含甘草酸和积雪草苷脂质体的可注射水凝胶促进伤口愈合

IF 2.3 4区 医学 Q2 DERMATOLOGY
Yunqi Zhang, Yu Xiong, Xiaochun Wu, Maofang Huang, Zhengjie Li, Tie Zhao, Peng Peng
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引用次数: 0

摘要

背景:开放性皮肤伤口会增加感染风险并损害健康。因此,在受伤部位使用药物促进伤口愈合至关重要。在实践中,直接给药往往由于吸收快或被擦掉而难以长期维持,从而降低了伤口愈合的效率。因此,开发兼具抗菌和伤口愈合特性的生物活性材料是非常可取的:方法:本研究采用薄膜分散-超声法合成了负载甘草酸(GA)和积雪草苷(AS)的脂质体,然后将其加入到 GelMA 溶液中,并通过紫外线交联形成一种用于伤口敷料的生物活性复合水凝胶:结果:这种水凝胶有利于营养物质的运输和气体交换。与 GelMA 水凝胶(膨胀率为 69.8% ± 5.7%)相比,GelMA/Lip@GA@AS 的膨胀率较低,为 52.1% ± 1.0%。GelMA/Lip@GA@AS还具有更好的压缩和流变特性,体外生物降解性与胶原酶处理组没有显著差异。此外,该水凝胶聚合物还具有稳定的药物释放率、良好的生物相容性和促进血管生成的作用。体外实验证明,在浓度为 0.5、1、2 和 3 mg/mL 时,GelMA/Lip@GA@AS 可抑制金黄色葡萄球菌的生长:我们合成了 GelMA/Lip@GA@AS 水凝胶,发现它具有良好的机械性能、流变性和生物降解性。体外实验结果表明,这种生物活性水凝胶能有效释放药物,具有生物相容性,并能增强血管生成和抗菌效果。这些结果表明,GelMA/Lip@GA@AS 水凝胶在伤口包扎材料中的应用前景广阔。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Injectable Hydrogel With Glycyrrhizic Acid and Asiaticoside-Loaded Liposomes for Wound Healing.

Background: Open skin wounds increase the risk of infections and can compromise health. Therefore, applying medications to promote healing at the injury site is crucial. In practice, direct drug delivery is often difficult to maintain for a long time due to rapid absorption or wiping off, which reduces the efficiency of wound healing. Consequently, the development of bioactive materials with both antibacterial and wound-healing properties is highly desirable.

Methods: This study synthesized liposomes loaded with glycyrrhizic acid (GA) and asiaticoside (AS) by film dispersion-ultrasonication method, which were then incorporated into a GelMA solution and cross-linked by ultraviolet light to form a bioactive composite hydrogel for wound dressings.

Results: This hydrogel is conducive to the transport of nutrients and gas exchange. Compared with GelMA hydrogel (swelling rate 69.8% ± 5.7%), the swelling rate of GelMA/Lip@GA@AS is lower, at 52.1% ± 1.0%. GelMA/Lip@GA@AS also has better compression and rheological properties, and the in vitro biodegradability is not significantly different from that of the collagenase-treated group. In addition, the hydrogel polymer has a stable drug release rate, good biocompatibility, and an angiogenic promoting effect. In vitro experiments prove that, at concentrations of 0.5, 1, 2, and 3 mg/mL, GelMA/Lip@GA@AS can inhibit the growth of Staphylococcus aureus.

Conclusion: We synthesized GelMA/Lip@GA@AS hydrogel and found it possesses advantageous mechanical properties, rheology, and biodegradability. Experimental results in vitro showed that the bioactive hydrogel could efficiently release drugs, exhibit biocompatibility, and enhance angiogenesis and antimicrobial effects. These results suggest the promising application of GelMA/Lip@GA@AS hydrogel in wound-dressing materials.

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来源期刊
CiteScore
4.30
自引率
13.00%
发文量
818
审稿时长
>12 weeks
期刊介绍: The Journal of Cosmetic Dermatology publishes high quality, peer-reviewed articles on all aspects of cosmetic dermatology with the aim to foster the highest standards of patient care in cosmetic dermatology. Published quarterly, the Journal of Cosmetic Dermatology facilitates continuing professional development and provides a forum for the exchange of scientific research and innovative techniques. The scope of coverage includes, but will not be limited to: healthy skin; skin maintenance; ageing skin; photodamage and photoprotection; rejuvenation; biochemistry, endocrinology and neuroimmunology of healthy skin; imaging; skin measurement; quality of life; skin types; sensitive skin; rosacea and acne; sebum; sweat; fat; phlebology; hair conservation, restoration and removal; nails and nail surgery; pigment; psychological and medicolegal issues; retinoids; cosmetic chemistry; dermopharmacy; cosmeceuticals; toiletries; striae; cellulite; cosmetic dermatological surgery; blepharoplasty; liposuction; surgical complications; botulinum; fillers, peels and dermabrasion; local and tumescent anaesthesia; electrosurgery; lasers, including laser physics, laser research and safety, vascular lasers, pigment lasers, hair removal lasers, tattoo removal lasers, resurfacing lasers, dermal remodelling lasers and laser complications.
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