Bioinspired Chitosan-Based Patches Enriched With Lipid-Casein Nanocarriers: An Innovative Approach for Wound Management and Evaluation in a Rat Model

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Madhu Kumari, Monika Dwivedi, K. Jayaram Kumar, Ashok Kumar Pattnaik
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引用次数: 0

Abstract

Purpose

Wounds are physical injuries that disrupt the skin’s structure and function, necessitating a complex healing process to restore integrity and functionality. Ursolic acid (UA), a naturally occurring compound, exhibits remarkable antioxidant, anti-inflammatory, and antimicrobial properties, making it a promising candidate for wound healing applications. However, its therapeutic potential is hindered by challenges such as poor solubility, limited permeability, and low bioavailability, which restrict its effectiveness in clinical settings. Delivering UA through nanocarriers provides a significant advantage in resolving these issues, we designed bioinspired milk protein casein-lipid nanocarriers (UA LCNPs) that were incorporated in a chitosan-based transdermal patch.

Method

UA LCNPs were prepared using the desolvation method utilizing casein and Phospholipon 90 ® G. UA LCNPs were characterized by dynamic light scattering (DLS), surface morphology, DSC, and FTIR parameters. The formulated nanoparticles were then incorporated into the chitosan patch using solvent-casting method. The UA LCNPs loaded patches were evaluated for the drug content, surface pH, FESEM, swelling index, hemolysis assay, antioxidant, etc. Furthermore, the developed transdermal patch was characterized and evaluated for in vitro permeation and in vivo wound treatment activity in rats.

Results

The formulated nanoparticles were spherical, with particle size (PS) 172.9 nm, zeta potential (ZP) -14.5 mV, and a PDI value were 0.336. The prepared patch from the nanoparticles was smooth, homogenous, and flexible having high drug content. The results showed that a transdermal patch can effectively control the UA release from the patch and the accumulation of UA in the skin. The hemolysis data provides insight into safety profile and invivo antioxidant activity showing strong antioxidant properties by inhibiting lipid peroxidation. The results showed that the transdermal patch UA LCNPs (test group) demonstrated effective wound healing compared to the control group and marketed ointment groups.

Conclusion

This work serves as a platform for the strategic management of wounds through phytomolecules shelled in casein nanocarriers subduing associated solubility and permeability hurdles. Moreover, accommodating them in patches for self-administration at the injury site presents an effective mode of wound management.

Graphical Abstract

Graphical representation of delivery of bioinspired hybrid nanocarriers UA LCNPs through a transdermal patch on excision wound model displaying fast healing

Abstract Image

富含脂质-酪蛋白纳米载体的壳聚糖生物启发贴片:在大鼠模型中进行伤口管理和评估的创新方法
伤口是破坏皮肤结构和功能的物理损伤,需要一个复杂的愈合过程来恢复完整性和功能。熊果酸(UA)是一种天然存在的化合物,具有显著的抗氧化、抗炎和抗菌特性,使其成为伤口愈合应用的有希望的候选者。然而,其治疗潜力受到诸如溶解度差、渗透性有限和生物利用度低等挑战的阻碍,这些挑战限制了其在临床环境中的有效性。通过纳米载体传递UA为解决这些问题提供了显著的优势,我们设计了生物启发牛奶蛋白酪蛋白脂质纳米载体(UA LCNPs),将其纳入基于壳聚糖的透皮贴剂中。方法以酪蛋白和磷脂90®g为原料,采用脱溶法制备UA LCNPs,通过动态光散射(DLS)、表面形貌、DSC和FTIR等参数对其进行表征。然后采用溶剂铸法制备壳聚糖贴片。对负载UA LCNPs的贴片进行药物含量、表面pH、FESEM、肿胀指数、溶血试验、抗氧化等评价。此外,我们还对所制备的透皮贴剂进行了表征,并对其体外渗透和体内创面治疗活性进行了评价。结果制备的纳米颗粒为球形,粒径(PS)为172.9 nm, ZP为-14.5 mV, PDI值为0.336。纳米颗粒制备的贴片光滑、均匀、柔韧性好,药物含量高。结果表明,透皮贴片能有效控制UA的释放和UA在皮肤中的蓄积。溶血数据提供了对安全性和体内抗氧化活性的深入了解,通过抑制脂质过氧化显示出强大的抗氧化特性。结果表明,与对照组和市售药膏组相比,UA LCNPs透皮贴片(试验组)的伤口愈合效果较好。结论本研究为利用酪蛋白纳米载体包裹的植物分子克服相关的溶解度和渗透性障碍,对创面进行策略性管理提供了平台。此外,将它们安置在补丁中,以便在损伤部位自我管理,这是一种有效的伤口管理模式。图示:仿生混合纳米载体UA LCNPs通过透皮贴片在切除伤口模型上快速愈合
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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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