Department of Pharmaceutical Sciences, Dr. Harisingh Gour University (A Central University), Sagar, MP, India.
Department of Pharmaceutical Sciences, Dr. Harisingh Gour University (A Central University), Sagar, MP, India; Use-inspired Biomaterials & Integrated Nano Delivery (U-BiND) Systems Laboratory Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, 259 Mack Ave, Wayne State University, Detroit, MI 48201, USA.
J Control Release. 2017 May 10;253:122-136. doi: 10.1016/j.jconrel.2017.03.023. Epub 2017 Mar 18.
Penetration enhancers coated biodegradable polymeric nanogels loaded with cytotoxic drugs applied via the topical route, can be a promising strategy for improving the chemotherapeutic efficiency of skin cancers. The major objective of proposed research was to investigate the in vitro and ex vivo chemotherapeutic potential of double walled PLGA-chitosan biodegradable nanogel entrapped with 5-fluororuacil (5-FU) coated with eucalyptus oil, topically applied onto the skin. 5-FU was first entrapped in PLGA core by solvent evaporation technique followed by coating with cationic chitosan for ionic interaction with anionic skin cancer cell membrane. A surface coating of eucalyptus oil (1%) was employed to improve the penetration efficacy of the nanogel into stratum corneum. The surface modified biodegradable double walled nanogel was characterized for particle size, charge and thermal properties followed by pH dependent in vitro analysis. Human keratinocyte (HaCaT) cell line was employed for the bio- and cyto-compatibility testing prior to the hemolysis assay and coagulation assessment. A porcine skin ex vivo screening was performed for assessing the penetration potential of the nanogels. DLS and TEM revealed a particle size about 170nm for the double walled nanogels. The nanogels also exhibited high thermal stability as analyzed by thermogravimetry (TG) and differential thermal analysis (DTA). The drug entrapment efficacy was about ~40%. The drug release showed sustained release pattern noted up to 24h. The low hemolysis of 2.39% with short prothrombin time (PT) and activated partial thromboplastin time (APTT) of 14.2 and 35.5s respectively, revealed high biocompatibility of the nanogels. The cellular uptake and localization was assessed by confocal microscopy. The cytotoxicity (MTT assay) on HaCaT cell line demonstrated high cytocompatibilty of the nanogels. An ex vivo evaluation using porcine skin displayed efficient and steady state flux of 5-FU from the biodegradable nanogles into the skin, while the histology of the porcine skin revealed enhanced penetration potential of eucalyptus oil coated PLGA-chitosan double walled nanogels. Taken together the in vivo and ex vivo results portend promising potential for the utility of the biodegradable nanogels for treating skin cancers.
经皮途径应用载细胞毒性药物的包被穿透增强剂的可生物降解聚合物纳米凝胶,可能是提高皮肤癌化疗效果的一种有前途的策略。本研究的主要目的是研究载有 5-氟尿嘧啶(5-FU)的双层 PLGA-壳聚糖可生物降解纳米凝胶的体外和离体化疗潜力,该纳米凝胶经皮给药应用于皮肤。首先通过溶剂蒸发技术将 5-FU 包埋在 PLGA 核中,然后用阳离子壳聚糖进行涂层,以与阴离子皮肤癌细胞膜进行离子相互作用。表面涂覆 1%桉树油以提高纳米凝胶进入角质层的渗透效果。对表面改性的生物可降解双层纳米凝胶进行粒径、电荷和热性能的表征,然后进行 pH 值依赖性体外分析。在进行溶血试验和凝血评估之前,用人角质形成细胞(HaCaT)细胞系进行生物和细胞相容性测试。进行猪皮离体筛选,以评估纳米凝胶的渗透潜力。DLS 和 TEM 显示双层纳米凝胶的粒径约为 170nm。热重分析(TG)和差示热分析(DTA)分析表明,纳米凝胶也表现出高的热稳定性。药物包封效率约为~40%。药物释放呈持续释放模式,直至 24 小时。溶血率低至 2.39%,凝血酶原时间(PT)短至 14.2s,部分凝血活酶时间(APTT)短至 35.5s,表明纳米凝胶具有很高的生物相容性。通过共聚焦显微镜评估细胞摄取和定位。在 HaCaT 细胞系上的细胞毒性(MTT 测定)表明纳米凝胶具有很高的细胞相容性。使用猪皮进行的离体评估显示,5-FU 从可生物降解纳米凝胶到皮肤的有效且稳定的通量,而猪皮的组织学显示桉树油包被的 PLGA-壳聚糖双层纳米凝胶具有增强的渗透潜力。综合体内和离体结果表明,可生物降解纳米凝胶在治疗皮肤癌方面具有有前途的应用潜力。