Lipid-Polymer Hybrid Nanoparticles as a Smart Drug Delivery System for Peptide/Protein Delivery.

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Alharith A A Hassan, Eslam Ramadan, Katalin Kristó, Géza Regdon, Tamás Sovány
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引用次数: 0

Abstract

The efficient oral delivery of therapeutic proteins and peptides poses a tremendous challenge due to their inherent instability, large molecular size, and susceptibility to enzymatic degradation. Several nanocarrier systems, such as liposomes, solid lipid nanoparticles, and polymeric nanoparticles, have been explored to overcome these problems. Liposomes and other lipid-based nanocarriers show excellent biocompatibility and the ability to encapsulate hydrophobic and hydrophilic drugs; however, they often suffer from poor structural stability, premature leakage of the loaded drugs, and poor encapsulation efficiency for macromolecular peptides and proteins. On the other hand, polymeric nanoparticles are more stable and allow better control over drug release; nevertheless, they usually lack the necessary biocompatibility and cellular uptake efficiency. Recently, lipid-polymer hybrid nanoparticles (LPHNs) have emerged as an advanced solution combining the structural stability of polymers and the biocompatibility and surface functionalities of lipids to enhance the controlled release, stability, and bioavailability of protein and peptide drugs. In this review, an attempt was made to set a clear definition of the LPHNs and extend the concept and area, so to our knowledge, this is the first review that highlights six categories of the LPHNs based on their anatomy. Moreover, this review offers a detailed analysis of LPHN preparation methods, including conventional and nonconventional one-step and two-step processes, nanoprecipitation, microfluidic mixing, and emulsification methods. Moreover, the material attributes and critical process parameters affecting the output of the preparation methods were illustrated with supporting examples to enable researchers to select the suitable preparation method, excipients, and parameters to be manipulated to get the LPHNs with the predetermined quality. The number of reviews focusing on the formulation of peptide/protein pharmaceutics usually focus on a specific drug like insulin. To our knowledge, this is the first review that generally discusses LPHN-based delivery of biopharmaceuticals. by discussing representative examples of previous reports comparing them to a variety of nanocarrier systems to show the potentiality of the LPHNs to deliver peptides and proteins. Moreover, some ideas and suggestions were proposed by the authors to tackle some of the shortcomings highlighted in these studies. By presenting this comprehensive overview of LPHN preparation strategies and critically analyzing literature studies on this topic and pointing out their strong and weak points, this review has shown the gaps and enlightened avenues for future research.

脂质-聚合物混合纳米颗粒作为肽/蛋白质传递的智能药物传递系统。
由于其固有的不稳定性、大分子大小和对酶降解的敏感性,治疗性蛋白质和肽的有效口服递送面临着巨大的挑战。一些纳米载体系统,如脂质体、固体脂质纳米颗粒和聚合物纳米颗粒,已经被探索来克服这些问题。脂质体和其他脂基纳米载体表现出优异的生物相容性和包封疏水和亲水药物的能力;但其结构稳定性较差,载药过早渗漏,对大分子多肽和蛋白质的包封效率较差。另一方面,聚合物纳米颗粒更稳定,可以更好地控制药物释放;然而,它们通常缺乏必要的生物相容性和细胞摄取效率。近年来,脂质-聚合物混合纳米颗粒(lphn)作为一种先进的解决方案,结合了聚合物的结构稳定性和脂质的生物相容性和表面功能,以提高蛋白质和肽类药物的控释、稳定性和生物利用度。在这篇综述中,我们试图明确lphn的定义,并扩展其概念和范围,因此,据我们所知,这是第一次根据lphn的解剖结构重点介绍6类lphn。此外,本文还详细分析了LPHN的制备方法,包括常规和非常规的一步法和两步法、纳米沉淀法、微流控混合法和乳化法。并举例说明了影响制备方法输出的材料属性和关键工艺参数,使研究人员能够选择合适的制备方法、辅料和操作参数,以获得具有预定质量的lphn。关于肽/蛋白制剂的综述通常集中在胰岛素等特定药物上。据我们所知,这是第一次普遍讨论基于lphn的生物药物递送的综述。通过讨论先前报告的代表性例子,将它们与各种纳米载体系统进行比较,以显示lphn递送肽和蛋白质的潜力。此外,针对这些研究中突出的一些不足,作者提出了一些想法和建议。本文通过对LPHN制备策略的全面概述,批判性地分析有关该主题的文献研究并指出其优缺点,指出了未来研究的差距和启示途径。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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