The Evaluation of Drug Delivery Nanocarrier Development and Pharmacological Briefing for Metabolic-Associated Fatty Liver Disease (MAFLD): An Update

被引:9
作者
Abou Assi, Reem [1 ,2 ]
Abdulbaqi, Ibrahim M. [2 ,3 ]
Siok Yee, Chan [1 ]
机构
[1] Univ Sains Malaysia, Sch Pharmaceut Sci, Discipline Pharmaceut Technol, Thoughts Formulat Lab, Minden 11800, Penang, Malaysia
[2] Al Kitab Univ, Coll Pharm, Discipline Pharmaceut Technol, Altun Kupri 36001, Kirkuk, Iraq
[3] Univ Sains Malaysia, Sch Pharmaceut Sci, Discipline Pharmaceut Technol, Pharmaceut Design & Simulat PhDS Lab, Minden 11800, Penang, Malaysia
关键词
non-alcoholic fatty liver disease (NAFLD); metabolic fatty liver disease (MAFLD); insulin resistance; obesity; nanoformulations; nanotechnology; nanocarrier; nanosystem; NANOSTRUCTURED LIPID CARRIERS; POLYMER HYBRID NANOPARTICLES; NANO-GRAPHENE OXIDE; NONALCOHOLIC STEATOHEPATITIS; CELLULAR UPTAKE; URSODEOXYCHOLIC ACID; HEPATIC STEATOSIS; ANTIINFLAMMATORY PROPERTIES; ORAL BIOAVAILABILITY; INSULIN-RESISTANCE;
D O I
10.3390/ph14030215
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Current research indicates that the next silent epidemic will be linked to chronic liver diseases, specifically non-alcoholic fatty liver disease (NAFLD), which was renamed as metabolic-associated fatty liver disease (MAFLD) in 2020. Globally, MAFLD mortality is on the rise. The etiology of MAFLD is multifactorial and still incompletely understood, but includes the accumulation of intrahepatic lipids, alterations in energy metabolism, insulin resistance, and inflammatory processes. The available MAFLD treatment, therefore, relies on improving the patient's lifestyle and multidisciplinary pharmacotherapeutic options, whereas the option of surgery is useless without managing the comorbidities of the MAFLD. Nanotechnology is an emerging approach addressing MAFLD, where nanoformulations are suggested to improve the safety and physicochemical properties of conventional drugs/herbal medicines, physical, chemical, and physiological stability, and liver-targeting properties. A wide variety of liver nanosystems were constructed and delivered to the liver, only those that addressed the MAFLD were discussed in this review in terms of the nanocarrier classes, particle size, shape, zeta potential and offered dissolution rate(s), the suitable preparation method(s), excipients (with synergistic effects), and the suitable drug/compound for loading. The advantages and challenges of each nanocarrier and the focus on potential promising perspectives in the production of MAFLD nanomedicine were also highlighted.
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页数:36
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