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开发用于百里酚的新型皮肤给药载体——囊泡磷脂凝胶的潜力与挑战

Potentials and Challenges in Development of Vesicular Phospholipid Gel as a Novel Dermal Vehicle for Thymol.

作者信息

Keser Sabina, Rukavina Zora, Jozić Marica, Pavlović-Mitrović Lea, Vodolšak Magda, Kranjčec Kristina, Stupin Polančec Darija, Maravić-Vlahoviček Gordana, Lovrić Jasmina, Šegvić Klarić Maja, Vanić Željka

机构信息

Department of Pharmaceutical Technology, Faculty of Pharmacy and Biochemistry, University of Zagreb, A. Kovačića 1, 10000 Zagreb, Croatia.

R&D, PLIVA Croatia Ltd., TEVA Group, Prilaz Baruna Filipovića 25, 10000 Zagreb, Croatia.

出版信息

Pharmaceutics. 2025 Jun 29;17(7):854. doi: 10.3390/pharmaceutics17070854.

Abstract

Thymol, one of the main compounds of thyme essential oil, has shown promising effects in treating various skin disorders owing to its anti-inflammatory, antimicrobial and antioxidative activities. Due to its limited solubility in water, thymol is commonly used in higher concentrations to achieve a suitable therapeutic effect, which can consequently lead to skin irritation. To overcome these limitations, we incorporated thymol into a vesicular phospholipid gel (VPG), a novel semisolid dermal vehicle consisting of highly concentrated dispersion of phospholipid vesicles (liposomes). Thymol was successfully loaded into two VPGs differing in bilayer fluidity, which were characterized for the physicochemical and rheological properties, storage stability, in vitro release, ex vivo skin permeability, in vitro compatibility with epidermal cells, wound healing potential, and antibacterial activity against skin-relevant bacterial strains. High pressure homogenization method enabled preparation of VPG-liposomes of neutral surface charge in the size range 140-150 nm with polydispersity indexes below 0.5. Both types of VPGs exhibited viscoelastic solid-like structures appropriate for skin administration and ensured skin localization of thymol. Although both types of VPGs enabled prolonged release of thymol, the presence of cholesterol in the VPG increased the rigidity of the corresponding liposomes and further slowed down thymol release. Loading of thymol into VPGs significantly reduced its cytotoxicity toward human keratinocytes in vitro even at very high concentrations, compared to free thymol. Moreover, it facilitated in vitro wound healing activity, proving its potential as a vehicle for herbal-based medicines. However, the antibacterial activity of thymol against and methicillin-resistant was hindered by VPGs, which represents a challenge in their development.

摘要

百里香酚是百里香精油的主要成分之一,因其具有抗炎、抗菌和抗氧化活性,在治疗各种皮肤疾病方面显示出良好的效果。由于百里香酚在水中的溶解度有限,通常使用较高浓度以达到合适的治疗效果,这可能会导致皮肤刺激。为了克服这些限制,我们将百里香酚掺入一种囊泡磷脂凝胶(VPG)中,这是一种新型半固体皮肤载体,由磷脂囊泡(脂质体)的高度浓缩分散体组成。百里香酚成功载入了两种双层流动性不同的VPG中,并对其理化性质、流变学性质、储存稳定性、体外释放、离体皮肤渗透性、与表皮细胞的体外相容性、伤口愈合潜力以及对与皮肤相关细菌菌株的抗菌活性进行了表征。高压均质法能够制备中性表面电荷、尺寸范围为140 - 150 nm且多分散指数低于0.5的VPG脂质体。两种类型的VPG均表现出适合皮肤给药的粘弹性固体状结构,并确保了百里香酚在皮肤中的定位。尽管两种类型的VPG都能使百里香酚实现长效释放,但VPG中胆固醇的存在增加了相应脂质体的刚性,并进一步减缓了百里香酚的释放。与游离百里香酚相比,将百里香酚载入VPG中即使在非常高的浓度下也能显著降低其对人角质形成细胞的细胞毒性。此外,它促进了体外伤口愈合活性,证明了其作为草药类药物载体的潜力。然而,VPG阻碍了百里香酚对[具体细菌名称1]和耐甲氧西林[具体细菌名称2]的抗菌活性,这在其开发过程中是一个挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baa2/12298122/5eb7093eea17/pharmaceutics-17-00854-g001.jpg

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