CN105267230A - Compound fenbendazole tablet - Google Patents
Compound fenbendazole tablet Download PDFInfo
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- CN105267230A CN105267230A CN201510654674.8A CN201510654674A CN105267230A CN 105267230 A CN105267230 A CN 105267230A CN 201510654674 A CN201510654674 A CN 201510654674A CN 105267230 A CN105267230 A CN 105267230A
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- fenbendazole
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- IRHZVMHXVHSMKB-UHFFFAOYSA-N fenbendazole Chemical compound [CH]1C2=NC(NC(=O)OC)=NC2=CC=C1SC1=CC=CC=C1 IRHZVMHXVHSMKB-UHFFFAOYSA-N 0.000 title claims abstract description 54
- 229960005473 fenbendazole Drugs 0.000 title claims abstract description 54
- 150000001875 compounds Chemical class 0.000 title claims abstract description 36
- AZSNMRSAGSSBNP-UHFFFAOYSA-N 22,23-dihydroavermectin B1a Natural products C1CC(C)C(C(C)CC)OC21OC(CC=C(C)C(OC1OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C1)C(C)C=CC=C1C3(C(C(=O)O4)C=C(C)C(O)C3OC1)O)CC4C2 AZSNMRSAGSSBNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 claims abstract description 28
- 229960002418 ivermectin Drugs 0.000 claims abstract description 28
- FSVJFNAIGNNGKK-UHFFFAOYSA-N 2-[cyclohexyl(oxo)methyl]-3,6,7,11b-tetrahydro-1H-pyrazino[2,1-a]isoquinolin-4-one Chemical compound C1C(C2=CC=CC=C2CC2)N2C(=O)CN1C(=O)C1CCCCC1 FSVJFNAIGNNGKK-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229960002957 praziquantel Drugs 0.000 claims abstract description 20
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- HMCCXLBXIJMERM-UHFFFAOYSA-N Febantel Chemical compound C1=C(NC(NC(=O)OC)=NC(=O)OC)C(NC(=O)COC)=CC(SC=2C=CC=CC=2)=C1 HMCCXLBXIJMERM-UHFFFAOYSA-N 0.000 description 2
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- LAOOXBLMIJHMFO-UHFFFAOYSA-N 1-[2-(diethylamino)ethylamino]-4-methylthioxanthen-9-one;hydron;chloride Chemical compound Cl.S1C2=CC=CC=C2C(=O)C2=C1C(C)=CC=C2NCCN(CC)CC LAOOXBLMIJHMFO-UHFFFAOYSA-N 0.000 description 1
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- Medicinal Preparation (AREA)
Abstract
The invention discloses a compound fenbendazole tablet. Specifically, each tablet is prepared from the following components by mass: 300-500mg of fenbendazole, 15-30mg of praziquantel, 0.01-0.05mg of ivermectin, 600-1000mg of a filler, 80-120mg of a disintegrating agent, 100-200mg of an adhesive, 10-20mg of a lubricant and 1-3mg of a flavoring agent. The compound fenbendazole tablet provided by the invention has significant repelling and killing effects on naturally infected worms of dogs, and single egg reduction rate reaches over 95%. The compound fenbendazole tablet can expel more species of parasites, can achieve better therapeutic effect, also is safe, has no toxic or side effect, good drug dissolution, high temperature resistance, sunlight resistance, good reproducibility, and stability.
Description
Technical field
The present invention relates to veterinary drug technical field, particularly relate to a kind of compound recipe fenbendazole tablet.
Background technology
Raising pets has long history in China.Along with growth in the living standard, the growth of people's economic capability, increasing people's pet feeding, is wherein no lack of famous and precious dog, cat kind, and pet owner also more and more pays close attention to the health problem of house pets.Dog, cat are all mammals, easily suffer from parasitic disease, if treat not in time, not only threaten the health of house pets, also can be transmitted to the mankind.
