Wang Pengyu, Gao Junwei, Guo Shijie, Liu Hongmei, Cao Can, Hong Shihao, Sun Yu, Wang Chen, Xiao Wei, Song Ping, Li Ning, Xu Ruodan
Department of Biomedical Engineering and Technology, Institute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, China.
Mater Today Bio. 2023 Aug 2;22:100756. doi: 10.1016/j.mtbio.2023.100756. eCollection 2023 Oct.
Indigo naturalis (IN) has been extensively used as a topical treatment for psoriasis. However, clinical applications of IN in ointment were hampered by its limited transdermal efficiency and dark stains. To address the aforementioned issues, nanopatches carrying IN were fabricated using poly(ε-caprolactone, PCL)/poly(ethylene oxide, PEO) and topically applied to psoriasiform skin. The ideal ratio of 5% PCL/PEO was established to be 80:20 (w/w), and 15% IN as payload was confirmed. Investigations on the three principal active components of IN release indicated that indirubin and tryptanthrin were released in bursts, while indigo was released in a limited and controlled manner. Further biological analyses confirmed a favorable biocompatibility of amphiphilic IN-PCL/PEO, which coincided with the intended therapeutic outcomes as measured by severity index scoring and pathological evaluations . The advantages of IN as nanopatches over ointment could be due to improved transdermal distribution of indirubin and tryptanthrin, resulting in effective management of epidermal hyperplasia and blood vessel remodeling. Meanwhile, due to the lower preservation of epidermal indigo, IN-PCL/PEO nanopatches caused no skin coloration. Similarly, during a 4-week topical treatment of IN-PCL/PEO nanopatches, the safety and anti-psoriatic benefits were obtained in an initial human test. The conversion of IN from topical cream to electrospun nanofibers opens up new avenues for bench-to-bedside translation of this herbal therapy and provides mechanistic insight into IN's roles in the management of psoriasis.
青黛已被广泛用作银屑病的局部治疗药物。然而,青黛软膏的临床应用受到其透皮效率有限和染色的限制。为了解决上述问题,使用聚(ε-己内酯,PCL)/聚(环氧乙烷,PEO)制备了载有青黛的纳米贴片,并将其局部应用于银屑病样皮肤。确定PCL/PEO的理想比例为80:20(w/w),并确认负载量为15%的青黛。对青黛释放的三种主要活性成分的研究表明,靛玉红和异吲哚酮以突发方式释放,而靛蓝以有限且可控的方式释放。进一步的生物学分析证实了两亲性青黛-PCL/PEO具有良好的生物相容性,这与通过严重程度指数评分和病理评估所测量的预期治疗结果一致。青黛作为纳米贴片相对于软膏的优势可能归因于靛玉红和异吲哚酮透皮分布的改善,从而有效管理表皮增生和血管重塑。同时,由于表皮中靛蓝的保留较少,青黛-PCL/PEO纳米贴片不会引起皮肤着色。同样,在对青黛-PCL/PEO纳米贴片进行为期4周的局部治疗期间,在初步人体试验中获得了安全性和抗银屑病益处。青黛从外用乳膏转变为电纺纳米纤维为这种草药疗法从实验室到临床的转化开辟了新途径,并为青黛在银屑病管理中的作用提供了机制性见解。