This paper describes the development and evaluation of albendazole nanosponges as an implicit strategy to enhance drug dissolution and increases the bioavailability of drug to the specific point of action. Nanotechnology interceded drug delivery has been reported to enhance the drug effectiveness, bioavailability, reduced poison and meliorate patient compliance by nanoparticles. The main end of the study was to formulate and estimate Albendazole loaded nanosponges.The FTIR test is conducted as the primary test, by this test there was no commerce between the drug and polymers. Also Nanosponges (NS) were estimated for flyspeck size, poly dispersive index (PDI), zeta eventuality, ruse effectiveness and Invitro drug release. The flyspeck size ranged from 111.7nm to 200nm, zeta eventuality from -17.7mv to 25.0mv and ruse effectiveness was ranged from 75.00%to 80.00%. Through logical system for albendazole absorbance at λmax 294nm ranges between 0.464 to 2.502 while the attention ranges between 10 to 50(µg/ml). This study appears to be a promising step in perfecting the delivery and effectiveness of albendazole using nanotechnology.
D. Christopher Vimalson*, M. Alagarraja, J. Mumtaj, T. Gowrishankar, C. Aparna, K.B. Arya, Khadeejathul Misriya, Reshma Reghunath, M. Selvakumar.
Matrix metalloproteinase-9 (MMP-9) is a vital enzyme involved in a variety of physiological activities, including tissue remodeling, immunological modulation and wound healing. However, dysregulation is linked to a wide range of clinical disorders, including cancer, cardiovascular disease and chronic inflammation. Because of its dual role in health and disease, MMP-9 has emerged as a promising therapeutic target and biomarker for disease detection and prognosis. While therapeutic techniques aimed at MMP-9, such as selective inhibitors, have showed promise, issues such as off-target effects and tissue-specific activities confound treatment approaches. Furthermore, MMP-9's potential as a biomarker opens up non-invasive diagnostic prospects, especially when paired with additional markers. Future research is required to address the limits of therapeutic interventions and improve the use of MMP-9 in clinical diagnostics and personalized medicine.