Silver Sulfadiazine Nanocrystal-Based Hydrogels: The Impact of Lipid Components on In-vitro and Ex-vivo Release, Bacterial Biofilm Permeability, and In-vitro Antibacterial Activity

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Anh Quang Luong, Hien Thanh-Thi Pham, Bao Ngoc Tran, Tiep Khac Nguyen, Chien Ngoc Nguyen
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引用次数: 0

Abstract

Purpose

This study developed a new formulation for silver sulfadiazine (SSD) nanocrystal-based hydrogels for in vitro antimicrobial activity.

Methods

SSD nanocrystals were prepared by using a wet-mill apparatus; effects of polymers, surfactants and lipid-based carriers were investigated. The gel-forming chemicals were subsequently dispersed in the SSD nanocrystal nanosuspensions, resulting in homogeneous hydrogels. The antibacterial activities of new formulations were tested in-vitro.

Results

The final SSD nanocrystal formulation (less than 300 nm, PDI: 0.300) containing glyceryl monostearate (GMS) or lecithin (Lec), combining with hydrophilic polymers (hydroxypropyl methyl cellulose and polyvinyl alcohol). The artificial neural network was utilized to confirm the effects of lipid ingredients in wet-milling process. Hydroxyethyl cellulose was chosen to formulate the hydrogel which formed the white, smooth, homogeneous, and stable hydrogel after 4 weeks at the room condition. The hydrogel also presented higher and more sustained drug release using Franz’s diffusion cells as compared with reference marketed drug and control hydrogels. The efficacy of antibacterial activity shown on the biofilm demonstrated effect of particle size, lipid carriers, and probably interaction between SSD with biofilm membrane.

Conclusion

These findings implied a potential application of SSD nanocrystal-lipid carrier-based hydrogels in clinical practice.

Abstract Image

Abstract Image

磺胺嘧啶银纳米晶水凝胶:脂质成分对体外和体内释放、细菌生物膜渗透性以及体外抗菌活性的影响
目的 本研究开发了一种新的磺胺嘧啶银(SSD)纳米晶体水凝胶配方,用于体外抗菌。方法 利用湿法研磨装置制备了磺胺嘧啶银纳米晶体;研究了聚合物、表面活性剂和脂质载体的影响。凝胶形成化学物质随后分散在 SSD 纳米晶体纳米悬浮液中,形成均匀的水凝胶。结果最终的 SSD 纳米晶体配方(小于 300 nm,PDI:0.300)含有单硬脂酸甘油酯(GMS)或卵磷脂(Lec),并与亲水性聚合物(羟丙基甲基纤维素和聚乙烯醇)相结合。利用人工神经网络确认了湿法研磨过程中脂质成分的影响。选用羟乙基纤维素配制的水凝胶在室温条件下放置 4 周后形成了白色、光滑、均匀和稳定的水凝胶。与市场上的参考药物和对照水凝胶相比,该水凝胶在弗朗兹扩散细胞中的药物释放率更高、更持久。在生物膜上显示的抗菌效果表明了粒度、脂质载体以及 SSD 与生物膜之间相互作用的影响。
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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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