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Journal ArticleDOI

Layer-by-Layer Assembly of Inactivated Poliovirus and N-Trimethyl Chitosan on pH-Sensitive Microneedles for Dermal Vaccination

TLDR
Topical administration of pH-sensitive microneedles coated with polyelectrolyte multinanolayers of antigens and oppositely charged polymers may be a useful approach for micronedle-based vaccination.
Abstract
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 μm 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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Recent advances of controlled drug delivery using microfluidic platforms.

TL;DR: This article reviews recent advances of controlled drug delivery using microfluidic platforms which can be implanted in human bodies to control drug release in real time through an on‐demand feedback mechanism.
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Transdermal drug delivery

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Chitin and Chitosans: Characteristics, Eco-Friendly Processes, and Applications in Cosmetic Science.

TL;DR: In this paper, the physicochemical and biological properties of chitin and chitosans are discussed, focusing on enzymatic deproteinization, bacteria fermentation, and enzymastic deacetylation methods.
Journal ArticleDOI

Materials for Immunotherapy

TL;DR: An overview of the materials used to enable or improve the success of immunotherapies in preclinical studies is presented, from immunosuppressive to proinflammatory strategies, with particular emphasis on technologies poised for clinical translation.
Journal ArticleDOI

Microneedles for painless transdermal immunotherapeutic applications

TL;DR: Microneedles possess many outstanding properties, such as the ability for the painless traverse of the stratum corneum, minimal invasiveness, facile fabrication, excellent biocompatibility, convenient administration, and bypassing first-pass metabolism that allows direct translocation of therapeutics into the systematic circulation.
References
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Journal ArticleDOI

Transdermal drug delivery

TL;DR: Third-generation delivery systems target their effects to skin's barrier layer of stratum corneum using microneedles, thermal ablation, microdermabrasion, electroporation and cavitational ultrasound for delivery of macromolecules and vaccines.
Journal ArticleDOI

Microneedles for drug and vaccine delivery.

TL;DR: Building off a strong technology base and multiple demonstrations of successful drug delivery, microneedles are poised to advance further into clinical practice to enable better pharmaceutical therapies, vaccination and other applications.
Journal ArticleDOI

Microfabricated microneedles: a novel approach to transdermal drug delivery.

TL;DR: These microneedle arrays could be easily inserted into skin without breaking and were shown to increase permeability of human skin in vitro to a model drug, calcein, by up to 4 orders of magnitude.
Journal ArticleDOI

Microneedle technologies for (trans)dermal drug and vaccine delivery.

TL;DR: This review describes different production methods for solid and hollow microneedles as well as conditions that influence skin penetration and the view on research and development that is needed to rendermicroneedle-based (trans)dermal drug delivery technologies clinically useful in the near future.
Journal ArticleDOI

Micro-scale devices for transdermal drug delivery

TL;DR: This review focuses on the recent trends and developments in this field of micro-scale devices for transdermal macromolecular delivery, which include liquid jet injector, powder injectors, microneedles and thermal microablation.
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