CN1562001A - Carbazochrome sodium sulfoate dripping pill and its preparing method - Google Patents

Carbazochrome sodium sulfoate dripping pill and its preparing method Download PDF

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Publication number
CN1562001A
CN1562001A CN 200410030367 CN200410030367A CN1562001A CN 1562001 A CN1562001 A CN 1562001A CN 200410030367 CN200410030367 CN 200410030367 CN 200410030367 A CN200410030367 A CN 200410030367A CN 1562001 A CN1562001 A CN 1562001A
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China
Prior art keywords
sodium sulfonate
carbazochrome sodium
carbazochrome
coolant
sulfonate
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Pending
Application number
CN 200410030367
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Chinese (zh)
Inventor
钱进
许军
彭红
李平
朱丹
刘孝乐
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Nanchang Hongyi Technology Co Ltd
Original Assignee
Nanchang Hongyi Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nanchang Hongyi Technology Co Ltd filed Critical Nanchang Hongyi Technology Co Ltd
Priority to CN 200410030367 priority Critical patent/CN1562001A/en
Publication of CN1562001A publication Critical patent/CN1562001A/en
Pending legal-status Critical Current

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Abstract

A dripping pill of carbazochrome sodium sulfonate is prepared through superfine pulverizing and conventional steps for preparing dripping pills.

