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基于无水脂质制剂系统的夫西地酸钠抗生素皮肤喷雾剂的临床前开发。

Preclinical development of sodium fusidate antibiotic cutaneous spray based on water-free lipid formulation system.

机构信息

Department of Materials and Environmental Chemistry, Stockholm University, Svante Arrhenius väg 16C, Stockholm SE-106 91, Sweden; Lipidor AB, Svärdvägen 13, Danderyd SE-182 33, Sweden.

Department of Materials and Environmental Chemistry, Stockholm University, Svante Arrhenius väg 16C, Stockholm SE-106 91, Sweden; Lipidor AB, Svärdvägen 13, Danderyd SE-182 33, Sweden.

出版信息

Eur J Pharm Sci. 2022 Sep 1;176:106250. doi: 10.1016/j.ejps.2022.106250. Epub 2022 Jun 30.

Abstract

Topical antibiotics are a key component in the management of mild to moderate skin and soft tissue infections. There are, however, concerns about the emerging bacterial resistance against topical antibacterial agents such as fusidic acid, due to the prolonged treatment period of its marketed dosage forms. Improving the efficacy of topical formulations could potentially shorten the treatment period and avoid the resistance growth. To provide a more effective drug delivery, a water-free lipid-based formulation system (AKVANO®) which can be applied by spraying, has been developed. In the current paper, different formulations containing sodium fusidate were evaluated for their in vitro skin permeability using artificial skin mimicking membranes and antibacterial properties using ex vivo and in vivo skin wound infection models. The novel formulations containing sodium fusidate showed a much higher skin permeation (up to 60% of nominal amount) than the commercially available Fucidin® cream (3%). These formulations also gave a significantly stronger antibacterial effect than Fucidin cream showing a clear dose-response relationship for the sodium fusidate content. A spray product based on the described formulation technology would therefore require a shorter treatment time and thereby lower the risk for the development of bacterial resistance. Spray administration of these formulations provides an even layer on the skin surface from which the solvent quickly evaporates and thereby facilitates a non-touch application where no rubbing is required.

摘要

局部用抗生素是治疗轻度至中度皮肤和软组织感染的关键组成部分。然而,由于其市售剂型的治疗期延长,人们对局部抗菌药物(如夫西地酸)的细菌耐药性不断出现感到担忧。提高局部制剂的疗效可能会缩短治疗期并避免耐药性的产生。为了提供更有效的药物递送,已经开发出一种无水的基于脂质的制剂系统(AKVANO®),可通过喷涂进行应用。在目前的论文中,使用模拟皮肤的人工膜评估了含有夫西地酸钠的不同制剂的体外皮肤渗透性,使用离体和体内皮肤创伤感染模型评估了其抗菌性能。与市售的 Fucidin®乳膏(3%)相比,含有夫西地酸钠的新型制剂显示出更高的皮肤渗透性(高达名义量的 60%)。这些制剂还表现出比 Fucidin 乳膏更强的抗菌作用,显示出夫西地酸钠含量的明显剂量反应关系。因此,基于所描述的制剂技术的喷雾产品将需要更短的治疗时间,从而降低细菌耐药性发展的风险。这些制剂的喷雾给药在皮肤表面形成均匀的层,溶剂迅速蒸发,从而便于非接触式应用,无需摩擦。

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