Pharmacodynamics and pharmacokinetics
Pharmacodynamics
A medicine with antibacterial and anti-inflammatory effect for local use in ENT practice and ophthalmology. The therapeutic effect is due to the antibacterial effect of ciprofloxacin and the anti-inflammatory effect of dexamethasone.
Ciprofloxacin is an antibacterial drug, a fluoroquinolone, which has a broad spectrum of action and has a bactericidal effect. Inhibits DNA gyrase , which disrupts DNA reproduction and the biosynthesis of cellular bacterial proteins. Active regarding:
- gram-negative bacteria Legionella pneumophila, Moraxella catarrhalis, Pasteurella multocida, Morganella morganii, Haemophilus influenzae, Esherichia coli, Providencia stuartii, as well as bacteria of the genera Shigella, Salmonella, Proteus, Klebsiella, Citrobacter, Enterobacter, Campylobacter, Vibrio, Hafnia, Gardnerella, Pseudomonas, Neisseria , Brucella, Acinetobacter, Chlamydia;
- gram-positive microorganisms Streptococcus pyogenes and agalactiae, Listeria monocytogenes, Corynebacterium diphtheriae, as well as bacteria of the genus Staphylococcus.
Dexamethasone is an artificial glucocorticoid . When applied locally, the therapeutic activity of dexamethasone is caused by antiallergic, anti-inflammatory and antiproliferative effects. Reduces capillary permeability, collagen , local exudation, phagocytic activity, cellular infiltration and fibroblast activity, and inhibits the development of scar tissue.
Pharmacokinetics
When used in ophthalmology, ciprofloxacin quickly penetrates into the tissues of the eye, except the lens. The highest concentration is recorded after half an hour. Systemic absorption is observed. But the content of the drug in the blood is significantly less than the detection limit and is not clinically significant. After dexamethasone into the conjunctival sac, it actively penetrates the eye tissue.
When using the drug in the ear canal in otorhinolaryngological practice, the half-life for ciprofloxacin is about 3 hours, and for dexamethasone - 2.8 hours.
Pharmacological properties
Combinil-Duo solution is used in ophthalmic practice as a local antimicrobial and anti-inflammatory agent. Its therapeutic effect is due to the presence of the fluoroquinolone antibiotic ciprofloxacin and the glucocorticosteroid dexamethasone.
Ciprofloxacin has an antibacterial effect and has a bactericidal effect. The effect of the substance inhibits the enzyme DNA gyrase of bacterial microflora, as a result of which DNA replication is disrupted and the synthesis of bacterial cellular proteins stops. Ciprofloxacin is active against reproducing microorganisms, as well as those in the dormant stage. Its antibacterial effect extends to Esherichia coli, Shigella spp., Salmonella spp., most species of Proteus spp., Morganella morganii, Klebsiella spp., Citrobacter spp., Enterobacter spp., Campylobacter spp., Vibrio spp., Hafnia spp., Haemophilus influenzae, Providencia stuartii, Pasteurella multocida, Gardnerella spp., Pseudomonas spp., Legionella pneumophila, Moraxella catarrhalis, Neisseria spp., Acinetobacter spp., Chlamidia spp., Brucella spp. (Gram-negative bacteria). And also: Staphylococcus spp., St. agalactiae, Streptococcus pyogenes, Corynebacterium diphtheria. The toxicity of the substance is negligible.
Dexamethasone is a synthetic glucocorticosteroid commonly used as an anti-inflammatory and immunosuppressive agent. When applied topically, its therapeutic activity is due to its anti-inflammatory, antiallergic, and antiproliferative properties. It reduces the permeability of capillary walls, local exudation, phagocytic activity, and cellular infiltration. Prevents collagen deposition and fibroblast activity, prevents the formation of scar tissue.
The auxiliary component hydroxypropyl betacyclodextrin contained in Combinil-Duo promotes long-term preservation of active substances on the surface of the eye, which increases the effectiveness of the solution.
Indications for use
Ear diseases of an infectious-inflammatory nature:
- otitis media with eardrum shunt, including with granulations and otorrhea ;
- acute otitis externa
Infectious-inflammatory eye diseases:
- keratitis;
- conjunctivitis;
- blepharitis and other inflammatory diseases of the eyelids;
- anterior uveitis;
- prevention and treatment of infectious complications during operations and after eye injuries.
