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Berberine hydrochloride-loaded liposomes-in-hydrogel microneedles achieve the efficient treatment for psoriasis

盐酸小檗碱 小檗碱 脂质体 银屑病 自愈水凝胶 药理学 材料科学 化学 医学 纳米技术 皮肤病科 高分子化学
作者
Si Shen,Shen Wang,Lu Wang,Bin Sun,Yongli Zhang,Yong Zhang,Ruoyang Jia,Wu Yang,Xue Chen,Keang Cao,Yuqing Fang,Hongmei Xia
出处
期刊:Materials today bio [Elsevier BV]
卷期号:32: 101795-101795 被引量:19
标识
DOI:10.1016/j.mtbio.2025.101795
摘要

Psoriasis is a common immune-mediated squamous skin disease, primarily characterized by the over proliferation of keratinocytes and a significant thickening of the stratum corneum. Traditional systemic drug delivery therapies often fall short due to low drug bioavailability and significant toxic side effects. Topical medications, while capable of achieving local or systemic treatment via transdermal routes, face limitations in psoriasis patients due to the abnormal thickening of the epidermis, which reduces skin permeability and hampers drug penetration efficiency. Hydrogel microneedles, as an emerging transdermal drug delivery technology, offer significant advantages such as high permeability, ease of use, low toxicity and side effects, and controlled release. Therefore, this study developed a liposome-hydrogel microneedle delivery system for the administration of berberine hydrochloride. We successfully prepared berberine hydrochloride-loaded liposomes (Ber-LPs) with high encapsulation efficiency and good stability, and integrated them into hydrogel microneedles crosslinked with PVA and PEGDA (Ber-LPs-PEGDA&PVA MNs) through a photocuring method. These microneedles exhibit an intact structure, high mechanical strength, and effective skin penetration. In vivo studies on anti-psoriatic effects showed that, compared to the model group, Ber-LPs-PEGDA&PVA MNs significantly alleviated imiquimod-induced psoriasis-like symptoms in mice, reduced skin epidermal thickness, decreased the expression levels of inflammatory cytokines, and lowered the expression of CD31 and VEGF, demonstrating excellent therapeutic efficacy. Additionally, the microneedles exhibited good drug release properties, antioxidant capacity, and biocompatibility. The novel hydrogel microneedle drug delivery system developed in this study offers a safe and effective solution for the treatment of psoriasis, with significant potential for clinical application. Encapsulating drugs into liposomes can enhance the solubility and bioavailability of berberine hydrochloride. The hydrogel microneedles prepared through crosslinking of poly (ethylene glycol) diacrylate (PEGDA) and polyvinyl alcohol (PVA) represent a highly promising painless transdermal drug delivery device. Liposomes-in-Hydrogel Microneedles loaded with berberine hydrochloride alleviated psoriasis lesions in mice, achieving sustained and controlled drug delivery.
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