Calixarene-Guest Complexes: The Next Innovation in Delivery of Drugs and Biologics

IF 3.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY Advanced Therapeutics Pub Date : 2024-07-17 DOI:10.1002/adtp.202400207
Sheetal Muley, Hozefa Dhila, Meghana Gote
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Abstract

Calixarenes are third generation of macrocyclic molecules with excellent biocompatibility currently being researched extensively for their diverse potential as therapeutic candidates and for delivery of drugs and biologics. This review discusses the unique structural features which allow them to selectively bind to a wide variety of guest molecules within their hydrophobic cavity, as well as complex with other molecules on their upper and lower rims to enable their application for encapsulation of drugs for targeted and controlled release, molecular carriers for antigens and nucleic acids, and as biomedical sensors. The calixarenes’ unique host–guest chemistry enables encapsulation of lipophilic drugs in the latter's cavity, while the head groups and side chains on the upper and lower rim can be functionalized readily with various targeting moieties as peptides and biological ligands which specifically recognize and bind to cancer cells via surface receptors. The design of calixarene constructs help incorporation of multiple functionalities into a single platform. This active targeting approach enhances the accumulation of the drug at the tumor site while reducing its distribution in healthy tissues, thereby minimizing side effects. Ongoing research in exploration and optimization of calixarenes for application as targeted drug and gene delivery agents has been discussed.

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卡利卡林-客体复合物:药物和生物制剂递送领域的下一次创新
钙杂烯类是第三代大环分子,具有极佳的生物相容性,目前正被广泛研究用于治疗候选药物以及药物和生物制剂的输送。本综述将讨论钙钛矿类化合物的独特结构特征,这些特征使钙钛矿类化合物能够在其疏水空腔内选择性地与各种客体分子结合,并在其上下边缘与其他分子复合,从而使其能够应用于药物的封装以实现定向和控制释放、抗原和核酸的分子载体以及生物医学传感器。钙杂烯类化合物独特的主客化学性质可将亲脂性药物封装在后者的空腔中,而上下边缘的头部基团和侧链则可随时与各种靶向分子进行官能化,如肽和生物配体,它们可通过表面受体特异性地识别癌细胞并与之结合。卡利卡尼构建体的设计有助于在单一平台上整合多种功能。这种主动靶向方法可增强药物在肿瘤部位的蓄积,同时减少其在健康组织中的分布,从而将副作用降至最低。会上还讨论了在探索和优化钙钛矿作为靶向药物和基因递送剂的应用方面正在进行的研究。
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来源期刊
Advanced Therapeutics
Advanced Therapeutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.10
自引率
2.20%
发文量
130
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