10 research outputs found
BREEDING MAIZE FOR RESISTANCE TO NORTHERN LEAF BLIGHT (Exserohilum turcicum Pass.)
Siva pjegavost lista kukuruza koju uzrokuje gljiva Exserohilum turcicum
(Pass.) najvažnija je lisna bolest kukuruza u humidnom podruÄju. Prvi
hibridi kukuruza u SAD-u bili su osjetljivi prema ovoj bolesti. Zbog toga je
zapoÄet program oplemenjivanja na otpornost koji se pokazao vrlo
uspjeÅ”nim. Rabljena je poligenetska i monogenetska otpornost. MeÄutim
nakon 15 godina Ŕiroke i neprekidne uporabe monogenetske otpornosti u
SAD-u dolazi do pojave novog patotipa Exserohilum turcicum, rase 2, koja
je kasnije nazvana rasa 1 buduÄi da protiv nje gen Ht 1 nije djelotvoran.
Nova rasa se brzo raŔirila u Americi, a kasnije i u Hrvatskoj. U svrhu
prouÄavanja otpornosti kukuruza prema rasi 1 Exserohilum turcicum posijan
je 2008. godine pokus sa 75 linija razliÄitog porijekla. Linije iz heterotiÄne
grupe BSSS su bile osjetljive prema rasi 1 Exserohilum turcicum s
prosjeÄnom ocjenom 3,0, dok su linije iz heterotiÄne grupe Lancaster otporne
s prosjeÄnom ocjenom 2,0. U drugom pokusu 2012. godine ispitana je
otpornost 25 linija kukuruza prema rasi 0 i rasi 1 s ciljem da se utvrdi koje su
linije otporne prema obje rase Exserohilum turcicum. Linije Pa875, Bc210K,
H102, Bc1411, Pa887P, H111 i H95 otporne su p rema obje rasi 0 i r asi 1
Exserohilum turcicum. Monogenetska otpornost prema rasi 1 unesena je u 4
linije kukuruza (A632, Bc31002, Bc703-19 i Bc14).Northern leaf blight, caused by the fungus Exserohilum turcicum (Pass.) is the
most important leaf disease of maize in humid environments. The first maize hybrids in
the United States were susceptible to this disease. Therefore, breeding program for
resistance was initiated and proved to be very successful. Polygenic and monogenic
resistance were used. However, after 15 years of continuous and extensive use of
monogenic resistance in the United States occurrence of a new pathotype of E.turcicum. race 2 was reported, which was later named race 1, because Ht 1 gene was not
effective against it. New race quickly spread throughout the United States, and later in
Croatia. To study maize resistance to race 1 of E. turcicum a trial was planted with 75
lines of different origin in 2008. The lines from the BSSS heterotic group were
susceptible to race 1 of Exserohilum turcicum with average rating 3,0, while the lines
from the Lancaster heterotic group were resistant with average rating 2,0. In the second
experiment in 2012., 25 maize lines were tsted for resistance to race 0 and race 1 to
detect lines resistant to both races of Exserohilum turcicum. Lines Pa875, Bc210K,
H102, Bc1411, Pa887P, H111 and H95 appear to be resistant to both race 0 and race 1
of Exserohilum turcicum. Monogenic otpornost resistance to race 1 was incorporated
into four maize lines (A632, Bc31002, Bc703-19 i Bc14)
BREEDING MAIZE FOR RESISTANCE TO NORTHERN LEAF BLIGHT (Exserohilum turcicum Pass.)
Siva pjegavost lista kukuruza koju uzrokuje gljiva Exserohilum turcicum
(Pass.) najvažnija je lisna bolest kukuruza u humidnom podruÄju. Prvi
hibridi kukuruza u SAD-u bili su osjetljivi prema ovoj bolesti. Zbog toga je
zapoÄet program oplemenjivanja na otpornost koji se pokazao vrlo
uspjeÅ”nim. Rabljena je poligenetska i monogenetska otpornost. MeÄutim
nakon 15 godina Ŕiroke i neprekidne uporabe monogenetske otpornosti u
SAD-u dolazi do pojave novog patotipa Exserohilum turcicum, rase 2, koja
je kasnije nazvana rasa 1 buduÄi da protiv nje gen Ht 1 nije djelotvoran.