Description

Carbazochrome sodium sulfonate drop pill and preparation method thereof
Technical field
The present invention relates to a kind of pharmaceutical product and preparation method thereof, specifically carbazochrome sodium sulfonate drop pill and preparation method thereof.
Background technology
Carbazochrome sodium sulfonate can increase the resistance of blood capillary to damage, reduces the permeability of blood capillary, promotes the retraction of blood capillary fracture end and stops blooding.
Behind the oral carbazochrome sodium sulfonate 150mg of the man of health adult, in 0.5~1 hour blood Cmax greater than 25mg/ml, half-life (t 1/2) be 1.5 hours, it is the highest that oral back reached urine Chinese medicine concentration in 0.5~1 hour, and drainage in about 24 hours finishes.Clinical in hemorrhage.
The carbazochrome sodium sulfonate odorless, easily molten in hot water, molten in the water part omitted, its disintegration of tablet time is long, and dissolution and dissolution rate are low, absorption difference, bioavailability is low, and the supplementary product consumption ratio is big, and child, old people, bed patient and dysphagia patients are taken inconvenience, compliance is poor, has influenced the performance of carbazochrome sodium sulfonate therapeutical effect.
The present invention makes the carbazochrome sodium sulfonate drop pill by using ultramicro communication technique and dropping pill formulation Technology exactly, thereby overcomes the above defective of carbazochrome sodium sulfonate sheet, and the therapeutical effect of carbazochrome sodium sulfonate is given full play to.
Summary of the invention
The carbazochrome sodium sulfonate drop pill of making by using ultramicro communication technique and dropping pill formulation Technology not only have disintegrate molten loose fast, dissolution and dissolution rate improve, steady quality, the pill volume is little, both can swallow also can buccal, easy to carry and use, onset is rapid, compliance is good, be particularly suitable for the characteristics that child, old people, bed patient and dysphagia patients are taken, but also have working condition and production equipment is simple, production cost is low, compare the advantage that supplementary product consumption reduces with tablet, demonstrated fully the new drug research exploitation spirit that people-oriented.
For achieving the above object, the present invention by the following technical solutions: the carbazochrome sodium sulfonate fine powder of 1 weight portion through micronizing is added in 1~10 weight portion molten matrix, abundant mixing, dropping preparation method is condensed into ball in coolant, remove coolant, drying, promptly.
The chemical name of carbazochrome sodium sulfonate among the present invention (Carbazochrome Sodium Sulfonate) is 1-methyl-6-oxo-2,3,5,6-tetrahydro indole-5-semicarbazone-2-sulfonate sodium trihydrate, and structural formula is Molecular formula is C 10H 11N 4NaO 5S3H 2O, molecular weight are 367.32.
Substrate among the present invention includes but not limited to polyethylene glycol 6000, Macrogol 4000, polyethylene glycol 1500, cetomacrogol 1000, sodium stearate, glycerin gelatine, poloxamer, stearic acid, glycerol monostearate acid, insect wax etc.
Coolant among the present invention includes but not limited to dimethicone, liquid paraffin, vegetable oil, water, alcoholic solution etc.
Below through detecting to beneficial effect of the present invention as directed
One, detects index and method
1. disintegrate (molten loosing) time limit: check according to inspection technique disintegration (two appendix XA of Chinese Pharmacopoeia version in 2000).
2. dissolution rate: sample thief, according to dissolution method (two appendix XC first methods of Chinese Pharmacopoeia version in 2000), 600ml is a solvent with phosphate buffer (pH7.0), and rotating speed is per 100 commentaries on classics, operation in accordance with the law, in the time of 10,20,30,40 minutes, get solution 10ml, filter, get filtrate, according to spectrophotography (two appendix IV of Chinese Pharmacopoeia version in 2000 A), measure absorption receipts degree at the wavelength place of 363nm, press C 10H 11N 4NaO 5Absorptance (the E of S 1cm 1%) be 862 calculating dissolution rates.
Two, commercially available carbazochrome sodium sulfonate sheet testing result
1. disintegration time: 62 minutes
2. dissolution rate:
Time (minute) 10 20 30 40
Dissolution (%) 23.6 35.4 53.5 74.5
Three, example 1 sample detection result
1. the molten diffusing time: 3 minutes
2. dissolution rate:
Time (minute) 10 20 30 40
Dissolution (%) 49.6 81.3 94.5 98.2
Four, example 2 sample detection results
1. the molten diffusing time: 3 minutes
2. dissolution rate:
Time (minute) 10 20 30 40
Dissolution (%) 43.4 84.5 92.3 97.6
Five, example 3 sample detection results
1. the molten diffusing time: 4 minutes
2. dissolution rate:
Time (minute) 10 20 30 40
Dissolution (%) 47.4 84.5 90.3 96.2
Six, example 4 sample detection results
1. the molten diffusing time: 5 minutes
2. dissolution rate:
Time (minute) 10 20 30 40
Dissolution (%) 41.4 82.3 90.6 99.1
Seven, example 5 sample detection results
1. the molten diffusing time: 8 minutes
2. dissolution rate:
Time (minute) 10 20 30 40
Dissolution (%) 38.5 84.4 93.1 97.2
Eight, example 6 sample detection results
1. the molten diffusing time: 12 minutes
2. dissolution rate
Time (minute) 10 20 30 40
Dissolution (%) 41.4 82.3 91.5 96.7
The specific embodiment
One, example 1
Prescription:
Carbazochrome sodium sulfonate 5g
Polyethylene glycol 6000 15g
Make 1000
Method for making: the carbazochrome sodium sulfonate fine powder that the micronizing of learning from else's experience is crossed 200 mesh sieves is added in the fused polyethylene glycol 6000 substrate, stirs evenly, and with the dimethicone coolant, the dropping preparation method pill, drying, promptly.
Two, example 2
Prescription:
Carbazochrome sodium sulfonate 5g
Macrogol 4000 15g
Make 1000
Method for making: the carbazochrome sodium sulfonate fine powder that the micronizing of learning from else's experience is crossed 200 mesh sieves is added in the fused Macrogol 4000 substrate, stirs evenly, and with the dimethicone coolant, the dropping preparation method pill, drying, promptly.
Three, example 3
Prescription:
Carbazochrome sodium sulfonate 5g
Polyethylene glycol 6000 5g
Macrogol 4000 10g
Make 1000
Method for making: the carbazochrome sodium sulfonate fine powder that the micronizing of learning from else's experience is crossed 200 mesh sieves is added in fused Macrogol 4000 and the polyethylene glycol 6000 mixed-matrix, stirs evenly, and with the dimethicone coolant, the dropping preparation method pill, drying, promptly.
Four, example 4
Prescription:
Carbazochrome sodium sulfonate 5g
Glyceryl monostearate 15g
Make 1000
Method for making: the carbazochrome sodium sulfonate fine powder that the micronizing of learning from else's experience is crossed 200 mesh sieves is added in the fused glyceryl monostearate substrate, and mixing is a coolant with the frozen water, the dropping preparation method pill, and drying, promptly.
Five, example 5
Prescription:
Carbazochrome sodium sulfonate 5g
Polyethylene glycol 6000 10g
Poloxamer 5g
Make 1000
Method for making: the carbazochrome sodium sulfonate fine powder that the micronizing of learning from else's experience is crossed 200 mesh sieves is added in fused polyethylene glycol 6000 and the poloxamer mixed-matrix, stirs evenly, and with the dimethicone coolant, the dropping preparation method pill, drying, promptly.
Six, example 6
Prescription:
Carbazochrome sodium sulfonate 5g
Glyceryl monostearate 15g
Poloxamer 1g
Make 1000
Method for making: get the mixing fine powders that carbazochrome sodium sulfonate and poloxamer cross 200 mesh sieves through micronizing and be added in the fused glyceryl monostearate substrate, mixing is a coolant with the frozen water, the dropping preparation method pill, and drying, promptly.

