Анализ на фенотиазинови производни

1. Анализ на фенотиазинови производни

2. С диметиламинопропилова верига при N10 • С пиперазинов хетероцикъл при N10 • С пиперидинов хетероцикъл при N10 Thioridazine Chlorpromazine Trifluoperazine

3. Antipsychotic — Chlorpromazine; Fluphenazine; Mesoridazine; Methotrimeprazine; Perphenazine; Pipotiazine; Prochlorperazine; Promazine; Thioproperazine; Thioridazine; Trifluoperazine; Triflupromazine; • Antipsychotic adjunct — Pericyazine; • Anesthetic adjunct — Chlorpromazine; Methotrimeprazine, intravenous; • Antidyskinetic, Huntington's chorea — Chlorpromazine; Thioridazine; • Antiemetic — Chlorpromazine; Methotrimeprazine; Perphenazine; Prochlorperazine; Trifluoperazine; Triflupromazine; • Antineuralgia adjunct — Fluphenazine; • Sedative — Chlorpromazine; Methotrimeprazine; Thioridazine; • Analgesic — Methotrimeprazine;

4. СВОЙСТВА:Фенотиазините са разтворими в липиди, бързо се разпределят в биомембраните. Съдържат един или два базични N атома, които дават възможност за образуване на водноразтворими соли. Представляват бели кристални вещества. Базите са оцветени от светло до тъмнокафяво и са гъсти масла, неразтворими във вода. рКа стойностите им са между 8.0 и 9.5. Всички фенотиазинови производни, използвани в терапията са много чувствителни на светлина (УВ), нагряване и окисление. Фенотиазинови производни

5. Мезомерни резонансни структури Висока електронна плътност при S атом, което обуславя лесно окисление Липса на базичност при N атом (малка ел. плътност)

6. Фенотиазинови производни Спрежение с p-системата от ароматното ядро 145 0 Тетрагонална сгъната конфигурация, доказана с квантово-химични изследвания

7. Стабилност при влияние на светлина (УВ) и окисление Елиминиране на електрон Мезомерно стабилизиран цветен радикал – 2а, 2b и 2c

8. феназатиониев йон Реакцията е обратима. Радикалите (непропорцинално) образуват феназатиониев йон, който във водна среда реагира като електрофилен реагент и образува моносулфоксид. Непропорционалността на радикалите се потиска в кисела среда – стабилизиране. моносулфоксид

9. В силно кисела среда радикалите образуват Chlorpromazinе и 3-хидрокси производно, от което при окисление се формира цветен продукт.

10. Chlorpromazine Hydrochloride 3-(2-chloro-10H-phenothiazin-10-yl)-N,N-dimethyl-propan-1-aminehydrochloride

12. IDENTIFICATION OF PHENOTHIAZINES (Ph. Eur. method 2.3.3) Carry out the method for thin-layer chromatography protected from light using kieselguhr G as the coating substance. Impregnate the dry plate by placing it in a tank containing a shallow layer of a solution containing 10% v/v of 2-phenoxyethanol and 5.0% w/v of polyethylene glycol 300 in acetone so that the plate dips about 5 mm beneath the surface of the liquid and allowing the impregnating solvent to ascend at least 17 cm above the line of application. Remove the plate from the tank and use it immediately. Carry out the chromatography in the same direction as the impregnation. For the mobile phase shake a mixture of 100 volumes of petroleum spirit (boiling range, 50° to 70°) and 2 volumes of diethylamine with 6 to 8 volumes of 2-phenoxyethanol until a persistent cloudiness is obtained, decant and use the supernatant layer even if cloudy. Apply separately to the plate 2 µl of each of two solutions in chloroform containing (1) 0.2% w/v of the substance being examined and (2) 0.2% w/v of the corresponding European Pharmacopoeia Chemical Reference Substance. After removal of the plate, examine under ultraviolet light (365 nm) and observe the fluorescence produced after a few minutes. The spot in the chromatogram obtained with solution (1) is similar in position, colour, fluorescence and size to that in the chromatogram obtained with solution (2). Spray the plate with ethanolic sulphuric acid ( 10%) and observe the colour produced. The colour of the spot in the chromatogram obtained with solution (1) is the same as that in the chromatogram obtained with solution (2) and has a similar stability over a period of at least 20 minutes after spraying.