Side effects
- Eye disorders: redness, burning, itching of the eyes, horny infiltrates, keratitis, conjunctivitis, periocular edema, photophobia, foreign body sensation, blurred vision, eyelid edema, dry eye, conjunctival hyperemia, glaucoma, decreased visual acuity, cataract , decrease visual fields, thinning of the cornea, secondary infection, perforation of the eye.
- Ear disorders: ear itching, ear congestion, ear pain.
- Other disorders: slow wound healing, facial swelling, skin rash, taste perversions.
Instructions for use (Method and dosage)
The instructions for Combinil-Duo provide the following regimens for ear and eye drops.
When treating infectious and inflammatory lesions of the eye and its appendages, it is recommended to instill 1-2 drops of the drug into the conjunctival sac 4-6 times a day. The first two days of treatment, instillations can be carried out every 2 hours. The duration of treatment for acute blepharitis and bacterial conjunctivitis is 5-14 days, for keratitis - 15-30 days, for the prevention of inflammatory disorders after surgery with perforation of the eye - 5-30 days. If the product is used for more than 10 days, it is necessary to monitor intraocular pressure.
When treating ear diseases of an infectious-inflammatory nature, 4 drops are instilled into the external auditory canal of the diseased ear twice a day for a week. You should not change the position of your head for another minute to ensure complete penetration of the medicine into the ear canal.
Directions for use and doses
The standard regimen for using the Combinil-Duo solution involves the conjunctival application of 1-2 drops of the drug every 4 or 6 hours. During the first two days, installations are prescribed every 2 hours.
Duration of treatment:
- Acute bacterial conjunctivitis and blepharitis - course 5 - 14 days.
- Keratitis - course 2 - 4 weeks.
- Prevention of surgical infections - course 5 - 30 days.
When using Combinil-Duo for more than 10 days, monitoring of intraocular pressure is mandatory.
Interaction
Absorption into the systemic circulation when applied locally is negligible, making the likelihood of pharmacological interactions very low.
Medicines that induce the activity of the CYP3A4 enzyme (phenytoin, barbiturates, Rifampicin, Carbamazepine) and can stimulate the metabolism of glucocorticosteroids.
Drugs that inhibit the activity of CYP3A4 (macrolides, ketoconazole) can potentially cause an increase in the level of corticosteroids in the blood.
Dexamethasone is a moderate inducer of the CYP3A4 enzyme. Combined use with drugs metabolized by CYP3A4 ( Erythromycin ) can increase their clearance, reducing their concentration in the blood.
When ciprofloxacin with other antimicrobial drugs ( aminoglycosides, beta-lactam antibiotics, Metronidazole, Clindamycin ), synergism is usually detected.
special instructions
Long-term use of the drug can lead to increased intraocular pressure with damage to the optic nerve, decreased acuity and reduced visual fields, as well as the development of posterior subcapsular cataracts . When using the drug for more than 10 days, intraocular pressure must be monitored.
For acute purulent infections of the organ of vision, corticosteroids can worsen or mask the signs of the disease.
Long-term use of the drug can reduce the immune response and cause secondary infections.
Before instilling the drug, contact lenses should be removed and put on again after 20 minutes, since the preservative in the drug has an adverse effect on the organ of vision.
The bottle must be closed after use. Do not touch the eye with the pipette.
Before instilling the medicine into the ear canal, it is necessary to warm it to human body temperature and sanitize the ear canal.
Immediately after use, it is not recommended to drive vehicles due to the high likelihood of decreased visual acuity.
Combinil-duo 5ml eye/ear drops
Release form
Eye and ear drops.