Nova rasa se brzo raŔirila u Americi, a kasnije i u Hrvatskoj. U svrhu
prouÄavanja otpornosti kukuruza prema rasi 1 Exserohilum turcicum posijan
je 2008. godine pokus sa 75 linija razliÄitog porijekla. Linije iz heterotiÄne
grupe BSSS su bile osjetljive prema rasi 1 Exserohilum turcicum s
prosjeÄnom ocjenom 3,0, dok su linije iz heterotiÄne grupe Lancaster otporne
s prosjeÄnom ocjenom 2,0. U drugom pokusu 2012. godine ispitana je
otpornost 25 linija kukuruza prema rasi 0 i rasi 1 s ciljem da se utvrdi koje su
linije otporne prema obje rase Exserohilum turcicum. Linije Pa875, Bc210K,
H102, Bc1411, Pa887P, H111 i H95 otporne su p rema obje rasi 0 i r asi 1
Exserohilum turcicum. Monogenetska otpornost prema rasi 1 unesena je u 4
linije kukuruza (A632, Bc31002, Bc703-19 i Bc14).Northern leaf blight, caused by the fungus Exserohilum turcicum (Pass.) is the
most important leaf disease of maize in humid environments. The first maize hybrids in
the United States were susceptible to this disease. Therefore, breeding program for
resistance was initiated and proved to be very successful. Polygenic and monogenic
resistance were used. However, after 15 years of continuous and extensive use of
monogenic resistance in the United States occurrence of a new pathotype of E.turcicum. race 2 was reported, which was later named race 1, because Ht 1 gene was not
effective against it. New race quickly spread throughout the United States, and later in
Croatia. To study maize resistance to race 1 of E. turcicum a trial was planted with 75
lines of different origin in 2008. The lines from the BSSS heterotic group were
susceptible to race 1 of Exserohilum turcicum with average rating 3,0, while the lines
from the Lancaster heterotic group were resistant with average rating 2,0. In the second
experiment in 2012., 25 maize lines were tsted for resistance to race 0 and race 1 to
detect lines resistant to both races of Exserohilum turcicum. Lines Pa875, Bc210K,
H102, Bc1411, Pa887P, H111 and H95 appear to be resistant to both race 0 and race 1
of Exserohilum turcicum. Monogenic otpornost resistance to race 1 was incorporated
into four maize lines (A632, Bc31002, Bc703-19 i Bc14)
RužiÄka days : International conference 16th RužiÄka Days āToday Science ā Tomorrow Industryā : Proceedings
Proceedings contains articles presented at Conference divided into sections: open lecture (1), chemical analysis and synthesis (3), chemical and biochemical engineering (8), food technology and biotechnology (8), medical chemistry and pharmacy (3), environmental protection (11) and meeting of young chemists (2)
Preparation and characterization of mini-tablets
Lurasidon-hidroklorid je djelatna tvar izrazito male topljivosti u vodenom mediju Å”to otežava njegovu primjenu u lijeÄenju psihiÄkih poremeÄaja. S ciljem poveÄanja njegove topljivosti pripravljene su Ävrste disperzije djelatne tvari u matrici hidrofilnog polimera, poli(etilen-glikola) (PEG) procesom liofilizacije. Dobivene Ävrste disperzije karakterizirane su diferencijalnom pretražnom kalorimetrijom, rendgenskom difrakcijskom analizom praha i infracrvenom spektroskopijom. Testirana je prividna topljivost djelatne tvari u Ävrstim disperzijama. U pripravi minitableta promjera 3 mm koriÅ”teni su liofilizati i granulirane mjeÅ”avine s ugraÄenom djelatnom tvari. KoriÅ”teni su manitol, natrijeva kroskarmeloza te mikrokristalna celuloza kao pomoÄne tvari. Karakterizacija minitableta ukljuÄivala je ispitivanje ujednaÄenosti masa te testiranje njihove raspadljivosti. Vrijeme raspadljivosti za sve tablete manje je od 3 minute. Profili oslobaÄanja ukazuju na poboljÅ”anu topljivost i brže oslobaÄanje djelatne tvari iz minitableta pripravljenih iz Ävrstih disperzija u odnosu na one koje sadrže Äisti netretirani lurasidon-hidroklorid (LRS HCl) i one s granuliranom mjeÅ”avinom djelatne tvari i polimera. Dodatno, minitablete pokazuju brže oslobaÄanje djelatne tvari u odnosu na raspadljiv oralni