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用于最大化口服药物递送的纳米颗粒工具。

Nanoparticle tools for maximizing oral drug delivery.

作者信息

Cahyani D M, Mubarok A S, Hariawan B S, Amalina I, Drake P, Parumasivam T, Sahu R K, Rijal M A S, Sari R, Miatmoko A

机构信息

Master Program of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.

Nanotechnology Engineering, Faculty of Advanced Technology and Multidiscipline, Universitas Airlangga, Campus C UNAIR Mulyorejo, Surabaya, Indonesia.

出版信息

Braz J Med Biol Res. 2025 Jun 16;58:e14459. doi: 10.1590/1414-431X2025e14459. eCollection 2025.

Abstract

The biological permeability and water solubility of drugs can pose substantial obstacles to oral drug delivery, the most common mode of drug administration for improving human health. Solubility determines the amount of drug that can be dissolved in solution, whereas permeability is the ability to permeate across biological membranes, determining therapeutic efficacy and safety. Some biological barriers, such as gastrointestinal pH, enzymes, and mucus, may affect the dissolution or absorption of therapeutic drugs. Physical or chemical approaches can be used to modify the water solubility or enhance the permeability. Moreover, nanocarriers, which can increase drug stability through encapsulation, enhance absorption due to their extensive surface area, and facilitate the targeted administration of medications to certain areas, could be useful for drug delivery systems. Nanoparticles can increase drug solubility by particle size reduction, complexation, and drug encapsulation and increase permeation by retention in tumors, opening of tight junctions, membrane fluidization, or intestinal mucoadhesion. Despite the many advantages of nanoparticle drug formulations, they also have several limitations, such as complicated manufacturing processes, nanotoxicity, and stability issues. In this article, we provide a comprehensive description of nanoparticle tools for maximizing oral drug delivery.

摘要

药物的生物渗透性和水溶性可能会对口服给药造成重大障碍,口服给药是改善人类健康最常见的药物给药方式。溶解度决定了可溶解在溶液中的药物量,而渗透性是指药物透过生物膜的能力,它决定了治疗效果和安全性。一些生物屏障,如胃肠道的酸碱度、酶和黏液,可能会影响治疗药物的溶解或吸收。可以采用物理或化学方法来改变水溶性或增强渗透性。此外,纳米载体可通过包裹提高药物稳定性,因其具有较大的表面积而增强吸收,并有助于将药物靶向递送至特定区域,对药物递送系统可能会很有用。纳米颗粒可通过减小粒径、络合和药物包裹来提高药物溶解度,并通过在肿瘤中滞留、打开紧密连接、使膜流化或肠黏膜黏附来增加渗透性。尽管纳米颗粒药物制剂有诸多优点,但它们也存在一些局限性,如复杂的制造工艺、纳米毒性和稳定性问题。在本文中,我们全面介绍了用于最大化口服药物递送的纳米颗粒工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b721/12172155/e572302efa0a/1414-431X-bjmbr-58-e14459-gf001.jpg

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