CN102274228A - Compound trimethoprim and sodium succinate florfenicol nanoemulsion preparation and preparation thereof - Google Patents
Compound trimethoprim and sodium succinate florfenicol nanoemulsion preparation and preparation thereof Download PDFInfo
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- CN102274228A CN102274228A CN 201110179278 CN201110179278A CN102274228A CN 102274228 A CN102274228 A CN 102274228A CN 201110179278 CN201110179278 CN 201110179278 CN 201110179278 A CN201110179278 A CN 201110179278A CN 102274228 A CN102274228 A CN 102274228A
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- trimethoprim
- sodium succinate
- florfenicol
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Abstract
The invention belongs to the technical field of antibacterial veterinary drugs, and in particular relates to a compound trimethoprim and sodium succinate florfenicol nanoemulsion preparation. The nanoemulsion preparation is in an oil-in-water type, has the grain size of between 1nm and 100nm and is prepared from trimethoprim, sodium succinate florfenicol, a surfactant, a cosurfactant, oil and distilled water. The compound trimethoprim and sodium succinate florfenicol nanoemulsion preparation has transparent appearance and can be used for treating various livestock and poultry infections caused by sensitive bacteria.
Description
Technical field
The invention belongs to anti-microbial type veterinary drug technical field, be specifically related to a kind of compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion preparation and preparation method thereof.
Background technology
Antimicrobial drug has advantages such as rapid-action, that production cost is low in treatment on the animal infectious disease, makes it that widely application enormous function be arranged on veterinary clinic.But the limitation of conventional dosage forms and chemical sproof increasing gradually rise and therapeutic effect decline its treatment cost.For this reason, in the clinical practice normal adopt to unite use two or more antibacterials, to reach the expansion antimicrobial spectrum, heighten the effect of a treatment, reduce dosage, reduce or avoid toxic and side effects, reduce or delay the purpose of the generation of Resistant strain.
Trimethoprim (TMP) belongs to synthetic broad spectrum antimicrobicide, is lipotropy weak base, and multiple gram positive bacteria and gram negative bacteria are all had antibacterial action.Single with easily producing drug resistance, its drug resistance mechanism may be that antibacterial changes metabolic pathway, for example produces more dihydrofolate synthetase, or directly utilizes exogenous folic acid.After antibacterial produces drug resistance, curative effect is reduced, and can cause the propagation of Resistant strain, bring difficulty to treatment.The sodium succinate florfenicol is the derivant of florfenicol, forms according to the principle design of prodrug, and it all has effect to multiple gram positive bacteria and gram negative bacteria and mycoplasma etc., is broad-spectrum antibacterial medicine, and high concentration has bactericidal action.This medicine clinical drug-resistant phenomenon is serious, and common fastbacteria is gram positive bacteria and gram negative bacterias such as staphylococcus.After antibacterial produces drug resistance, curative effect is reduced, and can cause the propagation of Resistant strain, bring difficulty to treatment.Therefore, how by drug combination and the shortcoming that the exploitation novel form solves trimethoprim and exists more than the sodium succinate florfenicol, improve two medicine clinical application curative effects and become current urgent problem.
Summary of the invention
The object of the present invention is to provide a kind of compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion preparation and preparation method thereof.
The present invention is by the following technical solutions:
A kind of compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion preparation, this nano-emulsion preparation is an oil-in-water type, particle diameter is made by following weight percentages between 1~100 nm:
Trimethoprim 0.01~1.75%
Sodium succinate florfenicol 0.04~6.99%
Surfactant 21.82~35.69%
Cosurfactant 7.94~11.90%
Oil 3.49~4.76%
Distilled water 47.59~63.54%
The total weight percent of above-mentioned raw materials is 100%.
Described surfactant is tween 80 or castor oil polyoxyethylene; Described cosurfactant is ethanol or 1, the 2-propylene glycol; Described oil is isopropyl myristate or ethyl acetate.
Described surfactant and cosurfactant mass ratio are 2-3:1; Described surfactant and cosurfactant quality sum are 9:1~7:3 with the mass ratio of oil.
A kind of method for preparing compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion preparation specifically may further comprise the steps:
1) gets each raw material in proportion;
2) the trimethoprim crude drug is dissolved in the cosurfactant, adds surfactant and oil phase mixing;
3) the sodium succinate florfenicol is dissolved in the distilled water;
4) room temperature drips down the solution of step 3) to step 2) in the solution of preparation, stir until the system that forms homogeneous transparent, i.e. compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion preparation.
When compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation used, every 100kg water added compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation 100ml, freely drinks water, and three days is a course of treatment.
The theory of constitution and the scientific basis thereof of compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation: because the trimethoprim crude drug is insoluble in water, the sodium succinate florfenicol is soluble in water, therefore with the aqueous solution of sodium succinate Florfenicol raw material medicine as aqueous portion, with trimethoprim as the oil phase part.
Select for use tween 80 or castor oil polyoxyethylene as surfactant in the raw material of compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation, be because tween 80 is relative with castor oil polyoxyethylene toxicity less, be not subject to the influence of electrolyte, inorganic salts and soda acid; Select ethanol or 1 for use, the 2-propylene glycol is during as cosurfactant, and the nano-emulsion preparation of formation is not only stable, and as the solvent of trimethoprim, has improved the content of trimethoprim in this compound nanometer emulsion; Isopropyl myristate or ethyl acetate are because the HLB value of isopropyl myristate, ethyl acetate and tween 80 is approaching as oil, easily form the stabilized nano breast.
When surfactant and cosurfactant mass ratio are 2-3:1, the nano-emulsion district maximum that the mass ratio of surfactant and cosurfactant sum and oil forms when being 9:1~7:3, the most stable, drug loading is the highest.
Compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation appearance transparent, particle diameter is between 1~100 nm, its viscosity can add the distilled water adjustment of arbitrary proportion as required, make things convenient for clinical administration, the structure of two kinds of crude drug trimethoprims and sodium succinate florfenicol does not all change.
Compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation can be used for treating poultry by the microbial all kinds of infection of sensitivity.Compared with prior art, compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation have the following advantages:
1) safely, efficiently, drug resistance is low;
2) absorb rapidly the bioavailability height; Targeting drug release, side effect is low; Particle diameter is little and even, the permeable membrane good absorbing;
3) viscosity is low, and pain is little during injection;
4) have good stability, but filtration sterilization is easy to preserve.
The specific embodiment
Embodiment 1
Castor oil polyoxyethylene 9.0g
1,2-propylene glycol 3.0g
Trimethoprim 0.003g
Sodium succinate florfenicol 0.012g
Isopropyl myristate 1.2g
Distilled water 12g
The concrete operations step is:
1) gets each raw material in proportion;
2) the trimethoprim crude drug is dissolved in 1, in the 2-propylene glycol, adds castor oil polyoxyethylene and isopropyl myristate mixing;
3) the sodium succinate florfenicol is dissolved in the distilled water;
4) room temperature drips down the solution of step 3) to step 2) in the solution of preparation, stir until the system that forms homogeneous transparent, promptly particle diameter is the compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of 1~100 nm, appearance transparent.
Embodiment 2
Composition of raw materials is as follows:
Tween 80 3.0g
Ethanol 1.0g
Trimethoprim 0.03 g
Sodium succinate florfenicol 0.12 g
Ethyl acetate 0..44g
Distilled water 8.0g
The concrete operations step is:
1) gets each raw material in proportion;
2) the trimethoprim crude drug is dissolved in the ethanol, adds tween 80 and ethyl acetate mixing;
3) the sodium succinate florfenicol is dissolved in the distilled water;
4) room temperature drips down the solution of step 3) to step 2) in the solution of preparation, stir until the system that forms homogeneous transparent, promptly particle diameter is the compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of 1~100 nm, appearance transparent.
Embodiment 3
Composition of raw materials is as follows:
Tween 80 6.0 g
1,2-propylene glycol 2.0g
Trimethoprim 0.4g
Sodium succinate florfenicol 1.6 g
Isopropyl myristate 0.88g
Distilled water 12 g
The concrete operations step is:
1) gets each raw material in proportion;
2) the trimethoprim crude drug is dissolved in 1, in the 2-propylene glycol, adds tween 80 and isopropyl myristate mixing;
3) the sodium succinate florfenicol is dissolved in the distilled water;
4) room temperature drips down the solution of step 3) to step 2) in the solution of preparation, stir until the system that forms homogeneous transparent, promptly particle diameter is the compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of 1~100 nm, appearance transparent.