Fenbendazole is wide spectrum, efficient, safe novel benzene thibenzazoline class contact-type anthelmintic, various parasite and larva and worm's ovum in growth in energy purged body, make infection loop termination before infecting early stage and maturation, thus prevention parasite multiplication, it not only has height anthelmintic activity to gastrointestinal nematode parasites adult and larva, and have good result to net filaria, fasciola and cestode, also have extremely strong killing egg effect.It is obvious to dog ancylostome, Trichocephalus, ascarid effect that dog takes 25mg/kg orally.50mg/kg is used in conjunction 14, can kill migratory stage ascaris alata larva; Be used in conjunction 3 and almost can drive clean cestode.Cat therapeutic dose 3 days, all has efficiently ascaris mystax, ancylostome, cestode.Ivermectin is the anti-parasite medicine of New-type wide-spectrum, efficient, low toxicity, to endoparasite, particularly nematicide and arthropod all have and good kill effect, effectively can drive away gastrointestinal nematode, also effectively can drive away the vermin such as demodicid mite, beer louse, the hematophagus etc. in feather.Dosing time can kill endoparasite and ectoparasite simultaneously, infects also effective, dog, cat skin hemostasis 200 μ g/kg dosage to some arthropod of dog, cat, again with the infection once getting rid of ear demodicid mite, acaricide, dog lung thorn demodicid mite after two weeks.Measure by 300 μ g/kg, be used in conjunction twice (2 weeks, interval) also very effective to the mite infestationss of Ji chela.Treatment demodicidosis disease is preferably by 600 μ g/kg subcutaneous injection amounts, and 7 days, interval, is used in conjunction 5 times.Praziquantel is as a kind of New-type wide-spectrum antiparasitic, to schistosomiasis japanica and taeniasis, clonorchiasis sinensis, paragonimiasis westermani etc. are all effective, because praziquantel also has killing effect to cercaria, miracidium, therefore also for preventing schistosomicide, be widely used in the parasiticide treatment of animal, poultry etc.
But due to house pet or mammal, there is cross infection in daily life, and the parasitic infection of different pathogenic bacteria, thus suffer from different diseases, disease causes reason also more complicated, therefore various medicine part the coming of single use carries out treatment anthelmintic, do not reach desired effect, if moreover too much take various medicine, the amount enlarged relative of medicine on the one hand, cause certain toxic and side effects and injury to body, the opposing party also result in very large waste.Therefore, how to realize comprehensive anthelminthic effect, reach wide and full effect, moreover improve effect, this is the problem that the present invention will consider.
Summary of the invention
The object of the present invention is to provide a kind of for multiple parasite, therapeutic effect better compound recipe fenbendazole tablet.
In order to achieve the above object, the invention provides a kind of compound recipe fenbendazole tablet, every sheet is obtained by the composition of following mass fraction: fenbendazole 300-500mg, praziquantel 15-30mg, ivermectin 0.01-0.05mg, filler 600-1000mg, disintegrating agent 80-120mg, binding agent 100-200mg, lubricant 10-20mg and correctives 1-3mg.
Wherein, every sheet is obtained by the composition of following mass fraction: fenbendazole 400-500mg, praziquantel 20-25mg, ivermectin 0.02-0.03mg, filler 800-1000mg, disintegrating agent 90-100mg, binding agent 150-200mg, lubricant 13-16mg and correctives 1-2mg.
Wherein, every sheet is obtained by the composition of following mass fraction: fenbendazole 454mg, praziquantel 23mg, ivermectin 0.027mg, filler 908mg, disintegrating agent 90mg, binding agent 150mg, lubricant 15mg and correctives 1.5mg.
Wherein, described filler is starch, sucrose or calcium hydrogen phosphate; Described disintegrating agent is PVPP, CMS-Na or L-HPC; Described binding agent is the mixed solution of mucialga of arabic gummy and gelatine size; Described lubricant is the micropowder silica gel of 1%; Described correctives is aspartame.
Preferably, described filler is starch; Described disintegrating agent is L-HPC.
Preferably, in described binding agent, the ratio of mucialga of arabic gummy and gelatine size solution is 1:3-1:1.
The preparation technology of compound recipe fenbendazole tablet of the present invention comprises:
The first step, fenbendazole mixed with filler after micronizing, cross 150-200 mesh sieve, mixture is for subsequent use, and praziquantel and ivermectin are pulverized and crossed 100-120 mesh sieve respectively, for subsequent use;
Second step, by the ivermectin after the first step is pulverized, add 20-40ml/ thousand anhydrous gelatine sizes, ultrasonic making it is dissolved completely, and the ivermectin gelatin serosity obtained is for subsequent use;
3rd step, praziquantel to be mixed homogeneously with the mixture that the first step obtains by equivalent method of progressively increasing in three-dimensional mixer, then add disintegrating agent and correctives to continue mixing 5-10min and obtain mixed powder, mixed powder is transferred to high speed one-step-granulating method, ivermectin gelatin serosity is sprayed in the mixed powder run up, mixing 10-15min, add binding agent again, obtain soft material, soft material is pulverized and crosses 20-25 mesh sieve and obtain granule;
4th step, the granule that the 3rd step obtains is placed in box drier at 50-65 DEG C, stirs dry 1.5-3 hour, be dried to water content in granule and, 3% ~ 5%, cross 24 mesh sieves and obtain granulate;
5th step, the granulate that the 4th step obtains is added lubricant, in blender, mix 10-15min evenly obtain waiting to press granule;
6th step, with 17mm dimple form punch die treat pressure granule carry out tabletting, obtain the Hardness Control of tablet at 6-10kgf;
7th step, the tablet the 6th step obtained, adopt brown plastic bottle packing.