dozirni oblik promjera 8 mm. Testirana je primjenjivost modela u opisu profila oslobaÄanja lurasidon-hidroklorida.Lurasidone hydrochloride is a drug of extremely low solubility in an aqueous medium, which makes it difficult to use in the treatment od mental disorders. In order to increase its solubility, solid dispersions of a drug in a hydrophilic polymer matrix, poly(ethylene glycol) (PEG) were prepared by the lyophilization process. Obtained solid dispersions were characterized by differential scanning calorimetry, X-ray powder difraction analysis and infrared spectroscopy. The apparent solubility of drug was tested in solid dispersions. Lyophilisates and granulated mixtures with incoporated active substance were used in the preparation of mini-tablets with 3 mm in diameter. Mannitol, sodium croscarmellose and microcrystalline cellulose were used as excipients. Characterization of mini-tablets involved testing the mass uniforimity and its disintegration. Disintegration time for all tablets was less than 3 minutes. Release profiles indicate improved solubility and faster drug release from mini-tablets prepared from solid dispersions in comparison to those containing pure untreated lurasidone hydrochloride (LRS HCl) and those with granulated mixture of drug and polymer. Additionally, mini-tablets show faster drug release in comparision to the disintegrated oral dosage form with 8 mm in diameter. The applicability of models was tested to describe release profiles for lurasidone hydrochloride
Fluidized bed drying - Influence of process parameters on drying kinetics and crystal morphology
U ovom je radu istražena kinetika suÅ”enja natrijeve soli cirkonija u razliÄitim laboratorijskim suÅ”ionicima. Odabrana su dva vakuum suÅ”ionika, jedan s pliticama i jedan rotacijski te suÅ”ionik s fluidiziranim slojem. Osim vrste suÅ”ionika, istražen je i utjecaj poÄetnog sadržaja vlage materijala kao i temperature na kinetiku suÅ”enja i morfoloÅ”ka svojstva osuÅ”enih kristala. Kinetika suÅ”enja praÄena je gravimetrijski u vakuum suÅ”ionicima te psihrometrijski u suÅ”ioniku s fluidiziranim slojem. U suÅ”ioniku s fluidiziranim slojem takoÄer je istraženo može li se bliskom infracrvenom spektroskopijom (NIR, engl. Near InfraRed) pratiti kinetika suÅ”enja. Mjerni podaci aproksimirani su Lewisovim i Pageovim matematiÄkim modelom te je za svaku vrstu suÅ”ionika odabran model koji uz najviÅ”i stupanj korelacije opisuje kinetiku suÅ”enja. Parametri oba modela dovedeni su u vezu s uvjetima provedbe procesa suÅ”enja. Rezultati su pokazali da vrsta suÅ”ionika i temperatura utjeÄu na kinetiku suÅ”enja i morfologiju kristala. VeÄe brzine suÅ”enja ostvarene su pri viÅ”im temperaturama. Pri nižim temperaturama suÅ”enje je brže u suÅ”ioniku s fluidiziranim slojem, a pri viÅ”im temperaturama u vakuum suÅ”ionicima. U rotacijskom vakuum suÅ”ioniku i u suÅ”ioniku s fluidiziranim slojem dolazi do loma kristala. Bliska infracrvena spektroskopija pokazala se kao dobra metoda praÄenja kinetike suÅ”enja u fluidiziranom sloju.This paper explores drying kinetics of zirconium sodium salt in different laboratory dryers. Drying was performed in two vacuum dryers, a tray dryer, a rotary dryer and a fluid bed dryer. Additionally, the effect of starting humidity levels and temperature on drying kinetics and morphological properties of dried crystals was explored. Drying kinetics was monitored gravimetrically in vacuum dryers and psychrometrically in fluid bed dryer. The possibility of monitoring drying kinetics with Near InfraRed spectroscopy in fluid bed dryer was also explored. Measurements were approximated with Lewis and Page mathematical models and the model with the highest correlation coefficient that was selected for each dryer. The parameters of both models were correlated with drying conditions. The results show that the type of dryer and the temperature affect drying kinetics and morphology of the crystals. At lower temperatures, drying was faster in fluid bed dryer whereas when the temperatures were higher, drying was faster in vacuum dryers. In rotational vacuum dryer and fluid bed dryer the crystals broke. Near InfraRed spectroscopy proved to be a good method for monitoring drying kinetics in a fluidized bed
