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立方液晶药物递送方法的洞察:解释性综述。

An Insight into Cubosomal Drug Delivery Approaches: An Explicative Review.

作者信息

Mukherjee Swarupananda, Dutta Ayon, Ash Dipanjana, Karati Dipanjan

机构信息

Department of Pharmaceutical Technology, NSHM Knowledge Campus, Kolkata-700053, West Bengal, India.

Department of Pharmaceutical Technology, Brainware University, 398, Ramkrishnapur Road, Barasat, Kolkata 700125, West Bengal, India.

出版信息

Pharm Nanotechnol. 2024 Jun 20. doi: 10.2174/0122117385306495240529052911.

Abstract

Cubosomes, a novel drug delivery system, have gained significant attention in recent years due to their unique self-assembled structures and enhanced drug encapsulation capabilities. They are administered by oral, ophthalmic, transdermal, and chemotherapeutic routes, to name a few. Due to their many potential benefits-which include high drug dispersal due to the cubic structure, a large surface area, a relatively simple manufacturing process, biodegradability, the capacity to encapsulate hydrophobic, hydrophilic, and amphiphilic compounds, targeted and controlled release of bioactive agents, and the biodegradability of lipids-cubosomes show enormous promise in drug nanoformulations for cancer therapeutics. The most common preparation method involves emulsifying a monoglyceride with a polymer, homogenizing, and then sonicating the mixture. Two distinct approaches to preparing are top-down and bottom-up. This evaluation will examine the materials, methods of preparation, cubosome-related drug encapsulating techniques, drug loading, release mechanism, and their uses. The following databases were used for literature searches: PubMed, Frontiers, Science Direct, Springer, Wiley, and MDPI. For the purpose of finding pertinent articles and contents (2015-2024), the keywords "cubosome; drug delivery systems, nano-carrier, theranostic, drug release mechanism" and others of a similar nature were utilized. This review will conduct a comprehensive analysis of the cubosome-related composition, production methods, drug encapsulating strategies, drug release mechanisms, and applications. Moreover, the difficulties encountered in fine-tuning different parameters to improve loading capabilities and prospects are also discussed. Innovation in pharmaceutical research and development can be stimulated by the knowledge gathered about cubosomal drug delivery methods. Through the clarification of the mechanisms involved in drug release from cubosomes and the investigation of innovative fabrication procedures, scientists can enhance the cubosomal formulation design for targeted therapeutic uses.

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摘要

立方液晶纳米粒作为一种新型药物递送系统,近年来因其独特的自组装结构和增强的药物包封能力而备受关注。它们可通过口服、眼部、透皮和化疗等途径给药,仅举几例。由于其具有许多潜在优势,包括立方结构导致的高药物分散性、大表面积、相对简单的制造工艺、生物可降解性、包封疏水、亲水和两亲性化合物的能力、生物活性剂的靶向和控释以及脂质的生物可降解性,立方液晶纳米粒在癌症治疗的药物纳米制剂中显示出巨大的前景。最常见的制备方法是将单甘油酯与聚合物乳化,均质化,然后对混合物进行超声处理。制备的两种不同方法是自上而下和自下而上。本评估将研究材料、制备方法、与立方液晶纳米粒相关的药物包封技术、载药量、释放机制及其用途。使用了以下数据库进行文献检索:PubMed、Frontiers、Science Direct、Springer、Wiley和MDPI。为了找到相关文章和内容(2015 - 2024年),使用了关键词“立方液晶纳米粒;药物递送系统、纳米载体、诊疗一体化、药物释放机制”以及其他类似性质的关键词。本综述将对与立方液晶纳米粒相关的组成、生产方法、药物包封策略、药物释放机制和应用进行全面分析。此外,还讨论了在微调不同参数以提高载药能力方面遇到的困难和前景。关于立方液晶纳米粒药物递送方法的知识可以激发药物研发的创新。通过阐明立方液晶纳米粒药物释放所涉及的机制以及研究创新的制备程序,科学家可以改进用于靶向治疗用途的立方液晶纳米粒制剂设计。

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