Package
There is 5 ml of the drug in a plastic dropper bottle. In a cardboard package there is 1 dropper bottle. 5 ml
pharmachologic effect
Combinil is intended for local use in ophthalmological and otorhinolaryngological practice. The therapeutic effect of the drug Combinilo is due to the antimicrobial effect of ciprofloxacin and the anti-inflammatory effect of dexamethasone. Ciprofloxacin is an antimicrobial drug from the fluoroquinolone group, has a wide spectrum of antibacterial action and has a bactericidal effect. The drug inhibits the enzyme DNA gyrase of bacteria, as a result of which DNA replication and the synthesis of bacterial cellular proteins are disrupted. Ciprofloxacin acts both on microorganisms that are reproducing and those in the dormant stage. The spectrum of antibacterial action of ciprofloxacin includes: Gram-negative microorganisms: Escherichia coli. Salmonella spp. Shigella spp. Proteus spp. (indole-positive and indole-negative). Morganella morganii. Citrobacter spp. Klebsiella spp. Enterobacter spp. Vibrio spp. Campylobacter spp. Hafnia spp. Providencia stuartii. Haemophilus influenzae. Pasteurella multocida. Pseudomonas spp. Gardnerella spp. Legionella pneumophila. Neisseria spp. Moraxella catarrhalis. Acinetobacter spp. Brucella spp. Chlamydia spp. Gram-positive microorganisms: Staphylococcus spp. Streptococcus pyogenes. St. agalactiae. Corynebacterium diphtheriae. Listeria monocitogenes. The drug is low toxic. Dexamethasone is a synthetic glucocorticosteroid primarily used as an anti-inflammatory and immunosuppressive agent. When applied topically, the therapeutic activity of dexamethasone is due to its anti-inflammatory, antiallergic and antiproliferative effects. It reduces capillary permeability and proliferation, local exudation, cellular infiltration, phagocytic activity, collagen deposition and fibroblast activity, and inhibits the formation of scar tissue. Thus, dexamethasone reduces the main symptoms of inflammation.
Pharmakinetics
Absorption and metabolism When used in ophthalmology, ciprofloxacin penetrates well into various tissues of the eye, with the exception of the lens. C max occurs within 30 minutes, the highest concentration is observed in the moisture of the anterior chamber. Systemic reabsorption is observed. However, the drug concentration achieved in the blood is well below the detection limit and has no clinical significance. Dexamethasone, after instillation into the conjunctival sac, penetrates well into the corneal epithelium and conjunctiva; at the same time, therapeutic concentrations are achieved in the aqueous humor of the eye; with inflammation or damage to the mucous membrane, the penetration rate increases. When used in otorhinolaryngological practice, when a fixed combination of ciprofloxacin and dexamethasone is administered into the ear canal, the maximum serum concentration for ciprofloxacin is 1.55 ng/l, and for dexamethasone 0.86. ng/l. Elimination The half-life of the drugs is 2.9 hours and 2.8 hours, respectively. Hydroxypropylbetacyclodextrin, which is part of the drug as an auxiliary component, promotes long-term preservation of the active substance on the front surface of the eye, thereby increasing the effectiveness and duration of action of the drug.
Indications
Bacterial inflammatory diseases of the eye and its appendages: Acute and subacute conjunctivitis. Keratitis. Anterior uveitis. Blepharitis and other inflammatory diseases of the eyelids. Prevention and treatment of infectious complications after injuries to the eye and its appendages and during operations on the eyeball. Bacterial inflammatory diseases of the ear: Acute external otitis. Acute otitis media with eardrum shunt. Acute otitis media with granulations and otorrhea in the presence of an eardrum shunt.
Contraindications
Hypersensitivity to the active substance of the drug or to any auxiliary ingredients included in this dosage form of the drug. Herpetic keratitis and other viral lesions of the cornea and conjunctiva. Tuberculosis of the eye. Fungal infections of the eyes. Viral infections of the ear canal. Perforation of the eardrum. Children under 18 years of age. Pregnancy. Breastfeeding period.
Use during pregnancy and breastfeeding
Contraindicated during pregnancy and breastfeeding.