Fluidized bed drying - Influence of process parameters on drying kinetics and crystal morphology
U ovom je radu istražena kinetika suÅ”enja natrijeve soli cirkonija u razliÄitim laboratorijskim suÅ”ionicima. Odabrana su dva vakuum suÅ”ionika, jedan s pliticama i jedan rotacijski te suÅ”ionik s fluidiziranim slojem. Osim vrste suÅ”ionika, istražen je i utjecaj poÄetnog sadržaja vlage materijala kao i temperature na kinetiku suÅ”enja i morfoloÅ”ka svojstva osuÅ”enih kristala. Kinetika suÅ”enja praÄena je gravimetrijski u vakuum suÅ”ionicima te psihrometrijski u suÅ”ioniku s fluidiziranim slojem. U suÅ”ioniku s fluidiziranim slojem takoÄer je istraženo može li se bliskom infracrvenom spektroskopijom (NIR, engl. Near InfraRed) pratiti kinetika suÅ”enja. Mjerni podaci aproksimirani su Lewisovim i Pageovim matematiÄkim modelom te je za svaku vrstu suÅ”ionika odabran model koji uz najviÅ”i stupanj korelacije opisuje kinetiku suÅ”enja. Parametri oba modela dovedeni su u vezu s uvjetima provedbe procesa suÅ”enja. Rezultati su pokazali da vrsta suÅ”ionika i temperatura utjeÄu na kinetiku suÅ”enja i morfologiju kristala. VeÄe brzine suÅ”enja ostvarene su pri viÅ”im temperaturama. Pri nižim temperaturama suÅ”enje je brže u suÅ”ioniku s fluidiziranim slojem, a pri viÅ”im temperaturama u vakuum suÅ”ionicima. U rotacijskom vakuum suÅ”ioniku i u suÅ”ioniku s fluidiziranim slojem dolazi do loma kristala. Bliska infracrvena spektroskopija pokazala se kao dobra metoda praÄenja kinetike suÅ”enja u fluidiziranom sloju.This paper explores drying kinetics of zirconium sodium salt in different laboratory dryers. Drying was performed in two vacuum dryers, a tray dryer, a rotary dryer and a fluid bed dryer. Additionally, the effect of starting humidity levels and temperature on drying kinetics and morphological properties of dried crystals was explored. Drying kinetics was monitored gravimetrically in vacuum dryers and psychrometrically in fluid bed dryer. The possibility of monitoring drying kinetics with Near InfraRed spectroscopy in fluid bed dryer was also explored. Measurements were approximated with Lewis and Page mathematical models and the model with the highest correlation coefficient that was selected for each dryer. The parameters of both models were correlated with drying conditions. The results show that the type of dryer and the temperature affect drying kinetics and morphology of the crystals. At lower temperatures, drying was faster in fluid bed dryer whereas when the temperatures were higher, drying was faster in vacuum dryers. In rotational vacuum dryer and fluid bed dryer the crystals broke. Near InfraRed spectroscopy proved to be a good method for monitoring drying kinetics in a fluidized bed
Fluidized bed drying - Influence of process parameters on drying kinetics and crystal morphology
U ovom je radu istražena kinetika suÅ”enja natrijeve soli cirkonija u razliÄitim laboratorijskim suÅ”ionicima. Odabrana su dva vakuum suÅ”ionika, jedan s pliticama i jedan rotacijski te suÅ”ionik s fluidiziranim slojem. Osim vrste suÅ”ionika, istražen je i utjecaj poÄetnog sadržaja vlage materijala kao i temperature na kinetiku suÅ”enja i morfoloÅ”ka svojstva osuÅ”enih kristala. Kinetika suÅ”enja praÄena je gravimetrijski u vakuum suÅ”ionicima te psihrometrijski u suÅ”ioniku s fluidiziranim slojem. U suÅ”ioniku s fluidiziranim slojem takoÄer je istraženo može li se bliskom infracrvenom spektroskopijom (NIR, engl. Near InfraRed) pratiti kinetika suÅ”enja. Mjerni podaci aproksimirani su Lewisovim i Pageovim matematiÄkim modelom te je za svaku vrstu suÅ”ionika odabran model koji uz najviÅ”i stupanj korelacije opisuje kinetiku