Background technology
Ceftazidime, chemistry entitled (6R, 7R)-7-[[(2-amino-4-thiazolyl)-[(1-carboxyl-1-methyl ethoxy)
Imino group] acetyl group] amino]-2-carboxyl-8-oxo-5-thia-1-azabicyclo [4.2.0] oct-2-ene-3-picoline
Inner salt pentahydrate, for applying wide cephalosporin clinically, its structural formula is:
In order to ensure human administration's safety, state-promulgated pharmacopoeia specifies, for ceftazidime antibiotic, it is desirable to ceftazidime five water
The content of compound is not less than 95%, and the content of polymer is not higher than 0.3%, and its color and luster is not higher than No. 6 colors.Ceftazidime antibiotic
During depositing, in the case of particularly suffering high temperature (> 50 DEG C), tend to occur degraded and polyreaction, generate cephalo he
Pyridine dimer, trimer and polymer etc. polymer, thus cause active constituents of medicine content to reduce, color and luster is strengthened, polymerization
Thing impurity content raises.It addition, expired ceftazidime antibiotic, owing to the resting period is long, pharmaceutically active is the most usually made to become
Dividing content to reduce, darken, polymer content raises.Further, in some cases, owing to controlling of production process is improper, institute
The ceftazidime pentahydrate obtained, ceftazidime dimer, trimer and polymer etc. polymer content is the highest.And gather
During compound content height, human body is easily made to produce anaphylaxis.So for high ceftazidime five water of this kind of polymeric impurities content
Compound or ceftazidime pharmaceutical preparation, it is necessary to be purified further, ceftazidime five water that obtain high-quality, that purity is high
Solvate crystal.
GB2063871 discloses the preparation method of ceftazidime pentahydrate crystal, and the method is regulation ceftazidime acid
The pH of salt or alkali salt aqueous solution is 3.3-4.0, makes ceftazidime pentahydrate crystal structure separate out.Above-mentioned polymeric impurities content
Higher ceftazidime pentahydrate or ceftazidime pharmaceutical preparation, such as, when polymeric impurities content is higher than 4%, according to
The method crystallization purifying of GB2063871, polymeric impurities is usually associated with ceftazidime pentahydrate crystal and separates out together, institute
With, in obtained ceftazidime pentahydrate crystal, the content of polymeric impurities remains unchanged the highest.
GB2157682 discloses the recovery method of a kind of ceftazidime, and the method is to use non-functional large hole mesh resin,
Be that 2.0-5.5 ceftazidime aqueous solution releases with pH, thus absorb ceftazidime, then carry out eluting, isolate ceftazidime or
Its salt or its hydrate.According to the method, end product may be ceftazidime or its salt or its hydrate, impurity polymer
Content reduces, and product color shoals, but the method needs to use non-functional large hole mesh resin, then carries out eluting, separation, operation
Many, complex operation, cost is high.
US4659813 discloses the preparation method of a kind of ceftazidime pentahydrate crystal, and the method is, about 5~15
At a temperature of DEG C, pH is about the ceftazidime aqueous solution of 5.5~about 6.5, regulates its pH with acid and is about 4.0~about 4.7, and at knot
By controlling the addition of acid during crystalline substance, make pH be maintained at about 4.0~about 4.7, thus separate out ceftazidime pentahydrate crystal.
Although this method is to improving product purity, reducing polymer content has certain help, but, color and luster the highest for polymer content
Very poor ceftazidime preparation, in this way, still can not get the ceftazidime pentahydrate crystal of high-quality.Meanwhile, this side
Material is first dissolved in the higher system of pH by method, causes ceftazidime to degrade, and such response rate reduces.
