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hfsr

银虫 (初入文坛)

[求助] 谁帮忙查个盐酸美金刚的标准,谢谢了。

谁帮忙查个盐酸美金刚的标准,谢谢了。
一定要USP36的,
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qiuqinglei5020

金虫 (小有名气)

硫酸大师


这个一定没有USP36,你也别找了!
4楼2013-10-20 12:24:43
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e_liang369

金虫 (正式写手)

【答案】应助回帖

感谢参与,应助指数 +1
直接到drugfuture上去查
http://www.drugfuture.com/standard/
悲催的研发!
2楼2013-10-18 12:28:32
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hfsr

银虫 (初入文坛)

引用回帖:
2楼: Originally posted by e_liang369 at 2013-10-18 12:28:32
直接到drugfuture上去查
http://www.drugfuture.com/standard/

那上面没有USP36版啊
3楼2013-10-19 20:33:53
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06药学

木虫 (著名写手)

【答案】应助回帖

★ ★ ★ ★ ★ ★ ★ ★ ★ ★
感谢参与,应助指数 +1
hfsr(zhychen2008代发): 金币+10, 多谢回帖交流 2013-10-20 23:08:46
Memantine Hydrochloride Tablets
DEFINITION

Memantine Hydrochloride Tablets contain an amount of memantine hydrochloride equivalent to NLT 90.0% and NMT 110.0% of the labeled amount of memantine hydrochloride (C12H21N ·HCl).
IDENTIFICATION
•  A. Infrared Absorption  197K
Analytical range:   4000 to 400 cm –1
Standard:   6.7 mg/mL of USP Memantine Hydrochloride RS in dichloromethane. Shake for 10 min, and pass through a suitable filter. Evaporate the solvent at room temperature. Collect the residue powder, and dry at 60 for 15 min. Prepare an approximate 1% (w/w) dispersion of the sample in potassium bromide.
Sample:   6.7 mg/mL of Memantine Hydrochloride in dichloromethane from NLT 20 crushed Tablets. Shake for 10 min, and centrifuge for 10 min. Pass the supernatant through a suitable filter. Evaporate the solvent at room temperature. Collect the residue powder, and dry at 60 for 15 min. Prepare an approximate 1% (w/w) dispersion of the sample in potassium bromide.
Acceptance criteria:   Fingerprint region of the Standard and Sample spectrum exhibit maxima at the same wave numbers.
•  B. The retention time of the memantine peak in the Sample solution corresponds to that of the memantine peak in the Standard solution, as obtained in the Assay.
ASSAY
•  Procedure
Solution A:   200 mg/mL of sodium hydroxide in water
Internal standard solution:   25 µg/mL of USP Amantadine Hydrochloride RS in water
Standard stock solution:   25 µg/mL of USP Memantine Hydrochloride RS prepared as follows. Weigh a suitable quantity of the Standard into a volumetric flask. Add methanol to fill 40% of the final flask volume, and sonicate. Dilute with water to volume.
Standard solution:   Pipet 4.0 mL each of Internal standard solution and Standard stock solution into a test tube. Add 2 mL of Solution A, and mix on a vortex mixer for 1 min. Add 4 mL of toluene, and mix on a vortex mixer for 3 min. Allow the two layers to separate. Inject the toluene layer.
Sample stock solution:   Nominally 20 µg/mL of memantine hydrochloride prepared as follows. Transfer a suitable number of Tablets to a volumetric flask to obtain a 0.1 mg/mL memantine hydrochloride solution. Add methanol to fill 40% of the final flask volume, and sonicate for 30 min with intermittent shaking. Add water to fill 40% of the final flask volume, and sonicate for 30 min with intermittent shaking. Dilute with water to volume, and centrifuge a portion for 10 min. Pipet a suitable volume of the clear centrifugate into a volumetric flask, and dilute with water to volume.
Sample solution:   Pipet 5.0 mL of the Sample stock solution, 4.0 mL of Internal standard solution, and 2 mL of Solution A into a test tube, and mix on a vortex mixer for 1 min. Add 4 mL of toluene, and mix on a vortex mixer for 5 min. Allow the two layers to separate. Inject the toluene layer.
Blank:   To 5.0 mL of 80 µL/mL of methanol in water add 2 mL Solution A, and mix on a vortex mixer for 1 min. Add 4.0 mL of tolune, and cyclomix on vortex for 5 min. Allow the two layers to separate. Inject the toluene layer.
Chromatographic system  
(See Chromatography  621 , System Suitability.)
Mode:   GC
Detector:   Flame ionization
Column:   30-m × 0.32-mm; 0.25-µm packing G27
Temperatures
Injection port:   210
Detector:   300
Oven:   See Table 1.
Table 1
Initial
Temperature
()        Temperature
Ramp
(/min)        Final
Temperature
()        Hold Time at Final
Temperature
(min)
50        0        50        2
50        20        140        0
140        30        200        5
Carrier gas:   Helium
Flow rate:   34.8 psi
Injection volume:   4 µL
Injection type:   Split ratio, 1:10
System suitability
Sample:   Standard solution
[ NOTE— The relative retention times for amantadine and memantine are 0.97 and 1.0, respectively. ]
Suitability requirements
Resolution:   NLT 2.0 between amantadine and memantine
Tailing factor:   NMT 2.5 for amantadine and NMT 2.0 for memantine
Relative standard deviation:   NMT 2.0% for the ratio of the peak areas of amantadine and memantine
Analysis
Samples:   Standard solution, Sample solution, and Blank