suÅ”enja. Parametri oba modela dovedeni su u vezu s uvjetima provedbe procesa suÅ”enja. Rezultati su pokazali da vrsta suÅ”ionika i temperatura utjeÄu na kinetiku suÅ”enja i morfologiju kristala. VeÄe brzine suÅ”enja ostvarene su pri viÅ”im temperaturama. Pri nižim temperaturama suÅ”enje je brže u suÅ”ioniku s fluidiziranim slojem, a pri viÅ”im temperaturama u vakuum suÅ”ionicima. U rotacijskom vakuum suÅ”ioniku i u suÅ”ioniku s fluidiziranim slojem dolazi do loma kristala. Bliska infracrvena spektroskopija pokazala se kao dobra metoda praÄenja kinetike suÅ”enja u fluidiziranom sloju.This paper explores drying kinetics of zirconium sodium salt in different laboratory dryers. Drying was performed in two vacuum dryers, a tray dryer, a rotary dryer and a fluid bed dryer. Additionally, the effect of starting humidity levels and temperature on drying kinetics and morphological properties of dried crystals was explored. Drying kinetics was monitored gravimetrically in vacuum dryers and psychrometrically in fluid bed dryer. The possibility of monitoring drying kinetics with Near InfraRed spectroscopy in fluid bed dryer was also explored. Measurements were approximated with Lewis and Page mathematical models and the model with the highest correlation coefficient that was selected for each dryer. The parameters of both models were correlated with drying conditions. The results show that the type of dryer and the temperature affect drying kinetics and morphology of the crystals. At lower temperatures, drying was faster in fluid bed dryer whereas when the temperatures were higher, drying was faster in vacuum dryers. In rotational vacuum dryer and fluid bed dryer the crystals broke. Near InfraRed spectroscopy proved to be a good method for monitoring drying kinetics in a fluidized bed
Preparation and characterization of mini-tablets
Lurasidon-hidroklorid je djelatna tvar izrazito male topljivosti u vodenom mediju Å”to otežava njegovu primjenu u lijeÄenju psihiÄkih poremeÄaja. S ciljem poveÄanja njegove topljivosti pripravljene su Ävrste disperzije djelatne tvari u matrici hidrofilnog polimera, poli(etilen-glikola) (PEG) procesom liofilizacije. Dobivene Ävrste disperzije karakterizirane su diferencijalnom pretražnom kalorimetrijom, rendgenskom difrakcijskom analizom praha i infracrvenom spektroskopijom. Testirana je prividna topljivost djelatne tvari u Ävrstim disperzijama. U pripravi minitableta promjera 3 mm koriÅ”teni su liofilizati i granulirane mjeÅ”avine s ugraÄenom djelatnom tvari. KoriÅ”teni su manitol, natrijeva kroskarmeloza te mikrokristalna celuloza kao pomoÄne tvari. Karakterizacija minitableta ukljuÄivala je ispitivanje ujednaÄenosti masa te testiranje njihove raspadljivosti. Vrijeme raspadljivosti za sve tablete manje je od 3 minute. Profili oslobaÄanja ukazuju na poboljÅ”anu topljivost i brže oslobaÄanje djelatne tvari iz minitableta pripravljenih iz Ävrstih disperzija u odnosu na one koje sadrže Äisti netretirani lurasidon-hidroklorid (LRS HCl) i one s granuliranom mjeÅ”avinom djelatne tvari i polimera. Dodatno, minitablete pokazuju brže oslobaÄanje djelatne tvari u odnosu na raspadljiv oralni dozirni oblik promjera 8 mm. Testirana je primjenjivost modela u opisu profila oslobaÄanja lurasidon-hidroklorida.Lurasidone hydrochloride is a drug of extremely low solubility in an aqueous medium, which makes it difficult to use in the treatment od mental disorders. In order to increase its solubility, solid dispersions of a drug in a hydrophilic polymer matrix, poly(ethylene glycol) (PEG) were prepared by the lyophilization process. Obtained solid dispersions were characterized by differential scanning calorimetry, X-ray powder difraction analysis and infrared spectroscopy. The apparent solubility of drug was tested in solid dispersions. Lyophilisates and granulated mixtures with incoporated active substance were used in the preparation of mini-tablets with 3 mm in diameter. Mannitol, sodium