CN1775784A discloses the purification process of a kind of ceftazidime, more particularly, it relates to by impure, containing polymerization
The ceftazidime that thing impurity is high prepares the method for the ceftazidime pentahydrate of high-quality by crystallization.Impure, polymer contains
Measure high ceftazidime pentahydrate, ceftazidime hydrochlorate, ceftazidime ambroxol salt or expired or from reclaiming on the market
The ceftazidime preparation come, is configured to ceftazidime aqueous solution, then with the pH of alkali or acid regulation ceftazidime aqueous solution is
1.5-2.5, now impurity, ceftazidime polymer separate out together with a small amount of ceftazidime, are filtered to remove these precipitates,
Obtained filtrate alkali regulation pH is 3.5-4.8, and ceftazidime pentahydrate crystal structure separates out.The method is easy and simple to handle,
Low cost, safety is good, and yield is high, and obtained ceftazidime pentahydrate crystal purity is high, and polymer content is low, reaches medicine
Allusion quotation regulation requirement.
CN101607966A discloses the preparation method of a kind of ceftazidime pentahydrate, carries out as steps described below: step
Rapid one, in a dissolving tank, inject water for injection, add ceftazidime hydrochlorate, after dissolving, put into activated carbon decolorizing, filter,
Filtrate is stand-by;Step 2, in another dissolving tank inject water for injection, add ceftazidime hydrochlorate, after dissolving, put into live
Property charcoal, decolouring, filter, filtrate proceeds to crystallizer;Step 3, drips aqueous slkali in the crystallizer in second step, regulation pH arrives
4.0-6.0, then drip the filtrate in the first step and make pH value pull back to 3.6, keep temperature 0-10 DEG C, stirring, crystallization;Step 4,
Growing the grain filtered after 3-4 hour, and filter cake cold water and acetone wash respectively, was vacuum dried 2-3 hour, obtained ceftazidime five hydration
Thing crystal.Its advantage is: save fund, Simplified flowsheet, minimizing waste gas discharge of wastewater;Easy and simple to handle, it is suitable for industrialized production;Pure
Degree is high, yield is high.
Visible, the method for prior art is mostly from improving stability, improving head with minimizing polyreaction as far as possible
The quality of his pyridine product of spore.But, ceftazidime poor fluidity prepared by the method for prior art, have a strong impact on its subpackage accurate
Really property and uniformity, be not suitable for commercial production.
In view of this, the special proposition present invention.
Summary of the invention
The primary and foremost purpose of the present invention is to provide a kind of ceftazidime compound, and this not only has preferable heat stability,
And mobility is preferable.
For achieving the above object, the present invention adopts the following technical scheme that
A kind of ceftazidime compound, it is characterised in that the structural formula such as formula I institute of described ceftazidime compound
Showing, this compound powder X-ray diffraction algoscopy measures, the X-ray powder diffraction pattern represented with the 2 θ ± 0.2 ° angles of diffraction
As shown in Figure 1.
The inside solid-state structure of compound has the biggest impact, same compound to its physicochemical property, and its crystal formation is not
With, cause its lattice energy different, thus cause its physical property the most different.
The invention provides a kind of ceftazidime unlike the prior art, have compared with the ceftazidime of prior art
Higher lattice energy, lattice is higher to the binding force of ceftazidime molecule, thus improves the stability of ceftazidime compound.
Inventor is by thermally-stabilised new test, and result shows that the special crystal form of ceftazidime compound provided by the present invention is with existing
The solid form having the ceftazidime of technology is compared, and has higher heat stability, which greatly improves the medication peace of patient
Entirely.It addition, present inventors have surprisingly found that, ceftazidime compound provided by the present invention has extraordinary mobility, easily
In subpackage.
Meanwhile, the present invention tests also by pharmacokinetics, surprisingly finds that the ceftazidime of the present invention has more preferable biology
Availability.
The present invention also aims to provide the preparation method of above-mentioned ceftazidime compound, the method to include walking as follows
Rapid:
1) crude product solution is prepared: ceftazidime crude product is added the mixed solvent formulated by dimethyl sulfoxide and methanol
In, control temperature 20~30 DEG C, add activated carbon decolorizing, filter, obtain ceftazidime crude product solution, standby;
2) nucleus generate process: control ceftazidime crude product solution temperature in the range of 20~30 DEG C, under agitation to
In this solution, stream adds deionized water, has muddy appearance, obtains turbid solution;
3) crystal growing process: by step 2) turbid solution of gained is placed under ultrasonic field, controls solution temperature 20~30
DEG C, drip chloroform wherein, separate out crystal;Closing ultrasonic field, be cooled to 0~5 DEG C, filter, filter cake is washed with deionized water
Washing, vacuum drying obtains described ceftazidime compound.
