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用于苄达明阴道控释的壳聚糖纳米颗粒负载纳米纤维混合系统的研制与表征

Development and characterization of chitosan nanoparticles loaded nanofiber hybrid system for vaginal controlled release of benzydamine.

作者信息

Tuğcu-Demiröz Fatmanur, Saar Sinem, Kara Adnan Altuğ, Yıldız Ayşegül, Tunçel Emre, Acartürk Füsun

机构信息

Gazi University, Faculty of Pharmacy, Department of Pharmaceutical Technology, 06330- Etiler, Ankara, Turkey.

Gazi University, Faculty of Pharmacy, Department of Pharmaceutical Technology, 06330- Etiler, Ankara, Turkey.

出版信息

Eur J Pharm Sci. 2021 Jun 1;161:105801. doi: 10.1016/j.ejps.2021.105801. Epub 2021 Mar 7.

Abstract

Vaginal infections caused by various pathogens such as fungi, viruses and protozoa are frequently seen. Systemic and local treatments can be applied to eliminate these infections. Novel vaginal drug delivery systems can be used to provide local treatment. Vaginal drug delivery systems prevent systemic side effects and can provide long-term drug release in the vaginal area. Nanofibers and nanoparticles have a wide range of applications and can also be preferred as vaginal drug delivery systems. Benzydamine is a non-steroidal anti-inflammatory and antiseptic drug which is used for treatment of vaginal infections. The aim of this study was to compare the nanofiber and gel formulations containing lyophilized benzydamine nanoparticles with nanofiber and gel formulations containing free benzydamine, and to provide prolonged release for protection from the vaginal infections. Ionic gelation method was used for the preparation of benzydamine loaded nanoparticles. To produce benzydamine nanoparticles loaded nanofiber formulations, polyvinylpyrrolidone (PVP) solutions were prepared at 10% concentrations and mixed with nanoparticles. Hydroxypropyl methylcellulose (HPMC) was used as a gelling agent at the concentration of 1% for the vaginal gel formulation. Nanoparticles were characterized in terms of zeta potential, polydispersity index and particle size. Viscosity, surface tension and conductivity values of the polymer solutions were measured for the electrospinning. Mechanical properties, contact angle and drug loading capacity of the fibers were determined. Scanning electron microscopy (SEM), differential scanning calorimetry (DSC), transmission electron microscopy (TEM), fourier-transform infrared (FT-IR) spectroscopy, mucoadhesion, ex vivo permeability studies and in vitro release studies were performed for the selected formulations. Ex vivo permeability studies were performed using Franz diffusion cell method. SEM and TEM images showed that fiber diameters increased with loading of nanoparticles. DSC studies showed no interaction between excipients used in the formulation. Tensile strength and elongation at break values of the fibers increased with the loading of nanoparticles, and the contact angle values of the fibers were found to be 0°. Addition of benzydamine nanoparticles to gel and nanofiber formulations increased mucoadhesion compared to free benzydamine loading formulations. Benzydamine nanoparticle loaded gel and nanofiber formulations penetrated slower than that of free benzydamine gel and fiber formulations. The results demonstrated that benzydamine and benzydamine nanoparticle loaded fibers and gels could be a potential drug delivery system for the treatment of vaginal infections. Chitosan nanoparticle loaded nanofiber formulations are offered as an alternative controlled release vaginal formulations for vaginal infections.

摘要

由真菌、病毒和原生动物等各种病原体引起的阴道感染很常见。可采用全身和局部治疗来消除这些感染。新型阴道给药系统可用于提供局部治疗。阴道给药系统可防止全身副作用,并能在阴道区域实现药物的长期释放。纳米纤维和纳米颗粒有广泛的应用,也可作为阴道给药系统的首选。苄达明是一种非甾体抗炎和抗菌药物,用于治疗阴道感染。本研究的目的是比较含有冻干苄达明纳米颗粒的纳米纤维和凝胶制剂与含有游离苄达明的纳米纤维和凝胶制剂,并实现延长释放以预防阴道感染。采用离子凝胶法制备负载苄达明的纳米颗粒。为制备负载苄达明纳米颗粒的纳米纤维制剂,制备了浓度为10%的聚乙烯吡咯烷酮(PVP)溶液,并与纳米颗粒混合。羟丙基甲基纤维素(HPMC)以1%的浓度用作阴道凝胶制剂的胶凝剂。对纳米颗粒的zeta电位、多分散指数和粒径进行了表征。测量了用于静电纺丝的聚合物溶液的粘度、表面张力和电导率值。测定了纤维的力学性能、接触角和载药量。对所选制剂进行了扫描电子显微镜(SEM)、差示扫描量热法(DSC)、透射电子显微镜(TEM)、傅里叶变换红外(FT-IR)光谱、粘膜粘附、体外渗透研究和体外释放研究。采用Franz扩散池法进行体外渗透研究。SEM和TEM图像显示,随着纳米颗粒的负载,纤维直径增加。DSC研究表明制剂中使用的辅料之间没有相互作用。纤维的拉伸强度和断裂伸长率值随着纳米颗粒的负载而增加,且纤维的接触角值为0°。与游离苄达明负载制剂相比,向凝胶和纳米纤维制剂中添加苄达明纳米颗粒可增加粘膜粘附性。负载苄达明纳米颗粒的凝胶和纳米纤维制剂的渗透速度比游离苄达明凝胶和纤维制剂慢。结果表明,负载苄达明和苄达明纳米颗粒的纤维和凝胶可能是治疗阴道感染的潜在给药系统。负载壳聚糖纳米颗粒的纳米纤维制剂可作为治疗阴道感染的另一种控释阴道制剂。

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