Topical analgesic composition
This invention concerns a synergistic combination of a topical anesthetic and wound barrier forming agent capable of providing extended analgesia of ‘significant open wounds’ (that being, for example, a laceration, surgical incision, abrasion, ulcer or burn, but not being a minor cut, scratch, sting, burn or abrasion) in which conventional management alternatives (such as suturing and/or administration of injected or systemic analgesia) are impractical, unaffordable or otherwise unavailable.
1. A topical analgesic composition for use on a significant open skin wound, said composition comprising:
about 40.0 mg/mL to 50.0 mg/mL of lignocaine HCl as a first local anesthetic agent having a rapid onset of action and present in an amount effective to anesthetize the open skin wound;
0 mg/mL to about 5.0 mg/mL bupivacaine HCl as a second local anesthetic agent having a long duration of action;
about 36.0 μg/mL to 45.0 μg/mL adrenaline tartrate as a vasoconstrictor present in an amount effective to reduce bleeding from the open skin wound and to decrease the rate of vascular absorption of the local anesthetic agents so as to reduce the risk of systemic toxicity;
up to about 5.0 mg/mL cetrimide as an antiseptic agent in an amount effective to minimize infection of the open skin wound;
about 1.5 mg/mL sodium metabisulfite as an antioxidant; and
about 100 mg/mL non-crystallizing liquid sorbitol (70%) and about 5.0 mg/mL hydroxy cellulose as a carrier applicable to the open skin wound in a fluid form, wherein said carrier:
adheres to the open skin wound;
forms a long-lasting viscous barrier over the open skin wound, that is capable of remaining firmly adhered to the open skin wound until the open skin wound has naturally sealed or pain due to the open skin wound has otherwise abated by way of a natural healing process;
promotes and prolongs contact of the anesthetic agents and the vasoconstrictor with the open skin wound; and
aids in healing of the open skin wound by minimizing or preventing water loss from the open skin wound and by acting as a barrier against microbial contamination, wherein the composition provides an analgesic effect beyond that attributable to the anesthetic agents alone whilst the barrier covers the skin wound, and wherein said long-lasting viscous barrier is capable of remaining intact over the open skin wound for at least 4 hours and is in a form selected from the group consisting of a gel and spray-solution.
2. The composition of claim 1 , wherein said open skin wound is selected from the group consisting of a laceration, a surgical incision, an ulcer, a major abrasion and a major burn.
3. The composition of claim 1 , wherein said barrier is in the form of a sticky, viscous gel.
4. The composition of claim 3 , wherein said composition is sprayable onto the open wound.
5. The composition of claim 1 , wherein said composition comprises one or more ingredients selected from the group consisting of an insecticide, an insect repellent, a skin penetrating enhancer, and a detectable marker for indicating the presence of the composition on the open wound.
6. A topical analgesic composition for use on a significant open skin wound, said composition comprising:
about 40.0 mg/mL to 50.0 mg/mL lignocaine HCl as a first local anesthetic agent having a rapid onset of action and present in an amount effective to anaesthetize the significant open skin wound;
up to about 5.0 mg/mL bupivacaine HCl as a second local anesthetic agent having a long duration of action and present in an amount effective to anaesthetize the significant open skin wound;
about 36.0 μg/mL to 45.0 μg/mL adrenaline tartrate as a vasoconstrictor present in an amount effective to reduce bleeding from the significant open skin wound and to decrease the rate of vascular absorption of the first and second local anesthetic agents so as to reduce the risk of systemic toxicity;
up to about 5.0 mg/mL cetrimide as an antiseptic agent in an amount effective to minimize infection of the significant open skin wound; and
a hydrophilic carrier comprising about 100 mg/mL non-crystallizing liquid sorbitol (70%) and about 5.0 mg/mL hydroxy cellulose that:
adheres to the significant open skin wound;
forms a long-lasting sticky, viscous, humectant gel barrier over the significant open skin wound that is capable of remaining firmly adhered to the significant open skin wound until the significant open skin wound has naturally sealed or pain due to the significant open skin wound has otherwise abated by way of a natural healing process;
promotes and prolongs contact of the first and second local anesthetic agents and the vasoconstrictor with the significant open skin wound; and
aids in healing of the significant open skin wound by minimizing or preventing water loss from the significant open skin wound and by acting as a barrier against microbial contamination, wherein the composition provides an analgesic effect beyond that attributable to the first and second anesthetic agents alone while the barrier covers the significant open skin wound.
7. The composition of claim 6 , wherein said hydrophilic carrier is applicable to the significant open skin wound as a sprayable solution.
8. The composition of claim 1 , wherein said open skin wound is caused by an animal husbandry procedure.
9. The composition of claim 6 , wherein said significant open skin wound is caused by an animal husbandry procedure.