In the present invention, described ceftazidime crude product can be the method such as CN102391289A institute public affairs using prior art
The ceftazidime pentahydrate that the synthetic method of the ceftazidime opened prepares, it is also possible to be commercially available ceftazidime five hydration
Raw material medicine.
Crystallization is a complicated process, and in different environments, the change of the either step of crystallization process all can be formed
Different crystallization effects.In the present invention, first for ensureing effective crystallize, step 1) purify former by activated carbon decolorizing, filtration
Material;Step 2) and step 3) it is that nucleus generates and crystal growing process.Wherein step 3) after nucleus is formed, introduce ultrasonic
, and in crystallization process introduce ultrasonic field have change crystal morphology, regulate crystal size, improve particle size distribution and shorten knot
The effect of brilliant time etc..In the present invention, by prepared ceftazidime compound crystal form XRD is characterized, obtained by discovery
Ceftazidime compound is a kind of ceftazidime being different from prior art crystal formation.
As the preferred version of the present invention, wherein, step 1) described in ceftazidime crude product and described mixed solvent
Amount ratio be 1g:5~8ml.
In described mixed solvent, dimethyl sulfoxide is 3~7:1 with the volume ratio of methanol.
Step 2) described in deionized water and step 1) described in the volume ratio of mixed solvent be 5:1~10:1.
Step 3) described in ultrasonic field be frequency be 3.5~6.5kHz, intensity be 0.6W cm-2~4W cm-2Super
Sound field.
Step 3) described in chloroform and step 1) described in the volume ratio of mixed solvent be 7:1~12:1.
Step 2) described in mixing speed be 130~200r/min.
Step 2) described in stream rate of acceleration be 10~15ml/min;Step 3) described in drop rate be 5~8ml/
min。
The present invention furthermore provides a kind of pharmaceutical composition, and described pharmaceutical composition contains head provided by the present invention
His acridine compound of spore.
In the present invention, described pharmaceutical composition can be prepared as any applicable various dosage forms of prior art, described
Various dosage forms are referred to prior art and are similar to dosage form and are prepared, and pay more creativeness without those skilled in the art
Work, can realize the purpose of the present invention.
The preferred injectable sterile powder of the present invention.
It is furthermore preferred that injectable sterile powder of the present invention is possibly together with natrium carbonicum calcinatum.
Most preferably, in described pharmaceutical composition, the consumption of natrium carbonicum calcinatum is the consumption of ceftazidime compound
11.2wt%, wherein the consumption of ceftazidime compound presses ceftazidime (C22H22N6O7S2) meter.
Described pharmaceutical composition is through nothing after ceftazidime crystalline compounds is mixed by described consumption with natrium carbonicum calcinatum
Aseptic powder injection is made after bacterium subpackage.
The sterilized powder of the present invention can carry out subpackage by the specification of 0.5g/ bottle, 1.0g/ bottle, 2.0g/ bottle etc..Here rule
Lattice are with ceftazidime (C22H22N6O7S2) meter.
Compared with prior art, present invention have the advantage that
(1) ceftazidime compound provided by the present invention has preferable heat stability, and polymer content change is little;
(2) ceftazidime provided by the present invention has preferable mobility, is conducive to improving the accuracy of subpackage, and
It is easily mixed when mixing with other composition uniformly;
(3) ceftazidime provided by the present invention has preferable bioavailability.
Detailed description of the invention
Be below the detailed description of the invention of the present invention, described embodiment be in order to further describe the present invention rather than
Limit the present invention.
