智能脂质:开创脂质纳米颗粒给药新时代

Bhawna Sharma, Iti Chauhan, Gaurav Kumar, Raj kumar Tiwari
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引用次数: 0

摘要

在给药领域,脂质纳米粒子已成为一种多功能载体,可增强治疗剂的封装、保护和靶向给药。在这些创新系统中,SmartLipids 是一项突破性进展,代表了最新一代的脂质纳米粒子。SmartLipids 以其独特的 "混沌 "和无序颗粒基质结构为特征,表现出不同于传统给药系统的显著特性。本综述深入探讨了智能脂质错综复杂的世界,揭示了其与众不同的特点,并探索了其在给药领域的巨大潜力。综述细致概述了其生产方法,阐明了确保生物相容性和安全性的无溶剂高压均质化技术。该综述细致研究了 SmartLipids 的理化特性,深入探讨了它们的颗粒大小、形态和封装效率。该研究共同强调了 SmartLipids 的多功能性和可定制性,强调了它们适用于广泛的给药应用。从封装亲水性、亲脂性和两亲性化合物到定制特定的释放曲线,SmartLipids 为给药策略提供了极大的灵活性。
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SmartLipids: Ushering in a New Era of Lipid Nanoparticles for Drug Delivery
In the realm of drug delivery, lipid nanoparticles have emerged as versatile carriers, offering enhanced encapsulation, protection, and targeted delivery of therapeutic agents. Among these innovative systems, SmartLipids stands out as a groundbreaking advancement, representing the latest generation of lipid nanoparticles. Characterized by their unique "chaotic" and disordered particle matrix structure, SmartLipids exhibit remarkable properties that set them apart from conventional drug delivery systems. This comprehensive review delves into the intricate world of SmartLipids, unraveling their distinctive features and exploring their immense potential in the field of drug delivery. It meticulously outlines their production methods, shedding light on the solvent-free, highpressure homogenization technique that ensures biocompatibility and safety. The review meticulously examines the physicochemical characterization of SmartLipids, providing insights into their particle size, morphology, and encapsulation efficiency. It further delves into their in vitro and in vivo performance, highlighting their ability to enhance drug solubility, permeability, and bioavailability. The study collectively underscores the versatility and customizable nature of SmartLipids, emphasizing their suitability for a wide range of drug delivery applications. From encapsulating hydrophilic, lipophilic, and amphiphilic compounds to tailoring specific release profiles, SmartLipids offer a remarkable degree of flexibility in drug delivery strategies.
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来源期刊
Micro and Nanosystems
Micro and Nanosystems Engineering-Building and Construction
CiteScore
1.60
自引率
0.00%
发文量
50
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