Swarupananda Mukherjee, Ayon Dutta, Dipanjana Ash, Dipanjan Karati
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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. 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引用次数: 0
摘要
立方体是一种新型给药系统,近年来因其独特的自组装结构和更强的药物封装能力而备受关注。它们可通过口服、眼科、透皮和化疗等途径给药。由于它们具有许多潜在的优点--包括立方结构带来的高药物分散性、大表面积、相对简单的制造工艺、生物可降解性、封装疏水性、亲水性和两性化合物的能力、生物活性剂的定向和控制释放以及脂质的生物可降解性--在癌症治疗药物纳米制剂方面显示出巨大的前景。最常见的制备方法是将单甘酯与聚合物乳化、均质,然后对混合物进行超声处理。自上而下和自下而上是两种不同的制备方法。本评估将研究材料、制备方法、立方体相关的药物封装技术、药物负载、释放机制及其用途。文献检索使用了以下数据库:PubMed、Frontiers、Science Direct、Springer、Wiley 和 MDPI。为了查找相关文章和内容(2015-2024 年),使用了关键词 "cubosome; drug delivery systems, nano-carrier, theranostic, drug release mechanism "及其他类似性质的关键词。本综述将全面分析立方体的相关组成、生产方法、药物封装策略、药物释放机制和应用。此外,还将讨论在微调不同参数以提高装载能力方面遇到的困难和前景。有关立方体给药方法的知识可以促进药物研发的创新。通过阐明立方体释放药物的机制和研究创新的制造程序,科学家们可以提高立方体配方设计的针对性治疗用途。.
An Insight into Cubosomal Drug Delivery Approaches: An Explicative Review.
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.
期刊介绍:
Pharmaceutical Nanotechnology publishes original manuscripts, full-length/mini reviews, thematic issues, rapid technical notes and commentaries that provide insights into the synthesis, characterisation and pharmaceutical (or diagnostic) application of materials at the nanoscale. The nanoscale is defined as a size range of below 1 µm. Scientific findings related to micro and macro systems with functionality residing within features defined at the nanoscale are also within the scope of the journal. Manuscripts detailing the synthesis, exhaustive characterisation, biological evaluation, clinical testing and/ or toxicological assessment of nanomaterials are of particular interest to the journal’s readership. Articles should be self contained, centred around a well founded hypothesis and should aim to showcase the pharmaceutical/ diagnostic implications of the nanotechnology approach. Manuscripts should aim, wherever possible, to demonstrate the in vivo impact of any nanotechnological intervention. As reducing a material to the nanoscale is capable of fundamentally altering the material’s properties, the journal’s readership is particularly interested in new characterisation techniques and the advanced properties that originate from this size reduction. Both bottom up and top down approaches to the realisation of nanomaterials lie within the scope of the journal.