Lipid-Based Nanocarriers for Oral Delivery of Proteins and Peptides: Opportunities, Challenges, and Future Prospects

Jannatul Naim, N. Sharmin, Madhabi Lata Shuma, S. Halder
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引用次数: 1

Abstract

Oral administration is the most common drug delivery route with high levels of patient acceptance. However, oral delivery of therapeutic proteins/peptides is extremely difficult, and improving the pharmacological bioavailability still is a challenging goal because of the poor membrane permeability, high molecular weight, and enzymatic degradation of these drugs. Lipid-based nanocarriers represent a viable means for enhancing the oral bioavailability of protein or peptide drugs while minimizing toxicity. Nowadays, like other macromolecules protein or peptide drugs are the promising candidates to be delivered employing liposomes and lipid nanoparticles including solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC). Generally, these drug delivery strategies can reduce protein or peptide drug degradation and improve membrane permeability thus enhance bioavailability. This review demonstrates various lipid-based formulation strategies used for successful oral delivery of peptides and proteins, assesses the hurdles and delivery efficiency and their clinical implications. Dhaka Univ. J. Pharm. Sci. 20(3): 395-416, 2022 (June) Centennial Special Issue
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用于蛋白质和多肽口服递送的脂基纳米载体:机遇、挑战和未来前景
口服给药是最常见的给药途径,患者接受程度高。然而,治疗性蛋白/肽的口服递送非常困难,并且由于这些药物的膜渗透性差,分子量高,酶降解,提高药理学生物利用度仍然是一个具有挑战性的目标。脂基纳米载体是提高蛋白质或肽药物的口服生物利用度同时最小化毒性的可行手段。目前,与其他大分子蛋白质或多肽药物一样,脂质体和脂质纳米颗粒是最有希望被用于递送的药物,包括固体脂质纳米颗粒(SLN)和纳米结构脂质载体(NLC)。一般来说,这些给药策略可以减少蛋白质或肽药物的降解,提高膜的通透性,从而提高生物利用度。这篇综述展示了各种基于脂质的配方策略,用于成功的口服递送多肽和蛋白质,评估障碍和递送效率及其临床意义。达卡大学药学院。科学通报,20(3):395-416,2022(6)百年特刊
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