Department of Chemical and Biomolecular Engineering, Chonnam National University, Yeosu 59626, Republic of Korea.
Department of Energy & Resources Engineering, Chonnam National University, Gwangju 61186, Republic of Korea.
Int J Biol Macromol. 2023 Mar 31;232:123382. doi: 10.1016/j.ijbiomac.2023.123382. Epub 2023 Jan 21.
The aim of this study was to prepare niacinamide (NA) imprinted biomaterials for treating hyperpigmentation using mungbean starch (MS), PVA, and plasticizers (glycerol (GL) and citric acid (CA)). Biomaterials and NA were characterized by FE-SEM, FT-IR, and H NMR. To evaluate the applicability of the NA imprinted biomaterials for a transdermal drug delivery system (TDDS), NA release experiment was conducted in different pH and temperature conditions. Results of NA release properties indicated that NA was released about 99 % rapidly in the initial 10 min. NA release in low pH and high temperature was also higher than that in high pH and low temperature. The determination of experimental conditions and the analysis of NA release results were achieved using response surface methodology (RSM). Results of NA release using artificial skin indicated that NA release from NA imprinted biomaterials was increased at a relatively steady rate for 90 min. To verify for treating hyperpigmentation of the prepared biomaterials, tyrosinase inhibitory and antioxidant inhibitory were performed. Results indicated that NA imprinted biomaterials with the addition of CA exhibited 55.8 % of tyrosinase inhibitory and 73.0 % of antioxidant inhibitory. In addition, their ability to inhibit melanin synthesis in B16F10 cells was evaluated.
本研究旨在利用绿豆淀粉(MS)、PVA 和增塑剂(甘油(GL)和柠檬酸(CA))制备用于治疗色素沉着过度的烟酰胺(NA)印迹生物材料。采用 FE-SEM、FT-IR 和 H NMR 对生物材料和 NA 进行了表征。为了评估 NA 印迹生物材料在经皮给药系统(TDDS)中的适用性,在不同 pH 值和温度条件下进行了 NA 释放实验。NA 释放性能的结果表明,NA 在最初的 10 分钟内迅速释放了约 99%。低 pH 值和高温下的 NA 释放也高于高 pH 值和低温下的释放。使用响应面法(RSM)确定了实验条件和分析了 NA 释放结果。使用人工皮肤进行的 NA 释放结果表明,NA 印迹生物材料中的 NA 释放以相对稳定的速率持续 90 分钟。为了验证所制备生物材料对治疗色素沉着过度的效果,进行了酪氨酸酶抑制和抗氧化抑制实验。结果表明,添加 CA 的 NA 印迹生物材料表现出 55.8%的酪氨酸酶抑制率和 73.0%的抗氧化抑制率。此外,还评估了它们在 B16F10 细胞中抑制黑色素合成的能力。