纳米杂交细胞团:靶向药物和基因递送的进步

Kalyani Pathak , Mohammad Zaki Ahmad , Riya Saikia , Partha Protim Borthakur , Pallab Pramanik , Md Ariful Islam , Aparoop Das , Basel A. Abdel-Wahab , Dibyajyoti Das , Saptasikha Gogoi
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摘要

纳米杂化吸附体是给药系统领域的一大进步,是传统吸附体和脂质体的优越替代品。Cerasomes 是一种生物相容性胶体纳米粒子,其特点是比传统脂质体多了一层聚有机硅氧烷网络层,从而增强了其稳定性。新型混合脂质体 Cerasome 具有部分陶瓷或二氧化硅涂层,因其独特的结构而备受关注。与传统脂质体相比,这种结构具有更好的形态稳定性,而且与二氧化硅纳米粒子相比,能显著降低整体硬度和密度。通过结合脂质体结构,cerasomes 比二氧化硅纳米粒子具有更好的生物相容性。这种独特的组合充分利用了脂质体和二氧化硅纳米粒子的优点,同时减轻了它们各自的缺点,使 cerasomes 成为一种最佳的药物输送系统。纳米杂化 cerasomes 可延长药物在血液循环中的停留时间,从而更有效地将药物输送到疾病部位,并促进特定疾病细胞的靶向治疗。它们作为蛋白质、肽、反义化合物、核糖酶和 DNA 的细胞内递送载体的潜力尤其值得注意。由于cerasomes中存在脂质体双分子层结构,因此降低了硬度和密度,增强了其作为药物和基因递送载体的稳定性和有效性。本文回顾了制备 cerasomes 的技术,并探讨了它们在靶向药物和基因递送系统中的应用,突出了它们与传统脂质体和二氧化硅纳米颗粒相比的优势。
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Nanohybrid cerasomes: Advancements in targeted drug and gene delivery

Nanohybrid cerasomes represent a significant advancement in the field of drug delivery systems, offering a superior alternative to traditional cerasomes and liposomes. Cerasomes are biocompatible colloidal nanoparticles characterized by an additional polyorganosiloxane network layer that enhances their stability compared to conventional liposomes. The novel hybrid liposomal cerasome, featuring a partial ceramic or silica coating, has garnered substantial interest due to its unique structure. This structure provides better morphological stability than traditional liposomes and, in comparison to silica nanoparticles, significantly reduces overall stiffness and density. By incorporating liposomal architecture, cerasomes achieve greater biocompatibility than silica nanoparticles. This unique combination leverages the benefits of both liposomes and silica nanoparticles while mitigating their respective drawbacks, positioning cerasomes as an optimal drug delivery system. Nanohybrid cerasomes offer extended circulation residence time, enabling more efficient drug delivery to disease sites and facilitating the targeting of specific disease cells. Their potential as intracellular delivery vehicles for proteins, peptides, antisense compounds, ribozymes, and DNA is particularly noteworthy. The presence of a liposomal bilayer structure in cerasomes reduces rigidity and density, enhancing their stability and effectiveness as drug and gene delivery vehicles. This article reviews the techniques for preparing cerasomes and explores their applications in targeted drug and gene delivery systems, highlighting their advantages over conventional liposomes and silica nanoparticles.

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