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用于博来霉素持续释放的pH响应性可生物降解纳米凝胶

pH responsive biodegradable nanogels for sustained release of bleomycin.

作者信息

Sahu Prashant, Kashaw Sushil K, Kushwah Varun, Sau Samaresh, Jain Sanyog, Iyer Arun K

机构信息

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, Wayne State University, Detroit, MI, USA.

出版信息

Bioorg Med Chem. 2017 Sep 1;25(17):4595-4613. doi: 10.1016/j.bmc.2017.06.038. Epub 2017 Jun 27.

Abstract

UNLABELLED

Site specific drug delivery with desired therapeutic effect still remains challenging task due to suboptimal release, tissue toxicity, low selectivity and meager therapeutic efficacy in skin cancers. The aim of the current study was to fabricate pH responsive, self-assembled, chemically cross-linked biodegradable chitosan nanogel loaded with bleomycin to target the dermal area of the skin. The nanogel synthesized by ion gelation technique and was characterized for drug loading, swelling and thermal stability followed by in vitro analysis. HaCaT (Human Keratinocyte cell) and HDF (Human dermal fibroblast) cell line were used for the biocompatibility and cytocompatibility evaluation prior to the hemolysis assay and coagulation assessment. The nanogel had a size range of 150nm as determined by TEM and DLS. The nanogel possessed optimum thermal stability as analyzed by thermogravimetry (TG) and differential thermal analysis (DTA). Biodegradation was confirmed by lysozyme enzyme degradation assays. The drug entrapment efficacy was about 55% in the swollen state. The In vitro drug release profile revealed sustained release pattern. The hemolysis of 2.39% and prothrombin time (PT) and activated partial thromboplastin time (APTT) of 12.9 and 31s revealed the biocompatibility of nanogels. The cell uptake and localization profile was validated by fluorescence and confocal microscopy using HDF and HaCaT cell lines. Finally, the MTT assay demonstrated the cytocompatibility of nanogels. In conclusion, the present findings suggest that biodegradable chitosan nanogels with stimuli responsive nature can release the anticancer drug cargo in a sustained and controlled manner and offer promising potentials for treating skin cancers.

STATEMENT OF SIGNIFICANCE

Drug delivery to the targeted site is a major challenge in clinical medicine. The newly constructed pH responsive biodegradable nanogel consisting of bleomycin revealed pH triggered drug release in a sustained manner to the dermal area offering novel approach against skin cancer. The nanogel system is biodegradable in nature possessing high drug entrapment efficiency and offers patient compliance with biocompatible and cytocompatible characteristics. This nanogel system can thus be highly useful for delivery of anticancer drugs to the skin in a controlled and sustained manner.

摘要

未标记

由于释放不理想、组织毒性、低选择性以及皮肤癌治疗效果不佳,实现具有理想治疗效果的位点特异性药物递送仍然是一项具有挑战性的任务。本研究的目的是制备负载博来霉素的pH响应性、自组装、化学交联的可生物降解壳聚糖纳米凝胶,以靶向皮肤的真皮区域。通过离子凝胶化技术合成纳米凝胶,并对其进行药物负载、溶胀和热稳定性表征,随后进行体外分析。在溶血试验和凝血评估之前,使用HaCaT(人角质形成细胞)和HDF(人皮肤成纤维细胞)细胞系进行生物相容性和细胞相容性评估。通过透射电子显微镜(TEM)和动态光散射(DLS)测定,纳米凝胶的尺寸范围为150nm。通过热重分析(TG)和差示热分析(DTA)分析,纳米凝胶具有最佳的热稳定性。通过溶菌酶降解试验证实了生物降解性。在溶胀状态下,药物包封率约为55%。体外药物释放曲线显示出持续释放模式。2.39%的溶血率以及凝血酶原时间(PT)为12.9秒和活化部分凝血活酶时间(APTT)为31秒,表明纳米凝胶具有生物相容性。使用HDF和HaCaT细胞系通过荧光和共聚焦显微镜验证了细胞摄取和定位情况。最后,MTT试验证明了纳米凝胶的细胞相容性。总之,本研究结果表明,具有刺激响应特性的可生物降解壳聚糖纳米凝胶能够以持续和可控的方式释放抗癌药物,为治疗皮肤癌提供了有前景的潜力。

重要性声明

将药物递送至靶位点是临床医学中的一项重大挑战。新构建的由博来霉素组成的pH响应性可生物降解纳米凝胶显示出pH触发的药物持续释放至真皮区域,为对抗皮肤癌提供了新方法。纳米凝胶系统本质上是可生物降解的,具有高药物包封效率,并具有生物相容性和细胞相容性,符合患者需求。因此,这种纳米凝胶系统对于以可控和持续的方式将抗癌药物递送至皮肤可能非常有用。

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