Answer:
1) 0.391 mg 2) By resizing the semi-permeable membrane and reducing the saturated drug concentration from 100% to 60% (i.e. from
to
).
Step-by-step explanation:
1) The total amount of released drug at time 't' is:
![M_(t) = [(2*3.142*H*D*K*C_(s) )/(ln(R_(0) )/(R_(i) ) )]*t](https://img.qammunity.org/2020/formulas/chemistry/college/lzpg97q40p3u5trcwxc2r87sxphzt2bd2a.png)
Where:
H is the length of the device = 1 cm,
D is the diffusion coefficient of the drug

K is the partition coefficient = 10
is the saturated drug concentration in the polymer matrix

is the radius of the device = 250 μm
is the radius of the cylindrical space = 100 μm
t is the released time = 48*3600 s = 172800 s
Therefore:
![M_(t) = [(2*3.142*1*2.2*10^(-10)*10*150 )/(ln(250)/(100) )]*172800 = (2.074*10^(-6)*172800 )/(0.9163) = 0.391 mg](https://img.qammunity.org/2020/formulas/chemistry/college/rerhsvbsufshb9zx99wmjxson7eoe7bj4n.png)
2) For a membrane-controlled device, the released rate can be controlled (i.e. decrease or increase) by resizing the semi-permeable membrane. In addition, the saturated drug concentration should be reduced from 100% to 60% (i.e. from
to
)