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This  study  will  contribute  to  increase  Zanamivir  bioavailability  using
                   nanotechnology drug delivery system.


                   1.5    Scope and limitation of the study



                          The  scope  of  this  study  is  to  formulate  a  better  formulation  for  increasing
                   Zanamivir  adsorption  through  oral  and  intranasal  administration  by  using

                   nanotechnology.  This  study  aims  in  increasing  Zanamivir  absorption  capability  and

                   develop a better Zanamivir drug delivery system through oral and intranasal. The use of
                   nano particle in drug delivery studies are increasingly becoming popular as it is a new

                   and improve technique for drug delivery system and formulation. The problem with using
                   nanotechnology in human medicine is that the nanoparticles could potentially be toxic as

                   they can translocate within and then damage living organisms as it is ridiculously small,
                   which allows them to penetrate physiological barriers and travel within the circulatory

                   systems of a host (Buzea et al., 2007).


                   2.0    LITERATURE REVIEW

                          Zanamivir which is a strong and highly selective antiviral is also safe to use and

                   has low acute toxicity and no significant systemic toxicity or respiratory tract irritancy

                   (Freund et al., 1999). Zanamivir are much more potent than amantadine and ribavirin in
                   animal studies to such a degree of 100 to 1000 times against influenza A and B (Cheer &

                   Wagstaff, 2002). It works by making the influenza virus unable to escape the host cell

                   and thus from infecting others by binding to the active site of the neuraminidase protein
                   (Zanamivir:  Uses,  Interactions,  Mechanism  of  Action  |  DrugBank  Online,  2020).

                   Zanamivir has very low bioavailability of only 2% for absolute oral and 10 to 20% for
                   oral and intranasal with maximum serum concentrations generally reached within 1 to 2

                   hours (Cass et al., 1999). Zanamivir which administered through intranasal in ferrets and
                   mouse shows inhibition of viral  replication with doses as low as 0.05mg/kg (Cheer &

                   Wagstaff, 2002).

                          The use of nanotechnology in formulating drug and its delivery system is a new
                   alternative which bring many benefits and new hope which it can enhanced therapeutic

                   effect  and  bioavailability  of  the  drug  (Al  Jbour,  2022).  The  use  of  nanoparticle
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