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  1. Article: Fast Absorbent and Highly Bioorthogonal Hydrogels Developed by IEDDA Click Reaction for Drug Delivery Application.

    Joo, Soo-Bin / Gulfam, Muhammad / Jo, Sung-Han / Jo, Yi-Jun / Vu, Trung Thang / Park, Sang-Hyug / Gal, Yeong-Soon / Lim, Kwon Taek

    Materials (Basel, Switzerland)

    2022  Volume 15, Issue 20

    Abstract: In this work, we engineered highly biocompatible and fast absorbent injectable hydrogels derived from norbornene (Nb)-functionalized hyaluronic acid (HA-Nb) and a water-soluble cross-linker possessing tetrazine (Tz) functional groups on both ends of ... ...

    Abstract In this work, we engineered highly biocompatible and fast absorbent injectable hydrogels derived from norbornene (Nb)-functionalized hyaluronic acid (HA-Nb) and a water-soluble cross-linker possessing tetrazine (Tz) functional groups on both ends of polyethylene glycol (PEG-DTz). The by-product (nitrogen gas) of the inverse electron demand Diels−Alder (IEDDA) cross-linking reaction carved porosity in the resulting hydrogels. By varying the molar ratio of HA-Nb and PEG-DTz (Nb:Tz = 10:10, 10:5, 10:2.5), we were able to formulate hydrogels with tunable porosity, gelation time, mechanical strength, and swelling ratios. The hydrogels formed quickly (gelation time < 100 s), offering a possibility to use them as an injectable drug delivery system. The experimental data showed rapid swelling and a high swelling ratio thanks to the existence of PEG chains and highly porous architectures of the hydrogels. The hydrogels were able to encapsulate a high amount of curcumin (~99%) and released the encapsulated curcumin in a temporal pattern. The PEG-DTz cross-linker, HA-Nb, and the resulting hydrogels showed no cytotoxicity in HEK-293 cells. These fast absorbent hydrogels with excellent biocompatibility fabricated from HA-Nb and the IEDDA click-able cross-linker could be promising drug carriers for injectable drug delivery applications.
    Language English
    Publishing date 2022-10-13
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2487261-1
    ISSN 1996-1944
    ISSN 1996-1944
    DOI 10.3390/ma15207128
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Multi-stimuli responsive hydrogels derived from hyaluronic acid for cancer therapy application.

    Jo, Yi-Jun / Gulfam, Muhammad / Jo, Sung-Han / Gal, Yeong-Soon / Oh, Chul-Woong / Park, Sang-Hyug / Lim, Kwon Taek

    Carbohydrate polymers

    2022  Volume 286, Page(s) 119303

    Abstract: One of the most promising strategies for the controlled release of therapeutic molecules is stimuli-responsive and biodegradable hydrogels developed from natural polymers. However, current strategies to development stimuli-responsive hydrogels lack ... ...

    Abstract One of the most promising strategies for the controlled release of therapeutic molecules is stimuli-responsive and biodegradable hydrogels developed from natural polymers. However, current strategies to development stimuli-responsive hydrogels lack precise control over drug release profile and use cytotoxic materials during preparation. To address these issues, multi-stimuli responsive hydrogels derived from hyaluronic acid and diselenide based cross-linker were developed for the controlled release of doxorubicin (DOX). Hydrogels were rapidly formed via an inverse electron demand Diels-Alder click chemistry and encapsulated DOX/indocyanine green (ICG) in their porous networks. The hydrogels showed a rapid release of DOX in acidic (pH 5), reducing (10 mmol DTT), and oxidizing medium (0.5% H
    MeSH term(s) Doxorubicin/chemistry ; Doxorubicin/pharmacology ; Drug Liberation ; Humans ; Hyaluronic Acid/chemistry ; Hyaluronic Acid/pharmacology ; Hydrogels/chemistry ; Hydrogels/pharmacology ; Hydrogen Peroxide ; Neoplasms/drug therapy
    Chemical Substances Hydrogels ; Doxorubicin (80168379AG) ; Hyaluronic Acid (9004-61-9) ; Hydrogen Peroxide (BBX060AN9V)
    Language English
    Publishing date 2022-03-01
    Publishing country England
    Document type Journal Article
    ZDB-ID 1501516-6
    ISSN 1879-1344 ; 0144-8617
    ISSN (online) 1879-1344
    ISSN 0144-8617
    DOI 10.1016/j.carbpol.2022.119303
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Dual cross-linked chitosan/alginate hydrogels prepared by Nb-Tz ‘click’ reaction for pH responsive drug delivery

    Hoang, Huong Thi / Vu, Trung Thang / Karthika, Viswanathan / Jo, Sung-Han / Jo, Yi-Jun / Seo, Jeong-Woo / Oh, Chul-Woong / Park, Sang-Hyug / Lim, Kwon Taek

    Carbohydrate polymers. 2022 Mar. 18,

    2022  

    Abstract: A novel physically and chemically double-crosslinked hydrogel derived from chitosan oligosaccharide/alginate (COS/Alg) was developed by using norbornene (Nb)-tetrazine (Tz) click reaction for ketoprofen delivery. The properties of the hydrogel were ... ...

