and anti-allergic agent.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2017.05.049</identifier><identifier>PMID: 28522399</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Administration, Topical ; Animals ; Anti-Allergic Agents - administration & dosage ; Anti-Allergic Agents - pharmacology ; Anti-Allergic Agents - therapeutic use ; Atopic dermatitis ; Cytokines - blood ; Dermatitis, Atopic - blood ; Dermatitis, Atopic - drug therapy ; Dermatitis, Atopic - genetics ; Dermatitis, Atopic - immunology ; Female ; Intermediate Filament Proteins - genetics ; Mice ; Polysaccharides - administration & dosage ; Polysaccharides - pharmacology ; Polysaccharides - therapeutic use ; Profilaggrin ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Sacran ; Skin - drug effects ; Skin - pathology ; T-Lymphocytes, Helper-Inducer - drug effects ; T-Lymphocytes, Helper-Inducer - metabolism ; Up-Regulation - drug effects</subject><ispartof>International journal of biological macromolecules, 2017-12, Vol.105 (Pt 2), p.1532-1538</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-e697c203f231a68a115293abfc2fb28f1a075d316c9e8f0deca540e4a7957fac3</citedby><cites>FETCH-LOGICAL-c434t-e697c203f231a68a115293abfc2fb28f1a075d316c9e8f0deca540e4a7957fac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijbiomac.2017.05.049$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28522399$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ngatu, Nlandu R.</creatorcontrib><creatorcontrib>Motoyama, Keiichi</creatorcontrib><creatorcontrib>Nishimura, Yasumitsu</creatorcontrib><creatorcontrib>Okajima, Maiko Kaneko</creatorcontrib><creatorcontrib>Hirota, Ryoji</creatorcontrib><creatorcontrib>Higashi, Taishi</creatorcontrib><creatorcontrib>Lee, Suni</creatorcontrib><creatorcontrib>Arima, Hidetoshi</creatorcontrib><creatorcontrib>Ikeda, Mitsunori</creatorcontrib><creatorcontrib>Nojima, Sayumi</creatorcontrib><creatorcontrib>Kaneko, Tatsuo</creatorcontrib><title>Anti-allergic and Profilaggrin (ProFLG)-mRNA expression modulatory effects of sacran</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>•Sacran is a sulfated glucosaminoglycan-like polysaccharide extracted from river alga Aphanothece sacrum.•Topical sacran markedly upregulates filaggrin production in hapten-induced murine model of contact hypersensitivity.•Topical sacran alleviates skin lesions in dust-mite extracts (DME)-induced atopic dermatitis-like disease in NC/Nga mice.•Sacran might serve as a natural skin barrier enhancer and anti-allergic agent.
Atopic dermatitis (AD) is a skin disorder characterized by filaggrin (FLG) defect. We evaluated sacran’s effects on dust-mite extracts (DME)-induced AD-like disease and also its effect on profilaggrin (proFLG) in a murine model of 2,4-dinitroflurobenze (DNFB)-induced contact hypersensitivity. In the murine AD-like disease model, allergic NC/Nga mice (N=60) were randomly divided into five treatment groups of 12 animals each: 0.2% and 1%sacran; 0.1% Tacrolimus; Vaseline and buffer-treated controls. Blood samples were drawn and serum levels of representative Th-1, Th-2 and also Th-17 (IL-17A) cytokines were assayed by Cytometric Bead Array (CBA). In the contact hypersensitivity model, diseased NC/Nga mice (N=20) were divided into four groups of five mice each [0.05%sacran, 0.05% chondroitin sulfate (CS), 0.5% prednisolone (PD), non-treated control group] and were treated for 14days. Skin biopsies were performed for the measurement of proFLG-mRNA by real-time PCR. Sacran solutions and 0.1%Tacrolimus reduced disease severity, suppressed histological changes and decreased the serum Th-1 (IFN-γ, TNF-α, IL-2) and Th-2 (IL-4, IL-6, IL-10) cytokines in allergic mice (vs. controls). Additionally, a marked increase of proFLG-mRNA expression was observed in 0.05%sacran group (vs. control 0.05% CS and 0.5% PD groups). Thus, Sacran might be useful as a natural skin barrier enhancer and anti-allergic agent.