Nanocochleates in Clinical Trials: A Review of Current Status, Challenges, and Future Directions.

IF 1.8 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Alka Singh, Sushma Verma
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引用次数: 0

Abstract

Nanocochleates are novel lipid-based nanoparticles with a distinctive, multilayered, rolled-up structure that resembles the spirals of a cochlea. They form when bivalent cations, such as calcium, interact with negatively charged lipid bilayers. These structures are gaining popularity in drug delivery due to their stability, biocompatibility, and ability to encapsulate and shield a wide range of bioactive substances, including hydrophobic drugs, peptides, and nucleic acids. Nanocochelates can withstand harsh environmental conditions, such as acidic pH or enzymatic degradation, making them suitable carriers for oral, injectable, and transdermal medication administration. Their unique construction ena-bles the gradual release of encapsulated medicines, thereby increasing bioavailability and therapeutic effectiveness. Additionally, nanocochleates can target specific tissues or cells, allowing for precision medical methods. A recent study demonstrates their promise for overcoming issues in the administration of poorly water-soluble medicines, gene therapy agents, and vaccines. Nanocochleates have shown promise in preclin-ical trials for the management of inflammatory diseases, cancer, and infectious diseases. Despite their potential, further research is needed to optimize large-scale manufacturing, maintain uniform quality, and address regulatory challenges. This review provides a detailed discussion of nanocochleate prepa-ration methods, with a particular focus on entrapment, hydrogel approaches, and dialysis methods. The paper reviews characterization experiments, including particle size measurements, encapsulation effec-tiveness, surface morphology, and in vitro release tests. Furthermore, the article discusses the feasibility of industrial-scale formation with pure lipid feedstock.

临床试验中的纳米螯合物:现状、挑战和未来方向的综述。
纳米耳蜗是一种新型的脂质纳米颗粒,具有独特的多层卷曲结构,类似于耳蜗的螺旋结构。当二价阳离子(如钙)与带负电荷的脂质双分子层相互作用时,它们就形成了。由于其稳定性、生物相容性以及包封和屏蔽多种生物活性物质(包括疏水药物、多肽和核酸)的能力,这些结构在药物输送中越来越受欢迎。纳米螯合物可以承受恶劣的环境条件,如酸性pH值或酶降解,使其成为口服、注射和透皮给药的合适载体。其独特的结构使胶囊化药物逐渐释放,从而提高生物利用度和治疗效果。此外,纳米藻酸盐可以针对特定的组织或细胞,从而实现精确的医疗方法。最近的一项研究表明,它们有望克服水溶性差的药物、基因治疗药物和疫苗的管理问题。纳米螯合物在治疗炎症性疾病、癌症和传染病的临床前试验中显示出前景。尽管它们具有潜力,但还需要进一步的研究来优化大规模生产,保持统一的质量,并应对监管挑战。这篇综述提供了纳米酸盐制备方法的详细讨论,特别侧重于包埋,水凝胶方法和透析方法。本文综述了表征实验,包括粒径测量、包封效果、表面形貌和体外释放试验。此外,本文还讨论了以纯油脂为原料进行工业规模合成的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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