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表面功能化脂质纳米粒子在促进治疗效果中的作用:动态药物传递系统的深入观察。

Surface Functionalized Lipid Nanoparticles in Promoting Therapeutic Outcomes: An Insight View of the Dynamic Drug Delivery System.

机构信息

Department of Pharmaceutics, School of Pharmaceutical Sciences, Delhi Pharmaceutical Sciences and Research University (DPSRU), Government of NCT of Delhi, Mehrauli-Badarpur Road, Pushp Vihar Sector-3, New Delhi-110017, Delhi (NCT), India.

Centre of Pharmaceutical Nanotechnology, Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), S.A.S Nagar, India.

出版信息

Curr Drug Targets. 2024;25(4):278-300. doi: 10.2174/0113894501285598240216065627.

Abstract

Compared to the conventional approach, nanoparticles (NPs) facilitate a non-hazardous, non-toxic, non-interactive, and biocompatible system, rendering them incredibly promising for improving drug delivery to target cells. When that comes to accomplishing specific therapeutic agents like drugs, peptides, nucleotides, , lipidic nanoparticulate systems have emerged as even more robust. They have asserted impressive ability in bypassing physiological and cellular barriers, evading lysosomal capture and the proton sponge effect, optimizing bioavailability, and compliance, lowering doses, and boosting therapeutic efficacy. However, the lack of selectivity at the cellular level hinders its ability to accomplish its potential to the fullest. The inclusion of surface functionalization to the lipidic NPs might certainly assist them in adapting to the basic biological demands of a specific pathological condition. Several ligands, including peptides, enzymes, polymers, saccharides, antibodies, ., can be functionalized onto the surface of lipidic NPs to achieve cellular selectivity and avoid bioactivity challenges. This review provides a comprehensive outline for functionalizing lipid-based NPs systems in prominence over target selectivity. Emphasis has been put upon the strategies for reinforcing the therapeutic performance of lipidic nano carriers' using a variety of ligands alongside instances of relevant commercial formulations.

摘要

与传统方法相比,纳米颗粒(NPs)促进了一种无危险、无毒、非相互作用和生物相容的系统,使它们在改善药物递送到靶细胞方面极具前景。当涉及到实现特定的治疗剂,如药物、肽、核苷酸等时,脂质纳米颗粒系统变得更加稳健。它们在绕过生理和细胞屏障、逃避溶酶体捕获和质子海绵效应、优化生物利用度和顺应性、降低剂量和提高治疗效果方面表现出了令人印象深刻的能力。然而,细胞水平缺乏选择性限制了它充分发挥潜力的能力。将表面功能化纳入脂质 NPs 肯定有助于它们适应特定病理状况的基本生物学需求。几种配体,包括肽、酶、聚合物、糖、抗体等,可以在脂质 NPs 的表面进行功能化,以实现细胞选择性并避免生物活性挑战。这篇综述为脂质 NPs 系统的靶向选择性功能化提供了全面的概述。重点介绍了通过使用各种配体和相关商业制剂的实例来增强脂质纳米载体治疗性能的策略。

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