{"id":31121,"date":"2025-11-12T17:23:49","date_gmt":"2025-11-12T10:23:49","guid":{"rendered":"https:\/\/nhathuocngocanh.com\/bp\/?p=31121"},"modified":"2025-11-12T17:48:14","modified_gmt":"2025-11-12T10:48:14","slug":"vincamine","status":"publish","type":"post","link":"https:\/\/nhathuocngocanh.com\/bp\/vincamine\/","title":{"rendered":"Vincamine"},"content":{"rendered":"

Edition: BP 2025 (Ph. Eur. 11.6 update)<\/p>\n

Action and use<\/strong><\/p>\n

Vasodilator.<\/p>\n

DEFINITION<\/h2>\n
Methyl 14-hydroxyvincane-14\u03b2-carboxylate.<\/p>\n
Content<\/strong><\/p>\n
99.0 per cent to 101.0 per cent (dried substance).<\/p>\n
CHARACTERS<\/h2>\n
Appearance<\/h3>\n
White or almost white, crystalline powder.<\/p>\n
Solubility<\/h3>\n
Practically insoluble in water, soluble in methylene chloride, slightly soluble in anhydrous ethanol.<\/p>\n
IDENTIFICATION<\/h2>\n
A. Specific optical rotation (see Tests).<\/p>\n
B. Infrared absorption spectrophotometry (2.2.24).<\/p>\n
Comparison\u00a0 vincamine CRS.<\/p>\n
TESTS<\/h2>\n
Specific optical rotation (2.2.7)<\/strong><\/p>\n
+ 44.3 to + 49.0 (dried substance).<\/p>\n
Dissolve 0.1 g in dimethylformamide R and dilute to 20.0 mL with the same solvent.<\/p>\n
Related substances<\/h3>\n
Liquid chromatography (2.2.29). Prepare the solutions immediately before use. Dissolve the samples using sonication, while avoiding any overheating.<\/p>\n
Test solution Dissolve 50.0 mg of the substance to be examined in 10 mL of tetrahydrofuran R and dilute to 100.0 mL with the mobile phase.<\/p>\n
Reference solution (a)\u00a0 Dilute 1.0 mL of the test solution to 200.0 mL with the mobile phase.<\/p>\n
Reference solution (b) Dissolve 5 mg of vincamine for system suitability CRS (containing impurities A, B and C) in 1 mL of tetrahydrofuran R and dilute to 10 mL with the mobile phase.<\/p>\n
Column:<\/p>\n
\u2014 size: l = 0.25 m, \u00d8 = 4.6 mm;<\/p>\n
\u2014 stationary phase: end-capped octadecylsilyl silica gel for chromatography with embedded polar groups R (5 \u00b5m).<\/p>\n
Mobile phase tetrahydrofuran R, acetonitrile R, 15.4 g\/L solution of ammonium acetate R (17:18:65 V\/V\/V). Flow rate 1.0 mL\/min.<\/p>\n
<\/p>\n
Detection\u00a0 Spectrophotometer at 272 nm.<\/p>\n
Injection\u00a0 20 \u00b5L.<\/p>\n
Run time\u00a0 3.5 times the retention time of vincamine.<\/p>\n
Identification of impurities Use the chromatogram supplied with vincamine for system suitability CRS and the chromatogram obtained with reference solution (b) to identify the peaks due to impurities A, B and C.<\/p>\n
Relative retention With reference to vincamine (retention time = about 10 min): impurity A = about 0.8; impurity B = about 0.9; impurity C = about 1.35.<\/p>\n
System suitability\u00a0 Reference solution (b):<\/p>\n
\u2014 resolution: minimum 2.0 between the peaks due to impurity B and vincamine.<\/p>\n
Calculation of percentage contents:<\/p>\n
\u2014 for each impurity, use the concentration of vincamine in reference solution (a).<\/p>\n
Limits:<\/p>\n
\u2014 impurities A, C: for each impurity, maximum 0.5 per cent;<\/p>\n
\u2014 unspecified impurities: for each impurity, maximum 0.10 per cent;<\/p>\n
\u2014 total: maximum 1.0 per cent;<\/p>\n
\u2014 reporting threshold: 0.05 per cent.<\/p>\n
Loss on drying (2.2.32)<\/strong><\/p>\n
Maximum 0.5 per cent, determined on 1.000 g by drying in an oven at 105 \u00b0C.<\/p>\n
Sulfated ash (2.4.14)<\/strong><\/p>\n
Maximum 0.2 per cent, determined on 1.0 g.<\/p>\n
ASSAY<\/h2>\n
Dissolve 0.300 g in 30 mL of a mixture of 1 volume of acetic anhydride R and 5 volumes of anhydrous acetic acid R. Titrate with 0.1 M perchloric acid, determining the end-point potentiometrically (2.2.20).<\/p>\n
1 mL of 0.1 M perchloric acid is equivalent to 35.45 mg of C_{21<\/sub>H_{26<\/sub>N_{2<\/sub>O_{3<\/sub>.<\/p>\n}}}}
IMPURITIES<\/h2>\n
Specified impurities\u00a0 A, C.<\/p>\n
Other detectable impurities (the following substances would, if present at a sufficient level, be detected by one or other of the tests in the monograph. They are limited by the general acceptance criterion for other\/unspecified impurities and\/or by the general monograph Substances for pharmaceutical use (2034). It is therefore not necessary to identify these impurities for demonstration of compliance. See also 5.10. Control of impurities in substances for pharmaceutical use) B, D.<\/p>\n
$\"Vincamine\"$ <\/p>\n
A. methyl 14-hydroxy-10-methoxyvincane-14\u03b2-carboxylate (10-methoxyvincamine),<\/p>\n
$\"Vincamine\"$ <\/p>\n
B. methyl 14-hydroxyvincane-14\u03b1-carboxylate (14-epi-vincamine),<\/p>\n
$\"Vincamine\"$ <\/p>\n
C. methyl 14-hydroxy-17,18-didehydrovincane-14\u03b2-carboxylate (17,18-didehydrovincamine),<\/p>\n
$\"Vincamine\"$ <\/p>\n
D. methyl 14,15-didehydrovincane-14-carboxylate (apovincamine).<\/p>\n","protected":false},"excerpt":{"rendered":"
Edition: BP 2025 (Ph. Eur. 11.6 update) Action and use Vasodilator. DEFINITION Methyl 14-hydroxyvincane-14\u03b2-carboxylate. Content 99.0 per cent to 101.0 per cent (dried substance). CHARACTERS Appearance White or almost white, crystalline powder. Solubility Practically insoluble in water, soluble in methylene chloride, slightly soluble in anhydrous ethanol. IDENTIFICATION A. Specific optical rotation (see Tests). B. Infrared…<\/p>\n","protected":false},"author":5,"featured_media":31122,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[174],"tags":[],"class_list":["post-31121","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medicinal-substances"],"acf":[],"_links":{"self":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/31121","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/comments?post=31121"}],"version-history":[{"count":4,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/31121\/revisions"}],"predecessor-version":[{"id":31177,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/posts\/31121\/revisions\/31177"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media\/31122"}],"wp:attachment":[{"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/media?parent=31121"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/categories?post=31121"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/nhathuocngocanh.com\/bp\/wp-json\/wp\/v2\/tags?post=31121"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}

