Problem of grafting of antituberculosis drugs to the high molecular copolymers based on N-vinylpyrrolidone
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2022-12-07 13:08
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IVANCIC, Albert, GHERCIU, Irina, ROBU, Stephan V.. Problem of grafting of antituberculosis drugs to the high molecular copolymers based on N-vinylpyrrolidone. In: Physical Methods in Coordination and Supramolecular Chemistry, 8-9 octombrie 2015, Chişinău. Chisinau, Republic of Moldova: 2015, XVIII, p. 81.
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Physical Methods in Coordination and Supramolecular Chemistry
XVIII, 2015
Conferința ""Physical Methods in Coordination and Supramolecular Chemistry""
Chişinău, Moldova, 8-9 octombrie 2015

Problem of grafting of antituberculosis drugs to the high molecular copolymers based on N-vinylpyrrolidone


Pag. 81-81

Ivancic Albert, Gherciu Irina, Robu Stephan V.
 
Moldova State University
 
Disponibil în IBN: 21 aprilie 2020


Rezumat

Nowadays the problem of pharmaceutical preparations with prolonged effect, which would release in the human body a sufficient amount of bioactive compound over an extended period of time, is the current one. In this work we set purpose to graft antituberculosis (anti-TB) drugs such as norfloxacin and others to N-vinylpyrrolidone with methacrylic acid copolymer. [1,2] Medicinal copolymer was synthesised based on N-vinylpyrrolidone with methacrylic acid copolymer (50:50 mol%) obtained after block copolymerization with characteristic viscosity ≈ 0,15Dl/g. Norfloxacin and its analogs grafting was performed according to the scheme:shemeObtained copolymers were purified by recrystallization from hexane, then diethyl ether. Chemical structures of copolymers were determined by IR spectroscopy: the occurrence of new absorption bands at wave numbers: 3200 cm-1 (group -NH-CO-), 1720 cm-1 ( = C=O from norfloxacin) and 750 cm-1 (≡C-F) demonstrates norfloxacin grafting. Preventive tests for antimicrobial activity of obtained copolymer, showed an activity comparable to that of norfloxacin. Studies of the prolongation effect of medicinal copolymer, by dialysis method, showed that the drug traverses the semipermiable membrane for 4-5 h, compared to 0,5-1 h for the control experiment (only norfloxacin). In conclusion we can mention that a macromolecular medicinal compound with noticiable antibiotic and potential anti-TB properties was obtained.