13. Chlorpromazine Hydrochloride

14. Abstract: An automated on-line method for simultaneous analysis of five phenothiazine drugs by high-performance liquid chromatography (HPLC)/sonic spray ionization mass spectrometry (SSI-MS) has been established, using backflush column switching. A 400-μl portion of serum sample diluted 81-fold with distilled water was subjected to the on-line system. In the system, an Oasis HLB cartridge was used as the precolumn for extraction; large molecules such as proteins in serum were discarded by use of distilled water containing 0.1% formic acid as a mobile phase. After switching a valve, the analytes trapped in the precolumn were eluted in the backflush mode and separated by a Chromolith Performance RP-18e column, which is composed of C18-bonded monolithic silica. The column effluents were then introduced into the SSI-MS. The present method provided successful separation and determination of six phenothiazines including an internal standard. Satisfactory linearities, reproducibility, and sensitivity were obtained at concentration levels that matched the toxic levels of phenothiazines. All drug peaks appeared within 18 min, and the system could be reequilibrated in only about 8 min for the next run. Because of the simplicity and rapidness of the method, it is likely to be useful in the fields of emergency medicine and forensic toxicology.

15. Metabolites of Chlorpromazine

17. Chromatogram of the separation of chlorpromazine and five metabolite standards

20. (Methotrimeprazine) (R)-10-[ 3-(dimethylamino)-2-methylpropyl]-2-methoxyphenothiazine

21. levomepromazine Acidity or alkalinity To 10 ml of solution S add 0.1 ml of bromocresol green solution R. Not more than 0.5 ml of 0.01M sodium hydroxide or 1.0 ml of 0.01M hydrochloric acid is required to change the colour of the indicator. Specific optical rotation (2.2.7). +9.5° to +11.5°, determined on solution S and calculated with reference to the dried substance. Related substances Carry out the test protected from bright light. Examine by thin-layer chromatography (2.2.27), using silica gel GF254 R as the coating substance. Loss on drying (2.2.32). Not more than 1.0 per cent, determined on 1.000 g by drying in an oven at 100°C to 105°C for 3 h. Sulphated ash (2.4.14). Not more than 0.1 per cent, determined on 1.0 g. Ph Eur

22. (RS)-10-[2-(1- methyl-2-piperidyl)ethyl]-2-(methylthio)phenothiazine 10-[3-(4- methyl-1-piperazinyl)propyl]-2-trifluoromethylphenothiazine

23. Тиоксантени Chlorprothixene (Z)-3-(2-Chloro-9H thioxanthen-9-ylidene)- N,N-dimethylpropan-1- amine hydrochloride.

24. Тиоксантени Стабилни в киселинна и алкална среда, както и при нагряване Промени под действие на UV-светлина:

25. IMPURITIES (E)-3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethylpropan-1-amine (E-isomer).

26. Flupentixol DEFINITION 2-[4-[3-[(EZ)-2-(trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl]piperazin -1-yl]ethanol dihydrochloride. Content - flupentixol dihydrochloride: 98.0 per cent to 101.5 per cent (dried substance), - Z-isomer: 42.0 per cent to 52.0 per cent. 2-(trifluoromethyl)-9H-thioxanthen-9-one.

27. The structure of flupentixol  is based on the thioxanthene ring to which the side chain is linked by a C=C double bond. Because of the double bond linking of the side chain to the thioxanthene ring structure, flupentixol exists as two geometric isomers, namely cis (Z) and trans (E) isomers. It is interesting to note that, in pharmacological studies, the neuroleptic activity is associated with the cis (Z) isomer, while the trans (E) isomer is practically inactive. The oral form of flupentixol, administered as tablets or drops, is an equimolar mixture of the active cis (Z) and the inactive trans (E) isomers, while the parenteral preparation for intramuscular injection is the decanoic acid ester of the isolated cis (Z) isomer.

29. Fluoroorganic compounds D. Mix about 5 mg with 45 mg of heavy magnesium oxide R and ignite in a crucible until an almost white residue is obtained ( usually less than 5 min). Allow to cool, add 1 ml of water R, 0.05 ml of phenolphthalein solution R1 and about 1 ml of dilute hydrochloric acid R to render the solution colourless. Filter. Add 1.0 ml of the filtrate to a freshly prepared mixture of 0.1 ml of alizarin S solution R and 0.1 ml of zirconyl nitrate solution R. Mix, allow to stand for 5 min and compare the colour of the solution with that of a blank prepared in the same manner. The test solution is yellow and the blank is red. Alizarine Ph Eur

30. Latest bibliographic data on file with the International Bureau

31. As a basis for quantitative determination of fluorinate species, flourine-19 nuclear magnetic resonance (19F NMR) offers several potential advantages compared to chromatography. 19F NMR spectroscopy has a large spectral window associated with it. Typically organofluorine nuclei lie within a window of 300 ppm, resulting in a small probability of peak overlap between molecules. Moreover, the spin 1/2 19F isotope is 100% abundant and possesses a sensitivity which is 81% of a 1H nucleus. The technique can be used for spectral identification of an analyte and for quantification, when an internal standard of known concentration is included

32. 19F NMR spectra of cis(Z)- (A), trans(E)-flupentixol (B), and their mixture (C) in acetonitrile/methanol (2:1 v/v) solvent