溶致液晶作为纳米载体递送系统治疗癌症的现状与展望

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Raj Baldha, G. S. Chakraborthy, Sachin Rathod
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引用次数: 0

摘要

多药耐药(MDR)降低了治疗的有效性,给癌症治疗带来了重大挑战。本文综述了溶致液晶(LLCs)作为克服耐多药耐药的创新纳米载体系统的潜力。llc的特点是其内部结构高度有序,可以自组装成各种相,包括层状、六边形和立方几何形状。这些结构允许llc封装和释放不同大小和极性的货物,使其成为药物输送应用的有希望的候选者。llc的相——无论是立方的、六边形的还是片状的——都可以影响被封装药物的物理化学性质,从而实现定制的释放特征,如持续、控制或靶向递送。本文还探讨了两亲化合物、添加剂和疏水分子在分子几何结构上的转变,这些转变会影响具有不同孔径和水通道的LLC相的形成和稳定性。该结论强调了正在进行的有限责任公司研究对解决包括耐多药在内的癌症治疗挑战的重要性。llc的多功能性从药物输送扩展到治疗和诊断应用。通过利用反应灵敏的智能药物输送系统或结合天然化合物,有限责任公司为癌症治疗提供了多方面的方法,突出了它们作为该领域突破的潜力。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current Status and Future Prospects of Lyotropic Liquid Crystals as a Nanocarrier Delivery System for the Treatment of Cancer

Multidrug resistance (MDR) poses a significant challenge in cancer treatment by reducing the efficacy of therapies. This review highlights the potential of lyotropic liquid crystals (LLCs) as innovative nanocarrier systems to overcome MDR. LLCs are characterized by their highly ordered internal structures, which can self-assemble into various phases, including lamellar, hexagonal, and cubic geometries. These structures allow LLCs to encapsulate and release cargo with diverse sizes and polarities, making them promising candidates for drug delivery applications. The phase of LLCs—whether cubic, hexagonal, or lamellar—can influence the physicochemical properties of encapsulated drugs, enabling tailored release profiles such as sustained, controlled, or targeted delivery. This review also explores the transitions in molecular geometry of amphiphilic compounds, additives, and hydrotrope molecules, which affect the formation and stability of LLC phases with varying pore sizes and water channels. The conclusion underscores the importance of ongoing research into LLCs for addressing cancer treatment challenges, including MDR. The versatility of LLCs extends beyond drug delivery to theranostic and diagnostic applications. By leveraging responsive smart drug delivery systems or incorporating natural compounds, LLCs offer a multifaceted approach to cancer therapy, highlighting their potential as a breakthrough in the field.

Graphical Abstract

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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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