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用于药物递送的固体脂质纳米粒:药理学和生物药剂学方面

Solid Lipid Nanoparticles for Drug Delivery: Pharmacological and Biopharmaceutical Aspects.

作者信息

Scioli Montoto Sebastián, Muraca Giuliana, Ruiz María Esperanza

机构信息

Laboratorio de Investigación y Desarrollo de Bioactivos, Departamento de Ciencias Biológicas, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina.

Consejo Nacional de Investigaciones Científicas y Técnicas, Buenos Aires, Argentina.

出版信息

Front Mol Biosci. 2020 Oct 30;7:587997. doi: 10.3389/fmolb.2020.587997. eCollection 2020.

Abstract

In the golden age of pharmaceutical nanocarriers, we are witnessing a maturation stage of the original concepts and ideas. There is no doubt that nanoformulations are extremely valuable tools for drug delivery applications; the current challenge is how to optimize them to ensure that they are safe, effective and scalable, so that they can be manufactured at an industrial level and advance to clinical use. In this context, lipid nanoparticles have gained ground, since they are generally regarded as non-toxic, biocompatible and easy-to-produce formulations. Pharmaceutical applications of lipid nanocarriers are a burgeoning field for the transport and delivery of a diversity of therapeutic agents, from biotechnological products to small drug molecules. This review starts with a brief overview of the characteristics of solid lipid nanoparticles and discusses the relevancy of performing systematic preformulation studies. The main applications, as well as the advantages that this type of nanovehicles offers in certain therapeutic scenarios are discussed. Next, pharmacokinetic aspects are described, such as routes of administration, absorption after oral administration, distribution in the organism (including brain penetration) and elimination processes. Safety and toxicity issues are also addressed. Our work presents an original point of view, addressing the biopharmaceutical aspects of these nanovehicles by means of descriptive statistics of the state-of-the-art of solid lipid nanoparticles research. All the presented results, trends, graphs and discussions are based in a systematic (and reproducible) bibliographic search that considered only original papers in the subject, covering a 7 years range (2013-today), a period that accounts for more than 60% of the total number of publications in the topic in the main bibliographic databases and search engines. Focus was placed on the therapeutic fields of application, absorption and distribution processes and current efforts for the translation into the clinical practice of lipid-based nanoparticles. For this, the currently active clinical trials on lipid nanoparticles were reviewed, with a brief discussion on what achievements or milestones are still to be reached, as a way of understanding the reasons for the scarce number of solid lipid nanoparticles undergoing clinical trials.

摘要

在药物纳米载体的黄金时代,我们正见证着最初概念和想法的成熟阶段。毫无疑问,纳米制剂是药物递送应用中极其有价值的工具;当前的挑战是如何对其进行优化,以确保它们安全、有效且可扩展,从而能够在工业规模上生产并推进到临床应用。在这种背景下,脂质纳米颗粒已获得认可,因为它们通常被视为无毒、生物相容且易于生产的制剂。脂质纳米载体的药物应用是一个新兴领域,可用于多种治疗剂的运输和递送,从生物技术产品到小分子药物。本综述首先简要概述了固体脂质纳米颗粒的特性,并讨论了进行系统的处方前研究的相关性。讨论了这类纳米载体的主要应用以及在某些治疗场景中所具有的优势。接下来描述了药代动力学方面,如给药途径、口服给药后的吸收、在生物体内的分布(包括脑渗透)以及消除过程。还探讨了安全性和毒性问题。我们的工作提出了一个独到的观点,即通过对固体脂质纳米颗粒研究现状的描述性统计来阐述这些纳米载体的生物制药方面。所有呈现的结果、趋势、图表和讨论均基于系统的(且可重复的)文献检索,该检索仅考虑该主题的原创论文,涵盖7年范围(2013年至今),这一时期占主要文献数据库和搜索引擎中该主题出版物总数的60%以上。重点放在治疗应用领域、吸收和分布过程以及当前将基于脂质的纳米颗粒转化为临床实践的努力上。为此,对目前关于脂质纳米颗粒的活跃临床试验进行了综述,并简要讨论了仍有待实现的成就或里程碑,以此来理解进行临床试验的固体脂质纳米颗粒数量稀少的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ed/7662460/d683e58b943c/fmolb-07-587997-g001.jpg

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