Appearance<\/h3>\nWhite or almost white, crystalline powder.<\/p>\n

Solubility<\/h3>\nPractically insoluble in water, soluble in methylene chloride, slightly soluble in anhydrous ethanol.<\/p>\n

IDENTIFICATION<\/h2>\nA. Specific optical rotation (see Tests).<\/p>\nB. Infrared absorption spectrophotometry (2.2.24).<\/p>\nComparison\u00a0 vincamine CRS.<\/p>\n

TESTS<\/h2>\nSpecific optical rotation (2.2.7)<\/strong><\/p>\n+ 44.3 to + 49.0 (dried substance).<\/p>\nDissolve 0.1 g in dimethylformamide R and dilute to 20.0 mL with the same solvent.<\/p>\n

Appearance<\/h3>\n
White or almost white, crystalline powder.<\/p>\n

Solubility<\/h3>\n
Practically insoluble in water, soluble in methylene chloride, slightly soluble in anhydrous ethanol.<\/p>\n

IDENTIFICATION<\/h2>\n
A. Specific optical rotation (see Tests).<\/p>\n
B. Infrared absorption spectrophotometry (2.2.24).<\/p>\n
Comparison\u00a0 vincamine CRS.<\/p>\n

TESTS<\/h2>\n
Specific optical rotation (2.2.7)<\/strong><\/p>\n
+ 44.3 to + 49.0 (dried substance).<\/p>\n
Dissolve 0.1 g in dimethylformamide R and dilute to 20.0 mL with the same solvent.<\/p>\n