special instructions
For bacterial inflammatory diseases of the ear Before using ear drops, the external auditory canal should be sanitized (rinse and dry the external auditory canal). Before instilling the drug into the external auditory canal, you should warm it to body temperature by holding it in your hands for 1-2 minutes. It is necessary to lie on your side or tilt your head back to facilitate instillation. Place the indicated number of drops into the external auditory canal. Allow the drops to drain into the external auditory canal, pulling the earlobe down and back. Keep your head tilted back for about 2 minutes. You can place a cotton wool pad in the external auditory canal. For bacterial inflammatory diseases of the eye and its appendages, long-term use can lead to an increase in intraocular pressure with subsequent damage to the optic nerve, a decrease in visual acuity and fields, as well as the formation of posterior subcapsular cataracts. When using the drug Combinil-Duo for more than 10 days, it is necessary to monitor intraocular pressure. For acute purulent eye infections, corticosteroids may worsen or mask symptoms. Long-term use of the drug may reduce the immune response and lead to the development of secondary eye infections. Patients using contact lenses should remove them before instillation of the drug and put them back on only after 20 minutes, since the preservative contained in the drug may have an adverse effect on the eye tissue. The bottle must be closed after each use. Do not touch the tip of the pipette to your eye. Effect on the ability to drive vehicles and machinery After using the drug, the clarity of visual perception may decrease; therefore, immediately after instillation, it is not recommended to drive a car or engage in activities that require increased attention and speed of psychomotor reactions.
Compound
1 ml contains: Active substances: dexamethasone 1 mg, ciprofloxacin (in the form of hydrochloride) 3 mg; Excipients: benzalkonium chloride, hydroxypropyl betadex, disodium edetate, mannitol, hydrochloric acid (up to pH 4.0), water for injection.
Directions for use and doses
For bacterial inflammatory diseases of the eye and its appendages, 1-2 drops are instilled into the conjunctival sac every four to six hours. The first 24-48 hours of installation can be done every two hours. For bacterial inflammatory diseases of the ear, 4 drops into the external auditory canal of the affected ear twice a day for 7 days. You should not change the position of your head for 60 seconds to ensure complete penetration of the drug into the ear canal. Course of treatment: for acute bacterial conjunctivitis, blepharitis - from 5 to 14 days. For keratitis - 2-4 weeks. For the prevention of inflammatory diseases after surgical interventions with perforation of the eyeball - from 5 days to 1 month. If the drug is used for more than 10 days, the patient's intraocular pressure should be monitored.
Side effects
On the part of the visual organs: Corneal infiltrates, burning, redness, itching of the eyes, conjunctivitis, keratitis, periocular edema, facial edema, foreign body sensation in the eye, photophobia, blurred vision, dry eye, eyelid edema, conjunctival hyperemia, glaucoma and optic nerve damage, decreased visual acuity and narrowing of visual fields, cataract formation, secondary infection (fungal and bacterial), thinning of the cornea and/or perforation of the eyeball, delayed wound healing. On the part of the hearing organs: Discomfort and pain in the ear, itching in the ear, ear congestion, taste perversions, skin rash.
Drug interactions
Systemic absorption when applied topically is negligible, so the likelihood of drug interactions is extremely low. Inducers, inhibitors and substrates of liver enzymes Drugs that induce the activity of cytochrome P450 3A4 (CYP 3A4) (barbiturates, phenytoin, carbamazepine, rifampicin) can enhance the metabolism of corticosteroids. Drugs that induce CYP3A4 activity (ketoconazole, macrolides) can potentially cause an increase in plasma corticosteroid levels. Dexamethasone is a moderate CYP3A4 inducer. Co-administration with drugs metabolized by CYP3A4 (erythromycin) may increase their clearance, reducing their plasma concentrations. Combination of ciprofloxacin with other antimicrobial drugs When ciprofloxacin is combined with other antimicrobial drugs (beta-lactam antibiotics, aminoglycosides, clindamycin, metronidazole), synergism is usually observed. Can be successfully used in combination with azlocillin and ceftazidime for infections caused by Pseudomonas spp. With mezlocillin and other beta-lactam antibiotics - for streptococcal infections. With isoxazolylpenicillins and vancomycin - for staphylococcal infections. With metronidazole and clindamycin - for anaerobic infections.
Overdose
Symptoms: the occurrence of punctate keratitis, erythema, increased lacrimation, swelling and itching of the eyelids. Treatment: there is no specific antidote. You should rinse your eyes with water, discontinue the drug and prescribe symptomatic therapy. There are no data on systemic manifestations of overdose.
Storage conditions
In a place protected from light, at a temperature not exceeding 25°C. Do not freeze. Shelf life: 2 years.
Conditions for dispensing from pharmacies
Dispensed with a doctor's prescription
