IP Library Granted Patent US 9,867,775
Granted Patent B2
US 9,867,775 · App. 14/830,945 · Granted Jan 16, 2018

Topical pharmaceutical bases for treating inflammatory disorders

Inventor: Daniel Banov (Sugar Land, TX)
Assignee: Professional Compounding Centers of America
A61K9/0014A61K31/015A61K36/32A61K36/47A61K45/06
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Quick Facts
Patent No.
US 9,867,775
App. No.
14/830,945
Granted
Jan 16, 2018
Kind
B2
Abstract

The present disclosure refers to topical pharmaceutical bases that possess anti-inflammatory properties. Further, these topical pharmaceutical bases are proposed for treating inflammatory disorders, such as swollen tissues within joints and muscles, and the like. The topical pharmaceutical bases include Amazonian oils and resins, such as pracaxi oil and breu-branco resin. The synergistic effect of pracaxi oil combined with breu-branco resin results in a highly effective anti-inflammatory treatment. Suitable active pharmaceutical ingredients (APIs) can be incorporated to the topical pharmaceutical bases to formulate topical pharmaceutical compositions, which improve anti-inflammatory effects. The synergistic effect provided by the combination of pracaxi oil and breu-branco resin enables lower dosage requirements of the associated APIs when topical pharmaceutical compositions are employed for treating inflammatory disorders.

Claims (13)

1. A transdermal pharmaceutical composition comprising:

about 1% w/w to about 95% w/w pracaxi oil,

a synergistically effective amount of breu-branco resin, and

a pharmaceutically effective amount of at least one active pharmaceutical ingredient.

2. The transdermal pharmaceutical composition of claim 1 , wherein the transdermal pharmaceutical composition comprises about 5% w/w to about 50% w/w breu-branco resin.

3. The transdermal pharmaceutical composition of claim 2 , wherein the transdermal pharmaceutical composition comprises about 10% w/w to about 20% w/w pracaxi oil.

4. The transdermal pharmaceutical composition of claim 2 , wherein the transdermal pharmaceutical composition comprises about 10% w/w breu-branco resin.

5. The transdermal pharmaceutical composition of claim 3 , wherein the transdermal pharmaceutical composition comprises about 10% w/w breu-branco resin.

6. The transdermal pharmaceutical composition of claim 1 , wherein the transdermal pharmaceutical composition further comprises at least one natural component selected from the group consisting of buriti oil, copaiba balsam, bacaba oil, acai oil, ojon oil, andiroba oil, murumuru butter, and tucuma oil.

7. The transdermal pharmaceutical composition of claim 1 , wherein the transdermal pharmaceutical composition further comprises at least one natural component selected from the group consisting of about 1% w/w to about 20% w/w buriti oil, about 1% w/w to about 20% w/w copaiba balsam, about 1% w/w to about 20% w/w bacaba oil, about 1% w/w to about 20% w/w acai oil, about 1% w/w to about 20% w/w ojon oil, about 1% w/w to about 20% w/w andiroba oil, about 1% w/w to about 20% w/w murumuru butter, and about 1% w/w to about 20% w/w tucuma oil.

8. The transdermal pharmaceutical composition of claim 3 , wherein the transdermal pharmaceutical composition further comprises at least one natural component selected from the group consisting of about 1% w/w to about 20% w/w buriti oil, about 1% w/w to about 20% w/w copaiba balsam, about 1% w/w to about 20% w/w bacaba oil, about 1% w/w to about 20% w/w acai oil, about 1% w/w to about 20% w/w ojon oil, about 1% w/w to about 20% w/w andiroba oil, about 1% w/w to about 20% w/w murumuru butter, and about 1% w/w to about 20% w/w tucuma oil.

9. The transdermal pharmaceutical composition of claim 1 , wherein the transdermal pharmaceutical composition further comprises at least one natural component selected from the group consisting of about 5% w/w buriti oil, about 5% w/w copaiba balsam, about 5% w/w bacaba oil, about 5% w/w acai oil, about 5% w/w ojon oil, about 5% w/w andiroba oil, about 5% w/w murumuru butter, and about 5% w/w tucuma oil.

10. The transdermal pharmaceutical composition of claim 1 , wherein the transdermal pharmaceutical composition is selected from the group consisting of a pharmaceutically acceptable liquid, a cream, an oil, a lotion, an ointment, a gel, a roll-on liquid, a skin patch, a spray, and a synthetic polymer dressing.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2016
From: BANOV, DANIEL
To: PROFESSIONAL COMPOUNDING CENTERS OF AMERICA (PCCA)
Reel/Frame 038216/0593 →
Continuity (2)
Provisional Application 62039782 · Aug 20, 2014
Related Publication 20160051609A1 · Feb 25, 2016