(i) It will help to minimize the toxicity of drug towards specific site of delivery. (ii) It provides reduction in fluctuations in therapeutic ranges by improving the bioavailability. (iii) Improves the stability of the drug. (iv) Reduce dosing frequency. (v) Smaller particle size reduce potent irritant at site.
(i) Proteins are able to show better action at minimum dose. (ii) It will also helps to decrease the drug resistance in the body. (iii) The rate of dissolution and surface area embedded in nanoparticles can also be enhanced. (iv) There will be less chemical reaction occurs.
(i) Clustering of nanoparticle into bigger arrangement may lead to change in morphology of the drug. (ii) Rupturing of small particles in bulk can occur. (iii) Once enter into the body can be forbidden by any action or adverse effects.
(i) There will be difficulty in controlling its molecular size. (ii) The ability to adjust the dose will be reduced. (iii) Due to lack of biological behavior unable to identify the nature of nanoparticles. (iv) Nanoparticles posses high energies due to their size.
(i) For tumor targeting a concentrated dose of drug will be given which will lead to enhance permeability and retention effect. (ii) Provide better permeability towards blood brain barrier with specific receptor –mediated transport system. For ex- poly (butyl cyanoacrylate) nanoparticles was able to deliver hexapeptide, doxorubicin into the brain. (iii) Nanoparticles loaded with plasmid DNA will also serve efficient gene delivery.
(i) Protein nanoparticles provide a new option for the oral intake of peptides via nanostructure drug delivery. For instance, Insulin loaded nanoparticles can preserve the insulin activity and produce blood glucose reduction. (ii) Nasal route offers an advantage by enhancing the surface area and lower enzymatic activity relative to GIT. (iii) In case of antibiotics protein nanoparticles show significant results via decreasing the toxicity after protein binding. (iv) For ocular therapy it exhibits the longer half life by prolonging the intraocular pressure.