Kwon Koo Chul, Kim Mi Jung, Yoon Sang A
SEORIN COMPANY Co., Roundlab R&D Center, Seoul, Republic of Korea.
J Cosmet Dermatol. 2025 Apr;24(4):e70195. doi: 10.1111/jocd.70195.
glutamine and linoleic acid (LA) can suppress inflammatory cytokine expression; however, studies on their simultaneous application are limited due to polarity differences.
To investigate the effect of glutamine linoleate vesicles (QLAsomes) on skin sensitization by assessing their impact on sensitization-related protein expression, bacterial growth, and clinical efficacy in relieving skin itchiness.
After synthesizing and analyzing QLAsomes, their inhibitory effects on capsaicin-induced cytokine expression and Staphylococcus aureus growth were evaluated. In a double-blind clinical trial, 24 participants (ages 22-63) with sensitized skin applied 10 wt% QLAsome cream on one side and a vehicle or no cream on the other twice daily for 2 weeks. Itchiness in the elbow area was assessed using a visual analog scale and expert evaluation. Skin barrier changes were measured using transepidermal water loss (TEWL), skin erythema, and stratum corneum (SC) hydration.
QLAsomes, formed by glutamine and LA through hydrogen bonding, were spherical vesicles (164.6 ± 3.1 nm). Based on the inhibitory effects of glutamine and LA on inflammation-related factors, QLAsomes inhibited the capsaicin-induced expression of these factors more effectively than the individual components. IL-4 inhibition was improved by over 26%. Matrix metalloproteinase-1, which degrades collagen, showed 32% and 23% improvements compared to glutamine and LA, respectively. In a clinical evaluation, 10 wt% QLAsome cream reduced itching by 45% compared to before application, which is a 67% improvement compared to placebo. Skin evaluations revealed improvements in erythema (12%), TEWL (15%), and SC hydration (19%), suggesting that QLAsomes enhance the skin barrier function.
QLAsomes showed up to 32% higher expression inhibition of key skin sensitization-related factors than individual components, and based on this, improved pruritus by 67% more than placebo. As nanovesicles with skin-soothing properties, they are effective for drug encapsulation and managing skin sensitivity in pharmaceutical and cosmetic industries.
谷氨酰胺和亚油酸(LA)可抑制炎性细胞因子表达;然而,由于极性差异,关于它们联合应用的研究有限。
通过评估谷氨酰胺亚油酸囊泡(QLAsomes)对致敏相关蛋白表达、细菌生长及缓解皮肤瘙痒临床疗效的影响,研究其对皮肤致敏的作用。
合成并分析QLAsomes后,评估其对辣椒素诱导的细胞因子表达和金黄色葡萄球菌生长的抑制作用。在一项双盲临床试验中,24名(年龄22 - 63岁)皮肤致敏的参与者,一侧每天两次涂抹10 wt% QLAsome乳膏,另一侧涂抹赋形剂或不涂抹乳膏,持续2周。使用视觉模拟评分法和专家评估法评估肘部区域的瘙痒情况。通过经表皮水分流失(TEWL)、皮肤红斑和角质层(SC)水合作用测量皮肤屏障变化。
谷氨酰胺和LA通过氢键形成的QLAsomes为球形囊泡(164.6 ± 3.1 nm)。基于谷氨酰胺和LA对炎症相关因子的抑制作用,QLAsomes比单一成分更有效地抑制辣椒素诱导的这些因子的表达。白细胞介素 - 4的抑制率提高了26%以上。降解胶原蛋白的基质金属蛋白酶 - 1与谷氨酰胺和LA相比,分别提高了32%和23%。在临床评估中,10 wt% QLAsome乳膏与涂抹前相比,瘙痒减轻了45%,与安慰剂相比改善了67%。皮肤评估显示红斑(改善12%)、TEWL(改善15%)和SC水合作用(改善19%)均有改善,表明QLAsomes增强了皮肤屏障功能。
QLAsomes对关键皮肤致敏相关因子的表达抑制比单一成分高出32%,基于此,与安慰剂相比瘙痒改善率高出67%。作为具有舒缓皮肤特性的纳米囊泡,它们在制药和化妆品行业中对药物封装和管理皮肤敏感性有效。