The beneficial effect that the present invention brings is: the compound recipe fenbendazole tablet that the present invention obtains, and a dog natural infection anthelmintic repelling and killing efficacy is obvious, and single Redution of eggs reaches more than 95%, more for anthelmintic kind, and reach better therapeutic effect, better effects if, and safety, there is no toxic and side effects, drug dissolution is good, high temperature resistant, resistance to illumination, favorable reproducibility is stable.
Detailed description of the invention
The present invention is described by the following example.
Embodiment 1
Three batches 1000 compound recipe fenbendazole sheets are prepared by the formula composition determined and preparation technology.
Often criticize formula composition: the mixed solution of fenbendazole 454g, praziquantel 23g, ivermectin 0.027g, starch 908g, L-HPC90mg, 50mg mucialga of arabic gummy and 100mg gelatine size, the micropowder silica gel 15g of 1% and aspartame 1.5g.
Preparation process:
The first step, fenbendazole mixed with starch after micronizing, cross 200 mesh sieves, mixture is for subsequent use, and praziquantel and ivermectin are pulverized and crossed 100 mesh sieves respectively, for subsequent use;
Second step, by the ivermectin after the first step is pulverized, add the anhydrous gelatine size of 40ml, ultrasonic making it is dissolved completely, for subsequent use;
3rd step, praziquantel to be mixed homogeneously with the mixture of the first step by equivalent method of progressively increasing in three-dimensional mixer, then add L-HPC and aspartame to continue mixing 10min and obtain mixed powder, mixed powder is transferred to high speed one-step-granulating method, ivermectin gelatin solution is sprayed in the mixed powder run up, mixing 10min, add the mixed solution of 50mg mucialga of arabic gummy and 100mg gelatine size again, obtain soft material, soft material was pulverized 24 mesh sieves and obtain granule;
4th step, the granule that the 3rd step obtains is placed in box drier at 60 DEG C, stirs dry 1.5 hours, be dried to water content in granule and, 3%, cross 24 mesh sieves and obtain granulate;
Add lubricant in 5th step, the granulate that obtains in the 4th step, in blender, mix 10min evenly obtain waiting to press granule;
6th step, with 17mm dimple form punch die treat pressure granule carry out tabletting, obtain the Hardness Control of tablet at 6kgf;
7th step, the tablet the 6th step obtained, adopt brown plastic bottle packing.
Quality testing is carried out to the compound recipe fenbendazole tablet second batch that embodiment 1 obtains.
Assay method: sample dissolution in vitro, related substance, uniformity of dosage units and content all adopt high effective liquid chromatography for measuring.
Instrument: Shimadzu LC-20AT type chromatograph of liquid (Japanese Shimadzu), DHA diode array, UV-detector and fluorescence detector; TU-1810 ultraviolet-uisible spectrophotometer, R-800C type intellectual drug digestion instrument (Radio Factory of Tianjin Univ.); TU-1810 ultraviolet-uisible spectrophotometer (Shanghai is general analyses); Shimadzu LC-20AT type chromatograph of liquid (Japanese Shimadzu).
Exposure experiments to light: get embodiments of the invention 1, removing outer package, be placed on illumination be 4500Lx illumination apparatus in place 10 days, in 0,5,10 day sampling, measure indices.
Hot test: get embodiments of the invention 1, removing outer package, is placed in surface plate, places 10 days under 60 DEG C of conditions, in sampling in 0,5,10 day, measures indices.
Result is as following table 1 and table 2:
Table 1 is the 0th day and the 5th day result of the test
Table 2 is the 0th day and the 10th day result:
Shown by table 1 and table 2 result, compound recipe fenbendazole sheet of the present invention was through illumination 5,10 days, and indices compared with 0 day and has no significant change; Place 10 days through 60 DEG C of high temperature, indices compared with 0 day, had no significant change, and all other index checking results are all in prescribed limit.Compound recipe fenbendazole tablet of the present invention is described, high temperature resistant, resistance to illumination.
The compound recipe fenbendazole tablet obtained to embodiment 1 three batches, carry out quality testing, testing result is:
Can be learnt by testing result, the compound recipe fenbendazole tablet that the present invention three crowdes prepares, rationally, stable, repeatability is high, and stability is high for formula composition.
Embodiment 2
1000 compound recipe fenbendazole sheets are prepared by the formula composition determined and preparation technology.
Often criticize formula composition: the mixed solution of fenbendazole 300mg, praziquantel 15mg, ivermectin 0.01mg, starch 600mg, L-HPC80mg, 25mg mucialga of arabic gummy and 75mg gelatine size, 1% micropowder silica gel 10mg and aspartame 1mg.