</description><subject>Administration, Topical</subject><subject>Animals</subject><subject>Anti-Allergic Agents - administration & dosage</subject><subject>Anti-Allergic Agents - pharmacology</subject><subject>Anti-Allergic Agents - therapeutic use</subject><subject>Atopic dermatitis</subject><subject>Cytokines - blood</subject><subject>Dermatitis, Atopic - blood</subject><subject>Dermatitis, Atopic - drug therapy</subject><subject>Dermatitis, Atopic - genetics</subject><subject>Dermatitis, Atopic - immunology</subject><subject>Female</subject><subject>Intermediate Filament Proteins - genetics</subject><subject>Mice</subject><subject>Polysaccharides - administration & dosage</subject><subject>Polysaccharides - pharmacology</subject><subject>Polysaccharides - therapeutic use</subject><subject>Profilaggrin</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Sacran</subject><subject>Skin - drug effects</subject><subject>Skin - pathology</subject><subject>T-Lymphocytes, Helper-Inducer - drug effects</subject><subject>T-Lymphocytes, Helper-Inducer - metabolism</subject><subject>Up-Regulation - drug effects</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v2zAMhoVhRZt2_QuBj93BHiVZtnVbUKwfQLAWRXcWaJkKFNhWJjnF-u_nLs2uPREknpcEH8aWHAoOvPq2Lfy29WFAWwjgdQGqgFJ_Ygve1DoHAPmZLYCXPG-4hDN2ntJ2nlaKN6fsTDRKCKn1gj2vxsnn2PcUN95mOHbZYwzO97jZRD9mV3N3s779mg9PP1cZ_dlFSsmHMRtCt-9xCvE1I-fITikLLktoI45f2InDPtHle71gv25-PF_f5euH2_vr1Tq3pSynnCpdWwHSCcmxapBzJbTE1lnhWtE4jlCrTvLKamocdGRRlUAl1lrVDq28YFeHvbsYfu8pTWbwyVLf40hhnwzXAI0sValntDqgNoaUIjmzi37A-Go4mDejZmuORs2bUQPKwL_g8v3Gvh2o-x87KpyB7weA5k9fPEWTrKfRUufjrMV0wX904y97rYqh</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Ngatu, Nlandu R.</creator><creator>Motoyama, Keiichi</creator><creator>Nishimura, Yasumitsu</creator><creator>Okajima, Maiko Kaneko</creator><creator>Hirota, Ryoji</creator><creator>Higashi, Taishi</creator><creator>Lee, Suni</creator><creator>Arima, Hidetoshi</creator><creator>Ikeda, Mitsunori</creator><creator>Nojima, Sayumi</creator><creator>Kaneko, Tatsuo</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>201712</creationdate><title>Anti-allergic and Profilaggrin (ProFLG)-mRNA expression modulatory effects of sacran</title><author>Ngatu, Nlandu R. ; Motoyama, Keiichi ; Nishimura, Yasumitsu ; Okajima, Maiko Kaneko ; Hirota, Ryoji ; Higashi, Taishi ; Lee, Suni ; Arima, Hidetoshi ; Ikeda, Mitsunori ; Nojima, Sayumi ; Kaneko, Tatsuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-e697c203f231a68a115293abfc2fb28f1a075d316c9e8f0deca540e4a7957fac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Administration, Topical</topic><topic>Animals</topic><topic>Anti-Allergic Agents - administration & dosage</topic><topic>Anti-Allergic Agents - pharmacology</topic><topic>Anti-Allergic Agents - therapeutic use</topic><topic>Atopic dermatitis</topic><topic>Cytokines - blood</topic><topic>Dermatitis, Atopic - blood</topic><topic>Dermatitis, Atopic - drug therapy</topic><topic>Dermatitis, Atopic - genetics</topic><topic>Dermatitis, Atopic - immunology</topic><topic>Female</topic><topic>Intermediate Filament Proteins - genetics</topic><topic>Mice</topic><topic>Polysaccharides - administration & dosage</topic><topic>Polysaccharides - pharmacology</topic><topic>Polysaccharides - therapeutic use</topic><topic>Profilaggrin</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Sacran</topic><topic>Skin - drug effects</topic><topic>Skin - pathology</topic><topic>T-Lymphocytes, Helper-Inducer - drug effects</topic><topic>T-Lymphocytes, Helper-Inducer - metabolism</topic><topic>Up-Regulation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ngatu, Nlandu R.