Seven day drug in adhesive transdermal delivery
A transdermal formulation and method of treatment includes providing an active pharmaceutical ingredient, a poly-isobutylene or silicone PSA, optionally, an oil, a crosslinked polyvinylpyrrolidone, and optionally, silicon dioxide, wherein said formulation is prepared on a backing in a three layer transdermal delivery system formulated to provide transdermal delivery and therapeutic levels for up to seven days and optionally with an overlay system required to show bioequivalence.
1. A transdermal formulation comprising:
an active pharmaceutical ingredient, wherein said active pharmaceutical ingredient is clonidine;
a polyisobutylene pressure sensitive adhesive, wherein said polyisobutylene pressure sensitive adhesive is present in an amount ranging from about 50-99.6% w/w;
a binder, wherein said binder is cross-linked polyvinylpyrrolidone;
a filler, wherein said filler comprises silicon dioxide, wherein the silicon dioxide is present in an amount ranging from about 2-5% w/w, further wherein the ratio of the silicon dioxide to cross-linked polyvinylpyrrolidone ranges from about 1:1 to about 1:5; and
mineral oil;
wherein said formulation is a component of a transdermal delivery system that delivers said active pharmaceutical ingredient for up to seven days, wherein delivery of the active pharmaceutical ingredient increases over the seven days.
2. The formulation of claim 1 wherein said active pharmaceutical ingredient is delivered at therapeutic levels for up to 7 days.
3. The formulation of claim 1 wherein said active pharmaceutical agent is present in an amount ranging from about 0.1-15% w/w.
4. The formulation of claim 1 wherein said binder is present in an amount ranging from about 0.1-15% w/w.
5. The formulation of claim 1 wherein said mineral oil is present in an amount ranging from 1-20% w/w.
6. The formulation of claim 1 wherein said formulation exhibits an increasing flux between 36 hours and 156 hours.
7. A method of providing transdermal delivery of an active pharmaceutical ingredient to a patient for up to seven days, the method comprising:
providing a transdermal delivery patch including the transdermal formulation of claim 1 , wherein the transdermal delivery patch includes a backing layer, a single adhesive layer comprising the transdermal formulation of claim 1 , and a release liner;
affixing said patch to the patient; and
transdermally delivering the active pharmaceutical ingredient to the patient.