Affiliation:
1. Department of Pharmaceutics, Guru Gobind Singh College of Pharmacy, Yamunanagar, (135001) Haryana, India
Abstract
Background:
A microsponge delivery system (MDS) is a cutting-edge and distinctive method of structured medication delivery. Regulated drug distribution is now possible with the use of microsponge technology. Techniques for drug release are created specifically to distribute medi-cations to the body's various locations. As a result, pharmacological therapy becomes more effec-tive, and patient compliance significantly affects the health care system.
Main Body:
MDS consists of porous microspheres with a substantially porous structure and a very small spherical shape, ranging in size from 5 to 300 microns. MDS is typically used to administer medications through topical channels, but new research has demonstrated the promise of this tech-nique for parenteral, oral, and ocular drug delivery. Topical formulations are an attempt to manage diseases like osteoarthritis, rheumatoid arthritis, psoriasis, etc. While reducing the drug's side ef-fects, MDS can readily change the pharmaceutical release shape and enhance formulation stability. Reaching the highest peak plasma concentration in the blood is the main goal of microsponge medi-cation delivery. The ability of MDS to self-sterilize is by far the most notable quality.
Conclusion:
In countless studies, MDS is employed as an anti-allergic, anti-mutagenic, and non-irritant. This review covers the overview of microsponges along with their release mechanism. The article focuses on the marketed formulation of microsponges and patent data of the same. This re-view will be helpful for researchers working in MDS technology.
Publisher
Bentham Science Publishers Ltd.
Reference167 articles.
1. Murphy L.; Helmick C.G.; The impact of osteoarthritis in the United States: A population-health perspective: A population-based review of the fourth most common cause of hospitalization in U.S. adults. Orthop Nurs 2012,31(2),85-91
2. Heidari B.; Knee osteoarthritis prevalence, risk factors, pathogenesis and features: Part I. Caspian J Intern Med 2011,2(2),205-212
3. Fang H.; Beier F.; Mouse models of osteoarthritis: modelling risk factors and assessing outcomes. Nat Rev Rheumatol 2014,10(7),413-421
4. Glyn-Jones S.; Palmer A.J.; Agricola R.; Carr AJ Osteoarthritis Lancet 2015,386(9991),376-387
5. Bijlsma J.W.J.; Berenbaum F.; Lafeber F.P.J.G.; Osteoarthritis: An update with relevance for clinical practice. Lancet 2011,377(9783),2115-2126
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献