Biologics and Biomaterials Laboratory, College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, China.
Biologics and Biomaterials Laboratory, College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, China.
Eur J Pharm Sci. 2018 Aug 30;121:330-337. doi: 10.1016/j.ejps.2018.06.014. Epub 2018 Jun 20.
We report a type of dissolving microneedles (DMNs) which was made of composite matrix materials of hydroxypropyl methyl cellulose (HPMC) and poly(methylvinylether‑co‑maleic anhydride) (PMVE/MA copolymer, Gantrez S-97), and was successfully loaded with lidocaine hydrochloride. The weight of lidocaine hydrochloride loaded in the microneedles tip was 70% of the weight of the whole tip. The content was 3.43 ± 0.12 mg in weight, which was determined by high performance liquid chromatography (HPLC). The results for mechanical test showed that these microneedles were able to penetrate into the skin of the experimental animals, that was proved using organic staining, texture analyzer and histological examination. The fracture force of the microneedles was 5.442 ± 0.412 N, which was much higher than the one required for the skin penetration. The DMNs with lidocaine hydrochloride could be dissolved inside of the rat skin in 5 min. The onset time would be faster (in <5 min) when it was applied to the guinea pig model, in comparing with a commercially available anesthesia cream that had an onset time for 100 min. However, the efficacy of the DMNs for the local anesthesia only lasted for 16 min. It was shorter than that of the commercially available anesthesia cream with which the efficacy could last for about 130 min. After the DMNs was packaged under the vacuum and dark condition, it was stable for 3 months under the condition of a temperature of 40 ± 2 °C and a humidity of 75 ± 5%. The result of the experiment for the safety evaluation showed that the microneedles were non-irritating and non-allergenic to the skin. In conclusion, the DMNs with lidocaine hydrochloride could be safely administered to the skin with a quick onset time for the local anesthesia.
我们报告了一种由羟丙甲纤维素(HPMC)和聚甲基乙烯基醚-马来酸酐共聚物(PMVE/MA 共聚物,Gantrez S-97)组成的复合基质材料制成的溶解微针(DMN),并成功负载了盐酸利多卡因。微针针尖中负载的盐酸利多卡因的重量为整个针尖重量的 70%。重量为 3.43±0.12mg,通过高效液相色谱法(HPLC)确定。机械测试结果表明,这些微针能够穿透实验动物的皮肤,这一点通过有机染色、纹理分析仪和组织学检查得到了证明。微针的断裂力为 5.442±0.412N,远高于皮肤穿透所需的力。含有盐酸利多卡因的 DMN 可在 5 分钟内在大鼠皮肤内溶解。与起效时间为 100 分钟的市售麻醉乳膏相比,当应用于豚鼠模型时,起效时间会更快(<5 分钟)。然而,DMNs 的局部麻醉效果仅持续 16 分钟。这比市售麻醉乳膏的起效时间(约 130 分钟)短。将 DMNs 包装在真空和黑暗的条件下,在 40±2°C 的温度和 75±5%的湿度条件下,3 个月内保持稳定。安全性评价实验结果表明,微针对皮肤无刺激性和过敏性。总之,载有盐酸利多卡因的 DMN 可安全地用于皮肤,具有快速起效的局部麻醉作用。