The preparation of [embodiment 1] ceftazidime compound
1) crude product solution is prepared: 20g ceftazidime crude product is added 110ml by formulated the mixing of dimethyl sulfoxide and methanol
In bonding solvent (wherein the volume ratio of dimethyl sulfoxide and methanol is 6:1), control temperature 22 DEG C, add ceftazidime crude product weight
The activated carbon decolorizing of 0.01%, filters, obtains ceftazidime crude product solution, standby;
2) nucleus generates process: the temperature of control ceftazidime crude product solution is in the range of 22 DEG C, and low whipping speed is
Under the stirring of 150r/min, in this solution, speed stream with 11ml/min adds deionized water, has muddy appearance, obtains muddy molten
Liquid;
3) nucleus crystal growing process: by step 2) turbid solution of gained be placed in frequency be 4kHz, intensity be 3W cm-2
Ultrasonic field under, control solution temperature 22 DEG C, drip 1210ml chloroform with the speed of 8ml/min wherein, separate out crystal;
Closing ultrasonic field, be cooled to 1 DEG C, filter, filter cake is washed with deionized 3 times, and vacuum drying obtains described ceftazidime
Compound.Purity 99.8%, loss on drying 14.1%.
The ceftazidime crystalline compounds powder X-ray diffraction algoscopy obtained is measured, with the 2 θ ± 0.2 ° angles of diffraction
The X-ray powder diffraction pattern represented is as shown in Figure 1.
The preparation of [embodiment 2] ceftazidime compound
1) crude product solution is prepared: 20g ceftazidime crude product is added 150ml by formulated the mixing of dimethyl sulfoxide and methanol
In bonding solvent (wherein the volume ratio of dimethyl sulfoxide and methanol is 4:1), control temperature 28 DEG C, add ceftazidime crude product weight
The activated carbon decolorizing of 0.01%, filters, obtains ceftazidime crude product solution, standby;
2) nucleus generates process: the temperature of control ceftazidime crude product solution is in the range of 28 DEG C, and low whipping speed is
Under the stirring of 180r/min, in this solution, speed stream with 14ml/min adds 1050ml deionized water, has muddy appearance, obtains
Turbid solution;
3) nucleus crystal growing process: by step 2) turbid solution of gained be placed in frequency be 4.8kHz, intensity be 1W
cm-2Ultrasonic field under, control solution temperature 28 DEG C, drip 1500ml chloroform with the speed of 7ml/min wherein, separate out crystalline substance
Body;Closing ultrasonic field, be cooled to 3 DEG C, filter, filter cake is washed with deionized 3 times, and vacuum drying obtains described ceftazidime
Compound.Purity 99.7%, loss on drying 14.0%.
The ceftazidime crystalline compounds powder X-ray diffraction algoscopy obtained is measured, with the 2 θ ± 0.2 ° angles of diffraction
The X-ray powder diffraction pattern represented is consistent with embodiment 1.
The preparation of [embodiment 3] ceftazidime compound
1) crude product solution is prepared: 20g ceftazidime crude product is added 130ml by formulated the mixing of dimethyl sulfoxide and methanol
In bonding solvent (wherein the volume ratio of dimethyl sulfoxide and methanol is 5:1), control temperature 25 DEG C, add ceftazidime crude product weight
The activated carbon decolorizing of 0.01%, filters, obtains ceftazidime crude product solution, standby;
2) nucleus generates process: the temperature of control ceftazidime crude product solution is in the range of 25 DEG C, and low whipping speed is
Under the stirring of 160r/min, in this solution, speed stream with 12ml/min adds 1040ml deionized water, has muddy appearance, obtains
Turbid solution;
3) nucleus crystal growing process: by step 2) turbid solution of gained be placed in frequency be 5.0kHz, intensity be 2W
cm-2Ultrasonic field under, control solution temperature 25 DEG C, drip 1170ml chloroform with the speed of 6ml/min wherein, separate out crystalline substance
Body;Closing ultrasonic field, be cooled to 2 DEG C, filter, filter cake is washed with deionized 3 times, and vacuum drying obtains described ceftazidime
Compound.Purity 99.8%, loss on drying 14.2%.
The ceftazidime crystalline compounds powder X-ray diffraction algoscopy obtained is measured, with the 2 θ ± 0.2 ° angles of diffraction
The X-ray powder diffraction pattern represented is consistent with embodiment 1.
