 |
|
|
|
|
 |
 |
 |
Guaranteed superior content
uniformity that cannot be achieved by other drug
formulation |
|
|
High-degree of precision of fill material |
|
|
Strong adhesion to prevent leakage |
|
|
Accommodates highly viscous compounds
and hydrophilic compounds as fill material |
|
|
Ability to quickly dissolve in the
digestive tract |
|
|
Enhanced absorption and bioavailability |
|
|
Masks strong odor and unpleasant taste |
|
|
Fill material capacity from 50 mg
to more than 2,000 mg |
|
|
Protects against oxidation and light/UV
for product stability |
|
|
Manufacturing process takes place
under room temperature, thus suitable for compounds
with a low melting point |
|
|
|
|
 |
| Gelatin sheets, G, are fed between two rotating
die rolls, and are simultaneously formed into two
halves of a capsule. The appropriate volume of fill
material is measured and dispensed by the fill injector
pump, P, and the fill material is instantly encapsulated.
Temperature necessary to adhere and encapsulate is
applied to gelatin sheet, G, by the wedge-shaped segment,
S, and necessary pressure for encapsulation is applied
by the die rolls, D. Movement of the die rolls and
fill injector pump, P, is perfectly synchronized so
that there is no fill material loss or air leakage
into the capsule. Precision of fill injector pump,
P, permits greater fill uniformity which leads to
higher yield. |
 |
 |
|
|
|
|
|
|
|
|