Claims (4)

1. carbazochrome sodium sulfonate drop pill and preparation method thereof is characterized in that: the carbazochrome sodium sulfonate fine powder of 1 weight portion through micronizing is added in 1~10 weight portion molten matrix, and abundant mixing, dropping preparation method is condensed into ball in coolant, remove coolant, drying, promptly.
2. the chemical name of the described carbazochrome sodium sulfonate Carbazochrome of claim 1 Sodium Sulfonate is 1-methyl-6-oxo-2,3,5,6-tetrahydro indole-5-semicarbazone-2-sulfonate sodium trihydrate, and structural formula is
Figure A2004100303670002C1
Molecular formula is C 10H 11N 4NaO 5S3H 2O, molecular weight are 367.32.
3. the described substrate of claim 1 includes but not limited to polyethylene glycol 6000, Macrogol 4000, polyethylene glycol 1500, cetomacrogol 1000, sodium stearate, glycerin gelatine, poloxamer, stearic acid, glycerol monostearate acid, insect wax etc.
4. the described coolant of claim 1 includes but not limited to dimethicone, liquid paraffin, vegetable oil, water, alcoholic solution etc.
CN 200410030367 2004-03-29 2004-03-29 Carbazochrome sodium sulfoate dripping pill and its preparing method Pending CN1562001A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200410030367 CN1562001A (en) 2004-03-29 2004-03-29 Carbazochrome sodium sulfoate dripping pill and its preparing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200410030367 CN1562001A (en) 2004-03-29 2004-03-29 Carbazochrome sodium sulfoate dripping pill and its preparing method

Publications (1)

Publication Number Publication Date
CN1562001A true CN1562001A (en) 2005-01-12

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Country Status (1)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104127388A (en) * 2014-02-21 2014-11-05 杭州长典医药科技有限公司 Special ultrafine carbazochrome sodium sulfonate powder freeze-dried preparation and preparation method thereof
CN104473864A (en) * 2014-11-25 2015-04-01 陈长潭 Carbazochrome sodium sulfonate semisolid preparation and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104127388A (en) * 2014-02-21 2014-11-05 杭州长典医药科技有限公司 Special ultrafine carbazochrome sodium sulfonate powder freeze-dried preparation and preparation method thereof
CN104473864A (en) * 2014-11-25 2015-04-01 陈长潭 Carbazochrome sodium sulfonate semisolid preparation and preparation method thereof
CN104473864B (en) * 2014-11-25 2017-02-22 陈长潭 Carbazochrome sodium sulfonate semisolid preparation and preparation method thereof

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