The preparation of [embodiment 4] ceftazidime compound
1) crude product solution is prepared: 20g ceftazidime crude product is added 160ml by formulated the mixing of dimethyl sulfoxide and methanol
In bonding solvent (wherein the volume ratio of dimethyl sulfoxide and methanol is 7:1), control temperature 30 DEG C, add ceftazidime crude product weight
The activated carbon decolorizing of 0.01%, filters, obtains ceftazidime crude product solution, standby;
2) nucleus generates process: the temperature of control ceftazidime crude product solution is in the range of 30 DEG C, and low whipping speed is
Under the stirring of 200r/min, in this solution, speed stream with 15ml/min adds 1600ml deionized water, has muddy appearance, obtains
Turbid solution;
3) nucleus crystal growing process: by step 2) turbid solution of gained be placed in frequency be 6.5kHz, intensity be 4W
cm-2Ultrasonic field under, control solution temperature 30 DEG C, drip 1920ml chloroform with the speed of 8ml/min wherein, separate out crystalline substance
Body;Closing ultrasonic field, be cooled to 5 DEG C, filter, filter cake is washed with deionized 3 times, and vacuum drying obtains described ceftazidime
Compound.Purity 99.7%, loss on drying 14.0%.
The ceftazidime crystalline compounds powder X-ray diffraction algoscopy obtained is measured, with the 2 θ ± 0.2 ° angles of diffraction
The X-ray powder diffraction pattern represented is consistent with embodiment 1.
The preparation of [embodiment 5] ceftazidime compound
1) crude product solution is prepared: 20g ceftazidime crude product is added 100ml by formulated the mixing of dimethyl sulfoxide and methanol
In bonding solvent (wherein the volume ratio of dimethyl sulfoxide and methanol is 3:1), control temperature 20 DEG C, add ceftazidime crude product weight
The activated carbon decolorizing of 0.01%, filters, obtains ceftazidime crude product solution, standby;
2) nucleus generates process: the temperature of control ceftazidime crude product solution is in the range of 20 DEG C, and low whipping speed is
Under the stirring of 130r/min, in this solution, speed stream with 10ml/min adds 500ml deionized water, has muddy appearance, obtains muddy
Turbid solution;
3) nucleus crystal growing process: by step 2) turbid solution of gained be placed in frequency be 3.5kHz, intensity be
0.6W·cm-2Ultrasonic field under, control solution temperature 20 DEG C, drip 700ml chloroform with the speed of 5ml/min wherein,
Separate out crystal;Closing ultrasonic field, be cooled to 0 DEG C, filter, filter cake is washed with deionized 3 times, and vacuum drying obtains described head
His acridine compound of spore.Purity 99.8%, loss on drying 14.2%.
The ceftazidime crystalline compounds powder X-ray diffraction algoscopy obtained is measured, with the 2 θ ± 0.2 ° angles of diffraction
The X-ray powder diffraction pattern represented is consistent with embodiment 1.
[example of formulations 1] ceftazidime for injection
Specification: 0.5g is (by ceftazidime C22H22N6O7S2Meter)
Preparation method:
1, interior packaging material processes
The cleaning of antibiotic glass bottle, plug, aluminium lid technique routinely, drying, sterilizing, standby;
2, concrete steps
(1) the ceftazidime compound prepared by the natrium carbonicum calcinatum of recipe quantity and embodiment 1 is weighed, in sterile chamber
Mix homogeneously;
(2) in the middle of, product examine is tested;
(3) carry out aseptic subpackaged by specification;
(4) evacuation, tamponade, lid is rolled;
(5) packaging, Quan Jian, warehouse-in.
[example of formulations 2] ceftazidime for injection
Specification: 1.0g is (by ceftazidime C22H22N6O7S2Meter)
Preparation method: with example of formulations 1, except that ceftazidime used is the cephalo prepared by embodiment 2
His acridine compound.
[example of formulations 3] ceftazidime for injection
Specification: 2.0g is (by ceftazidime C22H22N6O7S2Meter)
Preparation method: with example of formulations 1, except that ceftazidime used is the cephalo prepared by embodiment 3
His acridine compound.
[example of formulations 4] ceftazidime for injection
Specification: 0.5g is (by ceftazidime C22H22N6O7S2Meter)
Preparation method: with example of formulations 1, except that ceftazidime used is the cephalo prepared by embodiment 4
His acridine compound.