Preparation process:
The first step, fenbendazole mixed with starch after micronizing, cross 150 mesh sieves, mixture is for subsequent use, and praziquantel and ivermectin are pulverized and crossed 100 mesh sieves respectively, for subsequent use;
Second step, by the ivermectin after the first step is pulverized, add the anhydrous gelatine size of 20ml, ultrasonic making it is dissolved completely, and the ivermectin gelatin serosity obtained is for subsequent use;
3rd step, praziquantel to be mixed homogeneously with the mixture that the first step obtains by equivalent method of progressively increasing in three-dimensional mixer, then add L-HPC and aspartame to continue mixing 5min and obtain mixed powder, mixed powder is transferred to high speed one-step-granulating method, ivermectin gelatin solution is sprayed in the mixed powder run up, mixing 10min, add the mixed solution of mucialga of arabic gummy and gelatine size again, obtain soft material, soft material is pulverized and crosses 20 mesh sieves and obtain granule;
4th step, the granule that the 3rd step obtains is placed in box drier at 50 DEG C, stirs dry 1.5 hours, be dried to water content in granule and, 3%, cross 24 mesh sieves and obtain granulate;
5th step, the granulate that the 4th step obtains is added 1% micropowder silica gel, in blender, mix 10min evenly obtain waiting to press granule;
6th step, tabletting: treat pressure granule with 17mm dimple form punch die and carry out tabletting, obtain the Hardness Control of tablet at 6kgf;
7th step, packaging: the tablet the 6th step obtained, adopts brown plastic bottle packing.
Embodiment 3
1000 compound recipe fenbendazole sheets are prepared by the formula composition determined and preparation technology.
Often criticize formula composition: the mixed solution of fenbendazole 500mg, praziquantel 30mg, ivermectin 0.05mg, starch 1000mg, L-HPC120mg, 100mg mucialga of arabic gummy and 100mg gelatine size, 1% micropowder silica gel 20mg and aspartame 3mg.
Preparation process:
The first step, fenbendazole mixed with starch after micronizing, cross 200 mesh sieves, mixture is for subsequent use, and praziquantel and ivermectin are pulverized and crossed 120 mesh sieves respectively, for subsequent use;
Second step, by the ivermectin after the first step is pulverized, add the anhydrous gelatin of 40ml, ultrasonic making it is dissolved completely, and the ivermectin gelatin solution obtained is for subsequent use;
3rd step, praziquantel to be mixed homogeneously with the mixture that the first step obtains by equivalent method of progressively increasing in three-dimensional mixer, then add L-HPC and aspartame to continue mixing 10min and obtain mixed powder, mixed powder is transferred to high speed one-step-granulating method, ivermectin gelatin solution is sprayed in the mixed powder run up, mixing 15min, add the mixed solution of mucialga of arabic gummy and gelatine size again, obtain soft material, soft material is pulverized and crosses 25 mesh sieves and obtain granule;
4th step, the granule that the 3rd step obtains is placed in box drier at 65 DEG C, stirs dry 3 hours, be dried to water content in granule and, 5%, cross 24 mesh sieves and obtain granulate;
5th step, the granulate that the 4th step obtains is added 1% micropowder silica gel, in blender, mix 15min evenly obtain waiting to press granule;
6th step, tabletting: treat pressure granule with 17mm dimple form punch die and carry out tabletting, obtain the Hardness Control of tablet at 10kgf;
7th step, packaging: the tablet the 6th step obtained, adopts brown plastic bottle packing.
Clinical effect trial one
One, test objective
House pet is the dosage determination tests evaluating house pet antiCerbB2 monoclonal antibodies with the test of antiCerbB2 monoclonal antibodies evaluating drug effect, also II clinical trial phase is claimed, this test objective understands the test medicine of various dose to the anthelmintic effect of target animals, determines the therapeutic effect of test medicine, dosage and safety.
Two, experimental subject
(1) experimental animal
Zhengzhou, henan wandering dog rescue station, half a year does not do anthelmintic, finds that rare soft feces only appears in part dog in the recent period.
In May, 2015 goes to test site, indicates the feces gathering suspected infection dog, check worm's ovum with smear method through poultry raiser; Shave hair in veutro portion as numbering labelling, dog is only cooked clinical examination and drawn blood and does routine blood test, biochemical analysis, get rid of other diseases.
Field test selects experimental animal to be Chinese rural area dog, select body weight 5 ~ 15kg, the age dog between 6 monthly ages at monthly age to 12 only.Because test site condition limit, experimental animal body weight is bigness scale, and the age is introduced with poultry raiser and observes the estimation of tooth wear degree.
(2) test site
Graze and doctor Engineering Academy, HeNan agrigulture University, Zhengzhou pet clinic, house pet rescue station, Zhengzhou.
