Promising strategies for improving oral bioavailability of poor water-soluble drugs

被引:27
作者
Rocha, Bruna [1 ]
de Morais, Leticia Aparecida [1 ]
Viana, Mateus Costa [1 ]
Carneiro, Guilherme [1 ,2 ]
机构
[1] Fed Univ Jequitinhonha & Mucuri Valleys, Fac Biol & Hlth Sci, Dept Pharm, Diamantina, Brazil
[2] Fed Univ Jequitinhonha & Mucuri Valleys, Dept Pharm, Rodovia MGT 367,Km 583, BR-39100000 Diamantina, Brazil
关键词
Aqueous solubility; biological barriers; hydrophobic drugs; nanostructured systems; oral drug delivery; SOLID LIPID NANOPARTICLES; DELIVERY SYSTEM; IN-VITRO; VIVO EVALUATION; PHARMACOKINETICS; NANOCRYSTALS; FORMULATION; CURCUMIN; NANOSUSPENSIONS; OPTIMIZATION;
D O I
10.1080/17460441.2023.2211801
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionOral administration of poorly water-soluble drugs (PWSDs) is generally related to low bioavailability, leading to high drug doses, multiple side effects, and low patient compliance. Thus, different strategies have been developed to increase drug solubility and dissolution in the gastrointestinal tract, opening new venues for these drugs.Areas coveredThis review outlines the current challenges in PWSD formulation development and the strategies to overcome the oral barriers and increase their solubility and bioavailability. Conventional strategies include altering crystalline and molecular structures and modifying oral solid dosage forms. In contrast, novel strategies comprise micro- and nanostructured systems. Recent representative studies involving how these strategies have improved the oral bioavailability of PWSDs were also reviewed and reported.Expert opinionNew approaches to enhance PWSD bioavailability have sought to improve water solubility and dissolution rates, drug protection by overcoming biological barriers, and increased absorption. Still, only a handful of studies have focused on quantifying the increase in bioavailability. Improving the oral bioavailability of PWSDs remains an exciting unexplored field of research and has become an important issue for successfully developing pharmaceutical products.
引用
收藏
页码:615 / 627
页数:13
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