[example of formulations 5] ceftazidime for injection
Specification: 1.0g is (by ceftazidime C22H22N6O7S2Meter)
Preparation method: with example of formulations 1, except that ceftazidime used is the cephalo prepared by embodiment 5
His acridine compound.
[example of formulations 6] ceftazidime for injection
Specification: 2.0g is (by ceftazidime C22H22N6O7S2Meter)
Preparation method: with example of formulations 1, except that ceftazidime used is the cephalo prepared by embodiment 2
His acridine compound.
[example of formulations 7] ceftazidime for injection
Specification: 0.5g is (by ceftazidime C22H22N6O7S2Meter)
Preparation method: with example of formulations 1, except that ceftazidime used is the cephalo prepared by embodiment 3
His acridine compound.
Test example 1
Heat stabilization test
Ceftazidime is during depositing, and particularly under conditions of high temperature (> 50 DEG C), tends to occur degraded and polymerization
Reaction, thus cause active constituents of medicine content to reduce, color and luster is strengthened, and polymeric impurities content raises.This test example is used for examining
Examine the thermal stability difference of the ceftazidime crystalline compounds prepared by the present invention and ceftazidime of the prior art.
In this test example, each sample is numbered:
Trial target 1: the ceftazidime crystalline compounds prepared by the embodiment of the present invention 1;
Trial target 2: the ceftazidime crystalline compounds prepared by the embodiment of the present invention 5;
Reference substance 1: obtain after ceftazidime pentahydrate being purified according to the method for CN1775784A embodiment 1
Ceftazidime pentahydrate;
Reference substance 2: the ceftazidime pentahydrate crystal obtained according to the method for CN101607966A embodiment 1.
Each sample is respectively exposed to relative humidity be 75%, in the environment of temperature is 60 DEG C, use molecular-exclusion chromatography
Method measures the content of high molecular polymer, and (molecular exclusion chromatography is according to pharmacopeia in 2005 second, the relevant bar of annex VH
Part is measured), the results are shown in Table 1.
Table 1, heat stabilization test result
Time |
Content |
Trial target 1 |
Trial target 2 |
Reference substance 1 |
Reference substance 2 |
0 day |
The content (%) of polymer |
0.01 |
0.02 |
0.09 |
0.03 |
7 days |
The content (%) of polymer |
0.02 |
0.02 |
0.18 |
0.19 |
14 days |
The content (%) of polymer |
0.02 |
0.03 |
0.22 |
0.27 |
21 days |
The content (%) of polymer |
0.03 |
0.04 |
0.30 |
0.31 |
28 days |
The content (%) of polymer |
0.03 |
0.03 |
0.33 |
0.36 |
As can be seen from the above table, the heat stability of the ceftazidime compound that the method for the employing present invention prepares is significantly better than
The ceftazidime pentahydrate crystal that the method using prior art obtains after being purified.
The ceftazidime compound of other embodiments of the present invention has been also carried out above-mentioned test, and its result obtained is similar.
Test example 2
Fluidity test
This test example has investigated the mobility of the ceftazidime compound of the present invention and prior art.
This test example is by measuring the mobility evaluating sample angle of repose of sample, and concrete grammar is as follows: take sample
Grain, flows in the surface plate of circle from fixing little funnel, until obtain the highest cone, measure cone height H and
Radius R, calculates α angle of repose by tan α==H/R, the results are shown in Table 2, and angle of repose is the biggest, and mobility is the poorest.Refer to table 2.
Table 2, fluidity test result
|
Sample 1 |
Sample 2 |
Sample 3 |
Sample 4 |
Angle of repose (°) |
45° |
46° |
62° |
64° |
Wherein: sample 1 is the product of the embodiment of the present invention 1;
Sample 2 is the product of the embodiment of the present invention 2;
Sample 3 is the ceftazidime pentahydrate prepared according to the method for CN102391289A embodiment 8;
Sample 4 is the ceftazidime pentahydrate prepared according to the method for CN1775784A embodiment 1.