(3) key instrument equipment
Taiwan daybreak automatic clinical chemistry analyzer, steps auspicious full-automatic blood counting instrument for animals, microscope, Cecil McMaster egg count plate, routine clinical inspection apparatus equipment.
Three, for reagent thing and control drug
Test medicine: compound recipe fenbendazole tablet, Qingdao Agricultural University provides, embodiment 1, embodiment 2, embodiment 3.
Recommended dose: 4.5kg body weight a slice, once oral.
Drugs compared: compound recipe febantel sheet (visit and dote on clearly), Bayer Bitterfeld GmbH animal health, KP03AHB.
Specification: every sheet is containing febantel 150mg, Pyrantel Pamoate 144mg, praziquantel 50mg.
Using method: 10kg body weight a slice, once oral.
Four, EXPERIMENTAL DESIGN
(1) experimental animal grouping
Qualified sick dog is encoded.Specify according to " guideline ", this test arranges three large group altogether, embodiment 1 group, embodiment 2 groups and embodiment 3 groups, each group arranges five groups, namely be respectively blank group, drug control group, test medicine recommended dose reduce by half group, test medicine recommended dose group and test medicine doubling dosage group, wherein drug control group and test medicine recommended dose group often organize 30, reduce by half group, test medicine doubling dosage group of blank group, test medicine recommended dose often organizes 10, and each large group amounts to 90 cases (table 1-1/1-2/1-3).
The grouping of table 1-1. animal
The grouping of table 1-2. animal
The grouping of table 1-3. animal
(2) experimental technique
1. clinical examination
The body temperature (T) of sick dog, respiratory frequency (R), heart rate or pulse (P), fecaluria, diet is detected before administration, make a record according to numbering, body temperature is rectal temperature, breathing and heart rate carry out when sick dog is tranquil, respiratory frequency inspection adopts ocular estimate to observe dog chest rise number of times, and heart rate inspection adopts auscultation.After test medicine and the control drug of throwing something and feeding, equal conditions grouping is carried out to all experimental animals and raises.
2. worm's ovum inspection and counting
Feces collection: the fresh excreta taking experimental animal to discharge or internal rectum are got just.
Worm's ovum checks: cotton swab picks a small amount of feces and smoothens on microscope slide, and drip 1 ~ 2 normal saline, covered, is placed in basis of microscopic observation.This law is done case examination and is used.
Egg count: get 2 grams, feces and put into little conical flask or other glass container, add saturated brine 58 milliliters, add little bead 20, fully vibrate, make uniformly liquid manure, draw excrement juice with suction pipe and inject Cecil McMaster egg count plate, put on microscope, leave standstill 1 ~ 2 minute, under mirror, then count the worm's ovum sum in 1cm2 grid, obtain the average of worm's ovum number in two calibration chambers, be multiplied by 200 and be each worm kind worm's ovum number (E.P.G) in every gram of feces.
3. blood routine examination and biochemistry test
Extract 2mL venous blood from the forelimb radial veins of dog, remove syringe needle, blood is slowly pushed (containing anticoagulant) in 5mL centrifuge tube, prevent from injecting and too fastly cause haemolysis.Blood automatic blood analyzer detects routine blood indexes.With Special gun head and liquid-transfering gun draw above anticoagulation 200 μ L slowly inject reagent disc be placed in automatic clinical chemistry analyzer (from this laboratory belt to testing ground) do clinical biochemical detect.Clinical biochemical detects and is mainly liver function, renal function, muscle function, skeletal function and blood glucose.
4. drug use
Throwing something and feeding to often organizing dog respectively according to the scheme of table 1-1/1-2/1-3, throwing something and feeding once.
5. curative effect of medication
7th day to often organize dog use the same method carry out clinical examination, worm's ovum inspection, routine blood test and blood biochemical detect.
Judgement of medicine curative effect standard: by healing, the evaluation of effective, effective, invalid level Four.
Cure: clinical symptoms caused by parasitic infection (suffer from diarrhoea, become thin, feces character change or vomiting etc.) disappears, and Helminthic Eggs slip >=95% in feces, the sign of experimental animal recovers normal.
Effective: sb.'s illness took a favorable turn, the character of feces is close to normal (feces is shaped substantially), and Helminthic Eggs slip >=80% in feces, the sign of animal takes a turn for the better but do not recover normal completely.
Effective: sb.'s illness took a favorable turn, the character of feces is close to normal (being substantially shaped), and Helminthic Eggs slip >=60% in feces, the sign of animal takes a turn for the better but do not recover completely.
Invalid: after medication, the animal state of an illness even increases the weight of without obvious alleviation; Feces is shapeless, and Helminthic Eggs minimizing Shuai≤60% in feces, animal still has the clinical manifestations such as diarrhoea, vomiting.Calculate the corresponding percentage rate of each test group respectively.