Embodiment 4
Composition of raw materials is as follows:
Tween 80 6.0 g
Ethanol 3.0g
Trimethoprim 0.5g
Sodium succinate florfenicol 2.0g
Ethyl acetate 1.0g
Distilled water 15.0 g
The concrete operations step is:
1) gets each raw material in proportion;
2) the trimethoprim crude drug is dissolved in the ethanol, adds tween 80 and ethyl acetate mixing;
3) the sodium succinate florfenicol is dissolved in the distilled water;
4) room temperature drips down the solution of step 3) to step 2) in the solution of preparation, stir until the system that forms homogeneous transparent, promptly particle diameter is the compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of 1~100 nm, appearance transparent.
Adopt compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of embodiment 1 to carry out following test.
Test 1
Utilize speed that oil-soluble dyes tonyred and water-soluble dye methylene blue spread in compound recipe trimethoprim that embodiment 1 makes and sodium succinate florfenicol nano-emulsion preparation to judge the type of nano-emulsion, find that methylene blue solution has diffusion in compound recipe trimethoprim that embodiment 1 makes and sodium succinate florfenicol nano-emulsion preparation, tonyred solution is then not diffusion in compound recipe trimethoprim that embodiment 1 makes and sodium succinate florfenicol nano-emulsion preparation, shows that prepared compound nanometer emulsion is oil-in-water type (O/W).
Test 2Stability test
1) centrifugal acceleration test
Get the compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of embodiment 1 preparation, centrifugal with 20 000 r/min, to observe the nanoemulsions outward appearance behind 10 min and still keep clear, the profit lamination does not appear.
2) light stability test
The compound recipe trimethoprim of embodiment 1 preparation and sodium succinate florfenicol nano-emulsion preparation are packed in the vial in right amount, and room temperature placement under (4500 ± 500) the lx illumination condition of sealing back is respectively at 0 d, 5 d, the 10 d observation of taking a sample.The result shows that emulsion keeps the clear outward appearance, does not see phenomenons such as layering and breakdown of emulsion.
3) temperature stability test
The compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of embodiment 1 preparation are sub-packed in the vial, and placing respectively after the sealing keeps sample under 4 ℃, 25 ℃, 37 ℃, the 60 ℃ conditions investigates 3 months, observes every 10 d sampling.The result shows that emulsion all keeps the clear outward appearance under these four kinds of temperature conditions, do not see phenomenons such as layering and breakdown of emulsion.
Test 3The associating drug sensitive test of compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion
1) single medicinal chart sheet is put up a bridge and is tested
The trimethoprim drug sensitive test paper of preparation contains trimethoprim 5 μ g/ sheets, and sodium succinate florfenicol drug sensitive test paper contains trimethoprim 30 μ g/ sheets.Test strain is staphylococcus aureus ATCC
25923With escherichia coli ATCC
25922
With concentration is that the bacterium liquid of 1/2 Maxwell standard opacity tube is inoculated on the MHA culture medium, then each one of above-mentioned two kinds of drug sensitive test paper is attached to the MHA media surface respectively, and spacing 2~3 mm cultivate the antibacterial circle diameter and the form of observing behind 18 h between two scraps of paper for 35 ℃.The result shows that two kinds of antibacterials are to staphylococcus aureus ATCC
25923With escherichia coli ATCC
25922Angle, inhibition zone boundary straight, expression trimethoprim and sodium succinate florfenicol are synergetic antibacterial effect.
2) meat soup dilution chessboard test
According to measured single medicine trimethoprim and sodium succinate florfenicol nano-emulsion to staphylococcus aureus ATCC
25923With escherichia coli ATCC
25922Minimum inhibitory concentration MIC value, adopt micro-meat soup dilution chessboard method to carry out the associating antibacterial tests of medicine.
Adopt the compound recipe trimethoprim and the sodium succinate florfenicol nano-emulsion preparation of embodiment 1 preparation, become a series of concentration with the MHB doubling dilution respectively, two kinds of antibacterials with variable concentrations design by chessboard method then, combination in twos adds in the 96 hole flat boards, every kind of antibacterials are got 50 μ L, again with 1.5 * 10
5The bacterium liquid 100 μ L of CFU/mL add in the hand-hole, hatch 24 h for 37 ℃.Separately MIC when MIC when writing down two prescriptions and solely using and two medicine drug combinations, and calculate the FIC index.Process of the test repeats 5 times, and getting mode is the MIC value, the results are shown in Table 1.
