
![]() |
|||||||||||||
WJPR Citation
|
| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
VESICULAR DRUG DELIVERY SYSTEM (PHARMACOSOMES): A REVIEW
Shweta Yadav*, Shashi Kant Singh and Navneet Kumar Verma
. Abstract Numerous issues arise in the field of solubility augmentation. Pharmacosomes, a revolutionary lipid-based medication delivery method, have emerged. Pharmacosomes can be hexagon-shaped assemblies of colloidal drug dispersions covalently bonded to the phospholipid, or they can be colloidal, nanometric size micelles or vesicles. Because of their special qualities, which include tiny size, amphiphilicity, active drug loading, high entrapment efficiency, and stability, they function as suitable carriers for the precise delivery of pharmaceuticals. They aid in reduced therapy costs, drug leakage and toxicity, enhanced bioavailability of poorly soluble medications, and restorative benefits in addition to helping with regulated release of the drug at the site of action. The range of applications for this delivery technology has expanded to include many herbal medications as well as medications for cancer, heart conditions, inflammation, and protein delivery. Thus, pharmacosomes present fresh difficulties as well as chances for developing an enhanced innovative vesicular drug delivery system. Keywords: Vesicular Drug Delivery System, Pharmacosomes, Methods of Preparation, Uses etc. [Full Text Article] [Download Certificate] |
