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用于化疗药物肠胃外给药的热敏水凝胶功能化介孔二氧化硅纳米颗粒

Thermosensitive Hydrogel-Functionalized Mesoporous Silica Nanoparticles for Parenteral Application of Chemotherapeutics.

作者信息

Voycheva Christina, Slavkova Marta, Popova Teodora, Tzankova Diana, Stefanova Denitsa, Tzankova Virginia, Ivanova Ivelina, Tzankov Stanislav, Spassova Ivanka, Kovacheva Daniela, Tzankov Borislav

机构信息

Department Pharmaceutical Technology and Biopharmacy, Faculty of Pharmacy, Medical University-Sofia, 1000 Sofia, Bulgaria.

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University-Sofia, 1000 Sofia, Bulgaria.

出版信息

Gels. 2023 Sep 21;9(9):769. doi: 10.3390/gels9090769.

Abstract

Hydrogels can offer many opportunities for drug delivery strategies. They can be used on their own, or their benefits can be further exploited in combination with other nanocarriers. Intelligent hydrogels that react to changes in the surrounding environment can be utilized as gatekeepers and provide sustained on-demand drug release. In this study, a hybrid nanosystem for temperature- and pH-sensitive delivery was prepared from MCM-41 nanoparticles grafted with a newly synthesized thermosensitive hydrogel (MCM-41/AA-g-PnVCL). The initial particles were chemically modified by the attachment of carboxyl groups. Later, they were grafted with agar (AA) and vinylcaprolactam (VCL) by free radical polymerization. Doxorubicin was applied as a model hydrophilic chemotherapeutic drug. The successful formulation was confirmed by FT-IR and TGA. Transmission electron microscopy and dynamic light scattering analysis showed small particles with negative zeta potential. Their release behaviour was investigated in vitro in media with different pH and at different temperatures. Under tumour simulating conditions (40 °C and pH 4.0), doxorubicin was almost completely released within 72 h. The biocompatibility of the proposed nanoparticles was demonstrated by in vitro haemolysis assay. These results suggest the possible parenteral application of the newly prepared hydrogel-functionalized mesoporous silica nanoparticles for temperature-sensitive and pH-triggered drug delivery at the tumour site.

摘要

水凝胶可为药物递送策略提供诸多机遇。它们可单独使用,或者与其他纳米载体结合使用以进一步发挥其优势。对周围环境变化做出反应的智能水凝胶可用作守门人,并实现按需持续释药。在本研究中,通过用新合成的热敏水凝胶(MCM - 41/AA - g - PnVCL)接枝MCM - 41纳米颗粒,制备了一种用于温度和pH敏感递送的混合纳米系统。初始颗粒通过连接羧基进行化学修饰。随后,通过自由基聚合将琼脂(AA)和乙烯基己内酰胺(VCL)接枝到其上。阿霉素用作模型亲水性化疗药物。通过傅里叶变换红外光谱(FT - IR)和热重分析(TGA)证实了成功的配方。透射电子显微镜和动态光散射分析表明颗粒较小且具有负的zeta电位。在不同pH和不同温度的介质中对其体外释放行为进行了研究。在肿瘤模拟条件(40℃和pH 4.0)下,阿霉素在72小时内几乎完全释放。通过体外溶血试验证明了所提出的纳米颗粒的生物相容性。这些结果表明新制备的水凝胶功能化介孔二氧化硅纳米颗粒在肿瘤部位用于温度敏感和pH触发的药物递送具有肠胃外应用的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31ae/10530711/e69d40a7e684/gels-09-00769-g001.jpg

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