Table 1 is the MIC(mg/L of trimethoprim and sodium succinate florfenicol list usefulness and coupling) and the FIC index:
Table 1
As shown in Table 1, trimethoprim and sodium succinate florfenicol are to staphylococcus aureus ATCC
25923MIC during coupling is 1/16 and 1/4 times of single time spent, to escherichia coli ATCC
25922MIC during coupling all is 1/8 times for single time spent, and the two coupling is to staphylococcus aureus ATCC
25923With escherichia coli ATCC
25922The FIC index all be not more than 0.5.Results suggest, compound recipe trimethoprim of the present invention and sodium succinate florfenicol nano-emulsion preparation can improve the antibacterial activity of trimethoprim and sodium succinate florfenicol, medicament curative effect enhancement, thus can reduce dosage, reduce drug residue, delay or reduce bacterial resistance.
Claims (4)
1. compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion preparation is characterized in that this nano-emulsion preparation is an oil-in-water type, and particle diameter is made by following weight percentages between 1~100 nm:
Trimethoprim 0.01~1.75%
Sodium succinate florfenicol 0.04~6.99%
Surfactant 21.82~35.69%
Cosurfactant 7.94~11.90%
Oil 3.49~4.76%
Distilled water 47.59~63.54%
The total weight percent of above-mentioned raw materials is 100%.
2. compound recipe trimethoprim as claimed in claim 1 and sodium succinate florfenicol nano-emulsion preparation is characterized in that described surfactant is tween 80 or castor oil polyoxyethylene; Described cosurfactant is ethanol or 1, the 2-propylene glycol; Described oil is isopropyl myristate or ethyl acetate.
3. compound recipe trimethoprim as claimed in claim 1 or 2 and sodium succinate florfenicol nano-emulsion preparation is characterized in that: described surfactant and cosurfactant mass ratio are 2-3:1; Described surfactant and cosurfactant quality sum are 9:1~7:3 with the mass ratio of oil.
4. a method for preparing described compound recipe trimethoprim of claim 1 and sodium succinate florfenicol nano-emulsion preparation is characterized in that, specifically may further comprise the steps:
1) gets each raw material in proportion;
2) the trimethoprim crude drug is dissolved in the cosurfactant, adds surfactant and oil phase mixing;
3) the sodium succinate florfenicol is dissolved in the distilled water;
4) room temperature drips down the solution of step 3) to step 2) in the solution of preparation, stir until the system that forms homogeneous transparent, i.e. compound recipe trimethoprim and sodium succinate florfenicol nano-emulsion preparation.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103705528A (en) * | 2013-12-26 | 2014-04-09 | 南阳新先锋制药有限公司 | Compound colinflosaxin soluble powder for preventing and treating poultry colibacillosis |
CN105012304A (en) * | 2015-07-08 | 2015-11-04 | 河南牧业经济学院 | Complex florfenicol composition |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101653441A (en) * | 2009-09-24 | 2010-02-24 | 陈建波 | Veterinary compound florfenicol injection and preparation method thereof |
CN102028691A (en) * | 2010-12-08 | 2011-04-27 | 纽素乐必佳(天津)药业集团有限公司 | Composite florfenicol injection for livestock and preparation method thereof |
-
2011
- 2011-06-29 CN CN 201110179278 patent/CN102274228B/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101653441A (en) * | 2009-09-24 | 2010-02-24 | 陈建波 | Veterinary compound florfenicol injection and preparation method thereof |
CN102028691A (en) * | 2010-12-08 | 2011-04-27 | 纽素乐必佳(天津)药业集团有限公司 | Composite florfenicol injection for livestock and preparation method thereof |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103705528A (en) * | 2013-12-26 | 2014-04-09 | 南阳新先锋制药有限公司 | Compound colinflosaxin soluble powder for preventing and treating poultry colibacillosis |
CN105012304A (en) * | 2015-07-08 | 2015-11-04 | 河南牧业经济学院 | Complex florfenicol composition |
CN105012304B (en) * | 2015-07-08 | 2018-12-11 | 河南牧业经济学院 | A kind of compound florfenicol composition |
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