Lymphatic Drug Delivery System and Lipid-based Nanoformulations: Savior to Save for Patients Receiving Highly Hepatotoxic Drugs.

IF 2.3 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Vishal Kumar Vishwakarma, Prabhat Kumar Upadhyay, Nandini Dubey, Aditya Singh, Harlokesh Narayan Yadav
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Abstract

The liver plays a vital role in regulating normal physiological processes in the body. Liver dysfunction can lead to mild to severe pathological conditions and, in some cases, death. To date, more than 900 drugs, toxins, and herbs have been identified with the potential to cause various liver diseases, including acute liver damage, cholestatic jaundice, hepatic granulomas, active chronic hepatitis, and hepatic tumors. A wide range of liver dysfunction results from drug consumption and is referred to as drug-induced liver injury (DILI). DILI significantly contributes to the immediate withdrawal of drugs from the mar-ket. Due to its numerous advantages, the oral route has long been the preferred method of drug administration, although these medicines increase the risk of liver damage. Novel drug delivery approaches, such as the lymphatic drug delivery system and lipid-based nanofor-mulations-including solid lipid nanoparticles (SLNs) and nanostructured lipid carriers-can bypass the liver, reducing the toxic effects of various drugs. Therefore, SLNs represent a promising strategy for lymphatic drug delivery, particularly for hepatocompromised pa-tients and those taking hepatotoxic drugs. This review summarizes how lymphatic drug delivery systems and lipid-based nanoformulations can benefit hepatocompromised pa-tients and individuals on hepatotoxic medications.

淋巴给药系统和脂质纳米制剂:接受高肝毒性药物的患者的救星。
肝脏在调节人体正常生理过程中起着至关重要的作用。肝功能障碍可导致轻微到严重的病理状况,在某些情况下,甚至死亡。迄今为止,超过900种药物、毒素和草药已被确定有可能导致各种肝脏疾病,包括急性肝损伤、胆汁淤积性黄疸、肝肉芽肿、活动性慢性肝炎和肝肿瘤。广泛的肝功能障碍是由药物消耗引起的,被称为药物性肝损伤(DILI)。DILI极大地促进了药物立即从市场上撤出。由于其诸多优点,口服途径长期以来一直是首选的给药方法,尽管这些药物会增加肝损伤的风险。新的给药方法,如淋巴给药系统和基于脂质的纳米制剂——包括固体脂质纳米颗粒(sln)和纳米结构脂质载体——可以绕过肝脏,减少各种药物的毒性作用。因此,sln代表了淋巴给药的一种很有前景的策略,特别是对于肝受损患者和服用肝毒性药物的患者。本文综述了淋巴给药系统和脂质纳米制剂如何使肝损害患者和肝毒性药物个体受益。
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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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