| Literature DB >> 32175832 |
Shadab Md1,2, Shahid Karim3, Sanggetha R Saker4, Ooi A Gie4, Lim C Hooi4, Phua H Yee4, Alvin W C Kang4, Chen K Zhe4, Ng Ian4, Hibah M Aldawsari1,2, Khaled M Hosny1,5, Nabil A Alhakamy1,2.
Abstract
Rotigotine is a non-ergoline, high lipophilic dopamine agonist. It is indicated as the first-line therapy for Parkinson's disease (PD) and Restless Leg Syndrome (RLS). However, the precise mechanism of rotigotine is yet to be known. Rotigotine has similar safety and tolerability to the other oral non-ergolinic dopamine antagonists in clinical trials, which include nausea, dizziness and somnolence. Neupro® was the first marketed transdermal patch formulation having rotigotine. The transdermal delivery system is advantageous as it enables continuous administration of the drug, thus providing steady-state plasma drug concentration for 24-hours. Intranasal administration of rotigotine allows the drug to bypass the blood-brain barrier enabling it to reach the central nervous system within minutes. Rotigotine can also be formulated as an extended-release microsphere for injection. Some challenges remain in other routes of rotigotine administration such as oral, parenteral and pulmonary, whereby resolving these challenges will be beneficial to patients as they are less invasive and comfortable in terms of administration. This review compiles recent work on rotigotine delivery, challenges and its future perspective. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Parkinson's Disease (PD); Rotigotine; microemulsion; microspheres; nanoparticles; transdermal delivery.
Year: 2020 PMID: 32175832 DOI: 10.2174/1381612826666200316154300
Source DB: PubMed Journal: Curr Pharm Des ISSN: 1381-6128 Impact factor: 3.116