    Abstract A novel physically and chemically double-crosslinked hydrogel derived from chitosan oligosaccharide/alginate (COS/Alg) was developed by using norbornene (Nb)-tetrazine (Tz) click reaction for ketoprofen delivery. The properties of the hydrogel were evaluated by rheological, FTIR, TGA, XRD, SEM, swelling and drug release studies. The Nb-Tz chemical cross-linking facilitated outstanding hydrophobic drug loading (44% wt/wt of ketoprofen) and sustained release through a hydrophobic interaction mechanism between the drug and the used polysaccharides. The COS/Alg electrostatics network (10/10 of NH₂/COOH molar ratio) generated the pH responsiveness, suppressing the release in simulated gastric fluid (below 10% for 2 h) and enhancing the release in simulated intestinal fluids (up to 84% for 24 h). The prepared hydrogel was non-toxic to human HEK-293 cells (95% cell viability). This work opens up a potential approach for preparing hydrophilic hydrogels from natural polysaccharides that can be used in the delivery of hydrophobic drugs.
    Keywords alginates ; cell viability ; chitosan ; crosslinking ; gastric juice ; humans ; hydrogels ; hydrophilicity ; hydrophobic bonding ; hydrophobicity ; intestines ; ketoprofen ; oligosaccharides ; pH
    Language English
    Dates of publication 2022-0318
    Publishing place Elsevier Ltd
    Document type Article
    Note Pre-press version
    ZDB-ID 1501516-6
    ISSN 1879-1344 ; 0144-8617
    ISSN (online) 1879-1344
    ISSN 0144-8617
    DOI 10.1016/j.carbpol.2022.119389
    Database NAL-Catalogue (AGRICOLA)

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  4. Article: Multi-stimuli responsive hydrogels derived from hyaluronic acid for cancer therapy application

    Jo, Yi-Jun / Gulfam, Muhammad / Jo, Sung-Han / Gal, Yeong-Soon / Oh, Chul-Woong / Park, Sang-Hyug / Lim, Kwon Taek

    Carbohydrate polymers. 2022 June 15, v. 286

    2022  

    Abstract: One of the most promising strategies for the controlled release of therapeutic molecules is stimuli-responsive and biodegradable hydrogels developed from natural polymers. However, current strategies to development stimuli-responsive hydrogels lack ... ...

    Abstract One of the most promising strategies for the controlled release of therapeutic molecules is stimuli-responsive and biodegradable hydrogels developed from natural polymers. However, current strategies to development stimuli-responsive hydrogels lack precise control over drug release profile and use cytotoxic materials during preparation. To address these issues, multi-stimuli responsive hydrogels derived from hyaluronic acid and diselenide based cross-linker were developed for the controlled release of doxorubicin (DOX). Hydrogels were rapidly formed via an inverse electron demand Diels–Alder click chemistry and encapsulated DOX/indocyanine green (ICG) in their porous networks. The hydrogels showed a rapid release of DOX in acidic (pH 5), reducing (10 mmol DTT), and oxidizing medium (0.5% H₂O₂), and after NIR irradiation. The in vitro experiments demonstrated that hydrogels were highly cytocompatible and the DOX-loaded hydrogels induced similar anti-tumor effect as compared to that of the free-DOX. Furthermore, DOX + ICG loaded hydrogels increased the antitumor efficacy of DOX after NIR irradiation.
    Keywords antineoplastic activity ; biodegradability ; cancer therapy ; cycloaddition reactions ; cytotoxicity ; doxorubicin ; hyaluronic acid ; hydrogels ; irradiation ; pH
    Language English
    Dates of publication 2022-0615
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 1501516-6
    ISSN 1879-1344 ; 0144-8617
    ISSN (online) 1879-1344
    ISSN 0144-8617
    DOI 10.1016/j.carbpol.2022.119303
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: Dual cross-linked chitosan/alginate hydrogels prepared by Nb-Tz 'click' reaction for pH responsive drug delivery.

    Hoang, Huong Thi / Vu, Trung Thang / Karthika, Viswanathan / Jo, Sung-Han / Jo, Yi-Jun / Seo, Jeong-Woo / Oh, Chul-Woong / Park, Sang-Hyug / Lim, Kwon Taek

    Carbohydrate polymers

    2022  Volume 288, Page(s) 119389

    Abstract: A novel physically and chemically double-crosslinked hydrogel derived from chitosan oligosaccharide/alginate (COS/Alg) was developed by using norbornene (Nb)-tetrazine (Tz) click reaction for ketoprofen delivery. The properties of the hydrogel were ... ...

    Abstract A novel physically and chemically double-crosslinked hydrogel derived from chitosan oligosaccharide/alginate (COS/Alg) was developed by using norbornene (Nb)-tetrazine (Tz) click reaction for ketoprofen delivery. The properties of the hydrogel were evaluated by rheological, FTIR, TGA, XRD, SEM, swelling and drug release studies. The Nb-Tz chemical cross-linking facilitated outstanding hydrophobic drug loading (44% wt/wt of ketoprofen) and sustained release through a hydrophobic interaction mechanism between the drug and the used polysaccharides. The COS/Alg electrostatics network (10/10 of NH
    MeSH term(s) Alginates/chemistry ; Chitosan/chemistry ; Drug Carriers/chemistry ; Drug Delivery Systems ; Drug Liberation ; HEK293 Cells ; Humans ; Hydrogels/chemistry ; Hydrogen-Ion Concentration ; Ketoprofen ; Niobium ; Norbornanes
    Chemical Substances Alginates ; Drug Carriers ; Hydrogels ; Norbornanes ; Niobium (05175J654G) ; 2-norbornene (2Q51FLS550) ; Chitosan (9012-76-4) ; Ketoprofen (90Y4QC304K)
    Language English
    Publishing date 2022-03-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 1501516-6
    ISSN 1879-1344 ; 0144-8617
    ISSN (online) 1879-1344
    ISSN 0144-8617
    DOI 10.1016/j.carbpol.2022.119389
    Database MEDical Literature Analysis and Retrieval System OnLINE

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