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Cyclotide nanotubes as a novel potential Drug-Delivery System: Characterization and biocompatibility
[Display omitted] •Cyclotide nanotubes are stable even at 200 °C.•Cyclotide nanotubes could efficiently entrap coumarin.•Cyclotide nanotubes could be stable after 3 months keeping at −20 °C.•Cyclotide nanotubes are biocompatible agents.•Cyclotide nanotubes could be used as immunomodulatory agents. C...
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Published in: | International journal of pharmaceutics 2023-07, Vol.642, p.123104-123104, Article 123104 |
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container_title | International journal of pharmaceutics |
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creator | Dayani, Ladan Aliomrani, Mehdi Hashempour, Hossein Varshosaz, Jaleh Dinani, Masoud Sadeghi Taheri, Azade |
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•Cyclotide nanotubes are stable even at 200 °C.•Cyclotide nanotubes could efficiently entrap coumarin.•Cyclotide nanotubes could be stable after 3 months keeping at −20 °C.•Cyclotide nanotubes are biocompatible agents.•Cyclotide nanotubes could be used as immunomodulatory agents.
Cyclotides are a class of cyclic peptides that can be self-assembled. This study aimed to discover the properties of cyclotide nanotubes. We performed differential scanning calorimetric (DSC) to characterize their properties. Then, we incorporated the coumarin as a probe and identified the morphology of nanostructures. The stability of cyclotide nanotubes after 3 months of keeping at −20 °C was determined by field emission scanning electron microscopy (FESEM). The cytocompatibility of cyclotide nanotubes was evaluated on peripheral blood mononuclear cells. In vivo, studies were also conducted on female C57BL/6 mice by intraperitoneally administration of nanotubes at 5, 50, and 100 mg/kg doses. Blood sampling was done before and 24 h after nanotube administration and complete blood count tests were conducted. DSC thermogram showed that the cyclotide nanotubes were stable after heating until 200 °C. Fluorescence microscopy images proved that the self-assembled structures of cyclotide can encapsulate the coumarin. FESEM proved that these nanotubes were stable even after 3 months. The results of the cytotoxicity assay and in-vivo study confirmed that these novel prepared nanotubes were biocompatible. These results suggested that the cyclotide nanotubes could be considered as a new carrier in biological fields while they are biocompatible. |
doi_str_mv | 10.1016/j.ijpharm.2023.123104 |
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•Cyclotide nanotubes are stable even at 200 °C.•Cyclotide nanotubes could efficiently entrap coumarin.•Cyclotide nanotubes could be stable after 3 months keeping at −20 °C.•Cyclotide nanotubes are biocompatible agents.•Cyclotide nanotubes could be used as immunomodulatory agents.
Cyclotides are a class of cyclic peptides that can be self-assembled. This study aimed to discover the properties of cyclotide nanotubes. We performed differential scanning calorimetric (DSC) to characterize their properties. Then, we incorporated the coumarin as a probe and identified the morphology of nanostructures. The stability of cyclotide nanotubes after 3 months of keeping at −20 °C was determined by field emission scanning electron microscopy (FESEM). The cytocompatibility of cyclotide nanotubes was evaluated on peripheral blood mononuclear cells. In vivo, studies were also conducted on female C57BL/6 mice by intraperitoneally administration of nanotubes at 5, 50, and 100 mg/kg doses. Blood sampling was done before and 24 h after nanotube administration and complete blood count tests were conducted. DSC thermogram showed that the cyclotide nanotubes were stable after heating until 200 °C. Fluorescence microscopy images proved that the self-assembled structures of cyclotide can encapsulate the coumarin. FESEM proved that these nanotubes were stable even after 3 months. The results of the cytotoxicity assay and in-vivo study confirmed that these novel prepared nanotubes were biocompatible. These results suggested that the cyclotide nanotubes could be considered as a new carrier in biological fields while they are biocompatible.