用于肿瘤靶向的来曲唑负载纳米转运体凝胶的配方和统计优化。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sara Imtiaz, Saba Sohail, Fakhar Ud Din, Zakir Ali, Sibgha Batool, Maimoona Malik, Asif Nawaz, Ali H Alamri, Ahmed A Lahiq, Shaker T Alsharif, Abdullah Asiri
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引用次数: 0

摘要

来曲唑(LTZ)是绝经后妇女激素阳性乳腺癌(BC)的一线治疗药物。然而,由于其水溶性和渗透性较差,降低了其临床疗效。针对上述问题,我们开发了LTZ-纳米转运体(LTZ-NT)。我们使用 Design Expert® 对 LTZ-NT 进行了统计优化,然后通过动态光散射(DLS)、透射电子显微镜(TEM)、傅立叶变换红外光谱(FTIR)和差示扫描量热法(DSC)对其进行了表征。将优化后的 LTZ-NT 加入 1%壳聚糖凝胶中,开发出 LTZ-NTG。此外,还对 LTZ-NTG 进行了体外药物释放和体内渗透试验,并与 LTZ 分散体和 LTZ-NT 进行了比较。此外,还研究了 LTZ-NTG 的皮肤刺激性和组织病理学。此外,还在 BC 细胞系中对 LTZ-NTG 进行了体外抗肿瘤研究。优化后的 LTZ-NT 显示出合适的 zeta 电位(30.4 mV)、球形尺寸(162.5 nm)和出色的包埋效率(88.04%)。此外,LTZ-NT 还表现出合适的热行为,其辅料之间没有相互作用。此外,LTZ-NTG 具有最佳的 pH 值(5.6)和合适的粘度。从 LTZ-NTG 中可以观察到 LTZ 有意义的持续释放和更好的渗透性。此外,LTZ-NTG 还能明显增强 MCF-7 和 MCC-7 细胞的死亡。由此可以得出结论:LTZ-NTG 有潜力将化疗药物用于治疗 BC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and statistical optimization of letrozole loaded nanotransferosomal gel for tumor targeting.

Letrozole (LTZ) is used as first-line treatment for hormone-positive breast cancer (BC) in postmenopausal women. However, its poor aqueous solubility and permeability have reduced its clinical efficacy. Herein, we developed LTZ-nanotransferosomes (LTZ-NT) to address above mentioned issues. The LTZ-NT were optimized statistically using Design Expert® followed by their characterization via dynamic light scattering (DLS), Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), and Differential scanning calorimetry (DSC). The optimized LTZ-NT was incorporated into 1% chitosan-gel to develop LTZ-NTG. Moreover, in vitro drug release and ex vivo permeation of LTZ-NTG were performed and compared with LTZ-dispersion and LTZ-NT. Additionally, skin irritability and histopathology of LTZ-NTG were investigated. Furthermore, in vitro antitumor study of LTZ-NTG was investigated in BC cell lines. The optimized LTZ-NT showed suitable zeta potential (30.4 mV), spherical size (162.5 nm), and excellent entrapment efficiency (88.04%). Moreover, LTZ-NT exhibited suitable thermal behavior and no interactions among its excipients. In addition, LTZ-NTG had an optimal pH (5.6) and a suitable viscosity. A meaningfully sustained release and improved permeation of LTZ was observed from LTZ-NTG. Additionally, LTZ-NTG showed significantly enhanced cell death of MCF-7 and MCC-7 cells. It can be concluded that LTZ-NTG has the potential to deliver chemotherapeutic agents for possible treatment of BC.

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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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