Published
PLGA Based Nanoparticle:Best tool for Treatment of Visceral Leishmaniasis
Published in October 2013 Issue 5 (Vol. 3, Issue 5, 2013)

Abstract
Some of the natural macromolecules have been used to prepare NPs. These polymers include gelatin, alginate, chitosan and PLGA. They are hydrophilic natural polymers and have been used to synthesize biodegradable NPs by various method. Numerous techniques now exist for synthesizing different set of nanoparticles based on the type of drugs used, and the targeted organ and delivery mechanism selected. Depending upon the protocol of choice, the parameters can be tailored to create the best possible characteristics for the nanoparticles. In this manuscript we have reviewed a number of biodegradable nanoparticles currently in use, and the techniques of their preparation. We will also discuss advances in surface modifications, drug encapsulation and specific end applications of various types of NPs. Nanotechnology, although not a new concept, has gained significant momentum in recent years. Due to the recent advances in material science and nano-engineering in the last decade, the nanoparticles have become very attractive for their applications in the fields of biology and medicine. Nanostructured materials are materials with sizes in the 1-100 nm range, which demonstrate unique properties and functions due to their "size effect".Biodegradable nanoparticles (NPs) are gaining increased attention for their ability to serve as a viable carrier for site specific delivery of vaccines, genes, drugs and other biomolecules in the body.
Authors (3)
Vaibhav Prakash Srivastava
View all publications →Shaundarya Kumar
View all publications →Smriti Ojha Tripathi
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Article Information
Published in:
October 2013 Issue 5 (Vol. 3, Issue 5, 2013)- Article ID:
- AJPTR35011
- Paper ID:
- AJPTR-01-002064
- Published Date:
- 2013-10-01
Article Impact
Views:3,857
Downloads:2,499
How to Cite
Prakash, V., & Kumar & Ojha, S. (2013). PLGA Based Nanoparticle:Best tool for Treatment of Visceral Leishmaniasis. American Journal of PharmTech Research, 3(5), xx-xx. https://ajptr.scholarjms.com/articles/835
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