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2023.123104</identifier><identifier>PMID: 37277089</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Animals ; Biocompatibility ; Cyclotides ; Female ; Leukocytes, Mononuclear ; Mice ; Mice, Inbred C57BL ; Nanotubes ; Self-assembly ; Stability</subject><ispartof>International journal of pharmaceutics, 2023-07, Vol.642, p.123104-123104, Article 123104</ispartof><rights>2023 Elsevier B.V.</rights><rights>Copyright © 2023 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-792e814d48c61e33239f1bd31ba5719805f517bb820d629586a27488caa3b4713</citedby><cites>FETCH-LOGICAL-c365t-792e814d48c61e33239f1bd31ba5719805f517bb820d629586a27488caa3b4713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37277089$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dayani, Ladan</creatorcontrib><creatorcontrib>Aliomrani, Mehdi</creatorcontrib><creatorcontrib>Hashempour, Hossein</creatorcontrib><creatorcontrib>Varshosaz, Jaleh</creatorcontrib><creatorcontrib>Dinani, Masoud Sadeghi</creatorcontrib><creatorcontrib>Taheri, Azade</creatorcontrib><title>Cyclotide nanotubes as a novel potential Drug-Delivery System: Characterization and biocompatibility</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted]
•Cyclotide nanotubes are stable even at 200 °C.•Cyclotide nanotubes could efficiently entrap coumarin.•Cyclotide nanotubes could be stable after 3 months keeping at −20 °C.•Cyclotide nanotubes are biocompatible agents.•Cyclotide nanotubes could be used as immunomodulatory agents.
Cyclotides are a class of cyclic peptides that can be self-assembled. This study aimed to discover the properties of cyclotide nanotubes. We performed differential scanning calorimetric (DSC) to characterize their properties. Then, we incorporated the coumarin as a probe and identified the morphology of nanostructures. The stability of cyclotide nanotubes after 3 months of keeping at −20 °C was determined by field emission scanning electron microscopy (FESEM). The cytocompatibility of cyclotide nanotubes was evaluated on peripheral blood mononuclear cells. In vivo, studies were also conducted on female C57BL/6 mice by intraperitoneally administration of nanotubes at 5, 50, and 100 mg/kg doses. Blood sampling was done before and 24 h after nanotube administration and complete blood count tests were conducted. DSC thermogram showed that the cyclotide nanotubes were stable after heating until 200 °C. Fluorescence microscopy images proved that the self-assembled structures of cyclotide can encapsulate the coumarin. FESEM proved that these nanotubes were stable even after 3 months. The results of the cytotoxicity assay and in-vivo study confirmed that these novel prepared nanotubes were biocompatible. These results suggested that the cyclotide nanotubes could be considered as a new carrier in biological fields while they are biocompatible.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Biocompatibility</subject><subject>Cyclotides</subject><subject>Female</subject><subject>Leukocytes, Mononuclear</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Nanotubes</subject><subject>Self-assembly</subject><subject>Stability</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v2zAMhoVhw5qm_QkddOzFqT5sS96lGJJ-DAiww7azoA9mVWBbriQHcH_9HCTrdQAJAsRLvuSD0A0lK0pofbdf-f3womO3YoTxFWWckvIDWlApeMFLUX9EC8KFLCoq-AW6TGlPCKkZ5Z_RBRdMCCKbBXLrybYhewe4133Io4GE9Ry4Dwdo8RAy9NnrFm_i-KfYQOsPECf8c0oZuq94PZ-gbYbo33T2oce6d9j4YEM3zA3jW5-nK_Rpp9sE1-e6RL8fH36tn4vtj6fv62_bwvK6yoVoGEhaulLamgLnjDc7ahynRleCNpJUu_kZYyQjrmZNJWvNRCml1ZqbUlC-RLenvUMMryOkrDqfLLSt7iGMSTHJOCmPOUurk9TGkFKEnRqi73ScFCXqCFjt1RmwOgJWJ8Dz3JezxWg6cO9T_4jOgvuTAOZHDx6iStZDb8H5CDYrF_x_LP4Cp-ePLg</recordid><startdate>20230725</startdate><enddate>20230725</enddate><creator>Dayani, Ladan</creator><creator>Aliomrani, Mehdi</creator><creator>Hashempour, Hossein</creator><creator>Varshosaz, Jaleh</creator><creator>Dinani, Masoud