Because of its unique structural qualities a high surface area, pore diameters that may be altered, and biocompatibility mesoporous silica nanoparticles (MSNs) are attracting a lot of interest in the field of drug delivery. These features make MSNs ideal for enclosing medicinal substances and releasing them gradually. MSNs may be created to carry many different medications, including ones that either dislike water or ones that do. Their porous structure enables several medicinal molecules fit within. Surfaces of MSNs can also be altered to target certain cells or tissues, increase their stability, and assist in drug carrying capacity. MSNs have therefore been developed as effective means of delivering a variety of therapeutic drugs, including cancer therapies, gene therapy, and antibiotics. MSNs are among the finest as they allow encapsulated pharmaceuticals to remain unbroken. This maintains the medicinal agent's stability till it reaches its intended spot. Drug release from MSNs can frequently be triggered by external cues such variations in pH, temperature, or light. This allows one to control the release rate of medications. Targeting moieties to the surface of medications, such as peptides or antibodies, helps them to be delivered specifically to certain cells, therefore improving the therapeutic efficiency and lowering adverse effects. Though MSN-based medication delivery systems provide several advantages, their practical deployment is currently challenging. Among these issues include development, long-term safety, and maybe injury. Still, researchers are working hard to discover solutions to these challenges; MSNs are still viewed as a valuable and robust resource for developing improved drug delivery systems that may be applied in a range of therapeutic environments
Keywords: Mesoporous silica nanoparticles, drug delivery, controlled release, surface functionalization, targeted therapy
How to cite this article: Bansal K, Mundada K, Arya V, Suryavanshi NJ, Mohite A, Jagtap AD, Mesoporous Silica Nanoparticles for Drug Encapsulation.Int J Drug Deliv Technol. 2026;16(1s): 92-100; DOI: 10.25258/ijddt.16. 92-100