Author:
Gupta Yash,Shikha Riya,Rai Vishal,Bano Nisha,Khan Soban,Yadav Reena
Abstract
Bilirubin, a natural product of heme catabolism, has recently emerged as a promising candidate in nanomedicine for the treatment of Reactive Oxygen Species (ROS)-mediated diseases. ROS, including free radicals and other oxygen-derived molecules, play a pivotal role in various pathological conditions such as inflammation, neurodegenerative disorders, and cardiovascular diseases. Bilirubin's potent antioxidant properties make it an attractive therapeutic agent, and recent advancements in nanotechnology have paved the way for its effective delivery and application in treating ROS-related ailments.This abstract delves into the potential of bilirubin-based nanomedicines in combating ROS-induced damage. The encapsulation of bilirubin within nanocarriers enhances its stability, bioavailability, and targeted delivery to affected tissues. The utilization of nanoscale systems not only safeguards bilirubin from degradation but also allows for controlled release, ensuring sustained therapeutic effects.The multifaceted mechanisms of bilirubin action include its ability to scavenge free radicals, modulate inflammatory responses, and protect cellular components from oxidative stress. The encapsulation of bilirubin in nanoparticles further improves its pharmacokinetics, enabling efficient distribution and accumulation at disease sites. Moreover, the nanocarrier systems can be engineered to respond to specific stimuli, facilitating site-specific release of bilirubin in response to the elevated ROS levels characteristic of pathological conditions.This abstract also highlights the versatility of bilirubin nanomedicines in addressing diverse ROS-mediated diseases. From neuroprotection in conditions like Alzheimer's and Parkinson's diseases to alleviating oxidative stress in cardiovascular disorders, bilirubin-based nanotherapeutics exhibit a broad spectrum of applications. The tailored design of nanocarriers allows for personalized treatment approaches, catering to the unique characteristics of each disease state.
Reference32 articles.
1. Vaz AR, Silva SL, Barateiro A, et al. From the gut to the peripheral tissues: the multiple effects of butyrate. Nutr Res Rev. 2015 Dec;28(2): 109-25.
2. Jangi S, Gandhi R, Cox LM, et al. Alterations of the human gut microbiome in multiple sclerosis. Nat Commun. 2016;7:12015.
3. Mancuso C, Santangelo R. Alzheimer's disease and gut microbiota modifications: the long way between preclinical studies and clinical evidence. Pharmacol Res. 2018;129:329-36.
4. Sampson TR, Debelius JW, Thron T, et al. Gut Microbiota Regulate Motor Deficits and Neuroinflammation in a Model of Parkinson's Disease. Cell. 2016;167(6):1469-80.e12.
5. Cenit MC, Sanz Y, Codoner-Franch P. Influence of gut microbiota on neuropsychiatric disorders. World J Gastroenterol. 2017;23(30):5486-98.