Department of Biotechnology, School of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran.
Department of Biotechnology, School of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran.
Int J Biol Macromol. 2023 Apr 1;233:123621. doi: 10.1016/j.ijbiomac.2023.123621. Epub 2023 Feb 10.
5-Fluorouracil (5-FU) is a cytotoxic drug with a low half-life. These features can cause some problems such as burst drug release and numerous side effects. In the present study, a pH-sensitive nanocomposite of polyvinylpyrrolidone (PVP)/carboxymethyl cellulose (CMC)/γ-alumina developed by using water in oil in water (W/O/W) double emulsion method. The fabricated emulsion has been employed as the 5-FU carrier to investigate its effects on drug half-life, side effects, drug loading efficiency (DLE), and drug entrapment efficiency (DEE). Analyzing the FTIR and XRD indicated the successful loading of 5-FU into the nanocarrier and affirmed the synthesized nanocomposite's chemical bonding and crystalline features. Furthermore, by using DLS and Zeta potential assessment, size and undersize distribution, as well as the stability of the drug-loaded nanocomposite were determined, which demonstrated the monodisperse and stable nanoparticles. Moreover, the nanocomposites with spherical shapes and homogeneous surfaces were shown in FE-SEM, which indicated good compatibility for the constituents of the nanocomposites. Moreover, by employing BET analysis the porosity has been investigated. Drug release pattern was studied, which indicated a controlled drug release behavior with above 96 h drug retention. Besides, the loading and entrapment efficiencies were obtained 44 % and 86 %, respectively. Furthermore, the curve fitting technique has been employed and the predominant release mechanism has been determined to evaluate the best-fitted kinetic models. MTT assay and flow cytometry assessment has been carried out to investigate the cytotoxic effects of the fabricated drug-loaded nanocomposite on MCF-7 and normal cells. The results showed enhanced cytotoxicity and late apoptosis for the PVP/CMC/γ-alumina/5-FU. Based on the MTT assay outcomes on normal cell lines (L929), which indicated above 90 % cell viability, the biocompatibility and biosafety of the synthesized nanocarrier have been confirmed. Moreover, due to the porosity of the PVP/CMC/γ-alumina, this nanocarrier can exploit from high specific surface area and be more sensitive to environmental conditions such as pH. These outcomes propose that the novel pH-sensitive PVP/CMC/γ-alumina nanocomposite can be a potential candidate for drug delivery applications, especially for cancer therapy.
5-氟尿嘧啶(5-FU)是一种半衰期较短的细胞毒性药物。这些特性可能导致一些问题,如药物突释和许多副作用。在本研究中,采用水包油包水(W/O/W)双重乳液法制备了一种聚维酮(PVP)/羧甲基纤维素(CMC)/γ-氧化铝的 pH 敏感纳米复合材料。所制备的乳液被用作 5-FU 的载体,以研究其对药物半衰期、副作用、载药量(DLE)和药物包封率(DEE)的影响。分析 FTIR 和 XRD 表明 5-FU 成功负载到纳米载体中,并证实了合成纳米复合材料的化学键合和结晶特征。此外,通过使用 DLS 和 Zeta 电位评估、粒径和粒度分布以及载药纳米复合材料的稳定性,确定了单分散和稳定的纳米颗粒。此外,FE-SEM 显示纳米复合材料具有球形形状和均匀的表面,表明纳米复合材料成分具有良好的相容性。此外,通过 BET 分析研究了多孔性。研究了药物释放模式,结果表明药物保留超过 96 小时,具有控制药物释放行为。此外,载药量和包封率分别为 44%和 86%。此外,采用曲线拟合技术,确定了主导释放机制,以评估最佳拟合的动力学模型。MTT 测定和流式细胞术评估研究了制备的载药纳米复合材料对 MCF-7 和正常细胞的细胞毒性作用。结果表明,PVP/CMC/γ-氧化铝/5-FU 具有增强的细胞毒性和晚期细胞凋亡。基于对正常细胞系(L929)的 MTT 测定结果,细胞活力超过 90%,证实了合成纳米载体的生物相容性和生物安全性。此外,由于 PVP/CMC/γ-氧化铝的多孔性,这种纳米载体可以利用高比表面积,并对环境条件(如 pH 值)更敏感。这些结果表明,新型 pH 敏感的 PVP/CMC/γ-氧化铝纳米复合材料可能是药物输送应用的潜在候选物,特别是用于癌症治疗。
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