壳聚糖包被二氧化钛纳米管阵列纳米系统靶向鼻咽癌的局部递送顺铂。

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Wan Nuramiera Faznie Wan Eddis Effendy, Rabiatul Basria S M N Mydin, Amirah Mohd Gazzali, Srimala Sreekantan
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引用次数: 2

摘要

目的:顺铂(CDDP)虽然是目前公认的化疗药物之一,但已知具有局限性;缺乏单一的治疗方法和非特异性靶向治疗。因此,开发一种能够实现局部CDDP治疗的创新策略是一项紧迫的任务。二氧化钛纳米管阵列(tna)技术在局部化疗药物治疗中的应用前景广阔。本研究研究了TNA纳米系统在鼻咽癌(NPC)局部CDDP治疗中的效率。方法:制备了两种TNA纳米系统模型:一种是负载在TNA纳米系统表面的CDDP-TNA,另一种是壳聚糖包被的CDDP-TNA。研究了两种纳米体系在鼻咽癌细胞NPC/HK-1和C666-1上的CDDP释放情况。在孵育24、48和72小时后,对两种CDDP-TNA纳米系统的NPC细胞毒性进行了评估。用荧光显微镜分析Hoechst 33342、吖啶橙和碘化丙啶对细胞内损伤谱进行研究。结果:CDDP对NPC/HK-1的半最大抑制浓度(IC50)为0.50 mM,对C666-1的半最大抑制浓度为0.05 mM。CDDP-TNA和壳聚糖包被的CDDPTNA模型中的CDDP表现出显著程度的鼻咽癌抑制(结论:体外实验证明了TNA纳米系统对鼻咽癌细胞局部CDDP治疗的有效性。需要进一步的体内研究来支持这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Localised Delivery of Cisplatin from Chitosan-Coated Titania Nanotube Array Nanosystems Targeting Nasopharyngeal Carcinoma.

Localised Delivery of Cisplatin from Chitosan-Coated Titania Nanotube Array Nanosystems Targeting Nasopharyngeal Carcinoma.

Localised Delivery of Cisplatin from Chitosan-Coated Titania Nanotube Array Nanosystems Targeting Nasopharyngeal Carcinoma.

Localised Delivery of Cisplatin from Chitosan-Coated Titania Nanotube Array Nanosystems Targeting Nasopharyngeal Carcinoma.

Pupose: Cisplatin (CDDP), while amongst the recognised chemotherapeutic drugs currently available, is known to have limitations; the lack of a single treatment approach and non-specific targeted therapies. Therefore, the development of an innovative strategy that could achieve localised CDDP treatment is an urgent undertaking. Recent advances in titania nanotube arrays (TNAs) technology have demonstrated promising applications for localised chemotherapeutic drug treatment. The present work investigated the efficiency of a TNA nanosystem for the localised CDDP treatment of nasopharyngeal carcinoma (NPC). Methods: Two models of the TNA nanosystem were prepared: CDDP loaded onto the TNA nanosystem surface (CDDP-TNA) and the other consisted of chitosan-coated CDDP-TNA. CDDP release from these two nanosystems was comprehensively tested on the NPC cells NPC/HK-1 and C666-1. The NPC cytotoxicity profile of the two CDDP-TNA nanosystems was evaluated after incubation for 24, 48 and 72 hours. Intracellular damage profiles were studied using fluorescence microscopy analysis with Hoechst 33342, acridine orange and propidium iodide. Results: The half-maximal inhibitory concentrations (IC50) of CDDP at 24 hours were 0.50 mM for NPC/HK-1 and 0.05 mM for C666-1. CDDP in the CDDP-TNA and chitosan-coated CDDPTNA models presented a significant degree of NPC inhibition (P<0.05) after 24, 48 and 72 hours of exposure. The outcome revealed cellular damage and shrinkage of the cell membranes after 48 hours of exposure to CDDP-TNA. Conclusion: This in vitro work demonstrated the effectiveness of TNA nanosystems for the localised CDDP treatment of NPC cells. Further in vivo studies are needed to support the findings.

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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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