黄褐斑
材料科学
生物利用度
丝素
芯(光纤)
色素沉着
结晶度
控制释放
羧甲基纤维素
涂层
化学
化学工程
口腔给药
生物医学工程
药物输送
药品
动力学
生物物理学
PLGA公司
生物相容性材料
壳聚糖
扩散
透明质酸
纳米技术
毒品携带者
纤维素
乙酰化
图层(电子)
乙醇酸
作者
Tianshuo Jia,Yiyu Geng,Huiyan Shao,Yanai Chen,Guohongfang Tan,Subhas C. Kundu,Shenzhou Lu
标识
DOI:10.1002/adhm.202502052
摘要
Melasma is a facial hyperpigmentation disease that significantly impacts patients' quality of life. Clinical treatment is limited by the short half-lives and hydrophilicity of drugs, necessitating release curve optimization to maintain a stable therapeutic concentration for an extended period. This article utilizes natural biomaterials to design a core-shell structured microneedle, combining the "immediate release" and "delayed release" module to achieve programmed drug release. Silk fibroin with a crystalline structure is used as the shell to ensure the harmlessness of the accessible areas, which can provide a release channel for 24 h. The cellulose in the core layer undergoes acetylation treatment, endowing it with the ability to regulate the diffusion flux of hydrophilic drugs. Further, the release kinetics can be tuned based on the crystallinity of the shell layer and the degree of acetylation in the core layer. In the melasma model, glutathione and tranexamic acid play a major role at 0-4 h and 4-24 h, respectively, with bioavailability increased to 264% and 172%. The synergistic effect reduces the generation and transfer of melanin, and restores skin color to near normal. Therefore, this core-shell structure microneedle patch is expected to promote the long-term clinical treatment of melasma.
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