As known from Table 2, compared with ceftazidime of the prior art, the ceftazidime compound prepared by the present invention has
Preferably mobility, is conducive to improving the accuracy of subpackage, and is easily mixed when mixing with other composition uniformly.
Test example 3
Pharmacokinetics is tested
1, instrument and reagent
Agilent 1100Series high performance liquid chromatograph, Agilent company of the U.S. produces, including: G1310A HPLC
Pump, G1313A automatic sampler, G1314A ultraviolet wavelengthtunable detector, G1310A chromatographic work station.
Ceftazidime for injection investigational agent (ceftazidime for injection that invention formulation embodiment 2 prepares);Injection head
His pyridine of spore comparison medicine (ceftazidime for injection prepared according to prescription and the method for invention formulation embodiment 2, except that
Ceftazidime used is the ceftazidime pentahydrate prepared according to the method for CN1775784A embodiment 1).Used by test
Acetonitrile be chromatographically pure, other reagent are analytical pure, and test water is distilled water.Blank plasma is that Beijing Red Cross blood station carries
The Healthy Human Serum of confession.
2, method and result
2.1 chromatographic condition
Chromatographic column: A lltin a C18(53mm × 7mm, 3 μm, Alltech company of the U.S.);Chromatograph pre-column: Aichram-
Bond AQ C18(2.1mm × 10mm, 5 μm, Abel Industrise company of the U.S.);Flowing phase: 0.02mol L-1Di(2-ethylhexyl)phosphate
Hydrogen potassium-methanol (85:15, v/v);Flow velocity: 2mL min-1, detect wavelength: 254nm;Column temperature: room temperature;Sample size: 20 μ L.
2.2 sample pretreatment
Serum specimen processing method: accurate absorption blood serum sample 500 μ L, puts in 5mL centrifuge tube, adds perchloric acid
(0.5mol·L-1) 500 μ L, vortex oscillation 1min, in 10000r min-1Centrifugal 5min, Aspirate supernatant sample introduction measures.
2.3 pharmacokinetic studies
24 selected healthy male volunteers are university students, the mean age of experimenter be (21.7 ±
1.6) in year, height is (173.9 ± 2.8) cm, and body weight is (65.9 ± 4.4) kg, and Body Mass Index BMI is 21.8 ± 1.5, health check-up,
It is normal before electrocardiogram, blood biochemistry, routine blood test and routine urine test.Experimenter tests first 1 week and does not takes any medicine, without medicine
Thing allergies and habits of smoking and alcohol drinking.This test is ratified through Ethics Committee of institute, and the experimenter participating in test all signs written in the know
Letter of consent.
24 experimenters are randomly divided into two groups, test group and matched group, and often group 12, eats light respectively at the previous day of taking medicine
Fasting 12h after dinner, continued fasting to 4h after being administered tested morning on the same day, upon administration 4,10h fed standard meal, the most tested
Period can drink water, it is impossible to drinks tea, coffee and Other Drinks.Experimenter, can only be movable in special ward during testing, it is impossible to
Carry out aggravating activities.Can not drink during test, smoking.Test group and matched group give ceftazidime investigational agent and cephalo respectively
His pyridine comparison medicine, ceftazidime investigational agent and comparison medicine respectively with after a small amount of physiological saline solution, addition 250mL normal saline
In, constant rate intravenous drop 30min.Take a blood sample before being arranged to instil during test, the 5min during drop, drop 30min terminate
Can and be administered terminate after 5,15,30,45,60,90,120,180,240,360,480,720min extracting vein blood 5mL, be subject to
After examination person's blood sampling, can leave away.4000r·min-1Centrifugal 10min, separates serum, and the blood specimen after administration measures immediately,
The specimen do not surveyed is in-20 DEG C of preservations, and measures complete in the stable phase of sample.The mean blood plasma concentration curve recorded is shown in
Fig. 2.
From the mean blood plasma concentration-time graph of ceftazidime it can be seen that the C of investigational agentmaxIt is better than compareing medicine, uses
Trapezoidal method calculates AUC, result show by reagent AUC also superior to comparison medicine.
The ceftazidime for injection preparing other example of formulations of the present invention has been also carried out above-mentioned test, its knot obtained
The most similar.