Calculate the percentage of the labeled amount of memantine hydrochloride (C12H21N ·HCl) in the portion of Tablets taken:
Result = ( R U / R S ) × ( C S / C U ) × 100
R U        = peak area ratio of memantine to amantadine from the Sample solution
R S        = peak area ratio of memantine to amantadine from the Standard solution
C S        = concentration of USP Memantine Hydrochloride RS in the Standard solution (µg/mL)
C U        = nominal concentration of memantine hydrochloride in the Sample solution (µg/mL)
Acceptance criteria:   90.0%–110.0%
PERFORMANCE TESTS
•   Dissolution  711
Medium:   0.1 N hydrochloric acid with sodium chloride (2g/L of sodium chloride in water), adjusted with hydrochloric acid to a pH of 1.2; 900 mL
Apparatus 1:   100 rpm
Time:   30 min
Standard stock solution:   (L/900) mg/mL of USP Memantine Hydrochloride RS in Medium, where L is the label claim in mg/Tablet
Internal standard solution:   28 µg/mL of USP Amantadine Hydrochloride RS in Medium
Standard solution
For Tablets labeled to contain 5 mg:   Transfer 5 mL of the Standard stock solution to a test tube, add 1 mL of the Internal standard solution and 2 mL of 5 N sodium hydroxide, and mix for 1 min. Add 3 mL of toluene, and mix for 2 min. Use the toluene layer.
For Tablets labeled to contain 10mg:   Transfer 5 mL of the Standard stock solution to a test tube, add 2 mL of the Internal standard solution and 2 mL of 5 N sodium hydroxide, and mix for 1 min. Add 3 mL of toluene, and mix for 2 min. Use the toluene layer.
Sample solution:   Pass a portion of the solution under test through a suitable filter.
For Tablets labeled to contain 5 mg:   Transfer 5 mL of the filtrate to a test tube, add 1 mL of the Internal standard solution and 2 mL of 5 N sodium hydroxide, and mix for 1 min. Add 3 mL of toluene, and mix for 2 min. Use the toluene layer.
For Tablets labeled to contain 10 mg:   Transfer 5 mL of the filtrate to a test tube, add 2 mL of the Internal standard solution and 2 mL of 5 N sodium hydroxide, and mix for 1 min. Add 3 mL of toluene, and mix for 2 min. Use the toluene layer.
Chromatographic system  
(See Chromatography  621 , System Suitability.)
Mode:   GC, splitless
Detector:   Flame ionization
Column:   30-m × 0.32-mm; 0.25-µm packing G27
Flow rate:   34.8 psi
Temperatures
Injection port:   210
Detector:   300
Oven:   See Table 2.
Table 2
Initial
Temperature
()        Temperature
Ramp
(/min)        Final
Temperature
()        Hold Time at Final
Temperature
(min)
50        0        50        2
50        20        140        0
140        30        200        5
Carrier gas:   Helium
Injection volume:   4 µL
System suitability
Sample:   Standard solution
Suitability requirements
Resolution:   NLT 2.0 between amantadine and memantine
Tailing factor:   NMT 2.0 each for amantadine and memantine
Relative standard deviation:   NMT 2.0% for both the amantadine and memantine peaks
Analysis
Samples:   Standard solution and Sample solution