</creatorcontrib><creatorcontrib>Motoyama, Keiichi</creatorcontrib><creatorcontrib>Nishimura, Yasumitsu</creatorcontrib><creatorcontrib>Okajima, Maiko Kaneko</creatorcontrib><creatorcontrib>Hirota, Ryoji</creatorcontrib><creatorcontrib>Higashi, Taishi</creatorcontrib><creatorcontrib>Lee, Suni</creatorcontrib><creatorcontrib>Arima, Hidetoshi</creatorcontrib><creatorcontrib>Ikeda, Mitsunori</creatorcontrib><creatorcontrib>Nojima, Sayumi</creatorcontrib><creatorcontrib>Kaneko, Tatsuo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ngatu, Nlandu R.</au><au>Motoyama, Keiichi</au><au>Nishimura, Yasumitsu</au><au>Okajima, Maiko Kaneko</au><au>Hirota, Ryoji</au><au>Higashi, Taishi</au><au>Lee, Suni</au><au>Arima, Hidetoshi</au><au>Ikeda, Mitsunori</au><au>Nojima, Sayumi</au><au>Kaneko, Tatsuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-allergic and Profilaggrin (ProFLG)-mRNA expression modulatory effects of sacran</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2017-12</date><risdate>2017</risdate><volume>105</volume><issue>Pt 2</issue><spage>1532</spage><epage>1538</epage><pages>1532-1538</pages><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>•Sacran is a sulfated glucosaminoglycan-like polysaccharide extracted from river alga Aphanothece sacrum.•Topical sacran markedly upregulates filaggrin production in hapten-induced murine model of contact hypersensitivity.•Topical sacran alleviates skin lesions in dust-mite extracts (DME)-induced atopic dermatitis-like disease in NC/Nga mice.•Sacran might serve as a natural skin barrier enhancer and anti-allergic agent.
Atopic dermatitis (AD) is a skin disorder characterized by filaggrin (FLG) defect. We evaluated sacran’s effects on dust-mite extracts (DME)-induced AD-like disease and also its effect on profilaggrin (proFLG) in a murine model of 2,4-dinitroflurobenze (DNFB)-induced contact hypersensitivity. In the murine AD-like disease model, allergic NC/Nga mice (N=60) were randomly divided into five treatment groups of 12 animals each: 0.2% and 1%sacran; 0.1% Tacrolimus; Vaseline and buffer-treated controls. Blood samples were drawn and serum levels of representative Th-1, Th-2 and also Th-17 (IL-17A) cytokines were assayed by Cytometric Bead Array (CBA). In the contact hypersensitivity model, diseased NC/Nga mice (N=20) were divided into four groups of five mice each [0.05%sacran, 0.05% chondroitin sulfate (CS), 0.5% prednisolone (PD), non-treated control group] and were treated for 14days. Skin biopsies were performed for the measurement of proFLG-mRNA by real-time PCR. Sacran solutions and 0.1%Tacrolimus reduced disease severity, suppressed histological changes and decreased the serum Th-1 (IFN-γ, TNF-α, IL-2) and Th-2 (IL-4, IL-6, IL-10) cytokines in allergic mice (vs. controls). Additionally, a marked increase of proFLG-mRNA expression was observed in 0.05%sacran group (vs. control 0.05% CS and 0.5% PD groups). Thus, Sacran might be useful as a natural skin barrier enhancer and anti-allergic agent.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28522399</pmid><doi>10.1016/j.ijbiomac.2017.05.049</doi><tpages>7</tpages></addata></record> |
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subjects | Administration, Topical Animals Anti-Allergic Agents - administration & dosage Anti-Allergic Agents - pharmacology Anti-Allergic Agents - therapeutic use Atopic dermatitis Cytokines - blood Dermatitis, Atopic - blood Dermatitis, Atopic - drug therapy Dermatitis, Atopic - genetics Dermatitis, Atopic - immunology Female Intermediate Filament Proteins - genetics Mice Polysaccharides - administration & dosage Polysaccharides - pharmacology Polysaccharides - therapeutic use Profilaggrin RNA, Messenger - genetics RNA, Messenger - metabolism Sacran Skin - drug effects Skin - pathology T-Lymphocytes, Helper-Inducer - drug effects T-Lymphocytes, Helper-Inducer - metabolism Up-Regulation - drug effects |
title | Anti-allergic and Profilaggrin (ProFLG)-mRNA expression modulatory effects of sacran |
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