Worm reduction rate: worm's ovum classified counting worm reduction rate, before and after experiment, every gram of faecal egg number difference is divided by the percent of testing front worm's ovum number.
Five, test results and analysis
The change of contrast routine blood test, serum biochemistry and Redution of eggs etc. is with the curative effect and the drug safety that judge each group.
Clinical symptoms aspect, the front each group experimental animal infection symptoms of test is comparatively slight, and feces is shapeless, and diet declines, and has no other extremely.After test, A1/A2/A3 group experimental animal symptom has no obvious improvement, and B1/B2/B3 group part test animal symptom take a favorable turn, and C1/C2/C3, D1/D2/D3, E1/E2/E3 group experimental animal symptom is clearly better, and reaches criterion of cure.
(1) clinical examination and clinical basic index
All experimental animal hearts rate, breathing, body temperature are all measured under dog only quiet condition, and the data obtained is in normal range, also have no notable difference, do not have a statistical significance before and after test.Before test all there is not obvious helminthic infection symptom in each experimental animal, only with the deformed form performance of feces.
(2) worm's ovum inspection and anthelminthic effect contrast
Before and after test, the contrast of each group anthelminthic effect is in Table 2-1/2-2/2-3, and between each group, same insect infection strength difference is not remarkable.Analyzed by average EPG, C1/C2/C3, D1/D2/D3, E1/E2/E3 group worm group difference of the same race is not remarkable, significant difference in group, and all remarkable with A1/A2/A3 group group difference.B1/B2/B3 group is except ascarid, and in all the other worm kind groups, difference is not remarkable; B1/B2/B3 group whipworm and cestode the 7th day not remarkable with C1/C2/C3, D1/D2/D3, E1/E2/E3 group group difference; Ascarid and ancylostome first day remarkable with C1/C2/C3, D1/D2/D3, E1/E2/E3 group group difference.Analyzed by Redution of eggs, B1/B2/B3, C1/C2/C3, D1/D2/D3, E1/E2/E3 group ascarid worm's ovum decreased average rate is about 65.6%, 95.7%, 96.7%, 97.8%, ancylostome worm's ovum decreased average rate is about 47.7%, 93.4%, 93.6%, 96.6%, whipworm worm's ovum decreased average rate is about 69.2%, 94.4%, 93.8%, 96.4%, and cestode worm's ovum decreased average rate is about 42.5%, 32.3%, 42.7%, 41.8%.C1/C2/C3, D1/D2/D3, E1/E2/E3 group is not remarkable and all remarkable with A1/A2/A3 group group difference with worm kind group difference; B1/B2/B3 group cestode whipworm and C1/C2/C3, D1/D2/D3, E1/E2/E3 worm of the same race group difference not remarkable, ancylostome ascarid and C1/C2/C3, D1/D2/D3, E1/E2/E3 worm of the same race group difference remarkable, ancylostome whipworm and A1/A2/A3 group difference are not remarkable, ascarid cestode and A1/A2/A3 group significant difference.
Each group anthelminthic effect contrast (X ± SD) before and after table 2-1. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter
A*: these data are not remarkable with all data differences of going together.
B*: these data and BDE group same column data difference not remarkable.
Each group anthelminthic effect contrast (X ± SD) before and after table 2-2. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter
A*: these data are not remarkable with all data differences of going together.
B*: these data and BDE group same column data difference not remarkable.
Each group anthelminthic effect contrast (X ± SD) before and after table 2-3. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter
A*: these data are not remarkable with all data differences of going together.
B*: these data and BDE group same column data difference not remarkable.
Analyze from table 2-1/2-2/2-3, half amount group therapeutic effect does not reach best, and times amount group, dosage group, drug control group are not remarkable to worm anthelminthic effect difference of the same race.
According to experimental data, in test, cestode worm reduction rate is not fairly obvious, but test medicine still has the ability of killing to cestode.Its reason is as follows:
(1) cestode body segment after drug effect slowly comes off, or excretes with gravid proglottid or with worm's ovum or egg capsule form with feces.A large amount of hexacanth embryos is contained in gravid proglottid or egg capsule.And this process continuity 2 weeks or longer time.
(2) after the effect of deinsectization medicine, cestode gets rid of with the form of nodal plate or egg capsule, if do not get nodal plate or egg capsule when (so most) adopt excrement, worm's ovum is little; If got, spy is many, even cannot count.And worm's ovum is often little during spontaneous ovulation.
Found the nodal plate in feces during sampling on the (3rd) the 7th, some can also be wriggled.
(4) describe according to return visit poultry raiser, some cases were also shown in taeniasis proglottid in feces after one week.