Calculate the percentage of the labeled amount of memantine hydrochloride (C12H21N ·HCl) dissolved:
Result = ( R u / R s ) × ( C s /L) × V × 100
R U        = peak area ratio of memantine to amantadine from the Sample solution
R S        = peak area ratio of memantine to amantadine from the Standard solution
C S        = concentration of USP Memantine Hydrochloride RS from the Standard solution (µg/mL)
V        = volume of Medium, 900 mL
L        = label claim (mg/Tablet)
Tolerances:   NLT 80% (Q) of the labeled amount of memantine hydrochloride (C12H21N ·HCl) is dissolved.
•   Uniformity of Dosage Units  905 : Meet the requirements
IMPURITIES
•  Limit of Memantine–Lactose Adduct
[ NOTE— Perform this test if lactose is present in the formulation. ]
Solution A:   40 mg/mL of sodium hydroxide in water
Buffer:   Dissolve 3.3 g of monobasic potassium phosphate and 2.3 g of sodium 1-octane sulfonate in 1 L of water. Adjust with Solution A to a pH of 6.1.
Mobile phase:   Acetonitrile, methanol, and Buffer (26:4:70)
Standard solution:   0.2 mg/mL of USP Memantine Hydrochloride RS in Mobile phase
Sample solution:   Nominally 10 mg/mL of memantine hydrochloride from NLT 25 crushed Tablets, prepared as follows. Transfer an amount of powder equivalent to 100 mg of memantine hydrochloride to a 20-mL volumetric flask. Add 10 mL of Mobile phase, and sonicate for 30 min. Centrifuge, and pass a portion of the centrifugate through a suitable filter of 0.45-µm pore size.
Chromatographic system  
(See Chromatography  621 , System Suitability.)
Mode:   LC
Detector:   Refractive index
Column:   4.6-mm × 15-cm; 5-µm packing L1
Temperatures
Column:   40
Detector:   35
Flow rate:   1.3 mL/min
Injection volume:   50 µL
Run time:   1.3 times the retention time of the memantine peak
System suitability
Sample:   Standard solution
Suitability requirements
Tailing factor:   NMT 3.5
Relative standard deviation:   NMT 10.0%
Analysis
Samples:   Standard solution and Sample solution

