4.7 Article

Customized flexible hollow microneedles for psoriasis treatment with reduced-dose drug

Journal

Publisher

WILEY
DOI: 10.1002/btm2.10530

Keywords

drug delivery; dual-molding process; hollow microneedles

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Microneedles, especially hollow microneedles (HMNs), are crucial for drug delivery. However, current HMNs are mainly manufactured using silicon microfabrication, which lacks a low-cost and batch-scale customized approach, especially for flexible substrate HMNs. This study proposes using a high-precision 3D printed master mold and a dual-molding process to prepare HMNs with different shapes and sizes. The reuse of the molds significantly reduces costs. The drug delivery efficiency of the fabricated HMNs was verified through in situ treatment of psoriasis in mice, which resulted in reduced side effects and drug toxicity. This dual-molding process can revitalize HMNs development.
Microneedles, especially hollow microneedles (HMNs), play an important role in drug delivery, but most of the current HMNs are manufactured based on silicon microfabrication (lithography, etching, etc.), which are slightly conservative due to the lack of low-cost, batch-scale and customized preparation approach, especially for the HMNs with flexible substrate. For the first time, we propose the use of a high-precision 3D printed master mold followed by a dual-molding process for the preparation of HMNs with different shapes, heights, and inner and outer diameters to satisfy different drug delivery needs. The 3D printed master mold and negative mold can be reused, thereby significantly reducing the cost. HMNs are based on biocompatible materials, such as heat-curing polymers or light-curing resins. The thickness and rigidity/flexibility characteristics of the substrate can be customized for different applications. The drug delivery efficiency of the fabricated HMNs was verified by the in situ treatment of psoriasis on the backs of mice, which required only a 0.1-fold oral dose to achieve similar efficacy, and the associated side effects and drug toxicity were reduced. Thus, this dual-molding process can reinvigorate HMNs development.

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