(3) blood routine examination
Before and after test, each group routine blood indexes is in Table 3-1/3-2/3-3, and before and after dispensing, routine blood indexes is substantially all within normal range, and B1/B2/B3 group WBC organizes interior significant difference on the 7th, and to organize same column indicator difference remarkable with all the other.All the other indexs have no significant change.During helminthic infection, WBC slightly raises, and after getting rid of the cause of disease through treatment, WBC declines, and illustrates that treatment obtains certain effect.After treatment, overall WBC is still higher, but is in normal range, may be relevant with bad feeding environment.
Respectively routine blood indexes is organized before and after table 3-1. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter
Respectively routine blood indexes is organized before and after table 3-2. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter
Respectively routine blood indexes is organized before and after table 3-3. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter
(4) biochemical analysis
Before and after test, each group biochemical indicator is in Table 4-1/4-2/4-3, and before and after dispensing, biochemical rule index has no significant change.
Respectively biochemical indicator is organized before and after table 4-1. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter.
Respectively biochemical indicator is organized before and after table 4-2. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter.
Respectively biochemical indicator is organized before and after table 4-3. test
Note: significant difference (P<0.05) between the numerical value of colleague upper right corner mark different letter.
Six, discussion and conclusion
(1) EXPERIMENTAL DESIGN
This test has carried out clinical trial to compound recipe fenbendazole sheet, and test designs according to " house pet antiCerbB2 monoclonal antibodies evaluating drug effect field plot technique guideline " completely.
(2) result of the test
Compound recipe fenbendazole sheet is to dog natural infection anthelmintic clear curative effect.Dosage group, times amount group each worm kind repelling and killing efficacy of embodiment 1-3 are obvious, and with EPG significant difference average before dispensing, dosage group, times amount group anthelminthic effect and control drug difference on effect are not remarkable, and half amount group anthelminthic effect is not remarkable.Except cestode, most of experimental animal single Redution of eggs of dosage group, times amount group reaches more than 95%, reaches therapeutic effect.Illustrate that compound recipe fenbendazole sheet is obvious to a dog natural infection anthelmintic repelling and killing efficacy.
Experimental animal safety evaluatio shows, each dosage group of compound recipe fenbendazole sheet (half amount, recommended dose and times amount) is to suffering from dog all without ill effect.Illustrate that compound recipe fenbendazole sheet is safe to dog Clinical practice.
In sum, compound recipe fenbendazole tablet of the present invention, a dog natural infection anthelmintic repelling and killing efficacy is obvious, single Redution of eggs reaches more than 95%, therapeutic effect is reached, better effects if for anthelmintic, and safety, there is no toxic and side effects, drug dissolution is good, high temperature resistant, resistance to illumination, favorable reproducibility is stable.
Clinical comparison test two
Subjects: common dog only, and infects the parasite of following items respectively.
Pilot project: 1. for adult Toxocara canis; 2. for dog ancylostome; 3. for whipworm; 4. for Taenia elliptica; 5. for heart worm.
The recurrence fenbendazole tablet of trial drug: embodiment 1-3, fenbendazole medicament, praziquantel medicament and ivermectin medicament.
Test method:
The test dog of each project is only divided into 7 groups, often organizes 5 female dogs, 5 male dogs.
First group: 5 female dogs, 5 male dogs, the compound recipe fenbendazole tablet of feeding embodiment 1 is treated.
Second group: 5 female dogs, 5 male dogs, the compound recipe fenbendazole tablet of feeding embodiment 2 is treated.
3rd group: 5 female dogs, 5 male dogs, the compound recipe fenbendazole tablet of feeding embodiment 3 is treated.
4th group: 5 female dogs, 5 male dogs, feeding fenbendazole medicament is treated.
5th group: 5 female dogs, 5 male dogs, feeding praziquantel medicament is treated.
6th group: 5 female dogs, 5 male dogs, feeding ivermectin medicament is treated.
7th group: 5 female dogs, 5 male dogs, blank group.
Result of the test
By postmortem polypide counting contrast table 1:
As can be seen from Table 1, embodiments of the invention 1-3 tri-embodiment groups meet fenbendazole tablet, have higher effective percentage for adult Toxocara canis, dog ancylostome, whipworm and Taenia elliptica, and for heart worm, also there is good effect.It can thus be appreciated that compound fenbendazole tablet of the present invention, by proportioning and the component of science, can increase anthelmintic kind, improve drug effect.
The foregoing is only preferred embodiment of the present invention, not in order to limit the present invention, within the spirit and principles in the present invention all, any amendment done, equivalent replacement, improvement etc., all should be included within protection scope of the present invention.
Claims (6)
1. a compound recipe fenbendazole tablet, it is characterized in that, every sheet is obtained by the composition of following mass fraction: fenbendazole 300-500mg, praziquantel 15-30mg, ivermectin 0.01-0.05mg, filler 600-1000mg, disintegrating agent 80-120mg, binding agent 100-200mg, lubricant 10-20mg and correctives 1-3mg.
