Treatment of skin and mucosal superficial wounds using adrenergic receptor agonists
View Patent ↗The invention generally relates to the compositions and methods related to the use of adrenergic receptor agonists solutions for the treatment of skin and mucosal superficial wounds. Some of the preferred adrenergic receptor agonists include epinephrine, phenylephrine, norepinephrine, methoxamine, and mixtures thereof. The invention also relates to devices suitable for applying these solutions to the skin or the mucosal area. Methods according to the invention are especially effective to control superficial skin and mucosal bleeding and accelerate healing time.
1. A disposable dispenser comprising a cap cover, a sponge cap, a hollow shaft with a perforator, and a dispensing part comprising a sterile solution suitable for a topical application to a superficial skin or mucosal wound consisting essentially of: a) an adrenergic receptor agonist, wherein said adrenergic receptor agonist is selected from the group consisting of epinephrine hydrochloride, phenylephrine hydrochloride, norepinephrine hydrochloride, methoxamine hydrochloride, and mixtures thereof, at a concentration of about 0.1 mg/ml to about 2.5 mg/ml, b) an acidifying agent, wherein said acidifying agent is selected from the group consisting of sodium citrate, potassium citrate, sodium lactate, and mixtures thereof and c) one local anesthetic agent, wherein said anesthetic agent is selected from the group consisting of bupivacaine, lidocaine, chloroprocaine, dibucaine, etidocaine, tetracaine, and procaine.
2. A disposable solution applicator comprising a sealed aluminum foil or thin plastic pouch wherein said sealed aluminum foil or thin plastic pouch comprises a sterile solution consisting essentially of an adrenergic receptor agonist, wherein said adrenergic receptor agonist is selected from the group consisting of epinephrine hydrochloride, phenylephrine hydrochloride, norepinephrine hydrochloride, methoxamine hydrochloride, and mixtures thereof, at a concentration of about 0.1 mg/ml to about 2.5 mg/ml, b) an acidifying agent, wherein said acidifying agent is selected from the group consisting of sodium citrate, potassium citrate, sodium lactate, and mixtures thereof, and c) one local anesthetic agent, wherein said local anesthetic agent is selected from the group consisting of bupivacaine, lidocaine, chloroprocaine, dibucaine, etidocaine, tetracaine, and procaine, and a synthetic applicator, and wherein said synthetic applicator is soaked in said sterile solution.
3. The disposable dispenser of claim 1 , wherein said disposable dispenser is made of plastic.
4. An aqueous pharmaceutical composition formulated for the topical treatment of a superficial skin or mucosal wound, said pharmaceutical composition consisting essentially of: a) an adrenergic receptor agonist selected from the group consisting of epinephrine, phenylephrine, norepinephrine and mixtures thereof at a concentration of about 0.1 mg/ml to about 2.5 mg/ml; b) an acidifying agent; wherein said acidifying agent is selected from the group consisting of sodium citrate, potassium citrate, sodium lactate, and mixtures thereof, and c) an anesthetic agent; wherein said anesthetic agent is selected from the group consisting of bupivacaine, lidocaine, chloroprocaine, dibucaine, etidocaine, tetracaine, procaine, and mixtures thereof, and wherein said pharmaceutical composition is suitable for a topical application to a superficial skin or mucosal wound.
5. An aqueous pharmaceutical composition formulated for the topical treatment of a superficial skin or mucosal wound, said pharmaceutical composition consisting essentially of a) an adrenergic receptor agonist selected from the group consisting of epinephrine, phenylephrine, norepinephrine and mixtures thereof, at a concentration of about 0.1 mg/ml to about 2.5 mg/ml; b) sodium lactate, at a concentration of about 0.3 mg/ml; and c) bupivacaine hydrochloride at a concentration of about 0.75%; and wherein said pharmaceutical composition is suitable for a topical application to a superficial skin or mucosal wound.
6. An aqueous pharmaceutical composition formulated for the topical treatment of a superficial skin or mucosal wound consisting essentially of an adrenergic receptor agonist selected from the group consisting of epinephrine, phenylephrine, norepinephrine and mixtures thereof, at a concentration of about 0.1 mg/ml to about 2.5 mg/ml; b) sodium lactate, at a concentration of about 0.3 mg/ml; and c) bupivacaine hydrochloride at a concentration of about 0.75%; and d) a preservative, and wherein said pharmaceutical composition is suitable for a topical application to a superficial skin or mucosal wound.