croscarmellose and microcrystalline cellulose were used as excipients. Characterization of mini-tablets involved testing the mass uniforimity and its disintegration. Disintegration time for all tablets was less than 3 minutes. Release profiles indicate improved solubility and faster drug release from mini-tablets prepared from solid dispersions in comparison to those containing pure untreated lurasidone hydrochloride (LRS HCl) and those with granulated mixture of drug and polymer. Additionally, mini-tablets show faster drug release in comparision to the disintegrated oral dosage form with 8 mm in diameter. The applicability of models was tested to describe release profiles for lurasidone hydrochloride
Preparation and characterization of mini-tablets
Lurasidon-hidroklorid je djelatna tvar izrazito male topljivosti u vodenom mediju Å”to otežava njegovu primjenu u lijeÄenju psihiÄkih poremeÄaja. S ciljem poveÄanja njegove topljivosti pripravljene su Ävrste disperzije djelatne tvari u matrici hidrofilnog polimera, poli(etilen-glikola) (PEG) procesom liofilizacije. Dobivene Ävrste disperzije karakterizirane su diferencijalnom pretražnom kalorimetrijom, rendgenskom difrakcijskom analizom praha i infracrvenom spektroskopijom. Testirana je prividna topljivost djelatne tvari u Ävrstim disperzijama. U pripravi minitableta promjera 3 mm koriÅ”teni su liofilizati i granulirane mjeÅ”avine s ugraÄenom djelatnom tvari. KoriÅ”teni su manitol, natrijeva kroskarmeloza te mikrokristalna celuloza kao pomoÄne tvari. Karakterizacija minitableta ukljuÄivala je ispitivanje ujednaÄenosti masa te testiranje njihove raspadljivosti. Vrijeme raspadljivosti za sve tablete manje je od 3 minute. Profili oslobaÄanja ukazuju na poboljÅ”anu topljivost i brže oslobaÄanje djelatne tvari iz minitableta pripravljenih iz Ävrstih disperzija u odnosu na one koje sadrže Äisti netretirani lurasidon-hidroklorid (LRS HCl) i one s granuliranom mjeÅ”avinom djelatne tvari i polimera. Dodatno, minitablete pokazuju brže oslobaÄanje djelatne tvari u odnosu na raspadljiv oralni dozirni oblik promjera 8 mm. Testirana je primjenjivost modela u opisu profila oslobaÄanja lurasidon-hidroklorida.Lurasidone hydrochloride is a drug of extremely low solubility in an aqueous medium, which makes it difficult to use in the treatment od mental disorders. In order to increase its solubility, solid dispersions of a drug in a hydrophilic polymer matrix, poly(ethylene glycol) (PEG) were prepared by the lyophilization process. Obtained solid dispersions were characterized by differential scanning calorimetry, X-ray powder difraction analysis and infrared spectroscopy. The apparent solubility of drug was tested in solid dispersions. Lyophilisates and granulated mixtures with incoporated active substance were used in the preparation of mini-tablets with 3 mm in diameter. Mannitol, sodium croscarmellose and microcrystalline cellulose were used as excipients. Characterization of mini-tablets involved testing the mass uniforimity and its disintegration. Disintegration time for all tablets was less than 3 minutes. Release profiles indicate improved solubility and faster drug release from mini-tablets prepared from solid dispersions in comparison to those containing pure untreated lurasidone hydrochloride (LRS HCl) and those with granulated mixture of drug and polymer. Additionally, mini-tablets show faster drug release in comparision to the disintegrated oral dosage form with 8 mm in diameter. The applicability of models was tested to describe release profiles for lurasidone hydrochloride
RužiÄka days : International conference 18th RužiÄka Days āToday Science ā Tomorrow Industryā : Proceedings
Proceedings contains articles presented at Conference divided into sections: chemical analysis and synthesis, chemical and biochemical engineering, food technology and biotechnology, medical chemistry and pharmacy, environmental protection and meeting of young chemists