2. compound recipe fenbendazole tablet according to claim 1, it is characterized in that, every sheet is obtained by the composition of following mass fraction: fenbendazole 400-500mg, praziquantel 20-25mg, ivermectin 0.02-0.03mg, filler 800-1000mg, disintegrating agent 90-100mg, binding agent 150-200mg, lubricant 13-16mg and correctives 1-2mg.
3. compound recipe fenbendazole tablet according to claim 1 and 2, it is characterized in that, every sheet is obtained by the composition of following mass fraction: fenbendazole 454mg, praziquantel 23mg, ivermectin 0.027mg, filler 908mg, disintegrating agent 90mg, binding agent 150mg, lubricant 15mg and correctives 1.5mg.
4. the compound recipe fenbendazole tablet according to any one of claim 1-3, is characterized in that, described filler is starch, sucrose or calcium hydrogen phosphate; Described disintegrating agent is PVPP, CMS-Na or L-HPC; Described binding agent is the mixed solution of mucialga of arabic gummy and gelatine size; Described lubricant is the micropowder silica gel of 1%; Described correctives is aspartame.
5. the compound recipe fenbendazole tablet according to any one of claim 1-4, is characterized in that, described filler is starch; Described disintegrating agent is L-HPC.
6. compound recipe fenbendazole tablet according to claim 4, is characterized in that, in described binding agent, the ratio of mucialga of arabic gummy and gelatine size is 1:3-1:1.
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN107595871A (en) * | 2017-10-31 | 2018-01-19 | 佛山市南海东方澳龙制药有限公司 | Compound preparation containing ivermectin and preparation method thereof |
| CN107693532A (en) * | 2017-10-31 | 2018-02-16 | 佛山市南海东方澳龙制药有限公司 | Compound anti-parasitic preparation and preparation method thereof |
| CN107753498A (en) * | 2017-10-31 | 2018-03-06 | 佛山市雷米高动物营养保健科技有限公司 | Compound ivermectin tablet and preparation method thereof |
| CN107837238A (en) * | 2017-10-31 | 2018-03-27 | 佛山市南海东方澳龙制药有限公司 | The preparation method and ivermectin tablet of ivermectin tablet |
| CN108670974A (en) * | 2018-06-13 | 2018-10-19 | 四川农业大学 | A kind of broad-spectrum anti-parasite chewable tablets and preparation method thereof |
| CN109394713A (en) * | 2018-12-26 | 2019-03-01 | 湖北中博绿亚生物技术有限公司 | Compound Fenbendazole Pyrantel and preparation method thereof |
| CN113679681A (en) * | 2020-05-18 | 2021-11-23 | 湖北中博绿亚生物技术有限公司 | Compound fenbendazole tablet and preparation method thereof |
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| CN101966197A (en) * | 2010-07-26 | 2011-02-09 | 天津生机集团股份有限公司 | Composition for treating bovine severe compound parasitic infection and preparation method thereof |
| CN103933045A (en) * | 2014-05-14 | 2014-07-23 | 深圳市红瑞生物科技有限公司 | Anthelmintic and preparation method thereof |
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| CN101966197A (en) * | 2010-07-26 | 2011-02-09 | 天津生机集团股份有限公司 | Composition for treating bovine severe compound parasitic infection and preparation method thereof |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN107595871A (en) * | 2017-10-31 | 2018-01-19 | 佛山市南海东方澳龙制药有限公司 | Compound preparation containing ivermectin and preparation method thereof |
| CN107693532A (en) * | 2017-10-31 | 2018-02-16 | 佛山市南海东方澳龙制药有限公司 | Compound anti-parasitic preparation and preparation method thereof |
| CN107753498A (en) * | 2017-10-31 | 2018-03-06 | 佛山市雷米高动物营养保健科技有限公司 | Compound ivermectin tablet and preparation method thereof |
| CN107837238A (en) * | 2017-10-31 | 2018-03-27 | 佛山市南海东方澳龙制药有限公司 | The preparation method and ivermectin tablet of ivermectin tablet |
| CN108670974A (en) * | 2018-06-13 | 2018-10-19 | 四川农业大学 | A kind of broad-spectrum anti-parasite chewable tablets and preparation method thereof |
| CN109394713A (en) * | 2018-12-26 | 2019-03-01 | 湖北中博绿亚生物技术有限公司 | Compound Fenbendazole Pyrantel and preparation method thereof |
| CN113679681A (en) * | 2020-05-18 | 2021-11-23 | 湖北中博绿亚生物技术有限公司 | Compound fenbendazole tablet and preparation method thereof |
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