脂质体
渗透
化学
角质层
生物物理学
Zeta电位
阳离子脂质体
动态光散射
膜
色谱法
材料科学
纳米技术
生物化学
转染
病理
医学
纳米颗粒
基因
生物
作者
Mi So Lee,Ju Won Lee,Su Ji Kim,Oanh‐Vu Pham‐Nguyen,Jongmin Park,Ju Hyun Park,Young Mee Jung,Jun Bae Lee,Hyuk Sang Yoo
标识
DOI:10.1002/mabi.202000413
摘要
Abstract Charged phospholipids are employed to formulate liposomes with different surface charges to enhance the permeation of active ingredients through epidermal layers. Although 3D skin tissue is widely employed as an alternative to permeation studies using animal skin, only a small number of studies have compared the difference between these skin models. Liposomal delivery strategies are investigated herein, through 3D skin tissue based on their surface charges. Cationic, anionic, and neutral liposomes are formulated and their size, zeta‐potential, and morphology are characterized using dynamic light scattering and cryogenic‐transmission electron microscopy (cryo‐TEM). A Franz diffusion cell is employed to determine the delivery efficiency of various liposomes, where all liposomes do not exhibit any recognizable difference of permeation through the synthetic membrane. When the fluorescence liposomes are applied to 3D skin, considerable fluorescence intensity is observed at the stratum cornea and epithelium layers. Compared to other liposomes, cationic liposomes exhibit the highest fluorescence intensity, suggesting the enhanced permeation of liposomes through the 3D skin layers. Finally, the ability of niacinamide (NA)‐incorporated liposomes to suppress melanin transfer in pigmented 3D skin is examined, where cationic liposomes exhibit the highest degree of whitening effects.
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