Calculate the percentage of the memantine–lactose adduct in the portion of Tablets taken:
Result = ( r U / r S ) × ( C S / C U ) × (1/F) × 100
r U        = peak response of the memantine–lactose adduct from the Sample solution
r S        = peak response of memantine from the Standard solution
C S        = concentration of USP Memantine Hydrochloride RS in the Standard solution (mg/mL)
C U        = nominal concentration of memantine hydrochloride in the Sample solution (mg/mL)
F        = relative response factor of the memantine–lactose adduct (see Table 3)
Acceptance criteria:   See Table 3.
Disregard all peaks other than the memantine–lactose adduct peak.
Table 3
Name        Relative
Retention
Time        Relative
Response
Factor        Acceptance
Criteria,
NMT (%)
Memantine–lactose adduct        0.41        0.53        0.5
Memantine        1.0        1.0         —
•  Organic Impurities
Solution A:   1 N sodium hydroxide
Standard stock solution A:   0.5 mg/mL each of USP Memantine Related Compound A RS, USP Memantine Related Compound B RS, USP Memantine Related Compound C RS, USP Memantine Related Compound D RS, and USP Memantine Related Compound E RS in n-hexane
Standard stock solution B:   12.5 mg/mL of USP Memantine Hydrochloride RS prepared as follows. Weigh a suitable quantity of the Standard into a volumetric flask. Add Solution A to fill 15% of the final flask volume and n-hexane to fill 10% of the final flask volume. Mix for 10 min.
System suitability solution:   Pipet 4.0 mL of the n-hexane layer from Standard stock solution B into a 10-mL volumetric flask. Add 0.5 mL of Standard stock solution A, and dilute with n-hexane to volume.
Standard stock solution:   1.3 mg/mL of USP Memantine Hydrochloride RS in n-hexane prepared as follows. Weigh a suitable quantity of the Standard into a volumetric flask. Add Solution A to fill 30% of the final flask volume, and mix for 5 min. Add n-hexane to fill 40% of the final flask volume, and shake for 10 min. Transfer the contents of the flask into a separator. Allow the layers to separate, and filter a portion of the top n-hexane layer through anhydrous sodium sulfate. Use the clear solution.
Standard solution:   Pipet 2.0 mL of the clear solution from the Standard stock solution into a 100-mL volumetric flask, and dilute with n-hexane to volume.
Sample solution:   Nominally 5 mg/mL of memantine hydrochloride in n-hexane from NLT 20 crushed Tablets, prepared as follows. Transfer a weighed amount of powder equivalent to 100 mg of memantine hydrochloride to a suitable volumetric flask. Add Solution A to fill 15% of the final flask volume. Shake to disperse the material, and shake for 5 min. Sonicate for 5 min with intermittent shaking. Add n-hexane to fill 20% of the final flask volume, and shake for 10 min. Transfer the contents into a separator. Allow the layers to separate, and filter a portion of the top hexane layer through anhydrous sodium sulfate. Use the clear solution.
Chromatographic system  
(See Chromatography  621 , System Suitability.)
Mode:   GC
Detector:   Flame ionization
Column:   50-m × 0.32-mm; 0.52-µm packing G27
Temperatures
Injection port:   220
Detector:   300
Oven:   See Table 4.
Table 4
Initial
Temperature
()        Temperature
Ramp
(/min)        Final
Temperature
()        Hold Time at Final
Temperature
(min)
50        0        50        2
50        5        145        0
145        10        250        20
Carrier gas:   Helium
Flow rate:   4.0 ± 0.2 mL/min
Injection volume:   3 µL
Injection type:   Split ratio, 1:20
System suitability
Samples:   System suitability solution and Standard solution
[ NOTE— See Table 5 for the relative retention times. ]
Suitability requirements
Resolution:   NLT 2.0 between memantine and memantine related compound B, NLT 2.0 between memantine related compound B and memantine related compound C, System suitability solution
Tailing factor:   NMT 2.0, Standard solution
Relative standard deviation:   NMT 10.0%, Standard solution
Analysis
Samples:   Standard solution and Sample solution

Calculate the percentage of USP Memantine Related Compound E RS or any individual degradation product in the portion of Tablets taken:
Result = ( r U / r S ) × ( C S / C U ) × 100
r U        = peak response of USP Memantine Related Compound E RS or any individual degradation product from the Sample solution
r S        = peak response of memantine hydrochloride from the Standard solution
C S        = concentration of USP Memantine Hydrochloride RS in the Standard solution (mg/mL)
C U        = nominal concentration of memantine hydrochloride in the Sample solution (mg/mL)
Acceptance criteria:   See Table 5.
Table 5
Name        Relative
Retention
Time        Acceptance
Criteria,
NMT (%)
Memantine related compound Aa        0.77         —
Memantine        1.0         —
Memantine related compound Ba        1.03         —
Memantine related compound Ca        1.1         —
Memantine related compound Da        1.2         —
Memantine related compound E        1.4        0.15
Any individual unspecified degradation product         —        0.20
Total impuritiesb         —        0.5
a   Process impurities controlled in the drug substance and are included for identification only. Not reported for the drug product and not included in the total impurities
b   Excludes memantine–lactose adduct monitored in the test for Limit of Memantine–Lactose Adduct.
ADDITIONAL REQUIREMENTS
•  Packaging and Storage: Preserve in tight containers. Store at controlled room temperature.
•   USP Reference Standards  11
USP Amantadine Hydrochloride RS
USP Memantine Hydrochloride RS
USP Memantine Related Compound A RS
1,3-Dimethyladamantane.     
C12H20       164.29
USP Memantine Related Compound B RS  
3,5-Dimethyladamantane-1-ol.     
C12H20O       180.29
USP Memantine Related Compound C RS  
1-Chloro-3,5-dimethyladamantane.     
C12H19Cl       198.73
USP Memantine Related Compound D RS  
1-Bromo-3,5-dimethyladamantane.     
C12H19Br       243.18
USP Memantine Related Compound E RS  
N-3,5-Dimethyladamantan-1-yl formamide.     
C13H21NO       207.31

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