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Aptamer-Mediated Polymeric Vehicles for Enhanced Cell-Targeted Drug Delivery

适体 药物输送 靶向给药 治疗指标 药品 脂质体 化学 纳米载体 药代动力学 纳米技术 控制释放 毒品携带者 内吞作用 生物物理学 药理学 小分子 细胞生物学 医学 材料科学 生物化学 生物 分子生物学
作者
Kei Xian Tan,Michael K. Danquah,Amandeep S. Sidhu,Lau Sie Yon,Clarence M. Ongkudon
出处
期刊:Current Drug Targets [Bentham Science]
卷期号:19 (3) 被引量:9
标识
DOI:10.2174/1389450117666160617120926
摘要

Background: The search for smart delivery systems for enhanced pre-clinical and clinical pharmaceutical delivery and cell targeting continues to be a major biomedical research endeavor owing to differences in the physicochemical characteristics and physiological effects of drug molecules, and this affects the delivery mechanisms to elicit maximum therapeutic effects. Targeted drug delivery is a smart evolution essential to address major challenges associated with conventional drug delivery systems. These challenges mostly result in poor pharmacokinetics due to the inability of the active pharmaceutical ingredients to specifically act on malignant cells thus, causing poor therapeutic index and toxicity to surrounding normal cells. Aptamers are oligonucleotides with engineered affinities to bind specifically to their cognate targets. Aptamers have gained significant interests as effective targeting elements for enhanced therapeutic delivery as they can be generated to specifically bind to wide range of targets including proteins, peptides, ions, cells and tissues. Notwithstanding, effective delivery of aptamers as therapeutic vehicles is challenged by cell membrane electrostatic repulsion, endonuclease degradation, low pH cleavage, and binding conformation stability. Objective: The application of molecularly engineered biodegradable and biocompatible polymeric particles with tunable features such as surface area and chemistry, particulate size distribution and toxicity creates opportunities to develop smart aptamer-mediated delivery systems for controlled drug release. Results: This article discusses opportunities for particulate aptamer-drug formulations to advance current drug delivery modalities by navigating active ingredients through cellular and biomolecular traffic to target sites for sustained and controlled release at effective therapeutic dosages while minimizing systemic cytotoxic effects. Conclusion: A proposal for a novel drug-polymer-aptamer-polymer (DPAP) design of aptamer-drug formulation with stage-wise delivery mechanism is presented to illustrate the potential efficacy of aptamer- polymer cargos for enhanced cell targeting and drug delivery. Keywords: Aptamer, drug delivery, biodegradable polymer, encapsulation, cell targeting, DPAP.
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