开发和优化格拉布林负载型溶解微针,加强对瘢痕疙瘩的治疗

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics: X Pub Date : 2024-07-01 DOI:10.1016/j.ijpx.2024.100267
Juan Guo , Zhongtang Chen , Rong Huang , Dandan Tang , Yuhuan Wang , Pan Song , Liangyu Mei , Shuguang Hou , Wei Peng , Lisha He , Qiang Ren
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引用次数: 0

摘要

据报道,格拉布林(Gla)对疤痕治疗有显著效果,但由于格拉布林不溶于水,导致其透皮吸收能力差,影响了其生物活性。因此,我们尝试制备 Gla 溶解微针(Gla-MN)来改善 Gla 的吸收。在对针尖基质浓度、背衬材料处方浓度和 Gla 的溶解方法等 3 个因素进行研究后,我们最终确定了以 10%透明质酸(HA)为针尖、5% 聚乙烯醇(PVA)为背衬材料的工艺参数,据此制备出的 Gla-MN 具有硬度高、外观完整、体外溶解能力强等良好特性。此外,Gla-MN 还具有良好的皮肤穿透性,至少能穿透 4 至 5 层薄膜。穿刺 4 小时后,皮肤基本上可以恢复正常。重要的是,我们的研究结果表明,与相同剂量的 Gla 相比,Gla-MN 对瘢痕疙瘩的透皮给药和治疗效果更高。
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Development and optimization of the Glabridin-loaded dissolving microneedle for enhanced treatment of keloid

Glabridin (Gla) has been reported to have significant effects in scar treatment, and however, the water insolubility of Gla leads to its poor transdermal absorption ability, which affects its bioactivities. Therefore, we attempted to prepare the Gla dissolving microneedles (Gla-MN) to improve the absorbtion of Gla. After investigation of the 3 factors including the needle tip matrix concentration, the prescription concentration of backing material, and the dissolution method of Gla, we finally determined the process parameters of 10% hyaluronic acid (HA) as the needle tip and 5% polyvinyl alcohol (PVA) as the backing, according to which the Gla-MN was prepared with the good characteristics of high hardness, complete appearance and good in vitro dissolution ability. We then loaded Gla onto the microneedles and measured that the average drug loading of Gla-MN was 2.26 ± 0.11 μg/mg and the cumulative transdermal release of Gla-MN was up to 76.9% after 24 h. In addition, Gla-MN had good skin penetration properties, with Gla-MN penetrating at least 4 to 5 layers of parafilm. And the skin basically could return to normal after 4 h of piercing. Importantly, our results showed that Gla-MN had higher transdermal delivery and therapeutic effects against keloid than that of Gla at the same dosage.

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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
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