Sadeghi</creator><creator>Taheri, Azade</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>20230725</creationdate><title>Cyclotide nanotubes as a novel potential Drug-Delivery System: Characterization and biocompatibility</title><author>Dayani, Ladan ; Aliomrani, Mehdi ; Hashempour, Hossein ; Varshosaz, Jaleh ; Dinani, Masoud Sadeghi ; Taheri, Azade</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-792e814d48c61e33239f1bd31ba5719805f517bb820d629586a27488caa3b4713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Biocompatibility</topic><topic>Cyclotides</topic><topic>Female</topic><topic>Leukocytes, Mononuclear</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Nanotubes</topic><topic>Self-assembly</topic><topic>Stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dayani, Ladan</creatorcontrib><creatorcontrib>Aliomrani, Mehdi</creatorcontrib><creatorcontrib>Hashempour, Hossein</creatorcontrib><creatorcontrib>Varshosaz, Jaleh</creatorcontrib><creatorcontrib>Dinani, Masoud Sadeghi</creatorcontrib><creatorcontrib>Taheri, Azade</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 pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dayani, Ladan</au><au>Aliomrani, Mehdi</au><au>Hashempour, Hossein</au><au>Varshosaz, Jaleh</au><au>Dinani, Masoud Sadeghi</au><au>Taheri, Azade</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyclotide nanotubes as a novel potential Drug-Delivery System: Characterization and biocompatibility</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2023-07-25</date><risdate>2023</risdate><volume>642</volume><spage>123104</spage><epage>123104</epage><pages>123104-123104</pages><artnum>123104</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
•Cyclotide nanotubes are stable even at 200 °C.•Cyclotide nanotubes could efficiently entrap coumarin.•Cyclotide nanotubes could be stable after 3 months keeping at −20 °C.•Cyclotide nanotubes are biocompatible agents.•Cyclotide nanotubes could be used as immunomodulatory agents.
Cyclotides are a class of cyclic peptides that can be self-assembled. This study aimed to discover the properties of cyclotide nanotubes. We performed differential scanning calorimetric (DSC) to characterize their properties. Then, we incorporated the coumarin as a probe and identified the morphology of nanostructures. The stability of cyclotide nanotubes after 3 months of keeping at −20 °C was determined by field emission scanning electron microscopy (FESEM). The cytocompatibility of cyclotide nanotubes was evaluated on peripheral blood mononuclear cells. In vivo, studies were also conducted on female C57BL/6 mice by intraperitoneally administration of nanotubes at 5, 50, and 100 mg/kg doses. Blood sampling was done before and 24 h after nanotube administration and complete blood count tests were conducted. DSC thermogram showed that the cyclotide nanotubes were stable after heating until 200 °C. Fluorescence microscopy images proved that the self-assembled structures of cyclotide can encapsulate the coumarin. FESEM proved that these nanotubes were stable even after 3 months. The results of the cytotoxicity assay and in-vivo study confirmed that these novel prepared nanotubes were biocompatible. These results suggested that the cyclotide nanotubes could be considered as a new carrier in biological fields while they are biocompatible.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>37277089</pmid><doi>10.1016/j.ijpharm.2023.123104</doi><tpages>1</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Biocompatibility Cyclotides Female Leukocytes, Mononuclear Mice Mice, Inbred C57BL Nanotubes Self-assembly Stability |
title | Cyclotide nanotubes as a novel potential Drug-Delivery System: Characterization and biocompatibility |
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