Ionic Liquids Research Laboratory, Department of Chemistry, Sardar Vallabhbhai National Institute of Technology, Surat395007, Gujarat ,India.
Solid State Physics Division, Bhabha Atomic Research Centre, Trombay, Mumbai400085, India.
ACS Appl Bio Mater. 2024 May 20;7(5):3110-3123. doi: 10.1021/acsabm.4c00152. Epub 2024 Apr 15.
Transdermal drug delivery systems (TDDS) are a promising and innovative approach for breast cancer treatment, offering advantages such as noninvasiveness, potential for localized and prolonged drug delivery while minimizing systemic side effects through avoiding first-pass metabolism. Utilizing the distinctive characteristics of hydrogels, such as their biocompatibility, versatility, and higher drug loading capabilities, in the present work, we prepared ionic hydrogels through synergistic interaction between ionic liquids (ILs), choline alanine ([Cho][Ala]), and choline proline ([Cho][Pro]) with oleic acid (OA). ILs used in the study are biocompatible and enhance the solubility of 5-fluorouracil (5-FU), whereas OA is a known chemical penetration enhancer. The concentration-dependent (OA) change in morphological aggregates, that is, from cylindrical micelles to worm-like micelles to hydrogels was formed with both ILs and was characterized by SANS measurement, whereas the interactions involved were confirmed by FTIR spectroscopy. The hydrogels have excellent mechanical properties, which studied by rheology and their morphology through FE-SEM analysis. The in vitro skin permeation study revealed that both hydrogels penetrated 255 times ([Cho][Ala]) and 250 times ([Cho][Pro]) more as compared to PBS after 48 h. Those ionic hydrogels exhibited the capability to change the lipid and keratin arrangements within the skin layer, thereby enhancing the transdermal permeation of the 5-FU. Both ionic hydrogels exhibit excellent biocompatibility with normal cell lines (L-132 cells) as well as cancerous cell lines (MCF-7 cells), demonstrating over 92% cell viability after 48 h in both cell lines. In vitro, the cytotoxicity of the 5-FU-loaded hydrogels was evaluated on MCF-7 and HeLa cell lines. These results indicate that the investigated biocompatible and nontoxic ionic hydrogels enable the transdermal delivery of hydrophilic drugs, making them a viable option for effectively treating breast cancer.
经皮给药系统(TDDS)是一种有前途和创新的乳腺癌治疗方法,具有非侵入性、局部和延长药物输送的潜力,同时通过避免首过代谢最小化全身副作用。本工作利用水凝胶的独特特性,如生物相容性、多功能性和更高的药物负载能力,通过离子液体(ILs)、胆碱丙氨酸([Cho][Ala])和胆碱脯氨酸([Cho][Pro])与油酸(OA)的协同相互作用制备离子水凝胶。研究中使用的 ILs 具有生物相容性,并增强了 5-氟尿嘧啶(5-FU)的溶解度,而 OA 是一种已知的化学渗透增强剂。形态聚集体(OA)的浓度依赖性变化,即从圆柱状胶束到蠕虫状胶束到水凝胶,在两种 IL 存在的情况下形成,并通过小角中子散射(SANS)测量进行了表征,而涉及的相互作用通过傅里叶变换红外(FTIR)光谱进行了确认。水凝胶具有出色的机械性能,通过流变学和 FE-SEM 分析研究了它们的形态。体外皮肤渗透研究表明,与 PBS 相比,两种水凝胶在 48 小时后分别渗透了 255 倍([Cho][Ala])和 250 倍([Cho][Pro])。这些离子水凝胶具有改变皮肤层内脂质和角蛋白排列的能力,从而增强了 5-FU 的经皮渗透。两种离子水凝胶对正常细胞系(L-132 细胞)和癌细胞系(MCF-7 细胞)均表现出良好的生物相容性,在两种细胞系中,48 小时后细胞存活率均超过 92%。体外,用载有 5-FU 的水凝胶评估了对 MCF-7 和 HeLa 细胞系的细胞毒性。这些结果表明,所研究的生物相容性和无毒离子水凝胶能够实现亲水性药物的经皮递送,是有效治疗乳腺癌的可行选择。