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1.
J Chromatogr A ; 1554: 117-122, 2018 Jun 15.
Article in English | MEDLINE | ID: mdl-29699870

ABSTRACT

Chinoline alkaloids found in Cinchona bark still play an important role in medicine, for example as antimalarial and antiarrhythmic drugs. For the first time Supercritical Fluid Chromatography has been utilized for their separation. Six respective derivatives (dihydroquinidine, dihydroquinine, quinidine, quinine, cinchonine and cinchonidine) could be resolved in less than 7 min, and three of them quantified in crude plant extracts. The optimum stationary phase showed to be an Acquity UPC2 Torus DEA 1.7 µm column, the mobile phase comprised of CO2, acetonitrile, methanol and diethylamine. Method validation confirmed that the procedure is selective, accurate (recovery rates from 97.2% to 103.7%), precise (intra-day ≤2.2%, inter-day ≤3.0%) and linear (R2 ≥ 0.999); at 275 nm the observed detection limits were always below 2.5 µg/ml. In all of the samples analyzed cinchonine dominated (1.87%-2.30%), followed by quinine and cinchonidine. Their total content ranged from 4.75% to 5.20%. These values are in good agreement with published data, so that due to unmatched speed and environmental friendly character SFC is definitely an excellent alternative for the analysis of these important natural products.


Subject(s)
Alkaloids/analysis , Cinchona/chemistry , Alkaloids/chemistry , Chromatography, Supercritical Fluid , Cinchona/metabolism , Cinchona Alkaloids/analysis , Limit of Detection , Plant Bark/chemistry , Plant Bark/metabolism , Plant Extracts/chemistry , Quinidine/analogs & derivatives , Quinidine/analysis , Quinine/analysis
2.
Int J Mol Sci ; 12(11): 7846-60, 2011.
Article in English | MEDLINE | ID: mdl-22174637

ABSTRACT

Quinas contains several compounds, such as quinoline alkaloids, principally quinine, quinidine, cinchonine and cichonidine. Identified from barks of Cinchona, quinine is still commonly used to treat human malaria. Microwave-Integrated Extraction and Leaching (MIEL) is proposed for the extraction of quinoline alkaloids from bark of Cinchona succirubra. The process is performed in four steps, which ensures complete, rapid and accurate extraction of the samples. Optimal conditions for extraction were obtained using a response surface methodology reached from a central composite design. The MIEL extraction has been compared with a conventional technique soxhlet extraction. The extracts of quinoline alkaloids from C. succirubra obtained by these two different methods were compared by HPLC. The extracts obtained by MIEL in 32 min were quantitatively (yield) and qualitatively (quinine, quinidine, cinchonine, cinchonidine) similar to those obtained by conventional Soxhlet extraction in 3 hours. MIEL is a green technology that serves as a good alternative for the extraction of Cinchona alkaloids.


Subject(s)
Cinchona/chemistry , Plant Extracts/analysis , Quinolines/analysis , Antimalarials/analysis , Chromatography, High Pressure Liquid , Cinchona Alkaloids/analysis , Green Chemistry Technology , Microwaves , Plant Bark/chemistry , Quinidine/analysis , Quinine/analysis
3.
Indian J Med Res ; 113: 135-41, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11558322

ABSTRACT

BACKGROUND & OBJECTIVES: Though a number of barrier methods and potent spermicides are available, most of these have nonoxynol-9 (N-9) as the active ingredient which is observed to cause inflammation and genital ulceration on repeated use. The present study was undertaken to develop a safe spermicide with conjoint microbicidal properties. METHODS: A polyherbal pessary was formulated with purified ingredients from neem (Azadirachta indica) leaves, Sapindus mukerossi (pericarp of fruit) and Mentha citrata oil. Spermicidal action on human sperm was tested by Sander-Cramer slide test in vitro and by post coital tests in vivo. Contraceptive action was tested in rabbits. RESULTS: The combination of the three herbal ingredients resulted in the potentiation of the spermicidal action by 8-folds. The post coital tests confirmed the spermicidal properties of the Praneem polyherbal pessary (PPP) in women with high cervical mucous score around mid estrus. It also prevented in most women the migration of sperm into the cervical mucous. In 15 rabbits studied pregnancy was prevented by the intravaginal administration of PPP, whereas 13 of the 15 animals in the control group became pregnant. INTERPRETATION & CONCLUSION: The Praneem polyherbal pessary has potent spermicidal action on human sperm in vitro and in vivo. When applied in the vagina before mating, it prevented rabbits from becoming pregnant.


Subject(s)
Phytotherapy , Plant Extracts/analysis , Quinine/analysis , Spermatocidal Agents/analysis , Female , Humans , Male , Plant Extracts/pharmacology , Quinine/pharmacology , Spermatocidal Agents/pharmacology
6.
Pharmazie ; 39(8): 558-9, 1984 Aug.
Article in English | MEDLINE | ID: mdl-6504980

ABSTRACT

Diapulmon (Chinoin) which comprise camphor, 1-menthol, eucalyptus oil and quinine dissolved in sunflower oil (Oleum helianthi) is marketed in ampoules of 2 ml but utilized almost exclusively for inhalation therapy. Complexing the active ingredients of Diapulmon with beta-cyclodextrin (beta-CD) a stable non hygroscopic microcrystalline substance is obtained. When this powder sprinkled on hot water, the included volatile compounds are gradually released and the desired pharmacological effect can be brought about.


Subject(s)
Cyclodextrins , Dextrins , Starch , Camphor/analysis , Chromatography, Gas/methods , Drug Combinations/analysis , Drug Stability , Excipients , Menthol/analysis , Oils, Volatile/analysis , Quinine/analysis , Respiratory Therapy
8.
J Chromatogr ; 104(2): 417-24, 1975 Feb 12.
Article in English | MEDLINE | ID: mdl-1150768

ABSTRACT

Alkaloids are separated by liquid chromatography on resins having functional carboxyl groups combined with copper (II) ions. The eluent is aqueous alcohol containing ammonia. Some resins retain alkaloids much better than others. Alkaloids studied included morphine, codeine, strychnine, atropine, papaverine, narcotine, cocaine, quinine, cinchonine and methadone.


Subject(s)
Alkaloids/analysis , Chromatography, Ion Exchange/methods , Atropine/analysis , Cinchona/analogs & derivatives , Cinchona/analysis , Cinchona Alkaloids , Cocaine/analysis , Codeine/analysis , Copper , Hydrolysis , Ion Exchange Resins , Methadone/analysis , Methods , Morphine/analysis , Noscapine/analysis , Papaverine/analysis , Plants, Medicinal , Quinine/analysis , Strychnine/analysis
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