Dual chamber applicator

1. A dual chamber applicator for applying a medicine comprising a pharmaceutically active agent to a mucosal site or skin site, comprising:

an elongated tube having a sealed end and an open end;

a first ampoule disposed in the elongated tube and containing a first composition comprising a pharmaceutically active agent and a first volatile solvent, water, or a combination thereof;

a second ampoule disposed in the elongated tube and containing a second composition comprising a resin based tincture, a second volatile solvent and water,

the first composition configured to combine with the second composition within the elongated tube to form a medicine to be delivered to a mucosal site or a skin site; and

an applicator device provided at the open end of the elongated tube, the applicator device configured to control flow of the medicine out of the open end of the elongated tube and deliver the medicine via topical, transdermal or transmucosal delivery,

wherein the applicator device comprises a porous structure configured to allow passage of the medicine to be delivered to the mucosal site or the skin site, while simultaneously preventing passage of ruptured portions of the first and second ampoules or particulates from the resin based tincture that did not dissolve into solution, and

wherein an average pore size of the porous structure ranges from 1 μm to 300 μm.

2. The dual chamber applicator of claim 1 , wherein the first and second ampoules are non-concentric.

3. The dual chamber applicator of claim 1 , wherein a length of the second ampoule is greater than a length of the first ampoule.

4. The dual chamber applicator of claim 1 , wherein the first composition further comprises a second pharmaceutically active agent, different from the pharmaceutically active agent.

5. The dual chamber applicator of claim 1 , wherein the second composition further comprises a second resin based tincture, different from the resin based tincture.

6. The dual chamber applicator of claim 1 , wherein the pharmaceutically active agent is selected from the group consisting of bacitracin, polymyxin, chlorhexidine gluconate, fentanyl, retinoic acid (Retin-A), zolmitriptan, sumatriptan, naratriptan, rizatriptan, lorazepam, and mupirocin.

7. The dual chamber applicator of claim 1 , wherein the pharmaceutically active agent is selected from the group consisting of ondansetron, granisetron, zolmitriptan, dihydroergotamine, sumatriptan, rizatriptan, fentanyl, cocaine, alprazolam, clonazepam, lorazepam, diazepam, estazolam, apomorphine, risperidone, buprenorphine, naloxone, flumazenil, tadalafil, vardenafil, sildenafil, sildenafil mesylate, dolasetron, palonsetron, triazolam, naratriptan, diclofenac, etololac, meclofenamate, indocin, meloxicam, nabumetone, oxaprozin, prioxicam, sulindac, tolmetin, celecoxib, loratadine, desloratidine, cetirizine, morphine, hydromorphine, levorphanol, meperidine, oxycodone, oxymorphone, propanolol, calcitriol, and methylphenidate.

8. The dual chamber applicator of claim 1 , wherein the pharmaceutically active agent is selected from the group consisting of nicotine, scopolamine, lidocaine, benzocaine, ketorolac, ibuprofen, ketoprofen, flurbiprofen, naproxen, astemizole, terfenadine, cimetidine, testosterone, retin-A.

9. The dual chamber applicator of claim 1 , wherein the resin based tincture is selected from the group consisting of mastic gum and benzoin.

10. The dual chamber applicator of claim 1 , wherein the first composition comprises chlorhexidine gluconate, the first volatile solvent, and 1-40% (v/v) water, the second composition comprises mastic gum, the second volatile solvent and 1-40% (v/v) water, and a final amount of water in the medicine is up to 40% (v/v).

11. The dual chamber applicator of claim 1 , wherein the pharmaceutically active agent comprises bacitracin and the resin based tincture comprises mastic gum.

12. The dual chamber applicator of claim 1 , wherein the first composition and the second composition do not contain glycerin.

13. The dual chamber applicator of claim 1 , wherein the first volatile solvent, the second volatile solvent or a combination thereof are independently selected from the group consisting of ethyl acetate, n-propyl acetate, methanol, ethanol, propanol, isopropanol, isopropyl alcohol, acetone and dimethyl ether.

14. The dual chamber applicator of claim 1 , provided in a blister package configured to receive the dual chamber applicator in an interior of the blister package and be sealed prior to sterilization.

15. The dual chamber applicator of claim 14 , prepared by a process comprising:

disposing the dual chamber applicator in the blister package;

sealing the blister package; and

sterilizing the blister package such that the blister package and an exterior surface of the elongated tube are sterilized.

16. The dual chamber applicator of claim 1 ,

wherein a viscosity of the medicine is 10 to 30 centipoise, and

wherein the average pore size of the porous structure ranges from 1 μm to 100 μm.

17. The dual chamber applicator of claim 1 ,

wherein a viscosity of the medicine is 30 to 500 centipoise, and

wherein the average pore size of the porous structure ranges from 40 μm to 300 μm.

18. The dual chamber applicator of claim 1 , wherein a pore volume of the porous structure is less than or equal to 80%.

19. The dual chamber applicator of claim 1 , wherein the first composition is more stable against precipitation and degradation of the pharmaceutically active agent than the medicine.

20. The dual chamber applicator of claim 19 , wherein the pharmaceutically active agent is selected from bacitracin and chlorhexidine gluconate.

21. A method for delivery of a medicine comprising a pharmaceutically active agent to a mucosal site or a skin site using a dual chamber applicator including an elongated tube having a sealed end and an open end, a first ampoule and a second ampoule disposed within the elongated tube, the first ampoule containing a first composition comprising a pharmaceutically active agent and a first volatile solvent, water, or a combination thereof, and the second ampoule containing a second composition comprising a resin based tincture, a second volatile solvent, and water, and an applicator device provided at the open end of the elongated tube, the method comprising:

deforming the elongated tube to crush the first and second ampoules to release the first composition and the second composition into an interior of the elongated tube;

shaking the dual chamber applicator such that the first composition and the second composition combine to form the medicine to be delivered to the mucosal site or the skin site; and

applying the medicine topically, transdermally or transmucosally via a porous structure of the applicator device configured to allow passage of the medicine to be delivered to the mucosal site or the skin site, while simultaneously preventing passage of ruptured portions of the first and second ampoules or particulates from the resin based tincture that did not dissolve into solution, wherein an average pore size of the porous structure ranges from 1 μm to 300 μm.

22. The method of claim 21 , wherein the pharmaceutically active agent comprises chlorhexidine gluconate and the resin based tincture comprises mastic gum such that crushing the first and second ampoules and shaking the dual chamber applicator forms a medicine comprising chlorhexidine gluconate and mastic gum.

23. The method of claim 21 , wherein the pharmaceutically active agent comprises bacitracin and the resin based tincture comprises mastic gum such that crushing the first and second ampoules and shaking the dual chamber applicator forms a medicine comprising bacitracin and mastic gum.

24. The method of claim 21 , wherein the first composition is more stable against precipitation and degradation of the pharmaceutically active agent than the medicine.

25. The method of claim 24 , wherein the pharmaceutically active agent is selected from bacitracin and chlorhexidine gluconate.