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解决常规脂质体制剂 PK-PD 挑战的方法,特别针对癌症、阿尔茨海默病、糖尿病和青光眼:改良脂质体药物传递系统的最新进展。

Approaches to Address PK-PD Challenges of Conventional Liposome Formulation with Special Reference to Cancer, Alzheimer's, Diabetes, and Glaucoma: An Update on Modified Liposomal Drug Delivery System.

机构信息

Department of Pharmacy, Banasthali Vidyapith University, Banasthali, P.O. Rajasthan, India.

出版信息

Curr Drug Metab. 2022;23(9):678-692. doi: 10.2174/1389200223666220609141459.

Abstract

Liposomes nowadays have become a preferential drug delivery system since they provide facilitating properties to drugs, such as improved therapeutic index of encapsulated drug, target and controlled drug delivery, and less toxicity. However, conventional liposomes have shown some disadvantages, such as less drug loading capacity, poor retention, clearance by kidney or reticuloendothelial system, and less release of hydrophilic drugs. Thus, to overcome these disadvantages recently, scientists have explored new approaches and methods, viz., ligand conjugation, polymer coating, and liposome hybrids, including surface-modified liposomes, biopolymer-incorporated liposomes, guest-in-cyclodextrin-in-liposome, liposome-in-hydrogel, liposome-in-film, liposome-in-nanofiber, etc. These approaches have been shown to improve the physiochemical and pharmacokinetic properties of encapsulated drugs. Lately, pharmacokinetic-pharmacodynamic (PK-PD) computational modeling has emerged as a beneficial tool for analyzing the impact of formulation and system-specific factors on the target disposition and therapeutic efficacy of liposomal drugs. There has been an increasing number of liposome-based therapeutic drugs, both FDA approved and those undergoing clinical trials, having application in cancer, Alzheimer's, diabetes, and glaucoma. To meet the continuous demand of health sectors and to produce the desired product, it is important to perform pharmacokinetic studies. This review focuses on the physical, physicochemical, and chemical factors of drugs that influence the target delivery of drugs. It also explains various physiological barriers, such as systemic clearance and extravasation. A novel approach, liposomal-hybrid complex, an innovative approach as a vesicular drug delivery system to overcome limited membrane permeability and bioavailability, has been discussed in the review. Moreover, this review highlights the pharmacokinetic considerations and challenges of poorly absorbed drugs along with the applications of a liposomal delivery system in improving PKPD in various diseases, such as cancer, Alzheimer's, diabetes, and glaucoma.

摘要

如今,脂质体已成为一种优先的药物传递系统,因为它们为药物提供了一些有利的特性,如提高包封药物的治疗指数、靶向和控制药物传递、降低毒性。然而,传统的脂质体也表现出一些缺点,如载药量低、保留性差、被肾脏或网状内皮系统清除、以及亲水性药物的释放减少。因此,为了克服这些缺点,科学家们最近探索了新的方法和途径,例如配体偶联、聚合物涂层和脂质体杂化,包括表面修饰的脂质体、生物聚合物包埋的脂质体、客体-环糊精-脂质体、脂质体-水凝胶、脂质体-薄膜、脂质体-纳米纤维等。这些方法已被证明可以改善包封药物的物理化学和药代动力学性质。最近,药代动力学-药效学(PK-PD)计算模型已成为一种有益的工具,可用于分析制剂和系统特定因素对脂质体药物的靶分布和治疗效果的影响。越来越多的基于脂质体的治疗药物,包括 FDA 批准的和正在进行临床试验的,已应用于癌症、阿尔茨海默病、糖尿病和青光眼。为了满足卫生部门的持续需求并生产所需的产品,进行药代动力学研究非常重要。本文重点介绍了影响药物靶向传递的药物物理、物理化学和化学因素。它还解释了各种生理屏障,如全身清除率和外渗。本文还讨论了一种新的方法,即脂质体-杂化复合物,作为一种囊泡药物传递系统,以克服有限的膜通透性和生物利用度,这是一种创新的方法。此外,本文还强调了吸收不良药物的药代动力学考虑因素和挑战,以及脂质体传递系统在提高各种疾病(如癌症、阿尔茨海默病、糖尿病和青光眼)的 PKPD 方面的应用。

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