Layer-by-Layer Assembly of Inactivated Poliovirus and N-Trimethyl Chitosan on pH-Sensitive Microneedles for Dermal Vaccination
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van der Maaden, Koen
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Sekerdag, Emine
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Leiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, NetherlandsLeiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, Netherlands
Sekerdag, Emine
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Schipper, Pim
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Leiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, NetherlandsLeiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, Netherlands
Schipper, Pim
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Kersten, Gideon
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Leiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, Netherlands
Inst Translat Vaccinol Intravacc, NL-3720 AL Bilthoven, NetherlandsLeiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, Netherlands
Kersten, Gideon
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Jiskoot, Wim
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Bouwstra, Joke
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Leiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, NetherlandsLeiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, Netherlands
Bouwstra, Joke
[1
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[1] Leiden Univ, LACDR, Div Drug Delivery Technol, NL-2311 EZ Leiden, Netherlands
[2] Inst Translat Vaccinol Intravacc, NL-3720 AL Bilthoven, Netherlands
The aim of this work was to coat pH-sensitive microneedle arrays with inactivated polio vaccine (IPV) particles and N-trimethyl chitosan chloride (TMC) via electrostatic interactions, and assess the immunogenicity of the vaccine after topical application of the coated microneedles in rats. The surface of 200 mu m long microneedles was first chemically modified with pH-sensitive (pyridine) groups and then coated with negatively charged IPV and a positively charged polymer (TMC). To obtain a sufficient high antigen dose, 10 layers of IPV were alternately coated with TMC. The binding of IPV and TMC onto pH-sensitive microneedles was quantified and visualized by using fluorescently labeled TMC and IPV. The release of IPV and TMC from the microneedles was evaluated in ex vivo human skin by fluorescence and the immunogenicity of (unlabeled) IPV was assessed after topical application of the coated microneedles in rats. pH-sensitive microneedles were homogeneously coated with 10 layers of both IPV and TMC, resulting in 45 D antigen units IPV and 700 ng TMC per microneedle array. Fluorescence microscopy imaging revealed that both IPV and TMC were released into ex vivo human skin upon application of the coated microneedles. Finally, in vivo application of IPV-TMC-coated pH-sensitive microneedles in rats led to the induction of IPV specific antibody responses, illustrating that they are practically applicable. Topical administration of pH-sensitive microneedles coated with polyelectrolyte multinanolayers of antigens and oppositely charged polymers may be a useful approach for microneedle-based vaccination.
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Sharif Univ Technol, Dept Mat Sci & Engn, Polymer Mat Res Grp PMRG, POB 11365-9466, Tehran, IranSharif Univ Technol, Dept Mat Sci & Engn, Polymer Mat Res Grp PMRG, POB 11365-9466, Tehran, Iran
Pircheraghi, Gholamreza
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Bagheri, Reza
Saadatlou, Ghazaleh Azizi
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Koc Univ, Mat Sci & Engn Grad Program, TR-34450 Istanbul, TurkiyeSharif Univ Technol, Dept Mat Sci & Engn, Polymer Mat Res Grp PMRG, POB 11365-9466, Tehran, Iran
Saadatlou, Ghazaleh Azizi
Demirel, A. Levent
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Koc Univ, Chem Dept, TR-34450 Istanbul, TurkiyeSharif Univ Technol, Dept Mat Sci & Engn, Polymer Mat Res Grp PMRG, POB 11365-9466, Tehran, Iran