Antimicrobial prevention and treatment of human immunedeficience virus and other infectious diseases
View Patent ↗An improved medical treatment and medicine is provided to quickly and safely resolve HIV and other microbial infections. The inexpensive medicine can be self administered and maintained for the prescribed time. The attractive medicine comprises an antimicrobial concentrate comprising microbe inhibitors, phytochemicals or isolates. Desirably, the effective medicine comprises a surfactant and an aqueous carrier or solvent and a nutrient. In the preferred form, the medicine comprises: Echinacea and Commiphora myrrha phytochemicals, benzalkonium chloride, a sterile water solution, and folic acid.
1. A method for use in treating human immunodeficiency virus, comprising the steps of:
systemically applying an antimicrobial compound providing a medical composition into person infected with human immunodeficiency virus;
said antimicrobial compound comprises by weight:
from about 40% to about 60% of a phytochemical concentrate of herbaceous botanicals consisting of Commiphora myrrha and Echinacea purpurea;
from about 20% to about 60% water providing a diluent and carrier for said phytochemical concentrate;
systemically applying said antimicrobial compound into the person infected with human immunodeficiency virus in sufficient concentration and for a sufficient period of time to decrease human immunodeficiency virus in the person;
controlling viral load; and
said antimicrobial isolates of said phytochemical concentrate comprises by weight based upon the total weight of the medical composition;
from about 0.3% to about 9% echinacoside;
from about 0.1% to about 7% PS I is 4-O-methylglucoronoarabinoxylan, Mr 35 kD and PS II is acid rhamnoarabinogalactan, Mr 450 kD;
from about 0.1% to about 10% cynarin;
from about 0.2% to about 4% echinolone;
from about 0.2% to about 8% echinacin B;
from about 0.1% to about 6% echinaceine;
from about 2% to about 7% anthonocyanins comprising cynanidin 3-O-B-D-glucopyranoside and 3-O-(6-O-malonyl)-B-D-glucopyranoside;
from about 0.01% to about 0.06% pyrrolizidine alkaloids comprising tussilagine and isotussilagine;
from about 0.003% to about 0.009% isomeric dodeca isobutyalamides and tetroenoic acid; and
Commophora myyrha phytochemicals comprising members selected from the group consisting of: caryophylenes, sequiterpenes, curzerenone, dihydro fuanodien-6-one; 2-methoxyfuradine, elemol, lyndesterene, acetic acid, alpha-amyrone, arabinose, alpha-bisabolene, gamma-bisabolene, cadinene, campesterol, cholesterol, cinnamaldehyde, commiferin, alpha-commiphoric acid, beta-commiphoric acid, gamma-commiphoric acid, commiphorinic acid, m-cresol, cumic alcohol, cuminaldehyde, dipentene, 3epi-alpha-amyrin, eugenol, furanodiene, furanodienone, galactose, gum, heerabolene, alpha-heerabomyrrhol, beta-heerabomyrrhol, heeraboresene, limonene, 4-O-methyl-glucuronic acid, n-nonacesane, beta-sitosterol, and xylose.
2. A method for use in treating human immunodeficiency virus, comprising the steps of:
systemically applying an antimicrobial compound providing a medical composition into person infected with human immunodeficiency virus;
said antimicrobial compound comprises by weight:
from about 40% to about 60% of a phytochemical concentrate of herbaceous botanicals consisting of Commiphora myrrha and Echinacea purpurea;
from about 20% to about 60% water providing a diluent and carrier for said phytochemical concentrate;
systemically applying said antimicrobial compound into the person infected with human immunodeficiency virus in sufficient concentration and for a sufficient period of time to decrease human immunodeficiency virus in the person;
controlling viral load; and
said antimicrobial isolates of said phytochemical concentrate comprises by weight based upon the total weight of the medical composition:
from about 0.3% to about 9% echinacoside;
from about 0.1% to about 7% PS I is 4-O-methylglucoronoarabinoxylan, Mr 35 kD and PS II is acid rhamnoarabinogalactan, Mr 450 kD;
from about 0.1% to about 10% cynarin;
from about 0.2% to about 4% echinolone;
from about 0.2% to about 8% echinacin B;
from about 0.1to about 6% echinaceine;
from about 2% to about 7% anthonocyanins comprising cyananidin 3-O-B-D-glucopyranoside and 3-O-(6-O-malonyl)-B-D-glucopyranoside;
from about 0.01% to about 0.06% pyrrolizidine alkaloids comprising tussilagine and isoltussilagine;
from about 0.003% to about 0.009% isomeric dodeca isobutyalamides and tetroenoic acid; and
Commophora myrrha phytochemicals comprising members selected from the group consisting of: caryophylenes, sequiterpenes, curzerenone, dihydro fuanodien-6-one; 2-methoxyfuradine, elemol, lyndesterene, acetic acid, alpha-amyrone, arabinose, alpha-bisabolene, gamma-bisabolene, cadinene, campesterol, cholesterol, cinnamaldehyde, commiferin, alpha-commiphoric acid, beta-commiphoric acid, gamma-commiphoric acid, commiphorinic acid, m-cresol, cumic alcohol, cuminaldehyde, dipentene, 3-epi-alpha-amyrin, eugenol, furanodiene, furanodienone, galactose, gum, heerabolene, alpha-heerabomyrrhol, beta-heerabomyrrhol, heeraboresene, limonene, 4-O-methyl-glucuronic acid, n-nonacesane, beta-sitosterol, and xylose.
3. A method for use in treating human immunodeficiency virus in accordance with claim 2 , wherein:
said antimicrobial compound further comprises by weight from about 2% to about 12% folic acid providing a nutrient; and
said folic acid cooperates with said Commiphora myrrha and said Echinacea purpurea to help treat human immunodeficiency virus.
4. A method for use in treating human immunodeficiency virus in accordance with claim 2 , wherein said antimicrobial compound is systemically applied with a syringe into a rectal canal or vagina of a patient infected with human immunodeficiency virus.